SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs142481668 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080334 | GGCGAAACCCCACCT[C/T]TACAAAAAAAAAAAA | 26133 |
rs142515968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009856 | GCCACCAGGCAAGAA[A/G]GGAGCACATAAGCAA | 26133 |
rs142630362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060469 | GGTAGCATGCTCCTG[C/T]AGTCCCAGCTACTCA | 26133 |
rs142654947 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055234 | TTGCATATTGCTTTT[C/G]GTTTGATACAGCAGC | 26133 |
rs142659559 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062968 | TGATATGAAATATCC[C/G]TAACAGGTGATATGG | 26133 |
rs142674040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024892 | GTGACAGTCATTTGC[A/G]TTGTTTCCATATTTT | 26133 |
rs142680966 | in-del | -/GAGAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049485 | ACCAGTTCAGATAGC[-/GAGAA]GGTAAAGTGGTAAGA | 26133 |
rs142695706 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059422 | CCCAAGACTCTGGGC[A/G]GCTGAGGTGGGAGGA | 26133 |
rs142729534 | snp | C/T | 0.0019224 | 0.0309436 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002231 | GAATGTCTGCTGTTG[C/T]ACATCTGGCTGAGGC | 26133 |
rs142733643 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087435 | CATAAAGGAAGCAAC[A/G/T]ACTGCCATGTGGGAA | 26133 |
rs142751315 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021118 | CAGAAGGCCCAGTGG[A/G]GCACCTGGCATACCA | 26133 |
rs142771632 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073485 | GAGAGTTTTCAGCAT[A/G]AAGGGCTGTTGAATT | 26133 |
rs142807177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077812 | CAAAATAAACACACA[C/T]AGAGCCCAAAAGGAT | 26133 |
rs142904423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021549 | GAGACTCGGAAAAAT[A/G]GACTCTGCAATAGTT | 26133 |
rs142916187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040787 | TTGTCGCAGATGGCT[C/T]ATCATGGGACTCCTC | 26133 |
rs142923686 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074283 | CTTCAGTACTGCTCT[G/T]ATCTTAGTTATTTCT | 26133 |
rs142957063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005382 | TGCTGCACCACAGGG[C/G]ACCTGCGATGCCACG | 26133 |
rs142960867 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091975 | GAGTCCCTCTTAACC[A/G]TGACGCTCTACACTA | 26133 |
rs142961539 | snp | A/G | 0.00074339 | 0.0192651 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003481 | GCAGCAGGTTGTGGA[A/G]GTTGTTGAGCAGGAA | 26133 |
rs142977700 | in-del | -/TCTT | 0.145305 | 0.227022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030865 | CTTTACTTAAGGTGC[-/TCTT]TGTTTTTCATGTGGA | 26133 |
rs143031992 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037045 | TAAAATAAAACTACA[C/T]TGAGGTTCCTCAAAA | 26133 |
rs143127724 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034165 | TCAAAAAAAAAAAAA[A/T]AAAAAAAAAAAAAGA | 26133 |
rs143128862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007009 | CTTTGTGTTTATGAA[C/T]GAAATTGTTTAAATA | 26133 |
rs143163854 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015463 | CCTCAGGCAGGAACT[C/T]TTTTTTTTTTTTTTT | 26133 |
rs143166417 | snp | C/T | 9.885e-05 | 0.0070296 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005721 | ACCTGGTTTTCAAAT[C/T]GGTCCAGGGACAGAG | 26133 |
rs143183022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089344 | CGATCTTCCCACCTC[A/G]GGTTCCTGAGCAGCT | 26133 |
rs143221361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017352 | TAACTGGTAAAATTA[A/G]CTGCTTCATGGAACC | 26133 |
rs143351375 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040813 | TCCTCCGCCTGTGAT[A/C/T]GTGTGAGCCAATTCC | 26133 |
rs143371073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091190 | ACACAGGATTTTGCC[A/G]TGTTGCCTGGGCTGG | 26133 |
rs143384803 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073050 | CTTTGTAGCAATTGT[A/G]AATGGGAGTTCACTC | 26133 |
rs143453013 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081483 | CTGGTACCATACTCC[A/C]GCCCGGGCAACAGAA | 26133 |
rs143458044 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059281 | TTATAAGGAACTACT[-/A]ATGAACAACTGTATG | 26133 |
rs143476570 | snp | C/T | 1.65067e-05 | 0.00287282 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021258 | GTTTGTACATGATCT[C/T]ATGCATAATCTTCAT | 26133 |
rs143512216 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010530 | CCTGCCACATTCATC[A/G]ACAAGGCCCCTTCCC | 26133 |
rs143539865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023742 | GTGCTTGGCATCCTC[A/G]GCACCCAGCCCATGG | 26133 |
rs143543424 | snp | C/G | 0.000840066 | 0.0204775 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078109 | GGTGTGCAGCTTGAG[C/G]AGCAGCTGAGGAATT | 26133 |
rs143556936 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074566 | TTGTTCAGTTTCCAC[A/G]TAGTTGAGTGGTTTT | 26133 |
rs143600055 | in-del | -/A | 0.0966517 | 0.197444 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036053 | TTTTTTAAGGTAAAG[-/A]AAAAAAACTGAATAA | 26133 |
rs143645491 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067147 | TCAGAGAAATTCAAA[C/T]CAAGACCACAATGAG | 26133 |
rs143762177 | in-del | -/T | 0.0260105 | 0.111035 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047340 | CAACAAATAATTTGC[-/T]TTTTTGAGCTTTATG | 26133 |
rs143793854 | snp | C/G/T | 0.000469263 | 0.0153108 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050019 | GAAGAAAAGGCAGAA[C/G/T]AGGTTGTAAGTACAA | 26133 |
rs143818415 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056097 | TAGCTTGACTAGATG[-/G]GGTTGTCTCATAATC | 26133 |
rs143841821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012270 | TCAAATGCAAGGTTT[C/T]TAAAATATTTAAACC | 26133 |
rs143842297 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049234 | TGAAATTTTTAATTT[A/G]GTTTTCATTTCGATC | 26133 |
rs143866398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020684 | AGTCTTGAGGAGGGC[C/T]GCACTGTTCCAAGCC | 26133 |
rs143911959 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042753 | AATCTGTGCAGGCAA[C/T]AACATTTTAGATAGA | 26133 |
rs143975390 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053976 | TTGGCTGCTAAGAAG[C/T]TTGAAGCCAAATTTG | 26133 |
rs143995730 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046514 | GACCATACTTTGATG[A/G]AGGCATATATCCTAC | 26133 |
rs144041516 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004711 | AACGAAAGCTGACTG[-/T]GGCAGAAAGAAGGAC | 26133 |
rs144068930 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044783 | TGTGCCTCTCTTTCG[C/T]ATCCCCTTACATACG | 26133 |
rs144078848 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070229 | TGATTCTTGTTACTT[-/C]CGGCTGCTAGGTTTC | 26133 |
rs144127997 | in-del | -/CCA | 0.288646 | 0.246995 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071895 | AACTAGTTTACAGTC[-/CCA]CCAACAGTTTAAAAG | 26133 |
rs144147086 | snp | C/T | 0.00200491 | 0.031598 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006406 | CTGGACAACCCAGCA[C/T]ACTCCACAGAGCCCT | 26133 |
rs144188152 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028352 | CCTCCTCGGCCTCCC[A/G]AAGGGCTGGGACTAC | 26133 |
rs144241228 | in-del | -/AAAAAAC/AAC/AC/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068984 | CACACACACAAAAAA[-/AAAAAAC/AAC/AC/C]AACAAAACATCTTAA | 26133 |
rs144249405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083202 | TTTATATTACAGCTA[C/T]AATTTTTAAATGCAG | 26133 |
rs144262010 | snp | C/T | 0.000230715 | 0.010738 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044663 | TGCTGCTGATCGAAA[C/T]TGGATACTAAGGAAC | 26133 |
rs144329476 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027417 | TATACAATCCTTGTA[C/T]GTTGCTATACTTGGT | 26133 |
rs144344440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016209 | CAAAACCTCGTGCTC[A/G]GTACACACGATAATG | 26133 |
rs144348832 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076949 | TTTGTTTACCTACGC[A/G]AGTCTCAGCAGTTGT | 26133 |
rs144377533 | snp | C/G/T | 6.60572e-05 | 0.00574672 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035146 | TGCTCTGACTCCTCA[C/G/T]TGGCCACTCGCATCA | 26133 |
rs144378311 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033444 | TCTTTCCATGATCTC[C/T]CTGTTAAGCTTTCTA | 26133 |
rs144417578 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084536 | TGTATATATGTATAT[A/G]TGTATATGTATATAT | 26133 |
rs144433619 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070677 | TGCTGGGATTACAGG[C/T]GTGAGTCACTGCGCC | 26133 |
rs144489126 | in-del | -/TA | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084513 | ATATATGTATATACG[-/TA]TATATGTGTATATAT | 26133 |
rs144571525 | in-del | -/TTTAA | 0.114036 | 0.209795 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027027 | TCTAATTTGCATGCC[-/TTTAA]TTTCTTTTTCTTGCC | 26133 |
rs144606049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003998 | CTCGGTGGGGAAAGA[A/G]TTCTGCCCCACTCAC | 26133 |
rs144689243 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037715 | GCATTAACGCTGTTG[C/G/T]GGTCAACAACGACCA | 26133 |
rs144708101 | snp | A/G | 0.000824063 | 0.0202818 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057543 | CCCCGGATAGAGATC[A/G]TAGGCCTCATAAGAA | 26133 |
rs144720654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085060 | AAGTGAAAAGAAACA[C/G]CTTTATAACCATGTT | 26133 |
rs144753319 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013345 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCG | 26133 |
rs144782422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073537 | CCTATTATCATGTGG[A/T]TTTTGTCTTTGGTTC | 26133 |
rs144792110 | snp | C/T | 0.000515425 | 0.0160452 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069252 | TAAATTCCCAAACCA[C/T]TAAGCAGTAGTAACA | 26133 |
rs144795208 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011729 | CAATGGTCTTCCCTC[A/G]TTCAGGGGCTTCTGG | 26133 |
rs144797168 | snp | C/G | 0.148326 | 0.228391 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071509 | ATTGCTCAATTCCCA[C/G]CTATGAGTGAGAACA | 26133 |
rs144833757 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065965 | GTGGAGAGGGAATGC[A/G]GAGCAGCAGTTAAAG | 26133 |
rs144891524 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034859 | AATGCTCTGGTTACT[A/G]GTTCTTGTTAGTCCC | 26133 |
rs144910814 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084999 | GAATCGAATGTGTGA[A/G]TTAAATCCTAGTCTT | 26133 |
rs145099865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082285 | CACACCTCGAGCAGT[A/G]TATCTAGTAAATGCA | 26133 |
rs145122523 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086473 | TGTGTGTGTGTGTGT[A/G]TGTATGTGTGTGTAT | 26133 |
rs145123704 | in-del | -/TCT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076254 | ATCATCTGAAGCCTT[-/TCT]CTCTCAACTCATCAA | 26133 |
rs145174804 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064700 | CTGAACATATGCCTG[C/T]TTTGCTTTGTATAAT | 26133 |
rs145191394 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072157 | TTCTTGTAAATTTAA[A/G]TTCTTTGTAGATTCT | 26133 |
rs145238085 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038403 | GGAGGGTTAATTTGT[C/T]AACACTTACCAATTT | 26133 |
rs145383798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017185 | CACCAGTAAAAAAGA[A/G]TCAAGGTATTTTATA | 26133 |
rs145398923 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039797 | TCTAAATCGACAGAA[C/G]AACAACTGGTAGTTC | 26133 |
rs145433054 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062366 | AATTTATATGCCAAT[A/G]TTCATGGCAGCATTA | 26133 |
rs145462116 | snp | A/G | 5.64573e-05 | 0.00531276 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003611 | GTTGAGGCAGCTGAC[A/G]TTCTCCTGCAAGGCC | 26133 |
rs145472501 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007123 | TTACATTGATTTGGA[C/T]CAATTCTTTTCCACA | 26133 |
rs145478452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039663 | GCTGCATAATTCAGC[C/T]CCTCTCAGCTAAGTG | 26133 |
rs145481400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038106 | CTTAATGTGTACGGC[A/G]TTTCCTTTTGGGGTG | 26133 |
rs145490838 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059769 | AGACGAAGAAGACGA[A/C]GAAGACAAAGAAGAT | 26133 |
rs145524282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060006 | TTAGTGATTTAAAAA[A/C]AAACAAACAAAAACA | 26133 |
rs145576632 | snp | C/T | 0.00766365 | 0.0614255 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001919 | TCTCAGTCACCCAAG[C/T]GGAACCAAGGCCCTG | 26133 |
rs145679228 | in-del | -/TTG/TTGT/TTGTG/TTTG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080806 | TTGTACACTTCAGTT[-/TTG/TTGT/TTGTG/TTTG]TTTTTTTTTTTTACC | 26133 |
rs145733793 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017965 | AACCCAGCCTGGATC[A/T]ACCTTGCCCTGCTTA | 26133 |
rs145754990 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076335 | TTTGGAGGAGAAGAG[A/G]CGCTCTGATTTTTAG | 26133 |
rs145780927 | snp | G/T | 0.00398564 | 0.0444627 | | | GRCh38.p7 | 20:35090204 | AAAAAACTAAGAAAA[G/T]AAATATTTGAAAGAT | 26133 |
rs145820692 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085545 | TTGAGCCCAGGAGGC[A/G]GAGGTTTCAGTAGTT | 26133 |
rs145936088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059477 | CCACCCTGGCCAACA[C/T]AGCAAGACCCCATGT | 26133 |
rs145978249 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030706 | AACTTTGGTACCACC[C/T]GTTTTCTTTGTACAG | 26133 |
rs146003581 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009897 | TGCACGAGACAAGGC[A/G]GTGGGGCAGTGCGGA | 26133 |
rs146015606 | snp | C/T | 0.000494397 | 0.0157148 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006460 | GTGTTGATATATTTA[C/T]TGAATCTCTTGAATG | 26133 |
rs146015691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063066 | CCAGGTGGAGGTGAC[C/T]GGATCATGGAGGCAG | 26133 |
rs146250496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058342 | CACTCCATGCAGCAA[G/T]AACAGAGTATACATT | 26133 |
rs146268170 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024518 | TGCTGAATAATATCC[A/G]CTAGTATAAATATAT | 26133 |
rs146268394 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079022 | AGTGAGCCAAGATCG[C/T]GCCATGGCACCCCAG | 26133 |
rs146307796 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025090 | ATTCTACATGCCCAC[-/T]TAATAGTGACTGAGG | 26133 |
rs146338517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055334 | TTTTCCCTTAATGTC[C/T]TGCTTAGGATATATC | 26133 |
rs146363619 | in-del | -/T | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073433 | CATAAATAGCTCCTA[-/T]TATTTTAAGATACGT | 26133 |
rs146371379 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031718 | TATGCATATCTTGGT[C/G]TGCTTAATAGTGCCC | 26133 |
rs146419473 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002511 | GGCTCAGGCAGGAGC[A/G]GCTGCCTCAGGCAGA | 26133 |
rs146430782 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054288 | GTTTACACAGTTTAT[A/C]ATAAGTTTCTAAAAG | 26133 |
rs146444280 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047782 | ACTGACTTTACAACC[C/T]TCTGGGTTTCAATCC | 26133 |
rs146490187 | snp | A/G | 1.65089e-05 | 0.00287301 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049891 | CCCAAAATATCTTCA[A/G]TGAGGGTTGCTGTTT | 26133 |
rs146555090 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028432 | TGATCTCCTGTTTGA[A/C/T]CCACTGGTTATTTAG | 26133 |
rs146567484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023208 | CTACTGGGTTTGAAC[C/T]CCATTCACTAGCCGG | 26133 |
rs146682993 | snp | C/G | | | intron-variant, missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004198 | AGCAGGGCAGAAGGT[C/G]TGAGGGACGTGGACA | 26133 |
rs146699308 | in-del | -/TT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031391 | TACCCCTGGTTAACT[-/TT]TTTTTTTTTTTTTTT | 26133 |
rs146773849 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044554 | CAAGCTCTTCTTCTG[C/T]TGAGCATTTTTGGCA | 26133 |
rs146782388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008102 | CCAGAGGGCACAGCG[C/G]GTATCCACGACAGGG | 26133 |
rs146795075 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074703 | AACTATGTGGTCAAT[C/T]TTGGAATAAGTGCGA | 26133 |
rs146806038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072593 | GATCGGACAGTTGTA[A/G]ATATGCGGCATTATT | 26133 |
rs146813768 | snp | C/T | 3.33028e-05 | 0.00408048 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003525 | TTGCTGTGCTCCATC[C/T]GCTGCAGCAGCCGCA | 26133 |
rs146917369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004968 | GTCCTAGCGCAACTG[C/G]TTTTCCACACCAGCT | 26133 |
rs146917416 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060623 | AAACAAGAAAAGGAT[C/T]ATACACCATGACACT | 26133 |
rs146924519 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030986 | GATGTTTGTCTGTTA[C/T]TAATGAGTTCTTTCA | 26133 |
rs146932478 | snp | A/T | 0.000922676 | 0.021459 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069344 | ATTTGGATAAGTGGT[A/T]TCTTGGGTAAGTTTC | 26133 |
rs147031235 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008869 | AAGTCTGCAGGATGC[C/T]TTCCTGCTCCAACTG | 26133 |
rs147037674 | in-del | -/AG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086578 | TGTGTGTGTGTGTAT[-/AG]ATATATATGAATAAG | 26133 |
rs147054498 | in-del | -/GAC | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059818 | GAAGACAAAGATGAA[-/GAC]GAAGAAGATGAAGAC | 26133 |
rs147133728 | in-del | -/CCC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036306 | GGCTGCCACAGTAAA[-/CCC]CAGCCATAAGATGGA | 26133 |
rs147146528 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073340 | GTGCTGAGAGAGGGC[A/G]CCCCTGTCTTGTGCC | 26133 |
rs147155995 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071213 | CAAAACTTCACCTCT[A/G]AAGAACACTGTCATT | 26133 |
rs147249334 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050417 | TCAGTAAAATGATCA[C/T]CTTAAAAGTCTTTGA | 26133 |
rs147340492 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075089 | GCAACCCCTGCTTTT[-/T]TTTTTTGTTTTCCAC | 26133 |
rs147355930 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025755 | TTCCTCATTGTGTTT[A/C/T]CTGAAGAACAAAAAG | 26133 |
rs147366764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021134 | GCACCTGGCATACCA[C/T]GAGCACCCGGGCAGC | 26133 |
rs147411905 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086653 | AAAGCCAGGTAAGAT[A/T]TGTTTGACTTAAATG | 26133 |
rs147461437 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005431 | AGGGGGCCAACTCAT[C/T]GTGCCAGGCAATACC | 26133 |
rs147462448 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092264 | CCCACGCCCAATACA[C/T]GGGATAAACTCGAGG | 26133 |
rs147499555 | snp | C/T | 0.000247294 | 0.0111169 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003231 | GACTGCCGGTCCGGG[C/T]TCAACAGGATGGACA | 26133 |
rs147516805 | snp | C/T | 4.94923e-05 | 0.0049743 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021273 | CATGCATAATCTTCA[C/T]TGACTGGGGCAGCTG | 26133 |
rs147614901 | snp | A/G | 0.147321 | 0.227941 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084144 | ATCTCTACTAAAAAT[A/G]CAAAAAAATTAGCCA | 26133 |
rs147621511 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044400 | CCCATCTCAAAAAAG[A/G]AAAAAAAAAAAAAAA | 26133 |
rs147624655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078260 | CAGCCGACTTCCAAA[A/C]CCACCCAGGACAGTT | 26133 |
rs147706616 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091161 | CACCACCATGCCCGG[C/T]TAAATTTTTGGAGAC | 26133 |
rs147718745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065588 | CAGCAGGACAGCAAG[A/C]GAGTTCACTAACAAA | 26133 |
rs147726573 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060201 | ATACCAAAACCAAAC[A/G]AAGACATCACAAGAA | 26133 |
rs147830749 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033521 | CTGAATTCTCGACTG[C/T]TTTTGATAATGCCCT | 26133 |
rs147850360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080227 | GGGCACAGTGTCTCA[G/T]GCCTCTGATGCCAAA | 26133 |
rs147928168 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016217 | CGTGCTCAGTACACA[C/T]GATAATGATATTCAG | 26133 |
rs147938383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011949 | TGCTCAACGGTGGAA[A/T]CCTTGGATGAACAAC | 26133 |
rs147958050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061388 | AGAAGATTTAATATT[C/G]TTAAGATGATAATAC | 26133 |
rs147989682 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031050 | TTCATCTTTGAAACA[C/T]AGTTTTGTAAAATAC | 26133 |
rs147993758 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071174 | TATTACATTTTAAAA[C/T]AACTTACTATGTGAT | 26133 |
rs147999684 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081651 | ATGTAAACATATACC[A/G]AAAGGTAGTATAACT | 26133 |
rs148043882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023961 | TTCAAGAAACAGTCT[C/G]CAAAGCAATGGCCAG | 26133 |
rs148106873 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005546 | AGGCAGCAAAGCCAA[C/T]TGCCCTGGAAGCCGC | 26133 |
rs148116605 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057812 | CTCATTTTTGAAAAG[A/T]AGTATTTTAGATTAG | 26133 |
rs148122618 | in-del | -/GT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080807 | TGTACACTTCAGTTT[-/GT]TTTTTTTTTTTACCC | 26133 |
rs148161476 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085649 | AATTTTGTTTTCCTT[A/G]TGAACAGCTCAGCAC | 26133 |
rs148201466 | snp | A/C/G | 6.59602e-05 | 0.00574251 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005797 | TCTGCTTCAGGAATA[A/C/G]CTGGAACTATACAGA | 26133 |
rs148213045 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037074 | AAAGTTGGCCAGGCA[C/T]GGTGGCTCACGCCTG | 26133 |
rs148289137 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087161 | GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 26133 |
rs148325238 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009225 | ACTCTGGCCCCGTCA[C/T]GGGGGAAGGAAGACG | 26133 |
rs148368889 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041303 | CTCGTGATTTAATTA[C/T]GTCCACCAGCTTGGC | 26133 |
rs148378400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091509 | TTTCTCCCCCTTTAG[C/T]CCAATTCCCACCTCA | 26133 |
rs148432899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059879 | AGATGAAGAAAAGAC[A/G]AAGACAAAGATGAAG | 26133 |
rs148484518 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014648 | TAGAAATGCAAAATA[C/T]ATTTGCTTGAAATTA | 26133 |
rs148527991 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037924 | CAAGTACACTCTATG[A/C]CATTCACACAATGAC | 26133 |
rs148571535 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074092 | TTCTCTGATGGTAGT[C/T]TGTATTTCTGTGGGA | 26133 |
rs148629844 | in-del | -/TT | 0.397452 | 0.201886 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089396 | TTTTTTTTTTTTTTT[-/TT]GTAGTAGAGCTGGGG | 26133 |
rs148686950 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045195 | TCTGTGTTTATTATT[C/T]CCGTGCATGTTTTTA | 26133 |
rs148729224 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035181 | ATCTAGCACCAAAGC[A/G]TTGTCTAGCCATGTG | 26133 |
rs148781296 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027433 | GTTGCTATACTTGGT[A/G]TGCTAGTATTTTGTT | 26133 |
rs148844507 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007139 | CAATTCTTTTCCACA[C/T]GGATTTTATAATTCG | 26133 |
rs148866038 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075349 | TGCAGTTTCTTCCTA[A/G]CATCGAAGGTCTTTA | 26133 |
rs148886097 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073409 | GTATGATATTGGCTG[G/T]GGGTCTGTCATAAAT | 26133 |
rs149003941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048827 | ACACTGGCTGGAACA[C/T]ACAATTACTGGAATA | 26133 |
rs149020450 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035608 | TTCTGGGAATTTACC[A/G]TAACGAAATAACCAG | 26133 |
rs149056638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085055 | TCTAAAAGTGAAAAG[A/G]AACAGCTTTATAACC | 26133 |
rs149073793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030516 | GTTAAAAGCCCAACA[A/G]TACTTGTTCTAATTG | 26133 |
rs149168832 | in-del | -/AAGATGAAGAA | 0.0115144 | 0.0749975 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059852 | AAGAAGACGAAGATG[-/AAGATGAAGAA]AAGATGAAGAAAAGA | 26133 |
rs149170871 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023686 | CTGAAGAACTATCAC[A/G]CAGAATCCTGCCTCT | 26133 |
rs149213839 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004930 | AAGAAAAACAACGCA[A/C]AAGTTCCACTCCTTC | 26133 |
rs149218252 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091093 | CACTCTGTCAATCTC[C/T]GCCTCCCAGGCTCAG | 26133 |
rs149221907 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017223 | AACTGAACAATTGCC[A/G]AGAGATAATACTGGG | 26133 |
rs149341919 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037701 | TACAGTTATGCACTG[C/T]ATTAACGCTGTTGCG | 26133 |
rs149376668 | snp | C/T | 0.0102895 | 0.0709851 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057494 | GAAAACAAGGACCAG[C/T]AGCTAATAGGTATAC | 26133 |
rs149490637 | snp | A/C/G | 0.03685 | 0.130724 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027130 | AACGATCAGGAACTC[A/C/G]TCTTGTTCCTGATCT | 26133 |
rs149543957 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020592 | GGAAGGACTGCTGAG[C/T]CTCCAGCCTCTCCTG | 26133 |
rs149555462 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083199 | ATTTTTATATTACAG[A/C]TACAATTTTTAAATG | 26133 |
rs149575394 | in-del | -/AAAG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038595 | TACCATCTGTACAAA[-/AAAG]CAGGAGTCAATCTCT | 26133 |
rs149586704 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35009008 | AGACATGGCTTAGAA[C/T]TGCCAGAGGAGAGCT | 26133 |
rs149587164 | in-del | -/CCTGTGACTGTGACCCACAACAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011616 | TATATAAAATCCAGG[-/CCTGTGACTGTGACCCACAACAC]CCTGTGACTGTGACC | 26133 |
rs149596670 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062122 | CTTCATACCTACTAC[C/G]ATGGTTATAATGAAA | 26133 |
rs149666874 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059760 | AGAAGAAGAAGACGA[A/C]GAAGACGACGAAGAC | 26133 |
rs149720663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052022 | AGCACTAAAACAATA[C/T]ATAAAAGGTTGTATG | 26133 |
rs149805431 | snp | A/G | 0.000512714 | 0.0160029 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003500 | GTTGAGCAGGAAGCC[A/G]GGGTACTTCTTGCTG | 26133 |
rs149860942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022071 | TAGACTGCTCTGCAG[C/T]AGACAGCTAGGGTTA | 26133 |
rs149879474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011388 | TAATCACTGGCAACA[C/T]GGCAGGCACAGCACA | 26133 |
rs149906242 | in-del | -/CA | 0.145978 | 0.227331 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064560 | CCTAAACTACTACAC[-/CA]CAGATTGTCAATTCT | 26133 |
rs149921742 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044782 | ATGTGCCTCTCTTTC[A/G]CATCCCCTTACATAC | 26133 |
rs149925769 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078249 | GCAAAGGAGAGCAGC[C/T]GACTTCCAAACCCAC | 26133 |
rs149931816 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093805 | AATAAATAATTACAC[C/T]GGGACGGTAGGCATA | 26133 |
rs150020258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075226 | CCAATTTGCCAGTCT[A/G]TCTTTTAACTGGAGC | 26133 |
rs150022394 | in-del | -/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002774 | GCTTGGCTCACAGAT[-/G]GGGGGGTGGGGGTCA | 26133 |
rs150036146 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016512 | TAAACAAATTCCTTA[A/C]GATTTGTCTCCTCGT | 26133 |
rs150071144 | snp | C/T | 1.65198e-05 | 0.00287395 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035144 | TGTGCTCTGACTCCT[C/T]ATTGGCCACTCGCAT | 26133 |
rs150071543 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072087 | ATAAACGTCTTCTTT[A/T]GAAAAGTGTCTGTTC | 26133 |
rs150082447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039079 | CTGTGTCTCAAAATA[A/T]AACAAAGCAAAAAAA | 26133 |
rs150179620 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057542 | TCCCCGGATAGAGAT[C/T]GTAGGCCTCATAAGA | 26133 |
rs150195016 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012843 | GGAAGTCTGGAAAGA[C/T]GGGAGGTCCGACTGC | 26133 |
rs150231202 | in-del | -/TGTGTG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086432 | GAAATGAATGGCATA[-/TGTGTG]TGTGTGTGTGTGTGT | 26133 |
rs150239095 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048065 | CTATGGTATTGATTT[C/G]CATTTCCTTGATTGC | 26133 |
rs150291048 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084760 | TTTATATGCATATAT[A/G]TGTATATGTATATAT | 26133 |
rs150354358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019810 | TCATCCAGTGTCCTG[A/G]TTTTAAATACAACCA | 26133 |
rs150363968 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073017 | CCTTGTGAGTTGGAT[C/T]CCTAAGTATTTTAGT | 26133 |
rs150366156 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082000 | AAAAACAAAACAAAA[A/C]AAAAACAACAACAAC | 26133 |
rs150407327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061826 | GATGCACACCAATAC[C/G]CAAGTAACAAAAGAT | 26133 |
rs150515497 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015304 | CACGCCCGGGAGCAC[C/G]GTTCTATAGGTGGAT | 26133 |
rs150548251 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031440 | GGGGTTTTGCCACAT[G/T]CCCCAGGCTGGTCTT | 26133 |
rs150559917 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051809 | CCAGGCTGTCAAATA[C/T]ACAACCCTGCTGCTC | 26133 |
rs150647898 | in-del | -/TATA | 0.030665 | 0.119967 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044266 | GTGGTGGCACCTGCC[-/TATA]TATAGTTCCAGCTAC | 26133 |
rs150681505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037545 | GAAGGGATAAACAAA[C/T]TGTGGTATCTACATG | 26133 |
rs150681957 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074548 | CAGTCATTCAGGAGC[A/G]GGTTGTTCAGTTTCC | 26133 |
rs150714525 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010541 | CATCGACAAGGCCCC[C/T]TCCCTCAGCAGCTCT | 26133 |
rs150724629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063669 | TTGGAGACTGCCTAA[A/G]GAACAAAGCAAGACC | 26133 |
rs150756105 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007602 | GCATAGGAGGTGGTC[C/T]CTCGGAGGAAACTCT | 26133 |
rs150768023 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006087 | TACTTCAGCTAGCCT[A/G]AGCTGGGTTTCTGTC | 26133 |
rs150819680 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042230 | AGGAGGAAAAGCAAA[C/T]CTAGAGAGAGAATAA | 26133 |
rs150886303 | snp | A/T | 0.25045 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071931 | TCCTATTTCTCCACA[A/T]CCTCTCCAGCACCTG | 26133 |
rs150930337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087701 | GGATTTATAAGATCT[C/G]ATTTGCATTAAGCAT | 26133 |
rs150999034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038572 | TTATTTTATATTACC[C/T]ATTTACATTACCATC | 26133 |
rs151036154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012327 | TAAATCTTAATTTCT[A/G]CCTTTGCTTGGCAGA | 26133 |
rs151041246 | snp | A/G | 1.65304e-05 | 0.00287488 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003488 | GTTGTGGAAGTTGTT[A/G]AGCAGGAAGCCGGGG | 26133 |
rs151046304 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067356 | AAACACTTTCAAAAT[A/G]ACAGATAACAAGTGT | 26133 |
rs151054310 | snp | A/C/T | 0.00403224 | 0.0447215 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078154 | TTGTTTGTCCCTCTC[A/C/T]GTCAAAAAAGTCTCA | 26133 |
rs151089444 | snp | A/C/G | 0.000665101 | 0.0182247 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007508 | GCAACGCGTGGGCTG[A/C/G]GGGGAGACGGAACCC | 26133 |
rs151095089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021925 | ACATATTATCTACAG[A/G]CAGATTTTCATTTTA | 26133 |
rs151142516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046068 | CTGTGTACACATGTA[C/T]GTGACCATTTATCCA | 26133 |
rs151264300 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033073 | GTGGTGGCATGCACC[A/T]GTAACCCCAGCTACT | 26133 |
rs151331360 | in-del | -/TA | 0.225597 | 0.248806 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086486 | GTGTGTATGTGTGTG[-/TA]TATATATATGTGTAT | 26133 |
rs180783524 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010983 | AAACATATTGAGGCC[A/G]GGCGCGGTGGTTCAC | 26133 |
rs180795812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048531 | GCCTGTAAGAATTAT[A/T]GATAAATTCTGAATA | 26133 |
rs180801315 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078651 | TCACTGTAAATATCT[A/C]TGAATGGTCTAAACT | 26133 |
rs180810302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058500 | AAATCAGAACGAAAT[C/T]TGGGAAATTCATGAA | 26133 |
rs180811844 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019524 | GCTTTCTCAAGAATC[A/G]AGTGTGGGGACACAG | 26133 |
rs180821442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087308 | TGCACCATTGCCCTC[C/T]AGCCTGGGCAACAGA | 26133 |
rs180830928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038183 | AATGTACTAAATGCC[A/G]CTGAGTTGTTCACTT | 26133 |
rs180862290 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071985 | CGCCATTCTAACTAG[C/T]GTGAGATGGTATCTC | 26133 |
rs180872711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074834 | TATCCCTGTTAACTT[C/T]CTGTCTCGTTGATCT | 26133 |
rs180880118 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084205 | TACTCGGGGGGCATA[A/G]GTTGCAGGGAGCCGA | 26133 |
rs180897175 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043798 | TCTGGAATTTTTCAG[A/T]TAATATTTTCGGATT | 26133 |
rs180907070 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091681 | ATTCAACCTGGTTTA[C/G]CCTAAAGCAGTGTCC | 26133 |
rs180927239 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053604 | CATGGCTACCGAGCA[C/T]TTAAAAGGTGGCCAG | 26133 |
rs180935247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024761 | TGAGCCTGGGAGGTC[A/G]GGGCTGCAATGAGCT | 26133 |
rs181014942 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014405 | TCACTGCAACCTCTG[C/T]CTCCTGGGTTCAAGC | 26133 |
rs181042611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006294 | CAGACAGAGCAGGTT[C/G]CAATGAATGTTTGCC | 26133 |
rs181046824 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034525 | CAATTTGGAGCTGGA[A/G]GGAAGAAGAAAAGCT | 26133 |
rs181106348 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004355 | GAGCTGGGTCTCCAG[A/G]GACGCACTTCTGGAG | 26133 |
rs181117229 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023236 | CGGGTGGTCTTCAGT[A/C]AATCAGTGGACCTCT | 26133 |
rs181134889 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053909 | TTCAATTGCACAGCA[C/G]TATTATAGATGCTGA | 26133 |
rs181147289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064470 | TCGTGGCATGAATGT[A/G]ACACTATAATTCAAC | 26133 |
rs181154318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091966 | CTGACTCCAGAGTCC[C/T]TCTTAACCGTGACGC | 26133 |
rs181160367 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075537 | AGTTTGGCTGGATAT[A/G]AAACTCTGGGTTGAA | 26133 |
rs181164130 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014720 | GTCCCCAGAGTGCAG[C/T]GAAGAGAAGAGGGCC | 26133 |
rs181171909 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043107 | TTGGAGATTTTTCTA[C/T]AGCAGTACATAGAGA | 26133 |
rs181172530 | snp | A/C/T | 8.24904e-05 | 0.00642178 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035155 | TCCTCATTGGCCACT[A/C/T]GCATCAGGGCATCTA | 26133 |
rs181452590 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023704 | GAATCCTGCCTCTGT[C/T]GTGCACTGCTGTGAG | 26133 |
rs181462818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043522 | AAAGTGCTGGGATTA[C/T]AGGCGTTAAGCCACC | 26133 |
rs181479511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065133 | ACTTCAAATGGAAGA[C/T]AGACTATGTCAGTGA | 26133 |
rs181494240 | snp | A/C/T | 0.000148678 | 0.00862094 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005816 | GAACTATACAGAAAC[A/C/T]AAGCTCACAGCAGGC | 26133 |
rs181713102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054807 | AAATTCTGCCTCCCC[A/G]TAATTTCTACCAGTT | 26133 |
rs181723639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079038 | GCCATGGCACCCCAG[C/T]CTGGGCGACAGACCA | 26133 |
rs181745601 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038968 | AGTCCCAGCTACTTC[G/T]CAGACTGAGGCACGA | 26133 |
rs181765122 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020404 | CCAGGCTGTCCCGCG[C/T]TGCCTCACTGTTCCA | 26133 |
rs181769432 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039520 | GGTTAATGTTAAACT[A/G]ACAACTAAATCACTC | 26133 |
rs181787558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060863 | TAAAGGGCTTTTATT[A/T]AAAAACCCACAGCTA | 26133 |
rs181787932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075747 | TGTCTTGGAGTTCCT[C/T]TCCTCGAGGAGTATC | 26133 |
rs181799736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070649 | GTGATCCACCCGCCT[C/T]GGCCTCCCAGAGTGC | 26133 |
rs181932703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060540 | TGCAGTGAGCTGTGA[C/T]CACACCACTGCATTC | 26133 |
rs181981819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079209 | CAAAGGGGTTAATTC[G/T]CCAAGAAGACATAAC | 26133 |
rs181986250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029369 | AAGTGTGTTTTCTAT[A/G]GGCTGCATATAACTG | 26133 |
rs182159849 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020108 | CATCCAAACCATCAG[C/T]AAATCCTATCTTTCA | 26133 |
rs182162168 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060991 | AGTGTTCTAAGGCAA[A/C]TAGAGAAAAATAAAA | 26133 |
rs182168089 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032324 | GCCACCACACCTGGC[C/T]TGATTATTATACTAC | 26133 |
rs182198088 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040409 | CTGGAGTGGGAAGTT[C/T]TTCTCCTACTGCTCT | 26133 |
rs182198447 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079834 | CCAGCCTGAGCAACA[C/T]AGCGAGAGCTCGCCT | 26133 |
rs182203262 | snp | A/G | | | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012624 | GGGAAGAATCCTCCA[A/G]CTGCTCAGTAAGCAG | 26133 |
rs182209859 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036337 | AACAGCCAAAATGTC[C/T]GTCAAGTGGAAAAGG | 26133 |
rs182216109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056165 | CCTTTCAACCTACTG[A/G]GGCTCTGTGATTGAT | 26133 |
rs182243705 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016199 | AAAAATCTAGCAAAA[C/T]CTCGTGCTCAGTACA | 26133 |
rs182268016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010629 | CAGGTCCAATCACAC[C/T]CAAGCCTGGCCCTGC | 26133 |
rs182280338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047296 | CATCATTAATTATTA[C/T]TGCCTTGCCATTTAA | 26133 |
rs182368320 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088760 | AATCTGATTTTTTTT[C/T]CCAAGGAAATTCCAT | 26133 |
rs182540096 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008115 | CGGGTATCCACGACA[A/G]GGAGTTTGGACAAGG | 26133 |
rs182553395 | snp | A/G | 0.000131972 | 0.0081221 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021272 | TCATGCATAATCTTC[A/G]TTGACTGGGGCAGCT | 26133 |
rs182599601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077040 | CAGTGAGCAAGGCTC[C/T]GTGGGCATGGGACCC | 26133 |
rs182648904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046470 | GAACTTTTAATAATC[C/T]GTTCCTGCATCTATT | 26133 |
rs182651933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037316 | CGCGCCACTGCACTC[C/T]GGCCTGGGCGAAAGA | 26133 |
rs182658757 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057044 | TGTAAGTTATAAAAA[A/G]TAATAATAGAATATT | 26133 |
rs182660003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077521 | CAGGGGTGGGGCCCA[A/G]AACTCTGTGTTTTAA | 26133 |
rs182830291 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072925 | CATGAGCATGGGATG[G/T]TCTTCCATTTGTTTG | 26133 |
rs182832223 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025747 | TTTTCACTTTCCTCA[C/T]TGTGTTTTCTGAAGA | 26133 |
rs182875986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027752 | ATAGTTTGTGTCTTT[C/T]AACTTGCTCATTTCA | 26133 |
rs182903009 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086494 | GTGTGTGTATATATA[C/T]ATGTGTATATATATG | 26133 |
rs182908165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069181 | CTAAGCTTCTAAAAG[C/T]TAAAATCTGAAATGT | 26133 |
rs182919097 | snp | C/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094338 | AGCACTTTGGGAGGC[C/T]GAGGTAGTCAGATCA | 26133 |
rs182991146 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045531 | GCGTGTCATTACACC[C/T]GGCTACTTTTTTAAT | 26133 |
rs183026960 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085396 | GTAGGCCCATTGCTT[C/G]ATCCCAGGAGTTTAA | 26133 |
rs183029946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008482 | TGTGGGCTGCAGAAG[A/C]AGCTCTCACATACCT | 26133 |
rs183031797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068307 | ATACTTTGTTCCTGG[A/G]GATATAAACTGACAA | 26133 |
rs183032961 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026647 | ATCTGTAAGGCTGAT[C/G]TATAGATCAGAATGG | 26133 |
rs183040983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049398 | CTAATGAGAAAAAAT[A/G]GAGGCGGACTTCATA | 26133 |
rs183060459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087595 | TCCTTCAACTCGTAC[A/T]GATCATTTGGGGCCT | 26133 |
rs183063744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012132 | TGGTGCCATTTTTCA[A/G]AAGGTTAACATGCTT | 26133 |
rs183067150 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072297 | TTAATTAGATCCCAT[A/T]TGCCAATTCTGGCTT | 26133 |
rs183073621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030920 | ACCTGCTTTCAACCT[G/T]AAGAACTTCCTTTGG | 26133 |
rs183124192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067675 | GAAACATCATTTGAC[C/T]ATAAAAATGAGTGTT | 26133 |
rs183141782 | snp | C/T | 0.000536328 | 0.0163669 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044763 | AATTCACTCAAGAGA[C/T]TGGATGTGCCTCTCT | 26133 |
rs183343183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015331 | GGATGAAAATTACAA[C/T]AGGATAAAACAGCAA | 26133 |
rs183378629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084602 | TATATGCATATATGT[A/G]TATATGTATATATGT | 26133 |
rs183393646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017430 | ACTAATTTATATCTT[C/T]TAAAACAGAACTGCA | 26133 |
rs183447323 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041108 | CAGCACCTTGATCTT[G/T]GACTTCTAGCCTCCA | 26133 |
rs183499925 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080583 | CCAGTCTCAAAAGGC[A/C]ATATATTGTCTGATT | 26133 |
rs183517262 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080925 | AACTAAATAAATAAA[G/T]GAACATAAGTGAACT | 26133 |
rs183601720 | snp | A/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082380 | GCAAATGTCAATACA[A/T]TTAAATGAACTGAAA | 26133 |
rs183637277 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075012 | TCCCTTTACCATTAT[C/G]TAATGGCCTTGTCTC | 26133 |
rs183641846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035716 | AATGTTCATCAACAG[A/C]TGATTAATTAAATAC | 26133 |
rs183692655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021995 | ATATTTATGGGACAC[C/T]TGATATGTGTCAGAC | 26133 |
rs183716795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031983 | TGCAACCTCTGCCCC[A/G]GGTTCAATCGATTCT | 26133 |
rs183744897 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061440 | TCAATGCAATCACTA[C/T]CAAAATCTCAGCTGG | 26133 |
rs183874728 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078435 | AGTGGACTTAGACTC[A/C/G]TCGTAAATATATACT | 26133 |
rs183876495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019161 | CCAAGGAAACCCTTC[C/T]CCTTGCTACCCAGTG | 26133 |
rs183879571 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058172 | AAAAATACATGAAAC[A/G]AAAGCTGGCAGAAAT | 26133 |
rs183880851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038173 | CAACACTGTAAATGT[A/T]CTAAATGCCGCTGAG | 26133 |
rs183914531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012215 | GCATATGATGGAGGT[A/G]CCCTGGGGCCACAGC | 26133 |
rs184000437 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072582 | GGTTTGTCAAAGATC[A/G]GACAGTTGTAGATAT | 26133 |
rs184079931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028331 | CTCCTGACCTTAAGC[A/G]ACCCGCCTCCTCGGC | 26133 |
rs184114179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009697 | AAATCATGGCTCTTG[C/T]TGGATAAAGTCCACT | 26133 |
rs184122635 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063832 | TACCACTGCACTCCA[G/T]CCTGTGACACAGTGC | 26133 |
rs184134839 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091785 | TTCAGCCCTTAGTAT[A/G]CACCAGAAATGCACT | 26133 |
rs184168481 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070244 | CCGGCTGCTAGGTTT[C/T]GGGGTGACTAGTTCT | 26133 |
rs184173765 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073495 | AGCATGAAGGGCTGT[A/T]GAATTTTGTCGAAGG | 26133 |
rs184180585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050441 | TCTTTGAGGCCAGGC[A/G]TGGTGGCTCACACCT | 26133 |
rs184195072 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088015 | AAATGCTAGAAGGCA[A/C]TTGGATATACCTACC | 26133 |
rs184196064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028873 | CATACATGTTTATAA[C/T]TGTTGTATCTTCTTG | 26133 |
rs184203161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047040 | TGCTGGGCTAATTTT[C/T]ATATTTTTAGTAGAG | 26133 |
rs184205216 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087010 | GCACTCCAGCCTGGG[C/G]AACAGCACGAGACTC | 26133 |
rs184276864 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043085 | TCCTCTTTATCATTA[A/G]TATATCTTGGAGATT | 26133 |
rs184306488 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009917 | GGCAGTGCGGAGCAC[A/T]CATGACTTCTGGCAG | 26133 |
rs184312146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078801 | CCAGGCACGGTGGCT[C/T]ACACCTGTAATCCCA | 26133 |
rs184319498 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022304 | GGGACTACAGGCATG[C/T]GCCACCACGCCCAGC | 26133 |
rs184319772 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058784 | AACCTCCGCCTCCTG[C/G]GTTCAAGCGATTCTC | 26133 |
rs184368303 | snp | C/T | 0.00206044 | 0.0320309 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35008705 | CTTCATGACCTGCAG[C/T]AGACGAGTTAATAAG | 26133 |
rs184404302 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013209 | TAGTTAGAAAACCAT[C/T]TGTTCACTTCCACAT | 26133 |
rs184411755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033311 | GTTAGACTATTTTCG[C/T]AAAGTCTCCTTCCCC | 26133 |
rs184413200 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005316 | AAAAAAAGGAAACGC[A/G]TGCGCATACACATGG | 26133 |
rs184413374 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090433 | CCAGGCTGGAGTGCA[A/G]TGGCGTGATCTCAGC | 26133 |
rs184416578 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051741 | GAAGATCCAAAGAAA[A/C]AGAACAAAAAGAGAA | 26133 |
rs184420174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023317 | TACCTACCCCTTAAT[A/G]TTGTAAGGAGTAGAG | 26133 |
rs184420209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073611 | CCAGCCTTGTATCCC[A/G]GGGATGAAGCCAACT | 26133 |
rs184430340 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003673 | CCCCAGTGGCCCCTG[A/G]TGAACCTGGGTAGCC | 26133 |
rs184670952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082776 | AAGGAGAATAATTAT[C/T]TGATAACATAAAGGA | 26133 |
rs184949917 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038661 | GGCATGTATAGAATA[A/T]TTTTCGAAGGACGTT | 26133 |
rs184994848 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046963 | AACCTCTGCCTCCTG[G/T]GTTCAAGCAATTTTT | 26133 |
rs184997514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057875 | CTGAAAAGCTGCAGA[A/T]CATTATTACTATGAT | 26133 |
rs185001148 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019835 | CAACCATATGCTGAG[A/G]ACTCCCAAAGTGATA | 26133 |
rs185046445 | snp | C/T | 1.65949e-05 | 0.00288048 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003107 | CGTACCCACGCTCAC[C/T]CACACTGGCCCAGCA | 26133 |
rs185048622 | snp | A/G | 0.000841574 | 0.0204958 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022108 | AGACTGAATGGGAAC[A/G]TAAGAGAAGCCCAGC | 26133 |
rs185053796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063060 | GTGGGACCAGGTGGA[A/G]GTGACTGGATCATGG | 26133 |
rs185062296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042274 | TCCACAAACTTCTAC[C/T]TTTACATATGACTAC | 26133 |
rs185116793 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053829 | CACCACTTCTTCCTA[C/T]TTTTTTCTTTAAAAA | 26133 |
rs185126359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018694 | TACTTGTAGAATGCA[C/T]TATTCCTACTCTCAG | 26133 |
rs185150384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014495 | CTGAAGACCCAAACA[C/T]AAGCATTAGTGCCCC | 26133 |
rs185159298 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034567 | ACTCCCAATGAGAAA[C/T]CTATTCCTTGTTTGG | 26133 |
rs185230020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043286 | GAGTCTAATTATGTC[A/G]CCCAGGCTGAAGTGC | 26133 |
rs185250102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037769 | GATTATAATACTGTA[A/T]TTTTACTATACCTTT | 26133 |
rs185366095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064489 | CTATAATTCAACATC[C/T]TGAATTAAGAGAGAT | 26133 |
rs185495317 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032673 | GAGACGGGGTTTCAC[C/T]GTCTTAGCCAGGATA | 26133 |
rs185612849 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075648 | AGTCTGATGGGCTTC[C/T]CTTTGTGGGTAACCC | 26133 |
rs185638282 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053929 | ATAGATGCTGAATTA[C/T]GTAAGTGTTCAAACA | 26133 |
rs185652225 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045152 | CGCATTTTTTTCTCT[C/T]CCTGCAGACGTAAAC | 26133 |
rs185652245 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092145 | AATAACAATGGGGAC[C/T]TACTTTAGAAAGGGG | 26133 |
rs185665732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033647 | AGCTGTCTCCTTCCC[C/T]GGTTCTCTGGTGAAC | 26133 |
rs185720648 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074360 | CTTTTAATTGTGATG[G/T]TAGGGTGTCAATTTT | 26133 |
rs185766924 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025567 | TCTTCTTTGGAGAAA[C/T]ATCTATTCAGATCCT | 26133 |
rs185788491 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013833 | TACACTTGGTGAAAG[A/G]AGGGTTAGAAAGGCC | 26133 |
rs185809335 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053261 | TTATAAACTAAGTCA[A/C]CCTTACTGATTTATC | 26133 |
rs185827993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066827 | AACACAAATGACAAA[A/G]GCCTTTAAAAAATCA | 26133 |
rs185846339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048619 | TCCACTTTCTTTATG[A/G]TATCTATCCCCCTTT | 26133 |
rs185848655 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090738 | AAACAAATTAAGTTG[A/C]CTAAATTGCCTCATT | 26133 |
rs185883353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010999 | GGCGCGGTGGTTCAC[A/G]TCTGTAATCCCAGCA | 26133 |
rs185889534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006342 | CCCCGTCGTCTCTAA[C/T]GTAAAACCTGTGCCT | 26133 |
rs185903345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044246 | AAATACAAAAATTAG[C/T]CCGGTGTGGTGGCAC | 26133 |
rs185916891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031371 | GGGATTACAGGTGTG[C/T]ACTACTACCCCTGGT | 26133 |
rs185947850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087846 | AAAATCCAAGTAGAA[C/T]TGACCCATTACAAAT | 26133 |
rs185948201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084318 | TTAAAAGGATGCATT[A/G]TACCTGACTTCACCA | 26133 |
rs185959494 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072356 | CATGAAGTCCTTGCC[C/T]GTGCCTATGGCCTGA | 26133 |
rs186011171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010683 | CGGTCACACATCACA[C/T]AGAGGCCTGGTTAAC | 26133 |
rs186025581 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047873 | TAACCCATGGCAAAA[C/T]ACTGATGCCTCAGCC | 26133 |
rs186145725 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029780 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 26133 |
rs186163202 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060951 | AAGATGTCCACTCTC[A/G]CCACTTCAATTTAAC | 26133 |
rs186184673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020440 | TATGCACACTCCTCC[A/C]CAGGGCACTGCCCCC | 26133 |
rs186196619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040138 | CCTAAATATGACTGC[A/G]TTTTGAAACAGGCCC | 26133 |
rs186203179 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079288 | AAAAACTGCCTAAAA[C/G]AACTGCCAGACAAAA | 26133 |
rs186289349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084891 | ATATGGCCCTGCTGT[A/G]AATAATAATGCTAAC | 26133 |
rs186394380 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005864 | GTATGGCCATGGCCC[A/G]GGGGGATAGTCACTA | 26133 |
rs186418840 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065167 | AAAGTTCCTGAATGC[A/C]AAGCAATGGCTTACA | 26133 |
rs186439510 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024092 | CGGTCACCACTCTCT[A/G]TCTGCACTGCACTGT | 26133 |
rs186444352 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043527 | GCTGGGATTACAGGC[A/G]TTAAGCCACCGTGCC | 26133 |
rs186451019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084027 | AAAGCAGGCCGGGCG[C/T]GGTGGCTCACACCTG | 26133 |
rs186455591 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067833 | CAAAAAGTATACTAG[C/T]GTGGGGAGAGGGGGA | 26133 |
rs186477388 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016203 | ATCTAGCAAAACCTC[A/G]TGCTCAGTACACACG | 26133 |
rs186529653 | snp | G/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072058 | GAGCATTTTTTCCTG[G/T]GTCTGTTGGCTGCAT | 26133 |
rs186559026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036978 | ACACACACACACACA[C/T]ACCCCTCCCATAATT | 26133 |
rs186565747 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056214 | GCAGGGTGAAACACT[A/G]CTCTGCATGTCTCAC | 26133 |
rs186570044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077297 | CAGTGAGATGAACCC[A/G]GTACCTCAGTTGGAA | 26133 |
rs186576131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060802 | CCCAAAACACTTTCA[C/T]GATAAAACAATCAAC | 26133 |
rs186749006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087480 | CACAACCCAGTCTGT[C/T]ACCAGATTGCCAAAC | 26133 |
rs186773056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039346 | GTTGTGAGTCACTCA[C/T]CTCTTGAAAAGCTAA | 26133 |
rs186782338 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012199 | CTCACAGAGGATGGG[G/T]GCATATGATGGAGGT | 26133 |
rs186791300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079079 | TCAAAAAATAGAAAA[A/G]GGGATGGAGAAAGAT | 26133 |
rs186814749 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014772 | TGGGTGGCACTTTTA[C/G]GTCCCAGAGCACTTT | 26133 |
rs186979643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077766 | AATCACAGGATAGTG[C/T]TGACCTCCCAAAATT | 26133 |
rs187017830 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072943 | TTCCATTTGTTTGTG[C/G/T]CCTCTTTTATTTCAT | 26133 |
rs187031865 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080215 | CAGTGTCTAACTGGG[A/C]ACAGTGTCTCATGCC | 26133 |
rs187038762 | snp | A/G | 1.67778e-05 | 0.00289631 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035308 | ATGCTGAGAAGGGCC[A/G]CTGCCAGGGAAAGAA | 26133 |
rs187040768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032412 | TTATTCTCTATTTAA[C/T]GACACATTATCAAAT | 26133 |
rs187048548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051229 | ACACACACAGTTTGG[C/T]AAATGGGAACCCCAA | 26133 |
rs187095607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008136 | TTGGACAAGGCACTG[A/C]AGTGACAAAGGCCCA | 26133 |
rs187105726 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025815 | TTTATCTGGTTGCTT[A/G]TGCTTCAGATGTCAT | 26133 |
rs187106885 | snp | G/T | 0.103082 | 0.202275 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087210 | CAGGCGTGGTGGCGG[G/T]CACCTGTAGTCCCAG | 26133 |
rs187169831 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012832 | GCCTGCCATAAGGAA[C/G]TCTGGAAAGACGGGA | 26133 |
rs187235654 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073586 | CGTTTATTGATTTGC[A/G]TATGTTGAACCAGCC | 26133 |
rs187287908 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070690 | GGCGTGAGTCACTGC[A/G/T]CCCGGCCAAACCTAT | 26133 |
rs187377803 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035906 | AAATACACAAGGAAT[C/G]AAAGCATATATACCA | 26133 |
rs187399577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075905 | TACACCAATCAGACG[C/T]AGATTTGGTCTTTTC | 26133 |
rs187410376 | snp | C/T | 0.00336097 | 0.0408557 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002189 | CAGCACAAGGAGTGA[C/T]GGCCTGACCCCCTGG | 26133 |
rs187414163 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093617 | CAGGATGGCACTGAC[A/T]CCCCCCACCCAACAC | 26133 |
rs187417135 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022015 | ATGTGTCAGACTTGC[C/T]GGCTTTATGACTTTG | 26133 |
rs187476484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090553 | TAATTTTTGTATTTT[C/T]AGTAGAGACGGGGCT | 26133 |
rs187505889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069216 | AATTCTGAAATCTTT[C/T]CTATCTCCCATTTCA | 26133 |
rs187517083 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027786 | AGGTTATTTAGTTTA[C/T]TGGCTTATATTGTTT | 26133 |
rs187645835 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055490 | AAAGTAGAACTACTA[C/G]AATCTAAAGTATAGG | 26133 |
rs187672416 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015583 | TTCTGGTGCCTCAGC[C/T]TCCCGAAGAGTTGGG | 26133 |
rs187735097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046542 | TACCCTTTCTCCTGA[A/G]ACTCAATGCACAGGA | 26133 |
rs187763584 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRPC4AP | GRCh38.p7 | 20:35009089 | GAAAGACTCTGCCAA[C/T]AGGGTGAGGCCCAGC | 26133 |
rs187807496 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003194 | GTAGGGCTCCTCAAT[A/G]TAGCTAACGAGAGCA | 26133 |
rs187813514 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022302 | CTGGGACTACAGGCA[C/T]GTGCCACCACGCCCA | 26133 |
rs187854369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081006 | TTCATCAATTTGCTG[A/C]AAATCACTGAACTGT | 26133 |
rs187860748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063100 | CCCCATGCTGTTCTC[C/G]TGATAACGAGGGAGT | 26133 |
rs187870981 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042668 | ACTAGCTTTTAAGAC[A/C]CAAGTTTCAGTTCAA | 26133 |
rs187887456 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018128 | ATTCATCCAGTGCAA[C/T]TGCCTCACTGCACAG | 26133 |
rs187900668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085920 | TCTTATTTGTTTCTT[C/T]AATCCTAAATGTAAG | 26133 |
rs187903401 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057190 | TAAAAAAAATAGTTT[A/T]AAAAAAATAAAACAG | 26133 |
rs187908821 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068733 | CACCATCTTGGACAG[G/T]TTGGTCTCGAACTCC | 26133 |
rs187922221 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045549 | CTACTTTTTTAATAT[A/T]TTTTTTTTTGAGATG | 26133 |
rs187930335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018736 | TAGCCTGCTCTATAG[C/G]AGGATGGTAGGCAGG | 26133 |
rs187989856 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086459 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs188060987 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026862 | GGTTTGTTGATTGCT[A/C]CTCTATAGAAATACT | 26133 |
rs188142779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040499 | TGGGGTCCTCCAGCC[A/G]GGGAGCTACACCATT | 26133 |
rs188153510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019505 | CAGCCCAGTTTATGC[C/T]CTGGCTTTCTCAAGA | 26133 |
rs188161008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038182 | AAATGTACTAAATGC[C/T]GCTGAGTTGTTCACT | 26133 |
rs188178322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037474 | GTACACACATGTTCA[C/T]AGCAGCACTATTCCC | 26133 |
rs188271997 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062216 | ATATGTAAAATGGTG[C/T]AGCTGCTTCAGAAAG | 26133 |
rs188305113 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089715 | GTAGCCAGGTGTGGT[A/G]GCACACGACTGTAAT | 26133 |
rs188393113 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078441 | CTTAGACTCGTCGTA[A/G]ATATATACTGGAAAT | 26133 |
rs188399451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058302 | AACACAACGAACACA[G/T]ATATTCTAACAGACA | 26133 |
rs188421722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021658 | ATGCCCTTCTCCTGC[C/T]ACCAACCAGACCCCC | 26133 |
rs188441382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061090 | AGAATACAGAAAATT[C/T]CTAAAGAATCCACTC | 26133 |
rs188469679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009815 | AGCAGGTAAGAGGCT[C/T]CTGTCTGTCCTGCTT | 26133 |
rs188526770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028382 | CAGGTGTGAGCCACC[A/G]CGCCCGGCCTCAAGA | 26133 |
rs188534961 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046997 | TCCCAGCCTCCCAAG[C/T]AGCTGGGACTACAGG | 26133 |
rs188548684 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080599 | ATATATTGTCTGATT[C/G]TATTAATTTAAAATG | 26133 |
rs188558538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041613 | CAAAAAAGCCCAGCT[A/G]ACCAGAACAGTTCAT | 26133 |
rs188685427 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050568 | AAATATAAATATTAG[C/T]TGGGTGTGGTGGTGC | 26133 |
rs188686983 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014521 | GCCCCATGAGCAATC[A/G]AAAGAGACCTTAAGA | 26133 |
rs188695325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034819 | AAGAAAAAGAGACGA[A/G]GAGAGAAGTTTCTAG | 26133 |
rs188715843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012254 | GGCATGTTCTGTTAG[C/T]TCAAATGCAAGGTTT | 26133 |
rs188727075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091850 | AACAATCTTAAAAGG[C/T]AGGTTACTAATTCTC | 26133 |
rs188737373 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075353 | GTTTCTTCCTAGCAT[C/T]GAAGGTCTTTACAAT | 26133 |
rs188751037 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088172 | AAGTATGTTTCAGTC[A/G]CTATTTTAAGTGCTT | 26133 |
rs188755749 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053846 | TTTTTCTTTAAAAAA[A/T]TGTGGCTACAAGGAA | 26133 |
rs188806556 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005469 | AAGAGGAAGGTCTTT[C/T]TCTGGTTTTCTTTGC | 26133 |
rs188811883 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052453 | GGAGCTACAAACTAG[C/T]ATCCAGTAGGCCAAG | 26133 |
rs188815257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078250 | CAAAGGAGAGCAGCC[A/G]ACTTCCAAACCCACC | 26133 |
rs188817363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037911 | AGCTAGGTTTGTGCA[A/G]GTACACTCTATGACA | 26133 |
rs188934194 | snp | A/G | 0.000320186 | 0.0126487 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008631 | TGGCTCTGCAGCCCC[A/G]CAGAATCGGCAGGTA | 26133 |
rs188957875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032012 | CTCATGCCTCAGCAA[C/T]CCAAGTAGCTGGGAT | 26133 |
rs188984034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072753 | TTGGCTTAGGATTGT[A/C]TTGGCAATGTGGGCT | 26133 |
rs189056135 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073967 | TTATTGGTCTATTCA[A/G]GGATTCATTCAACTT | 26133 |
rs189057869 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058036 | AATTTTGCACAAACT[A/G]TTTAAAATAAGCATG | 26133 |
rs189062260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023394 | CAATTAGAAACTAAA[C/T]AGAAGTTAAGTTCTC | 26133 |
rs189070460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043427 | AATTTTTGTATTTTT[A/G]GTAGAGATGGGGTTT | 26133 |
rs189147897 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084171 | GCCAGACTTGGTGGC[A/G]GGCACCTGTAATCCC | 26133 |
rs189300937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065576 | AAATACTACCAGCAG[A/C]AGGACAGCAAGAGAG | 26133 |
rs189318394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071826 | GGCTGGGTCAAATGG[C/T]ATTTCTAGTTCTAGA | 26133 |
rs189341903 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047058 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCCTGTT | 26133 |
rs189386439 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087157 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 26133 |
rs189397112 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070560 | GGACTACAGGCGCCC[A/G]CCACTGCGCCCGGCT | 26133 |
rs189558886 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060178 | TCTTTGAGGCGAGTA[C/T]TACCCTGATACCAAA | 26133 |
rs189567480 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019877 | GCCATCTCCCCAACA[A/C]CAGGTGTAGGTAATC | 26133 |
rs189567500 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086763 | AATCTGGCTGGGCAC[A/G]GCGACTCACATCTGT | 26133 |
rs189577576 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043101 | TATATCTTGGAGATT[C/T]TTCTATAGCAGTACA | 26133 |
rs189582884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010750 | ACTGCTGGGTCCTGT[A/G]TTCCCAGGACACCAG | 26133 |
rs189592640 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087300 | GCTGAGATTGCACCA[C/T]TGCCCTCCAGCCTGG | 26133 |
rs189596703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082454 | ATGTTTGGAAAATAA[G/T]ATACTTCTCAAAAAT | 26133 |
rs189602221 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047994 | CATTTATCAGTAGTA[C/T]ACAAGTGTTTCCACT | 26133 |
rs189612303 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003823 | CCTTCCTCTTCCCCA[C/T]GCCCACCTCCCACCC | 26133 |
rs189639847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077361 | GCTGGGTACCATAGA[C/G]TGGAGCTGTTCCTAT | 26133 |
rs189797866 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038839 | GCACTTTGGGAGGCC[C/G]AGGTGGGTGGATCAC | 26133 |
rs189817318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020980 | AGACTGCCTAGAAAC[A/G]CTCCATACAGCAAGG | 26133 |
rs189823809 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078832 | ACACTTTGGGAAGCC[A/G]AGGCAGGTGGATCAC | 26133 |
rs189825883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040165 | GCCCTTTAGGGAATG[C/T]GGTGGTGTGATGGTT | 26133 |
rs189840810 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060981 | CATTGTACTGAGTGT[C/T]CTAAGGCAACTAGAG | 26133 |
rs189851319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033383 | AACCTTGGGCATGTA[C/T]AGAGTCTCCCTGGGA | 26133 |
rs189880629 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064372 | TGAGACTAGACAGTT[C/G]AGCTTGAGGGTCTGA | 26133 |
rs189883557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079815 | TCAGCTCAGGAGTTC[A/G]AGACCAGCCTGAGCA | 26133 |
rs189888727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022485 | TTTAAGAGGGCATTG[A/G]TCAGAGTCAGGAGAG | 26133 |
rs190050970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087560 | TATCCTAGAGCCCAG[C/T]GTTTACTCAGTCTAT | 26133 |
rs190060617 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072142 | GGGCTGTTTGCTTTT[C/T]TCTTGTAAATTTAAG | 26133 |
rs190072755 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049109 | AGGCTCAGGACAGAT[G/T]AGGACTGGGGAGGTG | 26133 |
rs190094050 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064983 | AGAGTCACAGAAATG[A/G]AAACAACAGGGCAAA | 26133 |
rs190099381 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013252 | AGATTAAGCTAATGT[C/G]GCCCCCTTCCTGCTA | 26133 |
rs190163287 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037304 | GTGAGCGGAGATCGC[A/G]CCACTGCACTCCGGC | 26133 |
rs190171564 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056854 | AGCCGGGTATGGTGG[A/T]GGGCGCCTGTAATCC | 26133 |
rs190202957 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011406 | CAGGCACAGCACAGA[C/G]TACTGGTTGTCTACC | 26133 |
rs190213238 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030670 | TTCAAGTTGCAATTT[A/G]GTGTCATGATACTCC | 26133 |
rs190367142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091642 | GGGGTGGGGGAGGGT[A/G]GAAGAAGTAGTGGAC | 26133 |
rs190370962 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013982 | TAAATAAGAAAACTG[A/G]CCCTGGGACAGCTGC | 26133 |
rs190384129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053571 | ATCTCCCTGTGCCTA[G/T]CTCTGTCATTGGCTA | 26133 |
rs190387430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083323 | ACACACTCTTGGCTG[G/T]GCACAGTGGTTCACA | 26133 |
rs190434074 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010040 | AGGTGACATGAATAC[A/G]ATGCCTGGCACACAG | 26133 |
rs190628499 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074519 | TTTCTGCCTTCATTT[C/T]GTTATGTACCCAGCA | 26133 |
rs190630503 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033783 | GATCACTTGAGGCCA[C/G]GAGTTTGAGACCAGC | 26133 |
rs190644960 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029026 | AGAGGCCAAGGCAGG[C/T]AGATCACCTGAGGCC | 26133 |
rs190685691 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040564 | TGAGCCATGCTAATG[A/G]CTTCTCAGGTTCTCC | 26133 |
rs190746195 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008381 | ACAGCACAGCTCTAG[A/C/G]GAATTCATGGCAGGG | 26133 |
rs190752530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026280 | AGTGCAGTGGCACAA[G/T]CACAGGTTACTGCAG | 26133 |
rs190758616 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045527 | AGGTGCGTGTCATTA[C/T]ACCTGGCTACTTTTT | 26133 |
rs190766899 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075664 | CTTTGTGGGTAACCC[A/G]ACCTTTCTCTCTGGC | 26133 |
rs190802534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068037 | TTAATAAAGCTGATT[A/T]AAAAAAACTATGGAA | 26133 |
rs190808765 | snp | A/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093005 | CACTGCCGGTTTCTC[A/T]GGCCCCCGGGCCCAG | 26133 |
rs190846123 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024529 | ATCCGCTAGTATAAA[C/T]ATATCACATTCTGGC | 26133 |
rs190856321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043696 | AATTTATAAATTAGG[C/T]ACACTAAGAGATTAA | 26133 |
rs190862131 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016079 | GCTTCCTCCAAATCA[A/G]TTTGTCAAACAAATT | 26133 |
rs190914770 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020392 | TGGCTGTTTGCTCCA[A/G]GCTGTCCCGCGCTGC | 26133 |
rs190970473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039380 | AAGCTAAGACCTTCT[A/C]CCCAGAAAAAAATTC | 26133 |
rs191029727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061104 | TCCTAAAGAATCCAC[C/T]CAAAAAAACTATTAG | 26133 |
rs191110375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087864 | ACCCATTACAAATTA[C/T]GTGGCCAGTAGTCAT | 26133 |
rs191117586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072483 | AGGAAAGGATCCAGT[G/T]TCAGCTTTCTACATG | 26133 |
rs191221587 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088741 | CAGGTCCACCTTACT[C/T]TAAAATCTGATTTTT | 26133 |
rs191263399 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080458 | GTGAGCCAAGACTGC[A/G]CCACTGCACTTCAGC | 26133 |
rs191264415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007154 | TGGATTTTATAATTC[A/G]TGGGTCAGTTTCTTG | 26133 |
rs191269294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040841 | TCCCCTAACAAATCC[C/T]ACCTCATAAATCCTA | 26133 |
rs191273910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084454 | AAAGGGTATATGTAT[A/G]TATGTGTGTATATAT | 26133 |
rs191278183 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044316 | GGATCACCTGAGCCT[A/G]GGGAGGTCAAGGCTG | 26133 |
rs191402076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012621 | GGAGGGAAGAATCCT[C/G]CAGCTGCTCAGTAAG | 26133 |
rs191488503 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032662 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTCT | 26133 |
rs191495043 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051544 | GACGATCACATTAAA[C/T]AGGACACTAAAGAAA | 26133 |
rs191506226 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025683 | TATTTGCAAAGATGT[C/T]CCACCCTGCCTTACC | 26133 |
rs191518816 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067365 | CAAAATGACAGATAA[C/G]AAGTGTTGGCAAGGA | 26133 |
rs191522672 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012920 | TCCAGGGCCTCCTCT[C/T]GAGCTGAGGTCAGGG | 26133 |
rs191545144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090167 | GAGCGGAAGGGCACA[A/G]CATGGAATAAATTAA | 26133 |
rs191551192 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073327 | GTTGAATAGGAGTGT[A/G]CTGAGAGAGGGCACC | 26133 |
rs191576947 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042832 | GAATAGTGTTTTGTT[C/T]TTAAGTAATATATTT | 26133 |
rs191599074 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081025 | TCACTGAACTGTACA[C/T]TTACAATGGGTAAAT | 26133 |
rs191607270 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063638 | GTGAGGCAGGAAGAT[C/T]ATTTGAGACCAGGAG | 26133 |
rs191693108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035456 | TGAATGTCAAACCAA[A/G]GTAAATAGTAATTAT | 26133 |
rs191736433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017013 | TCTAAAATTGCAAAT[C/T]CATAATCCCTTTAAA | 26133 |
rs191825008 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056108 | AGATGGGTTGTCTCA[C/T]AATCCTGAGACAACG | 26133 |
rs191826559 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094167 | AACAAAAACATAAAG[C/T]GGGGAAAGGACACCC | 26133 |
rs191988987 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054793 | TAACAACTGCTACAA[A/C]ATTCTGCCTCCCCGT | 26133 |
rs192008975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050234 | TGAGAACATAACACA[A/G]TGAGATGGTATTTCC | 26133 |
rs192024492 | snp | A/G | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090565 | TTTTAGTAGAGACGG[A/G]GCTTCGCCATGTTGG | 26133 |
rs192025420 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015303 | CCACGCCCGGGAGCA[C/T]GGTTCTATAGGTGGA | 26133 |
rs192037722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012202 | ACAGAGGATGGGTGC[A/G]TATGATGGAGGTGCC | 26133 |
rs192041157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084988 | CGAGTAAGAAGGAAT[C/T]GAATGTGTGAATTAA | 26133 |
rs192042327 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079178 | ATCAGAAATAAAGTG[C/G]GTCATTTCATAATGA | 26133 |
rs192077768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062464 | TGGATAAATAAGATG[A/T]GGTCTATCCATACAG | 26133 |
rs192089815 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076336 | TTGGAGGAGAAGAGG[C/T]GCTCTGATTTTTAGA | 26133 |
rs192112138 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086960 | ATCGCTTGAACCCGG[A/G]AAGCGGAGGTTGCAG | 26133 |
rs192115208 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036132 | GGTGGAAATTCTGAT[A/C/T]GGCATATTAGAACAT | 26133 |
rs192251783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028404 | GCCTCAAGACACTTC[C/T]TAATTTTGTTTGTGA | 26133 |
rs192252134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046772 | GTAACTTGTAGCTCA[A/C]CAGTTCCTCTAGCCC | 26133 |
rs192263301 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047025 | AGGCATGCACCACCA[C/T]GCTGGGCTAATTTTT | 26133 |
rs192267737 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086461 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs192276947 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069746 | AGGAGTTTGAGACCA[A/G]CCTGGCCAACATGGC | 26133 |
rs192285673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006223 | TCCCACCCTCACTCC[C/T]TACCCACAAGCAGCC | 26133 |
rs192297327 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009901 | CGAGACAAGGCGGTG[A/G]GGCAGTGCGGAGCAC | 26133 |
rs192349807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046345 | TGTACTACATCAACT[C/T]TTCTCATTTTGAACC | 26133 |
rs192355623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018974 | GGGCACTAAAAGAAA[C/G]GACTGCTATATGGAT | 26133 |
rs192355774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060821 | AAAACAATCAACAAG[A/G]AATAGAAGAGAACTT | 26133 |
rs192366502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038150 | ACTAGATAGAGGTGG[C/T]AGCTGCACAACACTG | 26133 |
rs192371182 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086340 | AACCACTGAATACTT[C/T]TGTGTCCTTTAATGG | 26133 |
rs192383127 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068785 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCG | 26133 |
rs192400825 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031519 | GGGATTACAGGTGTG[C/T]GCCAACATGCCAGGC | 26133 |
rs192474598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072754 | TGGCTTAGGATTGTC[C/T]TGGCAATGTGGGCTC | 26133 |
rs192501035 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032313 | TACAGGTGTGAGCCA[C/T]CACACCTGGCCTGAT | 26133 |
rs192559769 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002935 | GCATGGTACCCTGTC[C/T]TCATTATGGGGACTG | 26133 |
rs192568807 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022107 | CAGACTGAATGGGAA[C/T]GTAAGAGAAGCCCAG | 26133 |
rs192576015 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042084 | TGTTACATATGTATA[C/T]ATGTGCCATGTTGGA | 26133 |
rs192639285 | snp | C/T | 0.0164374 | 0.0891544 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069285 | AGTAGTAATAATAAA[C/T]AGCTACTTACATCAA | 26133 |
rs192656021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027974 | ACCTTTGGTTTTACA[A/G]ATTTTCTCTACTGTT | 26133 |
rs192736968 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | TRPC4AP | GRCh38.p7 | 20:35009112 | GGCCCAGCGTACTCC[A/G]TGCCTGAGGTTCACT | 26133 |
rs192808135 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050760 | AACAAAAAAACAAAA[C/T]CCCCAAGGGGTATGA | 26133 |
rs192810296 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022303 | TGGGACTACAGGCAT[A/G]TGCCACCACGCCCAG | 26133 |
rs192840123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082511 | GGATATATGAAAATA[C/T]CCTGAAAGATAATGA | 26133 |
rs192859482 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080626 | AATGTCCAGAATAAG[C/T]ATATCCAGAGACAGA | 26133 |
rs192866513 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013451 | AGGCATAGTTGCTGC[A/G]CCTGTAATTCTGGCT | 26133 |
rs192876714 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052551 | CCCACGCTGGAGTGC[A/G]GTGGTGCAATCTCAG | 26133 |
rs192997104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037733 | TCAACAACGACCACA[C/T]AGAAGACGGTGGTGC | 26133 |
rs192999132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077967 | TTTTAAAAGCCAACG[A/G]AAGGGAAAAAAAAAA | 26133 |
rs193023829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027609 | GTGTGAATTCTTCTT[C/G]AAACATTTGGTAGAA | 26133 |
rs193041532 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058077 | TTCATTCTACGGAGA[C/G]AAAGGATAGTTGATA | 26133 |
rs193079394 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033574 | CTAATTCAATTAAAT[G/T]CAGGAAGGGGTAATT | 26133 |
rs193081523 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074185 | ATTAGTCTTGCTAGC[A/G]GTCTTTCAATTTTGT | 26133 |
rs193200293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018195 | ACACAGCTGGGAAGA[A/G]AGGGGCCTTCTAAGG | 26133 |
rs193203917 | snp | A/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057516 | TAGGTATACTTACTT[A/T]TCAGTTTCTGTCCCC | 26133 |
rs193212641 | snp | A/G | 5.04172e-05 | 0.00502056 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008639 | CAGCCCCGCAGAATC[A/G]GCAGGTACTTTTCCC | 26133 |
rs193219935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078434 | GAGTGGACTTAGACT[C/T]GTCGTAAATATATAC | 26133 |
rs199646072 | snp | A/C | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056510 | AATATAAATCCTCTT[A/C]ATAACCACTACTGCA | 26133 |
rs199649804 | snp | A/G | 0.000202286 | 0.0100549 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035104 | CTCCCGATCACTCAG[A/G]GGACCCATCCTTCCA | 26133 |
rs199708625 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026042 | ACTACTACTGTTTCC[A/T]CCAATGAATGGTCTT | 26133 |
rs199716079 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049255 | ATTTCGATCATAGCT[-/G]GTTTTTTTTTTTTTT | 26133 |
rs199725379 | snp | C/T | 3.3168e-05 | 0.00407221 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003112 | CCACGCTCACCCACA[C/T]TGGCCCAGCAGCCTC | 26133 |
rs199725811 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076382 | GCTCTGGTTTCTCCC[C/T]ATCTTTGTGGTTTTA | 26133 |
rs199765862 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043809 | TCAGTTAATATTTTC[A/G]GATTGCAGTTGACCA | 26133 |
rs199774937 | in-del | -/A | 0.02016 | 0.0983543 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051433 | CACCTCAGCCTCCTG[-/A]AATCACTGGGACTAC | 26133 |
rs199804934 | snp | G/T | 0.000428456 | 0.0146303 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010225 | CACCTCAGGGATGTT[G/T]GCCTTGAGAGAGATG | 26133 |
rs199812167 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079896 | GGGTGGTGGTGCACA[C/T]CTCTGGTCTCAGCTA | 26133 |
rs199814033 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086190 | TCTTGAACTCCTGAG[C/G]TTAAAGAATCCGTCT | 26133 |
rs199840514 | in-del | -/T | 0.0217236 | 0.101931 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071574 | TGCTCAGAATGATGG[-/T]TTCCAGATTCATCCA | 26133 |
rs199848601 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034160 | CCGTCTCAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 26133 |
rs199856335 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074116 | TGTGGGATTGGTGGT[A/G]ATATCCCCTTTATCA | 26133 |
rs199859580 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090949 | GTACTTTTTCTAAAG[G/T]TTATGTGCTCACTAA | 26133 |
rs199888242 | snp | A/C | 3.30115e-05 | 0.00406259 | stop-gained, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069388 | CAAATGCCATAGCCT[A/C]CATGGAGAGAAGAGG | 26133 |
rs199958785 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070917 | TAGTAAGTTTCAAAT[-/T]AAGTACTTACTTAAT | 26133 |
rs199961940 | snp | C/T | 0.000201093 | 0.0100253 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035307 | AATGCTGAGAAGGGC[C/T]GCTGCCAGGGAAAGA | 26133 |
rs200035230 | snp | A/C/G | 0.00163032 | 0.0285102 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003550 | GCCGCAGGTACAGGG[A/C/G]CAGCCGCTCTTTCCG | 26133 |
rs200053799 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084664 | TTTATATGCATATAT[A/G]TGTATATGTATATAT | 26133 |
rs200073647 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049490 | GTTCAGATAGCGGTA[C/T]AGTGGTAAGAGAATG | 26133 |
rs200081917 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084496 | TATATATGTATATAT[A/C]TATATATGTATATAC | 26133 |
rs200117057 | in-del | -/TCT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076256 | CATCTGAAGCCTTCT[-/TCT]CTCAACTCATCAAAG | 26133 |
rs200126584 | in-del | -/AC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080542 | TCCATCTAAAAAAAA[-/AC]AAAAAAAAAAAAAAC | 26133 |
rs200155432 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047945 | TGCCTGTTCAACTAC[A/C]AAACAAAAAAAAAGA | 26133 |
rs200161670 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039794 | TCTTCTAAATCGACA[-/G]AAGAACAACTGGTAG | 26133 |
rs200170032 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086578 | GTGTGTGTGTGTGTA[G/T]ATATATATGAATAAG | 26133 |
rs200179978 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076127 | GTCATTTAAGGTCTT[C/T]TCTATGCTGTTTATT | 26133 |
rs200202509 | snp | G/T | 0.0869704 | 0.189529 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054969 | CCCCAGTGGCAGGGG[G/T]ACTTACACAGACACA | 26133 |
rs200230791 | snp | A/G | 1.97619e-05 | 0.00314333 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004579 | TCGGCAACTGTGGAG[A/G]GAGGCAGGGGTGCAG | 26133 |
rs200247321 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013160 | AGCCTGCTTCTCTAA[A/G]CCTCTGTCCTCATGT | 26133 |
rs200256872 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025770 | TCTGAAGAACAAAAA[-/G]TTTTAATTTTGATGA | 26133 |
rs200260477 | snp | A/C/G/T | 0.000348967 | 0.0132049 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001982 | ACCTGGCCAAGTATC[A/C/G/T]CAAGGCCCAGCACGA | 26133 |
rs200280850 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028224 | TCCTTTTTTTTTTTT[G/T]ATGGAATCTCACTCT | 26133 |
rs200305739 | snp | A/G | 4.9958e-05 | 0.00499765 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002066 | TGCGGGCACGGACCC[A/G]GGACGCCCTGGGCCC | 26133 |
rs200322275 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089549 | TATTATATATTTGTT[A/T]ACTACAATGAAAAAA | 26133 |
rs200326780 | snp | A/G | 0.000230897 | 0.0107422 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078155 | TGTTTGTCCCTCTCC[A/G]TCAAAAAAGTCTCAG | 26133 |
rs200383557 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012960 | GGAGATCGAGGCCTT[C/T]CGAAGACAGCCCAAC | 26133 |
rs200384977 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076545 | TCCAGACCCTGTTTG[C/T]CTGGGTATCACCAGC | 26133 |
rs200386644 | snp | A/G | 6.70443e-05 | 0.00578945 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008644 | CCGCAGAATCGGCAG[A/G]TACTTTTCCCCAGAC | 26133 |
rs200534243 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075541 | TGGCTGGATATGAAA[C/T]TCTGGGTTGAAAATT | 26133 |
rs200572611 | in-del | -/GTAGA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049486 | CCAGTTCAGATAGCG[-/GTAGA]GTAAAGTGGTAAGAG | 26133 |
rs200574010 | in-del | -/TG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048211 | GATTTGTAAGAATTC[-/TG]TTTTTTTTTTTTTTT | 26133 |
rs200641430 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049488 | CAGTTCAGATAGCGG[A/T]AAAGTGGTAAGAGAA | 26133 |
rs200642510 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080269 | ACTTTGGGAGGCCAA[A/G]GTGGACAGATCACTT | 26133 |
rs200642753 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086479 | TGTGTGTGTGTGTAT[A/G]TGTGTGTATATATAT | 26133 |
rs200658674 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051879 | CAATTTATCAAAGTG[C/G]TACTCCTTTTACAGA | 26133 |
rs200707079 | snp | A/G | 0.00014868 | 0.0086208 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003473 | CCAGAAGCGCAGCAG[A/G]TTGTGGAAGTTGTTG | 26133 |
rs200777856 | in-del | -/A/ACACACA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068963 | ACACACACACACACA[-/A/ACACACA]CACACACACACACAC | 26133 |
rs200798594 | snp | A/C | 5.00363e-05 | 0.00500156 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050008 | GTCTGTCACAAGAAG[A/C]AAAGGCAGAATAGGT | 26133 |
rs200803162 | snp | A/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056511 | ATATAAATCCTCTTA[A/T]TAACCACTACTGCAT | 26133 |
rs200832490 | in-del | -/T/TT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038289 | ACCATTTTTTTTTTT[-/T/TT]AACATATCAGCTTGG | 26133 |
rs200843794 | snp | C/T | 4.94645e-05 | 0.00497291 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049941 | TGTCATCAATGTAAA[C/T]AGGAAGATCACAAAG | 26133 |
rs200862858 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048210 | TGATTTGTAAGAATT[C/T]TGTTTTTTTTTTTTT | 26133 |
rs200883608 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077982 | AAGGGAAAAAAAAAA[-/A]CAGCAGACATCTTGT | 26133 |
rs200916753 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076854 | TCAGCTATGCCCTGC[C/T]CCCAGAGGTGGAGTC | 26133 |
rs200930585 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078163 | CCTCTCCGTCAAAAA[A/G]GTCTCAGTGAACTGT | 26133 |
rs201005202 | in-del | -/CT/TCTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030864 | CTTTACTTAAGGTGC[-/CT/TCTT]TCTTTGTTTTTCATG | 26133 |
rs201022117 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085100 | TACTGGCTCTCCTGT[A/T]TCCTGGATCCTTCTC | 26133 |
rs201023294 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036960 | ACGCGTGCGCACACA[A/C]ACACACACACACACA | 26133 |
rs201037229 | snp | A/G | 1.64955e-05 | 0.00287184 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021302 | TGGGTTCTGGCTGAC[A/G]TGTGAGGCAGGCCAT | 26133 |
rs201082619 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016797 | AACAGAGAACATACA[C/T]TGGCAATTCATGCCA | 26133 |
rs201093403 | snp | A/G | 0.00399202 | 0.044498 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003083 | GGAACAGGGCAGGGC[A/G]TGTGGCATCGTACCC | 26133 |
rs201107814 | snp | A/G | 5.41648e-05 | 0.00520379 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003602 | CAGGCTGGTGTTGAG[A/G]CAGCTGACGTTCTCC | 26133 |
rs201111349 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076220 | ATCCTCCTTTAGCTC[A/G]GAGAAGTTTGTTATT | 26133 |
rs201116259 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075104 | TTTTTTTGTTTTCCA[C/T]TTGCTTGGTAGATCT | 26133 |
rs201131995 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089550 | ATTATATATTTGTTT[A/T]CTACAATGAAAAAAT | 26133 |
rs201207284 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024824 | AGAGAGAGACCGTCT[-/C]CAAAAAAAAAAAAAA | 26133 |
rs201234738 | snp | C/T | 0.000627663 | 0.0177042 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006560 | ACTCGCTGTCCACAA[C/T]GCAGTAAAGGATGTG | 26133 |
rs201325275 | snp | A/G | 0.000379422 | 0.0137683 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010192 | CTGCACTCACCTGTC[A/G]GTGTTGAGGACAGCT | 26133 |
rs201340281 | snp | C/T | 4.94539e-05 | 0.00497238 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003202 | CCTCAATGTAGCTAA[C/T]GAGAGCAGAGGGTGA | 26133 |
rs201434451 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045071 | CATTCTTGCTACAGA[-/T]TTGCTTTTTTAAAAA | 26133 |
rs201484755 | in-del | -/TT | 0.0119091 | 0.0762411 | intron-variant, splice-acceptor-variant | TRPC4AP | GRCh38.p7 | 20:35007868 | CTGTCTGGAAGGGGC[-/TT]TGTGTCACAGAAAGG | 26133 |
rs201487624 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047983 | CTGCTGATAAACATT[C/T]ATCAGTAGTATACAA | 26133 |
rs201495843 | snp | A/G | 3.31807e-05 | 0.00407299 | downstream-variant-500B, synonymous-codon | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002010 | CGAGCTGGATGATGC[A/G]GAGGAGCGGGCAGAC | 26133 |
rs201507668 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055358 | TATATCTAGGATTTG[-/T]TTTTTTTTGTTTTTT | 26133 |
rs201508653 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086487 | TGTGTATGTGTGTGT[A/G]TATATATATGTGTAT | 26133 |
rs201517077 | snp | G/T | 0.0904765 | 0.19249 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008645 | CGCAGAATCGGCAGG[G/T]ACTTTTCCCCAGACT | 26133 |
rs201540883 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021584 | CTCATCAACTTTAAC[A/G]TAAAGTAAAAATATT | 26133 |
rs201554917 | in-del | -/TAT | 0.0279526 | 0.114869 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026816 | TTATTTTTTTGATCC[-/TAT]TATAAATAAAATTGT | 26133 |
rs201578373 | snp | C/T | 0.000148545 | 0.00861688 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035254 | GACTCTGACACCTTT[C/T]GAGTCGCCAGTTTGC | 26133 |
rs201625865 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085728 | CAGGTATCACATGGG[G/T]TTTCTCTTGAAGTAC | 26133 |
rs201683882 | in-del | -/TT | | | splice-acceptor-variant, intron-variant | TRPC4AP | GRCh38.p7 | 20:35044712 | TAGTCGGATCATTTC[-/TT]CTACAGAAGACAAAA | 26133 |
rs201736118 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079125 | AAAGATGGAGTAGTT[A/G]TATTAATTTCAGAGA | 26133 |
rs201750864 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083450 | CTAAAAATACCAAAA[-/T]AAAAAAAAATTAGCT | 26133 |
rs201781649 | in-del | -/CACAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068964 | ACACACACACACACA[-/CACAC]ACACACACACAAAAA | 26133 |
rs201783281 | snp | C/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094145 | CCAACTGATCTTCGA[C/T]AAAGCAAACAAAAAC | 26133 |
rs201797237 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002865 | ACAGAGCTAATGCTA[A/C]ATGTCCTCTTACCTC | 26133 |
rs201809090 | snp | A/C/G | 3.30252e-05 | 0.00406346 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049976 | TCTTTTCTGCCAAAC[A/C/G]CTTTGTAACTCCCTC | 26133 |
rs201842813 | snp | A/G | 1.6797e-05 | 0.00289797 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069451 | ATACATTGTTTTAGT[A/G]ACCAACACAGACCAG | 26133 |
rs201870674 | in-del | -/CTT | 0.364817 | 0.222075 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076251 | CTGATCATCTGAAGC[-/CTT]CTTCTCTCAACTCAT | 26133 |
rs201872741 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075924 | TTTGGTCTTTTCACA[C/T]AGTCCCATATTTCTT | 26133 |
rs201902537 | in-del | -/T | 0.450357 | 0.149522 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075085 | CCTGCTTTTTTTTTT[-/T]GTTTTCCACTTGCTT | 26133 |
rs201903754 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089551 | TTATATATTTGTTTA[A/C]TACAATGAAAAAATT | 26133 |
rs201920327 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084494 | TGTATATATGTATAT[A/C]TCTATATATGTATAT | 26133 |
rs201952218 | in-del | -/TTTA | 0.0126979 | 0.078662 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071263 | ATAACTTACATGGTT[-/TTTA]TTTATTTATTTTTGC | 26133 |
rs201983846 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009938 | CTTCTGGCAGGTGAC[A/C]TCTCTGAGGCTCACC | 26133 |
rs201995082 | snp | A/G/T | 0.000395755 | 0.0140615 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035236 | AAGCTGGCTGTGCCC[A/G/T]TTGACTCTGACACCT | 26133 |
rs201996680 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054594 | GCTCAATATATGGGC[A/G]GGGCTTCTGGTTCTC | 26133 |
rs202021508 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050392 | CACCTTTGGAACTCC[-/A]TTTTTTTCATCAGTA | 26133 |
rs202043337 | snp | A/G | 0.000131815 | 0.00811728 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044644 | CCGGCAGAAATTAGC[A/G]AGCTGCTGCTGATCG | 26133 |
rs202047781 | snp | A/G | 5.28788e-05 | 0.00514165 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003596 | GATCACCAGGCTGGT[A/G]TTGAGGCAGCTGACG | 26133 |
rs202055388 | snp | A/C/T | 6.6874e-05 | 0.00578209 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004604 | GTGCAGCAGGTCAGG[A/C/T]TTAGGCCCAGTGGCT | 26133 |
rs202059204 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060777 | AGAAAAAGCGTTTGG[-/A]AAAAAAAAACCCAAA | 26133 |
rs202081802 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086471 | TGTGTGTGTGTGTGT[A/G]TGTGTATGTGTGTGT | 26133 |
rs202104018 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024835 | GTCTCAAAAAAAAAA[-/C]AAAAAAAAAAAAAAA | 26133 |
rs202109042 | in-del | -/TG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084643 | ATATGTGTATATGTA[-/TG]TATGTTTATATGCAT | 26133 |
rs202151604 | snp | C/T | 8.2969e-05 | 0.00644031 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002009 | ACGAGCTGGATGATG[C/T]GGAGGAGCGGGCAGA | 26133 |
rs202197464 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045759 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 26133 |
rs202208296 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089546 | CTATATTATATATTT[A/G]TTTACTACAATGAAA | 26133 |
rs202216379 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083963 | TCAAATGATTTCTTT[-/A]AAAAAAAAAAAAAGT | 26133 |
rs202228156 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081813 | CAACATGATGAAACC[A/C]TGTCTCCACTAAAAA | 26133 |
rs367583493 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074059 | TTCTAGTTTATTTCC[A/G]TAGAGGTGTTTATAG | 26133 |
rs367584561 | snp | A/G/T | 9.97845e-05 | 0.00706281 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007500 | AGGACACAGCAACGC[A/G/T]TGGGCTGGGGGGAGA | 26133 |
rs367589701 | snp | A/G/T | 3.29773e-05 | 0.00406051 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049911 | GGTTGCTGTTTGTAA[A/G/T]AATGTCTTCTTACTT | 26133 |
rs367591346 | snp | C/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35092857 | CGGCGGAGGGGTCGC[C/T]GCAGCGCCCCCAGTG | 26133 |
rs367597577 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056955 | CATGCCACTGCACTC[C/T]AGCCTGGGCAACAGA | 26133 |
rs367598874 | in-del | -/AGA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059754 | CGACGAAGAAGAAGA[-/AGA]CGAAGAAGACGACGA | 26133 |
rs367601042 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029704 | GCAGTGGCGCGATCT[C/T]GGTTCACTGCAAGCT | 26133 |
rs367630083 | snp | A/C/G | 6.79999e-05 | 0.00583061 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035094 | CAAGGAAAAGCTCCC[A/C/G]ATCACTCAGGGGACC | 26133 |
rs367643359 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065042 | TATACTACACCAATT[C/T]TTCTCAAAAGAGATC | 26133 |
rs367651311 | snp | C/G | 5.01299e-05 | 0.00500624 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069435 | TTTTAAAAAAAAGTA[C/G]ATACATTGTTTTAGT | 26133 |
rs367661914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078794 | GAAAAGGCCAGGCAC[A/G]GTGGCTCACACCTGT | 26133 |
rs367672546 | snp | C/T | 5.3406e-05 | 0.00516722 | downstream-variant-500B, intron-variant, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002160 | TACTGCTCACTCAGC[C/T]ATCCCTTTCTCCTCA | 26133 |
rs367704685 | snp | C/T | 8.75818e-05 | 0.00661689 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004538 | CCTGGGATATGTAGG[C/T]GAGCAGGCGGCATTC | 26133 |
rs367725575 | snp | C/T | 6.60055e-05 | 0.00574442 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010258 | ACTGAGTTCATTCAG[C/T]TCCTGGTTGTTGAGT | 26133 |
rs367754330 | snp | C/G | 3.4353e-05 | 0.00414431 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003545 | CAGCAGCCGCAGGTA[C/G]AGGGGCAGCCGCTCT | 26133 |
rs367772252 | snp | A/C/G | 1.68105e-05 | 0.00289914 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050025 | AAGGCAGAATAGGTT[A/C/G]TAAGTACAAAATAAA | 26133 |
rs367802894 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029628 | TTCCCAAGTTACTTT[C/T]TTTTTTTTTTTTTTT | 26133 |
rs367824846 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079746 | AGGAGTATTATGAAC[C/T]GTTTGCCCCAATATT | 26133 |
rs367845366 | snp | A/C | 4.94238e-05 | 0.00497086 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044593 | GTGCTTGTCATCATT[A/C]CCTGTATCCATCTCT | 26133 |
rs367845912 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070928 | CAAATAAGTACTTAC[C/T]TAATGAATAAAGAAA | 26133 |
rs367885334 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008004 | ATGTGTGTGGGAAGC[A/G]GACGAACACATGCAG | 26133 |
rs367936626 | snp | C/T | 0.000613248 | 0.0174999 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078019 | TAGAGGCCCTGAATA[C/T]GCCCCTCCAAGGTCC | 26133 |
rs367979445 | in-del | -/TG | | | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012606 | GCACACCTCCTTGTG[-/TG]GAGGGAAGAATCCTC | 26133 |
rs368014526 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049115 | AGGACAGATTAGGAC[C/T]GGGGAGGTGAGCTCC | 26133 |
rs368016365 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066991 | TTTAAAAACTATGCA[C/G]AGAATTTATAAAGAA | 26133 |
rs368020204 | snp | A/C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028765 | TTATTAAAAGTAGTA[A/C/T]GTTAAGGTCTCCAGC | 26133 |
rs368071664 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075293 | GTGTGAATTTGATCC[C/T]GTCATTATGATGTTA | 26133 |
rs368083356 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011422 | TACTGGTTGTCTACC[C/T]TGGTGATCGTGTAGC | 26133 |
rs368130466 | snp | C/T | 1.66735e-05 | 0.00288729 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007528 | AGACGGAACCCAAGA[C/T]ACTGGCTGCTCCAGA | 26133 |
rs368221145 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004202 | GGGCAGAAGGTGTGA[C/G]GGACGTGGACATGGG | 26133 |
rs368237951 | snp | C/T | 1.65266e-05 | 0.00287455 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012959 | AGGAGATCGAGGCCT[C/T]CCGAAGACAGCCCAA | 26133 |
rs368271092 | snp | A/G | 0.000198 | 0.00994791 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003410 | GGGTGGGGCACTCAC[A/G]TTCTCTAGGCAGGTG | 26133 |
rs368283006 | in-del | -/AATTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027030 | AATTTGCATGCCTTT[-/AATTT]CTTTTTCTTGCCTAA | 26133 |
rs368334558 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051234 | CACAGTTTGGTAAAT[A/G]GGAACCCCAAGCTAG | 26133 |
rs368356624 | snp | C/G | 5.23876e-05 | 0.00511772 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002144 | GGGGGCTGACAGGTA[C/G]TACTGCTCACTCAGC | 26133 |
rs368378226 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032336 | GGCCTGATTATTATA[C/T]TACTCTTCAATTCTA | 26133 |
rs368385558 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078768 | TACATATAGATAGGT[C/T]AAAAGTAAGGGAAAA | 26133 |
rs368405065 | snp | A/G | 3.33167e-05 | 0.00408133 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044749 | CAATCCCCATGCTCA[A/G]TTCACTCAAGAGATT | 26133 |
rs368411374 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012792 | CTGGGGTGGCTATGA[A/G]GGTTAGAAGAAAGCT | 26133 |
rs368412846 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038412 | ATTTGTCAACACTTA[A/C]CAATTTCCATTAATG | 26133 |
rs368431855 | snp | C/T | 0.00165451 | 0.0287144 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021406 | GCTTGTGAGGAAACA[C/T]GTTTCTGCCCCTCGA | 26133 |
rs368448382 | snp | C/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093560 | CTATCCACCAGATAG[C/G]ATGTTGTCTCTAATA | 26133 |
rs368460867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074892 | GTCTCCCATTATTAT[C/T]GTGTGGGAGTCTAAG | 26133 |
rs368491904 | snp | C/T | 0.000149334 | 0.00863972 | downstream-variant-500B, synonymous-codon | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001995 | TCGCAAGGCCCAGCA[C/T]GAGCTGGATGATGCG | 26133 |
rs368499122 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034635 | CTGGCCAGAGTCAAA[G/T]GCTTTAAGGCTGGGC | 26133 |
rs368685510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077607 | ATAATGTCTCCGTGC[G/T]CTTTCCACTCATTTC | 26133 |
rs368714257 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086523 | TGTGTGTGTGTGTAT[A/G]TATGTGTGTGTGTGT | 26133 |
rs368732057 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050140 | GCATGGCTTAACTGT[A/G]GGAAACGCTCGTTAA | 26133 |
rs368738646 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042612 | GTACACAGTGATAGG[-/T]TTTTGTATTAACAAT | 26133 |
rs368744787 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075549 | TATGAAACTCTGGGT[C/T]GAAAATTCTTTTCTT | 26133 |
rs368757815 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059766 | AGAAGACGAAGAAGA[C/T]GACGAAGACAAAGAA | 26133 |
rs368763589 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019993 | CACCCCTTACCTGCT[A/G]GTCTTAACCACCTCA | 26133 |
rs368765112 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038860 | GGTGGATCACCTGAG[A/T]TTGGGAGTTCAAGAC | 26133 |
rs368769832 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049825 | AATCCAATGGTCTGA[C/G]ACACCCTTCCCCATC | 26133 |
rs368810018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023535 | ACTGGAGAAATTTTT[A/C]ATTTAAGAGATTCTA | 26133 |
rs368858341 | in-del | G/TT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048213 | TTTGTAAGAATTCTG[G/TT]TTTTTTTTTTTTTTT | 26133 |
rs368890640 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077876 | TGATGGGATTATAGG[C/T]GATGTATATTTTCTT | 26133 |
rs368924577 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069217 | ATTCTGAAATCTTTC[C/T]TATCTCCCATTTCAA | 26133 |
rs368957877 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059315 | ACAAATTAGATGACC[C/T]AGACGAAATGGACAC | 26133 |
rs368989056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090438 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACA | 26133 |
rs368992999 | snp | C/T | 0.000594845 | 0.0172357 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007685 | AAGGCTGCCCTCTTC[C/T]GGCCCATGTTCAGTT | 26133 |
rs368993921 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014105 | ATCTGCCCGCCTTGG[A/C]CTCTCAAAGTGCTGG | 26133 |
rs368997610 | snp | A/G | 3.30371e-05 | 0.00406417 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015991 | GCCCCATCTGTCCCC[A/G]GGGGTCTCCTGCTTA | 26133 |
rs369032490 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089099 | TCTCAAACTCCTGGG[-/G]CTCAAACAATCCGCT | 26133 |
rs369079230 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049137 | GTGAGCTCCAGGTCC[C/T]AACAAGCATTACACC | 26133 |
rs369086481 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029506 | AACTTTTTGTTTTCT[A/G]TATGTCTTGTGTGTT | 26133 |
rs369098171 | snp | C/T | 4.94458e-05 | 0.00497197 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035182 | TCTAGCACCAAAGCA[C/T]TGTCTAGCCATGTGT | 26133 |
rs369119465 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028949 | AACAGTTTTTGTTTT[A/T]AAGTCTCTCCAGCTT | 26133 |
rs369191711 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079615 | TAAAAAGATCAATAC[A/G]ATTGATAAACTCTAA | 26133 |
rs369241490 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086543 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs369263916 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013179 | CTGTCCTCATGTACC[A/G]TGAGGACTTTTCTTT | 26133 |
rs369277678 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072264 | GTAGTTTCTTTTGCT[A/G]TGCAGAAGCTCTTTA | 26133 |
rs369299529 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051290 | AGATATGTTGCAACA[A/C]ATTTAATTTTCTTTC | 26133 |
rs369306083 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009254 | CGGCCAGGCACGCAG[C/G]GGTCTGGGCCCTTCA | 26133 |
rs369325392 | snp | A/T | 9.89919e-05 | 0.00703464 | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35008719 | GCAGACGAGTTAATA[A/T]GCCCCTCTTCCCATC | 26133 |
rs369457090 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030097 | AAATACAAAATTAGC[C/T]GGGCATGGTGGCACA | 26133 |
rs369485330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032986 | GGTGGGTGGATTGCC[C/T]GAGCTCAGGAGTTCA | 26133 |
rs369503340 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040837 | CAATTCCCCTAACAA[A/C]TCCCACCTCATAAAT | 26133 |
rs369509109 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023949 | GTGATAAATATTTTC[A/G]AGAAACAGTCTCCAA | 26133 |
rs369517031 | snp | A/G | 0.000409507 | 0.0143034 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021143 | ATACCATGAGCACCC[A/G]GGCAGCACCTGCTCC | 26133 |
rs369550640 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018627 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAATAG | 26133 |
rs369550661 | snp | A/G | 6.32998e-05 | 0.00562547 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003629 | CTCCTGCAAGGCCAC[A/G]GGCCCACAGGGTCAG | 26133 |
rs369596742 | snp | A/C | 0.000437904 | 0.0147905 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002270 | CCGATCCTGCCATCT[A/C]TGCATCGCCCCCTGC | 26133 |
rs369640683 | snp | G/T | 4.94344e-05 | 0.00497139 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078102 | GGCTGGTGGTGTGCA[G/T]CTTGAGGAGCAGCTG | 26133 |
rs369712919 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084525 | ACGTATATATGTGTA[C/T]ATATGTATATATGTA | 26133 |
rs369719947 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021361 | CACAATGGAGGCTGA[C/G]ACAGCCACCGGAGAC | 26133 |
rs369742893 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062780 | TGTGGTGACAGTGGT[A/G]TATAACTCTGACTAT | 26133 |
rs369762574 | snp | C/T | 3.30808e-05 | 0.00406686 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057464 | GCTGGGAACTGCCAC[C/T]GTATCGGCAGGTTGG | 26133 |
rs369780830 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005853 | CTGCTGGCCAGGTAT[A/G]GCCATGGCCCGGGGG | 26133 |
rs369793283 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005716 | TATCCACCTGGTTTT[C/G]AAATCGGTCCAGGGA | 26133 |
rs369840973 | snp | A/G | 1.65083e-05 | 0.00287296 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003145 | GAGGCCTGGCCCAAG[A/G]TCACTCCTCAGTGAA | 26133 |
rs369903809 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002257 | GAGGCCACCTGCCCC[A/G]ATCCTGCCATCTCTG | 26133 |
rs369904330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040498 | CTGGGGTCCTCCAGC[C/T]GGGGAGCTACACCAT | 26133 |
rs369922714 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014808 | TCATGCTGGTAGGCA[G/T]GGTGCCGACTAGCCG | 26133 |
rs369971393 | snp | C/T | 1.65059e-05 | 0.00287275 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35013051 | GCCTCAAAAACTGTA[C/T]CTTCAAGGTGATGTC | 26133 |
rs369976764 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075845 | CTGGATAATATCCTG[A/C]AGAGTGTTTTCCAAC | 26133 |
rs370072488 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022964 | GAAGGTGAAGGTTGC[A/G]GTGAACCAACAGAGA | 26133 |
rs370142214 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030736 | GTTATTGCAAAATAT[A/G]TTTCCATATGTTATA | 26133 |
rs370142551 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061615 | ATTCAATGATGAAAG[A/C]GTAGTTTTTTCAATA | 26133 |
rs370164247 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011075 | ACCAGCCTGGCCAAC[A/G]TGGCGAAACCCCATC | 26133 |
rs370185618 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018384 | GCGGATCACTTGAGG[C/T]CAGGAGTTTCAGACC | 26133 |
rs370295838 | snp | A/T | 0.000149304 | 0.00863886 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003330 | TGGAGGACCCAGGTC[A/T]AGCCCAGCACCGGGA | 26133 |
rs370314822 | snp | C/T | 1.65007e-05 | 0.00287229 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057507 | AGTAGCTAATAGGTA[C/T]ACTTACTTTTCAGTT | 26133 |
rs370320579 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027689 | TCATTATTTATTCAA[C/T]CTCGTTGTTATACTT | 26133 |
rs370323979 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080769 | AGATGCATAACTTTG[G/T]GCATACAGTAAAAAC | 26133 |
rs370335376 | snp | C/T | 3.30551e-05 | 0.00406528 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016191 | TGTGCTTGAAAAATC[C/T]AGCAAAACCTCGTGC | 26133 |
rs370341827 | in-del | -/AC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029623 | TATATTTCCCAAGTT[-/AC]TTTCTTTTTTTTTTT | 26133 |
rs370365926 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032272 | TCAAATGCTCTGCCC[A/C/G]CCTCAGCCTCCCAAA | 26133 |
rs370366867 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056708 | TACCGAAGCTGGGTG[C/T]GGTGGCTCATGCCTG | 26133 |
rs370371907 | snp | A/G | 0.000236271 | 0.0108664 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003371 | AGAGGCCCTGGGTCC[A/G]CGGCCCACCCATCAC | 26133 |
rs370381100 | snp | C/T | 3.37969e-05 | 0.00411063 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069459 | TTTTAGTAACCAACA[C/T]AGACCAGACACTAAA | 26133 |
rs370395408 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037411 | CAGCAATTTCACTCC[C/T]ACATATATACCCAAA | 26133 |
rs370412346 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080779 | CTTTGTGCATACAGT[A/G]AAAACCACTGACTTG | 26133 |
rs370466123 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043019 | GTATGGTCTTATTCT[-/C]CCCCCTGACTTAATA | 26133 |
rs370546948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005974 | CTCACCACCCAGGTA[C/T]TAAGAGGCACTCCCC | 26133 |
rs370553791 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011507 | AGCATTGCAAGAGTA[C/T]TGAACTGTTTATCAT | 26133 |
rs370558652 | snp | C/T | 0.000115415 | 0.00759568 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044684 | ACTAAGGAACTCAGA[C/T]TGGGGACTTCATCTA | 26133 |
rs370575851 | in-del | -/CTT | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002332 | ACCACAGCCAGTTTC[-/CTT]CTTCTCATTCTTTTC | 26133 |
rs370594200 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073890 | TTCGGCTGTGAATCC[A/G]TCTGGTCCTGGACTT | 26133 |
rs370651373 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059721 | GAAATAAGAAGAAGA[A/G]GAAGAGGAAGAAGAC | 26133 |
rs370736251 | snp | C/G/T | 8.54349e-05 | 0.00653537 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002123 | CTCTCTGTGCAGGGG[C/G/T]ACTGTGGGGGCTGAC | 26133 |
rs370793030 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073232 | GCAAACAGGGACAAT[C/T]TGACTTCCTCTTTTC | 26133 |
rs370805700 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031912 | AAAAGTTTTTTTTGA[A/G]ACAAAGTCTCACTTT | 26133 |
rs370834271 | snp | A/C | 1.66333e-05 | 0.00288381 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008779 | ATATTGGTGACAGAT[A/C]TGAGAGGCTGACAGG | 26133 |
rs370841577 | snp | A/G | 1.65072e-05 | 0.00287286 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003446 | CTTGTCCTTGTGCAG[A/G]TAGTGCTGCTGCCAG | 26133 |
rs370895543 | snp | A/G | 1.69562e-05 | 0.00291167 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049816 | AGTTTTGAGAATCCA[A/G]TGGTCTGAGACACCC | 26133 |
rs370901590 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007174 | TCAGTTTCTTGTCCA[C/T]ATGAAAAAATCTGAA | 26133 |
rs370945652 | snp | C/T | 4.95209e-05 | 0.00497574 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069301 | AGCTACTTACATCAA[C/T]ACCTCCAAACAAGTC | 26133 |
rs370972695 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048639 | TATCCCCCTTTCAAA[A/C]TGCACCAAGATACCC | 26133 |
rs370988843 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007423 | ATCTAAGGCAGCCTG[A/C]ACAGGCATTTGGAAG | 26133 |
rs371020970 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071036 | AAGAAGCAAATAATG[G/T]GCAACTCTTTGAAAA | 26133 |
rs371048426 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025975 | GCAGGGGATCTAACT[-/T]CATTCTTTCGCATGT | 26133 |
rs371049908 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025244 | TTAAGTGCAGTGGCA[A/G]GATCACAGCTCACTG | 26133 |
rs371062748 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056926 | AGGAGGCGGAGGTTG[-/C]AGTGAGCCAAGATCA | 26133 |
rs371091315 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016221 | CTCAGTACACACGAT[A/G]ATGATATTCAGGACA | 26133 |
rs371134321 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052738 | CTCAAGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 26133 |
rs371142306 | snp | A/G | 6.62866e-05 | 0.00575664 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057569 | AAGAATTTCTACAAG[A/G]AGCTATAAAAAAAAT | 26133 |
rs371151350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047624 | GGGGCAGTGGCTTCT[A/G]AACTTTTTAGCTATC | 26133 |
rs371199403 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035435 | GCTAAAGCTACTCTT[C/T]TAAAATGAATGTCAA | 26133 |
rs371220374 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086535 | TATATATGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs371284276 | in-del | -/AGTT | 0.00478085 | 0.0486577 | utr-variant-3-prime, downstream-variant-500B | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002418 | TCATTTTTAAAATAA[-/AGTT]AGTTATTTAATAGTC | 26133 |
rs371293020 | snp | A/G | 1.65765e-05 | 0.00287888 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003515 | GGGGTACTTCTTGCT[A/G]TGCTCCATCCGCTGC | 26133 |
rs371366359 | snp | C/T | 8.42197e-05 | 0.00648867 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021172 | CCCCGTGTCCTGAGA[C/T]GCTGGAGAGGGGCCC | 26133 |
rs371366446 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077776 | TAGTGTTGACCTCCC[A/C]AAATTAAGCAAGCAC | 26133 |
rs371368495 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043236 | TATTACAAATAATGT[G/T]GCAATGAATAATTTT | 26133 |
rs371379270 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071053 | CAACTCTTTGAAAAG[A/C]ATTTTTAAACAAGTT | 26133 |
rs371397294 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053825 | ACTTCACCACTTCTT[A/C]CTACTTTTTTCTTTA | 26133 |
rs371406861 | snp | A/G | 0.000153988 | 0.00877328 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002029 | GAGCGGGCAGACATG[A/G]CGGAAACCCAGGCCA | 26133 |
rs371487351 | snp | C/G/T | 6.64027e-05 | 0.00576175 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077996 | AACAGCAGACATCTT[C/G/T]TGTCACCTAGAGGCC | 26133 |
rs371565199 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028165 | CTTTAGCTGCATCCC[A/G]TAAGTTTGATATATA | 26133 |
rs371574828 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029146 | ATCCCAACTACTTGG[G/T]AGGCTGAGGCATCAG | 26133 |
rs371612752 | snp | A/G | 7.09031e-05 | 0.0059537 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004547 | TGTAGGCGAGCAGGC[A/G]GCATTCAGACAGTAC | 26133 |
rs371635382 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038646 | CCCGTCCCATGATTG[G/T]GCATGTATAGAATAT | 26133 |
rs371661486 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054924 | TTCCCATCTTAAACA[C/T]TGCAGACCTGGTAGG | 26133 |
rs371702708 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052262 | TAACACCACGTCCAG[C/T]CAGTTTTTTATTTTT | 26133 |
rs371721115 | snp | C/G/T | 0.000199197 | 0.0099782 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007509 | CAACGCGTGGGCTGG[C/G/T]GGGAGACGGAACCCA | 26133 |
rs371785914 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053670 | AGGAAAGAAAAACAA[A/C]ACACACACACACATT | 26133 |
rs371798185 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013984 | AATAAGAAAACTGGC[C/G]CTGGGACAGCTGCCA | 26133 |
rs371826409 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028089 | TAAGGTAGACGTTTA[A/G]GCAATTTAGATTTAT | 26133 |
rs371827554 | in-del | -/CT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032835 | TTTCACAGGAAATTT[-/CT]GTTGCCTGCTTTTTC | 26133 |
rs371945025 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084580 | TATGTGTATATGTAT[A/G]TATGTTTATATGCAT | 26133 |
rs371950266 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059465 | AGAAGATTGAGACCA[C/T]CCTGGCCAACACAGC | 26133 |
rs371955726 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008045 | GGGCTCACAGACGAT[G/T]GGCTGGCCTAGGGAA | 26133 |
rs371957915 | snp | A/G | 2.01668e-05 | 0.00317537 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010338 | GGAACTGGGGCTGCT[A/G]GGTCAGCACCAGGCT | 26133 |
rs371961369 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007916 | AGGGCTGGCTCCTGC[A/G]AGCCCCCGTGAAACA | 26133 |
rs371962225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067392 | AGGATACAGAAAAAC[C/T]GAAACCCTTATACAC | 26133 |
rs371969033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038118 | GGCGTTTCCTTTTGG[A/G]GTGATGAAAACGTGC | 26133 |
rs371983247 | snp | C/T | 3.31159e-05 | 0.00406901 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054925 | TCCCATCTTAAACAT[C/T]GCAGACCTGGTAGGG | 26133 |
rs371993649 | in-del | -/AGA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059724 | ATAAGAAGAAGAAGA[-/AGA]GGAAGAAGACTACGA | 26133 |
rs372034532 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023841 | CTACTGAGAAATGAA[C/T]GTCTGCGAAGAAAGA | 26133 |
rs372082768 | snp | C/T | 1.75339e-05 | 0.00296085 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002148 | GCTGACAGGTAGTAC[C/T]GCTCACTCAGCTATC | 26133 |
rs372091131 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013597 | ATCCAACCAACCAAC[A/C]AACAAAACAACACGT | 26133 |
rs372093415 | snp | A/T | 3.33406e-05 | 0.00408279 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007529 | GACGGAACCCAAGAC[A/T]CTGGCTGCTCCAGAT | 26133 |
rs372119259 | in-del | -/TGAAGAAAAGA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059867 | AAGATGAAGAAAAGA[-/TGAAGAAAAGA]CGAAGACAAAGATGA | 26133 |
rs372139917 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088792 | ACATGCTATACCACA[C/G]ATGATCCTTGAGGAC | 26133 |
rs372143964 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054503 | TAACACTAAGTGCCA[C/T]CCTCTTTTGTTTCTA | 26133 |
rs372161656 | in-del | -/TATATA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086575 | GTGTGTGTGTGTGTG[-/TATATA]TATATATATATGAAT | 26133 |
rs372161833 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063738 | TGATGGCATGAACCT[A/G]TAGTCCCAGCTACTC | 26133 |
rs372178253 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044098 | CCATCTCTAGAGATA[C/T]TTAAAAGGGGTGCTA | 26133 |
rs372205155 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078990 | AGAACCGCTTGAACT[C/T]GGGAGGCAGAGGTTG | 26133 |
rs372205299 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056370 | CATGGAACCTATAAA[C/T]CTAGTGGGAAGAAGA | 26133 |
rs372269886 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060611 | AAAAAAAAAAAAAAA[-/C]AAGAAAAGGATTATA | 26133 |
rs372315048 | in-del | -/ACACA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068958 | TTTACACACACACAC[-/ACACA]ACACACACACACACA | 26133 |
rs372318612 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013083 | TGAAACACATGCACA[A/G]CCTCAATGTTAGGAC | 26133 |
rs372333788 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057138 | TTCACACCCTGGTAA[C/T]GCCTGAACTTTTTAC | 26133 |
rs372520839 | snp | A/C/G | 6.60567e-05 | 0.00574665 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004422 | AAGTGGTTTCCAATC[A/C/G]ACCTTCCCTGCTGTG | 26133 |
rs372531226 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082075 | GGCAAACTGGATAAT[A/G]TTAATGATCCTAAAT | 26133 |
rs372541691 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066149 | TTGCTCTGTCACCCA[C/G]GCTGCAGTTCATGGT | 26133 |
rs372554590 | snp | A/G | 3.30557e-05 | 0.00406531 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012962 | AGATCGAGGCCTTCC[A/G]AAGACAGCCCAACAA | 26133 |
rs372590052 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015296 | GTGACCACCACGCCC[A/G]GGAGCACGGTTCTAT | 26133 |
rs372664355 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055586 | AATCACAGCTCACTG[C/T]AGTCTCGAACTCCTA | 26133 |
rs372674769 | snp | A/C/T | 8.57558e-05 | 0.00654763 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035075 | AAGAATGGTCCCAGG[A/C/T]GCCCAAGGAAAAGCT | 26133 |
rs372696629 | snp | G/T | 1.67739e-05 | 0.00289597 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078206 | GAGAGAACATATTAT[G/T]GTATTATTGATGATA | 26133 |
rs372696978 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007601 | TGCATAGGAGGTGGT[C/T]CCTCGGAGGAAACTC | 26133 |
rs372734717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085972 | CACACTAAATGCAAG[A/G]GTCTCGCGCAATCTC | 26133 |
rs372741001 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065988 | AGTTAAAGAAGAAAG[A/G]CTGTGGCTGATGCCA | 26133 |
rs372782663 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076996 | GCTTTGCTGCCACCT[C/T]GCAGTTTGATCTCAG | 26133 |
rs372783719 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030628 | CCTCTTATTACCATT[C/T]TGGTTCTCCTCACCG | 26133 |
rs372797197 | snp | A/C | 3.29788e-05 | 0.00406058 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016162 | GGATAGGAAGGAAAA[A/C]GTATTAAGACAAATG | 26133 |
rs372827387 | snp | A/G | 6.67657e-05 | 0.0057774 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006414 | CCCAGCACACTCCAC[A/G]GAGCCCTGGGTTAAC | 26133 |
rs372861865 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086545 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs372876419 | snp | A/G | 3.29799e-05 | 0.00406065 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035226 | CTCCTGAAGGAAGCT[A/G]GCTGTGCCCGTTGAC | 26133 |
rs372913647 | snp | C/T | 1.6617e-05 | 0.00288239 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008778 | GATATTGGTGACAGA[C/T]CTGAGAGGCTGACAG | 26133 |
rs373014607 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033511 | TAACTGCTGACTGAA[C/T]TCTCGACTGTTTTTG | 26133 |
rs373043586 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044659 | GAGCTGCTGCTGATC[A/G]AAATTGGATACTAAG | 26133 |
rs373110411 | snp | A/C/G | 1.65919e-05 | 0.00288022 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001996 | CGCAAGGCCCAGCAC[A/C/G]AGCTGGATGATGCGG | 26133 |
rs373122109 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052239 | GAGGAGCTGGGACTA[-/A]TGGTATATAACACCA | 26133 |
rs373154849 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075878 | GGTTCCATTCTCCCC[A/G]TCACTTTCAGGTACA | 26133 |
rs373243411 | snp | C/T | 5.11924e-05 | 0.00505901 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021146 | CCATGAGCACCCGGG[C/T]AGCACCTGCTCCCCG | 26133 |
rs373262090 | snp | A/G | 3.29973e-05 | 0.00406172 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054962 | AACAGAGCCCCAGTG[A/G]CAGGGGTACTTACAC | 26133 |
rs373295554 | snp | A/G | 1.64909e-05 | 0.00287144 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057520 | TATACTTACTTTTCA[A/G]TTTCTGTCCCCGGAT | 26133 |
rs373330119 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064481 | ATGTGACACTATAAT[G/T]CAACATCCTGAATTA | 26133 |
rs373363028 | in-del | -/TCAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048021 | CACTGATACACACAC[-/TCAC]CAACATTTGCCCACT | 26133 |
rs373376388 | snp | A/G | 9.96214e-05 | 0.00705697 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003101 | TGGCATCGTACCCAC[A/G]CTCACCCACACTGGC | 26133 |
rs373386217 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037181 | GAAACCCCATCTCTA[C/T]TAAGAAGTACAAAAA | 26133 |
rs373417798 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079845 | AACATAGCGAGAGCT[C/T]GCCTCTACTAAAAAT | 26133 |
rs373424708 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091725 | AAATAACAATAATCA[C/T]ATGTTGGGCACCTGT | 26133 |
rs373504279 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014095 | ACCTCAAGTGATCTG[A/C]CCGCCTTGGCCTCTC | 26133 |
rs373603201 | snp | A/C | 0.000488683 | 0.0156238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092825 | GCGGCCTCGGGGCCG[A/C]GGAGATTTCTACGGG | 26133 |
rs373607769 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050454 | GCGTGGTGGCTCACA[A/C]CTGTAACCCCAGCAC | 26133 |
rs373641387 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070503 | GCAAGCTCTGCCTCC[C/T]GGGTTCACGCCATTC | 26133 |
rs373642235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068130 | CTTCTGGGTACTGGT[A/G]ATGTTCTATTTCCTA | 26133 |
rs373650126 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052457 | CTACAAACTAGCATC[A/C]AGTAGGCCAAGCTTT | 26133 |
rs373656467 | snp | G/T | 1.67351e-05 | 0.00289263 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002091 | GGGCCCCAAGGTGAG[G/T]AGTGGCAGGGGCATT | 26133 |
rs373666760 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022301 | GCTGGGACTACAGGC[A/G]TGTGCCACCACGCCC | 26133 |
rs373685367 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033147 | TGCAGTGAGCCGAGA[C/T]TGTGCCACTGCCCTC | 26133 |
rs373722628 | in-del | -/TTTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025607 | TTTTGAAATGGGTTT[-/TTTT]ATTATTGTTATGAGA | 26133 |
rs373737607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037129 | AGGCGGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 26133 |
rs373740764 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084066 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATTAC | 26133 |
rs373745235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017504 | ATTACTAGCCCTTCT[C/T]GGGGCTGTTGTAAGG | 26133 |
rs373757803 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073940 | TAATTATTGCCTCAA[C/T]TTCAGAGCCTGTTAT | 26133 |
rs373796507 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056829 | TACTAAAAAAAAAAA[C/T]ACAAAAATTAGCCGG | 26133 |
rs373821934 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080298 | TTGAGCTCACAAGTA[C/T]AAGACCAGCCTGAGC | 26133 |
rs373829023 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045165 | CTCCCTGCAGACGTA[A/C]ACATTATTTTGAACT | 26133 |
rs373849245 | in-del | -/CTGA | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005227 | ACAAGGAACAAGTGC[-/CTGA]CTTTTTGGGGGTGTG | 26133 |
rs373918807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077041 | AGTGAGCAAGGCTCC[A/G]TGGGCATGGGACCCT | 26133 |
rs373958975 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016174 | AAAAGTATTAAGACA[A/T]ATGTGCTTGAAAAAT | 26133 |
rs374012224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028291 | ACCTCTGCCTCGGGG[A/G]TTCAAGCAATTTTCC | 26133 |
rs374015860 | snp | C/T | | | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007816 | GTGCCCCCATCCTCA[C/T]AGAGAGCCAGCTCAG | 26133 |
rs374039578 | snp | A/G | 0.000153988 | 0.00877328 | stop-gained, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044703 | GGACTTCATCTAGTC[A/G]GATCATTTCCTACAG | 26133 |
rs374056068 | in-del | -/GCGAGACTCCATCT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080521 | AGAAACAAAAACAAA[-/GCGAGACTCCATCT]AAAAAAAAAAAAAAA | 26133 |
rs374152361 | snp | C/T | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010242 | CCTTGAGAGAGATGG[C/T]ACTGAGTTCATTCAG | 26133 |
rs374167272 | snp | C/T | 9.9744e-05 | 0.00706131 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001981 | AACCTGGCCAAGTAT[C/T]GCAAGGCCCAGCACG | 26133 |
rs374173310 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077657 | CCTTCAATCTTCTTA[C/T]GTTAGTAATAATATT | 26133 |
rs374174727 | snp | A/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093291 | TGGGGCTTTCTCTGC[A/G]CCCGACACCAAACCA | 26133 |
rs374190995 | in-del | -/TA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086499 | GTATATATATATGTG[-/TA]TATATATATGTGTGT | 26133 |
rs374281679 | snp | A/T | 1.65408e-05 | 0.00287578 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005667 | CTTACCCTGCATGAC[A/T]TGCCTTGACAGCCTG | 26133 |
rs374282031 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006350 | TCTCTAACGTAAAAC[C/T]TGTGCCTAAAGCCTG | 26133 |
rs374323873 | in-del | -/TGAAGAAGACGAAGACGAAGACAAAGA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059819 | AGACAAAGATGAAGA[-/TGAAGAAGACGAAGACGAAGACAAAGA]CGAAGAAGATGAAGA | 26133 |
rs374347170 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015623 | ACCCAACACCATACC[C/T]GGCCAATTTTTGTAT | 26133 |
rs374351292 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035644 | TTACACGAGAATATC[C/T]GTATAAGGAGGTTCA | 26133 |
rs374408746 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007474 | CTGATGAACTGTTTG[C/G]GGCTCAGGACAGGAC | 26133 |
rs374420135 | snp | C/T | 1.86086e-05 | 0.00305024 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057623 | TCAAAGTATAACTTA[C/T]AAAATGATTTTGCCA | 26133 |
rs374461010 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028348 | CCCGCCTCCTCGGCC[G/T]CCCAAAGGGCTGGGA | 26133 |
rs374488569 | snp | A/G | 3.30475e-05 | 0.00406481 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003479 | GCGCAGCAGGTTGTG[A/G]AAGTTGTTGAGCAGG | 26133 |
rs374492929 | snp | A/G | 3.30726e-05 | 0.00406635 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005826 | GAAACCAAGCTCACA[A/G]CAGGCAGTGGGCTGC | 26133 |
rs374493784 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057430 | ATTAAGAGTTAGGAA[C/G]GGAAGGAAGAAGGCA | 26133 |
rs374512290 | snp | C/G | 5.16978e-05 | 0.00508392 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001925 | TCACCCAAGCGGAAC[C/G]AAGGCCCTGTGTGTG | 26133 |
rs374565056 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010730 | ACTTGCCATCCAGGC[C/T]TGTCACTGCTGGGTC | 26133 |
rs374618620 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077469 | ATCCAAACTACAGCT[A/G]AAGTTTAGATACTCC | 26133 |
rs374660327 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075689 | TCTGGCTGCCCTTAA[C/T]ATTTTTTCCTTAATT | 26133 |
rs374664410 | snp | C/T | 1.65364e-05 | 0.0028754 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021219 | GCCCCATCAGCAGCA[C/T]GCAGAGGACATAGAG | 26133 |
rs374701715 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034609 | TCCTGGGTTTGTATA[C/T]TCTGAACCTGCTGGC | 26133 |
rs374714604 | snp | C/T | 1.66067e-05 | 0.00288151 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078000 | GCAGACATCTTGTGT[C/T]ACCTAGAGGCCCTGA | 26133 |
rs374749569 | multinucleotide-polymorphism | AAA/CAT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024852 | AAAAAAAAAAAAAAA[AAA/CAT]ATTCTGTTTATTCAT | 26133 |
rs374808046 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026054 | TCCACCAATGAATGG[C/T]CTTGGTACCCACTGA | 26133 |
rs374810415 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066122 | ACAATTTTTTTTTTT[-/T]GAGATGGGGTCTTGC | 26133 |
rs374852604 | snp | A/C/G | 9.51711e-05 | 0.00689768 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003386 | GCGGCCCACCCATCA[A/C/G]CCCCTTGAGGGTGGG | 26133 |
rs374884611 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069079 | GATGTACTTTTCACT[C/T]AGTATTTTTTTAAAA | 26133 |
rs374896059 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086537 | TATATGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs374906924 | in-del | -/ACA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068960 | TACACACACACACAC[-/ACA]ACACACACACACACA | 26133 |
rs374909428 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018635 | AAAAAAAGAAAGAAA[A/G]AAAATAGCAGCTTCT | 26133 |
rs374924202 | snp | G/T | 8.42368e-05 | 0.00648932 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035105 | TCCCGATCACTCAGG[G/T]GACCCATCCTTCCAT | 26133 |
rs374941328 | snp | A/G | 9.96099e-05 | 0.00705656 | downstream-variant-500B, synonymous-codon | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002031 | GCGGGCAGACATGGC[A/G]GAAACCCAGGCCAAC | 26133 |
rs374957700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073506 | CTGTTGAATTTTGTC[A/G]AAGGCCTTTTCTGCA | 26133 |
rs374963252 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037376 | AAAAAAAAAGTCAAA[A/C]ATAAAATTACCATAT | 26133 |
rs375001391 | in-del | -/CACAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067016 | AAAGAACTCTTACAA[-/CACAA]TATTCAAAAGAGATA | 26133 |
rs375003906 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003360 | ACACCCCTCTGAGAG[A/G]CCCTGGGTCCGCGGC | 26133 |
rs375018654 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008080 | TGGTTGATGCTGACC[A/G]AGGGACCCAGAGGGC | 26133 |
rs375019387 | snp | C/T | 3.37183e-05 | 0.00410585 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021404 | CAGCTTGTGAGGAAA[C/T]ACGTTTCTGCCCCTC | 26133 |
rs375079257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066359 | CAATCCGCCTGCTTC[A/G]GCCTCCTAAAGTGCT | 26133 |
rs375079551 | snp | A/G | | | intron-variant, missense | TRPC4AP | GRCh38.p7 | 20:35009176 | AAGCCTCAGCTTCCC[A/G]GTCTATGAAGCAAAG | 26133 |
rs375134231 | in-del | -/CTTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030866 | TTTACTTAAGGTGCT[-/CTTT]GTTTTTCATGTGGAG | 26133 |
rs375193688 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071638 | TATGGCTGCATAGTA[C/T]TCCATGGTGTATATG | 26133 |
rs375197519 | snp | A/G | 0.000155988 | 0.00883003 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002216 | CTGGGCTCTAAAGAG[A/G]AATGTCTGCTGTTGC | 26133 |
rs375204063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005337 | ATACACATGGAAGTG[C/T]GTTAGCAAGTCCAGG | 26133 |
rs375210165 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032941 | GGTGTGGTAGCTCAC[A/C/G]CCTGTAATCCTAGCA | 26133 |
rs375240443 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072224 | AATTTTCTCCCATTC[C/T]GTAGGTTGCCTGTTC | 26133 |
rs375250941 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033912 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAT | 26133 |
rs375275064 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081331 | CAGCCTAGGCAACAC[A/G]GTGAAACCCTGTCTC | 26133 |
rs375287395 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086521 | TATGTGTGTGTGTGT[A/G]TATATGTGTGTGTGT | 26133 |
rs375302723 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037716 | CATTAACGCTGTTGC[A/G]GTCAACAACGACCAC | 26133 |
rs375348784 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029928 | GGCGTGAGCCACCGC[A/G]CCCAGCCCCAAGTTA | 26133 |
rs375364633 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008559 | ACAGTAATTGTGCTT[C/T]AGGAGGCATGGACGC | 26133 |
rs375396964 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048996 | TGAACGCTGGGTTCA[C/G]CACAGTGCACATGAA | 26133 |
rs375422049 | snp | A/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094336 | CCAGCACTTTGGGAG[A/G]CCGAGGTAGTCAGAT | 26133 |
rs375424254 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007337 | CACCCTCCTGCATGG[C/G]CTGGCCACCCTCTAA | 26133 |
rs375425426 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044787 | CCTCTCTTTCGCATC[C/T]CCTTACATACGGGGC | 26133 |
rs375441133 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058537 | GGATAATTTTAAAAA[C/T]CCATCCTAAATAATA | 26133 |
rs375456440 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083277 | AATAAATCTAACAAA[A/G]TTATGCAAGACGGCT | 26133 |
rs375468674 | snp | C/G/T | 6.63761e-05 | 0.00576058 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002017 | GATGATGCGGAGGAG[C/G/T]GGGCAGACATGGCGG | 26133 |
rs375481022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047841 | CCCCACAAGTGTGTC[C/T]AGGCACAGGTTATAG | 26133 |
rs375501115 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083791 | CCCAGGAAAAAGGAA[C/G]ACAATTGAGGAAACA | 26133 |
rs375584281 | snp | C/T | 0.000199982 | 0.00999754 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007499 | CAGGACACAGCAACG[C/T]GTGGGCTGGGGGGAG | 26133 |
rs375590330 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045420 | CTGTTGCTCAAGCTG[C/T]GGAGCAGTAGTGTCA | 26133 |
rs375642441 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034255 | TGAACTTCCCTGGAC[C/T]CTGTTCTTATTAACT | 26133 |
rs375644375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061628 | AGAGTAGTTTTTTCA[A/G]TAAGTGGTGCTGTGA | 26133 |
rs375645552 | in-del | -/TTTT | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055363 | TCTAGGATTTGTTTT[-/TTTT]GTTTTTTGTGTTTTT | 26133 |
rs375664958 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041951 | GCAAATACTACCTTT[G/T]GTCAATGTATATGGA | 26133 |
rs375671403 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069732 | GATTACTTGAGGCCA[A/G]GAGTTTGAGACCAGC | 26133 |
rs375689681 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011257 | GCAAGATTCCGTCTT[A/G]AAAAAAAGAAAAAGA | 26133 |
rs375732962 | in-del | -/ATG | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002775 | CTTGGCTCACAGATG[-/ATG]GGGGGTGGGGGTCAC | 26133 |
rs375751115 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086962 | CGCTTGAACCCGGGA[A/G]GCGGAGGTTGCAGTG | 26133 |
rs375780392 | snp | A/C/T | 0.000363243 | 0.013472 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013084 | GAAACACATGCACAG[A/C/T]CTCAATGTTAGGACC | 26133 |
rs375801164 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020448 | CTCCTCCCCAGGGCA[A/C]TGCCCCCTCCCACCT | 26133 |
rs375820645 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059264 | TTATGGCAACAAAAG[C/T]GATTATAAGGAACTA | 26133 |
rs375831214 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012996 | TCCTTGCAGGGACAC[A/T]CTTGTACTTACTCGT | 26133 |
rs375894215 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067462 | CATTCTGGCAGTTCC[C/T]CAAACAATTAAACAT | 26133 |
rs375941111 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080707 | TGCTACTGAATACCA[C/G]GTTTCTTTTTTGGGT | 26133 |
rs375942169 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008525 | CTACACAAGATGGCA[A/G]TCAAACCACCTCTCC | 26133 |
rs375956715 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027560 | GGAACTGTTCCTTCC[C/T]CTTTTATTTTCTATT | 26133 |
rs375960624 | snp | C/T | 6.81257e-05 | 0.00583594 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035093 | CCAAGGAAAAGCTCC[C/T]GATCACTCAGGGGAC | 26133 |
rs375964853 | snp | C/T | | | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006456 | ATCGGTGTTGATATA[C/T]TTATTGAATCTCTTG | 26133 |
rs376007028 | in-del | -/AAAACAA/AACAC/CAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068986 | CACACACAAAAAAAA[-/AAAACAA/AACAC/CAC]CAAAACATCTTAAGC | 26133 |
rs376024090 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027964 | TAAAAAAATCACCTT[G/T]GGTTTTACAGATTTT | 26133 |
rs376042783 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014098 | TCAAGTGATCTGCCC[A/G]CCTTGGCCTCTCAAA | 26133 |
rs376074076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066462 | CATTCCTGTACAATC[A/G]CCACATAGATCAAGA | 26133 |
rs376081699 | snp | C/T | 0.000545639 | 0.0165082 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005827 | AAACCAAGCTCACAG[C/T]AGGCAGTGGGCTGCT | 26133 |
rs376084355 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005894 | ACAAGGGGCATCAGC[A/G]ACCTCTACCAGCCCC | 26133 |
rs376094667 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089455 | TGCCCAGGCTTGACT[C/T]AAACTGGCTCAGGTG | 26133 |
rs376117350 | snp | A/G | 0.000153988 | 0.00877328 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002026 | GAGGAGCGGGCAGAC[A/G]TGGCGGAAACCCAGG | 26133 |
rs376127660 | snp | C/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055214 | ATCAGAACCTACAAG[C/G]CCATTTGCATATTGC | 26133 |
rs376209935 | snp | A/C | 3.31543e-05 | 0.00407137 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003313 | AGGGGCTGGGGGGCG[A/C]CTGGAGGACCCAGGT | 26133 |
rs376219022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010098 | TGAGAGAGGACACGC[A/G]TGCATACCTGGATGT | 26133 |
rs376270828 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087065 | CCAGGCGCAGTGGCT[C/T]ACACCTGTAATCCCA | 26133 |
rs376312309 | in-del | -/AA | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050723 | ACTCAAAAAAAAAAA[-/AA]CAAAACAAAAAAACC | 26133 |
rs376328324 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075112 | TTTTCCACTTGCTTG[A/G]TAGATCTTCCTCCAT | 26133 |
rs376332483 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038139 | GAAAACGTGCAACTA[A/G]ATAGAGGTGGTAGCT | 26133 |
rs376334554 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031582 | GGATCTGAGTATTCC[A/G]ACTTGGATTCTTTGG | 26133 |
rs376336668 | snp | C/T | 0.000437904 | 0.0147905 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002268 | CCCCGATCCTGCCAT[C/T]TCTGCATCGCCCCCT | 26133 |
rs376437342 | in-del | -/TAATT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066791 | AATAACATCAAAATT[-/TAATT]CTCAAAATAGTAAAA | 26133 |
rs376464691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032663 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTCTT | 26133 |
rs376543118 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073857 | TGGTACCAGCTCCTC[C/T]TTGTACCTCTGGTAG | 26133 |
rs376580175 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064824 | TTACTATAACTTTAA[C/T]ATTATATTAACAACT | 26133 |
rs376635360 | snp | C/T | 0.000153988 | 0.00877328 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003104 | CATCGTACCCACGCT[C/T]ACCCACACTGGCCCA | 26133 |
rs376676022 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036016 | TTCCTGTAACATTTA[C/T]TAGCAGGATGAAAGA | 26133 |
rs376679194 | snp | C/T | 1.65021e-05 | 0.00287241 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010191 | CCTGCACTCACCTGT[C/T]GGTGTTGAGGACAGC | 26133 |
rs376711198 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082157 | GCTAAAAGGAGAAAT[A/G]AGGAAATCCATAATC | 26133 |
rs376711942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084339 | GACTTCACCACCATG[C/T]GATACACCAATGTAG | 26133 |
rs376756701 | snp | C/T | 0.000322507 | 0.0126945 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021160 | GCAGCACCTGCTCCC[C/T]GTGTCCTGAGACGCT | 26133 |
rs376786338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025764 | GTGTTTTCTGAAGAA[C/T]AAAAAGTTTTAATTT | 26133 |
rs376823057 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004862 | ACCCGTGCCCTCCAT[A/G]TCACACACAGAAGAG | 26133 |
rs376914568 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046892 | TTTTTTTTTTAAGGC[A/G]GAGTCTCACTGTGAT | 26133 |
rs376945990 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039604 | AAACATCAGTATTCC[C/T]CCCATACTCCTGTAG | 26133 |
rs376966472 | in-del | -/T/TT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031390 | CTACCCCTGGTTAAC[-/T/TT]TTTTTTTTTTTTTTT | 26133 |
rs376974308 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053816 | TTAAAATTAACTTCA[A/C]CACTTCTTCCTACTT | 26133 |
rs376978235 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007546 | TGGCTGCTCCAGATC[A/G]TACCTCCAAGAGGCC | 26133 |
rs376987642 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018604 | ACTGTCTCAAAAAAA[-/G]AAAAAAAAAAAAAAA | 26133 |
rs377000827 | snp | C/T | 1.6786e-05 | 0.00289702 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078208 | GAGAACATATTATTG[C/T]ATTATTGATGATAAT | 26133 |
rs377002739 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027023 | CTTTTCTAATTTGCA[C/T]GCCTTTAATTTCTTT | 26133 |
rs377061509 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068932 | AAACTAAGGTGGAGG[A/T]GGTGGGGAATATTTA | 26133 |
rs377096923 | snp | A/T | 1.64999e-05 | 0.00287222 | missense, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35055027 | CTTGGACATTTCATC[A/T]CTTACTGAAAGTGAA | 26133 |
rs377142719 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070603 | TTTCAGTAGAGACGG[G/T]GTTTCACCGTGGTCT | 26133 |
rs377226689 | snp | C/T | 0.000346795 | 0.0131635 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005679 | GACTTGCCTTGACAG[C/T]CTGCCTTTCATGTAC | 26133 |
rs377232516 | snp | C/T | 0.000216326 | 0.0103979 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002065 | CTGCGGGCACGGACC[C/T]GGGACGCCCTGGGCC | 26133 |
rs377257881 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041022 | AGAGAGGAAAATTCA[C/T]ATGTGGATACAATAA | 26133 |
rs377285273 | snp | C/G/T | 0.000148404 | 0.00861301 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007644 | GCTTGCCAAAACCTG[C/G/T]GACCCAAATACTGGC | 26133 |
rs377286159 | snp | C/T | 1.64795e-05 | 0.00287045 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078128 | AGCTGAGGAATTCCA[C/T]TCCACTTGGATTGTT | 26133 |
rs377318891 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055590 | ACAGCTCACTGTAGT[C/T]TCGAACTCCTAGGCT | 26133 |
rs377324163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034741 | AGTCTTCTGCCTAGT[C/G]CCATCAAGGGGACCA | 26133 |
rs377403157 | snp | C/T | 4.94442e-05 | 0.00497188 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044668 | CTGATCGAAATTGGA[C/T]ACTAAGGAACTCAGA | 26133 |
rs377569235 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010220 | GCTTCCACCTCAGGG[A/G]TGTTGGCCTTGAGAG | 26133 |
rs377620324 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069955 | TTAAAAAAAAATAAA[A/C]AGCCTGACAGACTTC | 26133 |
rs377630705 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049648 | TGAAGTTCTGAGTTT[A/T]AGAATTAGTTTGATT | 26133 |
rs377670693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073201 | GGGGTTTTCTAAATA[C/T]ACAATCATGTCATCT | 26133 |
rs377672145 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090327 | TTACCACAATAACCT[A/G]CCTTGCTTTTGTGGC | 26133 |
rs377673841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056087 | CCCTGCCAAGCTAGC[C/T]TGACTAGATGGGTTG | 26133 |
rs377683621 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063972 | GAATACTCCCGAATC[A/T]TAACAGTGGTTGAAT | 26133 |
rs377718868 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069609 | TGGTATGACACACCT[A/C]AACTAACAGCATGTG | 26133 |
rs377728916 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007870 | TGTCTGGAAGGGGCT[G/T]TGTCACAGAAAGGGT | 26133 |
rs377753023 | snp | A/C | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003254 | GATGGACACTGTCTC[A/C]TTCCAGTATGAGAAG | 26133 |
rs386393679 | in-del | -/TT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028212 | CTCAAAATATTTCCT[-/TT]TTTTTTTTTTTGATG | 26133 |
rs386393680 | in-del | -/TT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028222 | TTCCTTTTTTTTTTT[-/TT]TGATGGAATCTCACT | 26133 |
rs386813845 | multinucleotide-polymorphism | CTATATACGTATG/TTATATACGTATT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064164 | GTTTAAAGACATTCC[CTATATACGTATG/TTATATACGTATT]TATTTTTTATTATTG | 26133 |
rs386813846 | multinucleotide-polymorphism | AC/CA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065944 | CCTAGGACCACCGAC[AC/CA]TGCTGTGGAGAGGGA | 26133 |
rs386813847 | in-del | ATTG/TA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066076 | AAGGAAACTTTAATA[ATTG/TA]AAGTATAACGTGATA | 26133 |
rs386813848 | multinucleotide-polymorphism | CG/TA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068757 | GAACTCCTGACCTCA[CG/TA]ATCCACCTGCCTTGG | 26133 |
rs397757541 | in-del | -/C | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003397 | AACGTGAGTGCCCCA[-/C]CCCTCAAGGGGGTGA | 26133 |
rs397775709 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050399 | GGAACTCCATTTTTT[-/T]CATCAGTAAAATGAT | 26133 |
rs397782031 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054202 | TGTTTTTTTTTTTTT[-/T]ATTTCCACAGCATAC | 26133 |
rs397805820 | in-del | -/A | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009487 | CTCTACAAAAAAAAA[-/A]GTAAAAACACTAGCT | 26133 |
rs397810273 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038288 | CACCATTTTTTTTTT[-/T]TAACATATCAGCTTG | 26133 |
rs397865614 | in-del | -/CTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047177 | GCCAAGAATTTACTT[-/CTT]ATGTTTTAATTTTTG | 26133 |
rs397963996 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003310 | GGAGGGGCTGGGGGG[-/G]CGCCTGGAGGACCCA | 26133 |
rs398035623 | in-del | -/AA | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028223 | GAGTGAGATTCCATC[-/AA]AAAAAAAAAAAAGGA | 26133 |
rs398035624 | in-del | -/TTTTTTTTTTT | 0 | 0 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056998 | TTTTTAGGTATTCAA[-/TTTTTTTTTTT]TTTTTTTTTTTTTGA | 26133 |
rs398035625 | in-del | -/A | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058707 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 26133 |
rs398035626 | in-del | -/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085626 | ACAAAATTCTAATGA[-/T]TTTTTTTTTTTTTTT | 26133 |
rs398038439 | in-del | -/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044415 | TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 26133 |
rs398088417 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085096 | GAAATACTGGCTCTC[-/C]TGTTTCCTGGATCCT | 26133 |
rs398088418 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090949 | GTACTTTTTCTAAAG[-/G]TTATGTGCTCACTAA | 26133 |
rs398088610 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038773 | TGTGTATTATTTTTT[-/T]CTAAAAACAAATCAG | 26133 |
rs398101403 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033835 | TCTCTATTCAAAAAA[-/A]GAGAAAATATAAAAA | 26133 |
rs527267288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051754 | AACAGAACAAAAAGA[G/T]AACTAAATTTACACT | 26133 |
rs527301445 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018226 | CAGACTTGGACCTGA[C/T]CCTGGGTCTCCTAAG | 26133 |
rs527355372 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005127 | GCTGTTCCCCTGAAA[A/C]AGACCCTCTGGGGCA | 26133 |
rs527385886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086862 | GCATGGTGAAACCCT[A/G]TCTTTACTAAAAATA | 26133 |
rs527386063 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036431 | GCAGATTTTTTGGAA[C/T]CATGTGAATGTTACA | 26133 |
rs527395893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079078 | CTCAAAAAATAGAAA[A/C]GGGGATGGAGAAAGA | 26133 |
rs527397365 | snp | C/T | 0.00011574 | 0.00760635 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007690 | TGCCCTCTTCCGGCC[C/T]ATGTTCAGTTCTCCA | 26133 |
rs527408862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037163 | CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC | 26133 |
rs527468598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079686 | AATATGTGGTACATA[A/T]GAGGAGTTATTATTA | 26133 |
rs527472238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073218 | CAATCATGTCATCTG[C/T]AAACAGGGACAATTT | 26133 |
rs527481153 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048107 | AACATCTTCTCTTTT[A/G]TGTTTATGGACCATT | 26133 |
rs527497187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029745 | GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTCCC | 26133 |
rs527508872 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073767 | AGGCTTTGGTATCAG[C/G]ATGATGCTGGCCTCA | 26133 |
rs527514319 | snp | A/C | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055845 | GATCTATTACTAATT[A/C]TTATAAAGAAACTAC | 26133 |
rs527543791 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051998 | ACAAGTTCTTAACTG[A/G]GGCCAAAAAGCACTA | 26133 |
rs527596715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066749 | GATCAATCTGACAAT[C/T]TAAAAATTAAACATT | 26133 |
rs527621610 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081670 | GGTAGTATAACTATA[C/T]TAAAATCAGCAAGAG | 26133 |
rs527627969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013637 | AGCGGGGGAAGTCCA[C/T]AGGAGTTAGAAATGA | 26133 |
rs527663000 | in-del | -/GAT/GATG/GATGAT | 0.0330427 | 0.124565 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002771 | GAGGCTTGGCTCACA[-/GAT/GATG/GATGAT]GATGGGGGGTGGGGG | 26133 |
rs527683890 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043273 | TTTTTTTGAGACGGA[A/G]TCTAATTATGTCGCC | 26133 |
rs527701697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027261 | TTTTTACCATGAAAG[C/G]GTGTTGGATTTTGTC | 26133 |
rs527715135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078309 | ACTACTATAAAAAGC[C/T]TCTTTCTATAAATCT | 26133 |
rs527739952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028107 | AATTTAGATTTATTT[A/T]AAAATGTAGGCATTT | 26133 |
rs527744465 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023160 | GAGACACAGTGTGAC[A/G]CGGTAGTTAAGAGCA | 26133 |
rs527798722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064273 | AGGCCAATACTTAGG[C/T]AGCATGTCCAAGACA | 26133 |
rs527808494 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066089 | TAATTGAAGTATAAC[A/G]TGATACCGCATAAAG | 26133 |
rs527824047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020396 | TGTTTGCTCCAGGCT[C/G]TCCCGCGCTGCCTCA | 26133 |
rs527827043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011823 | TTGGCTGGCAAGCCA[C/T]TTCTGCAGGGGAGAG | 26133 |
rs527832935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065025 | TGTTTAAAGCTCTGA[A/C]GTATACTACACCAAT | 26133 |
rs527857944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012373 | TGCAACAGTGGGCCC[A/C]GTTTCCTGTGCACAC | 26133 |
rs527861886 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028974 | CAGCTTTTTTGGCTG[A/G]GTGGTGGTGGCTCAT | 26133 |
rs527938203 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051250 | GGAACCCCAAGCTAG[A/G]AGGCATTTCAGAATC | 26133 |
rs527945543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006330 | CTGCCCAGACTCCCC[C/T]GTCGTCTCTAACGTA | 26133 |
rs527974294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058544 | TTTAAAAACCCATCC[G/T]AAATAATAATGGGCC | 26133 |
rs527992118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006893 | GGGGAGCTGTCATCA[C/T]CAGGTCTAAAACACA | 26133 |
rs528028762 | snp | A/G/T | 0.000799864 | 0.0199829 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092818 | GAAGCAAGCGGCCTC[A/G/T]GGGCCGCGGAGATTT | 26133 |
rs528033876 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053061 | TATTTAAAAATACTT[C/T]TAGTTGATATATAAT | 26133 |
rs528040126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070693 | GTGAGTCACTGCGCC[C/T]GGCCAAACCTATGTT | 26133 |
rs528065567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010576 | CTTTCTCTTTGCCTA[C/T]ATTTCCACTTGTTTT | 26133 |
rs528068513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018332 | GGGCATGGTGGCTCA[C/T]GCCTGTTAATCCCAG | 26133 |
rs528080496 | in-del | -/AAG | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021828 | TTCCCCGTTTTTTAA[-/AAG]AAGAACCATCTAAAT | 26133 |
rs528131489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055711 | AATTGCTCTTGTTAT[A/G]AATTTCCATTGAAAG | 26133 |
rs528139393 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011061 | GTCAGGAGTTCGAGA[C/G]CAGCCTGGCCAACGT | 26133 |
rs528150989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056499 | CATTAAAAATGAATA[C/T]AAATCCTCTTAATAA | 26133 |
rs528153843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004624 | GCCCAGTGGCTGGGT[C/T]GCCCAGGCCTTTCGT | 26133 |
rs528176303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005149 | TCTGGGGCAGAAAAA[A/G]GAAGCAAACGGCTAA | 26133 |
rs528198364 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042328 | ATAACCTACAAAGTA[C/T]AGTTATGATCACCTC | 26133 |
rs528259937 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048796 | TGGAGTTTCCACTCT[A/G]GAGGTCCCCTTTCAC | 26133 |
rs528342451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091715 | GCTCACTCAAAAATA[A/C]CAATAATCATATGTT | 26133 |
rs528351541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084340 | ACTTCACCACCATGC[A/G]ATACACCAATGTAGC | 26133 |
rs528376215 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033916 | TTTGGGAGGCCGAGG[A/C]GGGTGGATCATGAGG | 26133 |
rs528377028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084673 | ATATATGTGTATATG[C/T]ATATATGTTTATATG | 26133 |
rs528402993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034590 | TTGTTTGGGAGCTGA[C/G]AATTCCTGGGTTTGT | 26133 |
rs528483298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003820 | GCACCTTCCTCTTCC[C/G]CACGCCCACCTCCCA | 26133 |
rs528566486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082759 | ACCACATTGATAACA[C/T]AAAGGAGAATAATTA | 26133 |
rs528571328 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031901 | CTACTTAAAAAAAAG[-/T]TTTTTTTTGAGACAA | 26133 |
rs528574588 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039092 | TAAAACAAAGCAAAA[A/G]AAACAAAAAAGAAAT | 26133 |
rs528580916 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090139 | ATAACTTATTCTGCA[C/G]GATGGGAGAGAGGAG | 26133 |
rs528612574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032086 | ATAGAGATGGGGTTT[C/T]GCCATGTTGGCCTGG | 26133 |
rs528651103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075882 | CCATTCTCCCCGTCA[C/T]TTTCAGGTACACCAA | 26133 |
rs528686940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076514 | GCAGGTCTGTCAGAG[C/T]TTGCTGGAGGTCCAC | 26133 |
rs528690506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032649 | AGCTAATTTTTTGTA[A/T]TTTTAGTAGAGACGG | 26133 |
rs528714472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023922 | GCTTGCGCAGGCCTG[A/C]CAAGACTTTCTGTGA | 26133 |
rs528795520 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070054 | AGAAATGAGGCCAAG[A/G]GCAACATCCTTAGTT | 26133 |
rs528815850 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094450 | GTGGCATGCACCTGT[A/G]GTCCCAGCTACTTGG | 26133 |
rs528838569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056559 | TACAGTATGTCGTAT[C/T]GGGGTAAAAAAAAAA | 26133 |
rs528860840 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026476 | CTGCCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 26133 |
rs528878575 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011668 | CCACAACGTCCTGTG[C/T]AGCCCAGCCCAGAGC | 26133 |
rs528927610 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057236 | TCAGCTAGTTATATG[G/T]GAGAAAGAAGAATTT | 26133 |
rs528930259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049009 | CACCACAGTGCACAT[A/G]AACATCCACCTCCCT | 26133 |
rs528935575 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047053 | TTTATATTTTTAGTA[A/G]AGACAGGGTTTCACC | 26133 |
rs529021429 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024206 | GTTAACCATGGTATC[A/G]TGATTTTTAGGACAT | 26133 |
rs529050509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084682 | TATATGTATATATGT[G/T]TATATGCATATATGT | 26133 |
rs529068509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041989 | ACACCAGCTCTGAGG[A/T]ATAATTTAGTTATAA | 26133 |
rs529074639 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022599 | CTCAAGTTCCTACAG[A/G]AACTGCTTCCCTAGA | 26133 |
rs529086845 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038685 | GGACGTTTAAGAAAC[-/T]GGTAAAAAGTTACCA | 26133 |
rs529107300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034648 | AATGCTTTAAGGCTG[C/G]GCACCTAACCAAAGA | 26133 |
rs529120415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077918 | TTCTGAATTTCTCAA[A/G]TTTTCTATAGCTCAC | 26133 |
rs529212791 | in-del | -/CT | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047069 | AGACAGGGTTTCACC[-/CT]GTTGGCCAGGCTGGT | 26133 |
rs529223845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039140 | TACATGAAAATCTTC[A/G]CATAGCTGGATTTTT | 26133 |
rs529261619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040091 | GTCCCCACCCCCCGC[A/G]CCCCCACAAATTCAT | 26133 |
rs529281558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090237 | AGGTCCCCATTTTAT[A/C]CTCACTATAGCTCCA | 26133 |
rs529388586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032695 | GCCAGGATAGTCTCG[A/G]TCTCCTGACCTCGTG | 26133 |
rs529440317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070261 | GGGTGACTAGTTCTG[C/T]AGCAATAACCAAGTC | 26133 |
rs529451231 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024043 | GAGGCCTGTGCTCCC[-/CT]GAGTCTCTTCAGCTC | 26133 |
rs529458661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077069 | CCTCCAAGCCAGGCG[C/T]AGGATATAATCTCCT | 26133 |
rs529464019 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072128 | CCCAGTTTTTGATGG[A/G]GCTGTTTGCTTTTTT | 26133 |
rs529473609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070773 | ACTTTGTATTCCCCA[C/G]AGATTCCAAGACAGA | 26133 |
rs529484451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025956 | ATTTTGTATATGACA[C/T]AAGGCAGGGGATCTA | 26133 |
rs529506242 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045349 | GATTCAATCACTTCC[C/T]GCCGTTTTACCCCAC | 26133 |
rs529559127 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063345 | GAGAACGGACTGACA[C/G]AACAGGCATATTATG | 26133 |
rs529662493 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071921 | TTAAAAGTGTTCCTA[C/T]TTCTCCACATCCTCT | 26133 |
rs529687101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075679 | GACCTTTCTCTCTGG[C/G]TGCCCTTAATATTTT | 26133 |
rs529699889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015311 | GGGAGCACGGTTCTA[C/T]AGGTGGATGAAAATT | 26133 |
rs529706967 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074997 | TTCTTGTTGAATTGA[C/T]CCCTTTACCATTATG | 26133 |
rs529714769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023143 | CTGAATGAAGTGTGA[A/C]TGAGACACAGTGTGA | 26133 |
rs529768767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060772 | AGATGCAGAAAAAGC[A/G]TTTGGAAAAAAAAAC | 26133 |
rs529807192 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087976 | ACATACTAAGTTTGA[A/G]ATGCCCATTAGACAT | 26133 |
rs529845813 | in-del | -/A | 0.476401 | 0.106032 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009478 | AGACCCCATCTCTAC[-/A]AAAAAAAAAGTAAAA | 26133 |
rs529846973 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090113 | TCTCAAAAAAAAAAA[A/C]GGGTAAGCAAATAAC | 26133 |
rs529849781 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061514 | AAATATAAGGGATGC[A/G]TAACAGCCAAAACAA | 26133 |
rs529910392 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019129 | TCTTTAAGGAGGAAG[C/G]CTTCTGTGAGGCCTG | 26133 |
rs529946927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054904 | TCTGCCATTCTACTC[A/G]AATATTCCCATCTTA | 26133 |
rs529954907 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038842 | CTTTGGGAGGCCGAG[A/G]TGGGTGGATCACCTG | 26133 |
rs529970125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003883 | CAGACCTGGGCTCAA[A/G]CATCACTCCTTCCGG | 26133 |
rs529972751 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046689 | AGGGGGCATTGGGGA[A/G]CAACTGCTTCCACTT | 26133 |
rs529989315 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042320 | ATTCCCTAATAACCT[A/G]CAAAGTATAGTTATG | 26133 |
rs529989575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067574 | CTGTGCAAGAATGTT[C/T]ATAGCACTGTTATTC | 26133 |
rs529995410 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059737 | GAAGAGGAAGAAGAC[G/T]ACGACGAAGAAGAAG | 26133 |
rs530022125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007924 | CTCCTGCGAGCCCCC[A/G]TGAAACATACTCTAG | 26133 |
rs530030854 | snp | C/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094801 | GCCTGGAGGAGGACA[C/T]GACCATAAGTCAGAG | 26133 |
rs530044600 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068799 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 26133 |
rs530052206 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033143 | AGGTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC | 26133 |
rs530056400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089661 | GGAGACCAGCCTGAC[C/T]GACATGGTGAAACCC | 26133 |
rs530086005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052541 | CACTCTGTCACCCAC[A/G]CTGGAGTGCAGTGGT | 26133 |
rs530097691 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014391 | GGCGTGATCTCAGCT[C/T]ACTGCAACCTCTGCC | 26133 |
rs530099415 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036205 | TCCATCATTTAACCT[C/T]CTTTAAAATGAGACT | 26133 |
rs530146835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059887 | AAAAGACGAAGACAA[A/G]GATGAAGATGAAGAA | 26133 |
rs530165534 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058106 | TAAAAGGGTCAATCC[A/T]TTAGAAAGATATAAC | 26133 |
rs530177729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008326 | GCTGCTATAGCTCCT[C/G]GGCCAACCCTGGCTC | 26133 |
rs530196827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053530 | AACTGTGCATTTCCT[C/G]AACAATTTGAAATTT | 26133 |
rs530259400 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002711 | ACCCACCACCCCTGC[C/T]CAGGGCTCAGAAGCC | 26133 |
rs530292545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045397 | CTTTTAAGAGACAGG[G/T]TCTCACTCTGTTGCT | 26133 |
rs530297517 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080883 | TTGTGCAATATGTGA[A/T]TTACATCTCAATAAA | 26133 |
rs530382192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088382 | AGCCATGAGATTGCT[C/T]GGCAAGTACAGACAG | 26133 |
rs530459769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031064 | ATAGTTTTGTAAAAT[A/G]CAAGATTCTTGGTTG | 26133 |
rs530468813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069894 | TGCAGTGAGCCAACA[A/T]AGAGCCACTGCACTC | 26133 |
rs530472170 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091302 | GAACACAAGGGGGAA[-/G]AAAGGCTGCTCATCT | 26133 |
rs530484782 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069387 | ACAAATGCCATAGCC[C/T]CCATGGAGAGAAGAG | 26133 |
rs530550599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016238 | TGATATTCAGGACAA[A/G]TATCAGTACTGTCAG | 26133 |
rs530566285 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010355 | GTCAGCACCAGGCTA[C/G]TGTAGGGAGTCTCCT | 26133 |
rs530566602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061577 | TCTATGATCAGTTGA[C/T]TTTTGACAAGGTTGC | 26133 |
rs530604151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062449 | CCATCAACTGATGAA[C/T]GGATAAATAAGATGT | 26133 |
rs530604947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004587 | TGTGGAGGGAGGCAG[A/G]GGTGCAGCAGGTCAG | 26133 |
rs530691678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055652 | GGCTAGGACTGCATG[C/T]GCGTGTACCACGCCT | 26133 |
rs530706863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048699 | TGGGGTACACAAAAA[A/G]GAATGAGAGGGAGTG | 26133 |
rs530770470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060491 | AGCTACTCAGGAGGC[C/T]GAGATAGGAGGCTCG | 26133 |
rs530783575 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019217 | CTCACGGTGCCCGGC[A/G]CACAGCAGAAACCCA | 26133 |
rs530792636 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015168 | AACATGCCTGGCTAA[C/T]TTTTGTATTTTTAGT | 26133 |
rs530796043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090296 | AATAGCTCCCACACC[C/T]ATATACAACCATCAG | 26133 |
rs530911081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008920 | CCTGCAGCCACAGAA[C/T]TAAACTGCCAAGTGC | 26133 |
rs530923452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088499 | TGAAAAATAAGACAC[A/G]GTCTCTTCAGGAAGC | 26133 |
rs530955255 | in-del | -/GAT | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059854 | GAAGACGAAGATGAA[-/GAT]GAAGAAAAGATGAAG | 26133 |
rs531017277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046083 | TGTGACCATTTATCC[A/G]GAGTGAGAGCAAGAA | 26133 |
rs531043230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082735 | TGAAAATTTTATTCA[A/G]TGCAATTCACCACAT | 26133 |
rs531044715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075023 | TTATGTAATGGCCTT[A/G]TCTCTTTTGATCTTT | 26133 |
rs531097503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038430 | ATTTCCATTAATGGG[A/G]GACTAATTAAATTAC | 26133 |
rs531136654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031267 | TGGAGGCAGGGTCTC[A/G]CTCTGTCACCCAGGC | 26133 |
rs531138281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038989 | TGAGGCACGAGAATC[A/G]CTTGAACCAGAAAGT | 26133 |
rs531179606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036566 | AGAAACACTGAAATA[C/T]ATGCAGGTGAAATTA | 26133 |
rs531218687 | in-del | -/TGTGTGTGTGTGTGTATGTGTGTGTATATATATA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086462 | GTGTGTGTGTGTGTG[lengthTooLong]TGTGTATATATATGT | 26133 |
rs531226897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031961 | CAGTGGCACCATCTC[A/T]GCACACTGCAACCTC | 26133 |
rs531237067 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028536 | GATTTGAGGACATAC[-/T]TTTGTACAGTTTTAA | 26133 |
rs531270974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023705 | AATCCTGCCTCTGTC[A/G]TGCACTGCTGTGAGA | 26133 |
rs531304103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029784 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCAGC | 26133 |
rs531305231 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044348 | AGTGAGCCACGATTG[C/T]GCCACTGCACTCCTG | 26133 |
rs531327604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073917 | ACTTTTTTTGGTTGG[C/T]AGGCTATTAATTATT | 26133 |
rs531331112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087005 | GCACTGCACTCCAGC[C/T]TGGGCAACAGCACGA | 26133 |
rs531336375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030209 | TGGTACCACTGCACT[C/T]CAGCCTGAGTAACAA | 26133 |
rs531420074 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034273 | GTTCTTATTAACTGC[C/T]TCTCTCTGTGGGCAA | 26133 |
rs531428360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013789 | GGACTAGACAGGGTG[C/T]CAGGTCCCAGTAAAG | 26133 |
rs531457311 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080556 | AAAAAAAAAAAAAAA[A/C]CCTAAAAGAAGCCAG | 26133 |
rs531484442 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060010 | TGATTTAAAAAAAAA[A/C]AAACAAAAACAACAA | 26133 |
rs531492158 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074468 | GATCCTGGTATGTCA[A/T]GTCTTTGTTCTCAAT | 26133 |
rs531526976 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059115 | ACAGAGAATAGAAAA[G/T]AACAGAAAATGAACA | 26133 |
rs531528042 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055317 | ATCATTTAATAAAGC[C/T]ATTTTCCCTTAATGT | 26133 |
rs531551594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015143 | TAGCAGGGATTACAG[A/G]TGCCCCACCAACATG | 26133 |
rs531652454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012568 | AAATAAATGAGCGCA[C/G]AATGTCTTTCAAGAA | 26133 |
rs531684397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008389 | GCTCTAGGGAATTCA[C/T]GGCAGGGCCCGTATC | 26133 |
rs531768774 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007753 | TACTCAACATTTACT[C/G]AACATCTACCAAGCA | 26133 |
rs531787820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020923 | CTCTTTAGTCTTCAC[C/T]TCACAGAGGCAACTG | 26133 |
rs531861980 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058104 | GATAAAAGGGTCAAT[C/T]CATTAGAAAGATATA | 26133 |
rs531867097 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029329 | TTCTGTCCTTTACTT[C/T]CAACCTATTTTATCT | 26133 |
rs531870332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078362 | TTACTATGTTATAAT[A/G]AGAAGGAGGGATTGG | 26133 |
rs531874120 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020283 | GTCAGAGGAATGACT[G/T]CTCACTTCACTCAGA | 26133 |
rs531998745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030238 | AAGAGCGAAACTCCA[C/T]ATCAAAAAAAAAAAA | 26133 |
rs532015832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052376 | TGAGATTATAGGTGT[A/G]AGCCACTGCGCCCAG | 26133 |
rs532017540 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093405 | GGGAAGACAGCAGAT[C/G]CATACACAAAGAAAC | 26133 |
rs532028730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022307 | ACTACAGGCATGTGC[C/T]ACCACGCCCAGCTAA | 26133 |
rs532113593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023116 | ATCACAACCTTGGAA[A/G]ACGACAAGCTGCTGA | 26133 |
rs532142881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080670 | GGCAAAGGCTGTGGG[G/T]ATGGGGAAACTGGGG | 26133 |
rs532234896 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061515 | ATATAAGGGATGCAT[-/A]AACAGCCAAAACAAT | 26133 |
rs532298664 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061140 | ATAAGCAAGAGTTCA[A/G]CAAGATTTCACGATA | 26133 |
rs532305296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009470 | AACATAGTGAGACCC[C/T]ATCTCTACAAAAAAA | 26133 |
rs532310084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015251 | AGTGATCTGCCCGCC[G/T]TGGCCTTTCAAACTG | 26133 |
rs532322160 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036979 | CACACACACACACAC[A/C]CCCCTCCCATAATTA | 26133 |
rs532355470 | in-del | -/CAGT | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083661 | TTATACTTCTATACC[-/CAGT]CAAACTAAATATATG | 26133 |
rs532363768 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040427 | CTCCTACTGCTCTTG[A/G]ATATCAGACTCCAGG | 26133 |
rs532401957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008931 | AGAATTAAACTGCCA[A/G]GTGCATTCCCACCAC | 26133 |
rs532450467 | snp | C/G | 1.6684e-05 | 0.00288821 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003366 | CTCTGAGAGGCCCTG[C/G]GTCCGCGGCCCACCC | 26133 |
rs532464401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007223 | GCCATTCTGCTCTAA[C/G]TTTTACTTTTTCTGA | 26133 |
rs532498381 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073684 | TTTGCCAGTATTTTA[C/T]TGAGGATTTTTGCAT | 26133 |
rs532564234 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057863 | CGGCTTTAATTTCTG[A/G]AAAGCTGCAGAACAT | 26133 |
rs532576867 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094273 | AAAATAAACTCAGCC[A/G]GGTGCAGTGGCTCAC | 26133 |
rs532590736 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058877 | TATTTTTAGTAGAAA[A/C]GAGGTTTTGCCATGT | 26133 |
rs532599217 | snp | C/G | 1.64789e-05 | 0.0028704 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044520 | CTTGATTGATTTCAG[C/G]TGCAGAAGGCCCCAA | 26133 |
rs532600594 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081488 | ACCATACTCCAGCCC[C/G]GGCAACAGAATGCAA | 26133 |
rs532602484 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013576 | GATGGAGACTCTGTC[C/G]CAAAAATCCAACCAA | 26133 |
rs532640075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007857 | TTCTATCTGGGTCTG[C/T]CTGGAAGGGGCTGTG | 26133 |
rs532642040 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002659 | ACAGGAAAATGAGGC[A/C]GAGGGGCAGGCTTGG | 26133 |
rs532661234 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087060 | GTCAGCCAGGCGCAG[C/T]GGCTCACACCTGTAA | 26133 |
rs532702502 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055633 | CCTCCTCACCCTCCC[A/G]AGTGGCTAGGACTGC | 26133 |
rs532717153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052456 | GCTACAAACTAGCAT[C/T]CAGTAGGCCAAGCTT | 26133 |
rs532732929 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057892 | ATTATTACTATGATT[A/C]TTCTGTTTAAAGAAC | 26133 |
rs532732982 | snp | A/G | 1.67806e-05 | 0.00289656 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050021 | AGAAAAGGCAGAATA[A/G]GTTGTAAGTACAAAA | 26133 |
rs532756386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053275 | ACCCTTACTGATTTA[C/T]CTAACACTAGGTCTT | 26133 |
rs532832873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045262 | CTCTGCATGCACAGT[A/G]TGAATGATACCATAC | 26133 |
rs532841947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026927 | CTTTGTTGAACCTAT[A/T]TATTAGTTTACTGGT | 26133 |
rs532880016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042801 | CTGAACAGAAATAGG[C/T]GGGCTAGATTGGTTA | 26133 |
rs532914870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035415 | TAATTCTTACTCTGA[C/T]AGTAGCTAAAGCTAC | 26133 |
rs532924845 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003044 | CAAAGACCTGGGGCA[C/G]GCAGAGAGCAGCAGG | 26133 |
rs533054984 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093223 | CACTGCGCCTGTGTC[C/T]TCGTCAGGTCACTCC | 26133 |
rs533076219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043283 | ACGGAGTCTAATTAT[A/G]TCGCCCAGGCTGAAG | 26133 |
rs533099070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073165 | GCTCATCAGTTTAAG[A/G]GGATTTTGGGCTGAG | 26133 |
rs533166755 | in-del | -/GAT | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059782 | GACGAAGACAAAGAA[-/GAT]GAAGAAGAAGGCGAA | 26133 |
rs533171558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033702 | TCTTAATTAAGAAGA[A/G]GGTACCTGGCCAGGC | 26133 |
rs533175414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028335 | TGACCTTAAGCGACC[C/T]GCCTCCTCGGCCTCC | 26133 |
rs533214614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028839 | GCTTCATGTATTTTT[G/T]GGGGGCTGTTTTTGG | 26133 |
rs533248727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034561 | CCCCCCACTCCCAAT[A/G]AGAAACCTATTCCTT | 26133 |
rs533322660 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071633 | TTTTTTATGGCTGCA[C/T]AGTACTCCATGGTGT | 26133 |
rs533384448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019291 | GGTTTTGGGGGGCCA[A/G]GATTTCAAGGTCATT | 26133 |
rs533396119 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084599 | GTTTATATGCATATA[C/T]GTGTATATGTATATA | 26133 |
rs533403021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077111 | TGCTAAGGCCGTTGG[A/G]AAAGTGCAGTTATTA | 26133 |
rs533420281 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011789 | TCACTCAATTCACTA[A/C]AAGCTGACACTTCAG | 26133 |
rs533424806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057309 | ACAAAGATGCATTCT[C/T]TTAACCCAGATCTGA | 26133 |
rs533434704 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072601 | AGTTGTAGATATGCG[A/G]CATTATTTCTGAGGG | 26133 |
rs533484980 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077726 | ATGTAATCTTCTAAA[A/C]CCTTTTCAAAAAGAA | 26133 |
rs533608727 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072072 | GTGTCTGTTGGCTGC[A/G]TAAACGTCTTCTTTT | 26133 |
rs533646314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072752 | TTTGGCTTAGGATTG[A/T]CTTGGCAATGTGGGC | 26133 |
rs533696344 | snp | A/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35092974 | GTAGGTGGGAAAAGA[A/G]ATGTGGCCTTTCCTG | 26133 |
rs533719933 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005959 | GCTGAGGGACCTCCC[C/G]TCACCACCCAGGTAC | 26133 |
rs533739048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065448 | GTCATGTTATGGATA[A/G]GGTCAGGCTGACAAG | 26133 |
rs533762564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085526 | GCTGAGGTGGGAGGA[C/T]TGCTTGAGCCCAGGA | 26133 |
rs533765564 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066079 | GAAACTTTAATAATT[A/G]AAGTATAACGTGATA | 26133 |
rs533780897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058294 | AAGACTTGAACACAA[C/T]GAACACATATATTCT | 26133 |
rs533838459 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052436 | GTCAAGTATCTAAAT[C/G]AGGAGCTACAAACTA | 26133 |
rs533853210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078468 | AAATTCTAGGGCAAC[C/T]GCTAAAAGTATTTTT | 26133 |
rs533883362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028358 | CGGCCTCCCAAAGGG[C/T]TGGGACTACAGGTGT | 26133 |
rs533907684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020638 | TCCTCCCTAGAAGGG[C/T]GCGGTCTGCAGGAAA | 26133 |
rs533948054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018790 | ACCAGAGGAGGCAGC[A/G]GGTACAGGCTCAGGC | 26133 |
rs533949729 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022506 | GTCAGGAGAGGCTAG[A/G]TGATCTTAGCAGAGT | 26133 |
rs533950231 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048945 | TTGTGCTGGGCAATG[A/T]CAAGCAAGGCCTGGG | 26133 |
rs533966646 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063595 | GAGGCAGGGTGGCTC[A/C/G]TGCCTATAATCCCAG | 26133 |
rs533997180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012687 | CCTGGGAATAGCCAC[A/G]CTGTCCACTCTTGCT | 26133 |
rs534028259 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070808 | TTGATACAGCACACA[C/T]AGGGTAGTAGTTCTC | 26133 |
rs534034033 | snp | A/G | 8.25471e-05 | 0.00642392 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35013022 | CTCGTGGTGGTCACT[A/G]AAGCTCTGAAGAAGC | 26133 |
rs534057577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056859 | GGTATGGTGGTGGGC[A/G]CCTGTAATCCCAGCT | 26133 |
rs534060481 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045953 | GGATTACATGTATGA[A/G]CCACTGTGCCTGACC | 26133 |
rs534075991 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005384 | CTGCACCACAGGGCA[A/C]CTGCGATGCCACGCA | 26133 |
rs534102018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051414 | CTGGGCTCAAGCGAT[C/G]CCCCCACCTCAGCCT | 26133 |
rs534116589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058997 | CCCGGCCAAAGAAAA[C/T]TGTTTCTAATCGATA | 26133 |
rs534138714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007348 | ATGGCCTGGCCACCC[A/T]CTAAACCTGTCACCC | 26133 |
rs534172551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050083 | GACACTGAAAAGCAG[C/T]TTCACCTCTGAAAAC | 26133 |
rs534179090 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024868 | AAATTCTGTTTATTC[A/G]TTAATCAGGTGACAG | 26133 |
rs534206442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042244 | ATCTAGAGAGAGAAT[A/T]AACTGGGGTTGGAGT | 26133 |
rs534215279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010869 | TCCCGGTGAAAACAC[A/T]TCCACAGCTTCCCAC | 26133 |
rs534301210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004132 | AGAAGGGAAGGCTGC[A/G]TGACTATTCAGTGAG | 26133 |
rs534363918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057341 | TTTCTACGCAGTACA[C/G]AATGAATAAAGACAG | 26133 |
rs534395068 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081946 | GCCAAGAATGCACCA[C/T]TGCACTCCAGCCTGG | 26133 |
rs534419564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091473 | TAAATAAAGTTACAC[C/T]GTGAAAAGTCTCACT | 26133 |
rs534462603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090437 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 26133 |
rs534478946 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006156 | CTCCCTACAGCGGCT[C/T]CCACCGTGGCACCCA | 26133 |
rs534483385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040253 | GTTTCTGGGTGTGTC[C/T]GTGAAGGTGATTCCA | 26133 |
rs534561186 | snp | G/T | 1.65261e-05 | 0.0028745 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055054 | TGAAAGGGTAATGAC[G/T]GGTTATTTTTCTCAA | 26133 |
rs534654503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047294 | ACCATCATTAATTAT[C/T]ATTGCCTTGCCATTT | 26133 |
rs534663267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042991 | CTTTAGGCATACCAT[A/G]TATGTGGGCAAACGT | 26133 |
rs534673809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081034 | TGTACACTTACAATG[A/G]GTAAATTTTATTGTA | 26133 |
rs534683306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048058 | TCCCTCACTATGGTA[C/T]TGATTTGCATTTCCT | 26133 |
rs534701487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039451 | GGGCTGACATCCCAG[C/T]ATATCCAGTCCTTGT | 26133 |
rs534709611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038471 | TATAATAGAATATTA[C/T]ATAATTACAAAAAGG | 26133 |
rs534738275 | in-del | -/TATA | 0.0944967 | 0.195752 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084667 | ATATGCATATATGTG[-/TATA]TGTATATATGTTTAT | 26133 |
rs534755106 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019531 | CAAGAATCGAGTGTG[A/G]GGACACAGAGTCACC | 26133 |
rs534756982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074743 | GAGAAGAATGTATAT[C/T]CTGTTGATTTGGGGT | 26133 |
rs534758086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083189 | AATCTATCTTATTTT[A/T]ATATTACAGCTACAA | 26133 |
rs534879359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076932 | TCGAGCTTCCCGGCC[A/G]CTTTGTTTACCTACG | 26133 |
rs534919104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070572 | CCCGCCACTGCGCCC[A/G]GCTAATTTTTTGTAT | 26133 |
rs534933075 | snp | A/G | 3.30595e-05 | 0.00406554 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069395 | CATAGCCTCCATGGA[A/G]AGAAGAGGAGAAATT | 26133 |
rs534982726 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038130 | TGGGGTGATGAAAAC[G/T]TGCAACTAGATAGAG | 26133 |
rs535019716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061737 | AAGATCTAAATGTAA[A/G]ATACAAAATATAAAA | 26133 |
rs535048696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009896 | ATGCACGAGACAAGG[C/T]GGTGGGGCAGTGCGG | 26133 |
rs535063156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048164 | CATAACATTGCCCAT[C/T]TGTCTACTGGGCTAT | 26133 |
rs535069563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090509 | CTCCAGAGTAGCTGG[A/G]ATTACAGGTGCTTAC | 26133 |
rs535114460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022703 | AACACAGTGATACTC[C/T]TTAAAGTATCAAGAC | 26133 |
rs535151593 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002761 | CAGGGACAAGGGAGG[C/T]TTGGCTCACAGATGG | 26133 |
rs535152072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023235 | CCGGGTGGTCTTCAG[C/T]AAATCAGTGGACCTC | 26133 |
rs535209390 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068908 | TATCACTCTATGTGC[A/G]GAGAAAATAAACTAA | 26133 |
rs535251322 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015541 | GATCTCAGCTCACTG[A/C]AACCTCTGCCTCCTG | 26133 |
rs535277916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009250 | AAGACGGCCAGGCAC[A/G]CAGGGGTCTGGGCCC | 26133 |
rs535290514 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016290 | GAAAACATCCGTGTA[A/T]CCCCTATGCCCAGCA | 26133 |
rs535363737 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054498 | GGTCCTAACACTAAG[G/T]GCCATCCTCTTTTGT | 26133 |
rs535384580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018899 | CCTTGATAGAAAAGG[C/T]GATGGGGGACGATGG | 26133 |
rs535459132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082920 | AAAACCCACTGCAAA[C/T]ATCATACTTAATGGC | 26133 |
rs535488335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069010 | CTTAAGCAGGACACA[A/C]AAGAAACTAGTAATC | 26133 |
rs535493661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032240 | ATGTTGGCCTGGCCA[A/G]TCTTGAACTCCTGGC | 26133 |
rs535497280 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022100 | TACTGTGCAGACTGA[A/G]TGGGAACGTAAGAGA | 26133 |
rs535544456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075909 | CCAATCAGACGTAGA[C/T]TTGGTCTTTTCACAC | 26133 |
rs535545466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076948 | CTTTGTTTACCTACG[C/G]AAGTCTCAGCAGTTG | 26133 |
rs535571121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024050 | GTGCTCCCCTGAGTC[G/T]CTTCAGCTCTACCAC | 26133 |
rs535612368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025698 | CCCACCCTGCCTTAC[C/G]CACAAAAAACGTTCT | 26133 |
rs535614899 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033989 | TCTCTACTAAAAATA[C/G]AAAAAATTAGCCGGG | 26133 |
rs535678354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071102 | TCTATCAGACTGTGA[A/G]ATTCAAAATATGAAA | 26133 |
rs535682676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062579 | AAAGAAGCCAGTCAC[A/G]AAAGACCACGTATTG | 26133 |
rs535777428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019667 | ACATATAAGCAACTG[C/T]GAAAGTGCCTCAAAA | 26133 |
rs535792344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055809 | CTGTTATCTGTGTTG[C/G]GCAAATGGCTCTTAA | 26133 |
rs535818232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004698 | TCAAAACAGCTTCAA[C/T]GAAAGCTGACTGTGG | 26133 |
rs535837661 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075356 | TCTTCCTAGCATCGA[A/C]GGTCTTTACAATTTG | 26133 |
rs535854365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023299 | CAGCAATACTGACAA[C/G]CATACCTACCCCTTA | 26133 |
rs535901576 | snp | C/T | 1.68613e-05 | 0.00290351 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008630 | CTGGCTCTGCAGCCC[C/T]GCAGAATCGGCAGGT | 26133 |
rs535971557 | in-del | -/TG | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012602 | GGGAGCACACCTCCT[-/TG]TGTGGAGGGAAGAAT | 26133 |
rs535986695 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016661 | TAAGAGTTGGAAAAG[C/G]CTTTCTGAAGGATTA | 26133 |
rs535993926 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062033 | AACAGACATTTCTCC[A/G]AAAGTCCAATAATAA | 26133 |
rs536001485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045606 | TGCAGTGGCGCAATC[C/T]TGACTCACTGCAAAC | 26133 |
rs536005947 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055961 | GTATGAACCATGGAC[-/A]AAAGTGCTTTATTTG | 26133 |
rs536019447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054368 | GTGTTTTCACATCTA[C/T]TATCTCATTTCTCAC | 26133 |
rs536074027 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019741 | ATTTTTTATTAAAAA[C/T]ATGTTCCGTATTGAA | 26133 |
rs536076303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009926 | GAGCACACATGACTT[A/C]TGGCAGGTGACCTCT | 26133 |
rs536105313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004224 | GGACATGGGGGAGGC[A/G]GGGAGAGCACTGGCC | 26133 |
rs536123762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038589 | TTTACATTACCATCT[A/G]TACAAACAGGAGTCA | 26133 |
rs536167020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047402 | CTGGCTTCTACCACT[C/T]GATTATTTCAATTAC | 26133 |
rs536299596 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094382 | TCGAGACCAGCCTGG[C/G]CAACATGGTGAAACC | 26133 |
rs536302483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086586 | GTGTGTATATATATA[C/T]GAATAAGACTTTATC | 26133 |
rs536335463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036900 | GCAGTGAGCTGAGAC[C/T]GCACCACTGTACTCC | 26133 |
rs536387355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079383 | TTTGTGGGATGCAGC[A/G]AAAGCAGTAATAAGC | 26133 |
rs536412178 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083496 | CGCCTGTAATCCCAG[C/T]TACTAGGGGAGGCTG | 26133 |
rs536414285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029286 | CTCTCCAGCTTTCTC[A/G]TGGATGCTGCCTGCA | 26133 |
rs536431869 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023118 | CACAACCTTGGAAGA[C/T]GACAAGCTGCTGAAT | 26133 |
rs536519017 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047545 | TTCAGTTTTTTGTTC[C/T]GAAACAACGAAGCTA | 26133 |
rs536522796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088804 | ACAGATGATCCTTGA[A/G]GACATTATGTTAAGT | 26133 |
rs536576632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022444 | TACAGGCGTGAGCCA[C/T]GGTGCCCAGCGTAGA | 26133 |
rs536582996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013941 | AACCCTGGGCTCATA[C/T]GACTGGGGCAGTAGG | 26133 |
rs536610012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051978 | TCCTTCCTTTCCTCT[A/G]TATCACAAGTTCTTA | 26133 |
rs536618849 | snp | A/C | 1.69516e-05 | 0.00291127 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001945 | CCCTGTGTGTGCCCC[A/C]AGGAGCAGCAGGCCA | 26133 |
rs536652417 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053014 | TAATTGAACCATATC[A/G]CCCTATGTTCCTCAA | 26133 |
rs536662388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016917 | ACCGTGTTGGTGACT[C/T]GGGCATTGGGTACAT | 26133 |
rs536774236 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039875 | AATCTCAAAAAATAA[C/T]GACTTACGCTATCTT | 26133 |
rs536791897 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087211 | AGGCGTGGTGGCGGG[C/T]ACCTGTAGTCCCAGC | 26133 |
rs536799306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003981 | AGCACTAGCCTGCGC[A/G]CCTCGGTGGGGAAAG | 26133 |
rs536811905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047247 | CTAGCTGTGTGTGCC[C/T]TTCCTATTGCATCTC | 26133 |
rs536852683 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031579 | TGTGGATCTGAGTAT[A/T]CCGACTTGGATTCTT | 26133 |
rs536861550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029857 | TAGCCAGGGTGGTCT[C/T]GATCTCCTGACCTCG | 26133 |
rs536912281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074155 | TGCATCTATTTGATT[A/C]TTCTCTCTTTTCTTA | 26133 |
rs536950822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067219 | GGCTGGAGCGGGGGC[C/T]CATGCTTGTAATCCC | 26133 |
rs536976055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024135 | TGCACACTCACTTTT[G/T]TTTTTTTTTAACAGC | 26133 |
rs536999487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053899 | TGCATTATATTTCAA[C/T]TGCACAGCACTATTA | 26133 |
rs537010838 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067152 | GAAATTCAAATCAAG[A/G]CCACAATGAGATGTC | 26133 |
rs537047380 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083962 | TTCAAATGATTTCTT[A/T]AAAAAAAAAAAAAAG | 26133 |
rs537085900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054459 | TGGGAGGTGTACTAA[A/G]CCAAGGGCCAGAACA | 26133 |
rs537101219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011120 | AAAAAATTAGCTGGG[C/T]GTGGTGGCACACGCC | 26133 |
rs537122824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080358 | AAAAAAAAATTAGCC[A/G]GATGTAGTGGCACAT | 26133 |
rs537128107 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046461 | AGATCACATGAACTT[G/T]TAATAATCTGTTCCT | 26133 |
rs537159709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080958 | TTAGGATGACAATGT[C/T]CTAAAACCAGATTGT | 26133 |
rs537160224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074289 | TACTGCTCTGATCTT[A/G]GTTATTTCTCGCCTT | 26133 |
rs537177173 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014253 | CCCTCCCTGCCTGGA[A/G]TGAAATGAGATCCCC | 26133 |
rs537189553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088956 | GAAGTTGTTCAATGG[C/T]AGTTTCAGATTTGCA | 26133 |
rs537209106 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083468 | AAAAAAATTAGCTGG[G/T]CGTGATGGTGGGCGC | 26133 |
rs537218474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038761 | AAAAAATTTTAGGTG[C/T]GTATTATTTTTTCTA | 26133 |
rs537261688 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091739 | ATATGTTGGGCACCT[A/G]TTATAAGTCAGATGC | 26133 |
rs537315600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083030 | GTAAGGCAAGATATA[C/T]AGAAGACATAAGATT | 26133 |
rs537361322 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057770 | CCAGCTTGGCCACCT[-/A]ACTTGCCCTTCTCTG | 26133 |
rs537363627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076077 | CTTGTGCATGCGTCA[C/T]GTAGTTTTCGAGCCA | 26133 |
rs537364226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068816 | TGAGCCACTGCGCCC[A/G]GCCTAAAATTGTTTT | 26133 |
rs537384964 | snp | C/G | 1.6522e-05 | 0.00287414 | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35008680 | TGAAAGACGACTCTG[C/G]TGGCTCCTTCTTCAT | 26133 |
rs537419536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044790 | CTCTTTCGCATCCCC[G/T]TACATACGGGGCTTA | 26133 |
rs537438767 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072859 | ATGGCATTGAATCTA[C/T]CAATTACCTCGGGCA | 26133 |
rs537458521 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029065 | CCAACCTGGCCAACA[A/T]GCTGAAACCCCATCT | 26133 |
rs537481055 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065581 | CTACCAGCAGCAGGA[C/G]AGCAAGAGAGTTCAC | 26133 |
rs537569119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066097 | GTATAACGTGATACC[A/G]CATAAAGAGTACAAT | 26133 |
rs537604538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059217 | ACAGATTACTATACT[C/T]AGAAATAAAGGAGAG | 26133 |
rs537643512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062543 | TGACACGGATTAACC[C/T]TGAGAACATTATGTT | 26133 |
rs537665720 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022594 | GTCCTCTCAAGTTCC[C/T]ACAGGAACTGCTTCC | 26133 |
rs537687590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052052 | GCAACTACATTTTTC[A/G]GGGGAGAGTTTTTTC | 26133 |
rs537692806 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059754 | CGACGAAGAAGAAGA[A/C]GACGAAGAAGACGAC | 26133 |
rs537706380 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093800 | GACACAATAAATAAT[C/T]ACACCGGGACGGTAG | 26133 |
rs537762684 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060206 | AAAACCAAACAAAGA[C/T]ATCACAAGAAAACTA | 26133 |
rs537794359 | in-del | -/CCTCAG | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026328 | CAAGCTACCCTCCCA[-/CCTCAG]CCTCTTGAGTAGCTG | 26133 |
rs537865920 | snp | A/C/T | 1.83977e-05 | 0.00303291 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002200 | GTGACGGCCTGACCC[A/C/T]CTGGGCTCTAAAGAG | 26133 |
rs537867017 | snp | A/G | | | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002101 | GTGAGGAGTGGCAGG[A/G]GCATTGCTCTCTGTG | 26133 |
rs537871003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005535 | AGTGTTGAACAAGGC[A/G]GCAAAGCCAATTGCC | 26133 |
rs537909505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006063 | TCCTTTAATTTTTAC[C/T]TTTAATTTTACTTCA | 26133 |
rs537982840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013125 | GGTTCCAAAATAACA[C/T]AAGCAGACACTCTGG | 26133 |
rs538058741 | snp | A/C | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008600 | AGGAGGTATTCCTAA[A/C]CTCCTGAGAAACACC | 26133 |
rs538061473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007471 | CTCCTGATGAACTGT[C/T]TGGGGCTCAGGACAG | 26133 |
rs538095413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034820 | AGAAAAAGAGACGAG[A/G]AGAGAAGTTTCTAGG | 26133 |
rs538098444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008041 | CACTGGGCTCACAGA[C/T]GATGGGCTGGCCTAG | 26133 |
rs538115478 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020298 | TCTCACTTCACTCAG[A/C]GTAAAAACCAAAGTC | 26133 |
rs538124151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052558 | TGGAGTGCAGTGGTG[C/T]AATCTCAGCTCACTG | 26133 |
rs538133878 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035701 | AGGTGAAGGTAACTA[A/T]ATGTTCATCAACAGC | 26133 |
rs538140956 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002338 | AGCCAGTTTCCTTCT[A/C]ATTCTTTTCTTTGGG | 26133 |
rs538194582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056960 | CACTGCACTCCAGCC[C/T]GGGCAACAGAGCGAG | 26133 |
rs538236052 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005085 | CTGGGAGGCAGGGCA[A/G]TAACCGAAGGTACCA | 26133 |
rs538243574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066289 | TTTTTTAATTTTTAG[G/T]AGTGATGGGGTTTTG | 26133 |
rs538256171 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027699 | TTCAATCTCGTTGTT[A/C]TACTTCAGGTTTTCT | 26133 |
rs538366375 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051762 | AAAAAGAGAACTAAA[C/T]TTACACTTTCTCAAA | 26133 |
rs538379811 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057167 | ACAAAGAGCATGTAT[C/T]ACCTTTCTAAAAAAA | 26133 |
rs538390363 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084612 | TATGTGTATATGTAT[A/G]TATGTTTATATGCAT | 26133 |
rs538417548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060094 | AACAATACAAGACAT[A/T]TAAAGAATGATCAAT | 26133 |
rs538428494 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35092839 | GCGGAGATTTCTACG[G/T]GGCGGCGGAGGGGTC | 26133 |
rs538442181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013697 | GCCAAGGAACTGATA[C/T]TCAGCAGCTGTGGGC | 26133 |
rs538472922 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094649 | TGAATATAACATCTT[A/G]AAATTTGTCCCTGAG | 26133 |
rs538477894 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043097 | TTAATATATCTTGGA[G/T]ATTTTTCTATAGCAG | 26133 |
rs538521023 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045547 | GGCTACTTTTTTAAT[A/T]TTTTTTTTTTTGAGA | 26133 |
rs538608420 | in-del | -/TACA | 0.011808 | 0.0759249 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084728 | TTATATGCATATATG[-/TACA]TGTATATGTATATAT | 26133 |
rs538624237 | snp | A/G/T | 3.29496e-05 | 0.00405881 | missense, synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006486 | GAATGCATCAACGTT[A/G/T]AACTTCATCAGCTCC | 26133 |
rs538636881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074007 | TTAGTCTTGGGAGGG[C/T]GTATGTGTCCAGGAA | 26133 |
rs538679676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013835 | CACTTGGTGAAAGAA[C/G]GGTTAGAAAGGCCTG | 26133 |
rs538712087 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35092919 | GGGACCGTGTGCGGC[A/G]TGGAGGCTACTGGGA | 26133 |
rs538734240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043117 | TTCTATAGCAGTACA[C/T]AGAGATCTTCATTTT | 26133 |
rs538766953 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008101 | CCCAGAGGGCACAGC[A/G]GGTATCCACGACAGG | 26133 |
rs538805434 | snp | C/G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004089 | CTAAGATCACCCTCA[C/G/T]TCTAGAAAAGAGGGG | 26133 |
rs538809046 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002417 | AGTCATTTTTAAAAT[A/G]AAGTTATTTAATAGT | 26133 |
rs538819995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035750 | GACACATTTATACAA[C/T]GGAATACTGCATAGA | 26133 |
rs538857284 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052961 | CCCTGAGAGCCCCAG[C/G/T]TTCTCTACATTAACA | 26133 |
rs538869191 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080220 | TCTAACTGGGCACAG[G/T]GTCTCATGCCTCTGA | 26133 |
rs538939947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029175 | AGAATTGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 26133 |
rs538966839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087989 | GAGATGCCCATTAGA[C/T]ATCAAAGTGGAAATG | 26133 |
rs538972428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029838 | AGACGGGGTTTCACC[A/G]CGTTAGCCAGGGTGG | 26133 |
rs539030921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041211 | TGACTGATACACACA[C/T]CTGAGATAAAGGCAT | 26133 |
rs539031796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084486 | TATATATGTGTATAT[A/G]TGTATATATCTATAT | 26133 |
rs539103489 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006008 | ATTCAGCACAGATCC[A/G]ACACTCTCTCCAGTG | 26133 |
rs539113624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051862 | CACCTTTCTCCTCTC[C/T]TCAATTTATCAAAGT | 26133 |
rs539119738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077516 | AATTTCAGGGGTGGG[G/T]CCCAGAACTCTGTGT | 26133 |
rs539156533 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077984 | AGGGAAAAAAAAAAC[A/G]GCAGACATCTTGTGT | 26133 |
rs539210903 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077658 | CTTCAATCTTCTTAC[A/G]TTAGTAATAATATTC | 26133 |
rs539291394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064502 | TCCTGAATTAAGAGA[A/G]ATGTGTTATTTTAGC | 26133 |
rs539307681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011993 | AGACTCTGCCCTTCA[C/T]GAGAGCAGGGGCCAT | 26133 |
rs539342366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073457 | GATACGTCCCATCAA[C/T]ACCTAGTTTATTGAG | 26133 |
rs539387103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006108 | GGTTTCTGTCACACA[C/T]ACTCGGTGAGCCTAA | 26133 |
rs539404232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091853 | AATCTTAAAAGGTAG[A/G]TTACTAATTCTCATC | 26133 |
rs539483300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062016 | AATGGAGAAAGCAGA[C/T]GAACAGACATTTCTC | 26133 |
rs539501013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017771 | ACCTCTTCCTTCAAC[A/G]TATTAGGTTGTGTAA | 26133 |
rs539508823 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024957 | AACAAATTTTTGTGT[A/C]ACATATATTTTCATT | 26133 |
rs539530329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071204 | TATAATAATCAAAAC[G/T]TCACCTCTGAAGAAC | 26133 |
rs539532617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034716 | CTGGGAGTCTTCTTA[C/T]TTAATAGGCAGTCTT | 26133 |
rs539566093 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027551 | AGTAAGTTGGGAACT[A/G]TTCCTTCCTCTTTTA | 26133 |
rs539581458 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068571 | TCATCACCCAGGCTA[C/G]AGTGCAGTGGTATGA | 26133 |
rs539586932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010763 | GTGTTCCCAGGACAC[C/T]AGCTCCCTTTACTAA | 26133 |
rs539605010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063491 | TTGGCGTGATAAAAA[C/T]GTTCTGGTTATCACT | 26133 |
rs539685377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056759 | CTGAGGTGGGCAGAT[A/C]ACTTGAGGTCAGGAG | 26133 |
rs539695160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020525 | AAATGGGGGTAACTG[C/T]ACCTCTGTTGCCCAG | 26133 |
rs539705749 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045675 | TCCCAAGTAGTGGGG[A/C]TTACAGGCGCCCGCC | 26133 |
rs539792018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091297 | TCTTAAGAACACAAG[A/G]GGGAAAAAGGCTGCT | 26133 |
rs539815856 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046827 | AAAACAGGTCCCACC[A/G]CCCCCAGCCCACTTC | 26133 |
rs539922358 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042576 | GTATAATTTTACCTT[C/G]TTTATTTGGTGTACC | 26133 |
rs539959999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057116 | AAAACACTCTGACTT[C/T]TTACCATTCACACCC | 26133 |
rs539999289 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011174 | CTGAGGTAGAATTGC[A/T]TGAACCCAGAAGGTG | 26133 |
rs540064233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048325 | CAAGCAATTCTCATG[C/T]CTTAGCCTCCCAAGT | 26133 |
rs540078483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090570 | GTAGAGACGGGGCTT[C/T]GCCATGTTGGCCAGG | 26133 |
rs540086541 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019891 | ACCAGGTGTAGGTAA[C/T]CAATCCAAGTGTCAA | 26133 |
rs540097098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092311 | CAAACACGACAGGGT[C/T]CCCCAGACGTGTAGA | 26133 |
rs540102212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005342 | CATGGAAGTGCGTTA[C/G]CAAGTCCAGGAGGGT | 26133 |
rs540184024 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093009 | GCCGGTTTCTCTGGC[C/T]CCCGGGCCCAGCATT | 26133 |
rs540193433 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074272 | GTCTCTATATCCTTC[A/C]GTACTGCTCTGATCT | 26133 |
rs540195556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026720 | CATGGGATGTCTTTA[C/T]ATTTATTTAGGGTTT | 26133 |
rs540204515 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018370 | GGAGGCCAAGGCGGG[C/T]GGATCACTTGAGGCC | 26133 |
rs540320663 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018707 | CATTATTCCTACTCT[C/T]AGGTCCAGCCCCGTA | 26133 |
rs540324489 | in-del | -/ATAAC | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082753 | CAATTCACCACATTG[-/ATAAC]ATAAAGGAGAATAAT | 26133 |
rs540351771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039955 | GCCCCAGGAAGATAG[C/T]GTAAATCATTATTTT | 26133 |
rs540388708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040523 | CACCATTAGCTTTCC[C/T]GGTTCTAAGTTTTCC | 26133 |
rs540400232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090688 | CTCTGGTGGGCTTTT[C/G]TAGGCTCCTCCCATT | 26133 |
rs540418291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057687 | TTACAAGACCCTTTT[G/T]TTCCAGGAGGCAGTT | 26133 |
rs540424437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049628 | CTACATTCACAGAGT[A/C]AATCTGAAGTTCTGA | 26133 |
rs540466237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050530 | GACCAGCCTGGCCAA[C/T]GTGCCAAAACCCTGT | 26133 |
rs540478936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077054 | CCGTGGGCATGGGAC[A/C]CTCCAAGCCAGGCGC | 26133 |
rs540486424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084218 | TAGGTTGCAGGGAGC[C/T]GAGATTGCGCCATTC | 26133 |
rs540562330 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002478 | AAATTGGCAACACAA[C/G]GAAGGGCCCCATGTC | 26133 |
rs540566676 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077541 | CTGTGTTTTAACACG[A/C]TCTTCAGGTGATTCA | 26133 |
rs540567181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070759 | CACAAACAGATCCCA[C/T]TTTGTATTCCCCACA | 26133 |
rs540678705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004895 | CCCTCCACAGGAAGA[C/T]GGATCCATGACGCTG | 26133 |
rs540683596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089112 | GGGCTCAAACAATCC[A/G]CTCACCTCAGCTTCC | 26133 |
rs540714310 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031270 | AGGCAGGGTCTCGCT[C/G]TGTCACCCAGGCTGT | 26133 |
rs540836090 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024258 | ACCACAATCAATTTT[A/T]GAATATCTTCATCAC | 26133 |
rs540876047 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084532 | TATGTGTATATATGT[A/C]TATATGTATATGTAT | 26133 |
rs540908583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034433 | TAGAGCTTCCACACC[A/G]TGAGTACAGTATGGA | 26133 |
rs540948261 | snp | C/G | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092727 | CCGCCACTGTGGCTG[C/G]CGACCGTCTCCCTCG | 26133 |
rs540978211 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066076 | AAGGAAACTTTAATA[-/AT]TGAAGTATAACGTGA | 26133 |
rs540984207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038293 | ATTTTTTTTTTTAAC[A/G]TATCAGCTTGGCAAA | 26133 |
rs541003673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074324 | TAGCTTTTGAATGTG[C/T]TTGCTCTTGCTTTTC | 26133 |
rs541008731 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057891 | CATTATTACTATGAT[A/T]CTTCTGTTTAAAGAA | 26133 |
rs541044199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066653 | AAAAACTGTAAAATA[G/T]TAGAAGGAAATAGGC | 26133 |
rs541045251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081544 | ATAAAATAAAATAAA[A/T]ATAAAATAAAATAAA | 26133 |
rs541070105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030990 | TTTGTCTGTTACTAA[C/T]GAGTTCTTTCAGTTT | 26133 |
rs541125908 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092389 | CACGCCATCAGTGTC[C/T]ACAGCAGCCCAGCCC | 26133 |
rs541168983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068371 | ACAATAAAAAACATA[C/T]GTTCTTGTTCCAAAG | 26133 |
rs541170109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075600 | CCCCACTCTCTTCTG[A/G]CTTGTAGAGTTTCTG | 26133 |
rs541206903 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076192 | TTTTAGCTTCTTTAT[C/G]ATGGGTTCAAACATC | 26133 |
rs541220144 | in-del | -/CT | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033926 | GAGGCGGGTGGATCA[-/CT]TGAGGTCAGGAGATC | 26133 |
rs541254420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060350 | CCAGCACTTTGAGAC[A/G]TCAAGGCAGGAGGAC | 26133 |
rs541259359 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002664 | AAAATGAGGCAGAGG[A/G]GCAGGCTTGGGGGAA | 26133 |
rs541283014 | snp | A/G | 1.66885e-05 | 0.00288859 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008796 | GAGAGGCTGACAGGG[A/G]CCCTGGGGATGGGTC | 26133 |
rs541299644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069693 | CACCTGTAATCCCAG[A/C]ACTTTGGGAGGCTAA | 26133 |
rs541314313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009514 | AGCTGGGAATGGTGG[C/T]GCACACCTGTAGTCC | 26133 |
rs541403794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030100 | TACAAAATTAGCTGG[A/G]CATGGTGGCACATGC | 26133 |
rs541403883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021530 | CAGGAGCCAGGTGAG[C/T]GCAGAGACTCGGAAA | 26133 |
rs541442895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060506 | CGAGATAGGAGGCTC[A/G]CTTGAGCCCAGGAGA | 26133 |
rs541470817 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011946 | TAATGCTCAACGGTG[A/G]AATCCTTGGATGAAC | 26133 |
rs541530056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076329 | TGTTCCTTTGGAGGA[A/G]AAGAGGCGCTCTGAT | 26133 |
rs541545530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008295 | CCAGCCCTAGCAGCG[C/G]AAGAGGCTTTCCTTT | 26133 |
rs541567238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014945 | TCAGAGCTCTCTCAA[G/T]GGGACTGTGAGAGAC | 26133 |
rs541626179 | snp | A/C/T | 1.65102e-05 | 0.00287312 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044697 | GATTGGGGACTTCAT[A/C/T]TAGTCGGATCATTTC | 26133 |
rs541632627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017205 | GGTATTTTATATGTC[A/G]TGAACTGAACAATTG | 26133 |
rs541737100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088295 | GATTAAATAACTTGC[C/T]TAAAGACACATAGTA | 26133 |
rs541775157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056163 | CACCTTTCAACCTAC[C/T]GGGGCTCTGTGATTG | 26133 |
rs541796993 | snp | G/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093143 | CAGGCCCTCGAGTCC[G/T]CTTCCTGCCTGCTTC | 26133 |
rs541816447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068607 | GCTCACGGCAACCTC[C/T]GCCTCCCGGCTTCAA | 26133 |
rs541833974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022891 | AGCTGGGCATGGTGG[C/T]ATGCGCCTGTAGTCC | 26133 |
rs541948497 | in-del | -/AAGTT | 0.00279162 | 0.0372561 | utr-variant-3-prime, downstream-variant-500B | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002418 | GTCATTTTTAAAATA[-/AAGTT]ATTTAATAGTCTCCA | 26133 |
rs542080116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089172 | CCACACTGGGCCTGA[C/T]CTATACACTTATAAA | 26133 |
rs542089871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046633 | CATGAATCCCATACT[C/T]GCCTCTATTTCTAGT | 26133 |
rs542105264 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004488 | CACGTGGATGATGTT[G/T]ATGAGGCGGAAGAGG | 26133 |
rs542121683 | in-del | -/TA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068901 | TATGGTATATCACTC[-/TA]TGTGCGGAGAAAATA | 26133 |
rs542287760 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060799 | AAACCCAAAACACTT[C/T]CATGATAAAACAATC | 26133 |
rs542307914 | snp | G/T | | | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007709 | TTCAGTTCTCCAAGG[G/T]GTTGGGAGATGTTTG | 26133 |
rs542319278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086880 | TTTACTAAAAATACA[A/G]AAAGTAGCCGGGCAT | 26133 |
rs542326991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054057 | CAATTCCTGGCTATA[C/T]GTTATGTCCCCACCT | 26133 |
rs542334446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037164 | ATCCTGGCTAACACG[A/G]TGAAACCCCATCTCT | 26133 |
rs542336320 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045082 | CAGATTTGCTTTTTT[A/T]AAAAATAAAATACTT | 26133 |
rs542341937 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008829 | TCTGCTGGCTTAGGC[A/G]GTGAAAAACCATGGG | 26133 |
rs542393205 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083961 | TTCAAATGATTTCTT[-/A]TAAAAAAAAAAAAAA | 26133 |
rs542397362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046040 | TTGCAATGAACATTC[C/T]TACAGGTACTCTCTG | 26133 |
rs542409200 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085209 | CTGCTGTTTTTTTGT[C/T]ACAAGCTCCATGATA | 26133 |
rs542458877 | in-del | -/TCACCCAG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013569 | CTGGGTGATGGAGAC[-/TCACCCAG]TCTGTCCCAAAAATC | 26133 |
rs542485637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074430 | AAATTTCCCTCTACA[C/T]ACTGCTTTAAATGTG | 26133 |
rs542520313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067614 | AAAAGACGGAGGCAA[C/T]CCAAATGCCTCTCAA | 26133 |
rs542527732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081226 | CCAATTAAAAACAAA[A/G]TTTGGGCCGGTTACA | 26133 |
rs542539829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030747 | ATATGTTTCCATATG[C/T]TATAGGTTCAACAAT | 26133 |
rs542546360 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088708 | ACTTAATCTTGGTCA[-/C]CCTGCTAGGATTCAA | 26133 |
rs542553909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082641 | AGTTTCACTAACGAC[A/G]ATGTAAGGGAAAAAC | 26133 |
rs542560447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038931 | ACAAAAAAATTAGTC[A/G]GGCCTGGTGGCGCAT | 26133 |
rs542612102 | snp | C/T | 6.59326e-05 | 0.00574125 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035193 | AGCATTGTCTAGCCA[C/T]GTGTACCACTCTTCC | 26133 |
rs542638677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078314 | TATAAAAAGCCTCTT[A/T]CTATAAATCTTCAAA | 26133 |
rs542669633 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093854 | GAACTGGCACTATGG[C/T]TACCATCCTCACACC | 26133 |
rs542817251 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007376 | CCCCGTAAGCACCCA[C/T]GGGGAACCCACAGTT | 26133 |
rs542821336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012882 | ACCTGCTAACACTGA[A/G]GGGACAGTGGGCTTC | 26133 |
rs542855411 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057318 | CATTCTCTTAACCCA[G/T]ATCTGAATTTCTACG | 26133 |
rs542863525 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042076 | TGCAGGTTTGTTACA[A/T]ATGTATATATGTGCC | 26133 |
rs542895370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022233 | TGACCTTGGCTCACT[A/G]CAACTTCCGCTTGCT | 26133 |
rs542909565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013322 | GTGGTGGTTACACCT[A/G]TAATCACAGCACTTT | 26133 |
rs542920712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058586 | CACAAGGGGAAGTAT[A/G]AAGTATCCAAGAAGG | 26133 |
rs542991797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086009 | ACCTCCGTCTCCTGG[A/G]CTCAAGTGATCCTCC | 26133 |
rs543000979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043145 | TTTTTCAAAGCTACA[C/T]AATTTTCCATTATAT | 26133 |
rs543002187 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045141 | CCCCATCCAGTCGCA[-/T]TTTTTTCTCTCCCTG | 26133 |
rs543061320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078841 | GAAGCCGAGGCAGGT[G/T]GATCACCTGAAGTCA | 26133 |
rs543089606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028614 | TGTCCTGGAGAATGT[G/T]CATGTGCACTTGAGA | 26133 |
rs543092345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045687 | GGGATTACAGGCGCC[C/T]GCCACCACGCCTGGC | 26133 |
rs543142345 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012303 | CATTTAAAATCAGGA[A/C]CTTTCACATAAATCT | 26133 |
rs543222241 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063753 | GTAGTCCCAGCTACT[C/T]GGGAGACTGAGGCAG | 26133 |
rs543224506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073527 | CTTTTCTGCACCTAT[C/T]ATCATGTGGTTTTTG | 26133 |
rs543224552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065865 | TCAGTTCTTACTAAG[C/T]AGATTTCTTGATGAA | 26133 |
rs543225213 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089576 | AAAATTTTGGCTAGG[C/T]GCAGTGGCTCACACC | 26133 |
rs543301413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023352 | ATACTGAAGGTGCCT[A/G]GAACATAGCCCCAAG | 26133 |
rs543312454 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066367 | CTGCTTCGGCCTCCT[A/G]AAGTGCTGGGATTAC | 26133 |
rs543338598 | snp | A/G | 1.65072e-05 | 0.00287286 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007557 | GATCATACCTCCAAG[A/G]GGCCTCGCTTCAGCA | 26133 |
rs543364278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069100 | TTTTTTAAAAAGGTA[C/T]ACACCAATTTAAATA | 26133 |
rs543423908 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028780 | TGTTAAGGTCTCCAG[C/G]TGTTGTTTTTGAACT | 26133 |
rs543439804 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073059 | AATTGTGAATGGGAG[A/T]TCACTCATGATTTGG | 26133 |
rs543457398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087511 | TGAAGGGCATCCAGG[A/G]ATGGCGGGTCATGAC | 26133 |
rs543588210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074880 | TGGGGTGTTAAAGTC[C/T]CCCATTATTATTGTG | 26133 |
rs543589159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081447 | TGATGCTAGGAGGCC[A/G]AGACTGCAGTGACCT | 26133 |
rs543604128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023006 | CACTCCAGCCTGGGC[A/G]ACAGAGCTGGACTGT | 26133 |
rs543653296 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067336 | TACTTTTTTTTTAAA[A/T]TTTAAAACACTTTCA | 26133 |
rs543675501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068711 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATCTT | 26133 |
rs543683804 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052409 | TAATCATAAGCTCTT[C/G]ACCTAGTATCTGTCA | 26133 |
rs543689860 | snp | A/G | 0.000973947 | 0.022046 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015145 | GCAGGGATTACAGGT[A/G]CCCCACCAACATGCC | 26133 |
rs543709841 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059998 | AGACTGACTTAGTGA[C/T]TTAAAAAAAAACAAA | 26133 |
rs543786670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079546 | TGAGAGCAAACATCA[C/T]TGAAATTGAAAACAA | 26133 |
rs543801559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064922 | TGTTACACCTAACGG[C/T]CTTGGTATACACAAG | 26133 |
rs543803075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028690 | CTGTTAGTCCTTGTT[A/G]GTATACAGTGTTATT | 26133 |
rs543849075 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083738 | AAAAAAAGTTACCTC[C/T]CATGTACTCTTTCTT | 26133 |
rs543873161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073612 | CAGCCTTGTATCCCA[C/G]GGATGAAGCCAACTT | 26133 |
rs543878348 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077232 | TGAGGCAATGCCCCG[C/T]CCTGCTTCAGCTCAC | 26133 |
rs543936160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092386 | GTACACGCCATCAGT[A/G]TCCACAGCAGCCCAG | 26133 |
rs543947955 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050293 | GCCATTCTTAAATCT[C/G]AAATCAAACAGTGCC | 26133 |
rs544020328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059580 | GGAGGATTACTTGAG[C/T]CCAGAAGGTTGAGGC | 26133 |
rs544022854 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093130 | TCAGGTCAGGAGTCA[A/G]GCCCTCGAGTCCGCT | 26133 |
rs544032514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042790 | TTCTTTTGCTACTGA[A/G]CAGAAATAGGTGGGC | 26133 |
rs544064724 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059826 | AGATGAAGACGAAGA[A/T]GATGAAGACAAAGAA | 26133 |
rs544110291 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053212 | CATTCAAATTCTCTT[C/T]TAGCTATTTTGAAAT | 26133 |
rs544126988 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057775 | CTTGGCCACCTACTT[A/G]CCCTTCTCTGGCCTC | 26133 |
rs544158669 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052614 | GATTCTCTTGCCTCT[C/T]CTGAGTAGCTGGGAC | 26133 |
rs544162394 | in-del | -/AA/AAA | 0.499891 | 0.00738737 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090180 | AGCATGGAATAAATT[-/AA/AAA]AAAAAAAAAAAAAAC | 26133 |
rs544197782 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028571 | TTAAATTTGCTGAAC[-/T]TTTTTTTTAACAGCC | 26133 |
rs544227624 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078981 | TGAGGCAGGAGAACC[A/G]CTTGAACTCGGGAGG | 26133 |
rs544241349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040709 | CCTGGGTTCAAGCAA[C/T]TCTCCTGCTTCAGCC | 26133 |
rs544278916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041507 | TCACACAGATATGAA[A/G]GTGAATCTAGATTAT | 26133 |
rs544323387 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006185 | CACCATGCTGCGTCA[C/T]GGCAGGCGCACAAGC | 26133 |
rs544359585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006786 | CAGACTGGGAATGCA[C/G]CACAATCTCTCCCCT | 26133 |
rs544366511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034541 | GGAAGAAGAAAAGCT[G/T]ATGGCCCCCCACTCC | 26133 |
rs544465764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077635 | TTCCCAATCATCAAA[C/G]CTGGCCCCTTCAATC | 26133 |
rs544480505 | snp | A/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093478 | GTGAAATTAAATAAT[A/G]GAAGGGAAAGGGATT | 26133 |
rs544482110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026976 | AGATTTTTCTACATA[C/T]AAGATCATCCCATCT | 26133 |
rs544497769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036101 | CCACCAATCTCATTT[C/T]ATTCACAATGAGTGA | 26133 |
rs544507803 | snp | A/C/G | 0.000105234 | 0.00725309 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004539 | CTGGGATATGTAGGC[A/C/G]AGCAGGCGGCATTCA | 26133 |
rs544551761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071527 | ATGAGTGAGAACACA[C/T]GGTGTTTGGTTTTCT | 26133 |
rs544582022 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017032 | AATCCCTTTAAACCA[G/T]CAATTCCACTTTAGG | 26133 |
rs544636139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049470 | TGAATGAAGGCTTCA[C/T]ACCAGTTCAGATAGC | 26133 |
rs544641295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059421 | TCCCAAGACTCTGGG[A/C]GGCTGAGGTGGGAGG | 26133 |
rs544641377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051668 | CATACAGTACCTACA[C/T]TGGCTATGATATGTG | 26133 |
rs544669661 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029176 | GAATTGCTTGAACCC[A/G]GGAGGTGGAGGTTGC | 26133 |
rs544673573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091599 | GTCTTTAAATAAAGC[G/T]AATGTTTTACAGGTG | 26133 |
rs544679421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084291 | AAAAAGGTATACACA[A/G]GGCAAAACAATTTAA | 26133 |
rs544681235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023172 | GACACGGTAGTTAAG[A/G]GCACTGACCCTGAAG | 26133 |
rs544698304 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028870 | ATGCATACATGTTTA[C/T]AACTGTTGTATCTTC | 26133 |
rs544727180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052249 | GGACTATGGTATATA[A/C]CACCACGTCCAGCCA | 26133 |
rs544737066 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030584 | AGGAATGAAGAGCAA[A/G]TATACATTTATGGAG | 26133 |
rs544765974 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093226 | TGCGCCTGTGTCCTC[G/T]TCAGGTCACTCCATC | 26133 |
rs544766271 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084554 | TATATGTATATATGT[A/T]TATATGCATATATGT | 26133 |
rs544805923 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086247 | TACAGGTGTGAGCCA[A/C]CGCACCCAGCCTAAA | 26133 |
rs544836617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036294 | AGCCAAGAGCAGTGG[C/T]TGCCACAGTAAACAG | 26133 |
rs544860182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078183 | CAGTGAACTGTGAGT[C/T]AAAAAAAGAGAGAAC | 26133 |
rs544930073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087311 | ACCATTGCCCTCCAG[A/C]CTGGGCAACAGAGCG | 26133 |
rs544939247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080438 | CCCAGGAGGCAGAGG[C/T]TGCAGTGAGCCAAGA | 26133 |
rs544943369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073699 | TTGAGGATTTTTGCA[C/T]TGATGTTCATCAGGG | 26133 |
rs544952414 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037605 | GAAGTACTGACATGC[C/T]ACAACATTAATGAAC | 26133 |
rs545149910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043936 | TAGATCAAAAAGTAT[A/C]TGCATTTGTAATTCT | 26133 |
rs545205866 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053004 | AGATAGCACATAATT[C/G]AACCATATCGCCCTA | 26133 |
rs545289779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020793 | CTGGAGCTCCCTGTA[C/T]TTGCCCAGTTTTCCT | 26133 |
rs545308407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029711 | CGCGATCTCGGTTCA[C/T]TGCAAGCTCCGCCTC | 26133 |
rs545321039 | in-del | -/ACA/ACACACA/CC | 0.337158 | 0.234315 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068956 | TATTTACACACACAC[-/ACA/ACACACA/CC]ACACACACACACACA | 26133 |
rs545342154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064964 | TTTGACTTACGTCTT[C/T]ATCAGAGTCACAGAA | 26133 |
rs545370783 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012319 | CTTTCACATAAATCT[C/T]AATTTCTGCCTTTGC | 26133 |
rs545406270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006240 | ACCCACAAGCAGCCC[C/T]GGTTTTCATCCCTGC | 26133 |
rs545461400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034945 | ACTTTGGGGAGTTCA[A/G]TGAAGTTTCTGTAAC | 26133 |
rs545527417 | in-del | -/A | 0.494013 | 0.0543839 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044400 | CCATCTCAAAAAAGG[-/A]AAAAAAAAAAAAAAA | 26133 |
rs545544950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070689 | AGGCGTGAGTCACTG[C/T]GCCCGGCCAAACCTA | 26133 |
rs545554721 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077872 | GGGATGATGGGATTA[C/T]AGGTGATGTATATTT | 26133 |
rs545566325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075187 | CTCCTGAATACAGCA[C/T]GCTGATGGGTCTAGA | 26133 |
rs545609119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004997 | CTCTCAGGTGAGTCC[A/G]GCCCAGTGCTGAGAC | 26133 |
rs545610296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011017 | TGTAATCCCAGCACT[C/T]TGGAAGGTCCAGGCG | 26133 |
rs545645723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005574 | CGCCACCTTGAGGCC[A/G]GCCACGTGGGCATCT | 26133 |
rs545685460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065642 | AGGTGCATAATTACT[C/T]AAGCAGGAGCCCATG | 26133 |
rs545727090 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062286 | CAACTCCACTTCTAG[A/G]TATATACCAAGGGAA | 26133 |
rs545789815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017308 | TTCGCCTTTGTAAGC[A/C]TAAAAATGTCTCTAG | 26133 |
rs545791025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061307 | AAGACTTGTACAACA[A/G]AACATTTTTGAAAGA | 26133 |
rs545955044 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087769 | CCAAAGTATCACCCC[A/G]GCATATTTTATTGCC | 26133 |
rs545964825 | snp | C/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094668 | TTTGTCCCTGAGTGT[C/T]GTTTCTTAGAAACTC | 26133 |
rs545993637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011460 | CATTTTTCTTGAAAT[A/C]CATTCTGAGCTGCAG | 26133 |
rs546003960 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026001 | CATGTGGACATCAAA[C/T]GGTCCCAATACCATT | 26133 |
rs546008350 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068051 | TAAAAAAAACTATGG[A/G]AAAATATCACTTTTC | 26133 |
rs546033613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047689 | AATGTATATAGAAAT[A/G]TCAAACAAAAACTTA | 26133 |
rs546046349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057092 | CCAGCTTAAGAAATA[C/G]TGCATACCAAAACAC | 26133 |
rs546127357 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076378 | TTCTGCTCTGGTTTC[C/T]CCCTATCTTTGTGGT | 26133 |
rs546133183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049550 | ACATGCTACAAAGAA[A/C]TTGCCCCAACGGTGA | 26133 |
rs546195237 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077393 | TGGCCATCCTGGAAC[C/T]GGACCCCCACTTACA | 26133 |
rs546235240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009439 | TTGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGGC | 26133 |
rs546277562 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038579 | ATATTACCTATTTAC[A/G]TTACCATCTGTACAA | 26133 |
rs546314227 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015224 | CAGGCTGGTCTCGAA[C/G]TCCTGACCTCAAGTG | 26133 |
rs546325122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091110 | CCTCCCAGGCTCAGG[C/T]AATCCTCCCACCTCA | 26133 |
rs546330641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039056 | CCAGCCTGGGCAACA[C/T]AGCCAGACTGTGTCT | 26133 |
rs546358148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004315 | ACAATGGGACACTGA[C/T]TCCTCCTGAGCACAG | 26133 |
rs546412714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091743 | GTTGGGCACCTGTTA[C/T]AAGTCAGATGCTTAA | 26133 |
rs546495197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032584 | TCTCGCCATTCTCCT[A/G]CCTCAGGCCTCCCCA | 26133 |
rs546497710 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084389 | CATTAATACAAATTT[A/T]AAAACAGTAAAATAA | 26133 |
rs546510046 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033980 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAA | 26133 |
rs546524855 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089395 | CCACACCTGGTTAAT[-/G]TTTTTTTTTTTTTTT | 26133 |
rs546555405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063155 | AGTGTCTGGCATTTC[C/T]CCTGCTTGCACTCAC | 26133 |
rs546586985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022002 | TGGGACACTTGATAT[A/G]TGTCAGACTTGCTGG | 26133 |
rs546627925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011078 | AGCCTGGCCAACGTG[A/G]CGAAACCCCATCTCT | 26133 |
rs546699320 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045129 | CCTCTGTGTATCCCC[C/T]ATCCAGTCGCATTTT | 26133 |
rs546710261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039095 | AACAAAGCAAAAAAA[A/C]CAAAAAAGAAATAAA | 26133 |
rs546734423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075903 | GGTACACCAATCAGA[C/T]GTAGATTTGGTCTTT | 26133 |
rs546773802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069423 | ATTTCCTAGTTTTTT[A/T]AAAAAAAAGTACATA | 26133 |
rs546798135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032132 | TGGCCTCAAGTGCTC[C/T]GCCCACCTCAGCCTC | 26133 |
rs546832067 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084678 | TGTGTATATGTATAT[A/G]TGTTTATATGCATAT | 26133 |
rs546872806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077268 | GTGGACTGCACCCAC[C/T]GTCTGACAAGCCCCA | 26133 |
rs546893473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034626 | CTGAACCTGCTGGCC[A/G]GAGTCAAATGCTTTA | 26133 |
rs546920139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077838 | AGGATAACACAGGGA[A/G]CCTAATGGTGATTAT | 26133 |
rs546945952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021901 | AACTGATGCTACTGA[C/T]GCAGATGAACATATT | 26133 |
rs546967122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038563 | GAGCAGCACTTATTT[C/T]ATATTACCTATTTAC | 26133 |
rs546994193 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094527 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 26133 |
rs547000231 | in-del | -/GCATTCCA | 0.00874735 | 0.0655527 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060549 | TGTGATCACACCACT[-/GCATTCCA]GCATTCCAGCCTGGG | 26133 |
rs547021003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062533 | ATACACGTTATGACA[C/T]GGATTAACCTTGAGA | 26133 |
rs547039408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030293 | ACATCTTAATCTTTT[C/T]CAGATTTTTTTTAAA | 26133 |
rs547157084 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013752 | CTAGTCACACTAAGG[C/T]TTGGGTTTTAATGCC | 26133 |
rs547161369 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015292 | GGGTGTGACCACCAC[A/G]CCCGGGAGCACGGTT | 26133 |
rs547171622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053621 | TAAAAGGTGGCCAGG[C/T]CAAACTAAGATGTGC | 26133 |
rs547194037 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015587 | GGTGCCTCAGCCTCC[C/T]GAAGAGTTGGGATTA | 26133 |
rs547257149 | in-del | -/CT | 0.00716266 | 0.059414 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043024 | GGTCTTATTCTCCCC[-/CT]GACTTAATACAAAAA | 26133 |
rs547268641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037118 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACAAGGT | 26133 |
rs547424796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068002 | CAAATGGGTGAAATG[C/T]ATGGTATATGAACCA | 26133 |
rs547505128 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002274 | TCCTGCCATCTCTGC[A/G]TCGCCCCCTGCTGCC | 26133 |
rs547506968 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043758 | ACAAGATGCTGTAAT[A/G]AGAGTTATACGAATG | 26133 |
rs547512016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060099 | TACAAGACATTTAAA[C/G]AATGATCAATTCTTC | 26133 |
rs547540003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008501 | TCTCACATACCTGTC[A/G]AGTCAAAACTACACA | 26133 |
rs547546589 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059724 | ATAAGAAGAAGAAGA[A/G]GAGGAAGAAGACTAC | 26133 |
rs547568543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007905 | TCTGGGATCGAAGGG[C/T]TGGCTCCTGCGAGCC | 26133 |
rs547572851 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093607 | ACTTCTGTGGCAGGA[C/T]GGCACTGACTCCCCC | 26133 |
rs547619433 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063816 | CAGTGAGCTAGGATC[A/G]TACCACTGCACTCCA | 26133 |
rs547626026 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018524 | TCGCTTGAGCTGGGG[A/T]GGCAGAGGTTGCAGT | 26133 |
rs547739035 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012956 | ACAAGGAGATCGAGG[C/T]CTTCCGAAGACAGCC | 26133 |
rs547754923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058878 | ATTTTTAGTAGAAAC[A/G]AGGTTTTGCCATGTT | 26133 |
rs547776888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007267 | ATAAAGGAAAATTAA[C/T]TTTTAGTACAAAATA | 26133 |
rs547779098 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008243 | CTTAGATGTATCTAA[C/G]GACCTCAGAGAAGGT | 26133 |
rs547799296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037865 | AACATGCTGTACAGG[C/T]TTGCAGCCTAAGTGT | 26133 |
rs547869278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | TRPC4AP | GRCh38.p7 | 20:35009104 | TAGGGTGAGGCCCAG[C/T]GTACTCCGTGCCTGA | 26133 |
rs547890586 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066733 | ATTATAGTAAAACAC[C/T]GATCAATCTGACAAT | 26133 |
rs547891246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029839 | GACGGGGTTTCACCA[C/T]GTTAGCCAGGGTGGT | 26133 |
rs547891331 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055723 | TATAAATTTCCATTG[A/C]AAGTTCTACTGCAGC | 26133 |
rs547919641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043642 | ACCCTATATATACTA[C/T]GTTTTTTCTTATATA | 26133 |
rs547921873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052508 | TATTTTTTTATCTTT[C/T]ATTTTTTGAGAGACC | 26133 |
rs547958470 | in-del | -/CGACAAGGCCC | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010529 | GCCTGCCACATTCAT[-/CGACAAGGCCC]CTTCCCTCAGCAGCT | 26133 |
rs548009921 | snp | G/T | 1.64779e-05 | 0.00287031 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044521 | TTGATTGATTTCAGC[G/T]GCAGAAGGCCCCAAA | 26133 |
rs548020855 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087101 | TTGGGAGGCCGAGGT[A/G]GGCGGATCATGAGGT | 26133 |
rs548058349 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016370 | ACAAGGCATAATGTC[C/T]GGTAGTTCCTATCAC | 26133 |
rs548097326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039195 | AAAATAGCTCCTGCT[A/G]CTTGACCTGCTCCTC | 26133 |
rs548114288 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047149 | ATTACAGGCATGAGA[C/G]CCACTGTGGCTGGCC | 26133 |
rs548139233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074063 | AGTTTATTTCCGTAG[A/T]GGTGTTTATAGTATT | 26133 |
rs548186430 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094431 | CAAAAATTAGCTGGG[C/T]GTGGTGGCATGCACC | 26133 |
rs548269399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054387 | CTCATTTCTCACAAT[A/C]AATCTATGATGTTAA | 26133 |
rs548307701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087787 | ATATTTTATTGCCTT[C/G]ACAGAGGGCAGAACA | 26133 |
rs548314345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061535 | GCCAAAACAATCTTG[A/C]TCTGTAAATACAAAA | 26133 |
rs548318363 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090132 | TAAGCAAATAACTTA[C/G/T]TCTGCAGGATGGGAG | 26133 |
rs548344978 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002723 | TGCCCAGGGCTCAGA[A/G]GCCTTTGCCTGGGTC | 26133 |
rs548392977 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088402 | AGTACAGACAGAAAT[G/T]AGACTGAGGACACAG | 26133 |
rs548500086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089677 | GACATGGTGAAACCC[C/T]ATCTCTACTAAAAAT | 26133 |
rs548511589 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008404 | TGGCAGGGCCCGTAT[C/T]CTAGTTCTCTCCCAC | 26133 |
rs548523741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035630 | AATAACCAGTCATAT[C/T]ACACGAGAATATCTG | 26133 |
rs548562930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081764 | GACCGAGACAGGTAG[A/G]TCACTTAGGTCAGGA | 26133 |
rs548576795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007969 | CAAGAATGGGAGGAC[A/G]TGCAATTGAGGGGCC | 26133 |
rs548579350 | in-del | -/AT | 0.0023933 | 0.0345097 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094096 | GACCAATGGAACAGA[-/AT]AGAGAACACAGTATA | 26133 |
rs548584580 | snp | A/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055684 | GCTAAAAGTTAAAAG[A/T]ATAAGCATCTCAATT | 26133 |
rs548602872 | snp | A/C | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002319 | GGCCCTGAATAAACA[A/C]CACAGCCAGTTTCCT | 26133 |
rs548647777 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019280 | AGTGAAACAGTGGTT[C/T]TGGGGGGCCAGGATT | 26133 |
rs548714334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073318 | CGACACTATGTTGAA[C/T]AGGAGTGTGCTGAGA | 26133 |
rs548718819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045434 | GCGGAGCAGTAGTGT[C/T]ATCATAGCTTACTGC | 26133 |
rs548748673 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073768 | GGCTTTGGTATCAGG[A/C]TGATGCTGGCCTCAT | 26133 |
rs548750835 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066086 | TAATAATTGAAGTAT[A/T]ACGTGATACCGCATA | 26133 |
rs548787500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080903 | ATCTCAATAAAGCTG[C/T]TATAAAAACTAAATA | 26133 |
rs548805723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030474 | CATTCTTTTTGTGCT[C/G]TAATTGTGCATATTG | 26133 |
rs548807714 | in-del | -/TA | 0.0170251 | 0.090679 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084545 | GTATATATGTATATG[-/TA]TATATGTTTATATGC | 26133 |
rs548826060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074593 | TTTTGAGTGAGTTTC[C/T]TAATCCTGAGTTCTA | 26133 |
rs548837321 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066757 | TGACAATCTAAAAAT[C/T]AAACATTTCTAATTT | 26133 |
rs548850086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088056 | TAAAAGGAGAAACAC[A/G]AATGGAAACAGAAAC | 26133 |
rs548880167 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081837 | CTAAAAATGCAAAAT[G/T]AGCTGGGCATGGTGG | 26133 |
rs548947144 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058192 | CTGGCAGAAATGAAG[G/T]AAACAGATAATTTAA | 26133 |
rs548981752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086285 | CTTAAAGGATAATAA[A/G]GATAAAATACCTTGT | 26133 |
rs549050609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011903 | AGACCCCGTTCCTCT[C/T]CTCCTGAATACCATC | 26133 |
rs549052421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020401 | GCTCCAGGCTGTCCC[A/G]CGCTGCCTCACTGTT | 26133 |
rs549084255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028932 | CCCTATTTTGCTCTG[A/G]TAACAGTTTTTGTTT | 26133 |
rs549112736 | snp | A/C | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056072 | GATCCCAATGGGCAG[A/C]CCTGCCAAGCTAGCT | 26133 |
rs549128448 | snp | A/G | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003721 | GTGGCCCCAGGCCTC[A/G]GGCCACCCACAGAGC | 26133 |
rs549134232 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029014 | CCCAGCACTTTGAGA[A/G]GCCAAGGCAGGCAGA | 26133 |
rs549138542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012404 | GCAGCTGGCTGGAGC[C/T]GAGCTCACTGAAATT | 26133 |
rs549214717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057390 | AGAGAGCAACCTGTA[A/G]CTAAATGTAAGACAT | 26133 |
rs549224638 | in-del | -/AGTATTTGATAC | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070788 | CAGATTCCAAGACAG[-/AGTATTTGATAC]AGCACACATAGGGTA | 26133 |
rs549242558 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027613 | GAATTCTTCTTGAAA[C/T]ATTTGGTAGAATTAA | 26133 |
rs549268124 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059748 | AGACTACGACGAAGA[A/C]GAAGAAGACGAAGAA | 26133 |
rs549283534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042984 | TTTGTTTCTTTAGGC[A/C]TACCATATATGTGGG | 26133 |
rs549311379 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075307 | CTGTCATTATGATGT[C/T]AGCTGGTTATTTTGC | 26133 |
rs549409601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029787 | ACTACAGGCGCCCGC[C/T]ACCACGCCCAGCTAA | 26133 |
rs549419074 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051772 | CTAAATTTACACTTT[A/C]TCAAAGCTTAAAAAT | 26133 |
rs549449754 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003093 | AGGGCGTGTGGCATC[A/G]TACCCACGCTCACCC | 26133 |
rs549468248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072515 | GGCTAGCCAGTTTTC[C/T]CAGCACTATTTATTA | 26133 |
rs549469871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064366 | AATCTTTGAGACTAG[A/G]CAGTTCAGCTTGAGG | 26133 |
rs549540594 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059757 | CGAAGAAGAAGAAGA[C/T]GAAGAAGACGACGAA | 26133 |
rs549548236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058071 | TAAAAATTCATTCTA[C/T]GGAGAGAAAGGATAG | 26133 |
rs549638965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060040 | ATAACAAAAAACTAC[C/T]CATAAAGAAAAACCT | 26133 |
rs549647129 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059290 | AACTACTATGAACAA[C/T]TGTATGCCAACAAAT | 26133 |
rs549649469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074472 | CTGGTATGTCATGTC[C/T]TTGTTCTCAATGGTT | 26133 |
rs549828144 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021662 | CCTTCTCCTGCCACC[A/G]ACCAGACCCCCAGGA | 26133 |
rs549918172 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034429 | GGGATAGAGCTTCCA[A/C]ACCGTGAGTACAGTA | 26133 |
rs550007497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051279 | TCAGTGAAATGAGAT[A/G]TGTTGCAACAAATTT | 26133 |
rs550010942 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069548 | ATGAACCACACTTCC[C/T]AGTATTCAGGCCCCT | 26133 |
rs550043034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019991 | TCCACCCCTTACCTG[C/T]TAGTCTTAACCACCT | 26133 |
rs550089873 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008400 | TTCATGGCAGGGCCC[A/G]TATCCTAGTTCTCTC | 26133 |
rs550113292 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020449 | TCCTCCCCAGGGCAC[C/T]GCCCCCTCCCACCTG | 26133 |
rs550121954 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002837 | GACAGCCAAGAAACC[A/G]GCAGGAGCTCACACA | 26133 |
rs550164047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091232 | TGGATTCAAGCGATC[C/T]GCCTGCCTCGGCCTC | 26133 |
rs550198191 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094117 | AACACAGTATAAAAC[A/C]AAATACTTATAGCCA | 26133 |
rs550204478 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031266 | TTGGAGGCAGGGTCT[C/T]GCTCTGTCACCCAGG | 26133 |
rs550220667 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044411 | AAAGGAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 26133 |
rs550262929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058117 | ATCCATTAGAAAGAT[A/G]TAACAACTACAAATA | 26133 |
rs550273213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065964 | TGTGGAGAGGGAATG[C/T]GGAGCAGCAGTTAAA | 26133 |
rs550283782 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078369 | GTTATAATAAGAAGG[A/G]GGGATTGGAAATACT | 26133 |
rs550288801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084718 | TGTATATATGTTTAT[A/G]TGCATATATGTGTAT | 26133 |
rs550295882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049044 | CAGCAACCTCTAGGA[A/G]GCTGCTCAACAGGAA | 26133 |
rs550299426 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058792 | CCTCCTGGGTTCAAG[C/G]GATTCTCCTGCCTCA | 26133 |
rs550337345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051827 | AACCCTGCTGCTCTA[A/G]CTAGCTACCCTTGAC | 26133 |
rs550353583 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093418 | ATCCATACACAAAGA[A/C]ACGCAGTCTCAAACT | 26133 |
rs550377761 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083317 | ACTGTAACACACTCT[C/T]GGCTGGGCACAGTGG | 26133 |
rs550382898 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085379 | GCACTTGGGAGGCCA[A/C]GGTAGGCCCATTGCT | 26133 |
rs550522144 | snp | A/C | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094805 | GGAGGAGGACACGAC[A/C]ATAAGTCAGAGCTAA | 26133 |
rs550524842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077965 | ATTTTTAAAAGCCAA[C/T]GGAAGGGAAAAAAAA | 26133 |
rs550539303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027505 | TGATGTCTTTATCTG[C/G]TTTTGGTATCATGAT | 26133 |
rs550563397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071932 | CCTATTTCTCCACAT[C/G]CTCTCCAGCACCTGT | 26133 |
rs550598666 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002795 | GTGGGGGTCACCCAT[A/G]TCTTCCTCCCCACTC | 26133 |
rs550603900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032696 | CCAGGATAGTCTCGA[G/T]CTCCTGACCTCGTGA | 26133 |
rs550621807 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041141 | ACTGTGAGAAAAATA[A/T]ATGTCTGTTAGTTAA | 26133 |
rs550664309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042052 | GTTCTAGGGTACATG[G/T]GCACAACGTGCAGGT | 26133 |
rs550712158 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070373 | CTACAACTCATTTGT[A/G]ACATTTAGCACTTTT | 26133 |
rs550745962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034672 | CCAAAGATGGGCCAG[A/C]GTTCTTTACCAGGAA | 26133 |
rs550747256 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062699 | GGCCTTGGGAGGAAA[G/T]GGGGAGTGGCTACTG | 26133 |
rs550756949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076682 | GGCCCCTACTGGGAG[A/G]TGTCTCCCAGTTAGG | 26133 |
rs550812848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078374 | AATAAGAAGGAGGGA[C/T]TGGAAATACTCTTGT | 26133 |
rs550836768 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063430 | CTGCCAGAGCTGGGG[A/G]GAAGGGGAGATGGGG | 26133 |
rs550858747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017505 | TTACTAGCCCTTCTC[A/G]GGGCTGTTGTAAGGA | 26133 |
rs550867178 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045421 | TGTTGCTCAAGCTGC[A/G]GAGCAGTAGTGTCAT | 26133 |
rs550886179 | in-del | -/TAAAT | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084402 | TTAAAAACAGTAAAA[-/TAAAT]TAAAGGATGCACTAT | 26133 |
rs550904178 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022294 | CCGAGTAGCTGGGAC[C/T]ACAGGCATGTGCCAC | 26133 |
rs550993852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056565 | ATGTCGTATTGGGGT[A/G]AAAAAAAAATCTTTT | 26133 |
rs551019328 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049373 | ATTAACCAACTTTAA[C/T]TGTTGAAGACTAATG | 26133 |
rs551028596 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091780 | CTACCTTCAGCCCTT[A/C]GTATGCACCAGAAAT | 26133 |
rs551042192 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052478 | GCCAAGCTTTTTCTG[A/G]TGAGCAGTACTGTTT | 26133 |
rs551118142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026026 | ACCATTTGTTGAAAA[G/T]ACTACTACTGTTTCC | 26133 |
rs551126745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034721 | AGTCTTCTTATTTAA[C/T]AGGCAGTCTTCTGCC | 26133 |
rs551138695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070832 | AGTTCTCAAACTGAC[A/G]GCCACAGAATCCTTT | 26133 |
rs551178646 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072710 | TAGTTTGAAGTCAGG[C/T]AGCGTGATGCCTCCA | 26133 |
rs551283572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011132 | GGGCGTGGTGGCACA[C/T]GCCTATAATCCTAGC | 26133 |
rs551330888 | in-del | -/TAAAAG | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081606 | GAGAAACAGAAAGGC[-/TAAAAG]TAAAAGAATGGGAAA | 26133 |
rs551341292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065432 | AGACACACTTTTCAC[A/G]GTCATGTTATGGATA | 26133 |
rs551358134 | snp | A/G | 0.00133536 | 0.025805 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092782 | CGGCGCCGCCGCCAT[A/G]TCTCCTCGTCGGACA | 26133 |
rs551368038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012667 | GTCTGAAGTTCCTGC[C/T]GGCCCCTGGGAATAG | 26133 |
rs551391023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042820 | CTAGATTGGTTAGAA[C/T]AGTGTTTTGTTTTTA | 26133 |
rs551403530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026121 | CTGAACTCTCAACAA[C/T]ATTCCATTGATCAAT | 26133 |
rs551448368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085421 | GTTTAAGACCAGCCT[C/G]GGCAACATGGCAGAA | 26133 |
rs551509568 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079220 | ATTCTCCAAGAAGAC[A/G]TAACAATCCTTATCA | 26133 |
rs551535715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070865 | TCATATGGAACAAAG[C/T]TAAGAGGAAAAAAAA | 26133 |
rs551543953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056853 | TAGCCGGGTATGGTG[A/G]TGGGCGCCTGTAATC | 26133 |
rs551563311 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018724 | GGTCCAGCCCCGTAG[C/T]CTGCTCTATAGCAGG | 26133 |
rs551608296 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020943 | AGAGGCAACTGCCTG[A/C]TTCTGCCCTCAGCAC | 26133 |
rs551611811 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069564 | AGTATTCAGGCCCCT[A/G]TAAAGCCCCTTCTCA | 26133 |
rs551623379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063523 | CACAATACTGATGGG[C/T]GGTTACAAGAATTAA | 26133 |
rs551631180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057332 | AGATCTGAATTTCTA[C/T]GCAGTACAGAATGAA | 26133 |
rs551651821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011181 | AGAATTGCTTGAACC[C/T]AGAAGGTGGAGGTTG | 26133 |
rs551653918 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024582 | TAATTCCGGCACTTT[A/G]GAAGACCAAGACGGG | 26133 |
rs551667332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050060 | GAAAGTACAAGGCAT[C/T]CTTTACAGACACTGA | 26133 |
rs551683474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021039 | TCAGCCTGGTTTCCT[C/T]ATAGGTAGAACAGAA | 26133 |
rs551694535 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066037 | TCAATCTTTACTTTA[C/T]TGGAAAATGGTAGCT | 26133 |
rs551811595 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042371 | AAAACTAGACAATAA[C/T]AGAGTGAATGGCAGG | 26133 |
rs551812594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077230 | GGTGAGGCAATGCCC[C/T]GCCCTGCTTCAGCTC | 26133 |
rs551881908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004598 | GCAGGGGTGCAGCAG[A/G]TCAGGCTTAGGCCCA | 26133 |
rs551891530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071748 | TGCAATAAATATACA[C/T]GTGCATGTGTCTTTA | 26133 |
rs551893272 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019281 | TGAAACAGTGGTTTT[-/G]GGGGGGCCAGGATTT | 26133 |
rs552009413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005372 | TTCAGATGCCTGCTG[C/T]ACCACAGGGCACCTG | 26133 |
rs552076150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032902 | ATGTCTCAATTTTTG[C/T]TAAAAACTGGACATT | 26133 |
rs552122413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040203 | GCTGTCAACTTGACT[A/G]GACTATGGGATGCCT | 26133 |
rs552245473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088531 | CAGTCTAATTAACTA[C/T]TAGCTGAGAGCAACT | 26133 |
rs552251021 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031235 | TCTTATCTTTCAGGA[-/T]TTTTTTTTTTTCTTT | 26133 |
rs552262053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047290 | AACCACCATCATTAA[C/T]TATTATTGCCTTGCC | 26133 |
rs552279999 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082003 | AACAAAACAAAACAA[A/C]AACAACAACAACAAC | 26133 |
rs552284901 | in-del | -/C | 0.00835141 | 0.0640778 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040082 | TGGACTGTGTCCCCA[-/C]CCCCCCGCGCCCCCA | 26133 |
rs552314437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046126 | TCTTGACTTTACCAG[A/G]AATAATTCCAAAACA | 26133 |
rs552356040 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048108 | ACATCTTCTCTTTTA[C/T]GTTTATGGACCATTT | 26133 |
rs552367783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082755 | ATTCACCACATTGAT[A/C]ACATAAAGGAGAATA | 26133 |
rs552390024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013578 | TGGAGACTCTGTCCC[A/G]AAAATCCAACCAACC | 26133 |
rs552524884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084325 | GATGCATTATACCTG[A/G]CTTCACCACCATGCG | 26133 |
rs552529023 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076817 | GACATTTAAACCTGC[A/T]GAAGTTTCTGCTGCC | 26133 |
rs552533417 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079215 | GGTTAATTCTCCAAG[A/G]AGACATAACAATCCT | 26133 |
rs552547790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075770 | GGAGTATCTTTGTGG[C/T]GTTCTCTGTATTTCC | 26133 |
rs552567893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038107 | TTAATGTGTACGGCG[C/T]TTCCTTTTGGGGTGA | 26133 |
rs552619241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003358 | GGACACCCCTCTGAG[A/G]GGCCCTGGGTCCGCG | 26133 |
rs552683794 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067792 | AAATTTATACAAAAC[A/G]TCCACGACAGAGAAA | 26133 |
rs552706668 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089825 | CACTCCAGTCTGGGC[A/G]ACAGAGCGAGACTCC | 26133 |
rs552756435 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031307 | AGCTCACTACAGCCT[C/T]ATCCTCCTGGGTTGA | 26133 |
rs552782072 | snp | C/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093942 | AAAAATCATATGGAA[C/T]CAAAAAAGAGCCTGC | 26133 |
rs552786644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083190 | ATCTATCTTATTTTT[A/G]TATTACAGCTACAAT | 26133 |
rs552802641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032334 | CTGGCCTGATTATTA[C/T]ACTACTCTTCAATTC | 26133 |
rs552814535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015389 | GCAGTGGGCAGCCCC[C/T]GCCTGGAGTGAAATG | 26133 |
rs552884948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023741 | CGTGCTTGGCATCCT[C/T]GGCACCCAGCCCATG | 26133 |
rs552971800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074770 | GGGTGGAGAGTTCTG[C/T]AGATGTCTATTAGGT | 26133 |
rs552995640 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038845 | TGGGAGGCCGAGGTG[C/G]GTGGATCACCTGAGT | 26133 |
rs553000044 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077973 | AAGCCAACGGAAGGG[-/A]AAAAAAAAACAGCAG | 26133 |
rs553037898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062993 | ATATGGTTTGGCTGT[A/G]TGCCCTCACCCAAAT | 26133 |
rs553089501 | in-del | -/TATA | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084673 | ATATATGTGTATATG[-/TATA]TATGTTTATATGCAT | 26133 |
rs553112017 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040279 | TTCCAGAAGAGATTG[A/G]TGTATGAGTGTGTGA | 26133 |
rs553119844 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063074 | AGGTGACTGGATCAT[A/G]GAGGCAGGTCCCCCA | 26133 |
rs553136540 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076304 | TTGTTCCGTTGCTGG[A/T]GAGGAGCTGTGTTCC | 26133 |
rs553224372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076935 | AGCTTCCCGGCCGCT[C/T]TGTTTACCTACGCAA | 26133 |
rs553263173 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070605 | TCAGTAGAGACGGGG[G/T]TTCACCGTGGTCTCC | 26133 |
rs553338548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009279 | CCTTCAAACAGAGCA[C/G]CTCTGCTGTGATCCA | 26133 |
rs553364043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031424 | TTTTTTTCAAAGAGA[C/T]GGGGTTTTGCCACAT | 26133 |
rs553375698 | snp | C/G | 9.15793e-05 | 0.00676618 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003667 | TGGGAGCCCCAGTGG[C/G]CCCTGGTGAACCTGG | 26133 |
rs553397192 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013896 | ATGGTGCTGCTGGTG[G/T]GTGAAGGGGGCCCTC | 26133 |
rs553433530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086117 | ACGCACCACCACGCC[C/T]GGATAATTTTTTGTA | 26133 |
rs553466767 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057209 | AAAATAAAACAGAGT[G/T]ATCTTACTCTCTCAG | 26133 |
rs553495162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052923 | GTTTTCTGCCTGATC[C/T]CTGGAGGCATTGGTG | 26133 |
rs553528558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014984 | AAGGAGAGTGCTTGG[A/G]CTCAAAAAACCAAAG | 26133 |
rs553532244 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044900 | GAGTCTTTGCTTGTT[C/T]ATCTGTAAAACGGAA | 26133 |
rs553555197 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040590 | TCTCCAGCTTGCAGA[C/T]GGCTTATCTTTTATT | 26133 |
rs553599154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061769 | TCTCAGAAGAATACA[C/T]AGGTAAATCTTTGTG | 26133 |
rs553690214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013257 | AAGCTAATGTGGCCC[C/T]CTTCCTGCTAAAAAC | 26133 |
rs553760150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058276 | AGACGAGCAAAGAAA[C/T]AGAAGACTTGAACAC | 26133 |
rs553773995 | snp | G/T | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008984 | CAGGCCAGAAACATA[G/T]CCAGAATCAGACATG | 26133 |
rs553781261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087999 | TTAGACATCAAAGTG[A/G]AAATGCTAGAAGGCA | 26133 |
rs553813985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081065 | TATAAATCATGCCTC[A/G]ATAAAGTTGTTTAAG | 26133 |
rs553853116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092280 | GGGATAAACTCGAGG[C/T]CCACAGAGGCTAAAA | 26133 |
rs553868749 | snp | A/G | 3.32226e-05 | 0.00407556 | downstream-variant-500B, synonymous-codon | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002049 | AACCCAGGCCAACAA[A/G]CTGCGGGCACGGACC | 26133 |
rs553958301 | in-del | -/AGCAGGGA | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015129 | CTCAGCCTCCTGAGT[-/AGCAGGGA]TTACAGGTGCCCCAC | 26133 |
rs553982076 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020797 | AGCTCCCTGTACTTG[A/C]CCAGTTTTCCTAAGC | 26133 |
rs554029507 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024669 | TCTCTTTTTATTACA[A/G]AAAATAAAAAAATTA | 26133 |
rs554045492 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030110 | GCTGGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 26133 |
rs554066968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036674 | CAAGCTGGCCAGGCA[C/T]GGTGGCTCATGCCTG | 26133 |
rs554067666 | snp | C/G | 3.30453e-05 | 0.00406467 | synonymous-codon, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021232 | CACGCAGAGGACATA[C/G]AGCACTTCCAGTTTG | 26133 |
rs554099853 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083215 | TACAATTTTTAAATG[C/G]AGTTTTAAAAACACT | 26133 |
rs554108288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008116 | GGGTATCCACGACAG[G/T]GAGTTTGGACAAGGC | 26133 |
rs554147753 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35092982 | GAAAAGAGATGTGGC[C/T]TTTCCTGCACTGCCG | 26133 |
rs554185387 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006810 | CTCCCCTGCCCAGGG[C/G]GTACAGCTGAAGCCT | 26133 |
rs554208975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043119 | CTATAGCAGTACATA[C/G]AGATCTTCATTTTTT | 26133 |
rs554219098 | snp | A/C | | | intron-variant, synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004185 | GATTCCAAAGCCCAG[A/C]AGGGCAGAAGGTGTG | 26133 |
rs554247962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035785 | AAGAATGATGACACA[A/T]ACATCTTTATATAGT | 26133 |
rs554298125 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058504 | CAGAACGAAATTTGG[A/G]AAATTCATGAATTAT | 26133 |
rs554330546 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003092 | CAGGGCGTGTGGCAT[C/T]GTACCCACGCTCACC | 26133 |
rs554332995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053695 | CACATTGGATTTTGA[A/G]AGCTCAATACGAAAA | 26133 |
rs554333713 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080455 | GCAGTGAGCCAAGAC[C/T]GCGCCACTGCACTTC | 26133 |
rs554340394 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078829 | CCAACACTTTGGGAA[G/T]CCGAGGCAGGTGGAT | 26133 |
rs554353148 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035609 | TCTGGGAATTTACCA[C/T]AACGAAATAACCAGT | 26133 |
rs554363992 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056817 | AACCCCATCTCTACT[-/A]AAAAAAAAAAATACA | 26133 |
rs554369643 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045633 | AAACTCCACCTCCTG[A/G]GTTCAAGTGATTCTC | 26133 |
rs554399415 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022706 | ACAGTGATACTCTTT[A/C]AAGTATCAAGACAGA | 26133 |
rs554461939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031563 | TTACCATGTGTCTGC[A/C]TGTGGATCTGAGTAT | 26133 |
rs554493409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066298 | TTTTAGTAGTGATGG[A/G]GTTTTGCCGTGTTGC | 26133 |
rs554526147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053102 | AATTTCAGGGAGCAT[A/G]TAATTTAATACATTC | 26133 |
rs554552028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086613 | TATCCTAATCAGGAG[A/T]TTTTCAGTATCAAAT | 26133 |
rs554589871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060194 | TACCCTGATACCAAA[A/G]CCAAACAAAGACATC | 26133 |
rs554597666 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002561 | CCCCGTGCCCCAAGG[G/T]ATGGAGGGAAAGGCC | 26133 |
rs554602811 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075420 | CTTTCCATGTTTAGC[A/G]CTTCCTTCAGGAGCT | 26133 |
rs554613078 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092494 | CTCACAGGGAGGCCT[C/T]CCGGCCAGCCAAAAG | 26133 |
rs554639673 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087212 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 26133 |
rs554642856 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001961 | AGGAGCAGCAGGCCA[A/G]CACCAACCTGGCCAA | 26133 |
rs554723340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082189 | TAATGGGAGATTTTA[C/T]ACATCTCTTTCAAAA | 26133 |
rs554742348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046408 | CTTCATCCCACTAAT[C/T]TACTTCCACTGGATT | 26133 |
rs554752700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081235 | AACAAAGTTTGGGCC[A/G]GTTACAGGGCCTCAT | 26133 |
rs554771991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088070 | CGAATGGAAACAGAA[A/G]CTTAGGATCCGTCAG | 26133 |
rs554813107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088831 | AAGTAAAATAAGCCA[C/G]TCACAAAAAGACAAA | 26133 |
rs554816688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029969 | AGTTGCTGGCTGGCG[C/T]GGTGGCTCATACCCG | 26133 |
rs554817713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014077 | GGGAAACTAACCCCA[A/C]TGACCTCAAGTGATC | 26133 |
rs554995643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043760 | AAGATGCTGTAATAA[G/T]AGTTATACGAATGTG | 26133 |
rs555004995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064774 | TACAGTATATAACCA[C/T]TTTATAGCCTGTTTT | 26133 |
rs555045543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079434 | TGCATATAATAGAAA[A/G]GAAGAAATATCTATA | 26133 |
rs555072085 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067275 | GGACTGTTTGAGTCC[A/G]GGAGTTTGAGACCAG | 26133 |
rs555077289 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008394 | AGGGAATTCATGGCA[A/G]GGCCCGTATCCTAGT | 26133 |
rs555089854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065487 | CCACTGAGCTTTGGG[C/G]AGCATGACCAAGAGA | 26133 |
rs555095334 | snp | A/C/T | 4.9486e-05 | 0.00497403 | synonymous-codon, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021301 | CTGGGTTCTGGCTGA[A/C/T]GTGTGAGGCAGGCCA | 26133 |
rs555117954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037524 | TATCCCAAATGTCCA[C/T]TAACTGAAGGGATAA | 26133 |
rs555162902 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085023 | TAGTCTTTCAAGAGC[A/G]AAGAAAATAGATAGT | 26133 |
rs555301328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018803 | GCGGGTACAGGCTCA[A/G]GCATTTATCTCTGCA | 26133 |
rs555305588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076928 | CAGTTCGAGCTTCCC[A/G]GCCGCTTTGTTTACC | 26133 |
rs555350994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059797 | GATGAAGAAGAAGGC[A/G]AAGACGAAGACAAAG | 26133 |
rs555351029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068069 | AATATCACTTTTCTC[A/G]TAACTGCTTAGTAAA | 26133 |
rs555408045 | in-del | -/ATAG | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064857 | ATAAAATTCAACAAA[-/ATAG]ATAGAATAACCATTA | 26133 |
rs555521092 | in-del | -/TTTT | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051306 | ATTTAATTTTCTTTC[-/TTTT]AATTTTAGAGACAGG | 26133 |
rs555535006 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050123 | TCAACAAAACAGGAA[C/T]GGCATGGCTTAACTG | 26133 |
rs555553009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030146 | CTAGAGAGGCTGAGG[C/T]AGGGGAATCACTTGA | 26133 |
rs555554825 | snp | C/G | | | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004406 | GGCACCAGGACAAAG[C/G]AAGTGGTTTCCAATC | 26133 |
rs555561455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012693 | AATAGCCACGCTGTC[C/T]ACTCTTGCTTTAGAG | 26133 |
rs555569831 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042257 | ATAAACTGGGGTTGG[A/T]GTCCACAAACTTCTA | 26133 |
rs555687398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007365 | TAAACCTGTCACCCC[A/G]TAAGCACCCATGGGG | 26133 |
rs555695533 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025734 | TCTGTGGGTTCTCTT[C/T]TCACTTTCCTCATTG | 26133 |
rs555704014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043177 | AATATTGAATACACT[A/G]AGCAGTCCAGTGTTA | 26133 |
rs555786937 | snp | G/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056791 | TCGAGACCAGCCTGG[G/T]CAACATGGTGAAACC | 26133 |
rs555798356 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056873 | CGCCTGTAATCCCAG[C/T]TACTTGAGAGGGTGA | 26133 |
rs555801210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058372 | TCTACTCAAGTGCAC[A/G]TGAAACATTCTCCAG | 26133 |
rs555816660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005445 | TCGTGCCAGGCAATA[C/T]CAGCCCAGAAGAGGA | 26133 |
rs555860734 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080055 | TTATAACCAAAGAGT[C/G]AAACAACTCAAATGT | 26133 |
rs555889294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059230 | CTCAGAAATAAAGGA[A/G]AGGGCATTACCACCA | 26133 |
rs555898667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073389 | TTCCAGTTTTTGCCC[A/T]TTCAGTATGATATTG | 26133 |
rs555937251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066136 | TTGAGATGGGGTCTT[A/G]CTCTGTCACCCAGGC | 26133 |
rs555963966 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013180 | TGTCCTCATGTACCA[A/T]GAGGACTTTTCTTTA | 26133 |
rs556004257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092165 | TTAGAAAGGGGAAGG[A/G]AAGAGTGTCAAGGAA | 26133 |
rs556014110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052565 | CAGTGGTGCAATCTC[A/C]GCTCACTGCAACCTC | 26133 |
rs556025498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084959 | ATATAACTACATTGG[C/T]AGACTAGTGGAGACG | 26133 |
rs556053918 | in-del | -/TCAT | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008810 | GGCCCTGGGGATGGG[-/TCAT]TCTGCTGGCTTAGGC | 26133 |
rs556079138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020739 | GGCCCCTCCTCCTCC[A/G]TCTTGGAACTACTTC | 26133 |
rs556150413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003897 | AGCATCACTCCTTCC[A/G]GAAGGTCCGTCCCAG | 26133 |
rs556160287 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094516 | ACAGAGGTCACAGTG[A/G]GCCGAGATCACGCCA | 26133 |
rs556166385 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031897 | TTATACTACTTAAAA[A/G]AAAGTTTTTTTTGAG | 26133 |
rs556167485 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030424 | TGAAGCAAGCATTTT[C/T]GGATTTATTCTAACT | 26133 |
rs556213297 | snp | A/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093519 | GACATCATATTCTCT[A/G]TCAGATGAAAACCCT | 26133 |
rs556220592 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054114 | TAAGTTCGTGATCTT[A/G]GTAGATTTTGCATAC | 26133 |
rs556270436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049493 | CAGATAGCGGTAAAG[C/T]GGTAAGAGAATGGAG | 26133 |
rs556310832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052056 | CTACATTTTTCGGGG[C/G]AGAGTTTTTTCCATG | 26133 |
rs556365195 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024697 | TTAGCTGGGCGTGGT[A/G]GTGTGCACCTGTTTC | 26133 |
rs556405087 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006886 | TAGGTGAGGGGAGCT[A/G]TCATCACCAGGTCTA | 26133 |
rs556449080 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35092855 | GGCGGCGGAGGGGTC[G/T]CCGCAGCGCCCCCAG | 26133 |
rs556454384 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051816 | GTCAAATACACAACC[C/T]TGCTGCTCTAACTAG | 26133 |
rs556456775 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002369 | GTTCAGGAGGAAAAA[A/C]ACAGTCCTAGGGACA | 26133 |
rs556481923 | snp | A/T | 1.67346e-05 | 0.00289258 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078199 | AAAAAAAGAGAGAAC[A/T]TATTATTGTATTATT | 26133 |
rs556628946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084470 | TATGTGTGTATATAT[G/T]TATATATGTGTATAT | 26133 |
rs556675348 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092240 | GGGGCTGCAATGATG[A/C]CCCCCTCCCCCACGC | 26133 |
rs556796459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025727 | CTTCCATTCTGTGGG[C/T]TCTCTTTTCACTTTC | 26133 |
rs556804656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070655 | CACCCGCCTCGGCCT[A/C]CCAGAGTGCTGGGAT | 26133 |
rs556817242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011417 | CAGAGTACTGGTTGT[C/T]TACCTTGGTGATCGT | 26133 |
rs556897132 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065624 | CCAAACTGAAGGTCA[C/G]TGAGGTGCATAATTA | 26133 |
rs556960309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069024 | ACAAGAAACTAGTAA[C/T]CACAACTGGTTCTGA | 26133 |
rs556982986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068091 | CTTAGTAAATACTTA[A/G]AATACACTGTTTGTG | 26133 |
rs556983506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040424 | TTTCTCCTACTGCTC[C/T]TGGATATCAGACTCC | 26133 |
rs556997333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069533 | CAAAGACAGTCCCCA[A/G]TGAACCACACTTCCT | 26133 |
rs557056198 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091105 | CTCCGCCTCCCAGGC[C/T]CAGGTAATCCTCCCA | 26133 |
rs557074443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026452 | AACTCCTGAGGCCAA[C/G]TGATCTTCCTGCCTC | 26133 |
rs557082714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061870 | TCAAAATTAAAGACT[G/T]TGTGTTTCAAAGGAC | 26133 |
rs557105837 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034069 | AGAATGGCGTGAACC[C/T]GGGAAGCGGAGCTTG | 26133 |
rs557152711 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073068 | TGGGAGTTCACTCAT[G/T]ATTTGGCTGTCTGTT | 26133 |
rs557162392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018902 | TGATAGAAAAGGCGA[C/T]GGGGGACGATGGAGC | 26133 |
rs557168471 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049524 | TCACTGCATAGCATA[C/T]AATAGCACATACATG | 26133 |
rs557170680 | in-del | -/AGA | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063429 | CTGCCAGAGCTGGGG[-/AGA]AGAAGGGGAGATGGG | 26133 |
rs557291756 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086139 | TTTTTTGTATTTTTA[A/G]TAAAGATGGAGTTTC | 26133 |
rs557333971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047499 | GAAAGTACATTCATC[C/T]CTTCTCCTATTCATG | 26133 |
rs557347575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075990 | CTAAACTTCTCTTCT[C/T]GCTTCATTTCATTCA | 26133 |
rs557364091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024068 | TCAGCTCTACCACAC[C/T]GATTGGAGCGGTCAC | 26133 |
rs557403284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016905 | AAGCTTTATAAGACC[A/G]TGTTGGTGACTTGGG | 26133 |
rs557467367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009401 | GGTTCACACCTGTAA[C/T]CCCTGGACTTTGGGA | 26133 |
rs557554624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010011 | GCTGCTGTGAGGCTC[C/T]AATGAGAAAATGCAG | 26133 |
rs557598434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063854 | ACACAGTGCAACTCT[A/C]TCTCTAAAATCATCC | 26133 |
rs557627129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011496 | GCTCAGTGCCCAGCA[C/T]TGCAAGAGTATTGAA | 26133 |
rs557637712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048200 | TTTTTCATGCTGATT[A/T]GTAAGAATTCTGTTT | 26133 |
rs557675451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004706 | GCTTCAACGAAAGCT[A/G]ACTGTGGCAGAAAGA | 26133 |
rs557685429 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041737 | GCCAGAATAGATTCC[C/T]TAAATGGGAAACTAA | 26133 |
rs557689569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039697 | CTTATAAATTGACAA[C/T]TATCTAGCCTATAGC | 26133 |
rs557735303 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034396 | TCAGAGCCATAGAAT[G/T]CTTGGCCTCAAGTAT | 26133 |
rs557775825 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045681 | GTAGTGGGGATTACA[A/G]GCGCCCGCCACCACG | 26133 |
rs557785086 | in-del | -/CT | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076538 | GGTCCACTCCAGACC[-/CT]GTTTGTCTGGGTATC | 26133 |
rs557847456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068742 | GGACAGGTTGGTCTC[A/G]AACTCCTGACCTCAC | 26133 |
rs557876245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055918 | AACTTAATTTTCATG[A/G]GCCCAAAACCAAAAG | 26133 |
rs557906364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019030 | AAACTTGACAGCACA[C/T]GGGGAGCCTTTCCAG | 26133 |
rs557909357 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010096 | TGTGAGAGAGGACAC[A/G]CGTGCATACCTGGAT | 26133 |
rs557940856 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026273 | AGGCTGGAGTGCAGT[A/G]GCACAATCACAGGTT | 26133 |
rs557979157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012091 | CTCACTTCCTCAGGG[A/T]AAACAGCACAGTTCC | 26133 |
rs558003180 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049193 | ACAGAGATCTATGAA[G/T]GTATTTTTGGGTATC | 26133 |
rs558016419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006112 | TCTGTCACACACACT[C/T]GGTGAGCCTAACACA | 26133 |
rs558025237 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028010 | ATTCTCTATCTCACC[A/G]GTTTTCACTCTAATC | 26133 |
rs558025872 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084203 | GCTACTCGGGGGGCA[G/T]AGGTTGCAGGGAGCC | 26133 |
rs558041659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057653 | ATAACCATTCATGGC[C/T]CATGTATCTGTCACA | 26133 |
rs558077611 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090573 | GAGACGGGGCTTCGC[C/T]ATGTTGGCCAGGCTG | 26133 |
rs558100682 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049798 | AAGCTCTGTATATTA[C/T]TCAGTTTTGAGAATC | 26133 |
rs558121136 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064067 | TGAGAAAAATTAGGA[C/T]CTTTGTTTTCCAAAA | 26133 |
rs558149484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070505 | AAGCTCTGCCTCCCG[G/T]GTTCACGCCATTCTC | 26133 |
rs558173594 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033357 | TTTTCATGTTGTGCC[C/T]CAGAGAGTGCAACCT | 26133 |
rs558177947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017796 | GTGTAAAAGTAATTG[C/T]GATTTTTGCCACTGA | 26133 |
rs558221279 | snp | C/T | 0.00212782 | 0.0325481 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005680 | ACTTGCCTTGACAGC[C/T]TGCCTTTCATGTACC | 26133 |
rs558265369 | in-del | -/AACT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061047 | GAAAGGAATAAGTAA[-/AACT]AACTATTTACAGATG | 26133 |
rs558341232 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046466 | ACATGAACTTTTAAT[A/G]ATCTGTTCCTGCATC | 26133 |
rs558346975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089037 | CATTACTTAACTATA[C/T]ACCTTTTTTTTTTAA | 26133 |
rs558351858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004872 | TCCATATCACACACA[C/G]AAGAGTTCCCTCCAC | 26133 |
rs558365197 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032310 | GATTACAGGTGTGAG[A/C]CACCACACCTGGCCT | 26133 |
rs558407709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091321 | GGCTGCTCATCTATG[A/G]TTGTGTGATGGCCAG | 26133 |
rs558439935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041213 | ACTGATACACACACC[C/T]GAGATAAAGGCATTC | 26133 |
rs558465162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091781 | TACCTTCAGCCCTTA[G/T]TATGCACCAGAAATG | 26133 |
rs558495772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRPC4AP | GRCh38.p7 | 20:35009146 | AGCTGGCCTTGGGCA[A/C]GTGTCCACAACTCCA | 26133 |
rs558496104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016920 | GTGTTGGTGACTTGG[A/G]CATTGGGTACATTCA | 26133 |
rs558510597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045753 | CCATGTTGGCCAGGC[C/T]GGTCTTGAACTCCTG | 26133 |
rs558534226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080371 | CCGGATGTAGTGGCA[A/C]ATGCCTGTAGTCCCA | 26133 |
rs558615006 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055670 | GTGTACCACGCCTGG[C/T]TAAAAGTTAAAAGTA | 26133 |
rs558678606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037548 | GGGATAAACAAACTG[C/T]GGTATCTACATGATG | 26133 |
rs558682522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089771 | GAATTGCTTGAATCC[A/G]GGAGACGGAGGATGC | 26133 |
rs558787861 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075538 | GTTTGGCTGGATATG[A/C]AACTCTGGGTTGAAA | 26133 |
rs558809324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074716 | ATTTTGGAATAAGTG[C/G]GACGTGGCGCTGAGA | 26133 |
rs558883909 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076078 | TTGTGCATGCGTCAC[A/G]TAGTTTTCGAGCCAT | 26133 |
rs558927194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014775 | GTGGCACTTTTAGGT[A/C]CCAGAGCACTTTCCT | 26133 |
rs558950637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023119 | ACAACCTTGGAAGAC[A/G]ACAAGCTGCTGAATG | 26133 |
rs559001439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074290 | ACTGCTCTGATCTTA[G/T]TTATTTCTCGCCTTC | 26133 |
rs559037944 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023647 | TCCAGAACAGTTAAG[A/T]GTCAGCTAATCTGTG | 26133 |
rs559060275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081546 | AAAATAAAATAAAAA[G/T]AAAATAAAATAAAAT | 26133 |
rs559067493 | in-del | -/ATG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035774 | GCATAGACACTAAGA[-/ATG]ATGACACATACATCT | 26133 |
rs559121314 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063998 | TGAATTTTGGTGACA[A/C]GTCCCAAGACAGTTT | 26133 |
rs559148500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022606 | TCCTACAGGAACTGC[C/T]TCCCTAGAGGCCTTT | 26133 |
rs559149826 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019122 | GGAGGCCTCTTTAAG[A/G]AGGAAGCCTTCTGTG | 26133 |
rs559152292 | snp | A/C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062555 | ACCTTGAGAACATTA[A/C/T]GTTAAGCAAAAGAAG | 26133 |
rs559158604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017108 | TTACAACACTACTCA[C/T]TATAGCATTATTTGT | 26133 |
rs559246946 | snp | A/G | 4.99363e-05 | 0.00499657 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010139 | GAGCCCCCGGGGAAC[A/G]TGGGCAGCCGGGATG | 26133 |
rs559254519 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090607 | TCAAACTCCTGACCT[C/G]AGATGATCCACCCGC | 26133 |
rs559313418 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082635 | CAGGCCAGTTTCACT[A/T]ACGACGATGTAAGGG | 26133 |
rs559323613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009659 | AAAAAACAAAACAAA[A/G]CAAACAAACAAAAAA | 26133 |
rs559332769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060861 | GATAAAGGGCTTTTA[C/T]TAAAAAACCCACAGC | 26133 |
rs559336188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054845 | ATTTTCAGGCACACA[C/T]AAAATAAGCCCGATT | 26133 |
rs559403237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074940 | CTTTATGAACCTGGG[C/T]GCTCCTGTATTGGGT | 26133 |
rs559427989 | snp | C/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093067 | CTCCCATTTCTCTCG[C/G]CGATTTGGGCAGGAT | 26133 |
rs559546580 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059884 | AAGAAAAGACGAAGA[A/C]AAAGATGAAGATGAA | 26133 |
rs559593386 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057980 | TTTCTACAGGTTTGG[A/G]GGTTATATGCATGTG | 26133 |
rs559640978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055476 | AAGATACATTTTCAA[A/G]AGTAGAACTACTAGA | 26133 |
rs559662245 | in-del | -/AAG | 0.0462092 | 0.144808 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059674 | TAAAAGAAAAAAAAG[-/AAG]AAGAAGAAGAAGGAA | 26133 |
rs559679603 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002703 | TCTCTGGTACCCACC[A/C]CCCCTGCCCAGGGCT | 26133 |
rs559698009 | in-del | -/AATTT | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066787 | TTAAAATAACATCAA[-/AATTT]AATTCTCAAAATAGT | 26133 |
rs559712753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059734 | GAAGAAGAGGAAGAA[C/G]ACTACGACGAAGAAG | 26133 |
rs559735910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007923 | GCTCCTGCGAGCCCC[C/G]GTGAAACATACTCTA | 26133 |
rs559773065 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033746 | CCTATAAACCTGGCA[C/T]TCTGGGAGGCCAAGG | 26133 |
rs559782682 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043359 | TCAAGCAATTATCCT[C/G]CCTCAGCCTTCTGAG | 26133 |
rs559782927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013583 | ACTCTGTCCCAAAAA[C/T]CCAACCAACCAACAA | 26133 |
rs559799706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038322 | AATATAAAAAAGTTT[A/G]ATAATGCTCTGTACT | 26133 |
rs559813014 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010337 | AGGAACTGGGGCTGC[G/T]GGGTCAGCACCAGGC | 26133 |
rs559821655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014378 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 26133 |
rs559844522 | snp | A/G | 1.65809e-05 | 0.00287926 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007517 | GGGCTGGGGGGAGAC[A/G]GAACCCAAGACACTG | 26133 |
rs559854444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006843 | GACCTGCTCTGTGGT[C/T]ACCAAGATGGCCGGG | 26133 |
rs559890189 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079044 | GCACCCCAGCCTGGG[C/T]GACAGACCAAAACTC | 26133 |
rs559934883 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029267 | AACTTTTTAAAAGTA[C/G]AGCCTCTCCAGCTTT | 26133 |
rs559964679 | in-del | -/TTTT | 0.00676609 | 0.0577691 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025604 | ATATTTTGAAATGGG[-/TTTT]TTTATTATTGTTATG | 26133 |
rs559966931 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054001 | AATTTGTGCCCATCC[A/G]TAATACAGATGATTT | 26133 |
rs560010356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073702 | AGGATTTTTGCATTG[A/G]TGTTCATCAGGGATA | 26133 |
rs560056839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045921 | CAATCCTCCCACCTT[A/G]GCCTCCTAAACTGCT | 26133 |
rs560064920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086831 | AGAGATCAAGAGTTT[A/G]AGACCAGCCTAGCCA | 26133 |
rs560180174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086259 | CCACCGCACCCAGCC[C/T]AAATAGATATCTTAA | 26133 |
rs560202656 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033981 | AACCCCGTCTCTACT[-/C]AAAAATACAAAAAAT | 26133 |
rs560269746 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081615 | AAAGGCTAAAAGTAA[A/C]AGAATGGGAAATAAT | 26133 |
rs560285727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028877 | CATGTTTATAACTGT[C/T]GTATCTTCTTGATGG | 26133 |
rs560293230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085189 | GGTGCAAAGCAGGCA[A/G]GGCACTGCTGTTTTT | 26133 |
rs560340999 | in-del | -/CT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028900 | CTTGATGGTTTCACC[-/CT]GTTATTATCAAATAT | 26133 |
rs560354272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034988 | GAGTCTTAATAGTCA[C/T]GGTCTAGAATTGCCT | 26133 |
rs560373858 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062095 | GCAAATCAAAACCAC[A/T]ATGAGATACCTCTTC | 26133 |
rs560416679 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051132 | TTTAATATTTCTTTT[G/T]TTTAGCCTCTAAGCT | 26133 |
rs560457379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050878 | GGCTCACACCTGTAA[G/T]CCCAGCTACCCCGGA | 26133 |
rs560468284 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021531 | AGGAGCCAGGTGAGC[A/G]CAGAGACTCGGAAAA | 26133 |
rs560492006 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077767 | ATCACAGGATAGTGT[G/T]GACCTCCCAAAATTA | 26133 |
rs560507758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084666 | TATATGCATATATGT[G/T]TATATGTATATATGT | 26133 |
rs560565381 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071749 | GCAATAAATATACAC[A/G]TGCATGTGTCTTTAT | 26133 |
rs560793779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057971 | TAACACTGATTTCTA[C/T]AGGTTTGGGGGTTAT | 26133 |
rs560823815 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093880 | ACACCCCATCTAAAA[A/G]GAGTAGACTCACCAT | 26133 |
rs560874232 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068614 | GCAACCTCTGCCTCC[A/C/T]GGCTTCAAGCAATTC | 26133 |
rs560884652 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080512 | TCTCAAAACAGAAAC[A/G]AAAACAAAGCGAGAC | 26133 |
rs560911089 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067268 | GGCTGGGGGACTGTT[C/T]GAGTCCGGGAGTTTG | 26133 |
rs560919334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030182 | GGAGGCGGAGGTTGC[A/G]GGGAGCCAAGATGGT | 26133 |
rs560944608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087484 | ACCCAGTCTGTCACC[A/G]GATTGCCAAACTGAA | 26133 |
rs560958398 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060856 | AGCCTGATAAAGGGC[-/T]TTTATTAAAAAACCC | 26133 |
rs560983060 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082916 | ACAGAAAACCCACTG[C/T]AAACATCATACTTAA | 26133 |
rs561014523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079791 | GGAGGCTAAGGCGGG[A/G]GGATTGCTTCAGCTC | 26133 |
rs561027232 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019059 | AGTCCTGAGATTTCA[A/G]TTTGGCCAAGATTGG | 26133 |
rs561048073 | snp | C/T | 0.0142086 | 0.0830808 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092786 | GCCGCCGCCATGTCT[C/T]CTCGTCGGACAAACA | 26133 |
rs561052506 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071892 | TTGAACTAGTTTACA[A/G]TCCCACCAACAGTTT | 26133 |
rs561098311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012916 | CAGCTCCAGGGCCTC[C/T]TCTCGAGCTGAGGTC | 26133 |
rs561183276 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014396 | GATCTCAGCTCACTG[C/G]AACCTCTGCCTCCTG | 26133 |
rs561225240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074842 | TTAACTTTCTGTCTC[A/G]TTGATCTGTCTAATG | 26133 |
rs561229137 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032514 | TCTCGCACTGTCGCC[C/T]AGGCTGAAATGCAGT | 26133 |
rs561239126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020904 | CAGGCTTGCCAGCTT[G/T]CAACTCTTTAGTCTT | 26133 |
rs561260640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035961 | AGCAGGAGAGAATAC[A/T]AACAATTCTCTTAAA | 26133 |
rs561300777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078356 | AGCCTATTACTATGT[G/T]ATAATAAGAAGGAGG | 26133 |
rs561328799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028271 | TGTGATCTCGGCTCA[C/T]TGCAACCTCTGCCTC | 26133 |
rs561369311 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053228 | TAGCTATTTTGAAAT[A/G]TAAAACAGAACAGAA | 26133 |
rs561369770 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064050 | ACCTTTTCCTTTTAA[A/C]ATGAGAAAAATTAGG | 26133 |
rs561374315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059520 | AATAAATTAGCTGGG[C/T]GTGGTGGTACGCCTA | 26133 |
rs561404936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065919 | TTGAGCTAGCCAAGT[A/G]AGTAAATGCCCTAGG | 26133 |
rs561445937 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055210 | GCCCATCAGAACCTA[C/T]AAGCCCATTTGCATA | 26133 |
rs561489984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066373 | CGGCCTCCTAAAGTG[A/C]TGGGATTACAGGCAT | 26133 |
rs561500611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091744 | TTGGGCACCTGTTAT[A/C]AGTCAGATGCTTAAT | 26133 |
rs561543510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056558 | ATACAGTATGTCGTA[C/T]TGGGGTAAAAAAAAA | 26133 |
rs561544896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058656 | TCAGAGGGAAATTTA[C/T]AGCTGTAAATGCCTA | 26133 |
rs561573890 | in-del | -/A | 0.000452671 | 0.0150376 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057589 | TAAAAAAAATTAGAT[-/A]AAAATCTTCAAAATT | 26133 |
rs561579774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051791 | AAGCTTAAAAATCTA[C/T]CTCCAGGCTGTCAAA | 26133 |
rs561620210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011082 | TGGCCAACGTGGCGA[A/G]ACCCCATCTCTACTA | 26133 |
rs561649840 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029210 | GAGCTGATCGTGCCA[C/G]TGCACTCCAGCCTGG | 26133 |
rs561694752 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006152 | GTCCCTCCCTACAGC[A/G]GCTCCCACCGTGGCA | 26133 |
rs561703612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011659 | GACTGTGACCCACAA[C/T]GTCCTGTGCAGCCCA | 26133 |
rs561714994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026397 | TTTTTAAATTTTTTA[G/T]AGAGACAGGGGTCTC | 26133 |
rs561773082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084680 | TGTATATGTATATAT[A/G]TTTATATGCATATAT | 26133 |
rs561813483 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040042 | TTTTGGCAACATCCT[A/G]CATATTTCAGCTTTC | 26133 |
rs561835087 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019130 | CTTTAAGGAGGAAGC[C/T]TTCTGTGAGGCCTGG | 26133 |
rs561841319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041962 | CTTTTGTCAATGTAT[A/G]TGGAGGTGTGTACAC | 26133 |
rs561842976 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046876 | TCTTAAATTTTAAGA[-/T]TTTTTTTTTTAAGGC | 26133 |
rs561852246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040538 | TGGTTCTAAGTTTTC[C/T]GGACTTGGACTGAGC | 26133 |
rs561860832 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020377 | TCAGCCCTCCTCTCC[C/T]GGCTGTTTGCTCCAG | 26133 |
rs561861786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049674 | TGATTTCAATGTATG[C/T]CTGTTTAGGTTTTAC | 26133 |
rs561902937 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028781 | GTTAAGGTCTCCAGC[G/T]GTTGTTTTTGAACTA | 26133 |
rs561919927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076677 | CAGTCGGCCCCTACT[A/G]GGAGGTGTCTCCCAG | 26133 |
rs561994985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085291 | ACTATTTATACATTG[C/T]CTTACAAGGCATGTA | 26133 |
rs562026423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083536 | AATCGCTTGAACCTG[G/T]GAGGCGGAGGTTGCA | 26133 |
rs562043464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070770 | CCCACTTTGTATTCC[C/T]CACAGATTCCAAGAC | 26133 |
rs562076379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004359 | TGGGTCTCCAGAGAC[C/G]CACTTCTGGAGTGGG | 26133 |
rs562078185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071320 | AAGTTCTAGGGTACT[G/T]GTGCACAACATGCAG | 26133 |
rs562080195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063276 | AACTGTGAGTCAATT[A/C]AACCTCCTTCCTTTA | 26133 |
rs562146562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090702 | TCTAGGCTCCTCCCA[C/T]TCTAAGTCATTCAGC | 26133 |
rs562176849 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008134 | GTTTGGACAAGGCAC[C/T]GAAGTGACAAAGGCC | 26133 |
rs562233919 | snp | C/G/T | 0.000249465 | 0.0111658 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007507 | AGCAACGCGTGGGCT[C/G/T]GGGGGAGACGGAACC | 26133 |
rs562243981 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077599 | ATCCTAGCATAATGT[C/T]TCCGTGCTCTTTCCA | 26133 |
rs562263234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052870 | GTCACAGTTTACACA[A/G]GTCCCCACTCCAACA | 26133 |
rs562295905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085390 | GCCAAGGTAGGCCCA[C/T]TGCTTGATCCCAGGA | 26133 |
rs562317679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077067 | ACCCTCCAAGCCAGG[C/T]GCAGGATATAATCTC | 26133 |
rs562333802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025863 | TTGTTAAATCCAAGG[C/T]CATGAAGCTTTATCC | 26133 |
rs562377635 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050814 | TAAAAGACCTTAAAA[A/C]TTAGGTTCAAGAGTT | 26133 |
rs562462939 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002836 | TGACAGCCAAGAAAC[C/T]GGCAGGAGCTCACAC | 26133 |
rs562492217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051600 | TTCGGTTCTTCAGTC[A/G]TAGCACTGACACATT | 26133 |
rs562496408 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093153 | AGTCCGCTTCCTGCC[C/T]GCTTCTCTCTACACG | 26133 |
rs562510526 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006186 | ACCATGCTGCGTCAC[A/G]GCAGGCGCACAAGCC | 26133 |
rs562530332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043282 | GACGGAGTCTAATTA[G/T]GTCGCCCAGGCTGAA | 26133 |
rs562563787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050762 | CAAAAAAACAAAACC[C/T]CCAAGGGGTATGAAG | 26133 |
rs562651777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026066 | TGGTCTTGGTACCCA[A/C]TGAAAATCAATTGAT | 26133 |
rs562651984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034559 | GGCCCCCCACTCCCA[A/G]TGAGAAACCTATTCC | 26133 |
rs562658981 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035399 | ATCTGCATGATAGGA[A/G]TAATTCTTACTCTGA | 26133 |
rs562739649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027045 | AATTTCTTTTTCTTG[A/C]CTAACTGCCCTAGCC | 26133 |
rs562822256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077095 | CTCCTGCTGTGCCAT[C/T]TGCTAAGGCCGTTGG | 26133 |
rs562848387 | snp | C/T | 0.000166248 | 0.00911573 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010148 | GGGAACGTGGGCAGC[C/T]GGGATGGGCTGAGGG | 26133 |
rs562871061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064926 | ACACCTAACGGTCTT[A/G]GTATACACAAGCTTT | 26133 |
rs562877318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057295 | GGACTATCAAAAGTA[C/T]AAAGATGCATTCTCT | 26133 |
rs562908443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091605 | AAATAAAGCTAATGT[C/T]TTACAGGTGTTAGCA | 26133 |
rs562908648 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083256 | CCACTTTTAAAAACG[C/G]TAAGGAATAAATCTA | 26133 |
rs562951372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084572 | TATGCATATATGTGT[A/G]TATGTATATATGTTT | 26133 |
rs563066294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077697 | TAAGGCCTCTTCCAC[A/G]AGCCTTCAGCAGTAT | 26133 |
rs563099767 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071552 | TTTTCTGTCCTTAAC[G/T]ATAGTTTGCTCAGAA | 26133 |
rs563126582 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019269 | GAGAACACGCTAGTG[A/G]AACAGTGGTTTTGGG | 26133 |
rs563171868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042643 | ATTTCCAGCCTGTTA[A/C]CATTGAAAAACTAGC | 26133 |
rs563184582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011009 | TTCACGTCTGTAATC[C/T]CAGCACTTTGGAAGG | 26133 |
rs563380347 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093350 | ATACAGTGGTGAGCA[A/G]AACGGCCTGGGATCC | 26133 |
rs563386332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069893 | TTGCAGTGAGCCAAC[A/G]TAGAGCCACTGCACT | 26133 |
rs563399016 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062445 | ATGTCCATCAACTGA[C/T]GAATGGATAAATAAG | 26133 |
rs563446664 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036833 | CGCCTGTAGTCCCAG[A/C]TACTCAGGAGGCTGA | 26133 |
rs563465176 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063230 | CTTCTGCCATGATTG[G/T]GAGTTTCCTGAGGCC | 26133 |
rs563487715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063095 | AGGTCCCCCATGCTG[G/T]TCTCGTGATAACGAG | 26133 |
rs563496998 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088450 | TTTCCTGAATATCAA[A/C]TGGCTGGCAAGGTTT | 26133 |
rs563497918 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055597 | ACTGTAGTCTCGAAC[A/C/T]CCTAGGCTCAAGCAA | 26133 |
rs563503835 | in-del | -/GAG | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069038 | ATCACAACTGGTTCT[-/GAG]GAGGGGACACTGGGA | 26133 |
rs563585363 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060621 | AAAAACAAGAAAAGG[A/T]TTATACACCATGACA | 26133 |
rs563594413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054073 | GTTATGTCCCCACCT[C/T]TATCTTCTTCTTTCT | 26133 |
rs563615393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082648 | CTAACGACGATGTAA[A/G]GGAAAAACCACAATT | 26133 |
rs563629656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015140 | GAGTAGCAGGGATTA[C/T]AGGTGCCCCACCAAC | 26133 |
rs563630021 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013350 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCGCTTGA | 26133 |
rs563649457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048683 | GAACACCTCGCCATT[C/T]TGGGGTACACAAAAA | 26133 |
rs563651085 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036558 | TATCATGTAGAAACA[A/C]TGAAATATATGCAGG | 26133 |
rs563705511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077048 | AAGGCTCCGTGGGCA[C/T]GGGACCCTCCAAGCC | 26133 |
rs563721517 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015166 | CCAACATGCCTGGCT[A/G]ATTTTTGTATTTTTA | 26133 |
rs563803062 | in-del | -/A | 0.00127829 | 0.025249 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044463 | TTTAGTAAGGGCCTC[-/A]AGAGCTATAATCTCA | 26133 |
rs563837001 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003679 | TGGCCCCTGGTGAAC[C/G]TGGGTAGCCATCAGG | 26133 |
rs563843396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054617 | TGGTTCTCATTTTGT[C/T]TTCTAACAAGGAAAA | 26133 |
rs563849665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038414 | TTGTCAACACTTACC[A/C]ATTTCCATTAATGGG | 26133 |
rs563880028 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085610 | GCAAGACCCTGTCTA[-/A]AAAAAAAAAAAAAAA | 26133 |
rs563917701 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071656 | CATGGTGTATATGTG[C/T]CACATTTTCTTAATC | 26133 |
rs563945746 | in-del | -/T/TT/TTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015461 | GCCTCAGGCAGGAAC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 26133 |
rs563945958 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062467 | ATAAATAAGATGTGG[C/T]CTATCCATACAGTGG | 26133 |
rs563956420 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021740 | AGTCGCAAATGGCCC[A/T]GCTTACTTGGTTCTT | 26133 |
rs563974231 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031938 | ACTTTGTCACCCAGG[A/C]GCAACTGCAGTGGCA | 26133 |
rs564101036 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046744 | ATGTAAGCTACTACT[A/G]TTATTGGCAACTGTA | 26133 |
rs564103127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018262 | GCCAGTGCTTAGGTT[G/T]GAGGTTTCTACTACA | 26133 |
rs564159908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054768 | TACCTGCTGCAGCAG[C/T]CCTGGCTCTTAACAA | 26133 |
rs564175720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091036 | TTAAGAAGGAAAGAG[C/T]AAGTATTTCTAGGAT | 26133 |
rs564176281 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026513 | GAGTCACTGTACCCG[A/G]CCTAGTTCAAGACTG | 26133 |
rs564183789 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040814 | CCTCCGCCTGTGATC[C/G]TGTGAGCCAATTCCC | 26133 |
rs564200762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056442 | CTTGCTATGAGGGTA[C/T]ATAGAGAACATGAAA | 26133 |
rs564228243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011019 | TAATCCCAGCACTTT[C/G]GAAGGTCCAGGCGGG | 26133 |
rs564266889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005133 | CCCCTGAAACAGACC[C/G]TCTGGGGCAGAAAAA | 26133 |
rs564286921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047773 | ACCCGATGGACTGAC[C/T]TTACAACCTTCTGGG | 26133 |
rs564292719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048775 | TGCTGAGACTGCTAA[A/G]GAGTCTGGAGTTTCC | 26133 |
rs564304319 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092401 | TCCACAGCAGCCCAG[-/C]CCCCGCTCGGCCCCT | 26133 |
rs564311507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082756 | TTCACCACATTGATA[A/G]CATAAAGGAGAATAA | 26133 |
rs564348590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083327 | ACTCTTGGCTGGGCA[C/T]AGTGGTTCACACTTG | 26133 |
rs564390881 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023428 | AAACTGAGTTTTTCT[G/T]CGAATGCTTGCTTGT | 26133 |
rs564402660 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068438 | TCTTTACTGCAACCT[C/T]GTCTGTAAGAGAAAT | 26133 |
rs564432488 | snp | C/G | 9.95405e-05 | 0.0070541 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003359 | GACACCCCTCTGAGA[C/G]GCCCTGGGTCCGCGG | 26133 |
rs564435858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076472 | TCTGTTTGTTAGTTT[C/T]CCTTCTAACAGTCAG | 26133 |
rs564450793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041801 | AGGCATCCAATACAG[A/T]ACCTTTCTAGCCCTC | 26133 |
rs564460562 | in-del | -/CTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018646 | GAAAGAAAATAGCAG[-/CTT]CTTCATGTGTAAAAT | 26133 |
rs564462639 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009462 | GCCTGGGCAACATAG[G/T]GAGACCCCATCTCTA | 26133 |
rs564466457 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065430 | TAAGACACACTTTTC[A/G]CAGTCATGTTATGGA | 26133 |
rs564500453 | snp | A/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094435 | AATTAGCTGGGCGTG[A/G]TGGCATGCACCTGTA | 26133 |
rs564517050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003791 | GCCCCCAGCAGCCCC[A/C]GTTTCCTGACTGAGC | 26133 |
rs564526546 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083191 | TCTATCTTATTTTTA[A/T]ATTACAGCTACAATT | 26133 |
rs564577599 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042796 | TGCTACTGAACAGAA[A/C]TAGGTGGGCTAGATT | 26133 |
rs564616218 | snp | C/T | 1.65499e-05 | 0.00287657 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35008672 | GACTCACCTGAAAGA[C/T]GACTCTGCTGGCTCC | 26133 |
rs564659572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069967 | AAAAAGCCTGACAGA[C/T]TTCGCTCTTGCCATC | 26133 |
rs564712430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037816 | CACAAATACTTACCA[C/T]TATGGTACAACTGCC | 26133 |
rs564729455 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063811 | GGCTGCAGTGAGCTA[A/G]GATCGTACCACTGCA | 26133 |
rs564771329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032600 | CCTCAGGCCTCCCCA[A/G]TAGCTGGGACTACAG | 26133 |
rs564783003 | snp | A/C | 0.0887219 | 0.191022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024844 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAAATTCT | 26133 |
rs564822852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087524 | GGGATGGCGGGTCAT[G/T]ACCTGTAATGTGAGC | 26133 |
rs564868690 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017448 | AAACAGAACTGCAGG[A/C]ATGATTTCCCTGTTA | 26133 |
rs564897992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074891 | AGTCTCCCATTATTA[C/T]TGTGTGGGAGTCTAA | 26133 |
rs564902887 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079547 | GAGAGCAAACATCAC[C/T]GAAATTGAAAACAAA | 26133 |
rs564964246 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015208 | GTTTCACCATGTTGG[A/C]CAGGCTGGTCTCGAA | 26133 |
rs564973112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074481 | CATGTCTTTGTTCTC[A/G]ATGGTTTCAAAGAAC | 26133 |
rs564998972 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086617 | TAATCAGGAGTTTTT[-/C]CAGTATCAAATTACC | 26133 |
rs565053771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008924 | CAGCCACAGAATTAA[A/G]CTGCCAAGTGCATTC | 26133 |
rs565141285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073652 | GAATAAGCTTTTTGA[C/T]GTGCTGCTGGATTTG | 26133 |
rs565169078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021439 | CTGCTCTGAACAGAC[C/T]TGTAGCATGGCCATT | 26133 |
rs565179528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069121 | AATTTAAATAAATGA[A/G]TTCTTCTGAAGTAAA | 26133 |
rs565206434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015864 | TCCTACTCCAAGGTA[G/T]CTTCCAATTAGGGGA | 26133 |
rs565207301 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002620 | GAACACAGCGGCCAA[G/T]GAGCAAACAGAACCA | 26133 |
rs565224808 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066539 | CTTCAGGTAATGGGG[C/T]TAAGGGCAGATATCT | 26133 |
rs565248815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073100 | TTGGTGTATAGGAAT[A/G]CTTGCGACTTTTGCA | 26133 |
rs565272728 | snp | C/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055509 | CTAAAGTATAGGCAT[C/G]TTTTTTTTGTTCATT | 26133 |
rs565274928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029475 | ATTGATAAGGCTGGA[A/C]TGACTTCTGCCATTT | 26133 |
rs565327307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013919 | GGGCCCTCCCAAGAG[C/G]AGCAGAAACCCTGGG | 26133 |
rs565335807 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035391 | AACAAACAATCTGCA[A/T]GATAGGAATAATTCT | 26133 |
rs565362141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014614 | TAAGCAGTTTCCGAA[C/T]TGAGCCAGACAGAAC | 26133 |
rs565371037 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065963 | CTGTGGAGAGGGAAT[A/G]CGGAGCAGCAGTTAA | 26133 |
rs565383571 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080979 | ACCAGATTGTGGTGA[C/T]GGTTGCATAACTTCA | 26133 |
rs565456567 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033120 | AACTGCTTGAACATG[A/G]GAGACAGAGGTTGCA | 26133 |
rs565488754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045246 | AAAATACATGTTACT[A/G]CTCTGCATGCACAGT | 26133 |
rs565495406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059841 | AGATGAAGACAAAGA[A/C]GACGAAGATGAAGAT | 26133 |
rs565498148 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015801 | GCCTAGGAAGATCTT[A/T]AAAGGGATTTCTGCA | 26133 |
rs565520370 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012515 | TTTCCTTACAGCAGA[C/G]AGTAATTTTCCTTGT | 26133 |
rs565553830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045581 | TATCTCATTGTCGCC[C/T]AGGCTGGAGTGCAGT | 26133 |
rs565611683 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084741 | ATGTGTATATGTATA[C/T]ATGTTTATATGCATA | 26133 |
rs565637399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060135 | CTCTTCCAAAAAACA[G/T]AAGAGAAGGAAACAT | 26133 |
rs565651853 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008548 | ACCTCTCCCCAACAG[G/T]AATTGTGCTTCAGGA | 26133 |
rs565665986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053659 | GTTCAAACAAGAGGA[A/G]AGAAAAACAAAACAC | 26133 |
rs565748167 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080482 | CTTCAGCCTGGGCGA[C/T]AAAGCCAGACCTTGT | 26133 |
rs565770372 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093609 | TTCTGTGGCAGGATG[A/G]CACTGACTCCCCCCA | 26133 |
rs565773398 | in-del | -/CACT | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048018 | TTCCACTGATACACA[-/CACT]CACCAACATTTGCCC | 26133 |
rs565817200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35009040 | TTTATACCAAAAGTG[G/T]GTTGAAACAGGTCAT | 26133 |
rs565852529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088802 | CCACAGATGATCCTT[A/G]AGGACATTATGTTAA | 26133 |
rs565881756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054341 | ACTAACATTTATATA[A/T]TGTTTTACAAAGTGT | 26133 |
rs566033121 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021918 | CAGATGAACATATTA[C/T]CTACAGGCAGATTTT | 26133 |
rs566095546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051931 | GGAAAACCTTCCCAA[C/G]TCAACAGTGGCCACC | 26133 |
rs566118809 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027317 | CGATCATGTGGTTTT[C/T]GTCCTTTATTCTATT | 26133 |
rs566190579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080138 | TTCAGCAAAAAAAGT[A/C]ATGATGTACTGATAC | 26133 |
rs566190900 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002292 | GCCCCCTGCTGCCTT[C/T]AGCCTTCCCTGGGCC | 26133 |
rs566206629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029853 | ACGTTAGCCAGGGTG[A/G]TCTCGATCTCCTGAC | 26133 |
rs566216748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078449 | CGTCGTAAATATATA[A/C]TGGAAATTCTAGGGC | 26133 |
rs566303036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072714 | TTGAAGTCAGGTAGC[A/G]TGATGCCTCCAGCTT | 26133 |
rs566341053 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073214 | TATACAATCATGTCA[C/T]CTGCAAACAGGGACA | 26133 |
rs566348788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080800 | CACTGACTTGTACAC[C/T]TCAGTTTTTTTTTTT | 26133 |
rs566411471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035529 | GGCTTTTTATCTACT[A/G]GGAATATAAATTAGA | 26133 |
rs566424538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084832 | GAAGAGGACTGTTTT[C/T]AACACTACAAAAAAA | 26133 |
rs566442822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034734 | AATAGGCAGTCTTCT[A/G]CCTAGTCCCATCAAG | 26133 |
rs566513325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026152 | ATGTCTATCCTCAGG[C/T]CAGCAGCATAGTGTC | 26133 |
rs566513622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017797 | TGTAAAAGTAATTGC[A/G]ATTTTTGCCACTGAA | 26133 |
rs566548125 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053583 | CTATCTCTGTCATTG[A/G]CTATACATGGCTACC | 26133 |
rs566637515 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043944 | AAAGTATATGCATTT[G/T]TAATTCTGATAAAAA | 26133 |
rs566651491 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066077 | AGGAAACTTTAATAA[A/T]TGAAGTATAACGTGA | 26133 |
rs566662471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020596 | GGACTGCTGAGCCTC[C/T]AGCCTCTCCTGCCCC | 26133 |
rs566665763 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079468 | AATAATCTAAGCTTC[C/T]ACCTTAGTAAACTAC | 26133 |
rs566667960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065443 | TCACAGTCATGTTAT[C/G]GATAGGGTCAGGCTG | 26133 |
rs566681540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058985 | TGAGCCACCGCACCC[A/G]GCCAAAGAAAATTGT | 26133 |
rs566699719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021082 | CTATGCTTTGCCAGG[C/T]TAAAGCGAGAGCCAT | 26133 |
rs566700528 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005638 | CTGGAGACAGGGTGT[C/G]TGATGCCAGCATTCT | 26133 |
rs566728792 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072870 | TCTATCAATTACCTC[A/G]GGCAATATGGCCATT | 26133 |
rs566788889 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048885 | CAAAGGGTCTGTCTG[G/T]GGCCTGCACACATCT | 26133 |
rs566825727 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024749 | TAGAAGGATGGCTGA[A/G]CCTGGGAGGTCAGGG | 26133 |
rs566842519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077243 | CCCGCCCTGCTTCAG[C/T]TCACACTCCGTGGAC | 26133 |
rs566866280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070877 | AAGCTAAGAGGAAAA[A/C]AAATCTTACAAGAAA | 26133 |
rs566886781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064245 | AAATTCTTCCTTAGC[C/T]CCTTCTAGCTATAGG | 26133 |
rs566949461 | in-del | -/TA | 0.0279526 | 0.114869 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084577 | ATATATGTGTATATG[-/TA]TATATGTTTATATGC | 26133 |
rs566952927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063564 | ATTATATTTCAATAA[A/G]GCTGTTATTGCTGGG | 26133 |
rs566967311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011217 | AGCCAAGATCATGCC[A/G]CTGCACTCCAGCCTG | 26133 |
rs566969555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057335 | TCTGAATTTCTACGC[A/G]GTACAGAATGAATAA | 26133 |
rs566992945 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070678 | GCTGGGATTACAGGC[G/T]TGAGTCACTGCGCCC | 26133 |
rs567087497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066090 | AATTGAAGTATAACG[A/T]GATACCGCATAAAGA | 26133 |
rs567134748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059164 | TTGAAGACTGGCAAA[C/T]TCTTAACTAGACTGA | 26133 |
rs567174326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092076 | ACAACAAAGAAATAC[A/G]AAATTATAGACTAAG | 26133 |
rs567188787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079099 | TGGAGAAAGATAAAT[C/G]ACATAAAAAGAAAGA | 26133 |
rs567196762 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042234 | GGAAAAGCAAATCTA[C/G]AGAGAGAATAAACTG | 26133 |
rs567204734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078719 | AAAAACCAAGATCCA[A/T]CAATATGCTGTCTAC | 26133 |
rs567212090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059752 | TACGACGAAGAAGAA[G/T]AAGACGAAGAAGACG | 26133 |
rs567215823 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029059 | CTGAGACCAACCTGG[A/C/T]CAACATGCTGAAACC | 26133 |
rs567252594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021113 | TCTAACAGAAGGCCC[A/C]GTGGAGCACCTGGCA | 26133 |
rs567295023 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034540 | GGGAAGAAGAAAAGC[A/T]GATGGCCCCCCACTC | 26133 |
rs567314277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019664 | TTCACATATAAGCAA[C/T]TGCGAAAGTGCCTCA | 26133 |
rs567316153 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025462 | ACAGGTGCCAGCCAC[C/T]GTGCCTGGCCTCACT | 26133 |
rs567351536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011938 | CTTATCACTAATGCT[C/G]AACGGTGGAATCCTT | 26133 |
rs567355361 | snp | A/G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027676 | TGTGGGCAGTTTTTC[A/G/T]TTATTTATTCAATCT | 26133 |
rs567420064 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073816 | ATTCCCTCTTTTTCT[A/T]TTGATTGGAATAGCT | 26133 |
rs567437576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012561 | GGTTAAAAAATAAAT[A/G]AGCGCAGAATGTCTT | 26133 |
rs567448381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021640 | ACCCATCCCTCCCTG[C/T]TTATGCCCTTCTCCT | 26133 |
rs567461514 | snp | C/G | 1.65315e-05 | 0.00287498 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013114 | CACAGCCACAAGGTT[C/G]CAAAATAACACAAGC | 26133 |
rs567473616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006343 | CCCGTCGTCTCTAAC[A/G]TAAAACCTGTGCCTA | 26133 |
rs567484873 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034061 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAAGC | 26133 |
rs567485523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052555 | CGCTGGAGTGCAGTG[A/G]TGCAATCTCAGCTCA | 26133 |
rs567498716 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007463 | CTGCTCTGCTCCTGA[A/T]GAACTGTTTGGGGCT | 26133 |
rs567521946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054087 | TTTATCTTCTTCTTT[A/C]TTACCTGCTTCTAAG | 26133 |
rs567583329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008008 | GTGTGGGAAGCGGAC[A/G]AACACATGCAGACAG | 26133 |
rs567596643 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045325 | TTATCTACACTGATA[C/G]AAGCAGCTGATTCAA | 26133 |
rs567628784 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071875 | ACTGTCTTCCACAAT[A/G]GTTGAACTAGTTTAC | 26133 |
rs567659453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043514 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTT | 26133 |
rs567664458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064384 | GTTCAGCTTGAGGGT[A/C]TGAGAAAGCCTCTGC | 26133 |
rs567668995 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040794 | AGATGGCTTATCATG[A/G]GACTCCTCCGCCTGT | 26133 |
rs567747618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090501 | GCCTCAGCCTCCAGA[A/G]TAGCTGGGATTACAG | 26133 |
rs567748146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057397 | AACCTGTAGCTAAAT[G/T]TAAGACATGTCCTTA | 26133 |
rs567758119 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049411 | ATAGAGGCGGACTTC[A/G]TAAGTGAAAGCCAAA | 26133 |
rs567783335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050197 | TCCTGACGTGCAGGC[G/T]ACACAAGTGGGAACT | 26133 |
rs567831831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091171 | CCCGGCTAAATTTTT[A/G]GAGACACAGGATTTT | 26133 |
rs567847709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092238 | TGGGGGCTGCAATGA[C/T]GACCCCCTCCCCCAC | 26133 |
rs567889915 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092829 | CCTCGGGGCCGCGGA[A/G]ATTTCTACGGGGCGG | 26133 |
rs567906298 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083606 | CAGAGCGAGACTCCA[G/T]CTCAAAAAAAAAAAA | 26133 |
rs567911757 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022895 | GGGCATGGTGGCATG[C/T]GCCTGTAGTCCCAGC | 26133 |
rs567977410 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093361 | AGCAGAACGGCCTGG[C/G]ATCCTTTATCACGAA | 26133 |
rs568001403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004685 | TAGGAGCTCATCATC[A/G]AAACAGCTTCAACGA | 26133 |
rs568021183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018851 | TCACAAGATAGCTCT[A/G]TGACCCTGGGCAACA | 26133 |
rs568076452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048066 | TATGGTATTGATTTG[C/T]ATTTCCTTGATTGCC | 26133 |
rs568089939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039110 | ACAAAAAAGAAATAA[A/G]AAGAATTTGTATTCT | 26133 |
rs568113253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048955 | CAATGACAAGCAAGG[A/C]CTGGGGAAAGCACAG | 26133 |
rs568115460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040321 | ATCTGCCCTCAATGT[A/G]GGCAGGCACCATCCA | 26133 |
rs568200062 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084421 | TTAAAGGATGCACTA[C/T]TATGCTAATGAAAGT | 26133 |
rs568221946 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033987 | CGTCTCTACTAAAAA[A/T]ACAAAAAATTAGCCG | 26133 |
rs568240844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077874 | GATGATGGGATTATA[G/T]GTGATGTATATTTTC | 26133 |
rs568315956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082284 | ACACACCTCGAGCAG[C/T]ATATCTAGTAAATGC | 26133 |
rs568338488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031506 | TTCCTAAAGTGCAGG[A/G]ATTACAGGTGTGCGC | 26133 |
rs568396061 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089602 | ACACCTGTAATCCCA[A/C/G]CACTTTGGGAGGACA | 26133 |
rs568430667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023290 | TTTGTAAAACAGCAA[C/T]ACTGACAACCATACC | 26133 |
rs568474979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091238 | CAAGCGATCTGCCTG[A/C]CTCGGCCTCCCAAAG | 26133 |
rs568481680 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063542 | TACAAGAATTAACTT[C/T]ATGTAAATTATATTT | 26133 |
rs568559483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084480 | TATATGTATATATGT[A/G]TATATATGTATATAT | 26133 |
rs568597541 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045215 | GCATGTTTTTATACT[C/T]ACAAATATTTCCATT | 26133 |
rs568628250 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084724 | TATGTTTATATGCAT[A/G]TATGTGTATATGTAT | 26133 |
rs568637433 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043049 | ACAAAAACTATACCA[C/T]ATACACACTGTTCTG | 26133 |
rs568647979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055090 | AGATAGTACAACAGT[C/T]ACCACATTTTTTTCA | 26133 |
rs568674691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004214 | TGAGGGACGTGGACA[A/T]GGGGGAGGCGGGGAG | 26133 |
rs568697305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017476 | TTAAAATTTGTTTAT[A/T]TAACATAAGGCTATT | 26133 |
rs568742272 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027129 | AAACGATCAGGAACT[C/T]GTCTTGTTCCTGATC | 26133 |
rs568755884 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039434 | CTCATACACAATCTC[A/G]TGGGCTGACATCCCA | 26133 |
rs568762655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055785 | AACTGAGCATTTCTT[C/T]TTTTGTTGCTGTTAT | 26133 |
rs568819104 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043485 | CTCTGAACCTCAAGT[C/G]ATCCTCCTGCCTCGG | 26133 |
rs568854900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041170 | AAGCCACCTAGTCTA[C/T]GGTACCTTGTTATGG | 26133 |
rs568892564 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068100 | TACTTAAAATACACT[C/G]TTTGTGGAAGGGGGC | 26133 |
rs568896877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032752 | GCTGGGATTACAGGT[A/G]TGAGCCAACGCGCCC | 26133 |
rs568929951 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034223 | TTATTTGCTTACCAT[A/C]AAAATCTCCTCAGGC | 26133 |
rs569022547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034708 | AGCTGAGACTGGGAG[C/T]CTTCTTATTTAATAG | 26133 |
rs569038170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072616 | GCATTATTTCTGAGG[A/G]CTCTGTTCTGTTCCA | 26133 |
rs569054598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027525 | GGTATCATGATAATA[C/T]GACCTCAAAGAGTAA | 26133 |
rs569063024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020491 | CATTCTCTTCTGGAC[A/G]TTTTCATCCTCACTT | 26133 |
rs569075651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062700 | GCCTTGGGAGGAAAT[A/G]GGGAGTGGCTACTGA | 26133 |
rs569076606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071934 | TATTTCTCCACATCC[C/T]CTCCAGCACCTGTTG | 26133 |
rs569100359 | in-del | -/AC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048013 | AGTGTTTCCACTGAT[-/AC]ACACACTCACCAACA | 26133 |
rs569103350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019768 | TGAAGGAAGGGACAC[C/G]AATGCTGTGGCTATC | 26133 |
rs569110038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076060 | CGAATTGGCTACTGA[A/G]GCTTGTGCATGCGTC | 26133 |
rs569112258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063481 | AGATTTCTTTTTGGC[A/G]TGATAAAAATGTTCT | 26133 |
rs569116506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055850 | ATTACTAATTCTTAT[A/T]AAGAAACTACTACTT | 26133 |
rs569175717 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070245 | CGGCTGCTAGGTTTC[A/G]GGGTGACTAGTTCTG | 26133 |
rs569204802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056718 | GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 26133 |
rs569230016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083658 | AATTTATACTTCTAT[A/G]CCCAGTCAAACTAAA | 26133 |
rs569304757 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024929 | TATGAATATGCTGTG[A/G]TGAACATACCTGAAC | 26133 |
rs569312952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070392 | TTTAGCACTTTTACT[A/T]TGCACCTATTTACAA | 26133 |
rs569318498 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070853 | AGAATCCTTTGTTCA[C/T]ATGGAACAAAGCTAA | 26133 |
rs569342817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017742 | GACATCCCTGGCAGC[C/T]TCCATTTCCATGGAC | 26133 |
rs569360633 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020239 | TCGCCCTATTCCCTT[C/T]CTTGCTGTTTCCAGT | 26133 |
rs569380094 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024348 | AGCTCTAGGCAACCA[C/T]GAAACTATTTTCCAT | 26133 |
rs569423177 | snp | C/G | 0.000311085 | 0.0124678 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004518 | GAAGGACATCTGCGT[C/G]GGCACCTGGGATATG | 26133 |
rs569430482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009823 | AGAGGCTTCTGTCTG[C/T]CCTGCTTGGCTGCAG | 26133 |
rs569467173 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003926 | AGGCAGGGCTGGGTG[C/T]GTGTGTTGGGGCGGT | 26133 |
rs569505705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011163 | TACTCAGGAGGCTGA[C/G]GTAGAATTGCTTGAA | 26133 |
rs569567629 | in-del | -/CTGA | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057109 | GCATACCAAAACACT[-/CTGA]CTTTTTACCATTCAC | 26133 |
rs569568087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049091 | AACCAGCAACCAACA[C/T]GGAGGCTCAGGACAG | 26133 |
rs569576102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039283 | CAGATGGGAAGTGCC[C/T]GGTACTCAGGGTTCT | 26133 |
rs569625017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015366 | GGAAAAGCAGGCTGC[C/T]AGCTCATGCAGTGGG | 26133 |
rs569634756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068815 | GTGAGCCACTGCGCC[C/T]GGCCTAAAATTGTTT | 26133 |
rs569648808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054440 | TTGGTAAGAAACTAC[A/G]GCTTGGGAGGTGTAC | 26133 |
rs569672322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060820 | TAAAACAATCAACAA[A/G]GAATAGAAGAGAACT | 26133 |
rs569685859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046436 | ATTGGGTGTTTCTCT[C/T]TCACTGCACAGATCA | 26133 |
rs569703489 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094445 | GCGTGGTGGCATGCA[C/T]CTGTAGTCCCAGCTA | 26133 |
rs569740642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087271 | ATGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 26133 |
rs569774364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064171 | GACATTCCCTATATA[C/T]GTATGTATTTTTTAT | 26133 |
rs569776347 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030382 | ATGCTAATCTCTGTA[C/T]TGTTCCAATTTTGGA | 26133 |
rs569828260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087801 | TGACAGAGGGCAGAA[C/G]AAAACGAAGGGAAGA | 26133 |
rs569855365 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047230 | GCAGCACAACAAAAT[A/G]ACTAGCTGTGTGTGC | 26133 |
rs569871444 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051913 | ACTAAAATGACTCCT[C/T]TTGGAAAACCTTCCC | 26133 |
rs569872365 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019196 | CAGGATCTGGGAATC[C/T]AGATCCTCACGGTGC | 26133 |
rs569893225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089700 | CTAAAAATACAAAAA[G/T]TAGCCAGGTGTGGTG | 26133 |
rs569945548 | snp | C/G | 0.00199481 | 0.0315187 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002326 | AATAAACACCACAGC[C/G]AGTTTCCTTCTCATT | 26133 |
rs569983122 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083015 | GTCTCAGGCAGCAGA[A/G]TAAGGCAAGATATAT | 26133 |
rs570096854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045518 | TAGGACTACAGGTGC[A/G]TGTCATTACACCTGG | 26133 |
rs570105135 | in-del | -/T | 0.498611 | 0.0263212 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026222 | AGTTGTCTTAGGTTG[-/T]TTTTTTTTTTTTGAG | 26133 |
rs570124418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037542 | ACTGAAGGGATAAAC[A/G]AACTGTGGTATCTAC | 26133 |
rs570148778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004046 | TGCTTCACCTCAGAA[C/T]GGAACCAAAGACCAC | 26133 |
rs570151721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080278 | GGCCAAGGTGGACAG[A/C]TCACTTGAGCTCACA | 26133 |
rs570197534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074641 | TCTGAGAGACAGTTT[A/G]TTATAATTTCTGTTC | 26133 |
rs570211232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038105 | GCTTAATGTGTACGG[C/T]GTTTCCTTTTGGGGT | 26133 |
rs570224535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022495 | CATTGGTCAGAGTCA[A/G]GAGAGGCTAGGTGAT | 26133 |
rs570261165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014767 | ATGGCTGGGTGGCAC[C/T]TTTAGGTCCCAGAGC | 26133 |
rs570268704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081857 | GGGCATGGTGGCACA[A/G]GCCTGTAATCCCAGT | 26133 |
rs570305183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075013 | CCCTTTACCATTATG[C/T]AATGGCCTTGTCTCT | 26133 |
rs570330120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031258 | TTTTCTTTTTGGAGG[C/G]AGGGTCTCGCTCTGT | 26133 |
rs570415795 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019333 | CCCAAGGAACCAGCA[C/T]TGTAATCATACAGTT | 26133 |
rs570417325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025410 | TGAGCTGGTCTTGAA[C/T]AATCCTCCTGCCTTG | 26133 |
rs570473666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089802 | AGTGAACCGAGATTG[C/T]GCCACTGCACTCCAG | 26133 |
rs570479521 | snp | C/T | 4.94784e-05 | 0.00497361 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35055010 | AGGATACTCAAGCAG[C/T]CCTTGGACATTTCAT | 26133 |
rs570518144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047293 | CACCATCATTAATTA[C/T]TATTGCCTTGCCATT | 26133 |
rs570526152 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040084 | GGACTGTGTCCCCAC[C/T]CCCCGCGCCCCCACA | 26133 |
rs570583920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090339 | CCTGCCTTGCTTTTG[C/T]GGCTCCAGAATATTC | 26133 |
rs570594615 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082047 | AGATAGGCACTTTAA[C/T]AAGGATAAAAATGGC | 26133 |
rs570603468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048055 | CTCTCCCTCACTATG[C/G]TATTGATTTGCATTT | 26133 |
rs570605815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040228 | ATGCCTACATGGCTG[G/T]CACAGCACTGTTTCT | 26133 |
rs570708471 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083898 | CAGACCTAGTAAGCA[A/G]CTAAACTAAACTGCT | 26133 |
rs570718895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087960 | AGGATTTTGGCTTTC[A/G]ACATACTAAGTTTGA | 26133 |
rs570719537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075877 | TGGTTCCATTCTCCC[C/T]GTCACTTTCAGGTAC | 26133 |
rs570844553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046201 | AGTTAAATTTTAATA[A/C]ATACCCTATATATAG | 26133 |
rs570862538 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031864 | GAGTCTTTCTAGTGA[-/T]TTTTTTCATCTTGAT | 26133 |
rs570872941 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088713 | ATCTTGGTCACCCTG[A/C]TAGGATTCAATTCAG | 26133 |
rs570883132 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038454 | AAATTACAGTATGCC[G/T]GTATAATAGAATATT | 26133 |
rs570888050 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057103 | AATAGTGCATACCAA[A/G]ACACTCTGACTTTTT | 26133 |
rs570898185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029801 | CCACCACGCCCAGCT[A/G]ATTTTTTTGTATTTT | 26133 |
rs570961468 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077593 | ACAATTATCCTAGCA[C/T]AATGTCTCCGTGCTC | 26133 |
rs571009101 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088585 | ATGCCACACTGGCTA[C/T]GCTTTTAAAACATAT | 26133 |
rs571029554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015414 | GAAATGAGATCCCTA[C/T]CACAGAGATTACAAG | 26133 |
rs571042870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023223 | CCCATTCACTAGCCG[C/G]GTGGTCTTCAGTAAA | 26133 |
rs571115541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060077 | TGATGGCTCCATTGG[C/T]GAACAATACAAGACA | 26133 |
rs571117729 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069392 | TGCCATAGCCTCCAT[G/T]GAGAGAAGAGGAGAA | 26133 |
rs571154939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061716 | AAAGTCAATGCAAAT[A/G]GATCAAAGATCTAAA | 26133 |
rs571164334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073955 | CTTCAGAGCCTGTTA[C/T]TGGTCTATTCAGGGA | 26133 |
rs571202341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053599 | CTATACATGGCTACC[A/G]AGCACTTAAAAGGTG | 26133 |
rs571233744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079861 | GCCTCTACTAAAAAT[A/T]AAAAAAAAAAATAAG | 26133 |
rs571295748 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083198 | TATTTTTATATTACA[C/G]CTACAATTTTTAAAT | 26133 |
rs571348391 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011310 | TAACCCACTGAACCT[C/G]CTAGCTTAGCCTAGC | 26133 |
rs571352454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008084 | TGATGCTGACCGAGG[C/G]ACCCAGAGGGCACAG | 26133 |
rs571415094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014457 | GACATTACAAAACAC[A/G]AGGCAACACTCCACC | 26133 |
rs571483235 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002405 | CAGGTCCACAGCAGT[C/T]ATTTTTAAAATAAAG | 26133 |
rs571519579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065231 | TTTACCTACAAATCT[A/G]GATTTCCCATAACCT | 26133 |
rs571542291 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029738 | CCTCCTGGGTTCACG[C/T]CATTCTCCTGCCTCA | 26133 |
rs571583938 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021089 | TTGCCAGGCTAAAGC[A/G]AGAGCCATTCTAACA | 26133 |
rs571593554 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002863 | ACACAGAGCTAATGC[C/T]AAATGTCCTCTTACC | 26133 |
rs571654283 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042410 | CAGCCTCAGGAGAGG[A/T]GGCTGCTCTGAAGCA | 26133 |
rs571657106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029138 | CGCCTGTAATCCCAA[C/G]TACTTGGGAGGCTGA | 26133 |
rs571676070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058149 | GTATGTACCTAACAA[C/T]AGAGCCCAAAAATAC | 26133 |
rs571706434 | snp | A/G | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35009007 | CAGACATGGCTTAGA[A/G]CTGCCAGAGGAGAGC | 26133 |
rs571708538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052345 | ACAATTCTCCTGCCT[C/T]GGCCTATCAAAGTGT | 26133 |
rs571767101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043590 | TCCCTTAGTCAAGAC[A/C]CTCACAGTGGATACC | 26133 |
rs571798549 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044195 | CAGGAAGTCAAGACC[A/G]GCCTGGGCAACATGG | 26133 |
rs571799656 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091351 | GGAAAACATTTCTCA[C/T]TCACAACTGCTCCTT | 26133 |
rs571805818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036630 | AGGTGAAGTAGGGTA[C/T]AGTGAATGGGAGTAG | 26133 |
rs571909629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059453 | CTGATTGAAGCCAGA[A/G]GATTGAGACCACCCT | 26133 |
rs571954935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079191 | TGGGTCATTTCATAA[C/T]GACAAAGGGGTTAAT | 26133 |
rs571955106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087019 | CCTGGGCAACAGCAC[A/G]AGACTCCATCTCACA | 26133 |
rs571958075 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030550 | CTTTAAATAATTTTA[C/T]GTTAGAGAAACTGAG | 26133 |
rs571968878 | snp | A/G | 6.64838e-05 | 0.0057652 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002054 | AGGCCAACAAGCTGC[A/G]GGCACGGACCCGGGA | 26133 |
rs571983867 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088183 | AGTCACTATTTTAAG[C/T]GCTTTATATGTACAA | 26133 |
rs571994954 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018107 | TTCCAACAATGGCCC[A/C]AAAAAATTCATCCAG | 26133 |
rs572019342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059775 | AGAAGACGACGAAGA[C/T]AAAGAAGATGAAGAA | 26133 |
rs572021204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074385 | AATTTTAGATCTTTC[C/T]GGCTTTCTCTTGTGT | 26133 |
rs572079416 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057264 | TTTCCCAAGGAAACA[C/T]AGAAGCTGGATCACA | 26133 |
rs572084798 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056266 | ATCCTCCATTTTTAA[A/G]AGGAATTGGGATTCA | 26133 |
rs572138997 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093844 | TCTCCCAGGTGAACT[A/G]GCACTATGGTTACCA | 26133 |
rs572141509 | snp | C/G | 0.00517822 | 0.0506191 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002521 | GGAGCGGCTGCCTCA[C/G]GCAGAGGCAGGGCAG | 26133 |
rs572286117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020805 | GTACTTGCCCAGTTT[C/T]CCTAAGCAGACACAG | 26133 |
rs572343134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030741 | TGCAAAATATGTTTC[C/T]ATATGTTATAGGTTC | 26133 |
rs572367487 | snp | A/T | 1.6504e-05 | 0.00287258 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021260 | TTGTACATGATCTCA[A/T]GCATAATCTTCATTG | 26133 |
rs572371481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012867 | CGACTGCAGTGTCAC[A/C]CCTGCTAACACTGAG | 26133 |
rs572376233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085979 | AATGCAAGGGTCTCG[C/T]GCAATCTCACTGCAA | 26133 |
rs572401085 | in-del | -/AAAAAAA | 0.242775 | 0.249896 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030242 | GCGAAACTCCATATC[-/AAAAAAA]AAAAAAAAAAAAGAA | 26133 |
rs572408199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013321 | CGTGGTGGTTACACC[C/T]GTAATCACAGCACTT | 26133 |
rs572464751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077531 | GCCCAGAACTCTGTG[C/T]TTTAACACGCTCTTC | 26133 |
rs572486169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043134 | GAGATCTTCATTTTT[G/T]CAAAGCTACACAATT | 26133 |
rs572553804 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071219 | TTCACCTCTGAAGAA[A/C]ACTGTCATTCAGTTT | 26133 |
rs572735060 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074234 | AGCTTCTGGATTCAT[C/T]GATTTTTTGAAGGGT | 26133 |
rs572852383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026699 | ATTAATTTTCTGATT[A/C]AAAGACATGGGATGT | 26133 |
rs572879519 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020309 | TCAGAGTAAAAACCA[A/G]AGTCTTTAAAATGGC | 26133 |
rs572904276 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055377 | TTTTTGTTTTTTGTG[G/T]TTTTTGGCTATTTAA | 26133 |
rs572941188 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071862 | GAGGAATCGCCACAC[C/T]GTCTTCCACAATGGT | 26133 |
rs572954547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057682 | CAGTATTACAAGACC[C/T]TTTTGTTCCAGGAGG | 26133 |
rs572957547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057111 | ATACCAAAACACTCT[A/G]ACTTTTTACCATTCA | 26133 |
rs572975426 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041913 | AAGCAGTTACCCAGC[A/G]TTTGCCACATACCAG | 26133 |
rs572977901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019866 | CCTCCAGCCTTGCCA[G/T]CTCCCCAACACCAGG | 26133 |
rs572982810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005581 | TTGAGGCCGGCCACG[C/T]GGGCATCTGGTGCAG | 26133 |
rs573009650 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090704 | TAGGCTCCTCCCATT[C/G]TAAGTCATTCAGCAC | 26133 |
rs573097579 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092291 | GAGGCCCACAGAGGC[A/T]AAAACAAACACGACA | 26133 |
rs573165067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050513 | TGAGGCCAGGAGTTC[C/G]AGACCAGCCTGGCCA | 26133 |
rs573165822 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022684 | AGGTAAGGCTCATAC[A/C]GAAAACACAGTGATA | 26133 |
rs573179130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010097 | GTGAGAGAGGACACG[C/T]GTGCATACCTGGATG | 26133 |
rs573187389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052363 | CCTATCAAAGTGTTG[A/G]GATTATAGGTGTGAG | 26133 |
rs573200011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042656 | TAACATTGAAAAACT[A/T]GCTTTTAAGACACAA | 26133 |
rs573201882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051411 | CACCTGGGCTCAAGC[A/G]ATCCCCCCACCTCAG | 26133 |
rs573224787 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077050 | GGCTCCGTGGGCATG[C/G]GACCCTCCAAGCCAG | 26133 |
rs573229787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010858 | GATCCTGTCACTCCC[A/G]GTGAAAACACTTCCA | 26133 |
rs573255725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072111 | TCTGTTCATATCCTT[C/T]GCCCAGTTTTTGATG | 26133 |
rs573268542 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004877 | ATCACACACAGAAGA[A/G]TTCCCTCCACAGGAA | 26133 |
rs573342194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064825 | TACTATAACTTTAAC[A/G]TTATATTAACAACTT | 26133 |
rs573358111 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074288 | GTACTGCTCTGATCT[C/T]AGTTATTTCTCGCCT | 26133 |
rs573373174 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045786 | CTCAGATGATCCATC[C/T]ACCTTGGCCTCCCAA | 26133 |
rs573390155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091376 | CTCCTTTCGTCCACA[A/G]TCCTCCATACACACA | 26133 |
rs573401979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040521 | TACACCATTAGCTTT[C/T]CTGGTTCTAAGTTTT | 26133 |
rs573408517 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050146 | CTTAACTGTGGGAAA[C/T]GCTCGTTAACTCCCC | 26133 |
rs573481292 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084512 | TATATATGTATATAC[A/G]TATATATGTGTATAT | 26133 |
rs573539842 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019946 | CTTGTACAAAACACA[A/C]CTCCCCATCTTCCTC | 26133 |
rs573565128 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093082 | CCGATTTGGGCAGGA[C/T]GCAGGCAGCTGGCCA | 26133 |
rs573579919 | in-del | -/TACTGAAA | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065196 | CACCTGGCCCACAAT[-/TACTGAAA]AGCTGGAAGATTTTT | 26133 |
rs573601362 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093699 | GAGAGCTAAGTGTGA[G/T]GTAACAGGGAATGGT | 26133 |
rs573601667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086104 | TGGGATTACAGGCAC[A/G]CACCACCACGCCCGG | 26133 |
rs573664760 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064457 | GCCATGAGATTGCTC[A/G]TGGCATGAATGTGAC | 26133 |
rs573723075 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050226 | CTCACTTGTGAGAAC[A/G]TAACACAATGAGATG | 26133 |
rs573726453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058306 | CAACGAACACATATA[C/T]TCTAACAGACATCTA | 26133 |
rs573753571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050726 | TCAAAAAAAAAAACA[A/G]AACAAAAAAACCAAC | 26133 |
rs573764776 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051489 | ATTTAATTTTCAAAG[C/T]GAAGGCATCAATAAA | 26133 |
rs573785892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012715 | GCTTTAGAGGGGCAG[C/T]AGGTTGAGAAATCCA | 26133 |
rs573795789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040610 | TATCTTTTATTTTAT[G/T]TATTTATTTTTGGAG | 26133 |
rs573824034 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028530 | CACTGGGATTTGAGG[A/G/T]CATACTTTTGTACAG | 26133 |
rs573830697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041371 | AAGGGAATGGAGTAG[C/G]AATTATGGTCAGGGT | 26133 |
rs573873959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006756 | AGGCCTGACAGACCT[C/T]ACCAGGAGGTGGAGC | 26133 |
rs573887415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030150 | AGAGGCTGAGGTAGG[A/G]GAATCACTTGAACCC | 26133 |
rs573911650 | snp | A/T | 1.66999e-05 | 0.00288958 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001967 | AGCAGGCCAACACCA[A/T]CCTGGCCAAGTATCG | 26133 |
rs573951488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056128 | CTGAGACAACGCAGA[C/T]GCTCTGCATCCCTTA | 26133 |
rs573962383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056932 | CGGAGGTTGCAGTGA[G/T]CCAAGATCATGCCAC | 26133 |
rs573983567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043270 | TTTTTTTTTTGAGAC[A/G]GAGTCTAATTATGTC | 26133 |
rs573988897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048667 | CCCATAATGTTTGGT[C/G]GAACACCTCGCCATT | 26133 |
rs574020728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035989 | AAAATTACTCATCTA[C/T]AGTTTCTAATTTTCC | 26133 |
rs574056817 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072833 | AGAAAGTAATTGGTA[A/G]CTTGATGGGGATGGC | 26133 |
rs574087961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089828 | TCCAGTCTGGGCAAC[A/G]GAGCGAGACTCCGTC | 26133 |
rs574117291 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003319 | TGGGGGGCGCCTGGA[A/G]GACCCAGGTCAAGCC | 26133 |
rs574139002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007326 | AACCAAACTGTCACC[C/T]TCCTGCATGGCCTGG | 26133 |
rs574169850 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084551 | ATGTATATGTATATA[C/T]GTTTATATGCATATA | 26133 |
rs574299901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027810 | ATTGTTTATAGTATT[C/T]CCTTAGAGTCCTCTT | 26133 |
rs574347354 | snp | A/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093732 | AGATTGTGACTCATA[A/G]CTAAGATGACTGTAA | 26133 |
rs574357865 | snp | C/G | 0.000132446 | 0.00813667 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010168 | TGGGCTGAGGGAAAA[C/G]CTGCACCCCTGCACT | 26133 |
rs574444926 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082405 | CTGAAATACAGACTA[C/T]GTTCCACATCAGAAA | 26133 |
rs574445513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074788 | ATGTCTATTAGGTCC[A/G]CTTGGTGCAGAGCTG | 26133 |
rs574489445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076313 | TGCTGGTGAGGAGCT[A/G]TGTTCCTTTGGAGGA | 26133 |
rs574498195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076944 | GCCGCTTTGTTTACC[C/T]ACGCAAGTCTCAGCA | 26133 |
rs574499388 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039565 | TTTCTGCAGAAGCAG[G/T]CCTCTTCTCTCTTCT | 26133 |
rs574503694 | snp | G/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093124 | TGGGCTTCAGGTCAG[G/T]AGTCAGGCCCTCGAG | 26133 |
rs574509676 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059806 | GAAGGCGAAGACGAA[C/G]ACAAAGATGAAGACG | 26133 |
rs574516200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024497 | CCTATCAGCATTCCC[C/T]TTTATTGCTGAATAA | 26133 |
rs574525143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025665 | ATCCCTTATTAGATA[C/T]ATTATTTGCAAAGAT | 26133 |
rs574529761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068487 | ATGCCAGTCAACTGG[C/G]GCCTGGGTAAATAAA | 26133 |
rs574530898 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070933 | AAGTACTTACTTAAT[A/G]AATAAAGAAATGATG | 26133 |
rs574543365 | in-del | -/TCAAAAT | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011538 | GAGCCCAGGAAAAGA[-/TCAAAAT]TCAAAATTCTACTTC | 26133 |
rs574552111 | in-del | -/TTTC | 0.00279162 | 0.0372561 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002343 | TTTCCTTCTCATTCT[-/TTTC]TTTCTTTGGGGTTCA | 26133 |
rs574607920 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079865 | TACTAAAAATAAAAA[-/T]AAAAAAATAAGCCAA | 26133 |
rs574639644 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089296 | TAATGGTGTGATCAT[C/G]GCTCACTGCAGCCTT | 26133 |
rs574851986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084150 | ACTAAAAATACAAAA[A/G]AATTAGCCAGACTTG | 26133 |
rs574908746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054014 | CCGTAATACAGATGA[C/T]TTTATGGTCTTCATT | 26133 |
rs574939679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061026 | AAATTAAAGGCACCC[A/C]AATTGGAAAGGAATA | 26133 |
rs574955043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015092 | GCAACCTCTACCTCC[C/T]GGGTTCAAGTGATTC | 26133 |
rs574988878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054545 | TCTTTATTCACCATT[C/T]TTCCTGGCTCAGTGG | 26133 |
rs575005374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003668 | GGGAGCCCCAGTGGC[C/T]CCTGGTGAACCTGGG | 26133 |
rs575047475 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038214 | TAAGACGGCTAATTT[C/T]ATGTTACGTGACTTC | 26133 |
rs575183227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005560 | ATTGCCCTGGAAGCC[A/G]CCACCTTGAGGCCGG | 26133 |
rs575217233 | in-del | -/GTG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014952 | TCTCTCAAGGGGACT[-/GTG]AGAGACACAAGCTAA | 26133 |
rs575232286 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077432 | AACTGCATTAGAGCT[A/G]GTGCTCTAAATTCAA | 26133 |
rs575237675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047299 | CATTAATTATTATTG[C/T]CTTGCCATTTAAAAA | 26133 |
rs575277209 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061164 | CACGATATGTGATCA[A/T]TATACATAAATCAAC | 26133 |
rs575288711 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091281 | AGGGTCTTAAGTCAG[A/G]TCTTAAGAACACAAG | 26133 |
rs575314113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061951 | AATTACAAGGAATTA[A/G]TATCCAGAAACTAAT | 26133 |
rs575331809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033218 | TTTAAGTAATATACT[A/G]TAGCAACTCTGGATA | 26133 |
rs575332724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018910 | AAGGCGATGGGGGAC[A/G]ATGGAGCTGTTGAAA | 26133 |
rs575371326 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023237 | GGGTGGTCTTCAGTA[A/T]ATCAGTGGACCTCTC | 26133 |
rs575374394 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065765 | TGTCCGAAGATGGGA[C/T]AGGCTCCTACTAGAG | 26133 |
rs575381431 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011015 | TCTGTAATCCCAGCA[C/G]TTTGGAAGGTCCAGG | 26133 |
rs575403019 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055199 | GTTTTCATAGTGCCC[A/T]TCAGAACCTACAAGC | 26133 |
rs575419671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011437 | TTGGTGATCGTGTAG[C/G]TGGTCACCATTTTTC | 26133 |
rs575468374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090038 | GGTGGGAGGATCACT[G/T]GAGCCCAGGAAGTTG | 26133 |
rs575479891 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063099 | CCCCCATGCTGTTCT[C/T]GTGATAACGAGGGAG | 26133 |
rs575490151 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049527 | CTGCATAGCATACAA[A/C/T]AGCACATACATGCTA | 26133 |
rs575548704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069051 | CTGAGGAGGGGACAC[G/T]GGGAAATTTAGAGAT | 26133 |
rs575577063 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015657 | TAGTGAGAGACGCAA[C/G]TGTCTCTCACACTAG | 26133 |
rs575592446 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069535 | AAGACAGTCCCCAAT[A/G]AACCACACTTCCTAG | 26133 |
rs575618926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016908 | CTTTATAAGACCGTG[C/T]TGGTGACTTGGGCAT | 26133 |
rs575689272 | in-del | -/AAAAAAAAAAA | 0.375598 | 0.21616 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056985 | GCGAGAGACTGTCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAATT | 26133 |
rs575699498 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009538 | GTAGTCCCAGCTACT[C/T]GGGCGGCTGAGGCAG | 26133 |
rs575735128 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012175 | CTATGGCTTTCAGCC[A/G]GAAAACCTCTCACAG | 26133 |
rs575763719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038195 | GCCGCTGAGTTGTTC[A/C]CTTTAAGACGGCTAA | 26133 |
rs575765465 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011797 | TTCACTACAAGCTGA[A/C]ACTTCAGGTCTTGGC | 26133 |
rs575780824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009412 | GTAATCCCTGGACTT[C/T]GGGAGGCTCACTTGA | 26133 |
rs575817504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003698 | GTAGCCATCAGGCAG[A/G]GAGGAGAGTGGCCCC | 26133 |
rs575817569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010022 | GCTCCAATGAGAAAA[C/T]GCAGGTGACATGAAT | 26133 |
rs575844727 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048288 | ATAATCTTGGCTCAC[A/T]GCAACCTCTGCCTCC | 26133 |
rs575848053 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089492 | CCATCTTGGTCTCCC[A/G]AAGTGCTGGGATTAC | 26133 |
rs575856024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038656 | GATTGGGCATGTATA[A/G]AATATTTTTCGAAGG | 26133 |
rs575857869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030833 | ATTTACACAATCTCT[C/T]ACAATTACAGAATTA | 26133 |
rs575879679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040477 | TGAGACTTGCACCAG[C/G]AGTTTCTGGGGTCCT | 26133 |
rs575888378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039709 | CAATTATCTAGCCTA[C/T]AGCTTCATTTACATC | 26133 |
rs575903522 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002613 | CTTGGATGAACACAG[C/T]GGCCAATGAGCAAAC | 26133 |
rs575904949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004287 | GAGCCCTCCTTCCTT[A/G]GGCCCTGTCTGTACA | 26133 |
rs575956361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045161 | TTCTCTCCCTGCAGA[C/T]GTAAACATTATTTTG | 26133 |
rs576018387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086646 | CCTTTGAAAAGCCAG[A/G]TAAGATTTGTTTGAC | 26133 |
rs576142129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087485 | CCCAGTCTGTCACCA[C/G]ATTGCCAAACTGAAG | 26133 |
rs576187596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074850 | CTGTCTCGTTGATCT[A/G]TCTAATGTTGACAGT | 26133 |
rs576214379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022896 | GGCATGGTGGCATGC[A/G]CCTGTAGTCCCAGCT | 26133 |
rs576227059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088081 | AGAAACTTAGGATCC[A/G]TCAGCGTATAGAGCA | 26133 |
rs576250304 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027735 | TTCCTGAGTTAGCTG[C/T]AATAGTTTGTGTCTT | 26133 |
rs576294825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088945 | GGGAGAAATGGGAAG[G/T]TGTTCAATGGTAGTT | 26133 |
rs576298471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014082 | ACTAACCCCACTGAC[C/G]TCAAGTGATCTGCCC | 26133 |
rs576302321 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075512 | TACTTCTCCTTCACT[A/T]ATGAAGCTTAGTTTG | 26133 |
rs576334118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082369 | TAGGCCATACTGCAA[A/G]TGTCAATACATTTAA | 26133 |
rs576335615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008126 | GACAGGGAGTTTGGA[C/T]AAGGCACTGAAGTGA | 26133 |
rs576362784 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060761 | GTCATCTCAACAGAT[A/G]CAGAAAAAGCGTTTG | 26133 |
rs576375790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078980 | CTGAGGCAGGAGAAC[C/T]GCTTGAACTCGGGAG | 26133 |
rs576388372 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079488 | TAGTAAACTACAGAA[A/T]GAGCAGTTTAAGCCT | 26133 |
rs576417131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029442 | GAATTGTTAAATCTA[C/T]TCACATTTAATGTTA | 26133 |
rs576424246 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022224 | GCAGTGGCATGACCT[C/T]GGCTCACTGCAACTT | 26133 |
rs576486198 | in-del | -/T | 0.484066 | 0.0878235 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032468 | TTTAGTTCTTTGATC[-/T]TTTTTTTTTTTTTTT | 26133 |
rs576551072 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050434 | TTAAAAGTCTTTGAG[A/G]CCAGGCGTGGTGGCT | 26133 |
rs576655796 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029981 | GCGCGGTGGCTCATA[A/C]CCGTAATCCCAGCAC | 26133 |
rs576691659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024254 | CATTACCACAATCAA[C/T]TTTAGAATATCTTCA | 26133 |
rs576751662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067332 | TCAGTACTTTTTTTT[C/T]AAATTTTAAAACACT | 26133 |
rs576755890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059579 | AGGAGGATTACTTGA[C/G]CCCAGAAGGTTGAGG | 26133 |
rs576782006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038262 | TACACAGAAATAGAT[C/T]TTTGTTTGAGACACC | 26133 |
rs576783529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080407 | TCGGGAGGCTGAGGT[A/G]GGAGAATGGCTTGAG | 26133 |
rs576788235 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059802 | AGAAGAAGGCGAAGA[C/T]GAAGACAAAGATGAA | 26133 |
rs576801336 | in-del | -/AC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068946 | TGGTGGGGAATATTT[-/AC]ACACACACACACACA | 26133 |
rs576826047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038794 | AACAAATCAGTAGGC[A/G]GGGCATGGTGGCCCA | 26133 |
rs576909153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074724 | ATAAGTGCGACGTGG[C/T]GCTGAGAAGAATGTA | 26133 |
rs576940636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032311 | ATTACAGGTGTGAGC[C/T]ACCACACCTGGCCTG | 26133 |
rs576955064 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066423 | TGAGTATAAATTGCA[C/T]ATGTAGTTTTACACA | 26133 |
rs577029598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015886 | ATTAGGGGACTATAA[A/G]ATATGATTTTAGTTT | 26133 |
rs577075191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083115 | TGTACAGTATACAAT[C/G]CAAAAGAACCTAAAT | 26133 |
rs577075212 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075571 | TCTTTTCTTTAAGAA[C/T]GTTGAATATTGGCCC | 26133 |
rs577118583 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092120 | CGAAACGAATTCGCG[C/G]CTGTGACAGAATAAC | 26133 |
rs577156952 | snp | A/C | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003191 | CATGTAGGGCTCCTC[A/C]ATGTAGCTAACGAGA | 26133 |
rs577157755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076086 | GCGTCACGTAGTTTT[C/T]GAGCCATGGTGTTCA | 26133 |
rs577180821 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085701 | CAGTCATCTTCCCAG[C/T]TGAATTACTGGCAGG | 26133 |
rs577212497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074291 | CTGCTCTGATCTTAG[C/T]TATTTCTCGCCTTCT | 26133 |
rs577223604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058491 | ATGAAATTAAAATCA[C/G]AACGAAATTTGGGAA | 26133 |
rs577252922 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087590 | TCCTTTCCTTCAACT[C/T]GTACTGATCATTTGG | 26133 |
rs577269043 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052990 | CATGGAATTCAGCCA[A/G]ATAGCACATAATTGA | 26133 |
rs577311877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059404 | GTTGTTCATGCCTGT[A/C]ATCCCAAGACTCTGG | 26133 |
rs577311958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051607 | CTTCAGTCGTAGCAC[G/T]GACACATTAAAAAAA | 26133 |
rs577315104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014180 | GTGGATGAAAATTAC[A/G]ATAGGATAAAACAGC | 26133 |
rs577339984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068341 | TTCTTAGGTAGGTAA[A/C]CTTCAGATTTATAAA | 26133 |
rs577348656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052227 | ACCTCAGCCTCCTGA[A/G]GAGCTGGGACTATGG | 26133 |
rs577353420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008256 | AAGGACCTCAGAGAA[C/G]GTCTCCCTGTATTCA | 26133 |
rs577354154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014837 | CGGGGGGCCAATAGG[A/G]GAAAGAGTATTATCC | 26133 |
rs577358357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054497 | AGGTCCTAACACTAA[A/G]TGCCATCCTCTTTTG | 26133 |
rs577376974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060349 | CCCAGCACTTTGAGA[C/T]GTCAAGGCAGGAGGA | 26133 |
rs577441562 | snp | C/T | 3.31669e-05 | 0.00407215 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008765 | GAAATAGAAGAGAGA[C/T]ATTGGTGACAGATCT | 26133 |
rs577447299 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086737 | AATGAAATTTTTTTT[A/T]AAAGTTAGTGAATCT | 26133 |
rs577462600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022668 | GTTATCAGATATATT[C/T]AGGTAAGGCTCATAC | 26133 |
rs577495520 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045781 | CTGACCTCAGATGAT[C/G]CATCCACCTTGGCCT | 26133 |
rs577540456 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079592 | AACAAAACCAAAAGT[G/T]AGTTCTTTAAAAAGA | 26133 |
rs577550228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012759 | TAGTAAGGGGCCAAC[A/G]ACTTCCATACTCAGT | 26133 |
rs577565127 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060453 | AAAATTAGCCAAGCA[C/T]GGTAGCATGCTCCTG | 26133 |
rs577604981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053968 | TATTTGTGTTGGCTG[C/T]TAAGAAGCTTGAAGC | 26133 |
rs577611789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006089 | CTTCAGCTAGCCTGA[A/G]CTGGGTTTCTGTCAC | 26133 |
rs577650146 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062782 | TGGTGACAGTGGTAT[A/G]TAACTCTGACTATAC | 26133 |
rs577691305 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079363 | AAAATATAACTTATC[-/A]AAAATTTGTGGGATG | 26133 |
rs577747526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034866 | TGGTTACTGGTTCTT[A/G]TTAGTCCCTGAGACA | 26133 |
rs577756714 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093810 | ATAATTACACCGGGA[C/T]GGTAGGCATAAAAGT | 26133 |
rs577778790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043929 | GACTTAGTAGATCAA[A/G]AAGTATATGCATTTG | 26133 |
rs577813436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037075 | AAGTTGGCCAGGCAC[A/G]GTGGCTCACGCCTGT | 26133 |
rs577822656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044863 | CAGCTCTGAAACTTT[A/G]GTTAAGTTACAAAAA | 26133 |
rs577826968 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002242 | GTTGCACATCTGGCT[C/G]AGGCCACCTGCCCCG | 26133 |
rs577838482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027900 | TTTCTTTTTTGGTCA[A/G]TGTGGCTAAAAGTTT | 26133 |
rs577893479 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087310 | CACCATTGCCCTCCA[A/G]CCTGGGCAACAGAGC | 26133 |
rs577901803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037589 | AGCCATATAAAGGAA[C/T]GAAGTACTGACATGC | 26133 |
rs577963537 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003948 | TGGGGCGGTTATCCC[A/G]CTTCAGAAGTGCCAT | 26133 |
rs577966857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050338 | AGAGTCAGACCTAAG[G/T]TCTAATTCCAGCTGT | 26133 |
rs577969308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091635 | AAGGTTCGGGGTGGG[A/G]GAGGGTGGAAGAAGT | 26133 |
rs577976622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041621 | CCCAGCTGACCAGAA[C/T]AGTTCATTCCTCAAG | 26133 |
rs577986966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092247 | CAATGATGACCCCCT[C/T]CCCCACGCCCAATAC | 26133 |
rs578009910 | in-del | -/T | 0.0162398 | 0.0886349 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025974 | GGCAGGGGATCTAAC[-/T]TCATTCTTTCGCATG | 26133 |
rs578028419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029699 | GGAGTGCAGTGGCGC[A/G]ATCTCGGTTCACTGC | 26133 |
rs578029511 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068037 | TTAATAAAGCTGATT[-/A]AAAAAAACTATGGAA | 26133 |
rs578172879 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006041 | TTTACGCTCAAGGGT[A/G]CTGGATTCCTTTAAT | 26133 |
rs578186761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085835 | GACATTTCTAGACAT[C/T]TACAGTTTCCACTGA | 26133 |
rs578236043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078798 | AGGCCAGGCACGGTG[A/G]CTCACACCTGTAATC | 26133 |
rs578255407 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037780 | TGTATTTTTACTATA[A/C]CTTTTTTCTATGTTT | 26133 |
rs578262561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020768 | TCAAGGCTCAGGGAA[A/C]CTTGCACATCTGGAG | 26133 |
rs745317531 | snp | C/T | 1.65828e-05 | 0.00287943 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055081 | TCAATGAAAAGATAG[C/T]ACAACAGTTACCACA | 26133 |
rs745328899 | snp | C/T | 1.74087e-05 | 0.00295026 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001907 | CCAGAATAAGCATCT[C/T]AGTCACCCAAGCGGA | 26133 |
rs745432706 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088247 | AGGTCCTATGATACT[A/T]ACTTTACAAATAAAT | 26133 |
rs745435194 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052787 | GATAGCCACCGTGCC[C/T]GGCCAACAGTACTTT | 26133 |
rs745438185 | snp | A/G | 1.65274e-05 | 0.00287462 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021225 | TCAGCAGCACGCAGA[A/G]GACATAGAGCACTTC | 26133 |
rs745472608 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070230 | GATTCTTGTTACTTC[C/T]GGCTGCTAGGTTTCG | 26133 |
rs745491691 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062650 | CTATAAAGACAGAAA[A/G]TAGATTAGTGGTTGC | 26133 |
rs745514987 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006510 | CAGCTCCCCCAGGAG[A/G]TCAAAGTAACTCTGG | 26133 |
rs745518337 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039622 | CATACTCCTGTAGTT[G/T]CCCCTCCTGCTTTCC | 26133 |
rs745524338 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058858 | CACTCCTGGCTACTT[G/T]GTGTATTTTTAGTAG | 26133 |
rs745530051 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025556 | TTATTTATATATCTT[A/C]TTTGGAGAAACATCT | 26133 |
rs745550690 | snp | A/G | 1.64846e-05 | 0.0028709 | stop-gained, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078060 | CCTTGAGGATGTTTT[A/G]ACACTCAACAAAGTC | 26133 |
rs745551469 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072117 | CATATCCTTCGCCCA[A/G]TTTTTGATGGGGCTG | 26133 |
rs745598631 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004130 | AGAGAAGGGAAGGCT[A/G]CATGACTATTCAGTG | 26133 |
rs745618404 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037956 | AAATCACCTCACTGC[A/G]TTTCTCAGAAGGATA | 26133 |
rs745636414 | in-del | -/TT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089397 | ACACCTGGTTAATGT[-/TT]TTTTTTTTTTTTTTT | 26133 |
rs745638986 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038290 | CCATTTTTTTTTTTA[-/A]ACATATCAGCTTGGC | 26133 |
rs745650554 | snp | C/T | 1.64876e-05 | 0.00287116 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078151 | GGATTGTTTGTCCCT[C/T]TCCGTCAAAAAAGTC | 26133 |
rs745674492 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005522 | TTCACCTTATTAAAG[G/T]GTTGAACAAGGCAGC | 26133 |
rs745692015 | snp | C/T | 4.94376e-05 | 0.00497156 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044658 | CGAGCTGCTGCTGAT[C/T]GAAATTGGATACTAA | 26133 |
rs745707897 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015387 | ATGCAGTGGGCAGCC[C/T]CTGCCTGGAGTGAAA | 26133 |
rs745714110 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027410 | GTCATGGTATACAAT[C/T]CTTGTATGTTGCTAT | 26133 |
rs745764861 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032638 | CCACCACGCCCAGCT[A/G]ATTTTTTGTATTTTT | 26133 |
rs745768612 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047929 | TGGGGCACAAGATAT[A/G]TGCCTGTTCAACTAC | 26133 |
rs745800265 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081860 | CATGGTGGCACAGGC[C/T]TGTAATCCCAGTTAC | 26133 |
rs745816538 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078428 | CATTGAGAGTGGACT[C/T]AGACTCGTCGTAAAT | 26133 |
rs745818738 | snp | C/T | 1.64953e-05 | 0.00287182 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010255 | GGCACTGAGTTCATT[C/T]AGCTCCTGGTTGTTG | 26133 |
rs745819828 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046518 | ATACTTTGATGAAGG[C/T]ATATATCCTACCCTT | 26133 |
rs745856559 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017242 | GATAATACTGGGAAA[A/G]CAAGTGTGCTCATGC | 26133 |
rs745881125 | snp | A/G | 1.74619e-05 | 0.00295477 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004496 | TGATGTTGATGAGGC[A/G]GAAGAGGAAGGACAT | 26133 |
rs745897264 | snp | A/G | 1.6516e-05 | 0.00287362 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013000 | TGCAGGGACACTCTT[A/G]TACTTACTCGTGGTG | 26133 |
rs745997705 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023913 | TGGTGCCTGGCTTGC[A/G]CAGGCCTGACAAGAC | 26133 |
rs746052375 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014717 | GAAGTCCCCAGAGTG[-/C]AGTGAAGAGAAGAGG | 26133 |
rs746053860 | snp | A/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093813 | ATTACACCGGGACGG[A/T]AGGCATAAAAGTGAC | 26133 |
rs746058512 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043620 | CTGAAATGGCAGATA[A/G]CACCAAACCCTATAT | 26133 |
rs746063052 | snp | C/T | 1.66785e-05 | 0.00288773 | downstream-variant-500B, synonymous-codon | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002082 | GGACGCCCTGGGCCC[C/T]AAGGTGAGGAGTGGC | 26133 |
rs746068657 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056416 | CACCAACAAATAATT[A/G]CAATATGCTACTTGC | 26133 |
rs746108278 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042876 | ATCAAACAATATATG[A/G]AAGTATACAGTAAGG | 26133 |
rs746247683 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004047 | GCTTCACCTCAGAAC[A/G]GAACCAAAGACCACC | 26133 |
rs746254860 | in-del | -/TC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045375 | CCCACAGTTTAATCA[-/TC]TCTCTCTTTTAAGAG | 26133 |
rs746293016 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078485 | CTAAAAGTATTTTTA[C/G]AAGAAGAATAATTGA | 26133 |
rs746300243 | snp | A/G | 1.64868e-05 | 0.00287109 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035210 | TGTACCACTCTTCCA[A/G]CTCCTGAAGGAAGCT | 26133 |
rs746300460 | snp | A/T | 1.64966e-05 | 0.00287194 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007652 | AAACCTGCGACCCAA[A/T]TACTGGCTCAGGTGG | 26133 |
rs746340348 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020362 | GGTCCCTGTGAGCCC[G/T]CAGCCCTCCTCTCCT | 26133 |
rs746362229 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019321 | TAGTGGTCCCTTCCC[A/T]AGGAACCAGCACTGT | 26133 |
rs746366696 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046682 | GCTGTGCAGGGGGCA[C/T]TGGGGAACAACTGCT | 26133 |
rs746368649 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074456 | ATGTGTCCCAGAGAT[C/T]CTGGTATGTCATGTC | 26133 |
rs746368950 | snp | C/T | 1.65192e-05 | 0.00287391 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003470 | CTGCCAGAAGCGCAG[C/T]AGGTTGTGGAAGTTG | 26133 |
rs746379953 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086467 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTATGTGT | 26133 |
rs746409722 | snp | A/G | 3.64637e-05 | 0.00426972 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092769 | ACCCAGCCGCTACCG[A/G]CGCCGCCGCCATGTC | 26133 |
rs746445620 | snp | C/T | 1.65696e-05 | 0.00287828 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049991 | GCTTTGTAACTCCCT[C/T]TGTCTGTCACAAGAA | 26133 |
rs746450013 | in-del | -/G | 1.64931e-05 | 0.00287163 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044493 | AAATTCTGAGAACTT[-/G]GGAGACTTTACCTTG | 26133 |
rs746458615 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050188 | AAAAAAGTCTCCTGA[C/T]GTGCAGGCTACACAA | 26133 |
rs746461281 | snp | A/G | 0.000109792 | 0.00740836 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092806 | TCGGACAAACAGGAA[A/G]CAAGCGGCCTCGGGG | 26133 |
rs746562922 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019206 | GAATCCAGATCCTCA[C/T]GGTGCCCGGCACACA | 26133 |
rs746564270 | snp | C/T | 3.29679e-05 | 0.00405991 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016030 | CAGTCACAGTTCTGG[C/T]TGTGACCATGGAGGA | 26133 |
rs746570729 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063704 | TATCTCTAACAAATA[G/T]TAAAAAATTAGCCAC | 26133 |
rs746596075 | snp | A/G | 1.65211e-05 | 0.00287407 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054935 | AACATTGCAGACCTG[A/G]TAGGGGAGATAAACA | 26133 |
rs746601250 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085534 | GGGAGGATTGCTTGA[A/G]CCCAGGAGGCGGAGG | 26133 |
rs746631214 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037853 | ATTTAGTACAGAAAC[A/C]TGCTGTACAGGTTTG | 26133 |
rs746633729 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087133 | AGGAGATCGAGACCA[C/T]CCTGGCTAACACGGT | 26133 |
rs746647485 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022445 | ACAGGCGTGAGCCAC[A/G]GTGCCCAGCGTAGAT | 26133 |
rs746684323 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036541 | CGTTTCTTAAAAGTC[A/G]TTATCATGTAGAAAC | 26133 |
rs746686158 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088167 | TGAGAAAGTATGTTT[A/C]AGTCACTATTTTAAG | 26133 |
rs746688000 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089551 | TTATATATTTGTTTA[-/C]TACAATGAAAAAATT | 26133 |
rs746746447 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031862 | GCTGAGTCTTTCTAG[C/T]GATTTTTTCATCTTG | 26133 |
rs746764064 | snp | A/C | 1.67683e-05 | 0.00289549 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006391 | ACTCCAGGTGAACTT[A/C]TGGACAACCCAGCAC | 26133 |
rs746785737 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028212 | TCTCAAAATATTTCC[-/T]TTTTTTTTTTTGATG | 26133 |
rs746787903 | in-del | -/CAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071899 | AGTTTACAGTCCCAC[-/CAA]CAGTTTAAAAGTGTT | 26133 |
rs746802244 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034354 | AGTGTAAAACCTCTG[-/T]ACATGAGCAAGCTAG | 26133 |
rs746817941 | snp | G/T | 1.64923e-05 | 0.00287156 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078047 | TCCTTAAGAGTTACC[G/T]TGAGGATGTTTTGAC | 26133 |
rs746862479 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024997 | TATATACCTGGGAGT[A/T]GGATTTCTAGGCCCT | 26133 |
rs746865334 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069986 | GCTCTTGCCATCCTG[A/G]AACCCAAACATCATG | 26133 |
rs746893422 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045363 | CCGCCGTTTTACCCC[A/C]CAGTTTAATCATCTC | 26133 |
rs746917113 | snp | C/T | | | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004388 | GGGGACAGAAACCTG[C/T]TGGGCACCAGGACAA | 26133 |
rs746918303 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058495 | AATTAAAATCAGAAC[A/G]AAATTTGGGAAATTC | 26133 |
rs746918571 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063964 | TTAGAAAGGAATACT[C/T]CCGAATCTTAACAGT | 26133 |
rs746921798 | snp | C/G | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003230 | TGACTGCCGGTCCGG[C/G]TTCAACAGGATGGAC | 26133 |
rs746953582 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026349 | CCTCTTGAGTAGCTG[A/G]GACTATAGGTGGGTG | 26133 |
rs746964373 | in-del | -/GCCGCCCCATCCGCCCCAA | 0.000131173 | 0.0080975 | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092692 | ACCAGGCCGCGGCCG[-/GCCGCCCCATCCGCCCCAA]GCCGCCACTGTGGCT | 26133 |
rs746965377 | snp | C/T | 1.64955e-05 | 0.00287184 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044492 | CAAAATTCTGAGAAC[C/T]TGGAGACTTTACCTT | 26133 |
rs746979416 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012573 | AATGAGCGCAGAATG[G/T]CTTTCAAGAAAAATG | 26133 |
rs746988790 | snp | C/T | 3.29647e-05 | 0.00405971 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078139 | TCCACTCCACTTGGA[C/T]TGTTTGTCCCTCTCC | 26133 |
rs747006416 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038645 | CCCCGTCCCATGATT[G/T]GGCATGTATAGAATA | 26133 |
rs747014645 | snp | C/T | 0.000100008 | 0.00707066 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010138 | TGAGCCCCCGGGGAA[C/T]GTGGGCAGCCGGGAT | 26133 |
rs747018659 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044642 | ATCCGGCAGAAATTA[C/G]CGAGCTGCTGCTGAT | 26133 |
rs747086805 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081540 | GAAAATAAAATAAAA[A/T]AAAAATAAAATAAAA | 26133 |
rs747133769 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082948 | GCAAAATGTTTAAGG[-/A]TTTTTTCCCTCTTAG | 26133 |
rs747139507 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010229 | TCAGGGATGTTGGCC[C/T]TGAGAGAGATGGCAC | 26133 |
rs747152262 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066197 | TAGCCTCAACCTCCC[A/G]GACTCAACCAATCCT | 26133 |
rs747163543 | snp | A/G/T | 3.53727e-05 | 0.00420539 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004486 | TGCACGTGGATGATG[A/G/T]TGATGAGGCGGAAGA | 26133 |
rs747202266 | in-del | -/AAG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059714 | AGAAGAAGAAATAAG[-/AAG]AAGAAGAAGAGGAAG | 26133 |
rs747203412 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011416 | ACAGAGTACTGGTTG[C/T]CTACCTTGGTGATCG | 26133 |
rs747205192 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054256 | TCGTCTCATTCTGCC[A/G]TGTATTATGATTCAC | 26133 |
rs747212080 | in-del | -/ACACACA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068963 | CACACACACACACAC[-/ACACACA]CACACACACAAAAAA | 26133 |
rs747282746 | in-del | -/G | 1.65636e-05 | 0.00287776 | frameshift-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003511 | GCCGGGGTACTTCTT[-/G]GCTGTGCTCCATCCG | 26133 |
rs747300156 | snp | C/T | 1.65908e-05 | 0.00288012 | downstream-variant-500B, synonymous-codon | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002007 | GCACGAGCTGGATGA[C/T]GCGGAGGAGCGGGCA | 26133 |
rs747313466 | snp | C/T | 1.64879e-05 | 0.00287118 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057531 | TTCAGTTTCTGTCCC[C/T]GGATAGAGATCGTAG | 26133 |
rs747346702 | snp | C/T | 1.7708e-05 | 0.00297552 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004546 | ATGTAGGCGAGCAGG[C/T]GGCATTCAGACAGTA | 26133 |
rs747350203 | in-del | -/TATTTGTTTAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089540 | CTGGCCTATATTATA[-/TATTTGTTTAC]TATTTGTTTACTACA | 26133 |
rs747364720 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35002969 | CTCTCCATGACCTAG[C/G]GCCCTCAGACCCAGG | 26133 |
rs747418223 | snp | C/T | 6.661e-05 | 0.00577067 | downstream-variant-500B, synonymous-codon | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002070 | GGCACGGACCCGGGA[C/T]GCCCTGGGCCCCAAG | 26133 |
rs747433812 | snp | A/C | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093648 | ACACACACTTTTTCC[A/C]TTCCTAGCAGGGGGC | 26133 |
rs747451445 | snp | A/C | 1.711e-05 | 0.00292484 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035077 | GAATGGTCCCAGGCG[A/C]CCAAGGAAAAGCTCC | 26133 |
rs747468978 | snp | A/G | 1.65277e-05 | 0.00287464 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021342 | AAGCCCCTGGAGGAG[A/G]GAACACAATGGAGGC | 26133 |
rs747480268 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028813 | TGCTCTCTTCCAATC[C/T]GTTAGTTTTTGCTTC | 26133 |
rs747484762 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077583 | CAGTTTGAGAACAAT[C/T]ATCCTAGCATAATGT | 26133 |
rs747563063 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043538 | AGGCGTTAAGCCACC[A/G]TGCCTGGCCTCAGTG | 26133 |
rs747566213 | snp | A/G | 3.29674e-05 | 0.00405988 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007627 | AACTCTCCACAGCCC[A/G]AGCTTGCCAAAACCT | 26133 |
rs747569273 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062663 | AAGTAGATTAGTGGT[G/T]GCCTAAGGATGTGGG | 26133 |
rs747594404 | snp | C/G | 0.000184145 | 0.00959368 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092656 | GGTCAGCTGGCCCTG[C/G]CGCAGCTGCAGCAGA | 26133 |
rs747619622 | snp | A/C/T | 6.79019e-05 | 0.00582642 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003372 | GAGGCCCTGGGTCCG[A/C/T]GGCCCACCCATCACC | 26133 |
rs747649570 | snp | A/G | 5.06077e-05 | 0.00503004 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049842 | CACCCTTCCCCATCT[A/G]GTCAGCTAGAGGACA | 26133 |
rs747706444 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006984 | GACACATTTTGACCC[C/T]ATGGTTTGTCTTTGT | 26133 |
rs747712880 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028668 | GGGTGGAGGGTTCTA[A/C]AGTTCTCTGTTAGTC | 26133 |
rs747722275 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061470 | GCTTCTTTGCAGAAA[C/T]TGGCAAGCTGATCCT | 26133 |
rs747738013 | snp | A/G | 4.69274e-05 | 0.00484371 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092747 | CGTCTCCCTCGGCCG[A/G]CTCCAGACCCAGCCG | 26133 |
rs747744111 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017111 | CAACACTACTCACTA[C/T]AGCATTATTTGTAAT | 26133 |
rs747759541 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018062 | TCCAAAGGGCCCTAA[A/G]CCAGGCCCAGGTCAC | 26133 |
rs747769527 | snp | C/T | 1.69075e-05 | 0.00290748 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049833 | GGTCTGAGACACCCT[C/T]CCCCATCTGGTCAGC | 26133 |
rs747773461 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062480 | GGTCTATCCATACAG[G/T]GGAATATTTCTTGAC | 26133 |
rs747822581 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048680 | GTGGAACACCTCGCC[A/G]TTTTGGGGTACACAA | 26133 |
rs747869737 | snp | C/T | 3.29908e-05 | 0.00406132 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016008 | GGGTCTCCTGCTTAC[C/T]GGGCTACAGTCACAG | 26133 |
rs747873634 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022075 | CTGCTCTGCAGCAGA[C/T]AGCTAGGGTTACTGT | 26133 |
rs747907552 | in-del | -/A | 1.66856e-05 | 0.00288834 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069423 | TTTCCTAGTTTTTTT[-/A]AAAAAAAAGTACATA | 26133 |
rs747912797 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016177 | AGTATTAAGACAAAT[-/G]TGCTTGAAAAATCTA | 26133 |
rs747990600 | snp | C/T | 1.64955e-05 | 0.00287184 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016172 | GAAAAAGTATTAAGA[C/T]AAATGTGCTTGAAAA | 26133 |
rs748011866 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085287 | CTTTACTATTTATAC[A/G]TTGTCTTACAAGGCA | 26133 |
rs748015446 | snp | G/T | 7.30794e-05 | 0.00604436 | downstream-variant-500B, stop-lost | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002187 | CTCAGCACAAGGAGT[G/T]ACGGCCTGACCCCCT | 26133 |
rs748037263 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036134 | TGGAAATTCTGATCG[G/T]CATATTAGAACATCA | 26133 |
rs748042319 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037529 | CAAATGTCCATTAAC[C/T]GAAGGGATAAACAAA | 26133 |
rs748043710 | snp | C/T | 1.65466e-05 | 0.00287628 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005831 | CAAGCTCACAGCAGG[C/T]AGTGGGCTGCTGGCC | 26133 |
rs748056647 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056722 | GCGGTGGCTCATGCC[C/T]GTAATCCCAGCACTT | 26133 |
rs748067251 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069177 | GCCGCTAAGCTTCTA[A/C]AAGTTAAAATCTGAA | 26133 |
rs748132480 | snp | A/G | 1.66913e-05 | 0.00288883 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069432 | TTTTTTTAAAAAAAA[A/G]TACATACATTGTTTT | 26133 |
rs748142880 | in-del | -/AA | 0.000117468 | 0.00766292 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021401 | TCACAGCTTGTGAGG[-/AA]ACACGTTTCTGCCCC | 26133 |
rs748157479 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006585 | GATGTGCTGGGTGAG[A/G]AGGGACAGGGTGAAG | 26133 |
rs748177511 | snp | C/G | 3.3083e-05 | 0.00406699 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078026 | CCTGAATACGCCCCT[C/G]CAAGGTCCTTAAGAG | 26133 |
rs748180926 | in-del | -/T | 1.65934e-05 | 0.00288035 | downstream-variant-500B, frameshift-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002027 | AGGAGCGGGCAGACA[-/T]GGCGGAAACCCAGGC | 26133 |
rs748206967 | snp | C/T | 4.95765e-05 | 0.00497853 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003135 | GCAGCCTCCCGAGGC[C/T]TGGCCCAAGGTCACT | 26133 |
rs748280846 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079652 | TTATCAAGAAAAAAA[C/G]ACAGAAACACAAATT | 26133 |
rs748295543 | snp | A/G | 1.66701e-05 | 0.002887 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008792 | ATCTGAGAGGCTGAC[A/G]GGGGCCCTGGGGATG | 26133 |
rs748320318 | snp | C/T | 8.18833e-05 | 0.00639804 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092815 | CAGGAAGCAAGCGGC[C/T]TCGGGGCCGCGGAGA | 26133 |
rs748322210 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053105 | TTCAGGGAGCATATA[A/C]TTTAATACATTCGTA | 26133 |
rs748327816 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021552 | ACTCGGAAAAATGGA[C/T]TCTGCAATAGTTGTG | 26133 |
rs748329195 | snp | C/G | 1.66244e-05 | 0.00288304 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008659 | GTACTTTTCCCCAGA[C/G]TCACCTGAAAGACGA | 26133 |
rs748336467 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066140 | GATGGGGTCTTGCTC[C/T]GTCACCCAGGCTGCA | 26133 |
rs748338031 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081551 | AAAATAAAAATAAAA[A/T]AAAATAAAATAAAAA | 26133 |
rs748363017 | in-del | -/ACGAAGACA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059768 | AAGACGAAGAAGACG[-/ACGAAGACA]AAGAAGATGAAGAAG | 26133 |
rs748386755 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050616 | TACTCAGGAGGCTGA[C/G]GTAAAAGGATCATTT | 26133 |
rs748420522 | snp | C/T | 2.8437e-05 | 0.00377063 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003658 | AGGGGCTGGTGGGAG[C/T]CCCAGTGGCCCCTGG | 26133 |
rs748492743 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055259 | AGCAGCTGTTTTCTT[-/A]TTATGCTCCACAGTC | 26133 |
rs748505013 | snp | A/C | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010199 | CACCTGTCGGTGTTG[A/C]GGACAGCTTCCACCT | 26133 |
rs748517907 | snp | A/G | 0.000103684 | 0.0071994 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001920 | CTCAGTCACCCAAGC[A/G]GAACCAAGGCCCTGT | 26133 |
rs748530840 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054131 | TAGATTTTGCATACA[A/C]CCACAAGATGTCAGA | 26133 |
rs748558244 | snp | C/T | 1.8183e-05 | 0.00301515 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004475 | GGGTCAGCGTCTGCA[C/T]GTGGATGATGTTGAT | 26133 |
rs748590907 | snp | A/G | 4.98343e-05 | 0.00499146 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057465 | CTGGGAACTGCCACC[A/G]TATCGGCAGGTTGGA | 26133 |
rs748599481 | snp | C/T | | | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001915 | AGCATCTCAGTCACC[C/T]AAGCGGAACCAAGGC | 26133 |
rs748629391 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042646 | TCCAGCCTGTTAACA[C/T]TGAAAAACTAGCTTT | 26133 |
rs748642733 | snp | A/G | 8.30296e-05 | 0.00644266 | downstream-variant-500B, synonymous-codon | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001986 | GGCCAAGTATCGCAA[A/G]GCCCAGCACGAGCTG | 26133 |
rs748644216 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091738 | CATATGTTGGGCACC[C/T]GTTATAAGTCAGATG | 26133 |
rs748667007 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067255 | TTTGGGAGGCCAAGG[C/T]TGGGGGACTGTTTGA | 26133 |
rs748680548 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041291 | TTTCCTCATCCACTC[A/G]TGATTTAATTATGTC | 26133 |
rs748701664 | in-del | -/TT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074395 | CTTTCCGGCTTTCTC[-/TT]GTGTGCATTTAGTGC | 26133 |
rs748741981 | snp | A/G | 1.64982e-05 | 0.00287208 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006549 | CCTTGACTTACACTC[A/G]CTGTCCACAATGCAG | 26133 |
rs748790693 | in-del | -/AA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068978 | CACACACACACACAC[-/AA]AAAAAAAACAAAACA | 26133 |
rs748807313 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051616 | TAGCACTGACACATT[-/A]AAAAAAAAAAAAAAA | 26133 |
rs748861960 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060103 | AGACATTTAAAGAAT[G/T]ATCAATTCTTCACAA | 26133 |
rs748866280 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041240 | ATTCACTACTGGAGC[A/G]CAATTCAAGAATGAT | 26133 |
rs748889641 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026597 | TCCATTTGTGCAAAG[C/T]AGTCAGCTGAGAGTT | 26133 |
rs748938753 | snp | A/G | 0.000116763 | 0.00763989 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003367 | TCTGAGAGGCCCTGG[A/G]TCCGCGGCCCACCCA | 26133 |
rs748971706 | snp | C/G | 1.6486e-05 | 0.00287102 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044680 | GGATACTAAGGAACT[C/G]AGATTGGGGACTTCA | 26133 |
rs748973779 | snp | A/G | 0.00103595 | 0.0227354 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092625 | GTACCTGCACCGCCC[A/G]GACCAGGCCCCGGCC | 26133 |
rs748986534 | in-del | -/GACAGTACCTCG | 5.39321e-05 | 0.0051926 | cds-indel, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004555 | AGCAGGCGGCATTCA[-/GACAGTACCTCG]GCAACTGTGGAGGGA | 26133 |
rs749041992 | snp | A/G | 6.5999e-05 | 0.00574414 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003434 | GCAGGTGCTGTCCTT[A/G]TCCTTGTGCAGGTAG | 26133 |
rs749105969 | snp | C/T | 1.65113e-05 | 0.00287322 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35013011 | TCTTGTACTTACTCG[C/T]GGTGGTCACTGAAGC | 26133 |
rs749111270 | in-del | -/G | 0.000148661 | 0.00862023 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015991 | GCCCCATCTGTCCCC[-/G]GGGGTCTCCTGCTTA | 26133 |
rs749140862 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035958 | CTAAGCAGGAGAGAA[C/T]ACAAACAATTCTCTT | 26133 |
rs749150684 | snp | C/T | 1.64925e-05 | 0.00287158 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049957 | AGGAAGATCACAAAG[C/T]CATTCTTTTCTGCCA | 26133 |
rs749156381 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082279 | AATGGACACACCTCG[A/G]GCAGTATATCTAGTA | 26133 |
rs749161205 | snp | A/G | 2.13081e-05 | 0.00326399 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004597 | GGCAGGGGTGCAGCA[A/G]GTCAGGCTTAGGCCC | 26133 |
rs749197029 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067730 | TCTAGAAATCATTAC[A/G]CTAAGTGAAAAGAAG | 26133 |
rs749199324 | in-del | -/TTCTTATAAAGAAACTACTAC | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055843 | CTGATCTATTACTAA[-/TTCTTATAAAGAAACTACTAC]TTCCCTGTGAGCAGG | 26133 |
rs749229112 | snp | C/T | 1.6525e-05 | 0.00287441 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015977 | TCCAAGCCAGTGAGG[C/T]CCCATCTGTCCCCGG | 26133 |
rs749263834 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034601 | CTGAGAATTCCTGGG[G/T]TTGTATATTCTGAAC | 26133 |
rs749321257 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058225 | ATAAAAGTTGGACAC[A/G]TTAATAACTCTGCTT | 26133 |
rs749348823 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005714 | CATATCCACCTGGTT[C/T]TCAAATCGGTCCAGG | 26133 |
rs749421174 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013869 | CACCAGCCCAGGGAG[C/G]CTGGCTCTGCCATGG | 26133 |
rs749476913 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031328 | CCTGGGTTGAGGTGA[C/T]TGTCCCATCTCAGTC | 26133 |
rs749484121 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079607 | TAGTTCTTTAAAAAG[A/T]TCAATACGATTGATA | 26133 |
rs749487928 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078508 | ATAATTGATATGCTA[A/G]GAGATGAAAAATAAT | 26133 |
rs749498462 | snp | A/T | 1.64912e-05 | 0.00287147 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035229 | CTGAAGGAAGCTGGC[A/T]GTGCCCGTTGACTCT | 26133 |
rs749517265 | snp | C/T | 6.61737e-05 | 0.00575174 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003129 | GGCCCAGCAGCCTCC[C/T]GAGGCCTGGCCCAAG | 26133 |
rs749541441 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014294 | TTACAAGGGGAAGTG[A/G]CTAGAGGGCCTCAGG | 26133 |
rs749564748 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057436 | AGTTAGGAAGGGAAG[A/G]AAGAAGGCAGCTGCT | 26133 |
rs749587567 | snp | C/T | 1.66463e-05 | 0.00288494 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008655 | GCAGGTACTTTTCCC[C/T]AGACTCACCTGAAAG | 26133 |
rs749612745 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009194 | CTATGAAGCAAAGGC[A/C]GGAGATGAGGAAATG | 26133 |
rs749648915 | snp | A/G | 3.37427e-05 | 0.00410734 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021407 | CTTGTGAGGAAACAC[A/G]TTTCTGCCCCTCGAA | 26133 |
rs749682320 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065076 | TTCATCCAAGTAAGA[C/T]GTAAGATGCTCAAGT | 26133 |
rs749702114 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020463 | CTGCCCCCTCCCACC[A/T]GGTACACTCTTTCAT | 26133 |
rs749712118 | snp | C/T | 3.34739e-05 | 0.00409095 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003537 | ATCCGCTGCAGCAGC[C/T]GCAGGTACAGGGGCA | 26133 |
rs749712182 | snp | C/T | 1.66012e-05 | 0.00288103 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008771 | GAAGAGAGATATTGG[C/T]GACAGATCTGAGAGG | 26133 |
rs749746428 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010095 | ATGTGAGAGAGGACA[C/T]GCGTGCATACCTGGA | 26133 |
rs749750938 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088519 | CTTCAGGAAGCCCAG[C/T]CTAATTAACTACTAG | 26133 |
rs749784062 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039806 | ACAGAAGAACAACTG[A/G]TAGTTCTGAGAATCT | 26133 |
rs749803499 | snp | C/T | 0.000198406 | 0.0099581 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007689 | CTGCCCTCTTCCGGC[C/T]CATGTTCAGTTCTCC | 26133 |
rs749821435 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092218 | TGAAATGCTCGGGAA[C/T]CATTTGGGGGCTGCA | 26133 |
rs749835513 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052906 | AATTCCAAACATTTC[C/G]TGTTTTCTGCCTGAT | 26133 |
rs749843640 | snp | A/G | 3.30267e-05 | 0.00406353 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054942 | CAGACCTGGTAGGGG[A/G]GATAAACAGAGCCCC | 26133 |
rs749885297 | snp | A/C | 1.80909e-05 | 0.00300751 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010315 | TGGGTTGGAGGAGGT[A/C]AAGGACAGGAACTGG | 26133 |
rs749886584 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065628 | ACTGAAGGTCAGTGA[A/G]GTGCATAATTACTTA | 26133 |
rs749887412 | snp | C/G | 3.85825e-05 | 0.00439201 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004464 | GCCTCTCACCTGGGT[C/G]AGCGTCTGCACGTGG | 26133 |
rs749890041 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009913 | GTGGGGCAGTGCGGA[A/G]CACACATGACTTCTG | 26133 |
rs749906798 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080157 | ATGTACTGATACTAC[A/T]ACAAGGATAAATCTT | 26133 |
rs749933201 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005159 | AAAAAGGAAGCAAAC[A/G]GCTAAATTACCAACA | 26133 |
rs749935219 | in-del | -/ACACACA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068957 | TATTTACACACACAC[-/ACACACA]CACACACACACACAC | 26133 |
rs749940472 | snp | A/G | 1.73303e-05 | 0.00294361 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004528 | TGCGTGGGCACCTGG[A/G]ATATGTAGGCGAGCA | 26133 |
rs749945307 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021173 | CCCGTGTCCTGAGAC[A/G]CTGGAGAGGGGCCCA | 26133 |
rs750023489 | snp | A/G | 8.25035e-05 | 0.00642222 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057506 | CAGTAGCTAATAGGT[A/G]TACTTACTTTTCAGT | 26133 |
rs750082527 | snp | C/T | 1.83549e-05 | 0.00302937 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057619 | TAATTCAAAGTATAA[C/T]TTATAAAATGATTTT | 26133 |
rs750084852 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066879 | GAAAAAGGACAAATA[A/C]TCAAATCGAAAAAGG | 26133 |
rs750092541 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091422 | ATTTTATTCTATCCT[C/T]TTCGTCATTTGAGGA | 26133 |
rs750103662 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053772 | GAATGACAATATTCT[C/T]GATACACTGTGTTAA | 26133 |
rs750149205 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066351 | AACTCATGCAATCCG[C/T]CTGCTTCGGCCTCCT | 26133 |
rs750164370 | in-del | -/C | 3.67451e-05 | 0.00428616 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002197 | GGAGTGACGGCCTGA[-/C]CCCCTGGGCTCTAAA | 26133 |
rs750211451 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002486 | AACACAAGGAAGGGC[C/G]CCATGTCCAGGCTCA | 26133 |
rs750248599 | snp | A/C | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007565 | CTCCAAGAGGCCTCG[A/C]TTCAGCAGGAACATC | 26133 |
rs750259959 | snp | C/T | 5.37533e-05 | 0.00518399 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092581 | CTCCCGCCTGGTCCG[C/T]CCCGCCCCGCCCCTC | 26133 |
rs750281845 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050045 | TACAAAATAAATTAT[-/G]AAAGTACAAGGCATC | 26133 |
rs750304980 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017647 | CAACGGCACCTAACT[C/G]AGGTGTTCAGATCTT | 26133 |
rs750308390 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061152 | TCAGCAAGATTTCAC[A/G]ATATGTGATCAATAT | 26133 |
rs750318035 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029097 | TACTAAAAACACACA[C/T]AAAAATGAGCTGGGC | 26133 |
rs750322557 | snp | C/G | 6.76247e-05 | 0.00581444 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008612 | TAACCTCCTGAGAAA[C/G]ACCTGGCTCTGCAGC | 26133 |
rs750371131 | snp | C/T | 1.65004e-05 | 0.00287227 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003416 | GGCACTCACGTTCTC[C/T]AGGCAGGTGCTGTCC | 26133 |
rs750376073 | snp | C/T | 1.65359e-05 | 0.00287536 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003491 | GTGGAAGTTGTTGAG[C/T]AGGAAGCCGGGGTAC | 26133 |
rs750384665 | snp | C/T | 0.000259909 | 0.0113968 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092728 | CGCCACTGTGGCTGC[C/T]GACCGTCTCCCTCGG | 26133 |
rs750396266 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071240 | CATTCAGTTTCATTA[C/T]GTTCAATATAACTTA | 26133 |
rs750404526 | snp | C/T | 1.64876e-05 | 0.00287116 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049916 | CTGTTTGTAAGAATG[C/T]CTTCTTACTTGTCAT | 26133 |
rs750433159 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089257 | TTTGAGGCAGGGTCT[C/T]ATTCTGTTGCCCAGG | 26133 |
rs750469308 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038530 | GTAATTTTTGGCAAG[A/G]TAAGTTTAATAAAAA | 26133 |
rs750530404 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024636 | TGAGACCAGCTTGGG[A/C]AACACAGCAAGATCC | 26133 |
rs750576804 | snp | A/G | 1.67891e-05 | 0.00289729 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050022 | GAAAAGGCAGAATAG[A/G]TTGTAAGTACAAAAT | 26133 |
rs750618312 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013722 | GTGGGCAGTGTGGAG[A/C]GGTGGAGACAAGACC | 26133 |
rs750631732 | snp | A/C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016114 | AGTCCAGGGATCAGC[A/C/T]TGAACTCTGCAATCA | 26133 |
rs750644600 | snp | A/C | 1.65048e-05 | 0.00287265 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005683 | TGCCTTGACAGCCTG[A/C]CTTTCATGTACCTTT | 26133 |
rs750668578 | in-del | -/T | 1.66266e-05 | 0.00288323 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069416 | GGAGAAATTTCCTAG[-/T]TTTTTTTAAAAAAAA | 26133 |
rs750728808 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038162 | TGGTAGCTGCACAAC[A/G]CTGTAAATGTACTAA | 26133 |
rs750739945 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059252 | TTACCACCAACCTTA[C/T]GGCAACAAAAGTGAT | 26133 |
rs750743623 | snp | C/G | 3.31005e-05 | 0.00406807 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069403 | CCATGGAGAGAAGAG[C/G]AGAAATTTCCTAGTT | 26133 |
rs750755121 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083962 | TCAAATGATTTCTTT[-/A]AAAAAAAAAAAAAAG | 26133 |
rs750795942 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016367 | CCTACAAGGCATAAT[G/T]TCCGGTAGTTCCTAT | 26133 |
rs750810594 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013942 | ACCCTGGGCTCATAC[G/T]ACTGGGGCAGTAGGG | 26133 |
rs750821907 | snp | C/T | 1.65974e-05 | 0.0028807 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077999 | AGCAGACATCTTGTG[C/T]CACCTAGAGGCCCTG | 26133 |
rs750845633 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045027 | AAAAGGAAATGCCTA[C/T]CACTCAAGTTTTGGA | 26133 |
rs750907096 | snp | C/T | 5.27347e-05 | 0.00513465 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035337 | AACAAGCGAGGAAAT[C/T]TTCAAAATAGAGACC | 26133 |
rs750915910 | in-del | -/TATGTG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084724 | ATGTTTATATGCATA[-/TATGTG]TATGTGTATATGTAT | 26133 |
rs750930762 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079393 | GCAGCGAAAGCAGTA[A/C]TAAGCCAGAAGTGTA | 26133 |
rs750957719 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005833 | AGCTCACAGCAGGCA[C/G]TGGGCTGCTGGCCAG | 26133 |
rs750971244 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077372 | TAGACTGGAGCTGTT[A/C]CTATTTGGCCATCCT | 26133 |
rs750989340 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064682 | GCAACAATGAAAACT[A/G]CCCTGAACATATGCC | 26133 |
rs750991282 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080753 | AATTGATCGTGATGA[C/T]AGATGCATAACTTTG | 26133 |
rs751034061 | snp | A/G | 1.65608e-05 | 0.00287752 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008755 | CCAAACTCCTGAAAT[A/G]GAAGAGAGATATTGG | 26133 |
rs751078115 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031161 | GCAGTCAGCCACTAA[C/T]CTTATTGGAATATCC | 26133 |
rs751083158 | snp | A/G | 1.65745e-05 | 0.00287871 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010163 | CGGGATGGGCTGAGG[A/G]AAAAGCTGCACCCCT | 26133 |
rs751107315 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020225 | AGGGCCCCTAATGGT[C/T]GCCCTATTCCCTTCC | 26133 |
rs751128696 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045693 | ACAGGCGCCCGCCAC[A/C]ACGCCTGGCTAATTT | 26133 |
rs751190114 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052666 | CTGGCTAATTTTTGT[C/G]TTTTTAGTACAGACG | 26133 |
rs751209114 | snp | G/T | 1.66718e-05 | 0.00288715 | downstream-variant-500B, synonymous-codon | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001971 | GGCCAACACCAACCT[G/T]GCCAAGTATCGCAAG | 26133 |
rs751239648 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051466 | GCGTGCACCACCGCA[A/C]CTGGCAAATTTAATT | 26133 |
rs751247859 | snp | A/C | 3.30852e-05 | 0.00406712 | synonymous-codon, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021214 | CTGACGCCCCATCAG[A/C]AGCACGCAGAGGACA | 26133 |
rs751280840 | snp | A/G | 8.26945e-05 | 0.00642965 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055069 | TGGTTATTTTTCTCA[A/G]TGAAAAGATAGTACA | 26133 |
rs751333900 | snp | C/G | 8.25607e-05 | 0.00642445 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057496 | AAACAAGGACCAGTA[C/G]CTAATAGGTATACTT | 26133 |
rs751381145 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010825 | GGTGCCAAAAGTGAT[C/T]TTCAGAATCAGGACT | 26133 |
rs751392240 | snp | C/T | 3.31994e-05 | 0.00407414 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002036 | CAGACATGGCGGAAA[C/T]CCAGGCCAACAAGCT | 26133 |
rs751421513 | snp | G/T | 1.67242e-05 | 0.00289168 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021395 | ATTGAGTCACAGCTT[G/T]TGAGGAAACACGTTT | 26133 |
rs751423655 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071346 | TGCAGGTTTGTTACA[C/T]ATGTATACATGTGCC | 26133 |
rs751429283 | snp | A/C | 3.29935e-05 | 0.00406149 | synonymous-codon, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021283 | CTTCATTGACTGGGG[A/C]AGCTGGGTTCTGGCT | 26133 |
rs751445133 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027308 | CTATGGAAACGATCA[C/T]GTGGTTTTTGTCCTT | 26133 |
rs751488175 | snp | C/G | 1.69677e-05 | 0.00291266 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006626 | GGCTGCCCCCACCAG[C/G]GCCTGGCATGGAGCT | 26133 |
rs751490571 | snp | G/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094797 | GGGGGCCTGGAGGAG[G/T]ACACGACCATAAGTC | 26133 |
rs751525958 | snp | A/T | 1.6817e-05 | 0.0028997 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078211 | AACATATTATTGTAT[A/T]ATTGATGATAATAGC | 26133 |
rs751536885 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005536 | GTGTTGAACAAGGCA[A/G]CAAAGCCAATTGCCC | 26133 |
rs751541371 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073026 | TTGGATTCCTAAGTA[C/T]TTTAGTCTCTTTGTA | 26133 |
rs751548252 | snp | C/G | 0.00454129 | 0.0474344 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007537 | CCAAGACACTGGCTG[C/G]TCCAGATCATACCTC | 26133 |
rs751554240 | in-del | -/C | 1.65124e-05 | 0.00287331 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013083 | GAAACACATGCACAG[-/C]CCTCAATGTTAGGAC | 26133 |
rs751592821 | snp | A/C | 1.65795e-05 | 0.00287914 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003322 | GGGGCGCCTGGAGGA[A/C]CCAGGTCAAGCCCAG | 26133 |
rs751681455 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023609 | GTTACTCAATTTCCA[C/T]GTTAGCACTCCTTGG | 26133 |
rs751728259 | snp | C/T | 7.43246e-05 | 0.00609563 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092715 | ATCCGCCCCAAGCCG[C/T]CACTGTGGCTGCCGA | 26133 |
rs751745502 | snp | C/T | 3.33233e-05 | 0.00408173 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044750 | AATCCCCATGCTCAA[C/T]TCACTCAAGAGATTG | 26133 |
rs751745628 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049401 | ATGAGAAAAAATAGA[C/G]GCGGACTTCATAAGT | 26133 |
rs751784202 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036869 | GAGAATTGCTTGAAC[C/T]TGGGATGCAGAGGTT | 26133 |
rs751811785 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088812 | TCCTTGAGGACATTA[C/T]GTTAAGTAAAATAAG | 26133 |
rs751833416 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035647 | CACGAGAATATCTGT[A/G]TAAGGAGGTTCACTG | 26133 |
rs751854462 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069645 | AGTGACACTAGGCCA[C/T]TTCCAGCACAAGCCT | 26133 |
rs751856469 | snp | A/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056343 | TGGTGAGGGAAAAAA[A/T]GTCTCAGCCTTCATG | 26133 |
rs751897040 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015783 | CCTGAGTCACTGTGC[C/T]CAGCCTAGGAAGATC | 26133 |
rs751935186 | snp | A/C | 1.65288e-05 | 0.00287474 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013097 | AGCCTCAATGTTAGG[A/C]CCACAGCCACAAGGT | 26133 |
rs751942827 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013625 | CGTGTGGGGAGGAGC[A/G]GGGGAAGTCCATAGG | 26133 |
rs751986958 | snp | A/T | 1.6571e-05 | 0.0028784 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069281 | CAGCAGTAGTAATAA[A/T]AAATAGCTACTTACA | 26133 |
rs751992865 | snp | A/G | 1.72335e-05 | 0.00293538 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002131 | GCAGGGGGACTGTGG[A/G]GGCTGACAGGTAGTA | 26133 |
rs751997776 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024574 | CAGGCCTGTAATTCC[A/G]GCACTTTGGAAGACC | 26133 |
rs752032750 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035846 | GTAAATTATTAAACA[A/C]TATGAATTTAATTTT | 26133 |
rs752074177 | snp | C/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094365 | ATCATGAGGTCAGGA[C/G]TTCGAGACCAGCCTG | 26133 |
rs752112632 | snp | C/T | 1.64814e-05 | 0.00287061 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005783 | CAGGGAGCTGTTGAT[C/T]TGCTTCAGGAATACC | 26133 |
rs752120337 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037777 | TACTGTATTTTTACT[A/C]TACCTTTTTTCTATG | 26133 |
rs752144729 | snp | C/T | 1.85101e-05 | 0.00304216 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002236 | TCTGCTGTTGCACAT[C/T]TGGCTGAGGCCACCT | 26133 |
rs752183923 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003927 | GGCAGGGCTGGGTGC[A/G]TGTGTTGGGGCGGTT | 26133 |
rs752232950 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013529 | GTTGCAGTGAGCCGA[C/G]ATCGCACCACTGACT | 26133 |
rs752262808 | snp | A/G | 1.64993e-05 | 0.00287218 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35008716 | GCAGCAGACGAGTTA[A/G]TAAGCCCCTCTTCCC | 26133 |
rs752263020 | snp | C/T | 5.04842e-05 | 0.0050239 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008638 | GCAGCCCCGCAGAAT[C/T]GGCAGGTACTTTTCC | 26133 |
rs752274327 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010707 | GGTTAACTGTGACAC[A/T]TCCCCCGACTTGCCA | 26133 |
rs752317723 | snp | A/C | 3.55069e-05 | 0.00421334 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092801 | CCTCGTCGGACAAAC[A/C]GGAAGCAAGCGGCCT | 26133 |
rs752318343 | snp | C/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094190 | GGACACCCTATTCAA[C/T]AGCTGGTGATAACTG | 26133 |
rs752321772 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078922 | AATACAAAAATTAGC[C/T]GAGTGTGGTGGCAAG | 26133 |
rs752369369 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078384 | AGGGATTGGAAATAC[C/T]CTTGTACCACTCACA | 26133 |
rs752390633 | snp | C/T | 3.31203e-05 | 0.00406928 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003510 | AAGCCGGGGTACTTC[C/T]TGCTGTGCTCCATCC | 26133 |
rs752399147 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029182 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG | 26133 |
rs752419890 | snp | C/T | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008828 | TTCTGCTGGCTTAGG[C/T]GGTGAAAAACCATGG | 26133 |
rs752429186 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049016 | GTGCACATGAACATC[C/T]ACCTCCCTGCAACAG | 26133 |
rs752457643 | in-del | -/AAAG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059836 | GAAGAAGATGAAGAC[-/AAAG]AAGACGAAGATGAAG | 26133 |
rs752495149 | snp | G/T | 1.69123e-05 | 0.0029079 | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003574 | CTTTCCGTCGGGCCA[G/T]CATCAGGATCACCAG | 26133 |
rs752548458 | snp | C/T | 2.992e-05 | 0.0038677 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004434 | ATCGACCTTCCCTGC[C/T]GTGTGTCTGCCGGGG | 26133 |
rs752562836 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049795 | AAAAAGCTCTGTATA[C/T]TATTCAGTTTTGAGA | 26133 |
rs752578986 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019958 | ACAACTCCCCATCTT[C/G]CTCCCTAAGCCTGCT | 26133 |
rs752594062 | snp | A/G | 1.65132e-05 | 0.00287339 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055042 | ACTTACTGAAAGTGA[A/G]AGGGTAATGACTGGT | 26133 |
rs752598929 | snp | A/G | 1.65679e-05 | 0.00287814 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021204 | CCTGGTTTCGCTGAC[A/G]CCCCATCAGCAGCAC | 26133 |
rs752610658 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009734 | TGACGCCTGTGAGAC[G/T]AGCCCCCCACTGCCT | 26133 |
rs752646370 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088037 | ATACCTACCCATCCA[C/G]AGCTAAAAGGAGAAA | 26133 |
rs752673060 | snp | A/G | 1.67343e-05 | 0.00289255 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001963 | GAGCAGCAGGCCAAC[A/G]CCAACCTGGCCAAGT | 26133 |
rs752676298 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026953 | CTGGTTTTTATAGTA[C/G]ATTCCTTAGATTTTT | 26133 |
rs752694059 | in-del | -/TTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032468 | TTTAGTTCTTTGATC[-/TTT]TTTTTTTTTTTTTTT | 26133 |
rs752702057 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017538 | GAGTCAGAAAGCAGA[C/T]GTAAAGCTCTGCACA | 26133 |
rs752703530 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069856 | TGAAGTACAAGAAGC[A/C]CTTGAGCCACGGAGG | 26133 |
rs752720528 | snp | C/T | 8.24287e-05 | 0.00641931 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003222 | GCAGAGGGTGACTGC[C/T]GGTCCGGGTTCAACA | 26133 |
rs752721209 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006476 | TGAATCTCTTGAATG[C/T]ATCAACGTTGAACTT | 26133 |
rs752723504 | snp | A/C | 3.29962e-05 | 0.00406165 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021271 | CTCATGCATAATCTT[A/C]ATTGACTGGGGCAGC | 26133 |
rs752818614 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033461 | TGTTAAGCTTTCTAC[C/T]TCTTCTGGTATCACA | 26133 |
rs752888323 | in-del | -/AA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037875 | ACAGGTTTGCAGCCT[-/AA]GTGTATCATGGGCTA | 26133 |
rs752924507 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048930 | CAGACAATAGGCCAC[C/T]TGTGCTGGGCAATGA | 26133 |
rs752940741 | snp | C/T | 0.000115328 | 0.0075928 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044630 | GTGACAGCCAGAATC[C/T]GGCAGAAATTAGCGA | 26133 |
rs752942859 | snp | C/T | 6.70691e-05 | 0.00579051 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078200 | AAAAAAGAGAGAACA[C/T]ATTATTGTATTATTG | 26133 |
rs752947568 | snp | A/G | 8.30296e-05 | 0.00644266 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003312 | GAGGGGCTGGGGGGC[A/G]CCTGGAGGACCCAGG | 26133 |
rs752957091 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061820 | TTCTTAGATGCACAC[C/G]AATACCCAAGTAACA | 26133 |
rs752979301 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047670 | CAGTAAACATACATA[C/T]TGGAATGTATATAGA | 26133 |
rs753035703 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067133 | GTCATCATTGGCAAT[A/C]AGAGAAATTCAAATC | 26133 |
rs753069656 | snp | C/G | 1.6588e-05 | 0.00287988 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044730 | ACAGAAGACAAAAAT[C/G]AAACAATCCCCATGC | 26133 |
rs753142387 | snp | A/T | | | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012645 | CAGTAAGCAGTCGGC[A/T]TTGCCTGTCTGAAGT | 26133 |
rs753183405 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068534 | CCAGGAAACACTAAC[C/G]ATTTAATTTTTTTTT | 26133 |
rs753212891 | in-del | -/AAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082006 | AAACAAAACAAAAAC[-/AAC]AACAACAACAACAAA | 26133 |
rs753230041 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055319 | CATTTAATAAAGCCA[C/T]TTTCCCTTAATGTCT | 26133 |
rs753244944 | snp | C/T | 1.66374e-05 | 0.00288417 | downstream-variant-500B, synonymous-codon | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002064 | GCTGCGGGCACGGAC[C/T]CGGGACGCCCTGGGC | 26133 |
rs753262943 | in-del | -/GC | 1.6681e-05 | 0.00288794 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008795 | GAGAGGCTGACAGGG[-/GC]GCCCTGGGGATGGGT | 26133 |
rs753291418 | snp | C/T | 1.65789e-05 | 0.0028791 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005657 | TGCCAGCATTCTTAC[C/T]CTGCATGACTTGCCT | 26133 |
rs753317543 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060746 | GCCAAAAGCCACACG[G/T]TCATCTCAACAGATG | 26133 |
rs753319528 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011152 | ATAATCCTAGCTACT[C/G]AGGAGGCTGAGGTAG | 26133 |
rs753338708 | snp | G/T | 3.30398e-05 | 0.00406434 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054938 | ATTGCAGACCTGGTA[G/T]GGGAGATAAACAGAG | 26133 |
rs753338951 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029916 | GCTGGGATTACAGGC[G/T]TGAGCCACCGCGCCC | 26133 |
rs753349970 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091626 | GGTGTTAGCAAGGTT[C/T]GGGGTGGGGGAGGGT | 26133 |
rs753372047 | snp | G/T | 1.71805e-05 | 0.00293086 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002128 | TGTGCAGGGGGACTG[G/T]GGGGGCTGACAGGTA | 26133 |
rs753375073 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012542 | TTGTACATTCTCCAT[C/T]GAAGGTTAAAAAATA | 26133 |
rs753397027 | snp | A/C/T | 4.94624e-05 | 0.00497284 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035165 | CCACTCGCATCAGGG[A/C/T]ATCTAGCACCAAAGC | 26133 |
rs753450381 | snp | C/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094089 | GCACATAGACCAATG[C/G]AACAGAATAGAGAAC | 26133 |
rs753495807 | snp | A/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093234 | TGTCCTCGTCAGGTC[A/G]CTCCATCTATAGATT | 26133 |
rs753508409 | snp | A/G | 1.64787e-05 | 0.00287038 | stop-gained, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007606 | AGGAGGTGGTCCCTC[A/G]GAGGAAACTCTCCAC | 26133 |
rs753509077 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077142 | GGGTGGGAGTGTCCC[A/G]ATTTTCTGGGTACCA | 26133 |
rs753549077 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042416 | CAGGAGAGGAGGCTG[C/T]TCTGAAGCACTTGAT | 26133 |
rs753562571 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062324 | AGTAAGACAATCTAA[C/T]AGAAAATGAAAACAC | 26133 |
rs753562629 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078181 | CTCAGTGAACTGTGA[C/G]TCAAAAAAAGAGAGA | 26133 |
rs753563300 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019043 | CATGGGGAGCCTTTC[C/T]AGTCCTGAGATTTCA | 26133 |
rs753576653 | snp | C/G | 5.14152e-05 | 0.00507001 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092742 | CCGACCGTCTCCCTC[C/G]GCCGGCTCCAGACCC | 26133 |
rs753588125 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008293 | CCCCAGCCCTAGCAG[C/T]GGAAGAGGCTTTCCT | 26133 |
rs753663423 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073182 | GATTTTGGGCTGAGA[A/C]AATGGGGTTTTCTAA | 26133 |
rs753733667 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049616 | TGAGGCATCACCCTA[C/T]ATTCACAGAGTCAAT | 26133 |
rs753737032 | snp | A/C | 0.000206647 | 0.0101627 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092792 | GCCATGTCTCCTCGT[A/C]GGACAAACAGGAAGC | 26133 |
rs753749565 | snp | A/T | 1.69272e-05 | 0.00290918 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050036 | GGTTGTAAGTACAAA[A/T]TAAATTATGAAAGTA | 26133 |
rs753761664 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063429 | GCTGCCAGAGCTGGG[A/G]AGAAGGGGAGATGGG | 26133 |
rs753810636 | snp | C/T | 3.36593e-05 | 0.00410226 | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003567 | AGCCGCTCTTTCCGT[C/T]GGGCCAGCATCAGGA | 26133 |
rs753830024 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085178 | TGGAACTTAGAGGTG[C/G]AAAGCAGGCAGGGCA | 26133 |
rs753852749 | snp | C/T | | | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003575 | TTTCCGTCGGGCCAG[C/T]ATCAGGATCACCAGG | 26133 |
rs753872196 | snp | C/T | 1.64836e-05 | 0.0028708 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016150 | TGAACCTGAATGGGA[C/T]AGGAAGGAAAAAGTA | 26133 |
rs753912036 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040465 | GCTTTTGGTCTCTGA[C/G]ACTTGCACCAGCAGT | 26133 |
rs753918899 | in-del | -/AGA | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094219 | TGGCAAGCCACATGC[-/AGA]AGAATGAAACTGGAT | 26133 |
rs753925256 | snp | C/T | 3.33067e-05 | 0.00408072 | synonymous-codon, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021190 | TGGAGAGGGGCCCAC[C/T]TGGTTTCGCTGACGC | 26133 |
rs753962190 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014928 | GCCTTCCAATGTCCT[A/G]TTCAGAGCTCTCTCA | 26133 |
rs753991061 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059387 | AACAGAGGCTGAGCA[C/T]GGTTGTTCATGCCTG | 26133 |
rs754008642 | in-del | -/TATA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084489 | ATATGTGTATATATG[-/TATA]TATCTATATATGTAT | 26133 |
rs754045631 | in-del | -/TTTTTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031391 | CTACCCCTGGTTAAC[-/TTTTTT]TTTTTTTTTTTTTTT | 26133 |
rs754054402 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016488 | TACCATGTGCAAACT[C/T]TGTAACCTTAAACAA | 26133 |
rs754115100 | snp | C/G | 1.65902e-05 | 0.00288008 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078006 | ATCTTGTGTCACCTA[C/G]AGGCCCTGAATACGC | 26133 |
rs754117408 | in-del | -/CCTGTAATC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036686 | GCACGGTGGCTCATG[-/CCTGTAATC]CTAGCACTTTGGGAG | 26133 |
rs754117468 | in-del | -/ACCCACACTG | 1.65986e-05 | 0.0028808 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003105 | ATCGTACCCACGCTC[-/ACCCACACTG]GCCCAGCAGCCTCCC | 26133 |
rs754137459 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003208 | TGTAGCTAACGAGAG[C/T]AGAGGGTGACTGCCG | 26133 |
rs754145546 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041232 | ATAAAGGCATTCACT[A/G]CTGGAGCGCAATTCA | 26133 |
rs754167898 | snp | A/G | 3.31857e-05 | 0.00407329 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044470 | AAGGGCCTCAGAGCT[A/G]TAATCTCAAAATTCT | 26133 |
rs754182997 | snp | A/G | 3.31175e-05 | 0.00406911 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003309 | AGGGAGGGGCTGGGG[A/G]GCGCCTGGAGGACCC | 26133 |
rs754188537 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077662 | AATCTTCTTACGTTA[A/G]TAATAATATTCAACA | 26133 |
rs754215850 | snp | A/T | 1.64746e-05 | 0.00287002 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044590 | CGTGTGCTTGTCATC[A/T]TTCCCTGTATCCATC | 26133 |
rs754274784 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080480 | CACTTCAGCCTGGGC[A/G]ATAAAGCCAGACCTT | 26133 |
rs754277170 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083006 | ATACTGGAGGTCTCA[A/G]GCAGCAGAGTAAGGC | 26133 |
rs754282323 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047514 | CCTTCTCCTATTCAT[A/G]GATCAGAGACTTGGT | 26133 |
rs754286351 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022281 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 26133 |
rs754292627 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081072 | CATGCCTCAATAAAG[C/T]TGTTTAAGAAATATT | 26133 |
rs754314600 | snp | C/T | 1.6528e-05 | 0.00287467 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010178 | GAAAAGCTGCACCCC[C/T]GCACTCACCTGTCGG | 26133 |
rs754345962 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065941 | TGCCCTAGGACCACC[A/G]ACACTGCTGTGGAGA | 26133 |
rs754423344 | in-del | -/CT | 3.43e-05 | 0.00414112 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001932 | AGCGGAACCAAGGCC[-/CT]GTGTGTGCCCCCAGG | 26133 |
rs754431271 | snp | A/G | 1.71935e-05 | 0.00293197 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002129 | GTGCAGGGGGACTGT[A/G]GGGGCTGACAGGTAG | 26133 |
rs754439523 | in-del | -/TTA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083182 | ATATAAAAATCTATC[-/TTA]TTTTTATATTACAGC | 26133 |
rs754473330 | snp | A/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093265 | CTGGGAGCCTGATCA[A/G]TCGTAGTTCCTGGGG | 26133 |
rs754482008 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042617 | CAGTGATAGGTTTTT[A/G]TATTAACAATATTTC | 26133 |
rs754485143 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091659 | AAGAAGTAGTGGACT[A/G]GGTCCTATTCAACCT | 26133 |
rs754565015 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018001 | GGGTGGGGAGGTACG[C/G]CTGACATCTATGGTG | 26133 |
rs754566589 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077165 | GGGTACCATCTGTCA[A/T]GGCTTCCCTTGGCTA | 26133 |
rs754584084 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007619 | TCGGAGGAAACTCTC[C/T]ACAGCCCGAGCTTGC | 26133 |
rs754597419 | in-del | -/TA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086435 | TGAATGGCATATGTG[-/TA]TGTGTGTGTGTGTGT | 26133 |
rs754622148 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028600 | CCTAGCATATGGTCT[A/G]TCCTGGAGAATGTTC | 26133 |
rs754656432 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043921 | CCAGGAGAGACTTAG[C/T]AGATCAAAAAGTATA | 26133 |
rs754657725 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029168 | AGGCATCAGAATTGC[C/T]TGAACCCGGGAGGTG | 26133 |
rs754702083 | snp | C/G | 3.48074e-05 | 0.00417163 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092793 | CCATGTCTCCTCGTC[C/G]GACAAACAGGAAGCA | 26133 |
rs754706800 | snp | A/G | 0.000165066 | 0.00908326 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003440 | GCTGTCCTTGTCCTT[A/G]TGCAGGTAGTGCTGC | 26133 |
rs754712812 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043443 | GTAGAGATGGGGTTT[C/T]GCCATGTTGGCCAGG | 26133 |
rs754721635 | snp | C/G | 4.88508e-05 | 0.00494196 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092745 | ACCGTCTCCCTCGGC[C/G]GGCTCCAGACCCAGC | 26133 |
rs754734088 | snp | A/G | 1.65121e-05 | 0.00287329 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049973 | CATTCTTTTCTGCCA[A/G]ACGCTTTGTAACTCC | 26133 |
rs754759873 | snp | C/G | 1.65444e-05 | 0.00287609 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003501 | TTGAGCAGGAAGCCG[C/G]GGTACTTCTTGCTGT | 26133 |
rs754794274 | in-del | -/GA | 1.67697e-05 | 0.00289561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021177 | TGTCCTGAGACGCTG[-/GA]GAGGGGCCCACCTGG | 26133 |
rs754814225 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045795 | TCCATCCACCTTGGC[C/T]TCCCAAAGTGCTGGG | 26133 |
rs754856831 | snp | A/C | 1.69565e-05 | 0.00291169 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050039 | TGTAAGTACAAAATA[A/C]ATTATGAAAGTACAA | 26133 |
rs754858953 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015990 | GGCCCCATCTGTCCC[C/T]GGGGGTCTCCTGCTT | 26133 |
rs754861551 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037458 | GCACACACAAATATG[C/T]GTACACACATGTTCA | 26133 |
rs754870614 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019085 | ATTGGTCTGAGAACT[C/T]GGCCCAACTGCTCAT | 26133 |
rs754911868 | snp | A/G | 1.64846e-05 | 0.0028709 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016152 | AACCTGAATGGGATA[A/G]GAAGGAAAAAGTATT | 26133 |
rs754914726 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050923 | GACCGCTTGAGGCCA[A/G]GAGTGTGAGGCCGCA | 26133 |
rs754958748 | in-del | -/GTTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071336 | GTGCACAACATGCAG[-/GTTT]GTTACATATGTATAC | 26133 |
rs754984180 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035982 | TTCTCTTAAAATTAC[G/T]CATCTATAGTTTCTA | 26133 |
rs755005680 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058317 | TATATTCTAACAGAC[A/G]TCTACAGAACACTCC | 26133 |
rs755018699 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027234 | CTGAGGAAGTTCTCT[C/T]CTGAGTTTTTGTTTT | 26133 |
rs755033677 | snp | A/C | 1.65968e-05 | 0.00288065 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021199 | GCCCACCTGGTTTCG[A/C]TGACGCCCCATCAGC | 26133 |
rs755040377 | in-del | -/CCA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032310 | GATTACAGGTGTGAG[-/CCA]CCACACCTGGCCTGA | 26133 |
rs755052500 | snp | C/G | 6.59304e-05 | 0.00574116 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006462 | GTTGATATATTTATT[C/G]AATCTCTTGAATGCA | 26133 |
rs755102098 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071214 | AAAACTTCACCTCTG[A/G]AGAACACTGTCATTC | 26133 |
rs755124998 | snp | A/G | 1.65356e-05 | 0.00287533 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003130 | GCCCAGCAGCCTCCC[A/G]AGGCCTGGCCCAAGG | 26133 |
rs755146743 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047563 | AACAACGAAGCTACA[A/C]ATGTTCTTATGTGTT | 26133 |
rs755153532 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065605 | AGTTCACTAACAAAT[A/G]CACCCAAACTGAAGG | 26133 |
rs755155088 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059389 | CAGAGGCTGAGCATG[A/G]TTGTTCATGCCTGTA | 26133 |
rs755164840 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016668 | TGGAAAAGCCTTTCT[A/G]AAGGATTATAATAAA | 26133 |
rs755172966 | snp | A/C | 1.65855e-05 | 0.00287967 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044472 | GGGCCTCAGAGCTAT[A/C]ATCTCAAAATTCTGA | 26133 |
rs755214663 | snp | A/G | 3.31532e-05 | 0.0040713 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078014 | TCACCTAGAGGCCCT[A/G]AATACGCCCCTCCAA | 26133 |
rs755217384 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032400 | ATCTTTTTATTGTTA[G/T]TCTCTATTTAACGAC | 26133 |
rs755222595 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005893 | TACAAGGGGCATCAG[C/T]GACCTCTACCAGCCC | 26133 |
rs755236784 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033403 | TCTCCCTGGGATGAC[A/G]TTGAGCCAGGCTGTC | 26133 |
rs755249709 | snp | C/G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016516 | CAAATTCCTTAAGAT[C/G/T]TGTCTCCTCGTATTA | 26133 |
rs755261418 | snp | A/G | 3.2956e-05 | 0.00405918 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078108 | TGGTGTGCAGCTTGA[A/G]GAGCAGCTGAGGAAT | 26133 |
rs755263319 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077744 | TTTTCAAAAAGAATG[C/T]CATCCCAATCACAGG | 26133 |
rs755272374 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046295 | GCTATTTGGTTCTAT[G/T]CTCACTCATTACTCC | 26133 |
rs755274000 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005208 | ATCAATGACAGTGAC[C/T]GTGACAAGGAACAAG | 26133 |
rs755279761 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081209 | AAATATGCTAAAATG[A/C]TCCAATTAAAAACAA | 26133 |
rs755336851 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066014 | TGCCATGCATGCAGA[C/T]GTCACACTCAATCTT | 26133 |
rs755355369 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052950 | GGTGTTTGCAACCCT[A/G]AGAGCCCCAGGTTCT | 26133 |
rs755375111 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083051 | ACATAAGATTGGTAA[C/G]GGTAAGATAAAAGAT | 26133 |
rs755414402 | in-del | -/C | 5.1147e-05 | 0.00505676 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001941 | AAGGCCCTGTGTGTG[-/C]CCCCAGGAGCAGCAG | 26133 |
rs755454966 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011238 | CTCCAGCCTGGGCAA[C/T]AGAGCAAGATTCCGT | 26133 |
rs755460328 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067061 | AAGAAATTGAAAAAG[A/G]AGAGACAGACATTTC | 26133 |
rs755509676 | snp | C/T | 3.80525e-05 | 0.00436174 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004467 | TCTCACCTGGGTCAG[C/T]GTCTGCACGTGGATG | 26133 |
rs755534950 | in-del | -/C | 1.65518e-05 | 0.00287674 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003126 | CTGGCCCAGCAGCCT[-/C]CCCGAGGCCTGGCCC | 26133 |
rs755562413 | snp | C/T | 1.73661e-05 | 0.00294665 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004532 | TGGGCACCTGGGATA[C/T]GTAGGCGAGCAGGCG | 26133 |
rs755562950 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029927 | AGGCGTGAGCCACCG[C/T]GCCCAGCCCCAAGTT | 26133 |
rs755604387 | snp | C/T | 1.66043e-05 | 0.00288129 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055083 | AATGAAAAGATAGTA[C/T]AACAGTTACCACATT | 26133 |
rs755647335 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022091 | AGCTAGGGTTACTGT[A/G]CAGACTGAATGGGAA | 26133 |
rs755648280 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089902 | ACTATACCACATGCC[A/G]TAACAGTATAAAAAT | 26133 |
rs755680595 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065755 | GATCCAAAGATGTCC[A/G]AAGATGGGATAGGCT | 26133 |
rs755680999 | snp | C/T | 6.64949e-05 | 0.00576568 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002059 | AACAAGCTGCGGGCA[C/T]GGACCCGGGACGCCC | 26133 |
rs755688964 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052788 | ATAGCCACCGTGCCC[A/G]GCCAACAGTACTTTT | 26133 |
rs755764039 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041106 | GACAGCACCTTGATC[C/T]TGGACTTCTAGCCTC | 26133 |
rs755828499 | in-del | -/AT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082498 | AAGAAATCGAAGTGG[-/AT]ATATGAAAATATCCT | 26133 |
rs755834155 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007506 | CAGCAACGCGTGGGC[C/T]GGGGGGAGACGGAAC | 26133 |
rs755835890 | snp | C/T | 1.6914e-05 | 0.00290805 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021408 | TTGTGAGGAAACACG[C/T]TTCTGCCCCTCGAAC | 26133 |
rs755843025 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016938 | TTGGGTACATTCACA[C/T]GCTGTTGGTGGGAGG | 26133 |
rs755883820 | snp | C/T | 0.000209271 | 0.010227 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092623 | TCGTACCTGCACCGC[C/T]CGGACCAGGCCCCGG | 26133 |
rs755890311 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073336 | GAGTGTGCTGAGAGA[A/G]GGCACCCCTGTCTTG | 26133 |
rs755901076 | snp | G/T | 3.30153e-05 | 0.00406283 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003424 | CGTTCTCTAGGCAGG[G/T]GCTGTCCTTGTCCTT | 26133 |
rs755921645 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069047 | GGTTCTGAGGAGGGG[A/G]CACTGGGAAATTTAG | 26133 |
rs755956691 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062204 | CACTGCTGGTAGATA[C/T]GTAAAATGGTGCAGC | 26133 |
rs755966604 | snp | C/T | 1.69562e-05 | 0.00291167 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049817 | GTTTTGAGAATCCAA[C/T]GGTCTGAGACACCCT | 26133 |
rs755978382 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061190 | TCAACTGTATTTCTA[A/C]AATTGTAGCAAGAAG | 26133 |
rs756008602 | snp | A/G | 6.37004e-05 | 0.00564324 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092729 | GCCACTGTGGCTGCC[A/G]ACCGTCTCCCTCGGC | 26133 |
rs756012560 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006804 | CAATCTCTCCCCTGC[C/T]CAGGGCGTACAGCTG | 26133 |
rs756072064 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017818 | TGCCACTGAAAGTAA[C/T]AGAGGTGACTATTCT | 26133 |
rs756093774 | snp | A/T | 4.94588e-05 | 0.00497262 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049928 | ATGTCTTCTTACTTG[A/T]CATCAATGTAAACAG | 26133 |
rs756132952 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069142 | CTGAAGTAAAAACTA[C/T]GCTGCTTCAACATGT | 26133 |
rs756197066 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024702 | TGGGCGTGGTGGTGT[A/G]CACCTGTTTCCAGCT | 26133 |
rs756200304 | snp | C/T | 8.23852e-05 | 0.00641762 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016131 | GAACTCTGCAATCAT[C/T]CTGTGAACCTGAATG | 26133 |
rs756214347 | snp | C/T | 1.65509e-05 | 0.00287666 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015964 | TTGAAACAACTACTC[C/T]AAGCCAGTGAGGCCC | 26133 |
rs756222576 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063789 | TCACTAGAGCCCAGG[G/T]GTTCAAGGCTGCAGT | 26133 |
rs756256839 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069798 | GTACAAAAATTAGCC[A/G]GATGTGGTGCTACAC | 26133 |
rs756292451 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059269 | GCAACAAAAGTGATT[A/G]TAAGGAACTACTATG | 26133 |
rs756310155 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058150 | TATGTACCTAACAAT[A/G]GAGCCCAAAAATACA | 26133 |
rs756313685 | snp | C/T | 1.64958e-05 | 0.00287187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005688 | TGACAGCCTGCCTTT[C/T]ATGTACCTTTCATAT | 26133 |
rs756325401 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045048 | AAGTTTTGGAAATCA[C/T]AAATTACCATTCTTG | 26133 |
rs756349785 | snp | C/G | 1.65586e-05 | 0.00287733 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069405 | ATGGAGAGAAGAGGA[C/G]AAATTTCCTAGTTTT | 26133 |
rs756374863 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014751 | CCATGGCACCAGGCC[A/G]ATGGCTGGGTGGCAC | 26133 |
rs756379295 | in-del | -/T | 1.66266e-05 | 0.00288323 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069417 | GGAGAAATTTCCTAG[-/T]TTTTTTAAAAAAAAG | 26133 |
rs756413571 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046021 | TTTTCACTATTAAAC[A/C]ATGTTGCAATGAACA | 26133 |
rs756426127 | snp | C/T | 1.764e-05 | 0.00296979 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002152 | ACAGGTAGTACTGCT[C/T]ACTCAGCTATCCCTT | 26133 |
rs756428296 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026137 | ATTCCATTGATCAAT[A/G]TGTCTATCCTCAGGC | 26133 |
rs756439970 | snp | A/G | 1.64893e-05 | 0.0028713 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035222 | CCAACTCCTGAAGGA[A/G]GCTGGCTGTGCCCGT | 26133 |
rs756468054 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079470 | TAATCTAAGCTTCTA[C/T]CTTAGTAAACTACAG | 26133 |
rs756494275 | in-del | -/AC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036962 | CGTGCGCACACAAAC[-/AC]ACACACACACACACA | 26133 |
rs756568702 | snp | A/G | 3.58789e-05 | 0.00423535 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035346 | GGAAATTTTCAAAAT[A/G]GAGACCAGCAAAACT | 26133 |
rs756618035 | snp | A/G | 3.31494e-05 | 0.00407107 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008759 | ACTCCTGAAATAGAA[A/G]AGAGATATTGGTGAC | 26133 |
rs756625174 | snp | A/G | 8.31414e-05 | 0.006447 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021371 | GCTGACACAGCCACC[A/G]GAGACAGGATTGAGT | 26133 |
rs756632554 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064943 | TATACACAAGCTTTA[C/T]CTCATTTTGACTTAC | 26133 |
rs756632733 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077557 | TCTTCAGGTGATTCA[C/T]AAACACACTCCAGTT | 26133 |
rs756657609 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031930 | AAAGTCTCACTTTGT[C/T]ACCCAGGCGCAACTG | 26133 |
rs756665871 | in-del | -/CTG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004738 | GGACCTCCAGCTGTC[-/CTG]CTACCAGGCAAAGCC | 26133 |
rs756710715 | snp | C/T | 3.75954e-05 | 0.00433547 | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003610 | TGTTGAGGCAGCTGA[C/T]GTTCTCCTGCAAGGC | 26133 |
rs756743025 | snp | C/T | 3.73881e-05 | 0.0043235 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092807 | CGGACAAACAGGAAG[C/T]AAGCGGCCTCGGGGC | 26133 |
rs756760127 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064625 | GTATTTATTGTTAAC[C/T]GCACTTGCAGGAGGG | 26133 |
rs756778163 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049476 | AAGGCTTCACACCAG[G/T]TCAGATAGCGGTAAA | 26133 |
rs756792366 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088177 | TGTTTCAGTCACTAT[A/T]TTAAGTGCTTTATAT | 26133 |
rs756818689 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079217 | TTAATTCTCCAAGAA[C/G]ACATAACAATCCTTA | 26133 |
rs756834346 | snp | A/G | 0.000973537 | 0.0220413 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004446 | TGCTGTGTGTCTGCC[A/G]GGGCCTCTCACCTGG | 26133 |
rs756871074 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051477 | CGCACCTGGCAAATT[A/T]AATTTTCAAAGTGAA | 26133 |
rs756884729 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021157 | CGGGCAGCACCTGCT[C/G]CCCGTGTCCTGAGAC | 26133 |
rs756897399 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039104 | AAAAAAACAAAAAAG[A/G]AATAAAAAGAATTTG | 26133 |
rs756907021 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052672 | AATTTTTGTGTTTTT[A/G]GTACAGACGGGGTTT | 26133 |
rs756930057 | in-del | -/CAA | 0.00084655 | 0.0205562 | downstream-variant-500B, cds-indel | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002043 | GGCGGAAACCCAGGC[-/CAA]CAAGCTGCGGGCACG | 26133 |
rs756984999 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026441 | GGCTGGCCTCAAACT[A/C]CTGAGGCCAAGTGAT | 26133 |
rs756986111 | snp | A/G | 1.65064e-05 | 0.00287279 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057499 | CAAGGACCAGTAGCT[A/G]ATAGGTATACTTACT | 26133 |
rs756988376 | snp | C/T | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008948 | TGCATTCCCACCACA[C/T]CTCAGGCCAGCTTTC | 26133 |
rs756989061 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040899 | CCTAATACAGGGAAG[C/T]AATTAAGGTTAAATG | 26133 |
rs757033850 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091236 | TTCAAGCGATCTGCC[A/T]GCCTCGGCCTCCCAA | 26133 |
rs757086947 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066215 | CTCAACCAATCCTCC[A/C]ACCCAGCCCCCATCA | 26133 |
rs757091620 | snp | A/C | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003881 | TCCAGACCTGGGCTC[A/C]AGCATCACTCCTTCC | 26133 |
rs757101403 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078140 | CCACTCCACTTGGAT[C/T]GTTTGTCCCTCTCCG | 26133 |
rs757108989 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071349 | AGGTTTGTTACATAT[A/G]TATACATGTGCCATG | 26133 |
rs757115631 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016833 | AAAGAAATTCCTCTA[C/T]AAGGAGTCCTACAAA | 26133 |
rs757206599 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059561 | TACTTGGGAGACTGA[A/G]GCAGGAGGATTACTT | 26133 |
rs757217670 | in-del | -/AGCAGTAGTAAC | 3.32651e-05 | 0.00407817 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069255 | ATTCCCAAACCATTA[-/AGCAGTAGTAAC]AGCAGTAGTAATAAT | 26133 |
rs757271512 | snp | C/G | 1.65018e-05 | 0.00287239 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003400 | ACCCCCTTGAGGGTG[C/G]GGCACTCACGTTCTC | 26133 |
rs757276715 | snp | A/G | 1.70043e-05 | 0.0029158 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078219 | ATTGTATTATTGATG[A/G]TAATAGCTGATACGG | 26133 |
rs757329774 | snp | A/G | 5.02997e-05 | 0.00501471 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044761 | TCAATTCACTCAAGA[A/G]ATTGGATGTGCCTCT | 26133 |
rs757367893 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088902 | TCACAAAAACAGAAA[A/G]GAGAAGAATGGTTAC | 26133 |
rs757374243 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049914 | TGCTGTTTGTAAGAA[C/T]GTCTTCTTACTTGTC | 26133 |
rs757393097 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085030 | TCAAGAGCGAAGAAA[A/G]TAGATAGTATCTAAA | 26133 |
rs757425725 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086013 | CCGTCTCCTGGGCTC[A/C]AGTGATCCTCCCACC | 26133 |
rs757501638 | in-del | -/TG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086518 | ATATATGTGTGTGTG[-/TG]TATATATGTGTGTGT | 26133 |
rs757503669 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061023 | AAGAAATTAAAGGCA[C/T]CCAAATTGGAAAGGA | 26133 |
rs757508442 | snp | C/G | 1.65277e-05 | 0.00287464 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012967 | GAGGCCTTCCGAAGA[C/G]AGCCCAACAACTCTC | 26133 |
rs757513188 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043591 | CCCTTAGTCAAGACC[C/T]TCACAGTGGATACCT | 26133 |
rs757520931 | in-del | -/A | 1.65225e-05 | 0.00287419 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013108 | TAGGACCACAGCCAC[-/A]AGGTTCCAAAATAAC | 26133 |
rs757561911 | snp | A/C | 0.00205918 | 0.0320211 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013100 | CTCAATGTTAGGACC[A/C]CAGCCACAAGGTTCC | 26133 |
rs757614952 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056403 | GACTAAACAAGTGCA[C/T]CAACAAATAATTACA | 26133 |
rs757668094 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057848 | CTCTGGGATCTAATG[C/T]GGCTTTAATTTCTGA | 26133 |
rs757669910 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035925 | GCATATATACCAAGG[-/A]ATTTACTGTGGCTGT | 26133 |
rs757712795 | snp | A/G | 1.65274e-05 | 0.00287462 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069393 | GCCATAGCCTCCATG[A/G]AGAGAAGAGGAGAAA | 26133 |
rs757734177 | snp | C/T | 1.66139e-05 | 0.00288213 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003100 | GTGGCATCGTACCCA[C/T]GCTCACCCACACTGG | 26133 |
rs757740758 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004860 | AGACCCGTGCCCTCC[A/G]TATCACACACAGAAG | 26133 |
rs757744348 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030337 | TATGGAATGCATCAG[C/G]AATTTGCATGTCATC | 26133 |
rs757764214 | snp | A/G | 1.64833e-05 | 0.00287078 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035188 | ACCAAAGCATTGTCT[A/G]GCCATGTGTACCACT | 26133 |
rs757800893 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044960 | ACTAAATTTACCTTT[C/T]GAGCACCACTGTTTT | 26133 |
rs757883720 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078385 | GGGATTGGAAATACT[A/C]TTGTACCACTCACAA | 26133 |
rs757919992 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029365 | TTGAAAGTGTGTTTT[A/C]TATAGGCTGCATATA | 26133 |
rs757934862 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063635 | AAGGTGAGGCAGGAA[A/G]ATCATTTGAGACCAG | 26133 |
rs757966187 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003928 | GCAGGGCTGGGTGCG[C/T]GTGTTGGGGCGGTTA | 26133 |
rs757966823 | snp | C/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094313 | CCCAGTGGCTCACAC[C/T]TGTAATCCCAGCACT | 26133 |
rs758045970 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051171 | TCCAAGGTTTACTGC[A/G]ATAAACTTGACTTCT | 26133 |
rs758064676 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049275 | TTTTTTTTTTTTAAA[G/T]TTATGGGTCATCCGA | 26133 |
rs758082201 | snp | C/T | 1.65222e-05 | 0.00287417 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054932 | TTAAACATTGCAGAC[C/T]TGGTAGGGGAGATAA | 26133 |
rs758085545 | snp | A/G | 0.00025431 | 0.0112734 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092803 | TCGTCGGACAAACAG[A/G]AAGCAAGCGGCCTCG | 26133 |
rs758093194 | in-del | -/GA | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003826 | CCTCTTCCCCACGCC[-/GA]CACCTCCCACCCCAC | 26133 |
rs758097790 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019961 | ACTCCCCATCTTCCT[C/T]CCTAAGCCTGCTCCT | 26133 |
rs758104900 | snp | C/T | 1.7081e-05 | 0.00292237 | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003583 | GGGCCAGCATCAGGA[C/T]CACCAGGCTGGTGTT | 26133 |
rs758122930 | snp | A/G | 3.30437e-05 | 0.00406457 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055051 | AAGTGAAAGGGTAAT[A/G]ACTGGTTATTTTTCT | 26133 |
rs758150932 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031093 | TGACTGTTTTCTTTC[A/G]GCATTCTGAATATGT | 26133 |
rs758175776 | snp | C/T | 6.62438e-05 | 0.00575478 | synonymous-codon, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021205 | CTGGTTTCGCTGACG[C/T]CCCATCAGCAGCACG | 26133 |
rs758184955 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016176 | AAGTATTAAGACAAA[C/T]GTGCTTGAAAAATCT | 26133 |
rs758242375 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024617 | TCATTTGAGTGCAGG[A/T]GTTTGAGACCAGCTT | 26133 |
rs758243870 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088080 | CAGAAACTTAGGATC[C/T]GTCAGCGTATAGAGC | 26133 |
rs758253524 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026336 | CCTCCCACCTCAGCC[A/T]CTTGAGTAGCTGGGA | 26133 |
rs758349302 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069913 | GCCACTGCACTCCAG[C/T]CTCGGCAACAGAGGG | 26133 |
rs758353085 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090844 | ATCATCTAACCTCTC[C/T]GAGCCTCAGTTTCCT | 26133 |
rs758360809 | snp | A/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006478 | AATCTCTTGAATGCA[A/T]CAACGTTGAACTTCA | 26133 |
rs758427245 | in-del | -/T | 3.35093e-05 | 0.0040931 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069444 | AAAGTACATACATTG[-/T]TTTAGTAACCAACAC | 26133 |
rs758463359 | snp | A/G | 1.67863e-05 | 0.00289704 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006609 | GGTGAAGGTGTCAAC[A/G]TGGCTGCCCCCACCA | 26133 |
rs758466593 | in-del | -/ACAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051035 | ACTGCTATAGCTTAC[-/ACAC]ACACACACACACACA | 26133 |
rs758484338 | in-del | -/TTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038261 | TTACACAGAAATAGA[-/TTT]TTGTTTGAGACACCA | 26133 |
rs758500941 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047761 | CTTGGCTGGTAGACC[C/T]GATGGACTGACTTTA | 26133 |
rs758502576 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081647 | CTCAATGTAAACATA[C/T]ACCAAAAGGTAGTAT | 26133 |
rs758513860 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055352 | CTTAGGATATATCTA[-/G]GATTTGTTTTTTTTG | 26133 |
rs758519272 | snp | C/G/T | 3.29599e-05 | 0.00405944 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078133 | AGGAATTCCACTCCA[C/G/T]TTGGATTGTTTGTCC | 26133 |
rs758543253 | in-del | -/G | 5.53838e-05 | 0.00526202 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003305 | AAAGAGGGAGGGGCT[-/G]GGGGGCGCCTGGAGG | 26133 |
rs758552118 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046375 | CATCCCCGTGCTACT[C/G]AGATAACACCTGCTA | 26133 |
rs758568639 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017567 | CACAGCACCAGTGCT[C/T]GCTTATTGCTATTTT | 26133 |
rs758587672 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017072 | TCAGACAGATCCATA[C/T]AAACACTAAATGATA | 26133 |
rs758602171 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043360 | CAAGCAATTATCCTG[C/T]CTCAGCCTTCTGAGT | 26133 |
rs758611291 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061742 | CTAAATGTAAGATAC[-/A]AAATATAAAATTCTC | 26133 |
rs758640916 | snp | C/T | 3.29554e-05 | 0.00405914 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044640 | GAATCCGGCAGAAAT[C/T]AGCGAGCTGCTGCTG | 26133 |
rs758648547 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085414 | CCCAGGAGTTTAAGA[C/T]CAGCCTGGGCAACAT | 26133 |
rs758682451 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033481 | CTGGTATCACATCCA[A/G]CTGTTAGGCTCTACT | 26133 |
rs758698071 | snp | G/T | 1.66599e-05 | 0.00288611 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044746 | AAACAATCCCCATGC[G/T]CAATTCACTCAAGAG | 26133 |
rs758808081 | in-del | -/ATTTTGCCAT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057630 | ATAACTTATAAAATG[-/ATTTTGCCAT]AACCATTCATGGCCC | 26133 |
rs758840117 | snp | A/G | 1.65985e-05 | 0.00288079 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069270 | AGCAGTAGTAACAGC[A/G]GTAGTAATAATAAAT | 26133 |
rs758867279 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013532 | GCAGTGAGCCGAGAT[C/T]GCACCACTGACTGCA | 26133 |
rs758881774 | in-del | -/G | 1.65192e-05 | 0.00287391 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012989 | ACAACTCTCCTTGCA[-/G]GGACACTCTTGTACT | 26133 |
rs758893520 | snp | A/C | 1.64882e-05 | 0.00287121 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057528 | CTTTTCAGTTTCTGT[A/C]CCCGGATAGAGATCG | 26133 |
rs758909002 | snp | A/C | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093371 | CCTGGGATCCTTTAT[A/C]ACGAAATGCAGGTTA | 26133 |
rs758980745 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029965 | TAGAAGTTGCTGGCT[-/G]GCGCGGTGGCTCATA | 26133 |
rs759015525 | snp | C/T | 1.68977e-05 | 0.00290665 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069463 | AGTAACCAACACAGA[C/T]CAGACACTAAAGCAT | 26133 |
rs759021804 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056130 | GAGACAACGCAGACG[C/T]TCTGCATCCCTTATC | 26133 |
rs759033119 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005772 | TTGGAGTCCACCAGG[A/G]AGCTGTTGATCTGCT | 26133 |
rs759044968 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085740 | GGGTTTTCTCTTGAA[A/G]TACTTGTGGTTTAAC | 26133 |
rs759080326 | snp | C/G | 6.59489e-05 | 0.00574196 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069360 | TCTTGGGTAAGTTTC[C/G]TCTCTTCAGTAACAA | 26133 |
rs759082264 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020347 | AGCTTGACATGACCT[-/G]GTCCCTGTGAGCCCT | 26133 |
rs759091256 | snp | A/G | 3.29794e-05 | 0.00406061 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003171 | GTGAAGTCCCTGTCT[A/G]TGTCCATGTAGGGCT | 26133 |
rs759112669 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024261 | ACAATCAATTTTAGA[A/C]TATCTTCATCACCCC | 26133 |
rs759139680 | snp | A/C | 1.84718e-05 | 0.00303901 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002217 | TGGGCTCTAAAGAGG[A/C]ATGTCTGCTGTTGCA | 26133 |
rs759142142 | snp | C/T | 9.92474e-05 | 0.00704371 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035275 | GCCAGTTTGCAAAGC[C/T]GCTCAACAAAGCCAG | 26133 |
rs759147068 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014198 | AGGATAAAACAGCAA[A/G]TAAGGAAAAGCAGGC | 26133 |
rs759192114 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057378 | AGCTGGGGGAGGAGA[A/G]AGCAACCTGTAGCTA | 26133 |
rs759215986 | in-del | -/CTCT | | | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049989 | ACGCTTTGTAACTCC[-/CTCT]GTCTGTCACAAGAAG | 26133 |
rs759295826 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078809 | GGTGGCTCACACCTG[G/T]AATCCCAACACTTTG | 26133 |
rs759302030 | snp | A/G | 1.88018e-05 | 0.00306603 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004468 | CTCACCTGGGTCAGC[A/G]TCTGCACGTGGATGA | 26133 |
rs759317167 | snp | A/C | 5.01274e-05 | 0.00500612 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078197 | TCAAAAAAAGAGAGA[A/C]CATATTATTGTATTA | 26133 |
rs759335732 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045517 | CTAGGACTACAGGTG[C/T]GTGTCATTACACCTG | 26133 |
rs759344028 | snp | C/T | 1.65023e-05 | 0.00287244 | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35008698 | GCTCCTTCTTCATGA[C/T]CTGCAGCAGACGAGT | 26133 |
rs759374074 | in-del | -/TT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088695 | GAGAGGTTAAATAAC[-/TT]AATCTTGGTCACCCT | 26133 |
rs759412446 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019921 | ATTCTAACACACACC[C/T]CAAATCTACCTTGTA | 26133 |
rs759427145 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064147 | TATGACTAAGCCCAT[A/G]TGTTTAAAGACATTC | 26133 |
rs759464119 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048760 | ACTTCTAGACTCCTA[C/T]GCTGAGACTGCTAAG | 26133 |
rs759466803 | snp | A/G | 1.68428e-05 | 0.00290192 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003569 | CCGCTCTTTCCGTCG[A/G]GCCAGCATCAGGATC | 26133 |
rs759471465 | snp | G/T | 4.47698e-05 | 0.00473105 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092826 | CGGCCTCGGGGCCGC[G/T]GAGATTTCTACGGGG | 26133 |
rs759480208 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065298 | TCCTCCATAAAAGCA[A/G]GCACACACTCTCTAG | 26133 |
rs759482368 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029965 | AGAAGTTGCTGGCTG[-/G]GCGCGGTGGCTCATA | 26133 |
rs759485780 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020827 | CAGACACAGCTCTGG[A/G]CTCTGTCCCACTGCC | 26133 |
rs759490010 | snp | C/T | 3.35739e-05 | 0.00409705 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001958 | CCCAGGAGCAGCAGG[C/T]CAACACCAACCTGGC | 26133 |
rs759543938 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041662 | AATGCTGGTTTTACT[C/T]AAGTCAGTTTACAAA | 26133 |
rs759576248 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092104 | AAGAAAGTAATGTAA[A/T]CGAAACGAATTCGCG | 26133 |
rs759643402 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017475 | GTTAAAATTTGTTTA[C/T]ATAACATAAGGCTAT | 26133 |
rs759652143 | snp | C/T | 1.64999e-05 | 0.00287222 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021264 | ACATGATCTCATGCA[C/T]AATCTTCATTGACTG | 26133 |
rs759694804 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028193 | ATAGTATCATTTTCA[C/T]TTGTCTCAAAATATT | 26133 |
rs759719787 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007052 | AAATACTGAGTTTTC[A/G]TCAAGAGAATAAAGC | 26133 |
rs759751023 | snp | C/T | 6.63779e-05 | 0.0057606 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007516 | TGGGCTGGGGGGAGA[C/T]GGAACCCAAGACACT | 26133 |
rs759753746 | snp | A/G | 3.31835e-05 | 0.00407316 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002012 | AGCTGGATGATGCGG[A/G]GGAGCGGGCAGACAT | 26133 |
rs759774833 | snp | C/T | 4.9879e-05 | 0.0049937 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021370 | GGCTGACACAGCCAC[C/T]GGAGACAGGATTGAG | 26133 |
rs759814171 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043164 | TTTCCATTATATAAA[A/T]ATTGAATACACTAAG | 26133 |
rs759822360 | snp | G/T | 1.66482e-05 | 0.0028851 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006584 | GGATGTGCTGGGTGA[G/T]GAGGGACAGGGTGAA | 26133 |
rs759862254 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044943 | ACAGGATTAGTCTGA[A/G]GACTAAATTTACCTT | 26133 |
rs759862385 | snp | C/T | 1.65198e-05 | 0.00287395 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044702 | GGGACTTCATCTAGT[C/T]GGATCATTTCCTACA | 26133 |
rs759872384 | snp | A/G | 5.13853e-05 | 0.00506853 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003374 | GGCCCTGGGTCCGCG[A/G]CCCACCCATCACCCC | 26133 |
rs759875405 | snp | A/G | 1.65718e-05 | 0.00287848 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003310 | GGGAGGGGCTGGGGG[A/G]CGCCTGGAGGACCCA | 26133 |
rs759883608 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048911 | CATCTCCAATGTGTT[A/C]CTACAGACAATAGGC | 26133 |
rs759892961 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084834 | AGAGGACTGTTTTTA[A/G]CACTACAAAAAAATT | 26133 |
rs759935576 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036585 | CAGGTGAAATTATAC[A/G]ATGTCTGGGGTTTAC | 26133 |
rs759952271 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020996 | CTCCATACAGCAAGG[C/T]ACAGTGAAAAGACTC | 26133 |
rs759962428 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068255 | AATACACACATAAAC[A/G]CAGTATGTTGGTGAT | 26133 |
rs759971869 | snp | C/T | 3.34588e-05 | 0.00409002 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078198 | CAAAAAAAGAGAGAA[C/T]ATATTATTGTATTAT | 26133 |
rs759989133 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050352 | GTTCTAATTCCAGCT[A/G]TGTGATCCTGAGCAA | 26133 |
rs759991058 | snp | A/G | 1.82911e-05 | 0.0030241 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010319 | TTGGAGGAGGTAAAG[A/G]ACAGGAACTGGGGCT | 26133 |
rs760001924 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018495 | CAGCTACTTGGAGGG[C/T]TGAGGCAAGAGGATC | 26133 |
rs760025142 | snp | C/G | 0.000318624 | 0.0126179 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092698 | CCGCGGCCGGCCGCC[C/G]CATCCGCCCCAAGCC | 26133 |
rs760027329 | in-del | -/AACA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068975 | ACACACACACACACA[-/AACA]CACAAAAAAAACAAA | 26133 |
rs760039304 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006358 | GTAAAACCTGTGCCT[A/G]AAGCCTGGCAGACCA | 26133 |
rs760173943 | snp | C/T | 3.3024e-05 | 0.00406336 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013081 | CCTGAAACACATGCA[C/T]AGCCTCAATGTTAGG | 26133 |
rs760211829 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024100 | ACTCTCTGTCTGCAC[C/T]GCACTGTTTTCTGCG | 26133 |
rs760228175 | in-del | -/AAAG | 3.69106e-05 | 0.0042958 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002209 | GACCCCCTGGGCTCT[-/AAAG]AAAGAGGAATGTCTG | 26133 |
rs760244514 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069336 | ATGTAAGTATTTGGA[C/T]AAGTGGTTTCTTGGG | 26133 |
rs760277948 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084192 | CTGTAATCCCAGCTA[C/T]TCGGGGGGCATAGGT | 26133 |
rs760296054 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005746 | ACAGAGTGACACAGC[A/G]CACCAGCATGTTGGA | 26133 |
rs760323963 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043160 | CAATTTTCCATTATA[C/T]AAATATTGAATACAC | 26133 |
rs760335594 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012208 | GATGGGTGCATATGA[C/T]GGAGGTGCCCTGGGG | 26133 |
rs760390380 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022903 | TGGCATGCGCCTGTA[A/G]TCCCAGCTACTCAAG | 26133 |
rs760397280 | snp | A/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056775 | ACTTGAGGTCAGGAG[A/T]TCGAGACCAGCCTGG | 26133 |
rs760412785 | in-del | -/A | 1.66682e-05 | 0.00288684 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007499 | AGGACACAGCAACGC[-/A]GTGGGCTGGGGGGAG | 26133 |
rs760415510 | snp | A/C | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055892 | GGAACAGGAAAGTAG[A/C]ATAAAAACGAAACTT | 26133 |
rs760416646 | snp | C/T | 1.83431e-05 | 0.0030284 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002192 | CACAAGGAGTGACGG[C/T]CTGACCCCCTGGGCT | 26133 |
rs760440120 | in-del | -/AAAG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018967 | ACTCAGGGGGCACTA[-/AAAG]AAACGACTGCTATAT | 26133 |
rs760444641 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013306 | AAAAATAAGGCGGGG[C/T]GTGGTGGTTACACCT | 26133 |
rs760500360 | snp | A/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094028 | ACTTCAATCTATACA[A/G]TAAGGCCATAGTCAC | 26133 |
rs760557027 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029109 | ACACAAAAATGAGCT[C/G]GGCGTGGGCTCCCCG | 26133 |
rs760575963 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018769 | GGCGAGATGAAGTGC[C/T]ACTCTACCAGAGGAG | 26133 |
rs760585085 | snp | A/T | 1.68758e-05 | 0.00290476 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008620 | TGAGAAACACCTGGC[A/T]CTGCAGCCCCGCAGA | 26133 |
rs760595520 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002490 | CAAGGAAGGGCCCCA[A/T]GTCCAGGCTCAGGCA | 26133 |
rs760610574 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078685 | CAATCAAAGGAAAGA[A/G]ACTAAAAGAATGGAT | 26133 |
rs760616684 | snp | C/G | 3.41793e-05 | 0.00413382 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092789 | GCCGCCATGTCTCCT[C/G]GTCGGACAAACAGGA | 26133 |
rs760626994 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073138 | TTTGTATCCTGAGAC[C/T]TTGCTGAAGCTGCTC | 26133 |
rs760684979 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045391 | CTCTCTCTTTTAAGA[A/G]ACAGGGTCTCACTCT | 26133 |
rs760692786 | snp | A/C | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003784 | GAAGGGGGCCCCCAG[A/C]AGCCCCAGTTTCCTG | 26133 |
rs760735415 | snp | C/G | 4.28421e-05 | 0.00462809 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092819 | AAGCAAGCGGCCTCG[C/G]GGCCGCGGAGATTTC | 26133 |
rs760743645 | snp | C/T | 5.03893e-05 | 0.00501917 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050023 | AAAAGGCAGAATAGG[C/T]TGTAAGTACAAAATA | 26133 |
rs760779009 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027035 | GCATGCCTTTAATTT[A/C]TTTTTCTTGCCTAAC | 26133 |
rs760790391 | snp | A/G | 1.64936e-05 | 0.00287168 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35054986 | CTTACACAGACACAG[A/G]TATTATACAGGATAC | 26133 |
rs760809518 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010506 | CCCCACCCCCATCCC[C/T]GACCCCTGCCTGCCA | 26133 |
rs760832213 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040378 | TGGAGGAAAACAAAA[A/G]GGGATTCTCCCCCTT | 26133 |
rs760863687 | snp | C/T | 3.38129e-05 | 0.00411161 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004415 | ACAAAGGAAGTGGTT[C/T]CCAATCGACCTTCCC | 26133 |
rs760865706 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009612 | AACACCACTGCTCTG[C/T]AGCCTGAGAGAAAGA | 26133 |
rs760873613 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089295 | GTAATGGTGTGATCA[C/T]GGCTCACTGCAGCCT | 26133 |
rs760887275 | snp | C/T | 1.65078e-05 | 0.00287291 | synonymous-codon, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021256 | CAGTTTGTACATGAT[C/T]TCATGCATAATCTTC | 26133 |
rs760931240 | snp | C/T | 1.70554e-05 | 0.00292017 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001939 | CCAAGGCCCTGTGTG[C/T]GCCCCCAGGAGCAGC | 26133 |
rs760951709 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072805 | TTTAAAGTAGTTTTT[G/T]CCAATTCTGTGAAGA | 26133 |
rs761010298 | snp | A/G | 1.65762e-05 | 0.00287886 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006569 | CCACAATGCAGTAAA[A/G]GATGTGCTGGGTGAG | 26133 |
rs761040681 | snp | C/T | 1.65031e-05 | 0.00287251 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006440 | TTAACTTTACCTTTG[C/T]ATCGGTGTTGATATA | 26133 |
rs761041142 | snp | A/T | 6.59131e-05 | 0.0057404 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078093 | TGTGGAGGTGGCTGG[A/T]GGTGTGCAGCTTGAG | 26133 |
rs761051327 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061674 | ATGCAAAAGAATGAA[A/G]CTGGACCCCTGCCTC | 26133 |
rs761054227 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036420 | TTTTGAATCCGCAGA[-/T]TTTTTTGGAACCATG | 26133 |
rs761152291 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033091 | AACCCCAGCTACTCG[G/T]GAGGCTGAGAGAGAA | 26133 |
rs761167162 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027993 | TTCTCTACTGTTTTT[C/G]TATTCTCTATCTCAC | 26133 |
rs761178979 | snp | A/G | 3.29506e-05 | 0.00405884 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044576 | TTTTTGGCAAGAAGC[A/G]TGTGCTTGTCATCAT | 26133 |
rs761186907 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016434 | ATATGATTCAAGAGT[C/T]CTTTGGGATGCAAGA | 26133 |
rs761203682 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047312 | TGCCTTGCCATTTAA[A/C]AACTAGTTTTATCAA | 26133 |
rs761225392 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006333 | CCCAGACTCCCCCGT[C/T]GTCTCTAACGTAAAA | 26133 |
rs761239995 | snp | C/G | 1.65241e-05 | 0.00287433 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003293 | GGAGCTCTGGGCAAA[C/G]AGGGAGGGGCTGGGG | 26133 |
rs761246609 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047087 | TTGGCCAGGCTGGTC[G/T]CCTGACCTCAAGTGA | 26133 |
rs761253075 | snp | A/G | 1.65872e-05 | 0.00287981 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078179 | GTCTCAGTGAACTGT[A/G]AGTCAAAAAAAGAGA | 26133 |
rs761259010 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005860 | CCAGGTATGGCCATG[A/G]CCCGGGGGGATAGTC | 26133 |
rs761276787 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017265 | GCTCATGCTGTATTA[C/T]TGATTGTGTAAAAAA | 26133 |
rs761341540 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034987 | AGAGTCTTAATAGTC[A/G]TGGTCTAGAATTGCC | 26133 |
rs761341569 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018197 | ACAGCTGGGAAGAGA[A/G]GGGCCTTCTAAGGCA | 26133 |
rs761347957 | in-del | -/AGGT | 5.21272e-05 | 0.00510499 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002138 | ACTGTGGGGGCTGAC[-/AGGT]AGGTAGTACTGCTCA | 26133 |
rs761354826 | snp | A/G | 3.572e-05 | 0.00422596 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010309 | ACAAAATGGGTTGGA[A/G]GAGGTAAAGGACAGG | 26133 |
rs761450617 | snp | C/G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080745 | TATTCTAAAATTGAT[C/G/T]GTGATGATAGATGCA | 26133 |
rs761475072 | snp | A/C | 3.30109e-05 | 0.00406256 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35013044 | TGAAGAAGCCTCAAA[A/C]ACTGTATCTTCAAGG | 26133 |
rs761479939 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065590 | GCAGGACAGCAAGAG[A/G]GTTCACTAACAAATG | 26133 |
rs761485315 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075393 | TTTTGCAGTAGTTGG[C/T]ATCGGTTGTTCCTTT | 26133 |
rs761500280 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022041 | CTTTGGGCCAGTCAC[A/C]TCCTCACTAGGCCTT | 26133 |
rs761511580 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082501 | AAATCGAAGTGGATA[C/T]ATGAAAATATCCTGA | 26133 |
rs761528640 | snp | A/G | 2.27622e-05 | 0.00337351 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004608 | AGCAGGTCAGGCTTA[A/G]GCCCAGTGGCTGGGT | 26133 |
rs761554257 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029243 | GACAGAGTGAGACTC[C/T]GTCCCTCCAACTTTT | 26133 |
rs761562999 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066860 | AGCACTTACAGATCA[A/G]TAAGAAAAAGGACAA | 26133 |
rs761574683 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022787 | GGACTTTGGGAGGCC[A/G]AGGCAGGTGGACTGC | 26133 |
rs761609977 | in-del | -/GGCTAAGGTGGGC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069703 | CCCAGCACTTTGGGA[-/GGCTAAGGTGGGC]GGATTACTTGAGGCC | 26133 |
rs761686945 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042136 | TGTAAATTTCCTAAA[A/G]TGAGAACTCCCCCAA | 26133 |
rs761699628 | snp | C/T | 1.67729e-05 | 0.00289589 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057589 | ATAAAAAAAATTAGA[C/T]AAAATCTTCAAAATT | 26133 |
rs761710721 | snp | A/C | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056254 | CACTATTTCTAGATC[A/C]TCCATTTTTAAAAGG | 26133 |
rs761735507 | snp | A/G | 3.37234e-05 | 0.00410616 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002104 | AGGAGTGGCAGGGGC[A/G]TTGCTCTCTGTGCAG | 26133 |
rs761761044 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010944 | CTGATAAACCCATCG[C/T]ATTTGAAAATGCCGT | 26133 |
rs761768753 | snp | C/T | 7.19088e-05 | 0.00599577 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092719 | GCCCCAAGCCGCCAC[C/T]GTGGCTGCCGACCGT | 26133 |
rs761778429 | in-del | -/CT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081976 | GGTGACAGAGTGAGA[-/CT]CTGTCTCAAAAACAA | 26133 |
rs761778516 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055637 | CTCACCCTCCCGAGT[A/G]GCTAGGACTGCATGC | 26133 |
rs761788651 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042961 | CACTTTATGTTTCTT[C/G]TGTACCCTTTGTTTC | 26133 |
rs761791688 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002277 | TGCCATCTCTGCATC[A/G]CCCCCTGCTGCCTTC | 26133 |
rs761836634 | in-del | -/CCTTTCATGTA | 1.65049e-05 | 0.00287266 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005682 | TGCCTTGACAGCCTG[-/CCTTTCATGTA]CCTTTCATGTACCTT | 26133 |
rs761841971 | snp | C/T | 1.65496e-05 | 0.00287655 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007539 | AAGACACTGGCTGCT[C/T]CAGATCATACCTCCA | 26133 |
rs761854676 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064070 | GAAAAATTAGGACCT[C/T]TGTTTTCCAAAAAAG | 26133 |
rs761897677 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083715 | TGATCTGCAAGCTTT[-/A]AAAAAAAAAAAAAAG | 26133 |
rs761939295 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019820 | TCCTGGTTTTAAATA[A/C]AACCATATGCTGAGG | 26133 |
rs761947802 | snp | G/T | 1.65282e-05 | 0.00287469 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003485 | CAGGTTGTGGAAGTT[G/T]TTGAGCAGGAAGCCG | 26133 |
rs762000553 | snp | A/G | 1.71805e-05 | 0.00293086 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003546 | AGCAGCCGCAGGTAC[A/G]GGGGCAGCCGCTCTT | 26133 |
rs762136600 | snp | C/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35092924 | CGTGTGCGGCGTGGA[C/G]GCTACTGGGAATTGT | 26133 |
rs762185480 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072690 | GTTACAGTAGCCTTG[C/T]AGTATAGTTTGAAGT | 26133 |
rs762187854 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016291 | AAAACATCCGTGTAT[A/C]CCCTATGCCCAGCAC | 26133 |
rs762255605 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016081 | TTCCTCCAAATCAGT[C/T]TGTCAAACAAATTAT | 26133 |
rs762284993 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070694 | TGAGTCACTGCGCCC[A/G]GCCAAACCTATGTTA | 26133 |
rs762322072 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040777 | CAGCTAATTTTTGTC[A/G]CAGATGGCTTATCAT | 26133 |
rs762339321 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025955 | AATTTTGTATATGAC[A/G]TAAGGCAGGGGATCT | 26133 |
rs762399088 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014585 | CAGCAGAAAAAAGAT[A/G]TTAACATCATGGCTA | 26133 |
rs762423461 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026724 | GGATGTCTTTACATT[C/T]ATTTAGGGTTTAATT | 26133 |
rs762446837 | snp | A/G | 1.73881e-05 | 0.00294852 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035329 | AGGGAAAGAACAAGC[A/G]AGGAAATTTTCAAAA | 26133 |
rs762446932 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078082 | AACAAAGTCACTGTG[A/G]AGGTGGCTGGTGGTG | 26133 |
rs762499824 | snp | C/G | 1.64749e-05 | 0.00287005 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044566 | CTGTTGAGCATTTTT[C/G]GCAAGAAGCGTGTGC | 26133 |
rs762502339 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040107 | CCCCCACAAATTCAT[A/T]CGTTGAAGCTCTAGC | 26133 |
rs762540798 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005620 | GTCATTCTTGTCTCC[C/T]TGCTGGAGACAGGGT | 26133 |
rs762547558 | snp | C/G | 1.65979e-05 | 0.00288074 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010151 | AACGTGGGCAGCCGG[C/G]ATGGGCTGAGGGAAA | 26133 |
rs762583286 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058974 | GATTACAGGCATGAG[A/C]CACCGCACCCGGCCA | 26133 |
rs762600122 | snp | A/G | 5.93014e-05 | 0.00544492 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004435 | TCGACCTTCCCTGCT[A/G]TGTGTCTGCCGGGGC | 26133 |
rs762672056 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031838 | TTCTTCTGCCAGTTC[A/G]TATCTACTGCTGAGT | 26133 |
rs762675333 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016204 | TCTAGCAAAACCTCG[A/T]GCTCAGTACACACGA | 26133 |
rs762708319 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065537 | CTAGTTATTAGCAGA[G/T]GAAGAAATAACAAGC | 26133 |
rs762752638 | snp | A/C | 1.66021e-05 | 0.0028811 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010276 | CTGGTTGTTGAGTAA[A/C]AAGTACTTGTTCCTG | 26133 |
rs762803960 | snp | C/G | 1.65594e-05 | 0.0028774 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057568 | TAAGAATTTCTACAA[C/G]AAGCTATAAAAAAAA | 26133 |
rs762809061 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009835 | CTGTCCTGCTTGGCT[A/G]CAGATGCCACCAGGC | 26133 |
rs762855391 | snp | A/G | 3.30409e-05 | 0.0040644 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057492 | TGGAAAACAAGGACC[A/G]GTAGCTAATAGGTAT | 26133 |
rs762874019 | snp | C/T | 0.000120939 | 0.00777527 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004515 | GAGGAAGGACATCTG[C/T]GTGGGCACCTGGGAT | 26133 |
rs762893838 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054408 | ATGATGTTAATACAA[C/T]TGCTAACTGCATTCT | 26133 |
rs762905793 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032856 | CCTGCTTTTTCTTGT[A/G]TATAGGTTACACTTC | 26133 |
rs762929777 | snp | A/G | 1.66477e-05 | 0.00288506 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021379 | AGCCACCGGAGACAG[A/G]ATTGAGTCACAGCTT | 26133 |
rs762950642 | snp | C/T | 4.98029e-05 | 0.00498988 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002030 | AGCGGGCAGACATGG[C/T]GGAAACCCAGGCCAA | 26133 |
rs762988611 | in-del | -/GGGGGACTGTGGG | 8.50999e-05 | 0.00652248 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002119 | ATTGCTCTCTGTGCA[-/GGGGGACTGTGGG]GGCTGACAGGTAGTA | 26133 |
rs762993399 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078008 | CTTGTGTCACCTAGA[A/G]GCCCTGAATACGCCC | 26133 |
rs762994917 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021841 | AAAAGAAGAACCATC[C/T]AAATTTTTCTAAGGT | 26133 |
rs763020565 | snp | A/C | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093878 | TCACACCCCATCTAA[A/C]AGGAGTAGACTCACC | 26133 |
rs763060607 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081824 | AACCCTGTCTCCACT[-/A]AAAATGCAAAATTAG | 26133 |
rs763076916 | snp | A/C | 1.67354e-05 | 0.00289265 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002092 | GGCCCCAAGGTGAGG[A/C]GTGGCAGGGGCATTG | 26133 |
rs763084521 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076946 | CGCTTTGTTTACCTA[C/T]GCAAGTCTCAGCAGT | 26133 |
rs763175181 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061871 | CAAAATTAAAGACTT[G/T]GTGTTTCAAAGGACA | 26133 |
rs763188638 | snp | C/G | 1.65064e-05 | 0.00287279 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007672 | GGCTCAGGTGGCTAA[C/G]GCTGCCCTCTTCCGG | 26133 |
rs763188697 | snp | C/T | 3.7228e-05 | 0.00431423 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003389 | GCCCACCCATCACCC[C/T]CTTGAGGGTGGGGCA | 26133 |
rs763222154 | snp | C/T | 3.46374e-05 | 0.00416143 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092776 | CGCTACCGGCGCCGC[C/T]GCCATGTCTCCTCGT | 26133 |
rs763240010 | snp | C/T | 0.000183284 | 0.00957124 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092705 | CGGCCGCCCCATCCG[C/T]CCCAAGCCGCCACTG | 26133 |
rs763253759 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050598 | CATGCCTGTAGTCCT[A/G]GCTACTCAGGAGGCT | 26133 |
rs763291995 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084939 | TAACAACAGCCAAAG[C/T]TGTGATATAACTACA | 26133 |
rs763308511 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036767 | GCCTGGTCAACATGG[C/T]GAACTCCATCTCTAC | 26133 |
rs763367178 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088544 | TACTAGCTGAGAGCA[A/G]CTATTTACTAAACAA | 26133 |
rs763374118 | in-del | -/C | 1.66713e-05 | 0.0028871 | downstream-variant-500B, frameshift-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002078 | CCGGGACGCCCTGGG[-/C]CCCCAAGGTGAGGAG | 26133 |
rs763387338 | in-del | -/AGAAG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060825 | CAATCAACAAGGAAT[-/AGAAG]AGAACTTCTTCAGCC | 26133 |
rs763395144 | snp | G/T | 1.64901e-05 | 0.00287137 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049907 | TGAGGGTTGCTGTTT[G/T]TAAGAATGTCTTCTT | 26133 |
rs763448722 | snp | C/T | 1.6516e-05 | 0.00287362 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013090 | CATGCACAGCCTCAA[C/T]GTTAGGACCACAGCC | 26133 |
rs763461089 | snp | A/G | 1.66624e-05 | 0.00288633 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050005 | TCTGTCTGTCACAAG[A/G]AGAAAAGGCAGAATA | 26133 |
rs763480556 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045655 | GTGATTCTCCTGCCT[C/T]AGCCTCCCAAGTAGT | 26133 |
rs763483063 | in-del | -/A | 1.66117e-05 | 0.00288194 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057575 | TCTACAAGAAGCTAT[-/A]AAAAAAAATTAGATA | 26133 |
rs763519591 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079117 | ATAAAAAGAAAGATG[A/G]AGTAGTTATATTAAT | 26133 |
rs763523494 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074233 | GAGCTTCTGGATTCA[C/T]TGATTTTTTGAAGGG | 26133 |
rs763532397 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004716 | AAGCTGACTGTGGCA[C/G]AAAGAAGGACCTCCA | 26133 |
rs763539589 | snp | C/T | 1.65002e-05 | 0.00287225 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35008723 | ACGAGTTAATAAGCC[C/T]CTCTTCCCATCACAC | 26133 |
rs763573189 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059003 | CAAAGAAAATTGTTT[C/T]TAATCGATAACCTAA | 26133 |
rs763575596 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038205 | TGTTCACTTTAAGAC[A/G]GCTAATTTTATGTTA | 26133 |
rs763587461 | snp | G/T | 3.29549e-05 | 0.00405911 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016070 | ATGCTGAATGCTTCC[G/T]CCAAATCAGTTTGTC | 26133 |
rs763617564 | snp | A/C/T | 4.94249e-05 | 0.00497096 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044575 | ATTTTTGGCAAGAAG[A/C/T]GTGTGCTTGTCATCA | 26133 |
rs763629085 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031117 | AATATGTCACCCTAC[C/T]GCCTTCTGCCTTCCA | 26133 |
rs763669395 | in-del | -/TGTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068099 | ATACTTAAAATACAC[-/TGTT]TGTGGAAGGGGGCTT | 26133 |
rs763680581 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044897 | TTCGAGTCTTTGCTT[A/G]TTTATCTGTAAAACG | 26133 |
rs763716530 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064358 | AGCAGGCAAATCTTT[C/G]AGACTAGACAGTTCA | 26133 |
rs763776504 | in-del | -/TT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032469 | TTAGTTCTTTGATCT[-/TT]TTTTTTTTTTTTTTT | 26133 |
rs763852471 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053521 | AGTTGCAAGAACTGT[A/G]CATTTCCTGAACAAT | 26133 |
rs763867578 | snp | C/G | 5.69752e-05 | 0.00533707 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004439 | CCTTCCCTGCTGTGT[C/G]TCTGCCGGGGCCTCT | 26133 |
rs763872562 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054524 | TTTGTTTCTACCAGA[C/T]TGCTTTCTTTATTCA | 26133 |
rs763887142 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027281 | TGGATTTTGTCAAAT[C/G]CTTTTTTGCTCCTAT | 26133 |
rs763903910 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052636 | AGCTGGGACTATAGG[C/T]ATGTACCACCACACC | 26133 |
rs763920748 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065564 | AAGCTGTTTGGAAAA[C/T]ACTACCAGCAGCAGG | 26133 |
rs763952972 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089745 | TCCCAGCTACTCAGG[A/T]GGCTGAGGCAGAATT | 26133 |
rs763957780 | snp | C/G | 1.66863e-05 | 0.0028884 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001969 | CAGGCCAACACCAAC[C/G]TGGCCAAGTATCGCA | 26133 |
rs763988903 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090934 | CATATGCCTTGTACC[A/G]TACTTTTTCTAAAGG | 26133 |
rs764081620 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040749 | GTTGGGATTACAGGC[A/G]TGTCACCATGCCCAG | 26133 |
rs764087706 | snp | A/G | 1.68972e-05 | 0.0029066 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006621 | AACGTGGCTGCCCCC[A/G]CCAGGGCCTGGCATG | 26133 |
rs764141253 | snp | G/T | 1.66302e-05 | 0.00288355 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007531 | CGGAACCCAAGACAC[G/T]GGCTGCTCCAGATCA | 26133 |
rs764160529 | snp | C/T | 1.6729e-05 | 0.00289209 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021392 | AGGATTGAGTCACAG[C/T]TTGTGAGGAAACACG | 26133 |
rs764165080 | snp | A/G | 7.68551e-05 | 0.00619852 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092714 | CATCCGCCCCAAGCC[A/G]CCACTGTGGCTGCCG | 26133 |
rs764167749 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017596 | TTACAAGGGGGAGAA[A/G]TTCAGCAAGACCAGC | 26133 |
rs764198630 | in-del | -/TG | 1.65053e-05 | 0.0028727 | frameshift-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35013046 | AGAAGCCTCAAAAAC[-/TG]TGTATCTTCAAGGTG | 26133 |
rs764210486 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008497 | AAGCTCTCACATACC[C/T]GTCGAGTCAAAACTA | 26133 |
rs764221948 | in-del | -/TAAGTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071142 | CTTAAACGTAAAGAC[-/TAAGTT]TAATTAGTTTCTATT | 26133 |
rs764263935 | snp | A/G/T | 3.30651e-05 | 0.00406591 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003398 | TCACCCCCTTGAGGG[A/G/T]GGGGCACTCACGTTC | 26133 |
rs764276516 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045051 | TTTTGGAAATCATAA[A/T]TTACCATTCTTGCTA | 26133 |
rs764370691 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021520 | TCCACAATCCCAGGA[A/G]CCAGGTGAGCGCAGA | 26133 |
rs764437904 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088766 | ATTTTTTTTTCCAAG[A/G]AAATTCCATCACATG | 26133 |
rs764460185 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060893 | AGCATCACGCTTAAC[A/G]GTGAAGACTAAATGC | 26133 |
rs764477183 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050630 | AGGTAAAAGGATCAT[C/T]TGAGCCCAGAAGGTG | 26133 |
rs764537675 | in-del | -/A | 1.66117e-05 | 0.00288194 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057576 | TCTACAAGAAGCTAT[-/A]AAAAAAATTAGATAA | 26133 |
rs764545892 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063316 | CAGTCTCAGGTATTT[A/C]TTCATTGCAGCATGA | 26133 |
rs764565091 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036814 | AGCCAGGCGTGGTAT[C/T]GTGCGCCTGTAGTCC | 26133 |
rs764571900 | snp | G/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005778 | TCCACCAGGGAGCTG[G/T]TGATCTGCTTCAGGA | 26133 |
rs764576588 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003939 | TGCGTGTGTTGGGGC[A/G]GTTATCCCGCTTCAG | 26133 |
rs764577330 | snp | C/T | 3.30344e-05 | 0.004064 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013093 | GCACAGCCTCAATGT[C/T]AGGACCACAGCCACA | 26133 |
rs764623876 | snp | C/T | 1.64874e-05 | 0.00287113 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069361 | CTTGGGTAAGTTTCC[C/T]CTCTTCAGTAACAAA | 26133 |
rs764624854 | in-del | -/AGAA/AGAAAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035827 | CTGTTTACTTGTTAG[-/AGAA/AGAAAA]AGAGTAAATTATTAA | 26133 |
rs764630359 | snp | A/C | 3.2956e-05 | 0.00405918 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016073 | CTGAATGCTTCCTCC[A/C]AATCAGTTTGTCAAA | 26133 |
rs764649117 | in-del | -/TT/TTT/TTTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014314 | GGGCCTCAGGCAGAA[-/TT/TTT/TTTT]TTTTTTTTTTTTTTT | 26133 |
rs764654319 | snp | A/G | 3.29745e-05 | 0.00406031 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057532 | TCAGTTTCTGTCCCC[A/G]GATAGAGATCGTAGG | 26133 |
rs764657767 | snp | C/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094127 | AAAACCAAATACTTA[C/T]AGCCAACTGATCTTC | 26133 |
rs764674422 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013488 | GAGGCTGAGGCAGGA[C/G]AATCACTTGAACCTG | 26133 |
rs764675533 | snp | A/G | 1.64863e-05 | 0.00287104 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035166 | CACTCGCATCAGGGC[A/G]TCTAGCACCAAAGCA | 26133 |
rs764724065 | snp | C/G | 1.72308e-05 | 0.00293515 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002130 | TGCAGGGGGACTGTG[C/G]GGGCTGACAGGTAGT | 26133 |
rs764727299 | snp | A/C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024273 | AGAATATCTTCATCA[A/C/T]CCCCCAAAAGCAGCC | 26133 |
rs764747988 | snp | C/T | 3.3195e-05 | 0.00407387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077995 | AAACAGCAGACATCT[C/T]GTGTCACCTAGAGGC | 26133 |
rs764777204 | snp | G/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056144 | GCTCTGCATCCCTTA[G/T]CACCACCTTTCAACC | 26133 |
rs764814328 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043516 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTTAA | 26133 |
rs764839502 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003905 | TCCTTCCGGAAGGTC[C/T]GTCCCAGGCAGGGCT | 26133 |
rs764909732 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071797 | TCCTTTGGGTAAATA[C/T]CCAGTAATGGGATGG | 26133 |
rs764921139 | snp | A/G | 4.98583e-05 | 0.00499266 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010149 | GGAACGTGGGCAGCC[A/G]GGATGGGCTGAGGGA | 26133 |
rs764933769 | snp | A/G | 1.80991e-05 | 0.00300819 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004476 | GGTCAGCGTCTGCAC[A/G]TGGATGATGTTGATG | 26133 |
rs764974640 | snp | A/T | 1.81803e-05 | 0.00301494 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092831 | TCGGGGCCGCGGAGA[A/T]TTCTACGGGGCGGCG | 26133 |
rs764984190 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063582 | TGTTATTGCTGGGGA[C/G]GCAGGGTGGCTCGTG | 26133 |
rs764991823 | snp | A/T | 0.000520987 | 0.0161314 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092797 | GTCTCCTCGTCGGAC[A/T]AACAGGAAGCAAGCG | 26133 |
rs765042433 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019956 | ACACAACTCCCCATC[C/T]TCCTCCCTAAGCCTG | 26133 |
rs765048318 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024374 | TCCATCTCTATGCAA[C/T]TGCCTGTTCAGGACA | 26133 |
rs765060626 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041127 | TCTAGCCTCCAGAAC[-/T]TGTGAGAAAAATAAA | 26133 |
rs765079104 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009722 | TCCACTGTATTCTGA[C/T]GCCTGTGAGACTAGC | 26133 |
rs765090147 | snp | A/G | 1.68704e-05 | 0.00290429 | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003570 | CGCTCTTTCCGTCGG[A/G]CCAGCATCAGGATCA | 26133 |
rs765135020 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030999 | TACTAATGAGTTCTT[C/T]CAGTTTTTCTTTTCT | 26133 |
rs765136107 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020901 | GGCCAGGCTTGCCAG[C/T]TTTCAACTCTTTAGT | 26133 |
rs765187425 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016526 | AAGATTTGTCTCCTC[A/G]TATTAACATCAAAAT | 26133 |
rs765225621 | snp | C/T | 1.6577e-05 | 0.00287893 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021203 | ACCTGGTTTCGCTGA[C/T]GCCCCATCAGCAGCA | 26133 |
rs765229377 | snp | C/T | 3.08885e-05 | 0.0039298 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004431 | CCAATCGACCTTCCC[C/T]GCTGTGTGTCTGCCG | 26133 |
rs765240663 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027256 | TTTTGTTTTTACCAT[C/G]AAAGGGTGTTGGATT | 26133 |
rs765258102 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028265 | CTGTAGTGTGATCTC[A/G]GCTCACTGCAACCTC | 26133 |
rs765266018 | snp | A/C | 1.67531e-05 | 0.00289418 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001960 | CAGGAGCAGCAGGCC[A/C]ACACCAACCTGGCCA | 26133 |
rs765274745 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006473 | TATTGAATCTCTTGA[A/G]TGCATCAACGTTGAA | 26133 |
rs765278538 | snp | A/G | 3.29979e-05 | 0.00406175 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021266 | ATGATCTCATGCATA[A/G]TCTTCATTGACTGGG | 26133 |
rs765283921 | snp | A/C | 0.000948943 | 0.0217617 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057484 | CGGCAGGTTGGAAAA[A/C]AAGGACCAGTAGCTA | 26133 |
rs765369442 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018521 | GGATCGCTTGAGCTG[C/G]GGAGGCAGAGGTTGC | 26133 |
rs765387701 | snp | C/G | 1.66543e-05 | 0.00288563 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003311 | GGAGGGGCTGGGGGG[C/G]GCCTGGAGGACCCAG | 26133 |
rs765396111 | in-del | -/TTCT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074167 | TTCTTCTCTCTTTTC[-/TTCT]TTATTAGTCTTGCTA | 26133 |
rs765428682 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047649 | GCTATCACCAAGAAC[A/G]ACCACCAGTAAACAT | 26133 |
rs765458177 | snp | C/T | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007577 | TCGCTTCAGCAGGAA[C/T]ATCTGGTCTGCATAG | 26133 |
rs765482804 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035438 | AAAGCTACTCTTTTA[A/C]AATGAATGTCAAACC | 26133 |
rs765500366 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039975 | ATCATTATTTTTGCT[-/A]GACAAGAAAATGACC | 26133 |
rs765519905 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043221 | TTTCTAGTCTTTTGT[A/T]ATTACAAATAATGTT | 26133 |
rs765531558 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067069 | GAAAAAGGAGAGACA[A/G]ACATTTCTCCAAGGA | 26133 |
rs765584035 | in-del | -/A | 1.66749e-05 | 0.00288741 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008792 | ATCTGAGAGGCTGAC[-/A]GGGGCCCTGGGGATG | 26133 |
rs765625061 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061819 | TTTCTTAGATGCACA[C/G]CAATACCCAAGTAAC | 26133 |
rs765640988 | in-del | -/AAG | 3.32621e-05 | 0.00407798 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050002 | CCCTCTGTCTGTCAC[-/AAG]AAGAAAAGGCAGAAT | 26133 |
rs765652426 | snp | C/G | 1.6563e-05 | 0.00287771 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044721 | TCATTTCCTACAGAA[C/G]ACAAAAATGAAACAA | 26133 |
rs765707693 | snp | A/G | 5.80142e-05 | 0.00538551 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010331 | AAGGACAGGAACTGG[A/G]GCTGCTGGGTCAGCA | 26133 |
rs765772248 | snp | C/T | 1.65061e-05 | 0.00287277 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049892 | CCAAAATATCTTCAA[C/T]GAGGGTTGCTGTTTG | 26133 |
rs765773217 | snp | C/T | 1.65729e-05 | 0.00287857 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005656 | ATGCCAGCATTCTTA[C/T]CCTGCATGACTTGCC | 26133 |
rs765824679 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068115 | GTTTGTGGAAGGGGG[C/T]TTCTGGGTACTGGTA | 26133 |
rs765828887 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023089 | GGAACTATCTTTCCC[C/T]GTCATGTTAAAATCA | 26133 |
rs765836267 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068288 | TATGGGTAAACAGAC[A/G]CTCATACTTTGTTCC | 26133 |
rs765880680 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022169 | CTAGATCCTTTCTTT[A/G]CTTATTTACAGAGTC | 26133 |
rs765880902 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035102 | AGCTCCCGATCACTC[A/G]GGGGACCCATCCTTC | 26133 |
rs765881274 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066937 | AACTACTTATAAACA[C/G]AAGAAAAAATATCCA | 26133 |
rs765902275 | in-del | -/G | 3.32732e-05 | 0.00407866 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007507 | AGCAACGCGTGGGCT[-/G]GGGGGAGACGGAACC | 26133 |
rs765943433 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010719 | CACTTCCCCCGACTT[-/G]CCATCCAGGCCTGTC | 26133 |
rs765995798 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012240 | CACAGCTGTCTCCAG[A/G]CATGTTCTGTTAGCT | 26133 |
rs765996161 | snp | A/T | 1.64836e-05 | 0.0028708 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069337 | TGTAAGTATTTGGAT[A/T]AGTGGTTTCTTGGGT | 26133 |
rs766060860 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056028 | CTCCTAAGCTGCTAG[A/G]AATGCTAAAATGCTA | 26133 |
rs766066614 | snp | C/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35092987 | GAGATGTGGCCTTTC[C/T]TGCACTGCCGGTTTC | 26133 |
rs766069229 | snp | C/G | 1.71173e-05 | 0.00292547 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035073 | GCAAGAATGGTCCCA[C/G]GCGCCCAAGGAAAAG | 26133 |
rs766119888 | snp | C/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094077 | GTATAAAAATAGGCA[C/T]ATAGACCAATGGAAC | 26133 |
rs766120047 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077136 | TTATTAGGGTGGGAG[A/T]GTCCCGATTTTCTGG | 26133 |
rs766157501 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009973 | CTGTCAAGTGCAGGT[A/G]CTGATGGGGCTCCCC | 26133 |
rs766162089 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029124 | GGGCGTGGGCTCCCC[A/G]CCTGTAATCCCAACT | 26133 |
rs766173321 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071571 | TTTGCTCAGAATGAT[-/G]GGTTTCCAGATTCAT | 26133 |
rs766186088 | snp | C/T | 3.30956e-05 | 0.00406776 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003499 | TGTTGAGCAGGAAGC[C/T]GGGGTACTTCTTGCT | 26133 |
rs766242243 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034471 | GGAGGAAGGAAGCCT[C/T]TGACCTCTTTGCCAT | 26133 |
rs766254310 | snp | A/C/T | 1.68601e-05 | 0.00290341 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008628 | ACCTGGCTCTGCAGC[A/C/T]CCGCAGAATCGGCAG | 26133 |
rs766278500 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030961 | AAGTCGGTATGCTGC[C/T]TAATTTCCAGATGTT | 26133 |
rs766286075 | snp | A/G | 3.41758e-05 | 0.00413361 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092790 | CCGCCATGTCTCCTC[A/G]TCGGACAAACAGGAA | 26133 |
rs766292507 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063328 | TTTCTTCATTGCAGC[A/T]TGAGAACGGACTGAC | 26133 |
rs766300425 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008003 | AATGTGTGTGGGAAG[C/T]GGACGAACACATGCA | 26133 |
rs766322323 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052494 | TGAGCAGTACTGTTT[-/A]TTTTTTTATCTTTTA | 26133 |
rs766331307 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026167 | CCAGCAGCATAGTGT[C/G]TCGATTGCAGCTTTG | 26133 |
rs766342417 | in-del | -/C | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002700 | ATTCTCTGGTACCCA[-/C]CCACCCCTGCCCAGG | 26133 |
rs766347489 | snp | C/T | 8.67717e-05 | 0.00658622 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092822 | CAAGCGGCCTCGGGG[C/T]CGCGGAGATTTCTAC | 26133 |
rs766378908 | snp | A/G | 3.30333e-05 | 0.00406393 | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35008683 | AAGACGACTCTGCTG[A/G]CTCCTTCTTCATGAC | 26133 |
rs766389503 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018884 | CTTTGAACCCAAGTC[C/T]CTTGATAGAAAAGGC | 26133 |
rs766441877 | snp | A/G | 1.67576e-05 | 0.00289457 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021177 | TGTCCTGAGACGCTG[A/G]AGAGGGGCCCACCTG | 26133 |
rs766450067 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080013 | GTGACAGAGCAAGAT[-/A]AAAAAAAAAAAAAAA | 26133 |
rs766465723 | snp | C/G/T | 9.8991e-05 | 0.00703468 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35054987 | TTACACAGACACAGG[C/G/T]ATTATACAGGATACT | 26133 |
rs766471706 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065437 | CACTTTTCACAGTCA[C/T]GTTATGGATAGGGTC | 26133 |
rs766505933 | snp | C/T | 9.88826e-05 | 0.00703076 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016145 | TTCTGTGAACCTGAA[C/T]GGGATAGGAAGGAAA | 26133 |
rs766559612 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090763 | CTCATTTATCATGCT[A/G]AAGAACTTCTGTGGC | 26133 |
rs766561022 | snp | C/T | 1.6601e-05 | 0.00288101 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078002 | AGACATCTTGTGTCA[C/T]CTAGAGGCCCTGAAT | 26133 |
rs766566817 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006453 | TGCATCGGTGTTGAT[A/G]TATTTATTGAATCTC | 26133 |
rs766576217 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071034 | GCAAGAAGCAAATAA[C/T]GTGCAACTCTTTGAA | 26133 |
rs766626079 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047467 | CATTTCTACTATATA[A/G]TATTCCATTGTGTGA | 26133 |
rs766628478 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041181 | TCTACGGTACCTTGT[C/T]ATGGCAGCTCAAGCT | 26133 |
rs766656712 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080982 | AGATTGTGGTGATGG[C/T]TGCATAACTTCATCA | 26133 |
rs766679919 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027074 | CCAGAACCTCCAATA[C/T]GATGCTGAAGAGAAG | 26133 |
rs766688071 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059280 | GATTATAAGGAACTA[C/G]TATGAACAACTGTAT | 26133 |
rs766734987 | snp | A/G | 1.65866e-05 | 0.00287976 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006573 | AATGCAGTAAAGGAT[A/G]TGCTGGGTGAGGAGG | 26133 |
rs766742767 | snp | A/G | 1.66985e-05 | 0.00288946 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078195 | AGTCAAAAAAAGAGA[A/G]AACATATTATTGTAT | 26133 |
rs766800764 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078095 | TGGAGGTGGCTGGTG[C/G]TGTGCAGCTTGAGGA | 26133 |
rs766810952 | in-del | -/TGTC | 0.000221689 | 0.0105259 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002218 | GGCTCTAAAGAGGAA[-/TGTC]TGTCTGCTGTTGCAC | 26133 |
rs766818467 | snp | A/G | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003204 | TCAATGTAGCTAACG[A/G]GAGCAGAGGGTGACT | 26133 |
rs766853672 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044587 | AAGCGTGTGCTTGTC[A/G]TCATTCCCTGTATCC | 26133 |
rs766855029 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016447 | GTCCTTTGGGATGCA[A/G]GAGTCCTGGGTTTGA | 26133 |
rs766860111 | snp | C/T | 4.95291e-05 | 0.00497615 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044696 | AGATTGGGGACTTCA[C/T]CTAGTCGGATCATTT | 26133 |
rs766897214 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033061 | AATTAGCCGGGTGTG[A/G]TGGCATGCACCTGTA | 26133 |
rs766940341 | snp | C/T | 3.3071e-05 | 0.00406625 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010176 | GGGAAAAGCTGCACC[C/T]CTGCACTCACCTGTC | 26133 |
rs766941277 | snp | A/G | 8.27684e-05 | 0.00643252 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003307 | AGAGGGAGGGGCTGG[A/G]GGGCGCCTGGAGGAC | 26133 |
rs766950487 | in-del | -/GACTACCCAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051839 | TAACTAGCTACCCTT[-/GACTACCCAC]GACTACCCACCTTTC | 26133 |
rs766964032 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082995 | TTCTATTCATCATAC[C/T]GGAGGTCTCAGGCAG | 26133 |
rs766972127 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048751 | TGAAGGAGCACTTCT[A/G]GACTCCTATGCTGAG | 26133 |
rs766989613 | snp | C/G | 1.79226e-05 | 0.00299349 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010312 | AAATGGGTTGGAGGA[C/G]GTAAAGGACAGGAAC | 26133 |
rs766991716 | snp | C/T | 1.99051e-05 | 0.0031547 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004459 | CCGGGGCCTCTCACC[C/T]GGGTCAGCGTCTGCA | 26133 |
rs767009757 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053684 | AAACACACACACACA[C/T]TGGATTTTGAGAGCT | 26133 |
rs767030329 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047278 | TCTGCCTCTGGGAAC[C/G]ACCATCATTAATTAT | 26133 |
rs767035013 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006334 | CCAGACTCCCCCGTC[A/G]TCTCTAACGTAAAAC | 26133 |
rs767068491 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032065 | CATCTAGCTTTTGTA[C/T]TTTTAATAGAGATGG | 26133 |
rs767083281 | in-del | -/AC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010092 | TGCATGTGAGAGAGG[-/AC]ACGCGTGCATACCTG | 26133 |
rs767116131 | snp | A/G | 1.72794e-05 | 0.00293928 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004519 | AAGGACATCTGCGTG[A/G]GCACCTGGGATATGT | 26133 |
rs767128047 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022066 | GGCCTTAGACTGCTC[C/T]GCAGCAGACAGCTAG | 26133 |
rs767149555 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065609 | CACTAACAAATGCAC[C/T]CAAACTGAAGGTCAG | 26133 |
rs767151603 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082561 | TGATGAGGTACAACT[A/G]AAGCCATGCTTACTG | 26133 |
rs767167634 | snp | A/G | 1.6489e-05 | 0.00287128 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004609 | GCAGGTCAGGCTTAG[A/G]CCCAGTGGCTGGGTC | 26133 |
rs767179934 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068956 | ATATTTACACACACA[-/C]ACACACACACACACA | 26133 |
rs767203428 | snp | C/T | 1.66252e-05 | 0.00288311 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002053 | CAGGCCAACAAGCTG[C/T]GGGCACGGACCCGGG | 26133 |
rs767203930 | snp | C/T | 1.68775e-05 | 0.0029049 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002105 | GGAGTGGCAGGGGCA[C/T]TGCTCTCTGTGCAGG | 26133 |
rs767251414 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091336 | GTTGTGTGATGGCCA[A/G]GAAAACATTTCTCAC | 26133 |
rs767263171 | in-del | -/AAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082004 | ACAAAACAAAACAAA[-/AAC]AACAACAACAACAAA | 26133 |
rs767266249 | snp | C/T | 3.30104e-05 | 0.00406252 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057501 | AGGACCAGTAGCTAA[C/T]AGGTATACTTACTTT | 26133 |
rs767282257 | in-del | -/TCTCCTCAGCACA | 3.57974e-05 | 0.00423053 | downstream-variant-500B, intron-variant, frameshift-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002167 | ACTCAGCTATCCCTT[-/TCTCCTCAGCACA]TCTCCTCAGCACAAG | 26133 |
rs767308468 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092467 | CCGCTGCAGCTGAGA[C/G]CGTCCGGGCAGCTCA | 26133 |
rs767321200 | snp | A/G | 3.57929e-05 | 0.00423027 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057613 | CAAAATTAATTCAAA[A/G]TATAACTTATAAAAT | 26133 |
rs767321728 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054688 | GTCACAGTCTGCCAA[A/C]ACTTGTCACCTTTTG | 26133 |
rs767353009 | in-del | -/TTTTGT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042825 | TTGGTTAGAATAGTG[-/TTTTGT]TTTTAAGTAATATAT | 26133 |
rs767354186 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073164 | TGCTCATCAGTTTAA[A/G]AGGATTTTGGGCTGA | 26133 |
rs767365978 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012052 | CAGAGTACTCAGACT[A/G]AAGAGTCTGATGAAA | 26133 |
rs767414070 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076947 | GCTTTGTTTACCTAC[A/G]CAAGTCTCAGCAGTT | 26133 |
rs767463506 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021741 | GTCGCAAATGGCCCT[A/G]CTTACTTGGTTCTTC | 26133 |
rs767483163 | in-del | -/TA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084705 | ATATATGTGTATATG[-/TA]TATATGTTTATATGC | 26133 |
rs767494227 | snp | C/T | 3.67823e-05 | 0.00428833 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092721 | CCCAAGCCGCCACTG[C/T]GGCTGCCGACCGTCT | 26133 |
rs767502698 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028479 | TTGCATGTATTTATT[A/C]ATTTCCCAAGTTTGT | 26133 |
rs767518429 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050824 | TAAAACTTAGGTTCA[A/G]GAGTTTGGATTTAAA | 26133 |
rs767605737 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052316 | CCAGGCTGGTCTTGA[A/C]CTCCTGGACACACAC | 26133 |
rs767628478 | in-del | -/GAG | 1.65337e-05 | 0.00287517 | cds-indel, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069400 | CCTCCATGGAGAGAA[-/GAG]GAGAAATTTCCTAGT | 26133 |
rs767642467 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087806 | GAGGGCAGAACAAAA[C/T]GAAGGGAAGAAAATA | 26133 |
rs767667229 | snp | A/G | 1.64885e-05 | 0.00287123 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049915 | GCTGTTTGTAAGAAT[A/G]TCTTCTTACTTGTCA | 26133 |
rs767702571 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016093 | AGTTTGTCAAACAAA[C/T]TATTAAGTCCAGGGA | 26133 |
rs767725433 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055129 | ACTGTTATAATCCCC[C/T]CCAAGATGATTATTT | 26133 |
rs767726805 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014633 | GCCAGACAGAACATC[C/T]AGAAATGCAAAATAT | 26133 |
rs767741035 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070718 | TATGTTATTTCTTCC[C/T]TAGACTAAACGTTCC | 26133 |
rs767839417 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069715 | GGAGGCTAAGGTGGG[C/T]GGATTACTTGAGGCC | 26133 |
rs767873111 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038064 | GGTTGCCAGCAGTTG[A/G]GGAGAAGGGGTAATG | 26133 |
rs767889574 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059080 | AAGCAAAAGGGAGAA[G/T]AAGAGTTGAAACAAA | 26133 |
rs767904828 | snp | A/G | 1.69496e-05 | 0.0029111 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021161 | CAGCACCTGCTCCCC[A/G]TGTCCTGAGACGCTG | 26133 |
rs767948059 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004878 | TCACACACAGAAGAG[C/T]TCCCTCCACAGGAAG | 26133 |
rs767952144 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078088 | GTCACTGTGGAGGTG[A/G]CTGGTGGTGTGCAGC | 26133 |
rs767963088 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040884 | CTCTGGAGACTGCTG[C/T]CTAATACAGGGAAGT | 26133 |
rs767995353 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016210 | AAAACCTCGTGCTCA[A/G]TACACACGATAATGA | 26133 |
rs767998383 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025978 | GGGGATCTAACTTCA[C/T]TCTTTCGCATGTGGA | 26133 |
rs767999748 | snp | A/G | 1.66037e-05 | 0.00288125 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077998 | CAGCAGACATCTTGT[A/G]TCACCTAGAGGCCCT | 26133 |
rs768054090 | snp | C/T | | | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005749 | GAGTGACACAGCGCA[C/T]CAGCATGTTGGAGTC | 26133 |
rs768054859 | snp | A/G | 1.75406e-05 | 0.00296142 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035335 | AGAACAAGCGAGGAA[A/G]TTTTCAAAATAGAGA | 26133 |
rs768079515 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045890 | TGTTGCCCAGGCTGG[A/T]ACTCCTGGACTCAAG | 26133 |
rs768100324 | snp | A/T | 1.66532e-05 | 0.00288554 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006421 | CACTCCACAGAGCCC[A/T]GGGTTAACTTTACCT | 26133 |
rs768110167 | in-del | -/TC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038296 | TTTTTTTTTAACATA[-/TC]AGCTTGGCAAATATA | 26133 |
rs768130242 | snp | C/T | 0.000409836 | 0.0143091 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092628 | CCTGCACCGCCCGGA[C/T]CAGGCCCCGGCCGGT | 26133 |
rs768132681 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064897 | CCTGGTAGATAGTCA[C/T]TACAAATAATGTTAC | 26133 |
rs768155943 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027739 | TGAGTTAGCTGCAAT[A/C]GTTTGTGTCTTTTAA | 26133 |
rs768178377 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016294 | ACATCCGTGTATCCC[C/T]TATGCCCAGCACACA | 26133 |
rs768185991 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060109 | TTAAAGAATGATCAA[C/T]TCTTCACAAACTCTT | 26133 |
rs768221991 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031234 | TCTTATCTTTCAGGA[-/T]TTTTTTTTTTTTCTT | 26133 |
rs768234964 | snp | A/C/G | 6.59439e-05 | 0.0057418 | missense, synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044682 | ATACTAAGGAACTCA[A/C/G]ATTGGGGACTTCATC | 26133 |
rs768240987 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042727 | AAATACATCTATGCC[A/G]GTTTCTCCAAAATCT | 26133 |
rs768324118 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079683 | ACTAATATGTGGTAC[A/G]TAAGAGGAGTTATTA | 26133 |
rs768329632 | snp | C/T | 1.68315e-05 | 0.00290094 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003370 | GAGAGGCCCTGGGTC[C/T]GCGGCCCACCCATCA | 26133 |
rs768335659 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044182 | GATCACTTGAGACCA[-/G]GAAGTCAAGACCAGC | 26133 |
rs768355649 | snp | C/T | 1.67973e-05 | 0.00289799 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010286 | AGTAACAAGTACTTG[C/T]TCCTGAAACAAAATG | 26133 |
rs768357655 | snp | C/T | 5.07138e-05 | 0.00503531 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049835 | TCTGAGACACCCTTC[C/T]CCATCTGGTCAGCTA | 26133 |
rs768387317 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017060 | AGGAATTTACACTCA[C/G]ACAGATCCATATAAA | 26133 |
rs768411876 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046921 | ATGCCCAGGCCAGAG[C/T]GCAATGGCACAATCT | 26133 |
rs768436987 | in-del | -/CTGA | 1.72642e-05 | 0.00293799 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002133 | GGGGGACTGTGGGGG[-/CTGA]CTGACAGGTAGTACT | 26133 |
rs768481709 | snp | A/C | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005717 | ATCCACCTGGTTTTC[A/C]AATCGGTCCAGGGAC | 26133 |
rs768503855 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032936 | GGCTGGGTGTGGTAG[C/T]TCACGCCTGTAATCC | 26133 |
rs768544951 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069312 | TCAACACCTCCAAAC[A/G]AGTCAAAAATGTAAG | 26133 |
rs768571842 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045198 | GTGTTTATTATTCCC[A/G]TGCATGTTTTTATAC | 26133 |
rs768589608 | snp | A/G | 2.1885e-05 | 0.00330787 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004602 | GGGTGCAGCAGGTCA[A/G]GCTTAGGCCCAGTGG | 26133 |
rs768600263 | snp | C/T | 1.65833e-05 | 0.00287948 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035131 | TCCATACCTTGATTG[C/T]GCTCTGACTCCTCAT | 26133 |
rs768614535 | snp | G/T | 1.78851e-05 | 0.00299036 | downstream-variant-500B, intron-variant, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002166 | TCACTCAGCTATCCC[G/T]TTCTCCTCAGCACAA | 26133 |
rs768651040 | snp | C/G/T | 0.00268974 | 0.0365742 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002103 | GAGGAGTGGCAGGGG[C/G/T]ATTGCTCTCTGTGCA | 26133 |
rs768651059 | in-del | -/C | 2.00938e-05 | 0.00316962 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004583 | AACTGTGGAGGGAGG[-/C]CAGGGGTGCAGCAGG | 26133 |
rs768659542 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012089 | GACTCACTTCCTCAG[A/G]GAAAACAGCACAGTT | 26133 |
rs768694084 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064035 | TTTTCCTTGACAAAC[A/G]CCTTTTCCTTTTAAA | 26133 |
rs768705163 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023920 | TGGCTTGCGCAGGCC[A/T]GACAAGACTTTCTGT | 26133 |
rs768757921 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022741 | CCTAACTTATTCCGA[C/T]TAGGTGTGGTGGCTC | 26133 |
rs768852706 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020469 | CCTCCCACCTGGTAC[A/G]CTCTTTCATTCTCTT | 26133 |
rs768853823 | in-del | -/CT | | | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002108 | GTGGCAGGGGCATTG[-/CT]CTCTGTGCAGGGGGA | 26133 |
rs768887787 | snp | C/T | 8.24599e-05 | 0.00642053 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035235 | GAAGCTGGCTGTGCC[C/T]GTTGACTCTGACACC | 26133 |
rs768908423 | in-del | -/TTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089396 | CACACCTGGTTAATG[-/TTT]TTTTTTTTTTTTTTT | 26133 |
rs768923183 | snp | A/G | 7.98244e-05 | 0.00631711 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092812 | AAACAGGAAGCAAGC[A/G]GCCTCGGGGCCGCGG | 26133 |
rs768937042 | snp | A/C | 6.65979e-05 | 0.00577014 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008656 | CAGGTACTTTTCCCC[A/C]GACTCACCTGAAAGA | 26133 |
rs768961746 | snp | A/G | 6.89798e-05 | 0.0058724 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092777 | GCTACCGGCGCCGCC[A/G]CCATGTCTCCTCGTC | 26133 |
rs769000258 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009247 | AGGAAGACGGCCAGG[C/T]ACGCAGGGGTCTGGG | 26133 |
rs769005501 | in-del | -/TACA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051033 | AGTACTGCTATAGCT[-/TACA]CACACACACACACAC | 26133 |
rs769005982 | snp | A/G | 3.35048e-05 | 0.00409283 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003538 | TCCGCTGCAGCAGCC[A/G]CAGGTACAGGGGCAG | 26133 |
rs769022385 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090060 | AGGAAGTTGAGCTTG[C/G]CACTGCACTCCAGCC | 26133 |
rs769033049 | in-del | -/CTC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050181 | ATGGAAGAAAAAAGT[-/CTC]CTGACGTGCAGGCTA | 26133 |
rs769049479 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065155 | TGTCAGTGAATAAAA[C/G]TTCCTGAATGCCAAG | 26133 |
rs769059042 | snp | A/G | 2.39421e-05 | 0.00345983 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003644 | AGGCCCACAGGGTCA[A/G]GGGCTGGTGGGAGCC | 26133 |
rs769082208 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088888 | TAAAGTAGTCAAACT[C/T]ACAAAAACAGAAAGG | 26133 |
rs769103794 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038218 | ACGGCTAATTTTATG[C/T]TACGTGACTTCCATC | 26133 |
rs769173527 | snp | A/G | 3.46188e-05 | 0.00416032 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001918 | ATCTCAGTCACCCAA[A/G]CGGAACCAAGGCCCT | 26133 |
rs769209965 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026177 | AGTGTCTCGATTGCA[A/G]CTTTGTAGTAAGTTT | 26133 |
rs769220283 | snp | A/C | 3.30175e-05 | 0.00406296 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054954 | GGGAGATAAACAGAG[A/C]CCCAGTGGCAGGGGT | 26133 |
rs769228456 | in-del | -/AT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028173 | CATCCCATAAGTTTG[-/AT]ATATATAGTATCATT | 26133 |
rs769258829 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007078 | AAGCCAATTTACTCC[-/T]TTTATAAAGTTTTCT | 26133 |
rs769282952 | snp | C/T | 3.29777e-05 | 0.00406051 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006540 | GAGCACATCCCTTGA[C/T]TTACACTCGCTGTCC | 26133 |
rs769285441 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041256 | CAATTCAAGAATGAT[A/G]ACATTCAGAGGACTA | 26133 |
rs769318181 | snp | A/G | | | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004399 | CCTGCTGGGCACCAG[A/G]ACAAAGGAAGTGGTT | 26133 |
rs769319458 | snp | G/T | 1.67044e-05 | 0.00288997 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006409 | GACAACCCAGCACAC[G/T]CCACAGAGCCCTGGG | 26133 |
rs769336553 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039926 | CATTAGATAATTACA[C/T]GTAAATTATCTGAGC | 26133 |
rs769338101 | snp | G/T | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003256 | TGGACACTGTCTCCT[G/T]CCAGTATGAGAAGCT | 26133 |
rs769344905 | snp | G/T | 1.70284e-05 | 0.00291786 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021148 | ATGAGCACCCGGGCA[G/T]CACCTGCTCCCCGTG | 26133 |
rs769372537 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070287 | AAGTCACTGCTCAAA[C/T]ATAATCTCCTGCAGG | 26133 |
rs769419031 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015678 | CTCACACTAGTGAGA[C/T]AGGGTTTCACCATGT | 26133 |
rs769423581 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058891 | ACGAGGTTTTGCCAT[A/G]TTGGCCAGGCTGGTC | 26133 |
rs769441830 | snp | C/T | 3.29745e-05 | 0.00406031 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003175 | AGTCCCTGTCTATGT[C/T]CATGTAGGGCTCCTC | 26133 |
rs769442044 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037142 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 26133 |
rs769464886 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059763 | AGAAGAAGACGAAGA[A/C]GACGACGAAGACAAA | 26133 |
rs769472120 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014230 | GCTAGCTCATGCAGT[C/G]GGCAGCCCCCTCCCT | 26133 |
rs769506985 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005559 | AATTGCCCTGGAAGC[C/T]GCCACCTTGAGGCCG | 26133 |
rs769523796 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026524 | CCCGGCCTAGTTCAA[G/T]ACTGTTTTTGTTAAT | 26133 |
rs769558239 | in-del | -/TAT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038294 | TTTTTTTTTTTAACA[-/TAT]CAGCTTGGCAAATAT | 26133 |
rs769619617 | snp | A/G | 1.66796e-05 | 0.00288782 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003365 | CCTCTGAGAGGCCCT[A/G]GGTCCGCGGCCCACC | 26133 |
rs769637017 | snp | C/T | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35013009 | ACTCTTGTACTTACT[C/T]GTGGTGGTCACTGAA | 26133 |
rs769687799 | in-del | -/AC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068954 | AATATTTACACACAC[-/AC]ACACACACACACACA | 26133 |
rs769691055 | in-del | -/GCAGGGGCATTGCTCTCTGT | 6.71107e-05 | 0.00579231 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002096 | CCAAGGTGAGGAGTG[-/GCAGGGGCATTGCTCTCTGT]GCAGGGGGACTGTGG | 26133 |
rs769733487 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058839 | GATTACAGGTGCCTG[C/T]CACCACTCCTGGCTA | 26133 |
rs769742274 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006113 | CTGTCACACACACTC[A/G]GTGAGCCTAACACAC | 26133 |
rs769761798 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021696 | GCCCAGGCAGATGTA[G/T]GACAGCAAATTATGG | 26133 |
rs769793475 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065322 | TCTCTAGCCCAAAAC[A/G]TTCCCCATACTCATT | 26133 |
rs769827499 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009367 | CTTAGAAAAAAAAGA[C/T]TGGGAGGCCAGGAGA | 26133 |
rs769904866 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055588 | TCACAGCTCACTGTA[A/G]TCTCGAACTCCTAGG | 26133 |
rs769920323 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033259 | CTCCTTCAGGGTTTG[C/T]TGTTGTTATTTGCTT | 26133 |
rs769945991 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009466 | GGCAACATAGTGAGA[-/C]CCCCATCTCTACAAA | 26133 |
rs769981494 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077966 | TTTTTAAAAGCCAAC[A/G]GAAGGGAAAAAAAAA | 26133 |
rs769992424 | snp | A/G | 1.99209e-05 | 0.00315596 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004582 | GCAACTGTGGAGGGA[A/G]GCAGGGGTGCAGCAG | 26133 |
rs770031274 | snp | C/G | 1.66974e-05 | 0.00288936 | downstream-variant-500B, splice-donor-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002086 | GCCCTGGGCCCCAAG[C/G]TGAGGAGTGGCAGGG | 26133 |
rs770051176 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043695 | TAATTTATAAATTAG[A/G]TACACTAAGAGATTA | 26133 |
rs770061332 | snp | A/G | 5.06333e-05 | 0.00503131 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035103 | GCTCCCGATCACTCA[A/G]GGGACCCATCCTTCC | 26133 |
rs770116154 | snp | A/G | 1.64985e-05 | 0.0028721 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007654 | ACCTGCGACCCAAAT[A/G]CTGGCTCAGGTGGCT | 26133 |
rs770141732 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019334 | CCAAGGAACCAGCAC[C/T]GTAATCATACAGTTT | 26133 |
rs770162391 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050419 | AGTAAAATGATCATC[G/T]TAAAAGTCTTTGAGG | 26133 |
rs770172846 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078486 | TAAAAGTATTTTTAC[A/G]AGAAGAATAATTGAT | 26133 |
rs770239387 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020408 | GCTGTCCCGCGCTGC[C/G]TCACTGTTCCAGCAA | 26133 |
rs770241002 | snp | A/G | 6.68416e-05 | 0.00578068 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008646 | GCAGAATCGGCAGGT[A/G]CTTTTCCCCAGACTC | 26133 |
rs770262899 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062838 | TATATCTTTTAAATG[G/T]GTGACTTGTATGACA | 26133 |
rs770265048 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072734 | GCCTCCAGCTTTGGT[C/T]CTTTTGGCTTAGGAT | 26133 |
rs770303445 | in-del | -/GT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050926 | CGCTTGAGGCCAGGA[-/GT]GTGAGGCCGCAGTGA | 26133 |
rs770303723 | snp | A/C | 9.90344e-05 | 0.00703615 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092702 | GGCCGGCCGCCCCAT[A/C]CGCCCCAAGCCGCCA | 26133 |
rs770359197 | snp | C/G | 1.79644e-05 | 0.00299698 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092771 | CCAGCCGCTACCGGC[C/G]CCGCCGCCATGTCTC | 26133 |
rs770368793 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008422 | AGTTCTCTCCCACCC[A/G]TAAGGCACCAGCACA | 26133 |
rs770409071 | in-del | -/AG | 3.53651e-05 | 0.00420491 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092801 | CCTCGTCGGACAAAC[-/AG]GAAGCAAGCGGCCTC | 26133 |
rs770439767 | snp | C/T | 3.42179e-05 | 0.00413615 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021142 | CATACCATGAGCACC[C/T]GGGCAGCACCTGCTC | 26133 |
rs770440407 | snp | A/G | 3.29625e-05 | 0.00405958 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016040 | TCTGGTTGTGACCAT[A/G]GAGGACAAGGGCAGA | 26133 |
rs770479879 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051463 | CAGGCGTGCACCACC[A/G]CACCTGGCAAATTTA | 26133 |
rs770481667 | snp | C/G | 1.65767e-05 | 0.00287891 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049993 | TTTGTAACTCCCTCT[C/G]TCTGTCACAAGAAGA | 26133 |
rs770495998 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008388 | AGCTCTAGGGAATTC[A/G]TGGCAGGGCCCGTAT | 26133 |
rs770507110 | snp | C/T | 1.67609e-05 | 0.00289486 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006392 | CTCCAGGTGAACTTC[C/T]GGACAACCCAGCACA | 26133 |
rs770529488 | in-del | -/ATAG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085030 | TCAAGAGCGAAGAAA[-/ATAG]ATAGTATCTAAAAGT | 26133 |
rs770532902 | snp | C/T | 1.65211e-05 | 0.00287407 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054936 | ACATTGCAGACCTGG[C/T]AGGGGAGATAAACAG | 26133 |
rs770564877 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005747 | CAGAGTGACACAGCG[C/T]ACCAGCATGTTGGAG | 26133 |
rs770566055 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025319 | CCAAGTTGTCAGGAC[C/T]ATGGGCACGTGCCAC | 26133 |
rs770615103 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037894 | GTATCATGGGCTATA[C/G]CAGCTAGGTTTGTGC | 26133 |
rs770626264 | in-del | -/AA | 1.67133e-05 | 0.00289074 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044757 | ATGCTCAATTCACTC[-/AA]GAGATTGGATGTGCC | 26133 |
rs770713085 | snp | A/G | 1.64944e-05 | 0.00287175 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003161 | TCACTCCTCAGTGAA[A/G]TCCCTGTCTATGTCC | 26133 |
rs770736649 | snp | A/G | 3.29745e-05 | 0.00406031 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078052 | AAGAGTTACCTTGAG[A/G]ATGTTTTGACACTCA | 26133 |
rs770792235 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035512 | CAGGTACAGGGAAAC[-/A]AGGCTTTTTATCTAC | 26133 |
rs770807718 | snp | G/T | | | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004436 | CGACCTTCCCTGCTG[G/T]GTGTCTGCCGGGGCC | 26133 |
rs770813052 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044338 | TCAAGGCTGCAGTGA[G/T]CCACGATTGTGCCAC | 26133 |
rs770814823 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062315 | AAATTTTTTAGTAAG[A/T]CAATCTAATAGAAAA | 26133 |
rs770833244 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057289 | ATCACAGGACTATCA[A/G]AAGTACAAAGATGCA | 26133 |
rs770861546 | snp | A/C | 1.64871e-05 | 0.00287111 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044498 | TCTGAGAACTTGGAG[A/C]CTTTACCTTGATTGA | 26133 |
rs770886324 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058597 | GTATAAAGTATCCAA[A/G]AAGGATGAAAATACC | 26133 |
rs770895493 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083038 | AGATATATAGAAGAC[A/G]TAAGATTGGTAAGGG | 26133 |
rs770904647 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036948 | TACTCTGTCTCAACG[C/T]GTGCGCACACAAACA | 26133 |
rs770948134 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063782 | GGAGGATCACTAGAG[-/C]CCCAGGGGTTCAAGG | 26133 |
rs770978834 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066267 | TGTGCTACCACAATC[A/G]GCTAATTTTTTTAAT | 26133 |
rs771028388 | in-del | -/AG | 6.93105e-05 | 0.00588646 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003643 | CAGGCCCACAGGGTC[-/AG]GGGCTGGTGGGAGCC | 26133 |
rs771074432 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022710 | TGATACTCTTTAAAG[C/T]ATCAAGACAGAAGAC | 26133 |
rs771112300 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041585 | AAAACTGGGCTTTCC[A/G]TTCTCAGTTAATCAA | 26133 |
rs771127670 | snp | C/T | 0.000135094 | 0.00821759 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004417 | AAAGGAAGTGGTTTC[C/T]AATCGACCTTCCCTG | 26133 |
rs771169325 | snp | A/G | 1.65471e-05 | 0.00287633 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021353 | GGAGGGAACACAATG[A/G]AGGCTGACACAGCCA | 26133 |
rs771191903 | snp | A/G | 6.66267e-05 | 0.00577139 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002071 | GCACGGACCCGGGAC[A/G]CCCTGGGCCCCAAGG | 26133 |
rs771204130 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028078 | TTCCAATGACTTAAG[A/G]TAGACGTTTAGGCAA | 26133 |
rs771279798 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062769 | TTAAAATCAATTGTG[A/G]TGACAGTGGTATATA | 26133 |
rs771301013 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067521 | TATTCCTAGGTATGT[A/G]TATGCCTGAGAGAAA | 26133 |
rs771344474 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091959 | CCCAGGCCTGACTCC[A/C]GAGTCCCTCTTAACC | 26133 |
rs771354144 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061685 | TGAAACTGGACCCCT[A/G]CCTCACATGATAAAC | 26133 |
rs771393156 | snp | G/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093721 | GGGAATGGTGAAGAT[G/T]GTGACTCATAACTAA | 26133 |
rs771446647 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077602 | CTAGCATAATGTCTC[C/T]GTGCTCTTTCCACTC | 26133 |
rs771463865 | snp | A/G | 4.45127e-05 | 0.00471745 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092753 | CCTCGGCCGGCTCCA[A/G]ACCCAGCCGCTACCG | 26133 |
rs771531804 | snp | A/G | 2.07179e-05 | 0.00321846 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092658 | TCAGCTGGCCCTGCC[A/G]CAGCTGCAGCAGAAT | 26133 |
rs771533038 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048707 | ACAAAAAGGAATGAG[A/C]GGGAGTGAGAGGCAA | 26133 |
rs771548825 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007464 | TGCTCTGCTCCTGAT[G/T]AACTGTTTGGGGCTC | 26133 |
rs771586907 | snp | A/G | 1.6782e-05 | 0.00289668 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049854 | TCTGGTCAGCTAGAG[A/G]ACACAGCTCACCTTT | 26133 |
rs771594974 | snp | C/T | 1.65157e-05 | 0.0028736 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003465 | TGCTGCTGCCAGAAG[C/T]GCAGCAGGTTGTGGA | 26133 |
rs771602019 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018348 | GCCTGTTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 26133 |
rs771648884 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018084 | CCAGGTCACACAGCT[A/G]TAAAATGTTCCAACA | 26133 |
rs771707326 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023956 | ATATTTTCAAGAAAC[A/C]GTCTCCAAAGCAATG | 26133 |
rs771710742 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036266 | TTAAGTCTCCCTGGA[A/C]GGACAGAAAAGAAGC | 26133 |
rs771725072 | snp | C/T | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016015 | CTGCTTACCGGGCTA[C/T]AGTCACAGTTCTGGT | 26133 |
rs771752365 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022893 | CTGGGCATGGTGGCA[C/T]GCGCCTGTAGTCCCA | 26133 |
rs771763213 | in-del | -/G | 1.6492e-05 | 0.00287154 | frameshift-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005800 | GCTTCAGGAATACCT[-/G]GAACTATACAGAAAC | 26133 |
rs771787350 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006986 | CACATTTTGACCCCA[C/T]GGTTTGTCTTTGTGT | 26133 |
rs771809828 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035012 | ATTGCCTTGAGGACA[A/G]TTCTACTCTGAGCAA | 26133 |
rs771847914 | snp | C/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005723 | CTGGTTTTCAAATCG[C/G]TCCAGGGACAGAGTG | 26133 |
rs771898990 | snp | C/T | 1.65979e-05 | 0.00288074 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005846 | CAGTGGGCTGCTGGC[C/T]AGGTATGGCCATGGC | 26133 |
rs771931893 | snp | A/G | 3.30431e-05 | 0.00406454 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003137 | AGCCTCCCGAGGCCT[A/G]GCCCAAGGTCACTCC | 26133 |
rs771967682 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086850 | CCAGCCTAGCCAGCA[A/T]GGTGAAACCCTGTCT | 26133 |
rs771967936 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067947 | TGGTGATGGTTGCAC[A/G]TATCTGCAAATATAC | 26133 |
rs771971835 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056420 | AACAAATAATTACAA[C/T]ATGCTACTTGCTATG | 26133 |
rs772009566 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051893 | CTACTCCTTTTACAG[-/A]ACTGACTAAAATGAC | 26133 |
rs772018976 | snp | G/T | 1.64814e-05 | 0.00287061 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069324 | AACAAGTCAAAAATG[G/T]AAGTATTTGGATAAG | 26133 |
rs772022988 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069227 | CTTTCCTATCTCCCA[C/T]TTCAAAAGTTAAATT | 26133 |
rs772032579 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013962 | GGGCAGTAGGGCCAA[G/T]ACATTAAATAAGAAA | 26133 |
rs772058073 | snp | G/T | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093895 | GGAGTAGACTCACCA[G/T]CCATCTTCATAGAAC | 26133 |
rs772079764 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024975 | ATATATTTTCATTTC[G/T]CTTGGGTATATACCT | 26133 |
rs772100451 | in-del | -/C | 0.000203352 | 0.0100814 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035099 | AAAAGCTCCCGATCA[-/C]TCAGGGGACCCATCC | 26133 |
rs772136406 | snp | A/G | 1.67747e-05 | 0.00289605 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003548 | CAGCCGCAGGTACAG[A/G]GGCAGCCGCTCTTTC | 26133 |
rs772140897 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020681 | AATAGTCTTGAGGAG[A/G]GCCGCACTGTTCCAA | 26133 |
rs772154250 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016294 | ACATCCGTGTATCCC[-/C]TATGCCCAGCACACA | 26133 |
rs772168375 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065211 | TACTGAAAAGCTGGA[A/G]GATTTTTACCTACAA | 26133 |
rs772190656 | snp | C/T | 1.64933e-05 | 0.00287165 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035237 | AGCTGGCTGTGCCCG[C/T]TGACTCTGACACCTT | 26133 |
rs772194260 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031630 | ATTAATGATTTACAT[C/T]ACATTTGGGAGATTT | 26133 |
rs772221657 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066169 | CAGTTCATGGTGCGA[C/T]CTCGGCTCACTGTAG | 26133 |
rs772222399 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021609 | AATATTCGGACACAG[A/C]CAATACAGTAACATG | 26133 |
rs772243598 | snp | C/T | 1.65209e-05 | 0.00287405 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044484 | TATAATCTCAAAATT[C/T]TGAGAACTTGGAGAC | 26133 |
rs772266872 | snp | A/C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010409 | TGAGAAGCCACCAGG[A/C/G]ACTTTCCTCTAGCAC | 26133 |
rs772288138 | snp | A/G | 1.66813e-05 | 0.00288797 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008793 | TCTGAGAGGCTGACA[A/G]GGGCCCTGGGGATGG | 26133 |
rs772305900 | snp | C/T | 5.01015e-05 | 0.00500482 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057469 | GAACTGCCACCGTAT[C/T]GGCAGGTTGGAAAAC | 26133 |
rs772320049 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009409 | CCTGTAATCCCTGGA[A/C]TTTGGGAGGCTCACT | 26133 |
rs772332510 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040237 | TGGCTGGCACAGCAC[G/T]GTTTCTGGGTGTGTC | 26133 |
rs772354549 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011380 | GTTGGCCATAATCAC[C/T]GGCAACACGGCAGGC | 26133 |
rs772363935 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028520 | TAACTCACCCCACTG[A/G]GATTTGAGGACATAC | 26133 |
rs772420209 | snp | C/T | 1.65165e-05 | 0.00287367 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021245 | TAGAGCACTTCCAGT[C/T]TGTACATGATCTCAT | 26133 |
rs772423384 | snp | A/G | 5.17898e-05 | 0.00508844 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001921 | TCAGTCACCCAAGCG[A/G]AACCAAGGCCCTGTG | 26133 |
rs772435480 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041525 | GAATCTAGATTATTT[C/T]ATAGAGACTTTAAGA | 26133 |
rs772439803 | in-del | -/GAAGAAGACGAAGAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059896 | GACAAAGATGAAGAT[-/GAAGAAGACGAAGAC]GAAGAAGACGAAGAC | 26133 |
rs772491754 | in-del | -/TCGGCAGGTAC | 5.04753e-05 | 0.00502346 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008637 | TGCAGCCCCGCAGAA[-/TCGGCAGGTAC]TTTTCCCCAGACTCA | 26133 |
rs772494121 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054222 | CCACAGCATACAGGG[C/T]TCACATTTATAATAG | 26133 |
rs772500530 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060304 | TACAAAAAGGATTAT[A/G]CTCCACGCATGATGG | 26133 |
rs772508432 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072713 | TTTGAAGTCAGGTAG[C/T]GTGATGCCTCCAGCT | 26133 |
rs772544135 | snp | A/C | 1.67534e-05 | 0.0028942 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049858 | GTCAGCTAGAGGACA[A/C]AGCTCACCTTTTTAA | 26133 |
rs772565903 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086465 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTATGT | 26133 |
rs772601380 | snp | C/T | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35013065 | ATCTTCAAGGTGATG[C/T]CCTGAAACACATGCA | 26133 |
rs772609835 | snp | C/T | | | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004553 | CGAGCAGGCGGCATT[C/T]AGACAGTACCTCGGC | 26133 |
rs772643386 | snp | A/G | 1.65154e-05 | 0.00287358 | synonymous-codon, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021337 | CTCAGAAGCCCCTGG[A/G]GGAGGGAACACAATG | 26133 |
rs772644837 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058687 | ATTAAAAGAAAATTC[-/T]TTTTTTTTTTTTTTT | 26133 |
rs772693950 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017159 | GGTATGCCACTCAAT[A/G]GGATACAAGGCACCA | 26133 |
rs772697155 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018248 | TCTCCTAAGTTCAGG[C/T]CAGTGCTTAGGTTTG | 26133 |
rs772700787 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035058 | TTCTTGGAAAGAAGA[C/G]CAAGAATGGTCCCAG | 26133 |
rs772717236 | in-del | -/CAAAACA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020121 | GCAAATCCTATCTTT[-/CAAAACA]CAAAACATATCCAGA | 26133 |
rs772720623 | snp | C/T | 1.65149e-05 | 0.00287353 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006557 | TACACTCGCTGTCCA[C/T]AATGCAGTAAAGGAT | 26133 |
rs772752159 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048719 | GAGAGGGAGTGAGAG[G/T]CAAGTGGGAAAAGTT | 26133 |
rs772802487 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006329 | ACTGCCCAGACTCCC[A/C]CGTCGTCTCTAACGT | 26133 |
rs772814558 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013540 | CGAGATCGCACCACT[-/G]GACTGCACTCCAGCC | 26133 |
rs772822549 | in-del | -/GCT | 1.65548e-05 | 0.002877 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005837 | CACAGCAGGCAGTGG[-/GCT]GCTGGCCAGGTATGG | 26133 |
rs772836040 | snp | A/G | 4.74271e-05 | 0.00486942 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004614 | TCAGGCTTAGGCCCA[A/G]TGGCTGGGTCGCCCA | 26133 |
rs772888958 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005731 | CAAATCGGTCCAGGG[A/G]CAGAGTGACACAGCG | 26133 |
rs772893433 | snp | A/G | 1.67857e-05 | 0.00289699 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069449 | ACATACATTGTTTTA[A/G]TAACCAACACAGACC | 26133 |
rs772902554 | snp | C/G | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016028 | TACAGTCACAGTTCT[C/G]GTTGTGACCATGGAG | 26133 |
rs772903515 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034329 | CTAGTCTTCCGGGCT[G/T]GCCTCTCCCAGTGTA | 26133 |
rs772968610 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044249 | TACAAAAATTAGCCC[A/G]GTGTGGTGGCACCTG | 26133 |
rs773025016 | snp | A/G | 7.31997e-05 | 0.00604934 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002190 | AGCACAAGGAGTGAC[A/G]GCCTGACCCCCTGGG | 26133 |
rs773030419 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013262 | AATGTGGCCCCCTTC[C/T]TGCTAAAAACATGCC | 26133 |
rs773053983 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087090 | ATCCCAGCACCTTGG[A/G]AGGCCGAGGTGGGCG | 26133 |
rs773057144 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043115 | TTTTCTATAGCAGTA[C/T]ATAGAGATCTTCATT | 26133 |
rs773063754 | snp | C/T | 1.65149e-05 | 0.00287353 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003140 | CTCCCGAGGCCTGGC[C/T]CAAGGTCACTCCTCA | 26133 |
rs773074642 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059530 | CTGGGCGTGGTGGTA[C/T]GCCTATAGTTCCAGC | 26133 |
rs773083786 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024038 | CTCACGAGGCCTGTG[C/T]TCCCCTGAGTCTCTT | 26133 |
rs773091038 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055869 | AAACTACTACTTCCC[C/T]GTGAGCAGGAACAGG | 26133 |
rs773105360 | snp | A/G | 9.88891e-05 | 0.00703099 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069329 | GTCAAAAATGTAAGT[A/G]TTTGGATAAGTGGTT | 26133 |
rs773114787 | snp | A/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093956 | ACCAAAAAAGAGCCT[A/G]CATGTCCAAAGCAAG | 26133 |
rs773152037 | snp | C/T | 1.65113e-05 | 0.00287322 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035150 | CTGACTCCTCATTGG[C/T]CACTCGCATCAGGGC | 26133 |
rs773206797 | snp | C/T | 3.40234e-05 | 0.00412439 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092788 | CGCCGCCATGTCTCC[C/T]CGTCGGACAAACAGG | 26133 |
rs773218290 | in-del | -/AAGACA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059771 | ACGAAGAAGACGACG[-/AAGACA]AAGAAGATGAAGAAG | 26133 |
rs773248769 | snp | C/G | 3.40663e-05 | 0.00412698 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004411 | CAGGACAAAGGAAGT[C/G]GTTTCCAATCGACCT | 26133 |
rs773249248 | snp | C/T | 3.30611e-05 | 0.00406565 | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35008677 | ACCTGAAAGACGACT[C/T]TGCTGGCTCCTTCTT | 26133 |
rs773253780 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009449 | GAGTTCGAGACCAGC[C/G]TGGGCAACATAGTGA | 26133 |
rs773279796 | snp | A/G | 1.64953e-05 | 0.00287182 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35054985 | ACTTACACAGACACA[A/G]GTATTATACAGGATA | 26133 |
rs773402707 | snp | A/G | 1.68661e-05 | 0.00290392 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021169 | GCTCCCCGTGTCCTG[A/G]GACGCTGGAGAGGGG | 26133 |
rs773427916 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040345 | CCATCCAATTGGTGG[A/G]GGAGCAGTGGGAGGC | 26133 |
rs773485942 | in-del | -/TTAT | | | utr-variant-3-prime, downstream-variant-500B | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002420 | ATTTTTAAAATAAAG[-/TTAT]TTATTTAATAGTCTC | 26133 |
rs773486408 | snp | A/C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041562 | TCCCAAATAAAAAAA[A/C/T]AAAAACAAAAACTGG | 26133 |
rs773543160 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089239 | ATTTATATATGTATA[C/T]AGTTTGAGGCAGGGT | 26133 |
rs773586481 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060343 | TGTAATCCCAGCACT[C/T]TGAGACGTCAAGGCA | 26133 |
rs773627981 | snp | C/G | 1.65086e-05 | 0.00287298 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021253 | TTCCAGTTTGTACAT[C/G]ATCTCATGCATAATC | 26133 |
rs773705091 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017101 | TATATATTTACAACA[C/T]TACTCACTATAGCAT | 26133 |
rs773745343 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026980 | TTTTCTACATATAAG[A/G]TCATCCCATCTGTGA | 26133 |
rs773750408 | snp | C/G | 3.29554e-05 | 0.00405914 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078092 | CTGTGGAGGTGGCTG[C/G]TGGTGTGCAGCTTGA | 26133 |
rs773764350 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015741 | GTGATCTGCCCGCTC[A/G]GCCTCCCAAAGTGCT | 26133 |
rs773815980 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061609 | AAGACAATTCAATGA[C/T]GAAAGAGTAGTTTTT | 26133 |
rs773879303 | snp | A/C | 1.65663e-05 | 0.002878 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005661 | AGCATTCTTACCCTG[A/C]ATGACTTGCCTTGAC | 26133 |
rs773894861 | snp | C/T | 3.30295e-05 | 0.0040637 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003289 | TGCAGGAGCTCTGGG[C/T]AAAGAGGGAGGGGCT | 26133 |
rs773931946 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006161 | TACAGCGGCTCCCAC[C/T]GTGGCACCCACCATG | 26133 |
rs773937030 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048535 | GTAAGAATTATTGAT[A/G]AATTCTGAATACAAC | 26133 |
rs773990195 | snp | C/T | 1.73912e-05 | 0.00294877 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010300 | GTTCCTGAAACAAAA[C/T]GGGTTGGAGGAGGTA | 26133 |
rs773992184 | snp | C/T | 5.06376e-05 | 0.00503152 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049839 | AGACACCCTTCCCCA[C/T]CTGGTCAGCTAGAGG | 26133 |
rs774007378 | in-del | -/ACACACAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068947 | TGGTGGGGAATATTT[-/ACACACAC]ACACACACACACACA | 26133 |
rs774020899 | in-del | -/GACA | 1.73141e-05 | 0.00294223 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002135 | GGGACTGTGGGGGCT[-/GACA]GACAGGTAGTACTGC | 26133 |
rs774041027 | snp | A/C | 1.65056e-05 | 0.00287272 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35013043 | CTGAAGAAGCCTCAA[A/C]AACTGTATCTTCAAG | 26133 |
rs774046271 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056233 | TGCATGTCTCACTAT[A/G]TATCTCACTATTTCT | 26133 |
rs774102965 | snp | C/T | 1.72862e-05 | 0.00293987 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004517 | GGAAGGACATCTGCG[C/T]GGGCACCTGGGATAT | 26133 |
rs774125150 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080640 | GCATATCCAGAGACA[A/G]AAAGATCACTGGTTG | 26133 |
rs774139784 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054220 | TTCCACAGCATACAG[G/T]GTTCACATTTATAAT | 26133 |
rs774140095 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066826 | AAACACAAATGACAA[A/G]GGCCTTTAAAAAATC | 26133 |
rs774152758 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067798 | ATACAAAACGTCCAC[A/G]ACAGAGAAATCTATA | 26133 |
rs774179247 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092332 | GACGTGTAGACGTGG[C/T]GCAAAGAAGGGAGGA | 26133 |
rs774182270 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082376 | TACTGCAAATGTCAA[C/T]ACATTTAAATGAACT | 26133 |
rs774204063 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055626 | AATTTTCCCTCCTCA[C/T]CCTCCCGAGTGGCTA | 26133 |
rs774233460 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034764 | GGGGACCAGGAAAAG[A/G]TAGGGTACAGTGAGA | 26133 |
rs774311829 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011418 | AGAGTACTGGTTGTC[C/T]ACCTTGGTGATCGTG | 26133 |
rs774330414 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030778 | ATAATTAGATGGTTT[C/G]TGTAAGTTTTTTAAC | 26133 |
rs774346628 | snp | A/C | 1.66879e-05 | 0.00288855 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057582 | AGAAGCTATAAAAAA[A/C]ATTAGATAAAATCTT | 26133 |
rs774355622 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078678 | AACTTACCAATCAAA[A/G]GAAAGAGACTAAAAG | 26133 |
rs774362613 | in-del | -/A | 2.01428e-05 | 0.00317348 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004585 | ACTGTGGAGGGAGGC[-/A]GGGGTGCAGCAGGTC | 26133 |
rs774403556 | snp | A/C | 1.64852e-05 | 0.00287094 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069317 | ACCTCCAAACAAGTC[A/C]AAAATGTAAGTATTT | 26133 |
rs774405344 | snp | C/G | 1.81912e-05 | 0.00301584 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002183 | TCTCCTCAGCACAAG[C/G]AGTGACGGCCTGACC | 26133 |
rs774412606 | snp | C/T | 3.42612e-05 | 0.00413877 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092781 | CCGGCGCCGCCGCCA[C/T]GTCTCCTCGTCGGAC | 26133 |
rs774424611 | snp | G/T | 1.66316e-05 | 0.00288367 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008657 | AGGTACTTTTCCCCA[G/T]ACTCACCTGAAAGAC | 26133 |
rs774433781 | in-del | -/CTGT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073075 | TCACTCATGATTTGG[-/CTGT]CTGTTATTGGTGTAT | 26133 |
rs774488324 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012112 | GCACAGTTCCATAAC[A/G]TATGTGGTGCCATTT | 26133 |
rs774499920 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011955 | ACGGTGGAATCCTTG[G/T]ATGAACAACTGTCTC | 26133 |
rs774515739 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088998 | TTCTGGAAATCTGTT[C/T]CACAACAATGGGAAT | 26133 |
rs774545018 | snp | C/T | 1.65277e-05 | 0.00287464 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003483 | AGCAGGTTGTGGAAG[C/T]TGTTGAGCAGGAAGC | 26133 |
rs774642583 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048901 | GGCCTGCACACATCT[-/C]CAATGTGTTCCTACA | 26133 |
rs774669261 | in-del | -/A | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094572 | GAGACTCCATCTCAG[-/A]AAAAAAAAAAAAAAT | 26133 |
rs774712778 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009336 | ACAATTTTATTTGAA[C/T]GAAGAGTTCTGCTAC | 26133 |
rs774735747 | snp | C/T | 0.000280084 | 0.0118306 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092814 | ACAGGAAGCAAGCGG[C/T]CTCGGGGCCGCGGAG | 26133 |
rs774793062 | snp | A/C | 1.6504e-05 | 0.00287258 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054955 | GGAGATAAACAGAGC[A/C]CCAGTGGCAGGGGTA | 26133 |
rs774808916 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063480 | AAGATTTCTTTTTGG[C/T]GTGATAAAAATGTTC | 26133 |
rs774809734 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063024 | CTCACCTTCAATTGT[A/G]ATAATCCTCATGTGT | 26133 |
rs774878213 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072642 | TTCCACTGGTCTATA[C/T]CTCTGTTTTGGTAAT | 26133 |
rs774878624 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059009 | AAATTGTTTCTAATC[A/G]ATAACCTAATCTTCT | 26133 |
rs774895956 | snp | C/T | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003178 | CCCTGTCTATGTCCA[C/T]GTAGGGCTCCTCAAT | 26133 |
rs774897729 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037431 | ATATACCCAAAAGAA[G/T]TGAAAACAGGTGCAC | 26133 |
rs774898830 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065015 | TGAGTAGTAATGTTT[A/G]AAGCTCTGAAGTATA | 26133 |
rs774927351 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070328 | GATTTCCCCCAACCA[C/G]AAGCATGCTCTTCAG | 26133 |
rs774998553 | snp | C/T | 1.70345e-05 | 0.00291838 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021149 | TGAGCACCCGGGCAG[C/T]ACCTGCTCCCCGTGT | 26133 |
rs775003860 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058923 | TGAACTCCTGACCTC[A/C]GGTGATCTGCCCACC | 26133 |
rs775009909 | snp | C/G | 1.6554e-05 | 0.00287693 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057475 | CCACCGTATCGGCAG[C/G]TTGGAAAACAAGGAC | 26133 |
rs775011504 | in-del | -/TT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031396 | CTGGTTAACTTTTTT[-/TT]TTTTTTTTTTTTTTT | 26133 |
rs775039951 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078073 | TTGACACTCAACAAA[A/G]TCACTGTGGAGGTGG | 26133 |
rs775047688 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006413 | ACCCAGCACACTCCA[C/T]AGAGCCCTGGGTTAA | 26133 |
rs775093727 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025726 | TCTTCCATTCTGTGG[A/G]TTCTCTTTTCACTTT | 26133 |
rs775095019 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044526 | TGATTTCAGCTGCAG[A/G]AGGCCCCAAACTCAA | 26133 |
rs775126543 | in-del | -/CTCT | 1.68903e-05 | 0.00290601 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002107 | GTGGCAGGGGCATTG[-/CTCT]CTCTCTGTGCAGGGG | 26133 |
rs775150907 | snp | C/T | 1.64944e-05 | 0.00287175 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003270 | TTCCAGTATGAGAAG[C/T]TGATGCAGGAGCTCT | 26133 |
rs775157241 | snp | G/T | 1.65356e-05 | 0.00287533 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010268 | TTCAGCTCCTGGTTG[G/T]TGAGTAACAAGTACT | 26133 |
rs775172026 | snp | C/T | 3.29989e-05 | 0.00406182 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006548 | CCCTTGACTTACACT[C/T]GCTGTCCACAATGCA | 26133 |
rs775193408 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015709 | TGGCCAGGCTGGTCT[A/G]TAACTCTTGACCTCA | 26133 |
rs775195020 | snp | G/T | 1.72847e-05 | 0.00293974 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004511 | GGAAGAGGAAGGACA[G/T]CTGCGTGGGCACCTG | 26133 |
rs775216510 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065382 | TGCTTCACTCCACTT[-/A]AGTTACATACTTCAC | 26133 |
rs775236190 | in-del | -/A/AA/AAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050712 | GGGAGACCCTAACTC[-/A/AA/AAA]AAAAAAAAAAACAAA | 26133 |
rs775259762 | snp | A/G | 3.30879e-05 | 0.00406729 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057487 | CAGGTTGGAAAACAA[A/G]GACCAGTAGCTAATA | 26133 |
rs775263078 | in-del | -/A/AA/AAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030241 | GCGAAACTCCATATC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 26133 |
rs775276674 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081948 | CAAGAATGCACCATT[G/T]CACTCCAGCCTGGGT | 26133 |
rs775280311 | snp | C/T | 1.72826e-05 | 0.00293956 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004513 | AAGAGGAAGGACATC[C/T]GCGTGGGCACCTGGG | 26133 |
rs775308861 | snp | G/T | 1.66043e-05 | 0.00288129 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010150 | GAACGTGGGCAGCCG[G/T]GATGGGCTGAGGGAA | 26133 |
rs775333700 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066454 | CTGAACACCATTCCT[A/G]TACAATCGCCACATA | 26133 |
rs775363297 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053431 | ATAAAACTAGTGACT[A/G]TATGGAGTTGCCAAA | 26133 |
rs775488611 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065359 | ATGCAGATGAGCTTG[C/G]TCTGGGTCTGCTTCA | 26133 |
rs775534821 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007428 | AGGCAGCCTGCACAG[C/G]CATTTGGAAGTCACG | 26133 |
rs775536938 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028986 | CTGGGTGGTGGTGGC[A/T]CATGCCTGTAATCCC | 26133 |
rs775539562 | snp | A/G | 4.01869e-05 | 0.00448239 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004583 | CAACTGTGGAGGGAG[A/G]CAGGGGTGCAGCAGG | 26133 |
rs775551276 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009875 | GCACATAAGCAAAGG[A/G]GCTGAATGCACGAGA | 26133 |
rs775561834 | snp | C/G | 1.66346e-05 | 0.00288393 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021374 | GACACAGCCACCGGA[C/G]ACAGGATTGAGTCAC | 26133 |
rs775586175 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042953 | TTAATAACCACTTTA[C/T]GTTTCTTGTGTACCC | 26133 |
rs775600734 | snp | A/G | 9.8943e-05 | 0.0070329 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057552 | GAGATCGTAGGCCTC[A/G]TAAGAATTTCTACAA | 26133 |
rs775624775 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030614 | GTTTTTATATTTACC[C/T]TCTTATTACCATTTT | 26133 |
rs775713764 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036677 | GCTGGCCAGGCACGG[A/T]GGCTCATGCCTGTAA | 26133 |
rs775741648 | snp | C/T | 1.65026e-05 | 0.00287246 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007659 | CGACCCAAATACTGG[C/T]TCAGGTGGCTAAGGC | 26133 |
rs775742514 | snp | C/G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019537 | TCGAGTGTGGGGACA[C/G/T]AGAGTCACCACCTGT | 26133 |
rs775802915 | in-del | -/G | 0.000182966 | 0.00956292 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057473 | GCCACCGTATCGGCA[-/G]GGTTGGAAAACAAGG | 26133 |
rs775896451 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062940 | TAAAAAGCCACACAG[C/T]GGACGATTCTGTTGA | 26133 |
rs775908037 | snp | C/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35016046 | TGTGACCATGGAGGA[C/G]AAGGGCAGATGCTGA | 26133 |
rs775944951 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087410 | AGGGGCATTTAGATA[A/T]GCCAATAATCATAAA | 26133 |
rs775949314 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063927 | CAAATTCTAGGTTAA[C/T]ATAAACAGAAAAAAA | 26133 |
rs775955658 | snp | A/C | 9.76896e-05 | 0.00698822 | stop-gained, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092703 | GCCGGCCGCCCCATC[A/C]GCCCCAAGCCGCCAC | 26133 |
rs775956861 | snp | G/T | 3.30447e-05 | 0.00406464 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003478 | AGCGCAGCAGGTTGT[G/T]GAAGTTGTTGAGCAG | 26133 |
rs775987742 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037917 | GTTTGTGCAAGTACA[C/T]TCTATGACATTCACA | 26133 |
rs775992340 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051735 | GTTCTGGAAGATCCA[A/C]AGAAACAGAACAAAA | 26133 |
rs776009086 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088375 | TCTTTAAAGCCATGA[C/G]ATTGCTTGGCAAGTA | 26133 |
rs776010760 | snp | A/G | 1.65037e-05 | 0.00287256 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049893 | CAAAATATCTTCAAT[A/G]AGGGTTGCTGTTTGT | 26133 |
rs776010915 | snp | G/T | 3.54277e-05 | 0.00420863 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092774 | GCCGCTACCGGCGCC[G/T]CCGCCATGTCTCCTC | 26133 |
rs776011524 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069477 | ACCAGACACTAAAGC[A/G]TCAGTTTGAGCTTTA | 26133 |
rs776027051 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023302 | CAATACTGACAACCA[C/T]ACCTACCCCTTAATG | 26133 |
rs776032740 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005771 | GTTGGAGTCCACCAG[A/G]GAGCTGTTGATCTGC | 26133 |
rs776045372 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050462 | GCTCACACCTGTAAC[C/T]CCAGCACTTTGGGAG | 26133 |
rs776045858 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089891 | GGTCTTTTCCTACTA[C/T]ACCACATGCCATAAC | 26133 |
rs776135546 | snp | C/T | 3.32397e-05 | 0.00407661 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049999 | ACTCCCTCTGTCTGT[C/T]ACAAGAAGAAAAGGC | 26133 |
rs776140850 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069420 | GAAATTTCCTAGTTT[C/T]TTTAAAAAAAAGTAC | 26133 |
rs776144671 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068248 | CTATAAAAATACACA[C/T]ATAAACACAGTATGT | 26133 |
rs776154499 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036582 | ATGCAGGTGAAATTA[C/T]ACGATGTCTGGGGTT | 26133 |
rs776196024 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025433 | CTGCCTTGGCCTCCC[A/G]AAGTATTGGGATTAC | 26133 |
rs776204326 | snp | C/G | 5.52135e-05 | 0.00525392 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002201 | TGACGGCCTGACCCC[C/G]TGGGCTCTAAAGAGG | 26133 |
rs776216969 | in-del | -/CTCTGT | 1.65483e-05 | 0.00287644 | cds-indel, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049989 | ACGCTTTGTAACTCC[-/CTCTGT]CTGTCACAAGAAGAA | 26133 |
rs776291195 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008392 | CTAGGGAATTCATGG[C/T]AGGGCCCGTATCCTA | 26133 |
rs776292939 | snp | A/G | 1.64808e-05 | 0.00287057 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044509 | GGAGACTTTACCTTG[A/G]TTGATTTCAGCTGCA | 26133 |
rs776308875 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003168 | TCAGTGAAGTCCCTG[C/T]CTATGTCCATGTAGG | 26133 |
rs776314253 | snp | A/C | 0.00451659 | 0.0473064 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069462 | TAGTAACCAACACAG[A/C]CCAGACACTAAAGCA | 26133 |
rs776336698 | snp | A/G | 1.67581e-05 | 0.00289461 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006394 | CCAGGTGAACTTCTG[A/G]ACAACCCAGCACACT | 26133 |
rs776338352 | in-del | -/CACT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019691 | TCAAAAAAGTAATAG[-/CACT]CACTCAATGCATAAA | 26133 |
rs776371506 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031633 | AATGATTTACATTAC[A/G]TTTGGGAGATTTTCA | 26133 |
rs776390979 | in-del | -/TAAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091589 | TGAAAAAGCTGTCTT[-/TAAA]TAAAGCTAATGTTTT | 26133 |
rs776430220 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014179 | GGTGGATGAAAATTA[C/T]AATAGGATAAAACAG | 26133 |
rs776437789 | snp | G/T | 1.65255e-05 | 0.00287445 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035266 | TTTCGAGTCGCCAGT[G/T]TGCAAAGCCGCTCAA | 26133 |
rs776476593 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030971 | GCTGCTTAATTTCCA[C/G]ATGTTTGTCTGTTAC | 26133 |
rs776493199 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005518 | GATTTTCACCTTATT[A/G]AAGTGTTGAACAAGG | 26133 |
rs776523161 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058852 | TGCCACCACTCCTGG[C/T]TACTTTGTGTATTTT | 26133 |
rs776532120 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078793 | GGAAAAGGCCAGGCA[C/T]GGTGGCTCACACCTG | 26133 |
rs776556225 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010042 | GTGACATGAATACAA[C/T]GCCTGGCACACAGGA | 26133 |
rs776559864 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045447 | GTCATCATAGCTTAC[C/T]GCAGACTCAAACTCC | 26133 |
rs776568172 | snp | C/T | 1.6504e-05 | 0.00287258 | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35008695 | CTGGCTCCTTCTTCA[C/T]GACCTGCAGCAGACG | 26133 |
rs776587265 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064088 | TTTTCCAAAAAAGTC[C/T]AATTTTCACTTAAAG | 26133 |
rs776620007 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080337 | AAACCCCACCTCTAC[-/A]AAAAAAAAAAAAAAT | 26133 |
rs776629943 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028791 | CCAGCTGTTGTTTTT[C/G]AACTACTGCTCTCTT | 26133 |
rs776671665 | in-del | -/T/TTA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076255 | TCATCTGAAGCCTTC[-/T/TTA]TCTCAACTCATCAAA | 26133 |
rs776692708 | snp | C/T | 8.32189e-05 | 0.00645 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010140 | AGCCCCCGGGGAACG[C/T]GGGCAGCCGGGATGG | 26133 |
rs776695504 | in-del | -/TTCCT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051966 | AGGCCATCACAATCC[-/TTCCT]TTCCTCTATATCACA | 26133 |
rs776701773 | snp | G/T | 0.0011009 | 0.0234358 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057477 | ACCGTATCGGCAGGT[G/T]GGAAAACAAGGACCA | 26133 |
rs776717780 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030951 | TATTTCTCATAAGTC[A/G]GTATGCTGCTTAATT | 26133 |
rs776745557 | snp | C/T | 1.64925e-05 | 0.00287158 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004420 | GGAAGTGGTTTCCAA[C/T]CGACCTTCCCTGCTG | 26133 |
rs776763507 | snp | C/G | 1.66219e-05 | 0.00288283 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006579 | GTAAAGGATGTGCTG[C/G]GTGAGGAGGGACAGG | 26133 |
rs776784190 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090887 | GAAATGAGTCTTGAA[C/G]CATAACTCAAAAGCT | 26133 |
rs776789974 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043116 | TTTCTATAGCAGTAC[A/C]TAGAGATCTTCATTT | 26133 |
rs776806513 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061725 | GCAAATGGATCAAAG[A/T]TCTAAATGTAAGATA | 26133 |
rs776807307 | snp | C/G | 1.68352e-05 | 0.00290126 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001954 | TGCCCCCAGGAGCAG[C/G]AGGCCAACACCAACC | 26133 |
rs776870625 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022714 | ACTCTTTAAAGTATC[A/C]AGACAGAAGACCCTA | 26133 |
rs776885273 | snp | A/G | 1.75585e-05 | 0.00296293 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004491 | GTGGATGATGTTGAT[A/G]AGGCGGAAGAGGAAG | 26133 |
rs776886242 | snp | A/C | 1.66131e-05 | 0.00288206 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021368 | GAGGCTGACACAGCC[A/C]CCGGAGACAGGATTG | 26133 |
rs776890664 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028890 | GTTGTATCTTCTTGA[C/T]GGTTTCACCCTGTTA | 26133 |
rs776972875 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091987 | ACCGTGACGCTCTAC[A/G]CTAGCAAACCAGATA | 26133 |
rs777004966 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048850 | CTGGAATAACAACAA[A/C]GCCTTTTTATCAAAG | 26133 |
rs777028037 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075408 | TATCGGTTGTTCCTT[C/T]CCATGTTTAGCGCTT | 26133 |
rs777066750 | snp | A/G | 1.6516e-05 | 0.00287362 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003466 | GCTGCTGCCAGAAGC[A/G]CAGCAGGTTGTGGAA | 26133 |
rs777071624 | in-del | -/AG | 3.31197e-05 | 0.00406925 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007524 | GGGAGACGGAACCCA[-/AG]AGACACTGGCTGCTC | 26133 |
rs777081730 | snp | A/G | 1.65833e-05 | 0.00287948 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007514 | CGTGGGCTGGGGGGA[A/G]ACGGAACCCAAGACA | 26133 |
rs777103303 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062580 | AAGAAGCCAGTCACA[A/G]AAGACCACGTATTGT | 26133 |
rs777108609 | in-del | -/AGA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039793 | CTCTTCTAAATCGAC[-/AGA]AGAACAACTGGTAGT | 26133 |
rs777134122 | in-del | -/AT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084690 | TATATGTTTATATGC[-/AT]ATATGTGTATATGTA | 26133 |
rs777135091 | snp | A/G | 0.000102529 | 0.00715919 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003373 | AGGCCCTGGGTCCGC[A/G]GCCCACCCATCACCC | 26133 |
rs777225022 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084396 | ACAAATTTAAAAACA[A/G]TAAAATAAATTAAAG | 26133 |
rs777231055 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020820 | TCCTAAGCAGACACA[A/G]CTCTGGGCTCTGTCC | 26133 |
rs777242983 | snp | C/T | 0.00355513 | 0.042011 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092683 | CAGAATGTTACCAGG[C/T]CGCGGCCGGCCGCCC | 26133 |
rs777256108 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050151 | CTGTGGGAAACGCTC[A/G]TTAACTCCCCAGCTA | 26133 |
rs777290484 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078424 | ATATCATTGAGAGTG[A/G]ACTTAGACTCGTCGT | 26133 |
rs777329241 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072112 | CTGTTCATATCCTTC[A/G]CCCAGTTTTTGATGG | 26133 |
rs777330068 | snp | C/T | 1.65026e-05 | 0.00287246 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016181 | TTAAGACAAATGTGC[C/T]TGAAAAATCTAGCAA | 26133 |
rs777341223 | snp | A/T | 1.65578e-05 | 0.00287726 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049990 | CGCTTTGTAACTCCC[A/T]CTGTCTGTCACAAGA | 26133 |
rs777345745 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046144 | TAATTCCAAAACATT[A/T]AAATTAAGTTCAATA | 26133 |
rs777369510 | snp | C/T | 3.32662e-05 | 0.00407824 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003524 | CTTGCTGTGCTCCAT[C/T]CGCTGCAGCAGCCGC | 26133 |
rs777371976 | snp | A/G | 3.80279e-05 | 0.00436033 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092762 | GCTCCAGACCCAGCC[A/G]CTACCGGCGCCGCCG | 26133 |
rs777389084 | in-del | -/CAGA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004714 | GAAAGCTGACTGTGG[-/CAGA]AAGAAGGACCTCCAG | 26133 |
rs777406312 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024996 | GTATATACCTGGGAG[G/T]AGGATTTCTAGGCCC | 26133 |
rs777427427 | snp | A/G | 0.00021736 | 0.0104227 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092804 | CGTCGGACAAACAGG[A/G]AGCAAGCGGCCTCGG | 26133 |
rs777517251 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038873 | AGTTTGGGAGTTCAA[C/G]ACCAGCCTGGCCAAT | 26133 |
rs777518049 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085527 | CTGAGGTGGGAGGAT[C/T]GCTTGAGCCCAGGAG | 26133 |
rs777564354 | snp | C/T | 1.67781e-05 | 0.00289634 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006384 | GACCAGGACTCCAGG[C/T]GAACTTCTGGACAAC | 26133 |
rs777617404 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006484 | TTGAATGCATCAACG[C/T]TGAACTTCATCAGCT | 26133 |
rs777638311 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014075 | GGGGGAAACTAACCC[C/T]ACTGACCTCAAGTGA | 26133 |
rs777644836 | snp | C/G | 1.65482e-05 | 0.00287643 | synonymous-codon, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021211 | TCGCTGACGCCCCAT[C/G]AGCAGCACGCAGAGG | 26133 |
rs777644972 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090867 | AGTTTCCTCATCCAT[A/T]TTAAGAAATGAGTCT | 26133 |
rs777662631 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006587 | TGTGCTGGGTGAGGA[A/G]GGACAGGGTGAAGGT | 26133 |
rs777710962 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069957 | AAAAAAAAATAAAAA[C/G]CCTGACAGACTTCGC | 26133 |
rs777726341 | in-del | -/TGTG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086434 | AATGAATGGCATATG[-/TGTG]TGTGTGTGTGTGTGT | 26133 |
rs777741923 | snp | A/G | 0.000214329 | 0.0103498 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003228 | GGTGACTGCCGGTCC[A/G]GGTTCAACAGGATGG | 26133 |
rs777759466 | snp | A/G | 6.59924e-05 | 0.00574385 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078041 | CCAAGGTCCTTAAGA[A/G]TTACCTTGAGGATGT | 26133 |
rs777790575 | in-del | -/T | 1.68057e-05 | 0.00289872 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078210 | GAACATATTATTGTA[-/T]TATTGATGATAATAG | 26133 |
rs777811744 | snp | A/G | 1.65723e-05 | 0.00287852 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003318 | CTGGGGGGCGCCTGG[A/G]GGACCCAGGTCAAGC | 26133 |
rs777903024 | snp | G/T | 1.65165e-05 | 0.00287367 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044485 | ATAATCTCAAAATTC[G/T]GAGAACTTGGAGACT | 26133 |
rs777908205 | in-del | -/C | 1.66338e-05 | 0.00288386 | downstream-variant-500B, frameshift-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002063 | AGCTGCGGGCACGGA[-/C]CCGGGACGCCCTGGG | 26133 |
rs777913097 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058367 | TACATTCTACTCAAG[C/T]GCACATGAAACATTC | 26133 |
rs777936305 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032573 | GCCTCCCAGGTTCTC[A/G]CCATTCTCCTGCCTC | 26133 |
rs777945759 | in-del | -/AA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018604 | CTGTCTCAAAAAAAG[-/AA]AAAAAAAAAAAAAAA | 26133 |
rs777973975 | snp | C/T | 3.52057e-05 | 0.00419543 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004542 | GGATATGTAGGCGAG[C/T]AGGCGGCATTCAGAC | 26133 |
rs777978402 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033561 | ACTGCTCCAAAGTCT[A/T]ATTCAATTAAATTCA | 26133 |
rs778015599 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032674 | AGACGGGGTTTCACC[A/G]TCTTAGCCAGGATAG | 26133 |
rs778021063 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067317 | AAGCAAAACGCCATC[C/T]CAGTACTTTTTTTTT | 26133 |
rs778028750 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047865 | GTTATAGGTAACCCA[C/T]GGCAAAATACTGATG | 26133 |
rs778028972 | snp | A/C | 1.64779e-05 | 0.00287031 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044641 | AATCCGGCAGAAATT[A/C]GCGAGCTGCTGCTGA | 26133 |
rs778072539 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043537 | CAGGCGTTAAGCCAC[C/T]GTGCCTGGCCTCAGT | 26133 |
rs778074347 | snp | C/T | 1.66283e-05 | 0.00288338 | downstream-variant-500B, synonymous-codon | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001980 | CAACCTGGCCAAGTA[C/T]CGCAAGGCCCAGCAC | 26133 |
rs778089035 | snp | C/T | | | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35008684 | AGACGACTCTGCTGG[C/T]TCCTTCTTCATGACC | 26133 |
rs778109006 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057703 | TTCCAGGAGGCAGTT[-/A]AGGTTCAGTAAGGCT | 26133 |
rs778112956 | snp | C/T | 1.64882e-05 | 0.00287121 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057529 | TTTTCAGTTTCTGTC[C/T]CCGGATAGAGATCGT | 26133 |
rs778122051 | snp | A/C/G | 1.79528e-05 | 0.00299601 | missense, synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004479 | CAGCGTCTGCACGTG[A/C/G]ATGATGTTGATGAGG | 26133 |
rs778125704 | snp | A/G | 1.65151e-05 | 0.00287355 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021338 | TCAGAAGCCCCTGGA[A/G]GAGGGAACACAATGG | 26133 |
rs778127209 | snp | G/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056190 | ATTGATTTATTTAAC[G/T]ACTTCAGAGCAGGGT | 26133 |
rs778155092 | snp | G/T | | | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012698 | CCACGCTGTCCACTC[G/T]TGCTTTAGAGGGGCA | 26133 |
rs778161091 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024825 | GAGAGAGACCGTCTC[-/A]AAAAAAAAAAAAAAA | 26133 |
rs778181669 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042700 | TATGAATTATCTACA[A/C]TCTTATGACCAAAAT | 26133 |
rs778204518 | snp | C/T | 1.6534e-05 | 0.00287519 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012961 | GAGATCGAGGCCTTC[C/T]GAAGACAGCCCAACA | 26133 |
rs778210215 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023526 | GAAAAATTTACTGGA[G/T]AAATTTTTAATTTAA | 26133 |
rs778224888 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091794 | TAGTATGCACCAGAA[A/G]TGCACTAATGCTTTA | 26133 |
rs778236066 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087174 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAAAA | 26133 |
rs778236322 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074274 | CTCTATATCCTTCAG[C/T]ACTGCTCTGATCTTA | 26133 |
rs778237498 | snp | C/G | 1.65897e-05 | 0.00288003 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069274 | GTAGTAACAGCAGTA[C/G]TAATAATAAATAGCT | 26133 |
rs778290875 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080823 | TTTTTTTTTTTACCC[A/T]TTTATCTCCTTAGTT | 26133 |
rs778338561 | in-del | -/TGTGTGTGTGTG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086508 | ATATGTGTATATATA[-/TGTGTGTGTGTG]TATATATGTGTGTGT | 26133 |
rs778358835 | snp | A/G | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008636 | CTGCAGCCCCGCAGA[A/G]TCGGCAGGTACTTTT | 26133 |
rs778379583 | in-del | -/CTAAACTG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083903 | TAGTAAGCAGCTAAA[-/CTAAACTG]CTAAACTGCTAAACT | 26133 |
rs778379965 | snp | A/G | 1.71208e-05 | 0.00292577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035076 | AGAATGGTCCCAGGC[A/G]CCCAAGGAAAAGCTC | 26133 |
rs778397268 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061458 | AAATCTCAGCTGGCT[A/T]CTTTGCAGAAATTGG | 26133 |
rs778415523 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069704 | CCAGCACTTTGGGAG[A/G]CTAAGGTGGGCGGAT | 26133 |
rs778422159 | snp | G/T | 9.49307e-05 | 0.00688886 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092746 | CCGTCTCCCTCGGCC[G/T]GCTCCAGACCCAGCC | 26133 |
rs778439856 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044166 | GAAGATGAGGTGGGT[-/G]GATCACTTGAGACCA | 26133 |
rs778490070 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077228 | CAGGTGAGGCAATGC[C/T]CCGCCCTGCTTCAGC | 26133 |
rs778502585 | snp | C/G | 2.28809e-05 | 0.0033823 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092642 | ACCAGGCCCCGGCCG[C/G]TCAGCTGGCCCTGCC | 26133 |
rs778506654 | snp | A/C | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007621 | GGAGGAAACTCTCCA[A/C]AGCCCGAGCTTGCCA | 26133 |
rs778516528 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052256 | GGTATATAACACCAC[A/G]TCCAGCCAGTTTTTT | 26133 |
rs778532479 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008062 | GCTGGCCTAGGGAAG[C/T]AGTGGTTGATGCTGA | 26133 |
rs778537782 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028618 | CTGGAGAATGTTCAT[A/G]TGCACTTGAGAAGAA | 26133 |
rs778569446 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019792 | GGCTATCACCGTGGG[A/G]TCTCATCCAGTGTCC | 26133 |
rs778576877 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043993 | TGTGGTTCTGAGCCC[A/G]TTAACAAATCTAATG | 26133 |
rs778583111 | snp | C/T | 1.65127e-05 | 0.00287334 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35049975 | TTCTTTTCTGCCAAA[C/T]GCTTTGTAACTCCCT | 26133 |
rs778585467 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019123 | GAGGCCTCTTTAAGG[A/C]GGAAGCCTTCTGTGA | 26133 |
rs778588915 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027805 | CTTATATTGTTTATA[A/G]TATTCCCTTAGAGTC | 26133 |
rs778593392 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062416 | AATAATAGCCAAAAG[C/T]GGGAACAACCCAAAT | 26133 |
rs778627815 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008318 | TTTCCTTTGCTGCTA[C/T]AGCTCCTGGGCCAAC | 26133 |
rs778639752 | snp | C/T | 1.65072e-05 | 0.00287286 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003443 | GTCCTTGTCCTTGTG[C/T]AGGTAGTGCTGCTGC | 26133 |
rs778660735 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051007 | CCTATCTCTAAAAAG[A/G]AAGAAACTGCAGTAC | 26133 |
rs778664893 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045804 | CTTGGCCTCCCAAAG[G/T]GCTGGGATTACAAGC | 26133 |
rs778734979 | in-del | -/ACTC | | | | | GRCh38.p7 | 20:35024293 | CAAAAGCAGCCTTGT[-/ACTC]ACTACCAGTCACTTC | 26133 |
rs778762757 | snp | C/T | 1.6566e-05 | 0.00287797 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003509 | GAAGCCGGGGTACTT[C/T]TTGCTGTGCTCCATC | 26133 |
rs778774213 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006948 | ATTCAAGTAAATGAA[A/G]GACAGAATTTAAAAG | 26133 |
rs778782050 | snp | A/G | 1.65389e-05 | 0.00287562 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005829 | ACCAAGCTCACAGCA[A/G]GCAGTGGGCTGCTGG | 26133 |
rs778795335 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084021 | ATACAGAAAGCAGGC[C/T]GGGCGCGGTGGCTCA | 26133 |
rs778834242 | in-del | -/CTC | 1.64982e-05 | 0.00287208 | cds-indel, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021319 | GTGAGGCAGGCCATT[-/CTC]CTCAGAAGCCCCTGG | 26133 |
rs778834984 | snp | G/T | 0.000115702 | 0.00760509 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003132 | CCAGCAGCCTCCCGA[G/T]GCCTGGCCCAAGGTC | 26133 |
rs778852025 | snp | A/G | 6.59011e-05 | 0.00573988 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35005719 | CCACCTGGTTTTCAA[A/G]TCGGTCCAGGGACAG | 26133 |
rs778885158 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086579 | TGTGTGTGTGTGTAT[A/G]TATATATGAATAAGA | 26133 |
rs778889308 | in-del | -/A | 1.66856e-05 | 0.00288834 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069424 | TTTCCTAGTTTTTTT[-/A]AAAAAAAGTACATAC | 26133 |
rs778956293 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069162 | CTTCAACATGTAAAT[A/G]CCGCTAAGCTTCTAA | 26133 |
rs778980539 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037486 | TCATAGCAGCACTAT[A/T]CCCAACAGCCAAAAG | 26133 |
rs778987302 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085259 | TCCAAATATTTGACT[G/T]CACAAGCAATTTCTT | 26133 |
rs778993000 | in-del | -/TG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084642 | ATATGTGTATATGTA[-/TG]TGTATGTTTATATGC | 26133 |
rs779041450 | snp | C/T | 4.94238e-05 | 0.00497086 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044613 | TATCCATCTCTGAAA[C/T]GGTGACAGCCAGAAT | 26133 |
rs779084968 | in-del | -/GACATGGCG | 1.65932e-05 | 0.00288034 | downstream-variant-500B, cds-indel | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002023 | GCGGAGGAGCGGGCA[-/GACATGGCG]GAAACCCAGGCCAAC | 26133 |
rs779091416 | snp | A/C | 8.33424e-05 | 0.00645478 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069425 | TTCCTAGTTTTTTTA[A/C]AAAAAAGTACATACA | 26133 |
rs779097736 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005297 | CCACAAGCCCTCTCC[C/T]AGGAAAAAAAGGAAA | 26133 |
rs779102355 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079643 | TAACCAGGCTTATCA[A/T]GAAAAAAAGACAGAA | 26133 |
rs779140362 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080505 | GACCTTGTCTCAAAA[C/G]AGAAACAAAAACAAA | 26133 |
rs779153521 | snp | C/T | 3.29723e-05 | 0.00406018 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003218 | GAGAGCAGAGGGTGA[C/T]TGCCGGTCCGGGTTC | 26133 |
rs779179939 | snp | A/G | 1.65531e-05 | 0.00287686 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044478 | CAGAGCTATAATCTC[A/G]AAATTCTGAGAACTT | 26133 |
rs779217381 | snp | A/G | 1.65946e-05 | 0.00288046 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010155 | TGGGCAGCCGGGATG[A/G]GCTGAGGGAAAAGCT | 26133 |
rs779234207 | in-del | -/TA | 1.64898e-05 | 0.00287135 | frameshift-variant, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003170 | AGTGAAGTCCCTGTC[-/TA]TGTCCATGTAGGGCT | 26133 |
rs779264372 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021508 | TGCAAAACTCCCTCC[A/C]CAATCCCAGGAGCCA | 26133 |
rs779270593 | snp | C/G | 2.65389e-05 | 0.00364263 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003655 | GTCAGGGGCTGGTGG[C/G]AGCCCCAGTGGCCCC | 26133 |
rs779294315 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066093 | TGAAGTATAACGTGA[C/T]ACCGCATAAAGAGTA | 26133 |
rs779312334 | in-del | -/GAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059758 | GAAGAAGAAGAAGAC[-/GAA]GAAGACGACGAAGAC | 26133 |
rs779325255 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054058 | AATTCCTGGCTATAC[A/G]TTATGTCCCCACCTT | 26133 |
rs779326038 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091716 | CTCACTCAAAAATAA[A/C]AATAATCATATGTTG | 26133 |
rs779328851 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005949 | GCTCAGATAAGCTGA[A/G]GGACCTCCCCTCACC | 26133 |
rs779352605 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055223 | TACAAGCCCATTTGC[A/G]TATTGCTTTTGGTTT | 26133 |
rs779453856 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011251 | AATAGAGCAAGATTC[C/T]GTCTTGAAAAAAAGA | 26133 |
rs779482365 | in-del | -/AT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091724 | AAAATAACAATAATC[-/AT]ATGTTGGGCACCTGT | 26133 |
rs779484709 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089966 | CTCTACCAAAGATAC[A/G]AAAATTAATGGGGTG | 26133 |
rs779519306 | snp | A/G | 6.65347e-05 | 0.0057674 | downstream-variant-500B, missense | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002060 | ACAAGCTGCGGGCAC[A/G]GACCCGGGACGCCCT | 26133 |
rs779528256 | snp | C/T | 1.64942e-05 | 0.00287173 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057514 | AATAGGTATACTTAC[C/T]TTTCAGTTTCTGTCC | 26133 |
rs779569194 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011133 | GGCGTGGTGGCACAC[A/G]CCTATAATCCTAGCT | 26133 |
rs779607801 | in-del | -/TA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051033 | AGTACTGCTATAGCT[-/TA]CACACACACACACAC | 26133 |
rs779611520 | in-del | -/AT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082784 | TAATTATTTGATAAC[-/AT]AAAGGAGAATAATGA | 26133 |
rs779615898 | snp | C/T | 1.65233e-05 | 0.00287426 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021230 | AGCACGCAGAGGACA[C/T]AGAGCACTTCCAGTT | 26133 |
rs779674703 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061277 | AAAACACTTAGAAAT[A/C]AGTTTAACAAGTGCA | 26133 |
rs779677194 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072378 | ATGGCCTGAATAGTA[C/T]TGCCTAGATTTTCTT | 26133 |
rs779679288 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091482 | TTACACTGTGAAAAG[C/T]CTCACTCCCATTTTC | 26133 |
rs779701003 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048129 | TGGACCATTTCTTTC[C/T]TGTCTGTGAAATGCT | 26133 |
rs779706402 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028081 | CAATGACTTAAGGTA[C/G]ACGTTTAGGCAATTT | 26133 |
rs779727567 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028534 | GGGATTTGAGGACAT[A/G]CTTTTGTACAGTTTT | 26133 |
rs779777585 | snp | C/T | 0.000208225 | 0.0102014 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092624 | CGTACCTGCACCGCC[C/T]GGACCAGGCCCCGGC | 26133 |
rs779781535 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006138 | ACACACCAGGCCCAG[G/T]CCCTCCCTACAGCGG | 26133 |
rs779832508 | snp | A/C | 0.000158592 | 0.00890341 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092741 | GCCGACCGTCTCCCT[A/C]GGCCGGCTCCAGACC | 26133 |
rs779832558 | snp | C/T | 5.07267e-05 | 0.00503595 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049832 | TGGTCTGAGACACCC[C/T]TCCCCATCTGGTCAG | 26133 |
rs779840599 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017029 | CATAATCCCTTTAAA[C/T]CAGCAATTCCACTTT | 26133 |
rs779876351 | snp | C/T | 3.29984e-05 | 0.00406179 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003431 | TAGGCAGGTGCTGTC[C/T]TTGTCCTTGTGCAGG | 26133 |
rs779897505 | snp | A/G | 1.65261e-05 | 0.0028745 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015976 | CTCCAAGCCAGTGAG[A/G]CCCCATCTGTCCCCG | 26133 |
rs779931531 | in-del | -/C | 2.06132e-05 | 0.00321033 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004455 | TCTGCCGGGGCCTCT[-/C]ACCTGGGTCAGCGTC | 26133 |
rs779974768 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049438 | CAAACATTACTACCA[A/C]GGAGAACATATCCTA | 26133 |
rs779991192 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019642 | CAGAAGCTGTCCCTA[C/T]AATTATTTCACATAT | 26133 |
rs780009911 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058164 | TAGAGCCCAAAAATA[C/T]ATGAAACAAAAGCTG | 26133 |
rs780011734 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036403 | ACTTTTCAATAAATA[C/T]CTTTTTGAATCCGCA | 26133 |
rs780011915 | snp | A/C/G | 8.24458e-05 | 0.00642007 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069311 | ATCAACACCTCCAAA[A/C/G]AAGTCAAAAATGTAA | 26133 |
rs780014242 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006831 | GCTGAAGCCTGTGAC[C/T]TGCTCTGTGGTCACC | 26133 |
rs780020090 | snp | A/T | 1.6492e-05 | 0.00287154 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005690 | ACAGCCTGCCTTTCA[A/T]GTACCTTTCATATCC | 26133 |
rs780027923 | snp | A/G | 8.2558e-05 | 0.00642434 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35013010 | CTCTTGTACTTACTC[A/G]TGGTGGTCACTGAAG | 26133 |
rs780095532 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043714 | ACTAAGAGATTAACA[A/G]TAACTAATGATAAAA | 26133 |
rs780141246 | snp | C/T | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056652 | ATCTCTGGCTTTTAA[C/T]ACCAGAGTAAAGTGC | 26133 |
rs780180605 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078491 | GTATTTTTACAAGAA[G/T]AATAATTGATATGCT | 26133 |
rs780185627 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045072 | ATTCTTGCTACAGAT[C/T]TGCTTTTTTAAAAAA | 26133 |
rs780221911 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054940 | TGCAGACCTGGTAGG[C/G]GAGATAAACAGAGCC | 26133 |
rs780242121 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069830 | CCTGTAATCCCAGCT[A/G]CTCAGGAATTTGAAG | 26133 |
rs780257586 | snp | A/G | 1.65244e-05 | 0.00287436 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005819 | CTATACAGAAACCAA[A/G]CTCACAGCAGGCAGT | 26133 |
rs780275547 | in-del | -/CA | 1.74042e-05 | 0.00294988 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35001907 | CCAGAATAAGCATCT[-/CA]GTCACCCAAGCGGAA | 26133 |
rs780306372 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077603 | TAGCATAATGTCTCC[A/G]TGCTCTTTCCACTCA | 26133 |
rs780318434 | snp | A/G | 3.32149e-05 | 0.00407509 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044465 | TTAGTAAGGGCCTCA[A/G]AGCTATAATCTCAAA | 26133 |
rs780321045 | snp | C/T | 1.66269e-05 | 0.00288326 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069418 | GAGAAATTTCCTAGT[C/T]TTTTTAAAAAAAAGT | 26133 |
rs780364988 | snp | C/G | 1.77068e-05 | 0.00297541 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002156 | GTAGTACTGCTCACT[C/G]AGCTATCCCTTTCTC | 26133 |
rs780370547 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032303 | GTGCTGGGATTACAG[C/G]TGTGAGCCACCACAC | 26133 |
rs780400709 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074719 | TTGGAATAAGTGCGA[C/T]GTGGCGCTGAGAAGA | 26133 |
rs780419253 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079485 | CCTTAGTAAACTACA[C/G]AAAGAGCAGTTTAAG | 26133 |
rs780419985 | snp | C/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005043 | CTGCTCCGTCCACTA[C/G]TGTCGGAGCAACTGC | 26133 |
rs780431926 | snp | C/T | 0.00137103 | 0.0261464 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008652 | TCGGCAGGTACTTTT[C/T]CCCAGACTCACCTGA | 26133 |
rs780471466 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004262 | CAGCCTGTGACCTGA[A/G]GGCACTTGCGAGCCC | 26133 |
rs780481547 | snp | C/G | 1.65444e-05 | 0.00287609 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003128 | TGGCCCAGCAGCCTC[C/G]CGAGGCCTGGCCCAA | 26133 |
rs780484855 | snp | A/G | 1.67407e-05 | 0.00289311 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003535 | CCATCCGCTGCAGCA[A/G]CCGCAGGTACAGGGG | 26133 |
rs780492785 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046259 | TTTTATTAAGAATGA[C/T]AATTTTATGGAATGC | 26133 |
rs780534738 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089368 | AGCAGCTGGGACTAC[-/A]GGCATGCATTTCCAC | 26133 |
rs780587897 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050072 | CATCCTTTACAGACA[C/T]TGAAAAGCAGTTTCA | 26133 |
rs780604791 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051434 | CACCTCAGCCTCCTG[A/C]ATCACTGGGACTACA | 26133 |
rs780643282 | in-del | -/AGA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072268 | TTTCTTTTGCTATGC[-/AGA]AGCTCTTTAGTTTAA | 26133 |
rs780675696 | snp | A/C/G | 0.000153494 | 0.00875938 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092810 | ACAAACAGGAAGCAA[A/C/G]CGGCCTCGGGGCCGC | 26133 |
rs780696459 | snp | A/G | 3.30677e-05 | 0.00406605 | synonymous-codon, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021220 | CCCCATCAGCAGCAC[A/G]CAGAGGACATAGAGC | 26133 |
rs780731096 | in-del | -/GAT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059865 | TGAAGATGAAGAAAA[-/GAT]GAAGAAAAGACGAAG | 26133 |
rs780738246 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052678 | TGTGTTTTTAGTACA[A/G]ACGGGGTTTCACCAT | 26133 |
rs780752373 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049508 | TGGTAAGAGAATGGA[A/G]TCACTGCATAGCATA | 26133 |
rs780756218 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025463 | CAGGTGCCAGCCACT[A/G]TGCCTGGCCTCACTG | 26133 |
rs780757682 | in-del | -/AT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084562 | TATATGTTTATATGC[-/AT]ATATGTGTATATGTA | 26133 |
rs780768020 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090994 | TCTGCCTGTCTCTAC[A/G]CACCCAGCTCGGTAA | 26133 |
rs780784877 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089721 | AGGTGTGGTGGCACA[C/T]GACTGTAATCCCAGC | 26133 |
rs780810733 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064656 | AAAAGAAAGAAGTCT[C/T]ATGACTTGAGGCAAC | 26133 |
rs780814470 | snp | A/G | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35009047 | CAAAAGTGTGTTGAA[A/G]CAGGTCATGCCAGTC | 26133 |
rs780830060 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039402 | AAAAAATTCACTGGA[A/C]CAATCATACCTAGCA | 26133 |
rs780855707 | snp | A/C | 3.31378e-05 | 0.00407036 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055079 | TCTCAATGAAAAGAT[A/C]GTACAACAGTTACCA | 26133 |
rs780930887 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027395 | GCATAAATCCATTTG[A/G]TCATGGTATACAATC | 26133 |
rs780940591 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070213 | ATTGTTGACAGATAA[A/G]TGATTCTTGTTACTT | 26133 |
rs780983923 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026470 | ATCTTCCTGCCTCAG[C/T]CTCCCAAAGTGCTGG | 26133 |
rs780985971 | in-del | -/AAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059836 | GAAGAAGATGAAGAC[-/AAA]GAAGACGAAGATGAA | 26133 |
rs780988777 | snp | C/T | 1.70017e-05 | 0.00291558 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078220 | TTGTATTATTGATGA[C/T]AATAGCTGATACGGC | 26133 |
rs780990083 | snp | C/G | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003242 | CGGGTTCAACAGGAT[C/G]GACACTGTCTCCTTC | 26133 |
rs781001817 | snp | C/T | 1.66308e-05 | 0.00288359 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069253 | AAATTCCCAAACCAT[C/T]AAGCAGTAGTAACAG | 26133 |
rs781043770 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009909 | GGCGGTGGGGCAGTG[C/T]GGAGCACACATGACT | 26133 |
rs781044869 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078144 | TCCACTTGGATTGTT[C/T]GTCCCTCTCCGTCAA | 26133 |
rs781065282 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066266 | ATGTGCTACCACAAT[C/T]GGCTAATTTTTTTAA | 26133 |
rs781066642 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086028 | AAGTGATCCTCCCAC[C/T]TCAGCCCTGCCCCCT | 26133 |
rs781120142 | snp | C/T | 1.66045e-05 | 0.00288132 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003333 | AGGACCCAGGTCAAG[C/T]CCAGCACCGGGACAC | 26133 |
rs781160750 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016850 | AGGAGTCCTACAAAT[A/G]TCTCTGATTTTTCAC | 26133 |
rs781160961 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039241 | GGAGCTAGTCTTCCC[C/T]ATTCCTGCACACTCA | 26133 |
rs781214058 | in-del | -/T | 1.65162e-05 | 0.00287365 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015984 | CAGTGAGGCCCCATC[-/T]GTCCCCGGGGGTCTC | 26133 |
rs781256082 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055582 | GCACAATCACAGCTC[A/G]CTGTAGTCTCGAACT | 26133 |
rs781297898 | in-del | -/ACACACAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068973 | CACACACACACACAC[-/ACACACAA]AAAAAACAAAACATC | 26133 |
rs781329922 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35010249 | AGAGATGGCACTGAG[C/T]TCATTCAGCTCCTGG | 26133 |
rs781331362 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012829 | AGTGCCTGCCATAAG[A/G]AAGTCTGGAAAGACG | 26133 |
rs781378137 | snp | G/T | 3.49864e-05 | 0.00418234 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002145 | GGGGCTGACAGGTAG[G/T]ACTGCTCACTCAGCT | 26133 |
rs781411101 | snp | C/G | | | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003185 | TATGTCCATGTAGGG[C/G]TCCTCAATGTAGCTA | 26133 |
rs781435084 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033006 | TCAGGAGTTCAATAC[C/T]AGCAACTAGGTAAAA | 26133 |
rs781441339 | snp | A/G/T | 0.000132108 | 0.00812637 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069297 | AAATAGCTACTTACA[A/G/T]CAACACCTCCAAACA | 26133 |
rs781451566 | snp | A/C | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056413 | GTGCACCAACAAATA[A/C]TTACAATATGCTACT | 26133 |
rs781456452 | snp | A/C | 1.65162e-05 | 0.00287365 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012997 | CCTTGCAGGGACACT[A/C]TTGTACTTACTCGTG | 26133 |
rs781511521 | snp | C/G | 1.65266e-05 | 0.00287455 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013111 | GACCACAGCCACAAG[C/G]TTCCAAAATAACACA | 26133 |
rs781511577 | snp | C/T | 3.73755e-05 | 0.00432277 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004565 | ATTCAGACAGTACCT[C/T]GGCAACTGTGGAGGG | 26133 |
rs781530791 | snp | C/G | 6.66844e-05 | 0.00577389 | downstream-variant-500B, synonymous-codon | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002079 | CCGGGACGCCCTGGG[C/G]CCCAAGGTGAGGAGT | 26133 |
rs781546692 | in-del | -/CCTGTGACTGTGACCCACAACAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011615 | TATATAAAATCCAGG[-/CCTGTGACTGTGACCCACAACAC]CCTGTGACTGTGACC | 26133 |
rs781563273 | snp | A/G | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094528 | GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGT | 26133 |
rs781569322 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003986 | TAGCCTGCGCGCCTC[A/G]GTGGGGAAAGAGTTC | 26133 |
rs781617589 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031188 | ATCCTTGGGCATGAT[A/G]AGCCATTTTTCTCTT | 26133 |
rs781624335 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024631 | GAGTTTGAGACCAGC[C/T]TGGGCAACACAGCAA | 26133 |
rs781630496 | snp | C/G | 1.65049e-05 | 0.00287266 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005682 | TTGCCTTGACAGCCT[C/G]CCTTTCATGTACCTT | 26133 |
rs781704221 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049257 | TTTCGATCATAGCTG[-/T]TTTTTTTTTTTTTTA | 26133 |
rs781732878 | in-del | -/AAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050722 | TAACTCAAAAAAAAA[-/AAC]AAAACAAAAAAACCA | 26133 |
rs781754960 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019245 | CCAGGAAATGCTGAC[C/T]GTGCAAATGAGAACA | 26133 |
rs781777850 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074399 | CCGGCTTTCTCTTGT[A/G]TGCATTTAGTGCTAT | 26133 |
rs796068634 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035185 | AGCACCAAAGCATTG[C/T]CTAGCCATGTGTACC | 26133 |
rs796079689 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068964 | ACACACACACACACA[-/C]ACACACACACACACA | 26133 |
rs796095085 | in-del | -/TTTT | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055359 | TATATCTAGGATTTG[-/TTTT]TTTTGTTTTTTGTGT | 26133 |
rs796105097 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086551 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs796317066 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036048 | AAACATTTTTTTAAG[A/G]TAAAGAAAAAAACTG | 26133 |
rs796340976 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015149 | GGATTACAGGTGCCC[-/C]ACCAACATGCCTGGC | 26133 |
rs796355258 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002879 | AAATGTCCTCTTACC[G/T]CTGGGTGGCCCTGGG | 26133 |
rs796385645 | in-del | -/CTC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029861 | CAGGGTGGTCTCGAT[-/CTC]CTGACCTCGTGATCC | 26133 |
rs796411926 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083246 | ACTTACAATACCACT[C/T]TTAAAAACGCTAAGG | 26133 |
rs796423559 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023040 | AAAAAAAAAAAAAAA[-/A]GAGAGAATCTAACTT | 26133 |
rs796434038 | in-del | -/TATA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086583 | GTGTGTGTATATATA[-/TATA]TATGAATAAGACTTT | 26133 |
rs796460500 | in-del | AA/GAG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034159 | CCGTCTCAAAAAAAA[AA/GAG]AAAAAAAAAAAAAAA | 26133 |
rs796531486 | multinucleotide-polymorphism | CGT/GGG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051401 | AGCCTCAATCACCTG[CGT/GGG]TCAAGCGATCCCCCC | 26133 |
rs796534366 | in-del | -/A | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094571 | GAGACTCCATCTCAG[-/A]AAAAAAAAAAAAAAA | 26133 |
rs796596552 | multinucleotide-polymorphism | AAA/TAT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034165 | CAAAAAAAAAAAAAA[AAA/TAT]AAAAAAAAAAGAGTA | 26133 |
rs796606645 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080805 | ACTTGTACACTTCAG[-/T]TTTTTTTTTTTTTAC | 26133 |
rs796654363 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080530 | AACAAAGCGAGACTC[C/T]ATCTAAAAAAAAAAA | 26133 |
rs796660046 | in-del | -/CT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030864 | CCTTTACTTAAGGTG[-/CT]CTTTGTTTTTCATGT | 26133 |
rs796779840 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068978 | ACACACACACACACA[-/C]AAAAAAAACAAAACA | 26133 |
rs796791778 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037058 | CATTGAGGTTCCTCA[A/G]AAAGTTGGCCAGGCA | 26133 |
rs796861590 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091051 | CAAGTATTTCTAGGA[-/T]TTTTTTTTTTTTTTG | 26133 |
rs796877552 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080549 | TAAAAAAAAAAAAAA[A/C]AAAAAAACCTAAAAG | 26133 |
rs796935834 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058193 | TGGCAGAAATGAAGG[A/C]AACAGATAATTTAAA | 26133 |
rs796957735 | in-del | -/ACAAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067012 | TTATAAAGAACTCTT[-/ACAAC]ACAATATTCAAAAGA | 26133 |