SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9497 | snp | A/C | 0.143284 | 0.226079 | utr-variant-3-prime | HERPUD1 | GRCh38.p7 | 16:56943662 | GTGGTTCTGCTGGTA[A/C]GATTTGATTCCTGTT | 9709 |
rs15104 | snp | C/T | 0 | 0 | utr-variant-3-prime | HERPUD1 | GRCh38.p7 | 16:56943744 | CTAGACATGTTTTAG[C/T]AGGACTTTTCTAGGA | 9709 |
rs37023 | snp | A/T | 0.435694 | 0.167385 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56934195 | CAAATAATATTAACA[A/T]ATAATCTGTCTATTG | 9709 |
rs37024 | snp | A/C | 0.473368 | 0.11228 | utr-variant-5-prime | HERPUD1 | GRCh38.p7 | 16:56932159 | AATCTCTGCAACGAC[A/C]GTTCACGTCTCTGGG | 9709 |
rs37025 | snp | C/T | 0.417756 | 0.185359 | utr-variant-5-prime | HERPUD1 | GRCh38.p7 | 16:56932099 | TAGAAGCCCCGCGCC[C/T]GGCTCTGCGGACAGA | 9709 |
rs39718 | snp | A/G | 0.479177 | 0.0998894 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56935771 | ATTCAATAAAAACCC[A/G]ATTAGTGTTAGTTCA | 9709 |
rs247609 | snp | C/T | 0.423881 | 0.179625 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56939549 | ATCAGACAAAAGCAC[C/T]CTTGTGTCAATACAC | 9709 |
rs247610 | snp | A/C | 0.466204 | 0.125522 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56938433 | TGGGACTACGGGCAC[A/C]CGCCACCACACCTGG | 9709 |
rs866038 | snp | A/G | 0.491316 | 0.0653198 | downstream-variant-500B | HERPUD1 | GRCh38.p7 | 16:56944040 | ctcaaaaacaaaaaC[A/G]CCAACAAAAACTTTC | 9709 |
rs881598 | snp | A/G | 0.252421 | 0.249988 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56942832 | cctgggtgacagagc[A/G]agactctgtctcaaa | 9709 |
rs952439 | snp | G/T | 0.252421 | 0.249988 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56941365 | tgacaaccaaaaata[G/T]ctacacattgccaaa | 9709 |
rs952440 | snp | C/T | 0.491368 | 0.0651254 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56941193 | GGAAGGCAGCTGTGG[C/T]CTGATAAAGGCAAAT | 9709 |
rs1366544 | snp | C/T | 0.276267 | 0.248616 | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56930807 | AGGCTGTGCTCCTTA[C/T]GAGAATCGAATGCCT | 9709 |
rs1428847 | snp | C/T | 0.479095 | 0.100076 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56935942 | ACACAGCGAGACCAT[C/T]TTTAAAAAAAAAAAA | 9709 |
rs1802311 | snp | C/T | | | utr-variant-3-prime | HERPUD1 | GRCh38.p7 | 16:56943656 | GCAGAAGTGGTTCTG[C/T]TGGTACGATTTGATT | 9709 |
rs1820787 | snp | C/T | 0.434543 | 0.168653 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56934977 | TGCCTGTAATCCAAG[C/T]ACTGTGGGAGGCCAA | 9709 |
rs1820788 | snp | C/T | 0.425277 | 0.178263 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56934815 | CTGAGGCAGGGGAAT[C/T]GCTTGAACCAGGGAG | 9709 |
rs2133783 | snp | A/G | 0.491629 | 0.0641526 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56939423 | AAGGGAATTTTATCC[A/G]TGTTACCTGTAAAGT | 9709 |
rs2217332 | snp | C/T | 0.25515 | 0.249947 | missense | HERPUD1 | GRCh38.p7 | 16:56935236 | CTCTGGTCCTCTGGA[C/T]GCTGATCATGGAAAG | 9709 |
rs2270835 | snp | C/T | 0.198324 | 0.244601 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56939137 | TAAATTCCATTCTTC[C/T]GTCTCTTCGATTTGA | 9709 |
rs2291955 | snp | A/G | 0.0349115 | 0.127424 | utr-variant-3-prime | HERPUD1 | GRCh38.p7 | 16:56943768 | AAAAAGCAATTATAC[A/G]TAAGTCTTTCCTAGA | 9709 |
rs2518054 | snp | A/G | 0.243633 | 0.249919 | downstream-variant-500B | HERPUD1 | GRCh38.p7 | 16:56943986 | TTGTTTTTCAGAAGA[A/G]GACTGTTTGTGCCGG | 9709 |
rs2518057 | snp | C/T | | | intron-variant | HERPUD1 | GRCh38.p7 | 16:56932629 | GAGTCATTTCACCCT[C/T]CAAGCCTGTTTCTCC | 9709 |
rs2518058 | snp | C/T | 0.296619 | 0.245615 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56932642 | CTCCAAGCCTGTTTC[C/T]CCCCCAGCGGCCAGG | 9709 |
rs2562126 | snp | C/T | 0.305934 | 0.243663 | | | GRCh38.p7 | 16:56938801 | TCTTCCTCCATCCTC[C/T]ATCTGAATCTATAGT | 9709 |
rs3764262 | snp | C/G | 0.388021 | 0.208447 | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56931819 | TGAGGGCGCCCGAGG[C/G]AGGGGGTGGGGAGTG | 9709 |
rs3764263 | snp | C/T | 0.481242 | 0.0950111 | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56931795 | GGGAGTGGGGTATCC[C/T]AGCAGACCCCAGTTT | 9709 |
rs3833831 | in-del | -/ATT | 0.206947 | 0.246265 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56942292 | TAAAGGTTGAGGATT[-/ATT]GGAGAGCCTGGCATA | 9709 |
rs3903056 | snp | C/T | 0.252702 | 0.249985 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56940879 | CCTCTGCCTCCCCAG[C/T]TCAAGCAATTCTCCT | 9709 |
rs4474668 | snp | A/G | 0.491368 | 0.0651254 | downstream-variant-500B | HERPUD1 | GRCh38.p7 | 16:56944204 | TAAAACTTTCAAGCT[A/G]AGTGTGATGGCGCAT | 9709 |
rs4784738 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56942630 | GAGGCTGAGGCAGGT[A/G]GATCACCTGAGGTCA | 9709 |
rs7189637 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56936542 | TCAGACTATTTTTTA[C/T]ATAACGTTGCTTCTG | 9709 |
rs7204290 | snp | A/G | 0.404384 | 0.196635 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56934127 | ACACCTTTATTCCAG[A/G]TTTCGCATAATCAGT | 9709 |
rs7342710 | snp | C/T | 0.00183515 | 0.0302359 | utr-variant-3-prime | HERPUD1 | GRCh38.p7 | 16:56943291 | GCCATCGCAAACTGA[C/T]GGTGTTTGTGCTGTA | 9709 |
rs7500979 | snp | A/G | 0.404384 | 0.196635 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56933846 | CAGCTGTGGTTTTCC[A/G]GCCTTTTCTATTGGT | 9709 |
rs8044804 | snp | A/G | 0.396 | 0.202938 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56936291 | TAAATGATCAAAAAC[A/G]GTATCATACCAAGGC | 9709 |
rs8056195 | snp | C/G | 0.409041 | 0.192888 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56932504 | TGACGGCTGCGATCG[C/G]TCGGCCGGTCACCTC | 9709 |
rs8058509 | snp | A/C/T | 0.000313692 | 0.01252 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56942253 | GTATGGAGCCTCCCA[A/C/T]GAAGCCCAGGCGAGC | 9709 |
rs9788873 | snp | A/G | 0.404384 | 0.196635 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56933620 | ACATTGTAAACAAAT[A/G]CCTCTCAGGTATACA | 9709 |
rs9925054 | snp | C/T | 0.370568 | 0.219005 | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56930495 | accttgtgatccacc[C/T]gcctcggcctcccag | 9709 |
rs9925326 | snp | A/G | 0.198324 | 0.244601 | downstream-variant-500B | HERPUD1 | GRCh38.p7 | 16:56944270 | CCTGATTTAAACAGT[A/G]CTGGCTTATATAGGA | 9709 |
rs9931176 | snp | A/G | 0.427271 | 0.176281 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56942608 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG | 9709 |
rs9932164 | snp | G/T | 0.241627 | 0.24986 | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56930533 | ggattacaggcgtga[G/T]ccacctcgcccagcc | 9709 |
rs9935267 | snp | C/T | 0.0858192 | 0.188533 | downstream-variant-500B | HERPUD1 | GRCh38.p7 | 16:56944307 | CAAAGTTAAATTCCC[C/T]AAATTTAAATTTAGT | 9709 |
rs9938413 | snp | C/T | 0.210301 | 0.246828 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56938338 | ggaggccaaggtggg[C/T]ggatcacgaggtcag | 9709 |
rs11301089 | in-del | -/T | | | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56931236 | TTTGTTTTTCAAGCC[-/T]TTTTTTTTTTTTTTT | 9709 |
rs11863728 | snp | A/G | 0.377977 | 0.21476 | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56931030 | TCCGTGGCCCAGGGG[A/G]GTTGGGGACCCCGTC | 9709 |
rs11864751 | snp | C/T | 0.269267 | 0.249256 | downstream-variant-500B | HERPUD1 | GRCh38.p7 | 16:56944236 | TTTACTAAGAATATA[C/T]CTGTGTTTCCCCCCA | 9709 |
rs12445769 | snp | A/G | 0.409382 | 0.192607 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56932874 | TTCTCCTCCCTGGCC[A/G]CCTTCCGCCGTGCCC | 9709 |
rs16963989 | snp | A/G | 0.0182019 | 0.0936463 | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56931608 | CTTGCACTCGGGGTC[A/G]CCCAGCCGTTCTTTG | 9709 |
rs28405407 | snp | C/T | | | intron-variant | HERPUD1 | GRCh38.p7 | 16:56940675 | TAAATAGTATATCAC[C/T]CTGTGGCTGGGCGCA | 9709 |
rs34040285 | snp | C/G | 0.0266618 | 0.112339 | missense | HERPUD1 | GRCh38.p7 | 16:56942180 | GCCGGTTCAGAACTT[C/G]CCAAATGATGGTCCT | 9709 |
rs34098794 | in-del | -/TG | 0.434687 | 0.168495 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56941154 | CATGGAACAGAAAAC[-/TG]TATTTGTTTTGAATG | 9709 |
rs34104593 | in-del | -/C | | | intron-variant | HERPUD1 | GRCh38.p7 | 16:56942981 | GCCTAGGGCATCATT[-/C]CCCTGGGGTCCTGGC | 9709 |
rs34189116 | in-del | -/CCATT | | | intron-variant | HERPUD1 | GRCh38.p7 | 16:56937074 | AGGCGTTTTATCCTT[-/CCATT]GTGCTGACCGCTTGG | 9709 |
rs34439988 | in-del | -/A | | | intron-variant | HERPUD1 | GRCh38.p7 | 16:56934909 | TAGAGATGGGGTTTC[-/A]CCATGTTGGCCAGGC | 9709 |
rs35206035 | in-del | -/G | | | | | GRCh38.p7 | 16:56929842 | ACTGCTAGCACTTTT[-/G]GGAGGCCAAGGCAGC | 9709 |
rs35318182 | in-del | -/T | | | intron-variant | HERPUD1 | GRCh38.p7 | 16:56942427 | ACATTCTATCACATA[-/T]TTTTTGACGTGGCAA | 9709 |
rs35721729 | snp | C/G | 0.00347018 | 0.0415096 | missense, synonymous-codon | HERPUD1 | GRCh38.p7 | 16:56942199 | AATGATGGTCCTCCT[C/G]CTGACGTTGTAAATC | 9709 |
rs35730351 | in-del | -/A | 0.5 | 0 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56938563 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 9709 |
rs35753270 | in-del | -/T | 0.441977 | 0.16014 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56937618 | CTATTACCCTTTCCC[-/T]TTTTTTTAAAAAAAG | 9709 |
rs55906908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56938471 | GGGAGGCTGAGGCAG[A/G]AGAATGGTGTGAATC | 9709 |
rs56129100 | snp | A/G | 0.364817 | 0.222075 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56941862 | GGTAAGGTTTAGTTC[A/G]TCATAAGCATTTATT | 9709 |
rs56322302 | in-del | -/A | 0 | 0 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56938577 | CAAAAAAAAAAAAAA[-/A]GAAGCATGCATTTGA | 9709 |
rs57502215 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56938507 | GGTGGAGCTTGCAGT[A/G]AGCCGAGATTGCGCC | 9709 |
rs57627126 | snp | C/T | 0.0410537 | 0.137264 | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56931489 | TGAGGCCCAGGGAAA[C/T]TGGCAACAGCTGCCT | 9709 |
rs58139050 | in-del | -/TTT | | | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56930230 | ACATACTGTTTTTTT[-/TTT]GTTGTTGTTGTTGTT | 9709 |
rs58225093 | snp | A/C | | | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56931461 | TTAGGGTGATGTCCC[A/C]AACGTTCAAGTCTGA | 9709 |
rs60138278 | in-del | -/GT | | | intron-variant | HERPUD1 | GRCh38.p7 | 16:56941155 | ATGGAACAGAAAACT[-/GT]ATTTGTTTTGAATGA | 9709 |
rs60906687 | snp | A/C | 0.366266 | 0.221319 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56941864 | TAAGGTTTAGTTCGT[A/C]ATAAGCATTTATTGA | 9709 |
rs62035460 | snp | C/T | 0 | 0 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56934697 | ACTGGAGATAATTTG[C/T]CATTCTTTTTTTTTT | 9709 |
rs62035461 | snp | A/C | 0 | 0 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56934699 | TGGAGATAATTTGCC[A/C]TTCTTTTTTTTTTTT | 9709 |
rs62035462 | snp | A/C/T | 0.000263861 | 0.0114831 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56939399 | TGTGGCCAGGGCTCC[A/C/T]GGGAATTGAAGGGAA | 9709 |
rs67754228 | in-del | -/TAA | | | intron-variant | HERPUD1 | GRCh38.p7 | 16:56941864 | AAGGTTTAGTTCGTC[-/TAA]ATAAGCATTTATTGA | 9709 |
rs71268445 | in-del | ATATAA/GTC | 0.5 | 0 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56941862 | GGTAAGGTTTAGTTC[ATATAA/GTC]ATAAGCATTTATTGA | 9709 |
rs72786778 | snp | G/T | 0.0242165 | 0.10734 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56933265 | GTGAGTTCCAGCTTG[G/T]GGTAGCGCCTGTGTC | 9709 |
rs72786781 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56936298 | TCAAAAACAGTATCA[A/T]ACCAAGGCTTACTTA | 9709 |
rs73561709 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56937003 | ATACACAGCCTTTTA[A/G]TACACACAAATTTAA | 9709 |
rs73561722 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56941447 | TGCTGAATTTTCTAC[A/C]ATGCACAGGACAACT | 9709 |
rs74402821 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56936065 | GGCTCTAAAGACATA[C/T]ATGACACACGAAACC | 9709 |
rs74703214 | snp | A/G | 0 | 0 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56938575 | CTCAAAAAAAAAAAA[A/G]AAGAAGCATGCATTT | 9709 |
rs75163163 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56938151 | CTTTGGGCAATTCTA[G/T]TATGGTTTCAATTTT | 9709 |
rs75311016 | snp | A/G | 0.00874735 | 0.0655527 | downstream-variant-500B | HERPUD1 | GRCh38.p7 | 16:56944000 | AGGACTGTTTGTGCC[A/G]GTAAGAATGATCAGG | 9709 |
rs75312411 | snp | A/T | 0.0240643 | 0.107019 | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56931374 | GGGTGCATGTGTGAG[A/T]ATCTTATAAAGTGAC | 9709 |
rs75439444 | snp | C/T | 0.00493004 | 0.0494036 | synonymous-codon | HERPUD1 | GRCh38.p7 | 16:56940081 | AAATTTGCGGATGAA[C/T]GCACAAGGTGGCCCT | 9709 |
rs75452491 | snp | A/G | 0.00982753 | 0.0694059 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56942254 | TATGGAGCCTCCCAC[A/G]AAGCCCAGGCGAGCT | 9709 |
rs75874809 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56941934 | GTGCAATGATGAATA[A/C]AACACAGTCCCTGCC | 9709 |
rs75936299 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56933611 | GAAGACCTAACATTG[C/T]AAACAAATACCTCTC | 9709 |
rs76930080 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56932947 | GGTGGAGCCCCGTGC[A/T]CTTTCTGACCAAGAG | 9709 |
rs77542462 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56941296 | TTTTAGCTGTGGCCC[A/G]AAGCAGTAGTTCTCA | 9709 |
rs77665021 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56935873 | TTGGAAATTTTCATT[C/G]TGATTAGTTGGATAG | 9709 |
rs77821827 | in-del | -/CCT | | | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56931234 | GTTTTGTTTTTCAAG[-/CCT]TTTTTTTTTTTTTTT | 9709 |
rs78455295 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56930268 | TGTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 9709 |
rs78600549 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56930267 | TTGTTTTTTTTTTTT[G/T]GAGACGGAGTCTCGC | 9709 |
rs79099545 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56938919 | TGGGTTGAGACCTGC[A/C]GTGAGACTCAACAAG | 9709 |
rs79570175 | in-del | -/TTTTT | | | upstream-variant-2KB | HERPUD1 | GRCh38.p7 | 16:56931252 | TTTTTTTTTTTTTTT[-/TTTTT]CCTACAGAGGAGGAG | 9709 |
rs79876588 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56938222 | AAGCCAAAGATGACT[C/T]GCATACACCTGCCCT | 9709 |
rs111662103 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56936437 | CCAATGACAACTTCA[C/T]TGGAAGATTTTAATG | 9709 |
rs111973684 | snp | C/T | 0.5 | 0 | | | GRCh38.p7 | 16:56930058 | GCAGTGAGCCGAGAA[C/T]GTGCCATTGCACTTC | 9709 |
rs112344247 | in-del | -/TAA | 0.5 | 0 | intron-variant | HERPUD1 | GRCh38.p7 | 16:56942294 | TGCCAGGCTCTCCAA[-/TAA]TCCTCAACCTTTAGA | 9709 |