SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13478981 | snp | A/G | 0.369846 | 0.219401 | intron-variant | Sec13 | GRCm38.p3 | 6:113730642 | AAAGTGCTTAGAAAA[A/G]GAGCAAGGTGTTTGT | 110379 |
rs29925574 | snp | A/G | 0.5 | 0 | intron-variant | Sec13 | GRCm38.p3 | 6:113739988 | TCCAACTTGGCAACA[A/G]AAGAGCCAAAGGCCA | 110379 |
rs29976252 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Sec13 | GRCm38.p3 | 6:113737027 | AATTCTATCTCCTTA[G/T]CTTACCTGTTATACA | 110379 |
rs30014764 | snp | A/T | 0.495 | 0.0497494 | intron-variant, upstream-variant-2KB | Sec13, Ghrl | GRCm38.p3 | 6:113729185 | CACAAAGGGACATAA[A/T]GTAGAGTGGGTAGTG | 110379 |
rs30117735 | snp | A/G | 0.375 | 0.216506 | intron-variant | Sec13 | GRCm38.p3 | 6:113736271 | TAAGGGCTCACTGCT[A/G]AATGTACTCTGAGAT | 110379 |
rs30174449 | snp | C/T | 0.375 | 0.216506 | intron-variant | Sec13 | GRCm38.p3 | 6:113733947 | CAAACATGAAATTGT[C/T]AGATGGCCCAACTGT | 110379 |
rs30220110 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Sec13 | GRCm38.p3 | 6:113737103 | CTTAAGAAGGATCTA[C/T]GGAGCACAATGGCTT | 110379 |
rs30222738 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Sec13 | GRCm38.p3 | 6:113737371 | TGCCGGTGGTCAGCT[A/G]TGGAGGCCAGGGGCC | 110379 |
rs30267582 | snp | A/G | 0.32 | 0.24 | intron-variant | Sec13 | GRCm38.p3 | 6:113739378 | CTGGGAGAGTACGGC[A/G]GCAAGGCATTCAGAA | 110379 |
rs30317927 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Sec13 | GRCm38.p3 | 6:113733231 | TATGTGTATACACAC[A/C]CTAACTAAAATCAAC | 110379 |
rs30415584 | snp | C/G/T | 0.492188 | 0.0620098 | intron-variant | Sec13 | GRCm38.p3 | 6:113733332 | CATCAAGAAAACAGC[C/G/T]GCAAACTCCATCCAG | 110379 |
rs30468609 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Sec13 | GRCm38.p3 | 6:113740603 | GGACGTAGAGGTGGT[C/T]TGTCTCAAAGCCACG | 110379 |
rs30514710 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Sec13 | GRCm38.p3 | 6:113738465 | GATATGATCCAAGCA[C/G]GAAAGGTTAGCATGG | 110379 |
rs30852913 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Sec13 | GRCm38.p3 | 6:113740716 | CTTCCGGTGCCGGCC[C/G]GCAGCCGGCAGGCTG | 110379 |
rs30957042 | snp | C/T | 0.32 | 0.24 | intron-variant | Sec13 | GRCm38.p3 | 6:113739453 | TGCTCTGAAAAGTGT[C/T]GGCAAAGATTAGAGA | 110379 |
rs36278510 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113734707 | GGTACAGTGAGAAGG[C/T]TTTCATCCTATATCT | 110379 |
rs36279091 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113734985 | ACAACAAGAGAAGGG[C/T]CTGGGATGCGAGCAG | 110379 |
rs36284904 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Sec13 | GRCm38.p3 | 6:113742189 | CCTTCAACTGATCGG[A/G]CCAAGTTCTTTTTCT | 110379 |
rs36294446 | snp | C/T | 0.32 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113729864 | ATGTCCTGCTTCTGA[C/T]CCTTTCGCCCTGAAC | 110379 |
rs36314800 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Sec13 | Mm_Celera | 6:113737084 | TAACCTTCAGTTTCC[A/G]TATCTTAAGAAGGAT | 110379 |
rs36329856 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113727698 | TGCCAAATACTTAAA[C/T]AGCAGGCTTCAGTAG | 110379 |
rs36344325 | snp | A/G | 0.18 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113737708 | GACGACTGATTGTCA[A/G]ACCTCTGCAGCTTTA | 110379 |
rs36391574 | snp | C/T | 0.42 | 0.183303 | upstream-variant-2KB | Sec13 | Mm_Celera | 6:113742288 | TTATTGAGGGAATTT[C/T]CTGGTATAAATTCTG | 110379 |
rs36416667 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Sec13 | Mm_Celera | 6:113731779 | GGGAAGATGGCTCAG[G/T]ACTTGTTAAACCTGA | 110379 |
rs36430392 | snp | A/G | 0.32 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113736301 | TTGCAGGGAATCTGT[A/G]CTCTCCCCTTTCCTC | 110379 |
rs36444034 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113735358 | TGAGCTTGTGATCCT[C/G]CCAGATGTGCCACCA | 110379 |
rs36447339 | snp | A/G | 0.18 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113737270 | CTCTGGGTCCATGCC[A/G]GTTCCAGCCAAGTGG | 110379 |
rs36483756 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113734717 | GAAGGTTTTCATCCT[A/G]TATCTACTACTGCGC | 110379 |
rs36528400 | snp | C/T | 0.42 | 0.183303 | intron-variant | Sec13 | Mm_Celera | 6:113740190 | ACTCAGCTAGGCCTG[C/T]CATCAGTTTCCCGAA | 110379 |
rs36528451 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113728969 | ATTAATATCAGGTCC[C/T]GACTCTGGTACAAAG | 110379 |
rs36553016 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Sec13 | GRCm38.p3 | 6:113736428 | ATCGAAAATTTTGAC[A/G]GACCTATCCGAGGAG | 110379 |
rs36600669 | snp | C/G | 0.18 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113737206 | TCTGATCCTCAGGAG[C/G]AAACCAAGGTGGGTG | 110379 |
rs36610189 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Sec13 | Mm_Celera | 6:113738747 | ATTTCTCCATTTGAT[G/T]TAAATCAGCCTCCCT | 110379 |
rs36620340 | snp | C/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113728828 | CAACACTGCCCTGTG[C/G]CTCCTCAGAAGGGCA | 110379 |
rs36636285 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, upstream-variant-2KB | Sec13, Ghrl | GRCm38.p3 | 6:113728443 | CCACTGTCCGTCCAC[C/T]GACTCTTTCCACAGG | 110379 |
rs36749822 | snp | C/T | 0.18 | 0.24 | upstream-variant-2KB | Sec13 | GRCm38.p3 | 6:113741690 | AGTAGAACCTCCACT[C/T]CCATTAGCTAAATCC | 110379 |
rs36765095 | snp | C/T | 0.18 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113737594 | CTGGGGTAGCCTCTG[C/T]CCTACGCTTTCACTG | 110379 |
rs36784951 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113731007 | AGTTGTCAGGACTTG[A/G]GTTACAGCACACAGA | 110379 |
rs36856962 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113727951 | GAGGAGGGACTATTT[C/T]CCCCTTGCAGGTGGA | 110379 |
rs36870454 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113729455 | AGGTCAGGCTACACT[A/G]CAGCTATGCAAGTCC | 110379 |
rs36890863 | snp | G/T | 0.32 | 0.24 | upstream-variant-2KB | Sec13 | Mm_Celera | 6:113742075 | CTTTTACAGGGATTT[G/T]AGGAGGCGATACTTA | 110379 |
rs36902646 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113733746 | ATATAGGCATAAAAA[A/C]ACCAAGACATGGTAA | 110379 |
rs36985386 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113734468 | CAGCCAGGACACCCA[C/T]TCTCTTCCTAGGAGC | 110379 |
rs36992757 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113727739 | CTTTAGTGACTGCTA[A/G]TTCAGGTGAGGGTTC | 110379 |
rs37050858 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Sec13 | Mm_Celera | 6:113730128 | TACATGGACCCAAGG[C/T]GCCTCCATTCCTCCT | 110379 |
rs37055756 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113729251 | TTCTGAAGATCAGCC[A/G]CACAGTGTCACACAG | 110379 |
rs37137093 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Sec13 | Mm_Celera | 6:113738027 | CATTCTGTGAATTCA[C/T]CGACAGCAGCCACCA | 110379 |
rs37159435 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Sec13 | Mm_Celera | 6:113739174 | GTGGATTGAAAAGGT[A/G]GCTTCCATTTGAGAC | 110379 |
rs37259496 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113733900 | TTGTAATTTTACACA[A/G]TGAATATATACTAAT | 110379 |
rs37275592 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Sec13 | Mm_Celera | 6:113734955 | AAAAGCCAACAAATG[C/T]CCAAAGGATGGACAA | 110379 |
rs37310004 | snp | C/G | 0.42 | 0.183303 | intron-variant | Sec13 | Mm_Celera | 6:113738302 | TGCACAGTGTGGAGC[C/G]GCAGCTCTTGCCTCA | 110379 |
rs37332880 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113736355 | CTGTGGCCTTCTCCA[C/T]GTGTGTTTACACTTA | 110379 |
rs37341842 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113736129 | CCCTGGATAGAGTCA[A/G]GATTATCCCATCTGA | 110379 |
rs37459536 | snp | A/C | 0.18 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113739707 | TCCCCACAATCCCAA[A/C]TGGCTCAAGGAAAAG | 110379 |
rs37484490 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113733115 | AGATAGCAAAAGCAG[G/T]ACGAAGAGGGAGCTT | 110379 |
rs37489577 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113728899 | AATCCTTATTGCATA[C/T]ATAGGGTGAGAAATG | 110379 |
rs37583153 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Sec13 | Mm_Celera | 6:113730730 | TGTACACGGTAGCTG[A/T]GCAATGACAGGCAGC | 110379 |
rs37603286 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113729464 | TACACTGCAGCTATG[C/T]AAGTCCTGTTGTGTG | 110379 |
rs37657070 | snp | G/T | 0.18 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113738885 | TTTGATGCATTCGCT[G/T]TCTGTCTTAGTAAAT | 110379 |
rs37682807 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Sec13 | Mm_Celera | 6:113734748 | TAAAAACCACAGGAA[C/T]TGCCAGCAGTCTTTT | 110379 |
rs37745128 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Sec13 | GRCm38.p3 | 6:113735058 | CCAACTCTACATACC[C/T]GAGGAGTCGTGTCCC | 110379 |
rs37752970 | snp | C/T | 0.42 | 0.183303 | intron-variant | Sec13 | Mm_Celera | 6:113740583 | GCAGGACAAGCAAAC[C/T]TTGAGGACGTAGAGG | 110379 |
rs37826938 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Sec13 | Mm_Celera | 6:113734803 | TGAACACCTAACAGC[A/T]TTTGTCTGTCTTCAC | 110379 |
rs38066178 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113727744 | GTGACTGCTAGTTCA[A/G]GTGAGGGTTCCAAGA | 110379 |
rs38091019 | snp | A/T | 0.18 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113736620 | CAACCTCTCAAAGGA[A/T]GTGCGGTATGGACCC | 110379 |
rs38183326 | snp | C/G | 0.297521 | 0.245442 | upstream-variant-2KB | Sec13 | Mm_Celera | 6:113742333 | GAGGATCTGGGATAA[C/G]CAACAGCAACTTAAG | 110379 |
rs38217550 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113732151 | ACATTGATCTGCCTC[C/T]ATGGGTATGACCATG | 110379 |
rs38303906 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Sec13 | Mm_Celera | 6:113740997 | CTTTTCTGCGGGTTC[C/T]GGGTCCCACTGGCTT | 110379 |
rs38383611 | snp | A/G | 0.32 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113738264 | CTGAGGATCTTCTTG[A/G]CATTAAGCCCCGTGT | 110379 |
rs38478681 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Sec13 | Mm_Celera | 6:113739082 | TAGTAACTACCTACT[A/G]AGTTAATAAAAGAGC | 110379 |
rs38484645 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Sec13 | Mm_Celera | 6:113734371 | AACCTGGGTCTTAGT[A/T]GTAGAAACCAGTGCC | 110379 |
rs38514006 | snp | A/C | 0.18 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113738337 | AGCTCGCGTGTGAAC[A/C]ACCTACCAGTAGCCA | 110379 |
rs38549126 | snp | C/T | 0.18 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113739852 | CTTGGAGCAGTCCTC[C/T]GGAGCATCTTATAAG | 110379 |
rs38687308 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Sec13 | Mm_Celera | 6:113731353 | GTCCTGACAGAAAAT[A/G]ACAGGACTACAGTGC | 110379 |
rs38782746 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113727704 | ATACTTAAACAGCAG[A/G]CTTCAGTAGGTGGTA | 110379 |
rs38819329 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Sec13 | Mm_Celera | 6:113741021 | CTGGCTTATCATGAC[C/T]ATCGTAGAGGTTAAT | 110379 |
rs38843931 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Sec13 | GRCm38.p3 | 6:113731305 | TCAGTAAAAATCCTA[A/G]GGATCAGAAAGGCAT | 110379 |
rs38854025 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Sec13 | Mm_Celera | 6:113738377 | TACTGCGGTTTGTGT[A/G]GGCAGAAAGAGCCCA | 110379 |
rs38935548 | snp | C/T | 0.18 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113739377 | CCTGGGAGAGTACGG[C/T]GGCAAGGCATTCAGA | 110379 |
rs38948598 | snp | A/G | 0.18 | 0.24 | upstream-variant-2KB | Sec13 | Mm_Celera | 6:113742462 | AAGGGCTCATTCTTC[A/G]CCTCTTTGAGTGGCT | 110379 |
rs39199757 | snp | C/T | 0.32 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113740307 | GAGGAGAATTTGGAT[C/T]TTAGCTTGCCACTGC | 110379 |
rs39235766 | snp | C/T | 0.32 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113732188 | TGCATACTCTACACA[C/T]ACACAGATGGACTAA | 110379 |
rs39278848 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Sec13 | Mm_Celera | 6:113737299 | GGTCTCACAGCTAGA[C/T]CACTCACCGCCAAAC | 110379 |
rs40064594 | snp | C/T | 0.42 | 0.183303 | intron-variant | Sec13 | Mm_Celera | 6:113738567 | GGCCCAGACAGTTTA[C/T]GTGAAACAAGTTATA | 110379 |
rs40085139 | snp | A/G | 0.18 | 0.24 | intron-variant | Sec13 | Mm_Celera | 6:113737049 | TGTTATACAACCTTT[A/G]GAAAATTTGCTTATT | 110379 |
rs47027997 | snp | A/T | | | upstream-variant-2KB | Sec13 | GRCm38.p3 | 6:113741944 | AAGGAGTGTGAAGGC[A/T]TTTTGGAGAGGGGCC | 110379 |
rs47355624 | snp | A/G | | | utr-variant-5-prime | Sec13 | Mm_Celera | 6:113740676 | GCGACCCACGGCCTC[A/G]GACGTGGCAGCTCAA | 110379 |
rs48468949 | snp | A/C | | | intron-variant | Sec13 | GRCm38.p3 | 6:113735491 | AAGTAGCAGGTCTAA[A/C]AACATGTAATTTCAA | 110379 |
rs211704410 | in-del | -/TTT | | | intron-variant | Sec13 | Mm_Celera | 6:113739111 | GCAAAGACACACATC[-/TTT]TTTTTTTTCTTCTCT | 110379 |
rs211740390 | snp | A/G | | | intron-variant | Sec13 | Mm_Celera | 6:113736521 | TAGGGAAGCCTGCAG[A/G]ACGCGTGGCTAACCC | 110379 |
rs211995160 | snp | C/T | | | intron-variant, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113729059 | GAACAGAAAAGGCTA[C/T]GTGTAGAGGGTTAAG | 110379 |
rs212040335 | snp | C/G | | | intron-variant, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113728567 | AAGCATTTGACTCCC[C/G]CTACCTGCTACACTT | 110379 |
rs212329011 | snp | A/C | | | intron-variant | Sec13 | Mm_Celera | 6:113730300 | ACTGGAAGGAAGGAA[A/C]GAACTCTAGTGTGAA | 110379 |
rs212339255 | snp | A/C | | | intron-variant | Sec13 | Mm_Celera | 6:113738898 | CTGTCTGTCTTAGTA[A/C]ATAGGTCTAGCTGCC | 110379 |
rs212377293 | snp | C/T | | | intron-variant | Sec13 | Mm_Celera | 6:113739477 | TTAGAGAAAGAGGAG[C/T]AGCACCTGCCTGGAG | 110379 |
rs212750165 | in-del | -/TT | | | utr-variant-3-prime, upstream-variant-2KB | Sec13, Ghrl | Mm_Celera | 6:113728255 | CATGTGTGGGCACTC[-/TT]GGGTGTGGAATCTTG | 110379 |
rs213030717 | snp | A/T | | | intron-variant | Sec13 | Mm_Celera | 6:113735300 | TGTTCCCATTGTCTT[A/T]GTTTTTTGAGGCAGG | 110379 |
rs213143431 | snp | C/T | | | intron-variant | Sec13 | Mm_Celera | 6:113734121 | GTTCTTTCATGTGTG[C/T]GTATTTTATAGAATT | 110379 |
rs213377933 | in-del | -/AAAAAA/AAAAAAAA/AAAAAAAAAA/AAAAAAAAAAAAA | | | intron-variant | Sec13 | Mm_Celera | 6:113731731 | GAGAAACCCTGTCTC[lengthTooLong]AAAAAAAAAAAAAAA | 110379 |
rs213488506 | snp | C/T | | | intron-variant | Sec13 | Mm_Celera | 6:113735425 | TGAGAACTCTGCATC[C/T]TGAAATGACTTACTT | 110379 |