SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6197604 | snp | A/G | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34199577 | AGAGATTTGGCAAAG[A/G]TTTCCTATGAGAGGT | 76630 |
rs6198119 | snp | C/G | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34233093 | TGTTAACAGGGCCCA[C/G]AGTGATGCGTGCCTG | 76630 |
rs6198134 | snp | C/T | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34199686 | GGTCAGGATGACTTG[C/T]TTTGACCCTTTCTGG | 76630 |
rs6199098 | snp | C/G | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34233252 | TCTACTCTGATAATA[C/G]CCAGGTATTTTGTTA | 76630 |
rs6199630 | snp | C/G | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34233352 | AGTTTGGGATTCTCT[C/G]TGATTCCCCTCCACC | 76630 |
rs6199699 | snp | A/G | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34233402 | AGGCATGCTGTAGAC[A/G]AATACAGAAAGGCTC | 76630 |
rs6200166 | snp | C/T | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34233440 | CCCCAAGCAAAAGAA[C/T]GTCTTNGTATACAGC | 76630 |
rs6200173 | snp | A/T | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34233446 | GCAAAAGAANGTCTT[A/T]GTATACAGCAGCCGC | 76630 |
rs6200204 | snp | A/G | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34233469 | GCAGCCGCAGCCCGG[A/G]AAACTGCTGGGCAAC | 76630 |
rs6200234 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34233497 | AACTCAGAATGTGAC[G/T]AGTGTGCCTGAGAAC | 76630 |
rs6204497 | snp | A/G | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34194366 | AACAGAACAATCTAG[A/G]GAAGAAAATAAGAAA | 76630 |
rs6251813 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Stambpl1 | Mm_Celera | 19:34202671 | TAGGGGTTGCAACTA[A/G]TGCAAATATTACTTT | 76630 |
rs6252358 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Stambpl1 | Mm_Celera | 19:34202791 | GGCAGCGTGATGGGC[A/G]TGGCATCCTAGAACT | 76630 |
rs6252852 | snp | A/G | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34202905 | AACCACACTCAGGGC[A/G]GCCCCACCCCTAAGA | 76630 |
rs6293574 | snp | A/G | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34199249 | TTAAGCACAGACTTG[A/G]TTGCCTGAGTTCTAC | 76630 |
rs6293642 | snp | C/T | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34199281 | CGTCCAGTCTTGATA[C/T]TGTGTCTCACTAAAG | 76630 |
rs6294170 | snp | G/T | 0.5 | 0 | intron-variant | Stambpl1 | Mm_Celera | 19:34199367 | ATTATTGAAGATATT[G/T]TAAATATCACCCCTA | 76630 |
rs13483598 | snp | C/T | 0.42 | 0.183303 | intron-variant | Stambpl1 | Mm_Celera | 19:34204932 | TGTGAATTCTATGAG[C/T]ATTCTTCAGAATGTC | 76630 |
rs30314368 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Stambpl1 | GRCm38.p3 | 19:34234296 | GGCCCTAAAGCCAGC[A/G]GCCACCCTGAGTGCT | 76630 |
rs30319924 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34208221 | GTTTATAAGTTTATG[G/T]ACTGTCTGTTGGATA | 76630 |
rs30348826 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34205671 | CTTTTCACCAGGCTG[C/T]GCCTCTTAGAGATTC | 76630 |
rs30371367 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stambpl1 | Mm_Celera | 19:34235462 | ATTAACTCTTACATA[C/T]CCTTAAACTACTGAC | 76630 |
rs30371372 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34239741 | AAATTCAGAGATACC[A/C]ACCTGCCTCTGCCTC | 76630 |
rs30373653 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34208269 | TTATCTTTAAAGGTA[A/C/G]TGGATACTTTGAATT | 76630 |
rs30401804 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34210897 | GCTCAGAGAGGTCCT[C/T]CTCTGTGAATCTGTC | 76630 |
rs30402797 | snp | C/G | 0.32 | 0.24 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34209415 | GTACCTGTTACCACC[C/G]TGGCAGCCATTGTGC | 76630 |
rs30405307 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Stambpl1 | Mm_Celera | 19:34231794 | TAGAGCTTCCGACCG[A/G]CTCTTGCCAGTGTAA | 76630 |
rs30407879 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Stambpl1 | GRCm38.p3 | 19:34215234 | AGAGGTGGAAAATGT[A/G]GGTCTGAGCAGTGTG | 76630 |
rs30418335 | snp | A/G | 0.32 | 0.24 | intron-variant | Stambpl1 | Mm_Celera | 19:34208249 | ATACCACAACATTTA[A/G]AATTTTATCTTTAAA | 76630 |
rs30423857 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Stambpl1 | Mm_Celera | 19:34209916 | AAGGATTGAAATTAG[A/T]ACTTTCAGTGAGATA | 76630 |
rs30452670 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stambpl1 | Mm_Celera | 19:34235106 | AATGGAATGTGAAGC[A/G]CCCAGTAGTTTCAGT | 76630 |
rs30454120 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Stambpl1 | Mm_Celera | 19:34235313 | AGGAATAGAGACCTG[C/T]GGGATCCTCTGTGGA | 76630 |
rs30499784 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stambpl1 | Mm_Celera | 19:34236872 | TAACCACTGAGCCAT[C/T]TCTCCAGTCCCCTTA | 76630 |
rs30511698 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34222157 | AGTGGGAAATCAAGA[A/G]CAAAAGCAATAGACT | 76630 |
rs30525805 | snp | A/G | 0.375 | 0.216506 | missense | Stambpl1 | GRCm38.p3 | 19:34234196 | TTTCCACCCACCAGA[A/G]CAACTCTCTGAGGAA | 76630 |
rs30562428 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34219683 | TAGAAGACCCACTAG[A/G]ACAGGTCAGTCTTGT | 76630 |
rs30608728 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34215095 | AAGTCCCTGAGTCAT[A/G]CAAACCCAGGCCCAA | 76630 |
rs30610291 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Stambpl1 | Mm_Celera | 19:34208274 | TTTAAAGGTAGTGGA[A/T]ACTTTGAATTGAACT | 76630 |
rs30613367 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Stambpl1 | Mm_Celera | 19:34197235 | TTTTTTTTTTTTTTT[G/T]GGGGTTTCGAGACAG | 76630 |
rs30654313 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34214226 | GGGCATCAGGTAACC[A/G]GCTGGGCCAGAAAGG | 76630 |
rs30667844 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34218750 | GGACCGTCTTGTGAC[C/T]AAAGTCATGCAAAGG | 76630 |
rs30669622 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stambpl1 | Mm_Celera | 19:34222036 | TGACCTTTCTCCATC[A/G]GCAGCCTGAATAGTA | 76630 |
rs30744592 | snp | C/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | Acta2, Stambpl1 | Mm_Celera | 19:34240519 | GCTACCATGTGGGTA[C/G]TAGGAGTAGAGGCCA | 76630 |
rs30753346 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stambpl1 | Mm_Celera | 19:34227687 | TTGCTTGTTTGGACA[A/G]AGGCTTTCATGTAGC | 76630 |
rs30754595 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stambpl1 | Mm_Celera | 19:34235338 | TGTGGAAAACTGGTA[C/T]GATCTTATTCCATCT | 76630 |
rs30755159 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34239275 | AAAACTGTCTACTCG[G/T]GTGGAGGACACAGGT | 76630 |
rs30755374 | snp | C/T | 0.5 | 0 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34237445 | GAGGTCATTCGTTTC[C/T]TGCCTAGTACTTTAT | 76630 |
rs30794198 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34213305 | GAGAAGGCCAAGTAT[A/G]GTGGTGCATGCTTGC | 76630 |
rs30798293 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stambpl1 | Mm_Celera | 19:34235012 | TATAAAATAATTTGT[A/G]TATGATATGTACATG | 76630 |
rs30802747 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Stambpl1 | Mm_Celera | 19:34231979 | TAGAAGAGGCATAGT[C/T]AGAGTTTCAATGGAT | 76630 |
rs30859053 | snp | C/G | 0.375 | 0.216506 | intron-variant | Stambpl1 | Mm_Celera | 19:34227997 | AGAAGAAGGATTTAC[C/G]GGTTATTTAATTTCT | 76630 |
rs30869570 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, downstream-variant-500B | Acta2, Stambpl1 | GRCm38.p3 | 19:34240919 | CATTTTTTCCTGGAT[A/G]TTGGCCAAAGGAGGA | 76630 |
rs30869783 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Stambpl1 | Mm_Celera | 19:34235098 | AAAAAAAAAATGGAA[A/T]GTGAAGCGCCCAGTA | 76630 |
rs30884631 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stambpl1 | Mm_Celera | 19:34222565 | CCTTTCTTGTTTACT[A/G]GCTTCTACGTGCACC | 76630 |
rs30904874 | snp | G/T | 0.375 | 0.216506 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34222112 | AGAATATATAGTGTC[G/T]CCAGCAATAGGGTCT | 76630 |
rs30934349 | snp | G/T | 0.444444 | 0.157135 | missense | Stambpl1 | GRCm38.p3 | 19:34234122 | GGCTCGAGGCCAGAT[G/T]CGAGGTCAGGACTCT | 76630 |
rs31000021 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stambpl1 | Mm_Celera | 19:34222577 | ACTAGCTTCTACGTG[C/T]ACCTCAAGTTAAATA | 76630 |
rs31006187 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stambpl1 | Mm_Celera | 19:34235104 | AAAATGGAATGTGAA[A/G]CGCCCAGTAGTTTCA | 76630 |
rs31029019 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34239811 | GCCTGGATCACCAGC[A/G]GCGATTATCTCCATG | 76630 |
rs31053466 | snp | G/T | 0.375 | 0.216506 | intron-variant | Stambpl1 | Mm_Celera | 19:34209948 | TGGAAGGTTTTTTTT[G/T]TTTTTTTTTTTAACC | 76630 |
rs31082814 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34213348 | CAGTAGAGAGCAGAG[A/G]CAGACACATCCCTGA | 76630 |
rs31133947 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34237411 | CAGACCTTAGTGAGA[A/G]CTCTGTCATAATTCA | 76630 |
rs31139022 | snp | A/C | 0.375 | 0.216506 | intron-variant | Stambpl1 | Mm_Celera | 19:34208754 | TACCAACTAGGCCAT[A/C]TTCTGCTACATATGC | 76630 |
rs31140616 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Stambpl1 | Mm_Celera | 19:34210668 | TTTTAAGATTCAATT[A/C]TTAACTGGCAAGTTT | 76630 |
rs31141628 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34213881 | CCCTAAACAGTCAAT[C/T]AAAGCACTCAGCAGG | 76630 |
rs31143628 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stambpl1 | Mm_Celera | 19:34227999 | AAGAAGGATTTACGG[A/G]TTATTTAATTTCTAA | 76630 |
rs31152007 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34233623 | AAATGCCTTGCTCCA[C/T]GTGGTCTGAGGGGTC | 76630 |
rs31177869 | snp | A/T | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | Acta2, Stambpl1 | Mm_Celera | 19:34240513 | GTGCAAGCTACCATG[A/T]GGGTAGTAGGAGTAG | 76630 |
rs31194354 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34209506 | AGCTTGGCTCTTGCC[A/C]AGGAGACAAGAGAGC | 76630 |
rs31257028 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34210922 | TCTGTCCTTGAAGGC[C/T]TGGGAGTGGCCCTTT | 76630 |
rs31286522 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34234781 | GTTCCCCTCCCCCCC[A/C]AAAAATAGTGCTTTT | 76630 |
rs31287291 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34219278 | TATATTCATCTCAGG[G/T]TTTTTGTGAGACACG | 76630 |
rs45642127 | snp | A/G | | | intron-variant | Stambpl1 | GRCm38.p3 | 19:34228893 | CTAACCCTGTCATCA[A/G]GTAAAATAAAATGAA | 76630 |
rs45676998 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34217841 | GCTGCCCTTCAACTT[G/T]CTCTATAGCTAAAAC | 76630 |
rs45741179 | snp | C/G/T | | | intron-variant, utr-variant-5-prime | Stambpl1 | GRCm38.p3 | 19:34232446 | TGTTTTTTCCTCTCT[C/G/T]TCTCTCTCTCTCCTC | 76630 |
rs45746552 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Stambpl1 | Mm_Celera | 19:34224972 | GAGGAAGCATCACTG[C/T]CTTCAGCTTAATGGA | 76630 |
rs45750962 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Stambpl1 | Mm_Celera | 19:34205831 | GGATGCTTGCCTAGC[A/C]GATGAGAGGTCCTGG | 76630 |
rs45775709 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34214260 | AAGGGAGGCCTCTGA[A/G]GCAGCATTAGCAGGC | 76630 |
rs45777659 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Stambpl1 | Mm_Celera | 19:34205672 | TTTTCACCAGGCTGC[G/T]CCTCTTAGAGATTCC | 76630 |
rs45783761 | snp | C/T | 0.32 | 0.24 | intron-variant | Stambpl1 | Mm_Celera | 19:34213828 | TAACATGGCCATGGT[C/T]CCTAGGCTTTGCTTT | 76630 |
rs45810371 | snp | A/G | | | intron-variant | Stambpl1 | Mm_Celera | 19:34214791 | TGTGATAGGTCCCAA[A/G]TGCTAACTGATCTCA | 76630 |
rs45812752 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Stambpl1 | Mm_Celera | 19:34216654 | GGATAGCTGGTCTAT[A/G]CTTTGAGAGGCACTG | 76630 |
rs45856813 | snp | A/G | 0.32 | 0.24 | intron-variant | Stambpl1 | Mm_Celera | 19:34204357 | GTCACATAAGAGTTA[A/G]TCAGAAGCCGGGCAG | 76630 |
rs45859958 | snp | C/T | | | intron-variant, upstream-variant-2KB | Stambpl1 | GRCm38.p3 | 19:34216991 | CCCACCCTAAACACA[C/T]ACGTTTCTAAATTGG | 76630 |
rs45863462 | snp | C/T | | | intron-variant | Stambpl1 | GRCm38.p3 | 19:34221679 | GCCATAGACACTTAC[C/T]CTCTGCACTTTGCCC | 76630 |
rs45868857 | snp | C/G | | | intron-variant | Stambpl1 | Mm_Celera | 19:34229063 | TATCATTCTTCATAC[C/G]AGGGATACATTATAG | 76630 |
rs45891809 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stambpl1 | Mm_Celera | 19:34210111 | CATCATCATCATCAG[C/T]ATTGTGTCAACTCCG | 76630 |
rs45903286 | snp | A/G | | | intron-variant | Stambpl1 | GRCm38.p3 | 19:34238493 | TAATAATTGATTATT[A/G]CCATCATCATCATTG | 76630 |
rs45919415 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Stambpl1 | Mm_Celera | 19:34207921 | ATTATTTTTTTTAAA[A/G]AGCCATTTGGGGTAA | 76630 |
rs45926530 | snp | C/T | | | intron-variant | Stambpl1 | Mm_Celera | 19:34213526 | TAGGGACATAGAGTA[C/T]ACACACACACACACA | 76630 |
rs45949865 | snp | C/T | 0.32 | 0.24 | intron-variant | Stambpl1 | Mm_Celera | 19:34207585 | TAGTGTAACACCCAA[C/T]GTAAACGCTATTGCT | 76630 |
rs45979836 | snp | A/G | 0.32 | 0.24 | intron-variant | Stambpl1 | Mm_Celera | 19:34214130 | TGCATGTTATCACAA[A/G]TGTGAGGATGAGAAC | 76630 |
rs46087343 | snp | C/G | | | intron-variant | Stambpl1 | Mm_Celera | 19:34219699 | ACAGGTCAGTCTTGT[C/G]CATTCTCAAGGGGAG | 76630 |
rs46121118 | snp | A/G | | | intron-variant, utr-variant-5-prime | Stambpl1 | GRCm38.p3 | 19:34232716 | TGTCTCTTTGCTTTG[A/G]AGGTTGCTGGCTCTA | 76630 |
rs46162383 | snp | A/C | 0.32 | 0.24 | intron-variant | Stambpl1 | Mm_Celera | 19:34203774 | TAAAGAGGCTCCTGG[A/C]TCAGAATGACCTTTG | 76630 |
rs46212566 | snp | G/T | | | intron-variant | Stambpl1 | GRCm38.p3 | 19:34229582 | GGGTTATTATTTCAG[G/T]AGTCCAATAACAGAC | 76630 |
rs46222564 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B, utr-variant-3-prime | Acta2, Stambpl1 | Mm_Celera | 19:34240251 | TTGCTGCGTCTCAAA[C/T]GAGGCCACGTGGTGT | 76630 |
rs46298759 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Stambpl1 | GRCm38.p3 | 19:34212832 | CAGTACTCCTCTGAC[C/G]TTCTGCTTCAGTATA | 76630 |
rs46304248 | snp | A/G | | | intron-variant | Stambpl1 | GRCm38.p3 | 19:34221006 | AATCTGATGGCAGGT[A/G]ACAGAATCCAAAACA | 76630 |
rs46381471 | snp | C/T | | | intron-variant | Stambpl1 | Mm_Celera | 19:34238199 | GGGAGTCCAAGATCC[C/T]GGGCTTTCTGATCTC | 76630 |