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 |