SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4616 | snp | A/G | 0.469445 | 0.119766 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002555 | TCCCTCCATCCCTTG[A/G]GGCACGGGGCAGCTG | 26133 |
rs8501 | snp | C/T | 0.289424 | 0.246872 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002781 | CTCACAGATGGGGGG[C/T]GGGGGTCACCCATAT | 26133 |
rs14206 | snp | A/G | 0 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002721 | CCTGCCCAGGGCTCA[A/G]AAGCCTTTGCCTGGG | 26133 |
rs14329 | snp | A/G | 0 | 0 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006451 | TTTGCATCGGTGTTG[A/G]TATATTTATTGAATC | 26133 |
rs717593 | snp | C/G | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065161 | CCATTGCTTGGCATT[C/G]AGGAACTTTTATTCA | 26133 |
rs752075 | snp | A/C | 0.287867 | 0.247116 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003788 | GGGGCCCCCAGCAGC[A/C]CCAGTTTCCTGACTG | 26133 |
rs752448 | snp | A/G | 0.37382 | 0.217183 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004445 | CAGGTGAGAGGCCCC[A/G]GCAGACACACAGCAG | 26133 |
rs752449 | snp | C/T | 0.337386 | 0.23423 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004671 | TTGATGATGAGCTCC[C/T]AGCTTCAGAGTCAGG | 26133 |
rs1058003 | snp | A/G | 0.483199 | 0.0901004 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002614 | TTGGATGAACACAGC[A/G]GCCAATGAGCAAACA | 26133 |
rs1080925 | snp | C/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048802 | TTCCACTCTGGAGGT[C/G]CCCTTTCACACACTG | 26133 |
rs1358854 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045856 | ATACTTTATTTTTAT[A/G]GAGACAGGGTCTCAC | 26133 |
rs1407202 | snp | C/T | 0.473451 | 0.112115 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064164 | GTTTAAAGACATTCC[C/T]TATATACGTATGTAT | 26133 |
rs1407203 | snp | G/T | 0.48378 | 0.0885831 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064176 | TCCCTATATACGTAT[G/T]TATTTTTTATTATTG | 26133 |
rs1544047 | snp | C/T | 0.483563 | 0.0891524 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082950 | caaaatgtttaaggt[C/T]ttttccctcttagat | 26133 |
rs1885115 | snp | A/G | 0.366473 | 0.221211 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093453 | AAGTTGTGTAACTGG[A/G]TAGGTTGTTGTGAAA | 26133 |
rs1885116 | snp | A/G | 0.288906 | 0.246954 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012757 | GGTAGTAAGGGGCCA[A/G]CGACTTCCATACTCA | 26133 |
rs1885117 | snp | C/T | 0.287867 | 0.247116 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012937 | AGCTGAGGTCAGGGA[C/T]CAGACAAGGAGATCG | 26133 |
rs1885119 | snp | C/T | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057846 | ATCTCTGGGATCTAA[C/T]GCGGCTTTAATTTCT | 26133 |
rs1998231 | snp | G/T | 0.4862 | 0.0819127 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010616 | ACCAACACCTCAACA[G/T]GTCCAATCACACTCA | 26133 |
rs1998232 | snp | G/T | 0.390277 | 0.206936 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014156 | ATGCCCGGGAGCACG[G/T]TTCTATAGGTGGATG | 26133 |
rs1998233 | snp | A/G | 0.359975 | 0.224512 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35069323 | AAACAAGTCAAAAAT[A/G]TAAGTATTTGGATAA | 26133 |
rs2013125 | snp | C/T | 0.287606 | 0.247155 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013351 | CTCAAGCGATCTGCC[C/T]GCCTCGGCCTCCCAA | 26133 |
rs2038503 | snp | A/G | 0.485255 | 0.0845871 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088097 | tcagcgtatagaGCA[A/G]TTATTAATAACAATA | 26133 |
rs2038504 | snp | C/T | 0.483563 | 0.0891524 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060384 | ttaagcccaagagta[C/T]gcaaccagcctgggc | 26133 |
rs2057323 | snp | C/T | 0.334182 | 0.235401 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068757 | GAACTCCTGACCTCA[C/T]GATCCACCTGCCTTG | 26133 |
rs2057324 | snp | A/G | 0.483636 | 0.0889627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068758 | aactcctgacctcac[A/G]atccacctgccttgg | 26133 |
rs2104083 | snp | A/G | 0.483418 | 0.0895317 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061330 | ttgaaagaaattaaa[A/G]acaatctaaaaaaat | 26133 |
rs2104084 | snp | C/G | 0.483491 | 0.0893421 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061414 | aatactccctaaatt[C/G]acctacaaattcaat | 26133 |
rs2145557 | snp | A/G | 0.483708 | 0.088773 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079757 | gaaCCGTTTGCCCCA[A/G]TATTTGcctagcact | 26133 |
rs2145558 | snp | A/G | 0.147321 | 0.227941 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062266 | AAATTAAACAGAGTT[A/G]CCAGCAACTCCACTT | 26133 |
rs2145559 | snp | A/G | 0.470132 | 0.118498 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063922 | TTAAACAAATTCTAG[A/G]TTAATATAAACAGAA | 26133 |
rs2180847 | snp | G/T | 0.48378 | 0.0885831 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079960 | ttgggagaatgaggc[G/T]gcagtgagctatgac | 26133 |
rs2180848 | snp | A/G | 0.386504 | 0.209444 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031308 | GCTCACTACAGCCTC[A/G]TCCTCCTGGGTTGAG | 26133 |
rs2180849 | snp | A/C | 0.388021 | 0.208447 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060436 | tacaaaaattaaaac[A/C]aaaaattagccaagc | 26133 |
rs2180850 | snp | C/G | 0.387453 | 0.208822 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067505 | TATGACCCAGCAACT[C/G]TATTCCTAGGTATGT | 26133 |
rs2273636 | snp | C/T | 0.48178 | 0.0936921 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007497 | GACAGGACACAGCAA[C/T]GCGTGGGCTGGGGGG | 26133 |
rs2273637 | snp | A/G | 0.00246026 | 0.0349868 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007686 | AGGCTGCCCTCTTCC[A/G]GCCCATGTTCAGTTC | 26133 |
rs2281626 | snp | G/T | 0.322539 | 0.239245 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049803 | CTGTATATTATTCAG[G/T]TTTGAGAATCCAATG | 26133 |
rs2295700 | snp | A/G | 0.147656 | 0.228091 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003824 | CTTCCTCTTCCCCAC[A/G]CCCACCTCCCACCCC | 26133 |
rs2295701 | snp | C/G | 0.337386 | 0.23423 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008314 | AGGCTTTCCTTTGCT[C/G]CTATAGCTCCTGGGC | 26133 |
rs2378332 | snp | A/G | 0.482534 | 0.0918038 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029447 | gttaaatctattcac[A/G]tttaatgttactatt | 26133 |
rs2889873 | snp | A/G | 0.148661 | 0.22854 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059038 | CTACCTTAAGACACT[A/G]GAAAAAGAGCAGACT | 26133 |
rs3736802 | snp | C/T | 0.4941 | 0.0539917 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016239 | GATATTCAGGACAAG[C/T]ATCAGTACTGTCAGT | 26133 |
rs3746430 | snp | A/G | 0.390277 | 0.206936 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005871 | CCCCTTGTAGTGACT[A/G]TCCCCCCGGGCCATG | 26133 |
rs3746431 | snp | A/G | 0.463569 | 0.129955 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005654 | CAAGTCATGCAGGGT[A/G]AGAATGCTGGCATCA | 26133 |
rs3746432 | snp | A/G | 0.482309 | 0.0923707 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004960 | TGGAAAACCAGTTGC[A/G]CTAGGACCTCTGCAG | 26133 |
rs3803936 | snp | A/G | 0.482683 | 0.0914256 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044972 | CAAGAACAATTGAAA[A/G]CAGTGGTGCTCAAAA | 26133 |
rs3803937 | snp | G/T | 0.485799 | 0.0830599 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044884 | AACAAGCAAAGACTC[G/T]AAAGGTTTTTGTAAC | 26133 |
rs3803938 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044797 | TAGCCACTAAGCCCC[A/G]TATGTAAGGGGATGC | 26133 |
rs3818253 | snp | A/G | 0.295088 | 0.245901 | intron-variant, utr-variant-3-prime | TRPC4AP | GRCh38.p7 | 20:35009073 | CAGTCTGCCAGATGG[A/G]GAAAGACTCTGCCAA | 26133 |
rs3830959 | in-del | -/AGAGA/GAGAA | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049489 | GTTCAGATAGCGGTA[-/AGAGA/GAGAA]AAGTGGTAAGAGAAT | 26133 |
rs3830960 | in-del | -/GCCTG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092594 | gccccgccccgcccc[-/GCCTG]tcctggtccagcctc | 26133 |
rs4142034 | snp | A/G | 0.388021 | 0.208447 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055453 | TGTTTGTATTAAACT[A/G]GTTCCTCAAGATACA | 26133 |
rs4331589 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049038 | CTGCAACAGCAACCT[C/T]TAGGAGGCTGCTCAA | 26133 |
rs4387881 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012801 | CTATGAGGGTTAGAA[A/G]AAAGCTTGGGGCAGT | 26133 |
rs4616550 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085185 | TAGAGGTGCAAAGCA[A/G]GCAGGGCACTGCTGT | 26133 |
rs4621232 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074934 | gacttgctttatgaa[C/T]ctgggtgctcctgta | 26133 |
rs4911167 | snp | A/G | 0.482534 | 0.0918038 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002293 | CCCCCTGCTGCCTTC[A/G]GCCTTCCCTGGGCCC | 26133 |
rs4911168 | snp | C/G | 0.48435 | 0.0870631 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005986 | GTACTAAGAGGCACT[C/G]CCCGGAATTCAGCAC | 26133 |
rs4911169 | snp | A/G | 0.485118 | 0.0849685 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006031 | CTCCAGTGGTTTTAC[A/G]CTCAAGGGTGCTGGA | 26133 |
rs4911457 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021676 | CAACCAGACCCCCAG[G/T]AAGTGCCCAGGCAGA | 26133 |
rs4911458 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024219 | tcgtgatttttagga[A/C]attcatagagttgtg | 26133 |
rs4911460 | snp | A/G | 0.48378 | 0.0885831 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036527 | tacagtggcagttac[A/G]tttcttaaaagtcgt | 26133 |
rs4911461 | snp | A/C | 0.483418 | 0.0895317 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042190 | ACCGTACACAGACCA[A/C]GGAAGACCTTGTATC | 26133 |
rs4911462 | snp | G/T | 0.464631 | 0.128193 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054929 | ATCTTAAACATTGCA[G/T]ACCTGGTAGGGGAGA | 26133 |
rs4911463 | snp | A/G | 0.464689 | 0.128096 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054934 | AAACATTGCAGACCT[A/G]GTAGGGGAGATAAAC | 26133 |
rs4911464 | snp | A/T | 0.388021 | 0.208447 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071319 | TAAGTTCTAGGGTAC[A/T]TGTGCACAACATGCA | 26133 |
rs4911465 | snp | A/G | 0.388021 | 0.208447 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083053 | ataagattggtaagg[A/G]taagataaaagattc | 26133 |
rs5841189 | in-del | -/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052099 | GTTTTTTTTTTTTTT[-/T]GGAGACAGGGTCTCA | 26133 |
rs6058157 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009953 | ctctctgaggctcac[C/T]tcatctgtcaagtgc | 26133 |
rs6058158 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018237 | CTGACCCTGGGTCTC[C/T]TAAGTTCAGGCCAGT | 26133 |
rs6058159 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022946 | aaggatcgcttgagc[C/T]tggaaggtgaaggtt | 26133 |
rs6058160 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029126 | gcgtgggctccccgc[C/T]tgtaatcccaactac | 26133 |
rs6058161 | snp | C/T | 0.483491 | 0.0893421 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032223 | agagatggggttttg[C/T]catgttggcctggcc | 26133 |
rs6058163 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041269 | ATAACATTCAGAGGA[C/T]TAAGACTTTCCTCAT | 26133 |
rs6058165 | snp | A/T | 0.386694 | 0.20932 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053037 | TTCCTCAAATTTTTT[A/T]AAAAATTTTATTTAA | 26133 |
rs6058166 | snp | C/G | 0.48378 | 0.0885831 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068907 | ATATCACTCTATGTG[C/G]GGAGAAAATAAACTA | 26133 |
rs6058168 | snp | C/T | 0.388021 | 0.208447 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072909 | attgattcttcctat[C/T]catgagcatgggatg | 26133 |
rs6058174 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080533 | aaaGCGAGACTCCAT[C/T]Taaaaaaaaaaaaaa | 26133 |
rs6058175 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080558 | aaaaaaaaaaaaaaC[C/T]taaaagaagccagtc | 26133 |
rs6058176 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087609 | CTGATCATTTGGGGC[C/T]TTGTACGCCCATGGT | 26133 |
rs6058177 | snp | C/T | 0.327445 | 0.237702 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089114 | GCTCAAACAATCCGC[C/T]CACCTCAGCTTCCCA | 26133 |
rs6060151 | snp | G/T | 0.464472 | 0.128459 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006423 | CTCCACAGAGCCCTG[G/T]GTTAACTTTACCTTT | 26133 |
rs6060152 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006600 | GAGGGACAGGGTGAA[A/G]GTGTCAACGTGGCTG | 26133 |
rs6060154 | snp | A/C | 0.389903 | 0.207189 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011798 | TCACTACAAGCTGAC[A/C]CTTCAGGTCTTGGCT | 26133 |
rs6060155 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018034 | CACCAAGCCATGTGC[C/T]TTCCTGTCTCACTCC | 26133 |
rs6060156 | snp | C/G | 0.390464 | 0.206809 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022342 | tctatttttagtaga[C/G]atggggtttcaccat | 26133 |
rs6060157 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022647 | TCTATGTGTTATAGA[A/G]GAGTGGTTATCAGAT | 26133 |
rs6060158 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022739 | ACCCTAACTTATTCC[A/G]ACTAggtgtggtggc | 26133 |
rs6060159 | snp | A/G | 0.300169 | 0.244914 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022743 | TAACTTATTCCgact[A/G]ggtgtggtggctcat | 26133 |
rs6060160 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022847 | acaatacagtgagac[C/T]tcattgctataaaaa | 26133 |
rs6060161 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023064 | CTAACTTACTCTATC[C/T]TACAGACTTGGAACT | 26133 |
rs6060162 | snp | C/G | 0.484561 | 0.0864924 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023658 | TAAGTGTCAGCTAAT[C/G]TGTGAAGTGAACCTG | 26133 |
rs6060163 | snp | C/T | 0.299916 | 0.244966 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023935 | TGACAAGACTTTCTG[C/T]GATAAATATTTTCAA | 26133 |
rs6060164 | snp | A/G | 0.482534 | 0.0918038 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028511 | atttatttctaactc[A/G]ccccactgggatttg | 26133 |
rs6060165 | snp | A/C | 0.487558 | 0.0778863 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031677 | gataatttttctgtt[A/C]ctttatctccttctg | 26133 |
rs6060166 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031855 | atctactgctgagtc[C/T]ttctagtgatttttt | 26133 |
rs6060167 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032808 | ctgctgttaaatctg[A/G]tatctggaccctttc | 26133 |
rs6060168 | snp | C/T | 0.483418 | 0.0895317 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033214 | acattttaagtaata[C/T]actgtagcaactctg | 26133 |
rs6060169 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035514 | AGGTACAGGGAAACA[A/G]GCTTTTTATCTACTG | 26133 |
rs6060170 | snp | C/G | 0.48378 | 0.0885831 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036663 | ataaagtaagaCAAG[C/G]Tggccaggcacggtg | 26133 |
rs6060172 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041002 | ctccgtctctcctca[A/G]tgacagagaggaaaa | 26133 |
rs6060173 | snp | C/T | 0.387832 | 0.208572 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041279 | GAGGACTAAGACTTT[C/T]CTCATCCACTCGTGA | 26133 |
rs6060175 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044133 | tggtggctcacacct[A/G]taattctagcacttc | 26133 |
rs6060176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047131 | gcctcacaaagtgct[G/T]ggattacaggcatga | 26133 |
rs6060177 | snp | G/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048212 | ATTTGTAAGAATTCT[G/T]TTTTTTTTTTTTTTT | 26133 |
rs6060178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049173 | TGTAACACAGTAAGT[C/T]TCTAACAGAGATCTA | 26133 |
rs6060180 | snp | A/G | 0.334642 | 0.235236 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050210 | GCTACACAAGTGGGA[A/G]CTCACTTGTGAGAAC | 26133 |
rs6060181 | snp | A/C | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051644 | aaaaaGGTTGTTATT[A/C]CCGAACTACATACAG | 26133 |
rs6060182 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053485 | TGTCTTCTTCTATAA[A/G]GACAATTTCTTATTG | 26133 |
rs6060183 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055325 | ATAAAGCCATTTTCC[C/T]TTAATGTCTTGCTTA | 26133 |
rs6060184 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055431 | ATATATATGTGTATC[C/T]TTTTCATGTTTGTAT | 26133 |
rs6060185 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056748 | cacttgggaggctga[A/G]gtgggcagatcactt | 26133 |
rs6060186 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056766 | gggcagatcacttga[A/G]gtcaggagttcgaga | 26133 |
rs6060187 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056893 | tgagagggtgaggca[A/G]gaaaatcacttgagc | 26133 |
rs6060188 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056912 | aatcacttgagctca[A/G]gaggcggaggttgca | 26133 |
rs6060189 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056921 | agctcaggaggcgga[A/G]gttgcagtgagccaa | 26133 |
rs6060190 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058096 | GGATAGTtgataaaa[A/G]ggtcaatccattaga | 26133 |
rs6060191 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058191 | gctggcagaaatgaa[A/G]gaaacagataattta | 26133 |
rs6060193 | snp | C/T | 0.38821 | 0.208322 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060630 | aaaaggattatacac[C/T]atgacactatgacaa | 26133 |
rs6060194 | snp | C/T | 0.297636 | 0.24542 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062127 | tacctactacgatgg[C/T]tataatgaaaaagac | 26133 |
rs6060196 | snp | C/G | 0.388021 | 0.208447 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065814 | AATAGACACAGGCTA[C/G]AGACCTACATTATTA | 26133 |
rs6060197 | snp | C/T | 0.482534 | 0.0918038 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066512 | CCAGAAATGCCCTCT[C/T]CCTCATGTTCACTTC | 26133 |
rs6060199 | snp | A/G | 0.482534 | 0.0918038 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066970 | CTCAGTCATAGAAGA[A/G]TGAATTTTAAAAACT | 26133 |
rs6060201 | snp | A/G | 0.388021 | 0.208447 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068010 | tgaaatgtatggtat[A/G]tgaaccatatcttaa | 26133 |
rs6060202 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068110 | ACACTGTTTGTGGAA[A/G]ggggcttctgggtac | 26133 |
rs6060204 | snp | C/G | 0.332799 | 0.23589 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070620 | TTTCACCGTGGTCTC[C/G]ATCTCCTAACCTTGT | 26133 |
rs6060205 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071066 | AGCATTTTTAAACAA[A/G]TTTAAGAAGCTATAA | 26133 |
rs6060206 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074783 | tgtagatgtctatta[A/G]gtccgcttggtgcag | 26133 |
rs6060207 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074918 | ctaagtttctttgta[A/G]gacttgctttatgaa | 26133 |
rs6060209 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080809 | GTACACTTCAGTTTT[G/T]TTTTTTTTTACCCTT | 26133 |
rs6060212 | snp | C/T | 0.484491 | 0.0866827 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089148 | tgttgggattacagg[C/T]gtaagccaccacact | 26133 |
rs6060214 | snp | G/T | 0.484421 | 0.0868729 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089866 | TAAAAAATAAAAAAT[G/T]TTTAAATCTGGTCTT | 26133 |
rs6060215 | snp | A/T | 0.484491 | 0.0866827 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090057 | CCCAGGAAGTTGAGC[A/T]TGCCACTGCACTCCA | 26133 |
rs6060216 | snp | C/T | 0.48435 | 0.0870631 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090275 | GGTCTCTACTTCAAC[C/T]TCTGAAATAGCTCCC | 26133 |
rs6060217 | snp | G/T | 0.387263 | 0.208947 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090331 | CACAATAACCTGCCT[G/T]GCTTTTGTGGCTCCA | 26133 |
rs6060218 | snp | C/T | 0.332337 | 0.236052 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090833 | TTTAGGAACATATCA[C/T]CTAACCTCTCTGAGC | 26133 |
rs6060219 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092448 | CCAGCTGCTTCCCAC[A/G]GCCCCGCTGCAGCTG | 26133 |
rs6060220 | snp | A/G | 0.0696718 | 0.173152 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094344 | ttgggaggccgaggt[A/G]gtcagatcatgaggt | 26133 |
rs6060221 | snp | A/G | 0.0858192 | 0.188533 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094369 | tgaggtcaggagttc[A/G]agaccagcctggcca | 26133 |
rs6060222 | snp | A/C | 0.362523 | 0.223246 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094767 | cttctattttttgtt[A/C]taaatttcttcctag | 26133 |
rs6087658 | snp | G/T | 0.485255 | 0.0845871 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018401 | AGGAGTTTCAGACCA[G/T]CCTGGCCAACATGAT | 26133 |
rs6087659 | snp | A/C | 0.280785 | 0.248097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018580 | ctccagcctgggtgg[A/C]agagcaagactgtct | 26133 |
rs6087660 | snp | C/T | 0.482534 | 0.0918038 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028725 | tcttctgtttccctg[C/T]tgatcttctgcttag | 26133 |
rs6087662 | snp | A/G | 0.288386 | 0.247035 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037272 | gaatggcgtgaaccc[A/G]ggaggcagagcttgc | 26133 |
rs6087663 | snp | A/G | 0.387642 | 0.208697 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037723 | gctgttgcggtcaac[A/G]acgaccacacagaag | 26133 |
rs6087664 | snp | C/G | 0.484066 | 0.0878235 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038413 | TTTGTCAACACTTAC[C/G]AATTTCCATTAATGG | 26133 |
rs6087666 | snp | A/G | 0.289424 | 0.246872 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052439 | AAGTATCTAAATGAG[A/G]AGCTACAAACTAGCA | 26133 |
rs6087667 | snp | A/G | 0.288646 | 0.246995 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064084 | TTTGTTTTCCAAAAA[A/G]GTCCAATTTTCACTT | 26133 |
rs6087668 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065589 | AGCAGGACAGCAAGA[A/G]AGTTCACTAACAAAT | 26133 |
rs6087669 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067647 | aataaaaaatgtggc[A/G]tatccacactgtgaa | 26133 |
rs6087670 | snp | C/T | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074466 | gagatcctggtatgt[C/T]atgtctttgttctca | 26133 |
rs6087671 | snp | C/T | 0.332337 | 0.236052 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076739 | aggaggcagtctgtc[C/T]gttctcagatctcaa | 26133 |
rs6087673 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086258 | gccaccgcacccagc[C/T]TAAATAGATATCTTA | 26133 |
rs6088671 | snp | C/T | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002250 | TCTGGCTGAGGCCAC[C/T]TGCCCCGATCCTGCC | 26133 |
rs6088672 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004786 | CCAGGAGCACCCCAC[C/T]TCATCCTCCAGAACC | 26133 |
rs6088673 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008826 | CATTCTGCTGGCTTA[A/G]GCGGTGAAAAACCAT | 26133 |
rs6088674 | snp | A/G | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008863 | ATTTCCAAGTCTGCA[A/G]GATGCCTTCCTGCTC | 26133 |
rs6088675 | snp | A/G | 0 | 0 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012773 | CGACTTCCATACTCA[A/G]TTCCTGGGGTGGCTA | 26133 |
rs6088676 | snp | C/T | 0.485118 | 0.0849685 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019623 | AGTAATAGCACTCAA[C/T]GCACAGAAGCTGTCC | 26133 |
rs6088677 | snp | C/T | 0.330249 | 0.23677 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019661 | TATTTCACATATAAG[C/T]AACTGCGAAAGTGCC | 26133 |
rs6088678 | snp | C/T | 0.287346 | 0.247195 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019748 | ATTAAAAACATGTTC[C/T]GTATTGAAGGAAGGG | 26133 |
rs6088680 | snp | C/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024989 | ctcttgggtatatac[C/G]tgggagtaggatttc | 26133 |
rs6088682 | snp | A/C | 0.289942 | 0.246789 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027899 | ctttcttttttggtc[A/C]gtgtggctaaaagtt | 26133 |
rs6088683 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031462 | gctggtcttgaactc[C/T]tgagctcaagcaatc | 26133 |
rs6088684 | snp | C/G/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031494 | acccttcttggcttc[C/G/T]taaagtgcagggatt | 26133 |
rs6088685 | snp | A/G | 0.288646 | 0.246995 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032503 | ttgagacagagtctc[A/G]cactgtcgcccaggc | 26133 |
rs6088686 | snp | C/T | 0.289165 | 0.246913 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035634 | ACCAGTCATATTACA[C/T]GAGAATATCTGTATA | 26133 |
rs6088687 | snp | A/G | 0.483199 | 0.0901004 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036947 | atactctgtctcaaC[A/G]CGTGCGcacacaaac | 26133 |
rs6088688 | snp | A/G | 0.288646 | 0.246995 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037279 | gtgaacccaggaggc[A/G]gagcttgcagtgagc | 26133 |
rs6088689 | snp | G/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044453 | AAACTAGATGATTTA[G/T]TAAGGGCCTCAGAGC | 26133 |
rs6088690 | snp | A/G | 0.288906 | 0.246954 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045523 | CTACAGGTGCGTGTC[A/G]TTACACCTGGCTACT | 26133 |
rs6088691 | snp | C/T | 0.287867 | 0.247116 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045955 | ATTACATGTATGAGC[C/T]ACTGTGCCTGACCCT | 26133 |
rs6088692 | snp | A/G | 0.484066 | 0.0878235 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050785 | GTATGAAGGAAGTTA[A/G]GGAAACTAGCTGGTA | 26133 |
rs6088693 | snp | A/G | 0.334642 | 0.235236 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052539 | ctcactctgtcaccc[A/G]cgctggagtgcagtg | 26133 |
rs6088694 | snp | A/G | 0.289165 | 0.246913 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064568 | ACTACACCACAGATT[A/G]TCAATTCTAGAGAAG | 26133 |
rs6088695 | snp | C/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066909 | GTGCAAAACAGAAAA[C/G]TGGCAGAAAAGGAAC | 26133 |
rs6088696 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067399 | agaaaaactgaaacc[C/T]ttatacactgctggt | 26133 |
rs6088697 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067527 | taggtatgtatatgc[C/T]tgagagaaatgaaaa | 26133 |
rs6088698 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067559 | atgtccacaaagaac[C/T]tgtgcaagaatgttt | 26133 |
rs6088699 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071402 | tcgtcatttatatta[A/G]gtatatctcctaatg | 26133 |
rs6088700 | snp | C/T | 0.288906 | 0.246954 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072949 | ttgtttgtgtcctct[C/T]ttatttcattgagca | 26133 |
rs6088701 | snp | C/T | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074565 | gttgttcagtttcca[C/T]gtagttgagtggttt | 26133 |
rs6088702 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076427 | ttgatgatggtgaca[C/T]acagatggggttttg | 26133 |
rs6088703 | snp | A/T | 0.287085 | 0.247234 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088246 | CAGGTCCTATGATAC[A/T]TACTTTACAAATAAA | 26133 |
rs6088704 | snp | C/T | 0.484491 | 0.0866827 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089818 | GCCACTGCACTCCAG[C/T]CTGGGCAACAGAGCG | 26133 |
rs6088705 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091951 | gctttgaacccaggc[C/T]tgactccagagtccc | 26133 |
rs6088706 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092030 | CCGCTGGAACTCAGC[C/T]TAATGTGGGAGACGG | 26133 |
rs6119559 | snp | A/G | 0.396546 | 0.202545 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013798 | AGGGTGTCAGGTCCC[A/G]GTAAAGCCTGGGGAG | 26133 |
rs6119560 | snp | C/G | 0.288906 | 0.246954 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019174 | TCCCCTTGCTACCCA[C/G]TGTAGGCAGGATCTG | 26133 |
rs6119561 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046761 | TATTGGCAACTGTAA[C/T]TTGTAGCTCACCAGT | 26133 |
rs6119562 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050869 | aagtgcagtggctca[C/T]acctgtaatcccagc | 26133 |
rs6119563 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051751 | AGAAACAGAACAAAA[A/G]GAGAACTAAATTTAC | 26133 |
rs6119564 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059776 | GAAGACGACGAAGAC[A/G]AAGAAGATGAAGAAG | 26133 |
rs6119565 | snp | C/T | 0.484701 | 0.0861117 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059867 | AAGATGAAGAAAAGA[C/T]GAAGAAAAGACGAAG | 26133 |
rs6119566 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061417 | actccctaaattgac[C/T]tacaaattcaatgca | 26133 |
rs6119567 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061484 | attggcaagctgatc[C/T]tgaaattcacatgca | 26133 |
rs6119568 | snp | A/C | 0.483923 | 0.0882034 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084490 | tatgtgtatatatgt[A/C]tatatctatatatgt | 26133 |
rs6119569 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084568 | tttatatgcatAtat[A/G]tgtatatgtatatat | 26133 |
rs6119570 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084644 | tatgtgtatatgtat[A/G]tatgtttatatgcat | 26133 |
rs6119571 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089398 | CACCTGGTTAATGTT[G/T]TTTTTTTTTTTTTTT | 26133 |
rs6120789 | snp | C/T | 0.0143288 | 0.0834212 | missense, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35008664 | TTTCCCCAGACTCAC[C/T]TGAAAGACGACTCTG | 26133 |
rs6120790 | snp | A/T | 0.301177 | 0.244706 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011287 | aaagaaaacacattt[A/T]atatatctaacccac | 26133 |
rs6120791 | snp | G/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011675 | GTCCTGTGCAGCCCA[G/T]CCCAGAGCCAAGCCC | 26133 |
rs6120793 | snp | C/T | 0.288906 | 0.246954 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016604 | CAATTATTAAAAAAC[C/T]CTAAGATCTAGAAAA | 26133 |
rs6120794 | snp | A/G | 0.00481925 | 0.0488508 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017777 | TCCTTCAACATAtta[A/G]gttgtgtaaaagtaa | 26133 |
rs6120795 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017904 | AATCTGTTAGACTGA[A/G]GCTGATGTAAAATGA | 26133 |
rs6120796 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017938 | CTGTTCTGCCACTCA[A/G]GCCTTTACTAAAACC | 26133 |
rs6120797 | snp | A/G | 0.288646 | 0.246995 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018199 | AGCTGGGAAGAGAGG[A/G]GCCTTCTAAGGCAGA | 26133 |
rs6120798 | snp | G/T | 0.289424 | 0.246872 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023019 | GCGACAGAGCTGGAC[G/T]GTCTCAAAAAAAAAA | 26133 |
rs6120799 | snp | C/T | 0.288906 | 0.246954 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027152 | tcctgatcttagtgg[C/T]agaagctttcaattt | 26133 |
rs6120800 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030032 | ggaccacctgaggtc[A/G]ggagatcgagaccag | 26133 |
rs6120801 | snp | A/C | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030037 | acctgaggtcaggag[A/C]tcgagaccagcctga | 26133 |
rs6120802 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030054 | cgagaccagcctgac[C/T]aacatggagaaaccc | 26133 |
rs6120803 | snp | A/C | 0.288646 | 0.246995 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032283 | gcccgcctcagcctc[A/C]caaagtgctgggatt | 26133 |
rs6120804 | snp | A/C | 0.288646 | 0.246995 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035898 | CTTCTTCAAAATACA[A/C]AAGGAATGAAAGCAT | 26133 |
rs6120805 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036117 | ATTCACAATGAGTGA[A/G]GTGGAAATTCTGATC | 26133 |
rs6120806 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036351 | CCGTCAAGTGGAAAA[A/G]GGGATTTAGGTCACT | 26133 |
rs6120807 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036360 | GGAAAAGGGGATTTA[A/G]GTCACTGAGAGTAAC | 26133 |
rs6120808 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037831 | ttatggtacaactgc[C/T]tactgtatttagtac | 26133 |
rs6120809 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037873 | gtacaggtttgcagc[C/T]taagtgtatcatggg | 26133 |
rs6120810 | snp | A/G | 0.388021 | 0.208447 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038446 | GACTAATTAAATTAC[A/G]GTATGCCTGTATAAT | 26133 |
rs6120811 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038485 | ATATAATTACAAAAA[A/G]GAATCATATAATTCT | 26133 |
rs6120812 | snp | C/T | 0.288386 | 0.247035 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041624 | AGCTGACCAGAACAG[C/T]TCATTCCTCAAGAAT | 26133 |
rs6120813 | snp | C/T | 0.289683 | 0.24683 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054309 | TTTCTAAAAGACAGG[C/T]ACTGTATCTTTTAAA | 26133 |
rs6120814 | snp | C/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054365 | AAAGTGTTTTCACAT[C/G]TACTATCTCATTTCT | 26133 |
rs6120816 | snp | C/G | 0.483708 | 0.088773 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056555 | CTTATACAGTATGTC[C/G]TATTGGGGTAAAAAA | 26133 |
rs6120817 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059677 | aaagaaaaaaaagaa[A/G]aagaagaaGgaagaa | 26133 |
rs6120818 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062670 | ttagtggttgcctaa[A/G]gatgtgggagggagg | 26133 |
rs6120819 | snp | C/T | 0.290977 | 0.246619 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065235 | CCTACAAATCTAGAT[C/T]TCCCATAACCTCTCA | 26133 |
rs6120820 | snp | A/C | 0.498182 | 0.0300969 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068978 | ACACACACACACACA[A/C]AAAAAAAACAAAACA | 26133 |
rs6120821 | snp | C/T | 0.289683 | 0.24683 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072958 | tcctcttttatttca[C/T]tgagcagtggtttgt | 26133 |
rs6120824 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080543 | TCCATCTaaaaaaaa[A/C]aaaaaaaaaaaaaCC | 26133 |
rs6120825 | snp | A/C | 0.290201 | 0.246747 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083338 | ggcacagtggttcac[A/C]cttgtaatcccagca | 26133 |
rs6120826 | snp | A/G | 0.289424 | 0.246872 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084028 | AAGCAggccgggcgc[A/G]gtggctcacacctgt | 26133 |
rs6120827 | snp | A/T | 0.332337 | 0.236052 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084320 | AAAAggatgcattat[A/T]cctgacttcaccacc | 26133 |
rs6120828 | snp | C/T | 0.288906 | 0.246954 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086657 | CCAGGTAAGATTTGT[C/T]TGACTTAAATGCCTA | 26133 |
rs6120829 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086927 | agtcccagctactca[A/G]gaggctgaggcaggg | 26133 |
rs6120830 | snp | A/G | 0.332568 | 0.235971 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087196 | aaaaaaaaattagcc[A/G]ggcgtggtggcgggc | 26133 |
rs6120831 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089053 | accttttttttttaa[A/G]atacagggtttcacc | 26133 |
rs6141524 | snp | A/C | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008202 | CCCTGATGGAACTCT[A/C]CCTGTCCACTGACTT | 26133 |
rs6141525 | snp | A/C | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008405 | GGCAGGGCCCGTATC[A/C]TAGTTCTCTCCCACC | 26133 |
rs6141526 | snp | G/T | 0.468949 | 0.12067 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027452 | tagtattttgttgaa[G/T]atttttgcacctata | 26133 |
rs6141527 | snp | C/T | 0.444444 | 0.157135 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031415 | ttttttttttttttt[C/T]caaagagatggggtt | 26133 |
rs6141529 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068819 | gccactgcgcccggc[C/T]taaaattgttttAAT | 26133 |
rs6141530 | snp | C/T | 0.464096 | 0.129085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075344 | gttgatgcagtttct[C/T]cctagcatcgaaggt | 26133 |
rs6141531 | snp | C/T | 0.00668889 | 0.057443 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081246 | ggccggttacagggc[C/T]tcatgcatgttactg | 26133 |
rs6142269 | snp | A/G | 0 | 0 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002119 | ATTGCTCTCTGTGCA[A/G]GGGGACTGTGGGGGC | 26133 |
rs6142270 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003842 | CACCTCCCACCCCAC[C/T]TGAGGCAACAACACC | 26133 |
rs6142271 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014530 | GCAATCGAAAGAGAC[C/T]TTAAGAAAGTATTTT | 26133 |
rs6142272 | snp | A/G | 0.337841 | 0.23406 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025568 | cttctttggagaaac[A/G]tctattcagatcctt | 26133 |
rs6142273 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025924 | tagctcttacattta[G/T]gtctttgaccctttt | 26133 |
rs6142274 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026218 | atgtgagttgtctta[A/G]gttgttttttttttt | 26133 |
rs6142275 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032271 | ctcaaatgctctgcc[C/T]gcctcagcctcccaa | 26133 |
rs6142276 | snp | C/T | 0.483491 | 0.0893421 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032529 | caggctgaaatgcag[C/T]ggcaggatctcggct | 26133 |
rs6142277 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034158 | ctccgtctcaaaaaa[A/G]aaaaaaaaaaaaaaa | 26133 |
rs6142278 | snp | A/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034167 | aaaaaaaaaaaaaaa[A/T]aaaaaaaaaaaGAGT | 26133 |
rs6142279 | snp | A/T | 0.375 | 0.216506 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034174 | aaaaaaaaaaaaaaa[A/T]aaaaGAGTAAAAAAA | 26133 |
rs6142280 | snp | A/C | 0.473543 | 0.111932 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034439 | TTCCACACCGTGAGT[A/C]CAGTATGGAGCTGGG | 26133 |
rs6142281 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044822 | tggctagatcactta[A/G]gttcctatcccagct | 26133 |
rs6142282 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046874 | TGTCTTAAATTTTAA[A/G]Atttttttttttaag | 26133 |
rs6142283 | snp | G/T | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051403 | GCCTCAATCACCTGG[G/T]CTCAAGCGATCCCCC | 26133 |
rs6142284 | snp | A/G | 0.483418 | 0.0895317 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053564 | CTTATAGATCTCCCT[A/G]TGCCTATCTCTGTCA | 26133 |
rs6142285 | snp | G/T | 0.477175 | 0.104362 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055837 | TAATGTCTGATCTAT[G/T]ACTAATTCTTATAAA | 26133 |
rs6142286 | snp | A/G | 0.444444 | 0.157135 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059906 | GAAGATGAAGAAGAC[A/G]AAGACGAAGAAGACA | 26133 |
rs6142289 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064726 | ATAATAGAGACCTAA[A/G]GTCATCCTCTAGAAA | 26133 |
rs6142290 | snp | A/C | 0.482534 | 0.0918038 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066869 | AGATCAATAAGAAAA[A/C]GGACAAATAATCAAA | 26133 |
rs6142291 | snp | C/T | 0.332337 | 0.236052 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077084 | caggatataatctcc[C/T]gctgtgccatttgct | 26133 |
rs6142292 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077643 | CATCAAACCTGGCCC[C/T]TTCAATCTTCTTACG | 26133 |
rs6142293 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081320 | gagttaaagaccagc[C/T]taggcaacacagtga | 26133 |
rs6142294 | snp | A/G | 0.475348 | 0.108251 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083694 | gtgtcagaataagac[A/G]ttttctgatctgcaa | 26133 |
rs6579208 | snp | C/T | 0.250732 | 0.249999 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010809 | AACTGAGTCATCaca[C/T]ggtgccaaaagtgat | 26133 |
rs6579210 | snp | C/T | 0.253264 | 0.249979 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017999 | GGGGGTGGGGAGGTA[C/T]GGCTGACATCTATGG | 26133 |
rs6579211 | snp | A/G | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018054 | TGTCTCACTCCAAAG[A/G]GCCCTAAGCCAGGCC | 26133 |
rs6579215 | snp | C/T | 0.250168 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080457 | agtgagccaagactg[C/T]gccactgcacttcag | 26133 |
rs6579216 | snp | C/T | 0.250168 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080494 | cgataaagccagacc[C/T]tgtctcaaaacagaa | 26133 |
rs7261539 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091477 | TAAAGTTACACTGTG[A/G]AAAGTCTCACTCCCA | 26133 |
rs7263253 | snp | C/T | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061573 | cgtgtctatgatcag[C/T]tgatttttgacaagg | 26133 |
rs7264779 | snp | A/G | 0.168299 | 0.236273 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084728 | tttatatgcatatat[A/G]tgtatatgtatatat | 26133 |
rs7268447 | snp | C/G | 0.145305 | 0.227022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061790 | aatctttgtgacctt[C/G]gattaggaaatggtt | 26133 |
rs7269601 | snp | A/G | 0.123798 | 0.215808 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043404 | ggcgtgcaccaccac[A/G]cccagctaatttttg | 26133 |
rs7271729 | snp | C/T | 0.144969 | 0.226867 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023189 | CACTGACCCTGAAGC[C/T]AGACTACTGGGTTTG | 26133 |
rs7271781 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010765 | GTTCCCAGGACACCA[A/G]CTCCCTTTACTAAAA | 26133 |
rs7272635 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084498 | tatatgtatatatct[A/C]tatatgtatatacgt | 26133 |
rs7273151 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006832 | CTGAAGCCTGTGACC[C/T]GCTCTGTGGTCACCA | 26133 |
rs7273382 | snp | C/T | 0.38821 | 0.208322 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037341 | gaaagagcgagactc[C/T]gtctcaaaaaaaaaa | 26133 |
rs7273734 | snp | C/G | 0.251014 | 0.249998 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011600 | ctaagtggaccatcT[C/G]TATATAAAATCCAGG | 26133 |
rs7274866 | snp | A/G | 0.25045 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020813 | CCAGTTTTCCTAAGC[A/G]GACACAGCTCTGGGC | 26133 |
rs7346552 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042926 | ctaccttcccttacc[A/G]gctacttcctattaa | 26133 |
rs7354143 | snp | G/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047181 | AGAATTTACTTCTTA[G/T]GTTTTAATTTTTGAT | 26133 |
rs7354623 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057705 | CCAGGAGGCAGTTAA[A/G]GTTCAGTAAGGCTCC | 26133 |
rs7354641 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057737 | GACTGCAGCAagtca[A/G]gagacccaggttcta | 26133 |
rs7354644 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057827 | aagtattttagatta[A/G]gtaatctctgggatc | 26133 |
rs7354670 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057973 | ACACTGATTTCTACA[A/G]GTTTGGGGGTTATAT | 26133 |
rs7362221 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024835 | cgtctcaaaaaaaaa[A/C]aaaaaaaaaaaaaaa | 26133 |
rs7362222 | snp | A/C | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024842 | aaaaaaaaaaaaaaa[A/C]aaaaaaaaaaaaatt | 26133 |
rs7362224 | snp | A/C | 0.243633 | 0.249919 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024852 | aaaaaaaaaaaaaaa[A/C]aaattctgtttattc | 26133 |
rs7362225 | snp | A/T | 0.492871 | 0.0592773 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024854 | aaaaaaaaaaaaaaa[A/T]attctgtttattcat | 26133 |
rs7362281 | snp | G/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069589 | ttctcacactaaatc[G/T]gggctggtatgacac | 26133 |
rs7509593 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030192 | gttgcggggagccaa[A/G]atggtaccactgcac | 26133 |
rs8114128 | snp | A/T | 0.123798 | 0.215808 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038783 | TTTTTTCTAAAAACA[A/T]ATCAGTAggcggggc | 26133 |
rs8114191 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083290 | AAGTTATGCAAGACG[A/G]CTACATAGAAAACTG | 26133 |
rs8116257 | snp | C/G | 0.25045 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076780 | gggagaaccactact[C/G]tcttcaaagctgtca | 26133 |
rs8117847 | snp | C/T | 0.249603 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054677 | GAGTCTTAAAGGTCA[C/T]AGTCTGCCAACACTT | 26133 |
rs8118005 | snp | C/G | 0.250168 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048416 | ATGAGACTGGGTTTT[C/G]CCATGATGGCCAGGC | 26133 |
rs8118469 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066173 | tcatggtgcgatctc[A/G]gctcactgtagcctc | 26133 |
rs8119799 | snp | A/G | 0.123452 | 0.215605 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038634 | CTCCCTCCTTCCCCC[A/G]TCCCATGATTGGGCA | 26133 |
rs8121148 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042345 | GTTATGATCACCTCA[A/T]GTTCCTAACTAAAAC | 26133 |
rs8121710 | snp | C/T | 0.15698 | 0.23205 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022315 | catgtgccaccacgc[C/T]cagctaatttttcta | 26133 |
rs8121957 | snp | C/T | 0.254105 | 0.249966 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088306 | TTGCCTAAAGACACA[C/T]AGTAAGTAAATACCA | 26133 |
rs8122691 | snp | C/T | 0.123798 | 0.215808 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046354 | TCAACTTTTCTCATT[C/T]TGAACCATCCCCGTG | 26133 |
rs8123978 | snp | C/T | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010986 | catattgaggccggg[C/T]gcggtggttcacgtc | 26133 |
rs8124075 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086475 | tgtgtgtgtgtgtgt[A/G]tatgtgtgtgtatat | 26133 |
rs8124078 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086481 | tgtgtgtgtgtatgt[A/G]tgtgtatatatatat | 26133 |
rs8124081 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086497 | tgtgtatatatatat[A/G]tgtatatatatgtgt | 26133 |
rs8124662 | snp | A/G | 0.250732 | 0.249999 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051453 | ACTGGGACTACAGGC[A/G]TGCACCACCGCACCT | 26133 |
rs8183497 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023541 | GAAATTTTTAATTTA[A/G]GAGATTCTATCTACT | 26133 |
rs8184459 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083741 | aaaagttacctccca[G/T]gtactctttcttggg | 26133 |
rs9647044 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084702 | tgcatatatgtgtat[A/G]tgtatatatgtttat | 26133 |
rs9941751 | snp | A/G | 0.250732 | 0.249999 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057906 | TCTTCTGTTTAAAGA[A/G]CATTTGTAAGTTTAT | 26133 |
rs10485508 | snp | C/T | 0.144969 | 0.226867 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017295 | AAGAGGAATACAATT[C/T]GCCTTTGTAAGCATA | 26133 |
rs10558977 | in-del | -/TAA | 0.334871 | 0.235153 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056509 | GAATATAAATCCTCT[-/TAA]TAACCACTACTGCAT | 26133 |
rs10566932 | in-del | -/TTA | 0.0279526 | 0.114869 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039160 | GCTGGATTTTTACTC[-/TTA]TACTTCTGTTCTCAG | 26133 |
rs10583769 | in-del | -/AAT | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071032 | TTGCAAGAAGCAAAT[-/AAT]GTGCAACTCTTTGAA | 26133 |
rs10627358 | in-del | -/AGAGAA | 0.338211 | 0.235419 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035825 | AGCTGTTTACTTGTT[-/AGAGAA]AGAGAGTAAATTATT | 26133 |
rs10665320 | in-del | -/T/TT/TTT | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024144 | CTTTTTTTTTTTTTT[-/T/TT/TTT]AACAGCTTTGAGGTA | 26133 |
rs10666982 | in-del | -/TT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015462 | TTTTTTTTTTTTTTT[-/TT]TGAGACACAGTCTCA | 26133 |
rs10681837 | in-del | -/TTT | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014335 | TTTTTTTTTTTTTTT[-/TTT]GAGACACAGTCTCAC | 26133 |
rs10875491 | snp | A/G | 0.482534 | 0.0918038 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026342 | acctcagcctcttga[A/G]tagctgggactatag | 26133 |
rs10875492 | snp | C/T | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043604 | ccctcacagtggata[C/T]ctgaaatggcagata | 26133 |
rs10875493 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068984 | ACACACACACAAAAA[A/C]AACAAAACATCTTAA | 26133 |
rs11167253 | snp | C/T | 0.288906 | 0.246954 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026646 | aatctgtaaggctga[C/T]ctatagatcagaatg | 26133 |
rs11167254 | snp | C/T | 0.25045 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066781 | CTAATTTTAAAATAA[C/T]ATCAAAATTTAATTC | 26133 |
rs11167255 | snp | A/G | 0.25045 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068800 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 26133 |
rs11167256 | in-del | -/AA | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090181 | TAAAAAAAAAAAAAA[-/AA]CTAAGAAAAGAAATA | 26133 |
rs11418092 | in-del | -/T | 0.0974055 | 0.198028 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022108 | GACTGAATGGGAACG[-/T]TAAGAGAAGCCCAGC | 26133 |
rs11430339 | in-del | -/T | 0.293551 | 0.246177 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054189 | TGTTTTTTTTTTTTT[-/T]ATTTCCACAGCATAC | 26133 |
rs11467773 | in-del | -/TGTC | 0.0170251 | 0.090679 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046103 | GAGAGCAAGAATTCT[-/TGTC]TTTTTCTTGACTTTA | 26133 |
rs11469382 | in-del | -/TATC | 0.482459 | 0.0919928 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084493 | GTGTATATATGTATA[-/TATC]TATATATGTATATAC | 26133 |
rs11469575 | in-del | -/TA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084609 | ATATATGTGTATATG[-/TA]TATATGTTTATATGC | 26133 |
rs11469576 | in-del | -/TATGTGTATATGTATATATGTTTATATGCATATATGTG | 0.233235 | 0.249437 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084725 | ATGTTTATATGCATA[lengthTooLong]TATATGTATATATGT | 26133 |
rs11471478 | snp | A/C | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068987 | cacacacaAAAAAAA[A/C]AAAACATCTTAAGCA | 26133 |
rs11471950 | in-del | -/GTTTT/TTTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080803 | GACTTGTACACTTCA[-/GTTTT/TTTT]GTTTTTTTTTTTTTT | 26133 |
rs11473089 | in-del | -/T/TT/TTT | 0.398354 | 0.201224 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024130 | GACATGCACACTCAC[-/T/TT/TTT]TTTTTTTTTTTTTTA | 26133 |
rs11473643 | in-del | -/AAGAGA | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035830 | TTTACTTGTTAGAGA[-/AAGAGA]GTAAATTATTAAACA | 26133 |
rs11474630 | in-del | -/AGAGA | 0.388398 | 0.208197 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049488 | AGTTCAGATAGCGGT[-/AGAGA]TAAAGTGGTAAGAGA | 26133 |
rs11475714 | in-del | -/A | 0.490727 | 0.0674567 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023025 | GAGCTGGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 26133 |
rs11477460 | in-del | -/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090948 | CGTACTTTTTCTAAA[-/G]GTTATGTGCTCACTA | 26133 |
rs11478429 | in-del | -/A | 0.483923 | 0.0882034 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090102 | GCAAGATTCTGTCTC[-/A]AAAAAAAAAAAGGGT | 26133 |
rs11478871 | in-del | -/T | 0.334642 | 0.235236 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050393 | ACCTTTGGAACTCCA[-/T]TTTTTTCATCAGTAA | 26133 |
rs11479211 | in-del | -/A | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018626 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAATA | 26133 |
rs11480740 | in-del | -/A | 0.483708 | 0.088773 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052240 | AGGAGCTGGGACTAT[-/A]GGTATATAACACCAC | 26133 |
rs11481073 | in-del | -/G | 0.377656 | 0.214951 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003394 | CCATCACCCCCTTGA[-/G]GGGTGGGGCACTCAC | 26133 |
rs11481657 | in-del | -/A | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030242 | AAAAAAAAAAAAAAA[-/A]GAAGTTGCTTACCAC | 26133 |
rs11482143 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009479 | CTCTACAAAAAAAAA[-/A]GTAAAAACACTAGCT | 26133 |
rs11483432 | in-del | -/A | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087338 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 26133 |
rs11483863 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044401 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAA | 26133 |
rs11552600 | snp | A/T | | | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006474 | GTTCAACGTTGATGC[A/T]TTCAAGAGATTCAAT | 26133 |
rs11552601 | snp | C/T | 1.66871e-05 | 0.00288847 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003526 | CTGCGGCTGCTGCAG[C/T]GGATGGAGCACAGCA | 26133 |
rs11696204 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032557 | gctcactgcaacctc[C/T]gcctcccaggttctc | 26133 |
rs11696386 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091270 | gctgggattacaggG[G/T]CTTAAGTCAGGTCTT | 26133 |
rs11696609 | snp | A/C | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006237 | CCTACCCACAAGCAG[A/C]CCCGGTTttcatccc | 26133 |
rs11696652 | snp | G/T | 0.288386 | 0.247035 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049257 | TTTCGATCATAGCTG[G/T]TTTTTTTTTTTTTTA | 26133 |
rs11697686 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086493 | tgtgtgtgtatatat[A/G]tatgtgtatatatat | 26133 |
rs11697687 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086495 | tgtgtgtatatatat[A/G]tgtgtatatatatgt | 26133 |
rs11697882 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032545 | ggcaggatctcggct[C/T]actgcaacctctgcc | 26133 |
rs11697883 | snp | A/C | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032582 | gttctcgccattctc[A/C]tgcctcaggcctccc | 26133 |
rs11699584 | snp | A/G | 0.498253 | 0.0295011 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086509 | tatgtgtatatatat[A/G]tgtgtgtgtgtatat | 26133 |
rs11905081 | snp | C/T | 0.250168 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053117 | ATAATTTAATACATT[C/T]GTATAATTTATAAAA | 26133 |
rs11905175 | snp | G/T | 0.113334 | 0.209338 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030489 | gtaattgtgcatatt[G/T]tatctatgtatgtta | 26133 |
rs11905247 | snp | C/G/T | 3.29893e-05 | 0.00406125 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021287 | ATTGACTGGGGCAGC[C/G/T]GGGTTCTGGCTGACG | 26133 |
rs11905354 | snp | A/G | 0.253544 | 0.249975 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089361 | gttcctgagcagctg[A/G]gactacaggcatgca | 26133 |
rs11905797 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059758 | gaagaagaagaagac[A/G]aagaagacgacgaag | 26133 |
rs11906019 | snp | A/G | 0.00943375 | 0.0680285 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020365 | ccctgtgagccctca[A/G]ccctcctctcctggc | 26133 |
rs11906126 | snp | A/C | 0.123798 | 0.215808 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020344 | gacagcttgacatga[A/C]ctggtccctgtgagc | 26133 |
rs11906627 | snp | A/T | 0.0696718 | 0.173152 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094109 | gaatagagaacacag[A/T]ataaaaccaaatact | 26133 |
rs11906803 | snp | A/G | | | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003769 | GAGATAGGACTGGGG[A/G]AAGGGGGCCCCCAGC | 26133 |
rs11907019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049602 | TCAGCAAAGTAACAT[A/G]AGGCATCACCCTACA | 26133 |
rs11907438 | snp | A/T | 0.25045 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053417 | TTTAAAACGGCCTCA[A/T]AAAACTAGTGACTAT | 26133 |
rs11907594 | snp | C/T | 0.251014 | 0.249998 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086040 | CACCTCAGCCCTGCC[C/T]CCTTCCCCCTCCCAG | 26133 |
rs11907883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083655 | tccaatttatacttc[C/T]atacccagtcaaact | 26133 |
rs12106042 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083751 | tcccatgtactcttt[C/T]ttgggaggctaccag | 26133 |
rs12480068 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080544 | CCATCTaaaaaaaaa[A/C]aaaaaaaaaaaaCCt | 26133 |
rs12480291 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086477 | tgtgtgtgtgtgtgt[A/G]tgtgtgtgtatatat | 26133 |
rs12480442 | snp | C/G | 0.288906 | 0.246954 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060585 | gagagaccttgtctc[C/G]aaaaaaaaaaaaaaa | 26133 |
rs12624760 | snp | A/C | 0.00952359 | 0.0683454 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043735 | aatgataaaatagaa[A/C]aattgtaacaagatg | 26133 |
rs12624766 | snp | A/G | 0.483636 | 0.0889627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037317 | gcgccactgcactcc[A/G]gcctgggcgaaagag | 26133 |
rs12625172 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011637 | ACTGTGACCCACAAC[A/G]CCCTGTGACTGTGAC | 26133 |
rs12625215 | snp | C/G | 0 | 0 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008570 | GCTTCAGGAGGCATG[C/G]ACGCTGGTGACTAAA | 26133 |
rs12625863 | snp | A/G | 0.483491 | 0.0893421 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087326 | CCTGGGCAACAGAGC[A/G]AGACTCCATCTCAAA | 26133 |
rs12625985 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032397 | cctatctttttattg[G/T]tattctctatttaac | 26133 |
rs12626022 | snp | C/T | 0.46855 | 0.121392 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011638 | CTGTGACCCACAACA[C/T]CCTGTGACTGTGACC | 26133 |
rs13037736 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089659 | ttggagaccagcctg[A/C]ccgacatggtgaaac | 26133 |
rs13038162 | snp | C/T | 0.484632 | 0.086302 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090268 | GGCAGGGGGTCTCTA[C/T]TTCAACTTCTGAAAT | 26133 |
rs13041961 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074093 | tctctgatggtagtt[A/T]gtatttctgtgggat | 26133 |
rs13042358 | snp | A/G | 0.482459 | 0.0919928 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046676 | GAATTTGCTGTGCAG[A/G]GGGCATTGGGGAACA | 26133 |
rs13042653 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059362 | aaaactaaaaactga[C/T]ttaagaagaaacaga | 26133 |
rs13044339 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029889 | gatccgcccacctca[G/T]actcccaaagtgctg | 26133 |
rs13045538 | snp | C/T | 0.0244538 | 0.107838 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007722 | GGGGTTGGGAGATGT[C/T]TGTTGCCTTTTCATG | 26133 |
rs13433216 | snp | C/T | 0.288127 | 0.247076 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028498 | tcccaagtttgttat[C/T]tatttctaactcacc | 26133 |
rs17092208 | snp | C/T | 0.0277325 | 0.114443 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003227 | GGGTGACTGCCGGTC[C/T]GGGTTCAACAGGATG | 26133 |
rs17092209 | snp | A/G | 0.089084 | 0.191327 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004918 | TGACGCTGCATTAAG[A/G]AAAACAACGCAAAAG | 26133 |
rs17092210 | snp | A/C | 0.101658 | 0.201233 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005328 | CGCGTGCGCATACAC[A/C]TGGAAGTGCGTTAGC | 26133 |
rs17092212 | snp | A/G | 0.095934 | 0.196885 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005580 | CTTGAGGCCGGCCAC[A/G]TGGGCATCTGGTGCA | 26133 |
rs17092215 | snp | C/T | 0.25045 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008110 | CACAGCGGGTATCCA[C/T]GACAGGGAGTTTGGA | 26133 |
rs17092221 | snp | A/C | 0.0919752 | 0.193722 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011941 | ATCACTAATGCTCAA[A/C]GGTGGAATCCTTGGA | 26133 |
rs17092223 | snp | C/G | 0.0966517 | 0.197444 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039301 | TACTCAGGGTTCTAA[C/G]TCTGACTTCCCACCT | 26133 |
rs17092225 | snp | C/T | 0.0277811 | 0.114537 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044483 | CTATAATCTCAAAAT[C/T]CTGAGAACTTGGAGA | 26133 |
rs17092242 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065862 | ACATCAGTTCTTACT[A/G]AGTAGATTTCTTGAT | 26133 |
rs17092244 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066033 | ACACTCAATCTTTAC[C/T]TTACTGGAAAATGGT | 26133 |
rs17092274 | snp | A/G | 0.0107246 | 0.0724382 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093520 | CAGGGTTTTCATCTG[A/G]CAGAGAATATGATGT | 26133 |
rs17317888 | snp | G/T | 0.148661 | 0.22854 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007156 | GATTTTATAATTCGT[G/T]GGTCAGTTTCTTGTC | 26133 |
rs17319032 | snp | C/T | 0.288906 | 0.246954 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055493 | GTAGAACTACTAGAA[C/T]CTAAAGTATAGGCAT | 26133 |
rs17404569 | snp | A/C | 0.483636 | 0.0889627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086274 | TAAATAGATATCTTA[A/C]AGGATAATAAAGATA | 26133 |
rs28368375 | snp | A/T | 0.0836354 | 0.186609 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021829 | TCCCCGTTTTTTAAA[A/T]GAAGAACCATCTAAA | 26133 |
rs28416097 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086569 | TGTGTGTGTGTGTGT[A/G]TGTGTGTATATATAT | 26133 |
rs28520715 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086507 | TATATGTGTATATAT[A/G]TGTGTGTGTGTGTAT | 26133 |
rs28533393 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086517 | TATATATGTGTGTGT[A/G]TGTATATATGTGTGT | 26133 |
rs28536059 | snp | A/G | 0.192715 | 0.243348 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086525 | TGTGTGTGTGTATAT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs28680298 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086499 | TGTATATATATATGT[A/G]TATATATATGTGTGT | 26133 |
rs28712561 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086485 | TGTGTGTATGTGTGT[A/G]TATATATATATGTGT | 26133 |
rs28820635 | snp | A/G | 0.288906 | 0.246954 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029778 | GCAGCTGGGACTACA[A/G]GCGCCCGCCACCACG | 26133 |
rs28871333 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026540 | ACTGTTTTTGTTAAT[C/T]CAAGTCTCCTGCATT | 26133 |
rs33911641 | in-del | -/TTT/TTTT | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089050 | ACACCTTTTTTTTTT[-/TTT/TTTT]AAGATACAGGGTTTC | 26133 |
rs34052264 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054968 | CCCCAGTGGCAGGGG[-/G]TACTTACACAGACAC | 26133 |
rs34081482 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018723 | AGGTCCAGCCCCGTA[-/G]CCTGCTCTATAGCAG | 26133 |
rs34091819 | in-del | -/CA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051069 | ACACACACACACACA[-/CA]TATATATCCCACCCC | 26133 |
rs34177220 | in-del | -/A/AC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036961 | ACGTGCGCACACAAA[-/A/AC]CACACACACACACAC | 26133 |
rs34261821 | snp | A/C | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024843 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAAAATTC | 26133 |
rs34279472 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014434 | GCAATTCTGGTGGCC[A/G]CTCCACAGACATTAC | 26133 |
rs34293481 | in-del | -/TGTGTGTGTGTGTATATATGTGTGTGTG | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086535 | GTGTATATATATATA[-/TGTGTGTGTGTGTATATATGTGTGTGTG]TGTGTGTGTGTGTAT | 26133 |
rs34337249 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054239 | CACATTTATAATAGC[A/G]CTCGTCTCATTCTGC | 26133 |
rs34344985 | snp | A/C | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024836 | GTCTCAAAAAAAAAA[A/C]AAAAAAAAAAAAAAA | 26133 |
rs34370030 | in-del | -/GTTTT/TTTT/TTTTGT/TTTTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080804 | ACTTGTACACTTCAG[-/GTTTT/TTTT/TTTTGT/TTTTT]TTTTTTTTTTTTTTA | 26133 |
rs34387096 | in-del | -/T | 0.483708 | 0.088773 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038767 | TTTAGGTGTGTATTA[-/T]TTTTTTCTAAAAACA | 26133 |
rs34427070 | in-del | -/A | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35087353 | AAAAAAAAAAAAAAA[-/A]GTCAGTGAATCTAAA | 26133 |
rs34455434 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061245 | AATTCCATTTAAAGG[-/G]AGCATCAAAAACAGT | 26133 |
rs34481467 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006988 | ATTTTGACCCCATGG[-/G]TTTGTCTTTGTGTTT | 26133 |
rs34523684 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023581 | CTCCTGTACCTTGGG[-/G]CAAAAAACTATAGTT | 26133 |
rs34633366 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048136 | TTTCTTTCTTGTCTG[G/T]GAAATGCTTGTTCAT | 26133 |
rs34642944 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062749 | TTGGAGTGATGAAAA[-/A]TGTTTTAAAATCAAT | 26133 |
rs34678599 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047471 | CTACTATATAATATT[-/G]CCATTGTGTGAAGAA | 26133 |
rs34679450 | in-del | -/AGA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059917 | AGACGAAGACGAAGA[-/AGA]CAAAGACGAAGAAGA | 26133 |
rs34750023 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054371 | TTTCACATCTACTAT[-/G]CTCATTTCTCACAAT | 26133 |
rs34778468 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042098 | TATGTGCCATGTTGG[-/G]AAAGTCACATATTTT | 26133 |
rs34916579 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092511 | CGGCCAGCCAAAAGG[-/G]CTTTGGCCCGTCCAG | 26133 |
rs35003167 | in-del | -/A | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094586 | GAAAAAAAAAAAAAA[-/A]TAGCCAAAGAAGTTA | 26133 |
rs35047668 | in-del | -/A | | | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35007652 | AACCTGCGACCCAAA[-/A]TACTGGCTCAGGTGG | 26133 |
rs35143678 | in-del | -/A | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060610 | AAAAAAAAAAAAAAA[-/A]CAAGAAAAGGATTAT | 26133 |
rs35227212 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065328 | CCCAAAACATTCCCC[-/C]ATACTCATTTAATTT | 26133 |
rs35352745 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020224 | AGGGCCCCTAATGGT[-/G]CGCCCTATTCCCTTC | 26133 |
rs35372826 | in-del | -/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029629 | TCCCAAGTTACTTTC[-/T]TTTTTTTTTTTTTTT | 26133 |
rs35374751 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061402 | GTTAAGATGATAATA[-/A]CTCCCTAAATTGACC | 26133 |
rs35461400 | in-del | -/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089412 | TTTTTTTTTTTTTTT[-/T]GTAGTAGAGCTGGGG | 26133 |
rs35473399 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063017 | CCAAATCTCACCTTC[-/C]AATTGTAATAATCCT | 26133 |
rs35478505 | in-del | -/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038285 | ACCATTTTTTTTTTT[-/T]AACATATCAGCTTGG | 26133 |
rs35561710 | in-del | -/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017993 | TAACTGGGGGTGGGG[-/G]AGGTACGGCTGACAT | 26133 |
rs35593144 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012451 | CCACATCACCTCCCC[-/C]AATGCCAAGGTCAAG | 26133 |
rs35659686 | in-del | -/AT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084646 | TGTGTATATGTATAT[-/AT]GTTTATATGCATATA | 26133 |
rs35677907 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041043 | GATACAATAAAAAGG[-/T]GGCCTTCTACAAGCC | 26133 |
rs35697723 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037584 | ATTCAGCCATATAAA[-/A]GGAATGAAGTACTGA | 26133 |
rs35724723 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083739 | AAAAAGTTACCTCCC[-/C]ATGTACTCTTTCTTG | 26133 |
rs35755461 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018258 | TCAGGCCAGTGCTTA[A/G]GTTTGAGGTTTCTAC | 26133 |
rs35758054 | in-del | -/CTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047174 | CTGGCCAAGAATTTA[-/CTT]CTTATGTTTTAATTT | 26133 |
rs35771366 | in-del | -/TG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086508 | ATATGTGTATATATA[-/TG]TGTGTGTGTGTATAT | 26133 |
rs35794517 | in-del | -/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026223 | TTGTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 26133 |
rs35801271 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037767 | CAGATTATAATACTG[G/T]ATTTTTACTATACCT | 26133 |
rs35808832 | in-del | -/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032489 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 26133 |
rs35810831 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069841 | GCTACTCAGGAATTT[-/T]GAAGTACAAGAAGCA | 26133 |
rs36065765 | in-del | -/TT/TTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024143 | ACATGCACACTCACT[-/TT/TTT]TTTTTTTTTTTTTAA | 26133 |
rs41290906 | snp | A/G | 0.0611399 | 0.163804 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057470 | AACTGCCACCGTATC[A/G]GCAGGTTGGAAAACA | 26133 |
rs55633140 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093835 | AAAAGTGACTCTCCC[A/G]GGTGAACTGGCACTA | 26133 |
rs55703444 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086455 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs55776381 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086483 | TGTGTGTGTATGTGT[A/G]TGTATATATATATGT | 26133 |
rs55946144 | snp | C/T | 0.250732 | 0.249999 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041807 | CCAATACAGAACCTT[C/T]CTAGCCCTCAGTTTC | 26133 |
rs55993524 | snp | C/T | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086201 | TGAGCTTAAAGAATC[C/T]GTCTAGCTCGGCCTC | 26133 |
rs56108599 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086453 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs56363533 | snp | C/G | 0.251014 | 0.249998 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038202 | AGTTGTTCACTTTAA[C/G]ACGGCTAATTTTATG | 26133 |
rs56666362 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051633 | AAAAAAAAAAAAAAA[-/A]GGTTGTTATTCCCGA | 26133 |
rs56749221 | in-del | -/AT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084614 | TGTGTATATGTATAT[-/AT]GTTTATATGCATATA | 26133 |
rs57030277 | in-del | -/TTTGTTTACTA | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089543 | GGCCTATATTATATA[-/TTTGTTTACTA]CAATGAAAAAATTTT | 26133 |
rs57144406 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086577 | TGTGTGTGTGTGTGT[A/G]TATATATATGAATAA | 26133 |
rs57540562 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086527 | TGTGTGTGTATATAT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs57697362 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045683 | AGTGGGGATTACAGG[C/T]GCCCGCCACCACGCC | 26133 |
rs57896641 | in-del | -/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015480 | TTTTTTTTTTTTTTT[-/T]GAGACACAGTCTCAC | 26133 |
rs58076215 | in-del | -/GTATGTTTATATGCATATATGTGTATATGTAT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084644 | TATGTGTATATGTAT[lengthTooLong]ATATGTTTATATGCA | 26133 |
rs58208529 | snp | G/T | 0.123452 | 0.215605 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036623 | TAACCCAAGGTGAAG[G/T]AGGGTATAGTGAATG | 26133 |
rs58209783 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012341 | TGCCTTTGCTTGGCA[A/G]AAAAAATCAGAAGTT | 26133 |
rs58614584 | in-del | -/A | | | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094586 | AAAAAAAAAAAAAAA[-/A]TAGCCAAAGAAGTTA | 26133 |
rs58763520 | in-del | -/GT/GTTT | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080808 | GTACACTTCAGTTTT[-/GT/GTTT]TTTTTTTTTTACCCT | 26133 |
rs58968594 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35045353 | CAATCACTTCCCGCC[A/G]TTTTACCCCACAGTT | 26133 |
rs59492667 | in-del | -/AA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060609 | AAAAAAAAAAAAAAA[-/AA]CAAGAAAAGGATTAT | 26133 |
rs59579695 | in-del | -/AAAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034175 | AAAAAAAAAAAAAAA[-/AAAA]GAGTAAAAAAAAAGA | 26133 |
rs59685764 | in-del | -/AT | 0.00716266 | 0.059414 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051070 | CACACACACACACAC[-/AT]ATATATCCCACCCCT | 26133 |
rs59909520 | in-del | -/G | 5.53838e-05 | 0.00526202 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35003304 | AAAGAGGGAGGGGCT[-/G]GGGGGGCGCCTGGAG | 26133 |
rs59920318 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054203 | TGTTTTTTTTTTTTT[A/T]TTTCCACAGCATACA | 26133 |
rs59955315 | in-del | -/A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043056 | TATACCATATACACA[-/A/G]CTGTTCTGTATTTTC | 26133 |
rs60008149 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020640 | CTCCCTAGAAGGGCG[C/T]GGTCTGCAGGAAAAG | 26133 |
rs60911221 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054202 | ATGTTTTTTTTTTTT[A/T]ATTTCCACAGCATAC | 26133 |
rs60932055 | in-del | -/AGAAGA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059721 | GAAATAAGAAGAAGA[-/AGAAGA]GGAAGAAGACTACGA | 26133 |
rs60959870 | in-del | -/C | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016291 | AAAACATCCGTGTAT[-/C]CCCTATGCCCAGCAC | 26133 |
rs61542836 | in-del | -/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072425 | TTTAGGTCTAACATT[-/T]AAGTCTTTAATCAAT | 26133 |
rs61653757 | in-del | -/C | 0.448066 | 0.152544 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080543 | CCATCTAAAAAAAAA[-/C]AAAAAAAAAAAAACC | 26133 |
rs61745054 | snp | A/G | 0.0317056 | 0.121851 | downstream-variant-500B, intron-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002124 | TCTCTGTGCAGGGGG[A/G]CTGTGGGGGCTGACA | 26133 |
rs62213675 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018104 | ATGTTCCAACAATGG[A/C]CCAAAAAAATTCATC | 26133 |
rs62213676 | snp | A/T | 0.482757 | 0.0912364 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024873 | CTGTTTATTCATTAA[A/T]CAGGTGACAGTCATT | 26133 |
rs62213677 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032248 | CTGGCCAATCTTGAA[C/T]TCCTGGCCTCAAATG | 26133 |
rs62213678 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032369 | ACTTCCACTGGGCTC[C/T]TTTCAAATACTTCCT | 26133 |
rs62213708 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051069 | ACACACACACACACA[C/T]ATATATATCCCACCC | 26133 |
rs62213709 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054593 | TGCTCAATATATGGG[C/T]GGGGCTTCTGGTTCT | 26133 |
rs62213710 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059820 | AGACAAAGATGAAGA[C/T]GAAGAAGATGAAGAC | 26133 |
rs62213711 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059836 | GAAGAAGATGAAGAC[A/G]AAGAAGACGAAGATG | 26133 |
rs62213712 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059850 | CAAAGAAGACGAAGA[A/T]GAAGATGAAGAAAAG | 26133 |
rs62213713 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059890 | AGACGAAGACAAAGA[C/T]GAAGATGAAGAAGAC | 26133 |
rs62213714 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059896 | AGACAAAGATGAAGA[C/T]GAAGAAGACGAAGAC | 26133 |
rs62213715 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059905 | TGAAGATGAAGAAGA[C/T]GAAGACGAAGAAGAC | 26133 |
rs62213716 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059911 | TGAAGAAGACGAAGA[C/T]GAAGAAGACAAAGAC | 26133 |
rs62213718 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086511 | TGTGTATATATATGT[A/G]TGTGTGTGTATATAT | 26133 |
rs62213719 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086519 | TATATGTGTGTGTGT[A/G]TATATATGTGTGTGT | 26133 |
rs62213720 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086539 | TATGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs62213721 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086541 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs62213722 | snp | A/G | 0.495855 | 0.045338 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086571 | TGTGTGTGTGTGTGT[A/G]TGTGTATATATATAT | 26133 |
rs62213723 | snp | A/G | 0.495855 | 0.045338 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086573 | TGTGTGTGTGTGTGT[A/G]TGTATATATATATGA | 26133 |
rs62213724 | snp | A/G | 0.489259 | 0.0724914 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086575 | TGTGTGTGTGTGTGT[A/G]TATATATATATGAAT | 26133 |
rs62213736 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090983 | TTAGTCCTCTTTCTG[C/T]CTGTCTCTACACACC | 26133 |
rs66497534 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052241 | GGAGCTGGGACTATG[-/A]GTATATAACACCACG | 26133 |
rs66518839 | in-del | -/TTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014333 | GGCCTCAGGCAGAAT[-/TTT]TTTTTTTTTTTTTTT | 26133 |
rs66535333 | snp | A/G | 0.483491 | 0.0893421 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068863 | AGAAGAAGAAAGAAG[A/G]TACAGAATAGTGTAG | 26133 |
rs66539354 | in-del | -/C | 0.334642 | 0.235236 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048212 | AAAAAAAAAAAAAAA[-/C]AGAATTCTTACAAAT | 26133 |
rs67550472 | in-del | -/AAG | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059792 | AAGAAGATGAAGAAG[-/AAG]GCGAAGACGAAGACA | 26133 |
rs67554713 | in-del | -/AGAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038597 | CCATCTGTACAAACA[-/AGAA]GGAGTCAATCTCTCT | 26133 |
rs67627695 | in-del | -/A | 0.482459 | 0.0919928 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041128 | ATTTATTTTTCTCAC[-/A]GTTCTGGAGGCTAGA | 26133 |
rs67999415 | in-del | -/GTCTTCGTCTTCTTC | 0.49607 | 0.0441545 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059897 | GTCTTTGTCTTCTTC[-/GTCTTCGTCTTCTTC]ATCTTCATCTTTGTC | 26133 |
rs68050373 | in-del | -/GAAGACGAAGAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059906 | GAAGATGAAGAAGAC[-/GAAGACGAAGAC]AAAGACGAAGAAGAC | 26133 |
rs71196775 | in-del | -/AA | 0.478932 | 0.10045 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028211 | GAGTGAGATTCCATC[-/AA]AAAAAAAAAAAAGGA | 26133 |
rs71196778 | in-del | -/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037369 | AATTTTATGTTTGAC[-/T]TTTTTTTTTTTTTTT | 26133 |
rs71196779 | in-del | -/CTTT | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038598 | GAGAGAGATTGACTC[-/CTTT]CTGTTTGTACAGATG | 26133 |
rs71196781 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058688 | AAAAAAAAAAAAAAA[-/A]AGAATTTTCTTTTAA | 26133 |
rs71196782 | in-del | -/CTT | 0.4856 | 0.0836214 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059672 | TTCCTTCTTCTTCTT[-/CTT]TTTTTTCTTTTAAAG | 26133 |
rs71196783 | in-del | -/TGTG | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068971 | TTTTTTTTTTTTGTG[-/TGTG]TGTGTGTGTGTGTGT | 26133 |
rs71196784 | in-del | -/T | 0.482831 | 0.0910472 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079860 | ACCACCCTTGGCTTA[-/T]TTTTTTTTTTTTATT | 26133 |
rs71196785 | in-del | -/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080014 | GGTTATAATGATGTC[-/T]TTTTTTTTTTTTTTT | 26133 |
rs71196786 | in-del | -/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080556 | CTGGCTTCTTTTAGG[-/T]TTTTTTTTTTTTTTT | 26133 |
rs71196788 | in-del | -/T | 0.499527 | 0.0153681 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085609 | TTTTTTTTTTTTTTT[-/T]TAGACAGGGTCTTGC | 26133 |
rs71196792 | in-del | -/AAAAAAA | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090394 | GTGAGACTTCATCTC[-/AAAAAAA]AAAAAAAAAAAAAAA | 26133 |
rs71299218 | in-del | -/AA/G/GA | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031415 | AACCCCATCTCTTTG[-/AA/G/GA]AAAAAAAAAAAAAAA | 26133 |
rs71337964 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084676 | TATGTGTATATGTAT[A/G]TATGTTTATATGCAT | 26133 |
rs71337965 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086549 | TATGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 26133 |
rs71349784 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027313 | GAAACGATCATGTGG[G/T]TTTTGTCCTTTATTC | 26133 |
rs71349785 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086547 | TATATGTGTGTGTGT[A/G]TATGTGTGTGTGTGT | 26133 |
rs71891942 | in-del | -/AC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051034 | GTACTGCTATAGCTT[-/AC]ACACACACACACACA | 26133 |
rs72010225 | in-del | -/A | 0.387832 | 0.208572 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033829 | AACCCGTCTCTATTC[-/A]AAAAAAGAGAAAATA | 26133 |
rs72187724 | in-del | -/GAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059912 | GAAGAAGACGAAGAC[-/GAA]GAAGACAAAGACGAA | 26133 |
rs72216231 | in-del | -/TATTTGTTTAC | 0.484632 | 0.086302 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089541 | CTGGCCTATATTATA[-/TATTTGTTTAC]TACAATGAAAAAATT | 26133 |
rs72350296 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068962 | CACACACACACACAC[-/A]ACACACACACACACA | 26133 |
rs72363864 | in-del | -/TTT/TTTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089048 | CTTAACTATACACCT[-/TTT/TTTT]TTTTTTTTTAAGATA | 26133 |
rs73095147 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009890 | GGCTGAATGCACGAG[A/T]CAAGGCGGTGGGGCA | 26133 |
rs73095150 | snp | C/T | 0.0209421 | 0.100162 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012737 | AGAAATCCATTGATT[C/T]CAAAGGTAGTAAGGG | 26133 |
rs73095192 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048723 | GGGAGTGAGAGGCAA[C/G]TGGGAAAAGTTGTGA | 26133 |
rs73269566 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009394 | GAGAGGTGGTTCACA[C/T]CTGTAATCCCTGGAC | 26133 |
rs73273811 | snp | C/G | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028586 | CTTTTTTTTAACAGC[C/G]TAGCATATGGTCTGT | 26133 |
rs73273814 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028919 | TATTATCAAATATCC[C/T]TATTTTGCTCTGATA | 26133 |
rs73273826 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032413 | TATTCTCTATTTAAC[A/G]ACACATTATCAAATA | 26133 |
rs73273831 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033686 | CTGTAGATCACCCTG[C/T]TCTTAATTAAGAAGA | 26133 |
rs73273856 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046284 | GAATGCCTTGTGCTA[C/T]TTGGTTCTATTCTCA | 26133 |
rs73273857 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049740 | AGTTTTATACTTGAA[C/T]ACATCTGAGTAACAA | 26133 |
rs73273859 | snp | C/T | 0.095934 | 0.196885 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050080 | ACAGACACTGAAAAG[C/T]AGTTTCACCTCTGAA | 26133 |
rs73273863 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052255 | TGGTATATAACACCA[C/T]GTCCAGCCAGTTTTT | 26133 |
rs73273864 | snp | A/T | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052354 | CTGCCTCGGCCTATC[A/T]AAGTGTTGAGATTAT | 26133 |
rs73273874 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065070 | ATCACATTCATCCAA[A/G]TAAGACGTAAGATGC | 26133 |
rs73273898 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084253 | CCAGCCGGGCAACAG[C/T]GCGAGACTCCGTCCC | 26133 |
rs73275915 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093290 | CTGGGGCTTTCTCTG[A/C]GCCCGACACCAAACC | 26133 |
rs73616614 | snp | A/C | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024826 | GAGAGAGACCGTCTC[A/C]AAAAAAAAAAAAAAA | 26133 |
rs73616615 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031145 | CCATTATTCCTGATG[A/C]GCAGTCAGCCACTAA | 26133 |
rs73616616 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049246 | TTTAGTTTTCATTTC[A/G]ATCATAGCTGTTTTT | 26133 |
rs73616620 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077340 | CCTGTCTTAGGCATC[A/G]CTCATGCTGGGTACC | 26133 |
rs73616621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089111 | TGGGCTCAAACAATC[C/T]GCTCACCTCAGCTTC | 26133 |
rs73621678 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029964 | TAGAAGTTGCTGGCT[-/G]GGCGCGGTGGCTCAT | 26133 |
rs73621681 | in-del | -/A | 0.483199 | 0.0901004 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043055 | CTATACCATATACAC[-/A]ACTGTTCTGTATTTT | 26133 |
rs73622025 | in-del | -/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085095 | AGAAATACTGGCTCT[-/C]CTGTTTCCTGGATCC | 26133 |
rs73903005 | snp | C/T | 0.123798 | 0.215808 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066670 | AGAAGGAAATAGGCA[C/T]GGTTTAAATCCAACA | 26133 |
rs73903009 | snp | A/G | 0.250732 | 0.249999 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090929 | GATAACATATGCCTT[A/G]TACCGTACTTTTTCT | 26133 |
rs73905041 | snp | A/G | 0.243919 | 0.249926 | intron-variant, missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004345 | GTCCTCAGAAGAGCT[A/G]GGTCTCCAGAGACGC | 26133 |
rs73905045 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008461 | GCTTGGTGAATGCTC[A/G]GTCACTGTGGGCTGC | 26133 |
rs73905050 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020639 | CCTCCCTAGAAGGGC[A/G]CGGTCTGCAGGAAAA | 26133 |
rs73905055 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034583 | CTATTCCTTGTTTGG[C/G]AGCTGAGAATTCCTG | 26133 |
rs73905057 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040109 | CCCACAAATTCATAC[A/G]TTGAAGCTCTAGCCC | 26133 |
rs73905063 | snp | C/T | 0.0839998 | 0.186933 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056189 | GATTGATTTATTTAA[C/T]GACTTCAGAGCAGGG | 26133 |
rs74173926 | in-del | -/A | 0.5 | 0 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003782 | GGAAGGGGGCCCCCA[-/A]GCAGCCCCAGTTTCC | 26133 |
rs74173928 | in-del | -/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051470 | GCACCACCGCACCTG[-/G]CAAATTTAATTTTCA | 26133 |
rs74173929 | in-del | -/GAA | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059683 | AAAAAAGAAGAAGAA[-/GAA]GGAAGAAGAAGAAAG | 26133 |
rs74173931 | multinucleotide-polymorphism | GGT/TTC | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070507 | GCTCTGCCTCCCGGG[GGT/TTC]ACGCCATTCTCCTGC | 26133 |
rs74323250 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061105 | CCTAAAGAATCCACT[A/C]AAAAAAACTATTAGA | 26133 |
rs74543591 | snp | C/T | 0.148661 | 0.22854 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070855 | AATCCTTTGTTCATA[C/T]GGAACAAAGCTAAGA | 26133 |
rs74605061 | snp | A/T | 0.0201592 | 0.0983524 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069424 | TTTCCTAGTTTTTTT[A/T]AAAAAAAGTACATAC | 26133 |
rs74610303 | snp | A/G | 0 | 0 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094573 | AGACTCCATCTCAGA[A/G]AAAAAAAAAAAAATA | 26133 |
rs74637704 | snp | A/C | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059926 | CGAAGAAGACAAAGA[A/C]GAAGAAGACGAAGAA | 26133 |
rs74742197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021548 | AGAGACTCGGAAAAA[C/T]GGACTCTGCAATAGT | 26133 |
rs74747438 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051071 | ACACACACACACACA[C/T]ATATATCCCACCCCT | 26133 |
rs74883214 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063140 | TCTGATGATTTTATA[A/G]GTGTCTGGCATTTCC | 26133 |
rs74906646 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047956 | CTACAAAACAAAAAA[A/C]AAGAGGATATTCTGC | 26133 |
rs74998104 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004939 | AACGCAAAAGTTCCA[C/T]TCCTTCTGCAGAGGT | 26133 |
rs75063217 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062835 | TAATATATCTTTTAA[A/G]TGGGTGACTTGTATG | 26133 |
rs75159393 | snp | A/G | 0.0629771 | 0.165899 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093315 | CAAACCATGTCTAGG[A/G]GAAAGGGAGGGTGTC | 26133 |
rs75165171 | snp | A/G | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063650 | GATCATTTGAGACCA[A/G]GAGTTGGAGACTGCC | 26133 |
rs75225837 | snp | C/T | 0.0168055 | 0.0901129 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094627 | ATATTTTGTTCCCTA[C/T]AGAAACTGAATATAA | 26133 |
rs75227286 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091066 | TTTTTTTTTTTTTTT[G/T]AGACAGGGTCTCACT | 26133 |
rs75227887 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047642 | CTTTTTAGCTATCAC[A/C]AAGAACGACCACCAG | 26133 |
rs75229350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020324 | AAGTCTTTAAAATGG[C/T]CTGTGACAGCTTGAC | 26133 |
rs75304943 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043794 | TCTCTCTGGAATTTT[C/T]CAGTTAATATTTTCG | 26133 |
rs75377266 | snp | A/C | 0.279991 | 0.248195 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068980 | ACACACACACACACA[A/C]AAAAAACAAAACATC | 26133 |
rs75383229 | snp | C/T | 0.242201 | 0.249878 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35025848 | TGTATGACAGCTAAA[C/T]TGTTAAATCCAAGGT | 26133 |
rs75404979 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054473 | AGCCAAGGGCCAGAA[A/C]ACAAAATCAGGTCCT | 26133 |
rs75459464 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062562 | GAACATTATGTTAAG[A/C]AAAAGAAGCCAGTCA | 26133 |
rs75501571 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064447 | TAATTCACATGCCAT[A/G]AGATTGCTCGTGGCA | 26133 |
rs75513290 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020979 | AAGACTGCCTAGAAA[C/T]GCTCCATACAGCAAG | 26133 |
rs75535620 | snp | C/T | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35013695 | GAGCCAAGGAACTGA[C/T]ACTCAGCAGCTGTGG | 26133 |
rs75537616 | snp | C/T | 0.146985 | 0.227789 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004785 | CCCAGGAGCACCCCA[C/T]CTCATCCTCCAGAAC | 26133 |
rs75624842 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028687 | TCTCTGTTAGTCCTT[A/G]TTGGTATACAGTGTT | 26133 |
rs75632179 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023405 | TAAATAGAAGTTAAG[G/T]TCTCAGAAAACTGAG | 26133 |
rs75654531 | snp | G/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014333 | TTTTTTTTTTTTTTT[G/T]TTGAGACACAGTCTC | 26133 |
rs75820351 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094574 | GACTCCATCTCAGAA[A/G]AAAAAAAAAAAATAG | 26133 |
rs75887482 | snp | A/G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093824 | ACGGTAGGCATAAAA[A/G/T]TGACTCTCCCAGGTG | 26133 |
rs75910003 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006799 | CAGCACAATCTCTCC[C/T]CTGCCCAGGGCGTAC | 26133 |
rs75971237 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091821 | TTTACACAATTGCCC[C/T]CTTTGATCTCCACAA | 26133 |
rs76063978 | snp | A/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027956 | ATTACCTTTAAAAAA[A/T]TCACCTTTGGTTTTA | 26133 |
rs76223987 | snp | C/T | 0.147321 | 0.227941 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030669 | ATTCAAGTTGCAATT[C/T]GGTGTCATGATACTC | 26133 |
rs76238959 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064927 | CACCTAACGGTCTTG[A/G]TATACACAAGCTTTA | 26133 |
rs76262079 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054445 | AAGAAACTACGGCTT[G/T]GGAGGTGTACTAAGC | 26133 |
rs76280557 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026235 | TTGTTTTTTTTTTTT[G/T]AGACAGAGTCTTGCT | 26133 |
rs76363448 | snp | C/T | 0.147991 | 0.228242 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067732 | TAGAAATCATTACGC[C/T]AAGTGAAAAGAAGCC | 26133 |
rs76482035 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026103 | AAGCATGAGGGTTTA[C/T]TTCTGAACTCTCAAC | 26133 |
rs76507298 | snp | A/T | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035719 | GTTCATCAACAGCTG[A/T]TTAATTAAATACAAT | 26133 |
rs76513573 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008821 | TGGGTCATTCTGCTG[C/G]CTTAGGCGGTGAAAA | 26133 |
rs76622792 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037838 | ACAACTGCCTACTGT[A/T]TTTAGTACAGAAACA | 26133 |
rs76633046 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094571 | TGAGACTCCATCTCA[A/G]AAAAAAAAAAAAAAA | 26133 |
rs76665252 | snp | C/T | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35056184 | TCTGTGATTGATTTA[C/T]TTAACGACTTCAGAG | 26133 |
rs76762134 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037489 | TAGCAGCACTATTCC[A/C]AACAGCCAAAAGATG | 26133 |
rs76795850 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076625 | ATCCTTTCTCTGGAA[A/G]CTTCATCTCAGAGGG | 26133 |
rs76850134 | snp | A/C | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083922 | AACTGCTAAACTGCT[A/C]AACTGCAGTAGGGGA | 26133 |
rs76898922 | snp | A/C/G | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | TRPC4AP | GRCh38.p7 | 20:35009105 | AGGGTGAGGCCCAGC[A/C/G]TACTCCGTGCCTGAG | 26133 |
rs76903154 | snp | A/C | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085449 | GAACCTTATCTCTAC[A/C]AAAAAATACAAAAAT | 26133 |
rs76907781 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058414 | TTTCAGGCCACTGAA[A/C]AAGCCTCAATAAATT | 26133 |
rs77014858 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091065 | ATTTTTTTTTTTTTT[G/T]GAGACAGGGTCTCAC | 26133 |
rs77024009 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082114 | ATCTAATAAAAACTT[A/C/T]AACATACATAAAGCA | 26133 |
rs77063383 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002321 | CCCTGAATAAACACC[A/C]CAGCCAGTTTCCTTC | 26133 |
rs77085049 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033404 | CTCCCTGGGATGACA[C/T]TGAGCCAGGCTGTCT | 26133 |
rs77089953 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043264 | TTTTTTTTTTTTTTT[G/T]GAGACGGAGTCTAAT | 26133 |
rs77125017 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053447 | TATGGAGTTGCCAAA[A/G]ATGGAGTCATTATAT | 26133 |
rs77142686 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005313 | AGGAAAAAAAGGAAA[C/T]GCGTGCGCATACACA | 26133 |
rs77236645 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059921 | GAAGACGAAGAAGAC[A/G]AAGACGAAGAAGACG | 26133 |
rs77416002 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031927 | GACAAAGTCTCACTT[C/T]GTCACCCAGGCGCAA | 26133 |
rs77509444 | snp | A/C | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090101 | AGCAAGATTCTGTCT[A/C]AAAAAAAAAAAAGGG | 26133 |
rs77577905 | snp | A/C | 0.46875 | 0.121031 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068976 | ACACACACACACACA[A/C]ACAAAAAAAACAAAA | 26133 |
rs77642827 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093052 | CCCAAGGTCCACATT[A/C]TCCCATTTCTCTCGC | 26133 |
rs77653624 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024913 | TCCATATTTTGGCTG[G/T]TATGAATATGCTGTG | 26133 |
rs77729998 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091930 | CAAGCAAGAGAGAGG[A/G]GCAGGGCTTTGAACC | 26133 |
rs77947413 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060726 | CAATAGAATAAAGGA[A/C]AAAAGCCAAAAGCCA | 26133 |
rs77966079 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002318 | GGGCCCTGAATAAAC[A/C]CCACAGCCAGTTTCC | 26133 |
rs77989763 | in-del | -/A/CA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050722 | AACTCAAAAAAAAAA[-/A/CA]ACAAAACAAAAAAAC | 26133 |
rs78035764 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043265 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTAATT | 26133 |
rs78055011 | snp | A/G | 0.147991 | 0.228242 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030803 | TTTAACTGAAGAAAA[A/G]GAGAAGAAATATGCA | 26133 |
rs78099018 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040948 | CCCTAAACCGAGAGG[A/G]CTGGTGTCCTTCTAA | 26133 |
rs78119421 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055108 | CACATTTTTTTCAGC[A/G]TAAGAACTGTTATAA | 26133 |
rs78121704 | snp | A/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051617 | AGCACTGACACATTA[A/T]AAAAAAAAAAAAAAA | 26133 |
rs78202808 | snp | C/T | 0.25045 | 0.25 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079621 | GATCAATACGATTGA[C/T]AAACTCTAACCAGGC | 26133 |
rs78295806 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021760 | ACTTGGTTCTTCTGC[A/T]GAGACTCCATGAGGG | 26133 |
rs78324790 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085044 | AATAGATAGTATCTA[A/G]AAGTGAAAAGAAACA | 26133 |
rs78330058 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005158 | GAAAAAGGAAGCAAA[C/T]GGCTAAATTACCAAC | 26133 |
rs78353970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006124 | ACTCGGTGAGCCTAA[C/T]ACACCAGGCCCAGTC | 26133 |
rs78358750 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080038 | AAAAAAAAAAGACAT[A/C]ATTATAACCAAAGAG | 26133 |
rs78374088 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079860 | CGCCTCTACTAAAAA[A/T]AAAAAAAAAAAATAA | 26133 |
rs78434747 | in-del | -/TTTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049268 | GCTGTTTTTTTTTTT[-/TTTT]AAAGTTATGGGTCAT | 26133 |
rs78458685 | snp | G/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090392 | CTTTTTTTTTTTTTT[G/T]TTGAGATGAAGTCTC | 26133 |
rs78608549 | snp | A/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051618 | GCACTGACACATTAA[A/T]AAAAAAAAAAAAAAA | 26133 |
rs78704804 | snp | A/C | 0.177714 | 0.239321 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078028 | TGAATACGCCCCTCC[A/C]AGGTCCTTAAGAGTT | 26133 |
rs78801724 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053548 | CAATTTGAAATTTTA[C/T]CTTATAGATCTCCCT | 26133 |
rs78835838 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022672 | TCAGATATATTCAGG[C/T]AAGGCTCATACAGAA | 26133 |
rs78858961 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058687 | TATTAAAAGAAAATT[C/T]TTTTTTTTTTTTTTT | 26133 |
rs78930130 | in-del | -/CTAT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084496 | TATATATGTATATAT[-/CTAT]ATATGTATATACGTA | 26133 |
rs78992288 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090813 | ACTGATTATCAGGAT[G/T]GGTGTTTAGGAACAT | 26133 |
rs79101357 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092370 | ACTGGGCCCAGGGTT[C/T]GTACACGCCATCAGT | 26133 |
rs79186377 | snp | A/G | 0.00334586 | 0.0407644 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057480 | GTATCGGCAGGTTGG[A/G]AAACAAGGACCAGTA | 26133 |
rs79232133 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054189 | GAAATGGAGCTAAAT[G/T]TTTTTTTTTTTTTAT | 26133 |
rs79275258 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35091064 | GATTTTTTTTTTTTT[G/T]TGAGACAGGGTCTCA | 26133 |
rs79320789 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061973 | GAAACTAATACAACT[A/C]AATAATAAAAAGACA | 26133 |
rs79341480 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011393 | ACTGGCAACACGGCA[A/G]GCACAGCACAGAGTA | 26133 |
rs79398449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029266 | CAACTTTTTAAAAGT[A/C]CAGCCTCTCCAGCTT | 26133 |
rs79439610 | snp | A/C | 0.145978 | 0.227331 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066886 | GACAAATAATCAAAT[A/C]GAAAAAGGTGCAAAA | 26133 |
rs79539428 | snp | A/C | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085448 | AGAACCTTATCTCTA[A/C]AAAAAAATACAAAAA | 26133 |
rs79608518 | snp | G/T | 0.084728 | 0.187577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085475 | AAAATGAGCTGCGTA[G/T]GGTGGCATGCGCCTA | 26133 |
rs79791855 | snp | G/T | 0.188387 | 0.242289 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057476 | CACCGTATCGGCAGG[G/T]TGGAAAACAAGGACC | 26133 |
rs79818778 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083641 | ACAGGAAAATAACTT[A/C]CAATTTATACTTCTA | 26133 |
rs79871468 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027852 | GTTGGTTGTAACGTA[C/T]CTTCTTTCATTTCTA | 26133 |
rs79933608 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069596 | ACTAAATCTGGGCTG[A/G]TATGACACACCTCAA | 26133 |
rs79965102 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006044 | ACGCTCAAGGGTGCT[A/G]GATTCCTTTAATTTT | 26133 |
rs80029343 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028223 | TTCCTTTTTTTTTTT[G/T]GATGGAATCTCACTC | 26133 |
rs80046900 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042798 | CTACTGAACAGAAAT[A/G]GGTGGGCTAGATTGG | 26133 |
rs80124481 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049258 | TTCGATCATAGCTGT[G/T]TTTTTTTTTTTTTAA | 26133 |
rs80179041 | snp | A/C | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017850 | TTCCTACTAGAAATC[A/C]CAGCCTCTGGCCAGT | 26133 |
rs80226966 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092459 | CCACGGCCCCGCTGC[A/G]GCTGAGAGCGTCCGG | 26133 |
rs80325521 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006661 | CCATGCATTGGCTTT[A/G]AGCAAGCATCCTGGG | 26133 |
rs111155304 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059787 | AGACAAAGAAGATGA[A/T]GAAGAAGGCGAAGAC | 26133 |
rs111261076 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012473 | AAGGTCAAGGGTCAG[C/T]TGCTAGTCACCCCCT | 26133 |
rs111297408 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034970 | TGTAACAAGCTGTCA[A/G]AAGAGTCTTAATAGT | 26133 |
rs111309083 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024120 | TGTTTTCTGCGGACA[C/T]GCACACTCACTTTTT | 26133 |
rs111319785 | in-del | -/AGAA | 0.405776 | 0.195535 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038596 | ACCATCTGTACAAAC[-/AGAA]CAGGAGTCAATCTCT | 26133 |
rs111482242 | snp | C/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086754 | AAGTTAGTGAATCTG[C/G]CTGGGCACGGCGACT | 26133 |
rs111492502 | snp | C/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014277 | GATCCCCATCACAGA[C/G]ATTACAAGGGGAAGT | 26133 |
rs111519466 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018832 | CAGTCAGACAGCCCT[G/T]GGTTCACAAGATAGC | 26133 |
rs111528596 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029918 | TGGGATTACAGGCGT[G/T]AGCCACCGCGCCCAG | 26133 |
rs111552972 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048432 | CCATGATGGCCAGGC[C/T]GTTCTCAAACTCCTG | 26133 |
rs111562961 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029133 | CTCCCCGCCTGTAAT[C/G]CCAACTACTTGGGAG | 26133 |
rs111576127 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070144 | ATTCCAGATATCTCA[A/G]TACCACCCTACCCAA | 26133 |
rs111590598 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075447 | AGCTCTTGTAAGGCA[A/G]GCCTGGTGGTGACAA | 26133 |
rs111633517 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049563 | AACTTGCCCCAACGG[C/T]GATGAGTGAGGGGCA | 26133 |
rs111654277 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089832 | GTCTGGGCAACAGAG[C/T]GAGACTCCGTCTAAA | 26133 |
rs111735167 | snp | G/T | 0.0966517 | 0.197444 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083646 | AAAATAACTTCCAAT[G/T]TATACTTCTATACCC | 26133 |
rs111792816 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052035 | TATATAAAAGGTTGT[A/G]TGCAACTACATTTTT | 26133 |
rs111798362 | in-del | -/GAT | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059894 | GAAGACAAAGATGAA[-/GAT]GAAGAAGACGAAGAC | 26133 |
rs111843330 | snp | C/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086053 | CCCCCTTCCCCCTCC[C/G]AGCCCCCCACACCAC | 26133 |
rs111864249 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35020458 | GGGCACTGCCCCCTC[C/T]CACCTGGTACACTCT | 26133 |
rs111864745 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072528 | TCCCAGCACTATTTA[C/T]TAAATAGGGAATCCT | 26133 |
rs111877511 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084444 | ATGAAAGTCAAAAGG[G/T]TATATGTATATATGT | 26133 |
rs111896985 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084711 | GTGTATATGTATATA[C/T]GTTTATATGCATATA | 26133 |
rs111912172 | in-del | -/AA | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068991 | ACAAAAAAAACAAAA[-/AA]CATCTTAAGCAGGAC | 26133 |
rs111915008 | snp | A/C | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075608 | TCTTCTGGCTTGTAG[A/C]GTTTCTGCCAAGAGA | 26133 |
rs111922440 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031414 | TTTTTTTTTTTTTTT[C/T]TCAAAGAGATGGGGT | 26133 |
rs111947073 | snp | A/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076868 | CTCCCAGAGGTGGAG[A/T]CTACAGAGGCAGGCA | 26133 |
rs111990633 | in-del | -/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079859 | CGCCTCTACTAAAAA[-/T]TAAAAAAAAAAAATA | 26133 |
rs112004083 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059904 | ATGAAGATGAAGAAG[A/G]CGAAGACGAAGAAGA | 26133 |
rs112021223 | in-del | -/T/TT | 0.563585 | 0.166272 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038278 | TTGTTTGAGACACCA[-/T/TT]TTTTTTTTTTTAACA | 26133 |
rs112079634 | snp | C/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004780 | GAGTGCCCAGGAGCA[C/G]CCCACCTCATCCTCC | 26133 |
rs112088349 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068643 | TCTCCTGCCTCAGCC[C/T]CCTGAGTAGCTGGGA | 26133 |
rs112103992 | snp | C/T | 4.94564e-05 | 0.0049725 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078058 | TACCTTGAGGATGTT[C/T]TGACACTCAACAAAG | 26133 |
rs112134403 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35035327 | CCAGGGAAAGAACAA[A/G]CGAGGAAATTTTCAA | 26133 |
rs112141213 | in-del | -/TTTG | 0.39214 | 0.205661 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35080805 | CTTGTACACTTCAGT[-/TTTG]TTTTTTTTTTTTTAC | 26133 |
rs112143958 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076721 | GGGTCAGGGACCCAC[G/T]TGAGGAGGCAGTCTG | 26133 |
rs112200365 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067052 | ATCTCAACTAAGAAA[C/T]TGAAAAAGGAGAGAC | 26133 |
rs112212209 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042467 | GGGAATGCACACAAC[C/T]GGACTTTAGAAACAA | 26133 |
rs112256637 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014976 | ACAAGCTAAAGGAGA[A/G]TGCTTGGGCTCAAAA | 26133 |
rs112357112 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059689 | GAAGAAGAAGAAGGA[A/G]GAAGAAGAAAGAAGA | 26133 |
rs112368170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042950 | CTATTAATAACCACT[G/T]TATGTTTCTTGTGTA | 26133 |
rs112375673 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018627 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAATAG | 26133 |
rs112390694 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017335 | CTAGAAGGATACACT[A/G]ATAACTGGTAAAATT | 26133 |
rs112400096 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | TRPC4AP | GRCh38.p7 | 20:35009085 | TGGGGAAAGACTCTG[C/T]CAATAGGGTGAGGCC | 26133 |
rs112433439 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048508 | ACAGGCATGAGCCAC[C/T]GTGCCTGGCCTGTAA | 26133 |
rs112438364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078991 | GAACCGCTTGAACTC[A/G]GGAGGCAGAGGTTGC | 26133 |
rs112446595 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021137 | CCTGGCATACCATGA[A/G]CACCCGGGCAGCACC | 26133 |
rs112485032 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083289 | AAAGTTATGCAAGAC[A/G]GCTACATAGAAAACT | 26133 |
rs112582343 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35065843 | TATTTTTCCTCCCAT[A/G]AATACATCAGTTCTT | 26133 |
rs112617727 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRPC4AP, MYH7B | GRCh38.p7 | 20:35002767 | CAAGGGAGGCTTGGC[C/T]CACAGATGGGGGGTG | 26133 |
rs112621890 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010329 | TAAAGGACAGGAACT[A/G]GGGCTGCTGGGTCAG | 26133 |
rs112648423 | in-del | -/CC | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078020 | GAGGCCCTGAATACG[-/CC]CCCCTCCAAGGTCCT | 26133 |
rs112677737 | snp | C/G | 0.5 | 0 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044617 | CATCTCTGAAATGGT[C/G]ACAGCCAGAATCCGG | 26133 |
rs112701152 | snp | C/T | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35044078 | CTAGGAGCCTTCACA[C/T]GGATCCATCTCTAGA | 26133 |
rs112715301 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083892 | GTATAGCAGACCTAG[C/T]AAGCAGCTAAACTAA | 26133 |
rs112755483 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35088740 | TCAGGTCCACCTTAC[C/T]TTAAAATCTGATTTT | 26133 |
rs112765511 | snp | C/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073712 | CATTGATGTTCATCA[C/G]GGATATTGGTCTAAA | 26133 |
rs112773430 | snp | G/T | | | splice-acceptor-variant | TRPC4AP | GRCh38.p7 | 20:35013068 | TTCAAGGTGATGTCC[G/T]GAAACACATGCACAG | 26133 |
rs112788298 | in-del | -/C | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060436 | TACAAAAATTAAAAC[-/C]AAAAATTAGCCAAGC | 26133 |
rs112805608 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072599 | ACAGTTGTAGATATG[C/T]GGCATTATTTCTGAG | 26133 |
rs112867932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015737 | TCAAGTGATCTGCCC[A/G]CTCGGCCTCCCAAAG | 26133 |
rs112970499 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059687 | AAGAAGAAGAAGAAG[A/G]AAGAAGAAGAAAGAA | 26133 |
rs112973799 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047253 | GTGTGTGCCTTTCCT[A/G]TTGCATCTCTCTGCC | 26133 |
rs113022302 | snp | C/G | 0.5 | 0 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008897 | CTGGGTCCAGAGCCC[C/G]GGAGACCCCTGCAGC | 26133 |
rs113055632 | snp | C/T | 0.444444 | 0.157135 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048922 | TGTTCCTACAGACAA[C/T]AGGCCACTTGTGCTG | 26133 |
rs113061860 | snp | A/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35007430 | GCAGCCTGCACAGGC[A/T]TTTGGAAGTCACGAG | 26133 |
rs113071588 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059713 | AAGAAGAAGAAATAA[G/T]AAGAAGAAGAAGAGG | 26133 |
rs113229449 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009214 | ATGAGGAAATGACTC[C/T]GGCCCCGTCATGGGG | 26133 |
rs113267371 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35092631 | GCACCGCCCGGACCA[A/G]GCCCCGGCCGGTCAG | 26133 |
rs113296089 | snp | C/G/T | 0.0115144 | 0.0749975 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083524 | CTGAGGCAGGAGAAT[C/G/T]GCTTGAACCTGGGAG | 26133 |
rs113315967 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053788 | GATACACTGTGTTAA[A/G]CAGAATTTATCATTA | 26133 |
rs113331649 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076236 | GAGAAGTTTGTTATT[A/G]CTGATCATCTGAAGC | 26133 |
rs113338276 | snp | C/T | 0.02016 | 0.0983543 | intron-variant, missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004319 | TGGGACACTGATTCC[C/T]CCTGAGCACAGTCCT | 26133 |
rs113385627 | snp | A/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022912 | CCTGTAGTCCCAGCT[A/T]CTCAAGAGGGAGAGG | 26133 |
rs113403650 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059688 | AGAAGAAGAAGAAGG[A/G]AGAAGAAGAAAGAAG | 26133 |
rs113405986 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046359 | TTTTCTCATTTTGAA[C/T]CATCCCCGTGCTACT | 26133 |
rs113407747 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071194 | TACTATGTGATATAA[A/T]AATCAAAACTTCACC | 26133 |
rs113433814 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037674 | GAAGGCCACATGCTA[C/T]ATGATTCCATTTACA | 26133 |
rs113495751 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074128 | GGTAATATCCCCTTT[A/G]TCATTTTTTATTGCA | 26133 |
rs113505268 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35009017 | TTAGAACTGCCAGAG[A/G]AGAGCTGTTTATACC | 26133 |
rs113508464 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090948 | CGTACTTTTTCTAAA[A/G]GTTATGTGCTCACTA | 26133 |
rs113596363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028330 | CCTCCTGACCTTAAG[C/T]GACCCGCCTCCTCGG | 26133 |
rs113600328 | snp | A/C/G/T | 0.000153988 | 0.00877328 | splice-donor-variant | TRPC4AP | GRCh38.p7 | 20:35005694 | CCTGCCTTTCATGTA[A/C/G/T]CTTTCATATCCACCT | 26133 |
rs113611670 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031571 | TGTCTGCATGTGGAT[C/G]TGAGTATTCCGACTT | 26133 |
rs113614784 | snp | C/T | 0.444444 | 0.157135 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047154 | AGGCATGAGAGCCAC[C/T]GTGGCTGGCCAAGAA | 26133 |
rs113700195 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059636 | ACACTCCAGCCTGGA[G/T]GGCAGGGTGAGACTC | 26133 |
rs113715656 | snp | A/G | 0 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081753 | GCACTCTGGGAGACC[A/G]AGACAGGTAGATCAC | 26133 |
rs113720763 | in-del | -/TTT/TTTT | 0.495927 | 0.0449436 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089040 | ACTTAACTATACACC[-/TTT/TTTT]TTTTTTTTTTAAGAT | 26133 |
rs113761163 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075841 | TCTCCTGGATAATAT[C/T]CTGAAGAGTGTTTTC | 26133 |
rs113807224 | snp | A/C | 0 | 0 | intron-variant, downstream-variant-500B, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004011 | GAGTTCTGCCCCACT[A/C]ACCATGCACTCCCAC | 26133 |
rs113848444 | snp | A/T | 0.107694 | 0.205546 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030232 | AGTAACAAGAGCGAA[A/T]CTCCATATCAAAAAA | 26133 |
rs113897208 | snp | A/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089772 | AATTGCTTGAATCCG[A/G]GAGACGGAGGATGCA | 26133 |
rs113914549 | snp | G/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037885 | AGCCTAAGTGTATCA[G/T]GGGCTATACCAGCTA | 26133 |
rs113929036 | snp | C/G | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071926 | AGTGTTCCTATTTCT[C/G]CACATCCTCTCCAGC | 26133 |
rs113987460 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35029552 | ATCTCCTTTAGTGTT[C/T]CTTTTGATTAATATT | 26133 |
rs113988952 | snp | C/T | 0.5 | 0 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092323 | GGTCCCCCAGACGTG[C/T]AGACGTGGCGCAAAG | 26133 |
rs114007205 | snp | G/T | 0.146314 | 0.227484 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059700 | AGGAAGAAGAAGAAA[G/T]AAGAAGAAATAAGAA | 26133 |
rs114045370 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35068469 | GGTGTGGAAAAATTA[C/T]AAATGCCAGTCAACT | 26133 |
rs114202248 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023221 | ACCCCATTCACTAGC[C/T]GGGTGGTCTTCAGTA | 26133 |
rs114237757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049599 | ATTTCAGCAAAGTAA[C/T]ATGAGGCATCACCCT | 26133 |
rs114317226 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054493 | AATCAGGTCCTAACA[C/G]TAAGTGCCATCCTCT | 26133 |
rs114367106 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085670 | AGCTCAGCACTGTGA[C/T]AAAAGTGCCACCATT | 26133 |
rs114377251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034356 | TGTAAAACCTCTGTA[C/T]ATGAGCAAGCTAGGG | 26133 |
rs114415475 | snp | G/T | 0.0633504 | 0.166319 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35092910 | CGCGTGGCAGGGACC[G/T]TGTGCGGCGTGGAGG | 26133 |
rs114441807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042090 | ATATGTATATATGTG[C/T]CATGTTGGAAAGTCA | 26133 |
rs114448870 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092239 | GGGGGCTGCAATGAT[A/G]ACCCCCTCCCCCACG | 26133 |
rs114494638 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014244 | TGGGCAGCCCCCTCC[C/T]TGCCTGGAGTGAAAT | 26133 |
rs114555670 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009308 | CACTGCAGACATCAG[A/G]GCAGGACTGGGTACA | 26133 |
rs114570832 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034816 | AGAAAGAAAAAGAGA[C/T]GAGGAGAGAAGTTTC | 26133 |
rs114586832 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059684 | AAAAAGAAGAAGAAG[A/G]AGGAAGAAGAAGAAA | 26133 |
rs114641773 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066863 | ACTTACAGATCAATA[A/C]GAAAAAGGACAAATA | 26133 |
rs114675684 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024977 | ATATTTTCATTTCTC[C/T]TGGGTATATACCTGG | 26133 |
rs114677382 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35057076 | CCCATATATCTACCA[A/C]CCAGCTTAAGAAATA | 26133 |
rs114786577 | snp | G/T | 0.00456254 | 0.0475442 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006595 | GTGAGGAGGGACAGG[G/T]TGAAGGTGTCAACGT | 26133 |
rs114829197 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052049 | TATGCAACTACATTT[C/T]TCGGGGGAGAGTTTT | 26133 |
rs114859043 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046700 | GGGAACAACTGCTTC[C/T]ACTTTTCCTTTTCCC | 26133 |
rs114859261 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35023349 | GATATACTGAAGGTG[C/G]CTGGAACATAGCCCC | 26133 |
rs115043806 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012138 | CATTTTTCAGAAGGT[C/T]AACATGCTTCCTGGA | 26133 |
rs115116598 | snp | C/T | 0.00189643 | 0.0307347 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006608 | GGGTGAAGGTGTCAA[C/T]GTGGCTGCCCCCACC | 26133 |
rs115154966 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059686 | AAAGAAGAAGAAGAA[A/G]GAAGAAGAAGAAAGA | 26133 |
rs115291025 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062519 | GGAATGGAGTATTGA[C/T]ACACGTTATGACACG | 26133 |
rs115306300 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085345 | GGGGCTGGGCACAGC[A/G]GCTTACACTCATATC | 26133 |
rs115352129 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004981 | TGGTTTTCCACACCA[G/T]CTCTCAGGTGAGTCC | 26133 |
rs115396627 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008802 | CTGACAGGGGCCCTG[A/G]GGATGGGTCATTCTG | 26133 |
rs115467409 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35036133 | GTGGAAATTCTGATC[A/G]GCATATTAGAACATC | 26133 |
rs115559073 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046613 | GCATGATTCCTAGAA[A/G]CTCTCATGAATCCCA | 26133 |
rs115566706 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015386 | CATGCAGTGGGCAGC[C/T]CCTGCCTGGAGTGAA | 26133 |
rs115638204 | snp | C/T | 0.030665 | 0.119967 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006172 | CCACCGTGGCACCCA[C/T]CATGCTGCGTCACGG | 26133 |
rs115724902 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062945 | AGCCACACAGTGGAC[A/G]ATTCTGTTGATATGA | 26133 |
rs115842823 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35083883 | AACTCAGCTGTATAG[C/T]AGACCTAGTAAGCAG | 26133 |
rs115885194 | snp | C/G | 0.021333 | 0.101051 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034457 | GTATGGAGCTGGGTG[C/G]AGGAAGGAAGCCTCT | 26133 |
rs115917242 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015652 | ATTTTTAGTGAGAGA[C/T]GCAAGTGTCTCTCAC | 26133 |
rs116033567 | snp | C/T | 0.029116 | 0.117091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35009886 | AAGGGGCTGAATGCA[C/T]GAGACAAGGCGGTGG | 26133 |
rs116073608 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079115 | ACATAAAAAGAAAGA[C/T]GGAGTAGTTATATTA | 26133 |
rs116095487 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35052822 | ACTTTTGAATTCAAA[C/T]ATCTTTAGACAGGAC | 26133 |
rs116130126 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012668 | TCTGAAGTTCCTGCC[A/G]GCCCCTGGGAATAGC | 26133 |
rs116131280 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051401 | CAGCCTCAATCACCT[C/G]GGCTCAAGCGATCCC | 26133 |
rs116224501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055698 | GTATAAGCATCTCAA[C/T]TGCTCTTGTTATAAA | 26133 |
rs116281727 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028635 | GCACTTGAGAAGAAC[A/G]TGCATTCTGTAGTAG | 26133 |
rs116299131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041332 | GCCTTCCCAGGGCAT[C/T]TGAATGGAGAAAATC | 26133 |
rs116315378 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058494 | AAATTAAAATCAGAA[A/C]GAAATTTGGGAAATT | 26133 |
rs116332085 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35066603 | ATTACACCAAAATAA[A/T]CTTCAAATGATGCAA | 26133 |
rs116392543 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047972 | AAGAGGATATTCTGC[G/T]GATAAACATTTATCA | 26133 |
rs116410483 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064172 | ACATTCCCTATATAC[A/G]TATGTATTTTTTATT | 26133 |
rs116421189 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038204 | TTGTTCACTTTAAGA[C/T]GGCTAATTTTATGTT | 26133 |
rs116516921 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041102 | TCCTGACAGCACCTT[G/T]ATCTTGGACTTCTAG | 26133 |
rs116590256 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024528 | TATCCGCTAGTATAA[A/C]TATATCACATTCTGG | 26133 |
rs116717431 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021495 | AGACTCTGAAAGCTG[A/C]AAAACTCCCTCCACA | 26133 |
rs116719895 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055910 | AAAAACGAAACTTAA[C/T]TTTCATGAGCCCAAA | 26133 |
rs116753976 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048681 | TGGAACACCTCGCCA[C/T]TTTGGGGTACACAAA | 26133 |
rs116986414 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055974 | GACAAAGTGCTTTAT[G/T]TGGCACTTGCTTCTA | 26133 |
rs116997506 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060220 | ACATCACAAGAAAAC[C/T]ACAGATGAGTATCTC | 26133 |
rs117031110 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078549 | AAACTGCTCAGTTAA[A/G]CCCATAAAAGGCAGA | 26133 |
rs117046905 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028148 | AGTTCCCTCTAAGCA[C/T]GCTTTAGCTGCATCC | 26133 |
rs117057422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070884 | GAGGAAAAAAAATCT[C/T]ACAAGAAAACCTAAA | 26133 |
rs117089057 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030229 | CTGAGTAACAAGAGC[A/G]AAACTCCATATCAAA | 26133 |
rs117092869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35060412 | GGCAACATAGTGAGA[C/T]CCTGTCTCTACAAAA | 26133 |
rs117110721 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051011 | TCTCTAAAAAGAAAG[A/G]AACTGCAGTACTGCT | 26133 |
rs117132077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054167 | TATTTTGAATGAGGC[A/G]AGAAATGAAATGGAG | 26133 |
rs117136769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042735 | CTATGCCAGTTTCTC[C/T]AAAATCTGTGCAGGC | 26133 |
rs117236853 | snp | A/C | 0.146985 | 0.227789 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079980 | TGAGCTATGACAGCA[A/C]CACTGCACTCCAGCC | 26133 |
rs117252061 | snp | A/G | 0.0165278 | 0.0893908 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093421 | CATACACAAAGAAAC[A/G]CAGTCTCAAACTGGA | 26133 |
rs117320301 | snp | A/C | 0.145978 | 0.227331 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026334 | ACCCTCCCACCTCAG[A/C]CTCTTGAGTAGCTGG | 26133 |
rs117470487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078759 | ATTTAAATATACATA[C/T]AGATAGGTTAAAAGT | 26133 |
rs117487118 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024414 | AATGAACTCATGCAA[C/T]ATGCCATCTTTTGTG | 26133 |
rs117573845 | snp | A/G | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063818 | GTGAGCTAGGATCGT[A/G]CCACTGCACTCCAGC | 26133 |
rs117585914 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037977 | CAGAAGGATAGAGAC[A/T]GCTAAGTGACAACAT | 26133 |
rs117619601 | snp | A/G | 0.0616122 | 0.16492 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031805 | GTTTAATCTCTATCA[A/G]CCTATTTTGCTGAGT | 26133 |
rs117619919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089305 | GATCATGGCTCACTG[C/T]AGCCTTGACTTGCCA | 26133 |
rs117729108 | snp | C/G | 0.00609806 | 0.0548802 | missense, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003210 | TAGCTAACGAGAGCA[C/G]AGGGTGACTGCCGGT | 26133 |
rs117831363 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081110 | AGAAAGAAGAGAAAA[A/G]GGAACAAAGGATAGG | 26133 |
rs117904650 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35094684 | GTTTCTTAGAAACTC[A/G]AACCCCCACCAAATG | 26133 |
rs118017677 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35070095 | TGACAGCCAGCACCA[A/G]CCTGCCAGGGATGTG | 26133 |
rs118025025 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012603 | GGGAGCACACCTCCT[C/T]GTGGAGGGAAGAATC | 26133 |
rs118027108 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35079322 | TGGCAAATCAACTCT[C/T]ACAGTTAAAATATTT | 26133 |
rs118040773 | snp | A/G | 0.0225913 | 0.103852 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003203 | CTCAATGTAGCTAAC[A/G]AGAGCAGAGGGTGAC | 26133 |
rs118057529 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022145 | TTCTTAGGAAGCCCC[C/G]ATTCACTCCTAGATC | 26133 |
rs118147534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35064684 | AACAATGAAAACTGC[C/T]CTGAACATATGCCTG | 26133 |
rs118186611 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024986 | TTTCTCTTGGGTATA[C/T]ACCTGGGAGTAGGAT | 26133 |
rs137879852 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078068 | ATGTTTTGACACTCA[A/G]CAAAGTCACTGTGGA | 26133 |
rs137939507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35040776 | CCAGCTAATTTTTGT[C/T]GCAGATGGCTTATCA | 26133 |
rs137973902 | snp | A/G | 5.18354e-05 | 0.00509068 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004516 | AGGAAGGACATCTGC[A/G]TGGGCACCTGGGATA | 26133 |
rs137980750 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35026694 | ACAATATTAATTTTC[C/T]GATTCAAAGACATGG | 26133 |
rs138023248 | snp | A/G | 0.000132199 | 0.00812907 | synonymous-codon, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021226 | CAGCAGCACGCAGAG[A/G]ACATAGAGCACTTCC | 26133 |
rs138047349 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015851 | GAGTTCACTCAGATC[C/T]TACTCCAAGGTAGCT | 26133 |
rs138067635 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062828 | TATCTTTTAATATAT[A/C]TTTTAAATGGGTGAC | 26133 |
rs138072393 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35019928 | CACACACCTCAAATC[C/T]ACCTTGTACAAAACA | 26133 |
rs138093658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073029 | GATTCCTAAGTATTT[C/T]AGTCTCTTTGTAGCA | 26133 |
rs138130124 | in-del | -/G | 0.095934 | 0.196885 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063631 | GAAGAAGGTGAGGCA[-/G]GAAGATCATTTGAGA | 26133 |
rs138170831 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35008922 | TGCAGCCACAGAATT[A/G]AACTGCCAAGTGCAT | 26133 |
rs138180677 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075683 | TTTCTCTCTGGCTGC[C/T]CTTAATATTTTTTCC | 26133 |
rs138197829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35062102 | AAAACCACAATGAGA[C/T]ACCTCTTCATACCTA | 26133 |
rs138279356 | in-del | -/T | 0.483852 | 0.0883933 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072423 | GTTTTAGGTCTAACA[-/T]TTAAGTCTTTAATCA | 26133 |
rs138286700 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35004710 | CAACGAAAGCTGACT[A/G]TGGCAGAAAGAAGGA | 26133 |
rs138288731 | in-del | -/GAA | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059785 | GAAGACAAAGAAGAT[-/GAA]GAAGAAGGCGAAGAC | 26133 |
rs138295936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35090920 | AGGATTAAAGATAAC[A/T]TATGCCTTGTACCGT | 26133 |
rs138335819 | in-del | -/ATAG | 0.0260105 | 0.111035 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041470 | CAAGCAGAATCACAC[-/ATAG]ATAGACTGTCTACTA | 26133 |
rs138371700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35092367 | GAAACTGGGCCCAGG[A/G]TTCGTACACGCCATC | 26133 |
rs138519018 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055137 | AATCCCCTCCAAGAT[G/T]ATTATTTTTCCTTTA | 26133 |
rs138542460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35049245 | ATTTAGTTTTCATTT[C/T]GATCATAGCTGTTTT | 26133 |
rs138597638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085205 | GGCACTGCTGTTTTT[C/T]TGTTACAAGCTCCAT | 26133 |
rs138628775 | snp | A/G | 0.147991 | 0.228242 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35069707 | GCACTTTGGGAGGCT[A/G]AGGTGGGCGGATTAC | 26133 |
rs138711543 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35073447 | ATTATTTTAAGATAC[A/G]TCCCATCAATACCTA | 26133 |
rs138768181 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012947 | AGGGACCAGACAAGG[A/G]GATCGAGGCCTTCCG | 26133 |
rs138877577 | in-del | -/GAA | 0.031825 | 0.122064 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059857 | GACGAAGATGAAGAT[-/GAA]GAAAAGATGAAGAAA | 26133 |
rs138891459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030707 | ACTTTGGTACCACCC[A/G]TTTTCTTTGTACAGT | 26133 |
rs138909201 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35048282 | AGTGACATAATCTTG[A/G]CTCACTGCAACCTCT | 26133 |
rs138933534 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35024888 | TCAGGTGACAGTCAT[G/T]TGCGTTGTTTCCATA | 26133 |
rs138983950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082350 | TTGCAAAATGACCAG[C/G]TGCTAGGCCATACTG | 26133 |
rs139060292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010668 | TCCCACCAAGCACCA[C/T]GGTCACACATCACAC | 26133 |
rs139072476 | in-del | -/GAC | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059933 | GACAAAGACGAAGAA[-/GAC]GAAGAAGAAGAAAAA | 26133 |
rs139080738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063944 | TAAACAGAAAAAAAT[A/T]AATGTTAGAAAGGAA | 26133 |
rs139112105 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35050911 | CTGAGGTGAGAGGAC[A/C]GCTTGAGGCCAGGAG | 26133 |
rs139169193 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35006131 | GAGCCTAACACACCA[A/G]GCCCAGTCCCTCCCT | 26133 |
rs139171780 | snp | A/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35093628 | TGACTCCCCCCACCC[A/T]ACACACACACACTTT | 26133 |
rs139312615 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008185 | TGACAGCTCACGCCC[A/G]GCCCTGATGGAACTC | 26133 |
rs139313902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35033173 | CCCTCCAACCTGGGC[A/G]ACAAGAGACTCCATC | 26133 |
rs139353038 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005314 | GGAAAAAAAGGAAAC[A/G]CGTGCGCATACACAT | 26133 |
rs139390267 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058817 | GCCTCAGCCTCAGAG[C/T]AGCAGGGATTACAGG | 26133 |
rs139403823 | snp | C/T | 0.148326 | 0.228391 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35071947 | CCTCTCCAGCACCTG[C/T]TGTTTCCTGACTTTT | 26133 |
rs139428496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35053587 | CTCTGTCATTGGCTA[C/T]ACATGGCTACCGAGC | 26133 |
rs139466115 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077296 | CCAGTGAGATGAACC[C/T]GGTACCTCAGTTGGA | 26133 |
rs139467391 | in-del | -/CTT | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076252 | TGATCATCTGAAGCC[-/CTT]TTCTCTCAACTCATC | 26133 |
rs139594595 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051849 | ACCCTTGACTACCCA[C/T]CTTTCTCCTCTCTTC | 26133 |
rs139710788 | snp | C/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35038247 | TCTCCATAAAATAAT[C/T]ACACAGAAATAGATT | 26133 |
rs139727296 | in-del | -/A | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35074190 | CTTGCTAGCGGTCTT[-/A]TCAATTTTGTTGATC | 26133 |
rs139747041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031724 | TATCTTGGTGTGCTT[A/C]ATAGTGCCCCACATT | 26133 |
rs139767379 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082815 | ATATGAATACCTCAA[C/T]TGATACAGAAAAAGC | 26133 |
rs139767486 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028083 | ATGACTTAAGGTAGA[C/T]GTTTAGGCAATTTAG | 26133 |
rs139792737 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35086469 | TGTGTGTGTGTGTGT[A/G]TGTGTGTATGTGTGT | 26133 |
rs139800499 | snp | C/T | 0.0136162 | 0.081382 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078166 | CTCCGTCAAAAAAGT[C/T]TCAGTGAACTGTGAG | 26133 |
rs139867118 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35078153 | ATTGTTTGTCCCTCT[C/T]CGTCAAAAAAGTCTC | 26133 |
rs139911580 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35042422 | AGGAGGCTGCTCTGA[A/G]GCACTTGATAACTCT | 26133 |
rs139956627 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35010351 | CTGGGTCAGCACCAG[A/G]CTAGTGTAGGGAGTC | 26133 |
rs139961186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35022061 | CACTAGGCCTTAGAC[A/T]GCTCTGCAGCAGACA | 26133 |
rs139975509 | snp | C/T | 0.00540568 | 0.051707 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35006498 | GTTGAACTTCATCAG[C/T]TCCCCCAGGAGGTCA | 26133 |
rs139997857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35037664 | ACCAGATTCAGAAGG[C/T]CACATGCTATATGAT | 26133 |
rs140050862 | snp | C/T | 1.6498e-05 | 0.00287206 | missense, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35021314 | GACGTGTGAGGCAGG[C/T]CATTCTCCTCAGAAG | 26133 |
rs140134901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35016284 | TCTGAAGAAAACATC[C/T]GTGTATCCCCTATGC | 26133 |
rs140177971 | snp | A/G | 0.493748 | 0.0555599 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018604 | ACTGTCTCAAAAAAA[A/G]AAAAAAAAAAAAAAA | 26133 |
rs140192793 | in-del | -/TC | 0.0966517 | 0.197444 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032834 | CTTTCACAGGAAATT[-/TC]TGTTGCCTGCTTTTT | 26133 |
rs140196281 | snp | C/G/T | 8.24972e-05 | 0.00642204 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003274 | AGTATGAGAAGCTGA[C/G/T]GCAGGAGCTCTGGGC | 26133 |
rs140210666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35046360 | TTTCTCATTTTGAAC[C/T]ATCCCCGTGCTACTC | 26133 |
rs140212889 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35004272 | CCTGAGGGCACTTGC[A/G]AGCCCTCCTTCCTTA | 26133 |
rs140284031 | snp | A/G/T | 0.00518109 | 0.0506754 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35039747 | AGAATCTTGAAAGAC[A/G/T]TTACTTTCCCCCAGA | 26133 |
rs140342472 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35021088 | TTTGCCAGGCTAAAG[C/G/T]GAGAGCCATTCTAAC | 26133 |
rs140361914 | snp | C/T | 8.37949e-05 | 0.00647228 | missense, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003555 | AGGTACAGGGGCAGC[C/T]GCTCTTTCCGTCGGG | 26133 |
rs140381034 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015608 | GTTGGGATTACAGGC[A/C]CCCAACACCATACCT | 26133 |
rs140426374 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35061692 | GGACCCCTGCCTCAC[A/G]TGATAAACAAAGTCA | 26133 |
rs140455019 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084244 | CATTCCACTCCAGCC[A/G]GGCAACAGTGCGAGA | 26133 |
rs140526072 | snp | C/T | 4.96775e-05 | 0.0049836 | intron-variant, upstream-variant-2KB | TRPC4AP | GRCh38.p7 | 20:35055078 | TTCTCAATGAAAAGA[C/T]AGTACAACAGTTACC | 26133 |
rs140599073 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35017950 | TCAGGCCTTTACTAA[A/C]ACCCAGCCTGGATCT | 26133 |
rs140612284 | snp | C/G | 3.29576e-05 | 0.00405928 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35044652 | AATTAGCGAGCTGCT[C/G]CTGATCGAAATTGGA | 26133 |
rs140622086 | snp | A/G | 0.190519 | 0.242821 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072639 | CTGTTCCACTGGTCT[A/G]TATCTCTGTTTTGGT | 26133 |
rs140646600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085253 | TCACAGTCCAAATAT[C/T]TGACTTCACAAGCAA | 26133 |
rs140657366 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35089207 | TAAGATGGTAAATTT[C/T]ATGTTTACATATATA | 26133 |
rs140817919 | snp | C/G/T | 0.000131893 | 0.00811982 | missense, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35057535 | GTTTCTGTCCCCGGA[C/G/T]AGAGATCGTAGGCCT | 26133 |
rs140825259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35043825 | GATTGCAGTTGACCA[C/T]GGATAACTGAAACCA | 26133 |
rs140848050 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TRPC4AP | GRCh38.p7 | 20:35003023 | CCCTCCCACCAAGCC[C/T]GTACCCAAAGACCTG | 26133 |
rs140858990 | in-del | -/AAGAAG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059711 | GAAAGAAGAAGAAAT[-/AAGAAG]AAGAAGAAGAGGAAG | 26133 |
rs140884978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054517 | ATCCTCTTTTGTTTC[C/T]ACCAGATTGCTTTCT | 26133 |
rs140909956 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35012642 | GCTCAGTAAGCAGTC[A/G]GCTTTGCCTGTCTGA | 26133 |
rs140926257 | snp | A/G | 1.65359e-05 | 0.00287536 | synonymous-codon, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35003494 | GAAGTTGTTGAGCAG[A/G]AAGCCGGGGTACTTC | 26133 |
rs140929858 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35047864 | GGTTATAGGTAACCC[A/G]TGGCAAAATACTGAT | 26133 |
rs140982312 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35028579 | TGCTGAACTTTTTTT[G/T]AACAGCCTAGCATAT | 26133 |
rs141019632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008049 | TCACAGACGATGGGC[C/T]GGCCTAGGGAAGTAG | 26133 |
rs141132015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35063145 | TGATTTTATAAGTGT[C/T]TGGCATTTCCCCTGC | 26133 |
rs141167455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35072357 | ATGAAGTCCTTGCCC[A/G]TGCCTATGGCCTGAA | 26133 |
rs141201005 | snp | C/G | 0.0962929 | 0.197165 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35076681 | CGGCCCCTACTGGGA[C/G]GTGTCTCCCAGTTAG | 26133 |
rs141240222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35058282 | GCAAAGAAATAGAAG[A/T]CTTGAACACAACGAA | 26133 |
rs141292147 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35067891 | GATAAAACACATGGA[A/G]TTTCTTTTTTGAGGT | 26133 |
rs141380417 | in-del | -/GAA | 0.251014 | 0.249998 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059936 | AAAGACGAAGAAGAC[-/GAA]GAAGAAGAAAAAACA | 26133 |
rs141419906 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35034412 | CTTGGCCTCAAGTAT[A/G]TGGGATAGAGCTTCC | 26133 |
rs141460086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35030979 | ATTTCCAGATGTTTG[C/T]CTGTTACTAATGAGT | 26133 |
rs141487375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35051383 | TACGAATATAGCTCA[C/T]TACAGCCTCAATCAC | 26133 |
rs141590068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35041885 | AAGGATTAAATAAAA[C/T]CACTTCTAGGTAAAG | 26133 |
rs141611450 | snp | C/T | 0.030665 | 0.119967 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35015116 | GTGATTCTCCCACCT[C/T]AGCCTCCTGAGTAGC | 26133 |
rs141677317 | snp | G/T | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031169 | CCACTAATCTTATTG[G/T]AATATCCTTGGGCAT | 26133 |
rs141696642 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35081947 | CCAAGAATGCACCAT[C/T]GCACTCCAGCCTGGG | 26133 |
rs141703585 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35018691 | TTTTACTTGTAGAAT[C/G]CATTATTCCTACTCT | 26133 |
rs141839947 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35014394 | GTGATCTCAGCTCAC[C/T]GCAACCTCTGCCTCC | 26133 |
rs141844854 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011961 | GAATCCTTGGATGAA[C/G]AACTGTCTCTGTTTT | 26133 |
rs141884128 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35008353 | GCTCCATTCCTTCCC[A/G]CACTGCATTGAAACA | 26133 |
rs141908183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35005990 | TAAGAGGCACTCCCC[A/G]GAATTCAGCACAGAT | 26133 |
rs142027568 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35085694 | CACCATTCAGTCATC[G/T]TCCCAGTTGAATTAC | 26133 |
rs142059867 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35012951 | ACCAGACAAGGAGAT[C/T]GAGGCCTTCCGAAGA | 26133 |
rs142075881 | in-del | -/AAG | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35059711 | GAAAGAAGAAGAAAT[-/AAG]AAGAAGAAGAAGAGG | 26133 |
rs142083142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35011718 | TCAGCTGGCCACAAT[C/G]GTCTTCCCTCGTTCA | 26133 |
rs142109703 | snp | A/G | | | intron-variant | TRPC4AP | GRCh38.p7 | 20:35031628 | GCATTAATGATTTAC[A/G]TTACATTTGGGAGAT | 26133 |
rs142134547 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35054689 | TCACAGTCTGCCAAC[A/G]CTTGTCACCTTTTGA | 26133 |
rs142242696 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35082640 | CAGTTTCACTAACGA[C/G]GATGTAAGGGAAAAA | 26133 |
rs142266561 | snp | A/C/T | 0.000181653 | 0.00952867 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TRPC4AP | GRCh38.p7 | 20:35035259 | TGACACCTTTCGAGT[A/C/T]GCCAGTTTGCAAAGC | 26133 |
rs142267157 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35078959 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 26133 |
rs142275707 | snp | A/G | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35032654 | ATTTTTTGTATTTTT[A/G]GTAGAGACGGGGTTT | 26133 |
rs142281985 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35077253 | TTCAGCTCACACTCC[A/G]TGGACTGCACCCACT | 26133 |
rs142304991 | snp | C/T | 0.147656 | 0.228091 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35075712 | CCTTAATTTCAACTT[C/T]GGTGAATCTGACAAT | 26133 |
rs142373810 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35084000 | ATTTAGGAACAAATT[A/G]TAAGTATACAGAAAG | 26133 |
rs142454801 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | TRPC4AP | GRCh38.p7 | 20:35027738 | CTGAGTTAGCTGCAA[C/T]AGTTTGTGTCTTTTA | 26133 |