SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs31012741 | snp | A/G | 0.32 | 0.24 | intron-variant | Kctd13 | Mm_Celera | 7:126935360 | GCTCACTAAAATCTG[A/G]CCATGTTGTATGTAC | 233877 |
rs31014340 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126946906 | ACTCAATGGGCCTCA[C/T]AGGCCAGATTCTGTG | 233877 |
rs31046276 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B, intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126945782 | GAGGCAGGAGGATTT[C/T]TGAGTTCGAGGCCAG | 233877 |
rs31097944 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kctd13 | Mm_Celera | 7:126938715 | GTACGCAACAAAGGT[A/G]CTCAGTGAGGTACAG | 233877 |
rs31126222 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon, upstream-variant-2KB | Kctd13, Tmem219 | Mm_Celera | 7:126929273 | CATGTTCAGCGGCCG[C/T]GTTGAAGTGCTCACA | 233877 |
rs31167892 | snp | A/C | 0.5 | 0 | intron-variant | Kctd13 | GRCm38.p3 | 7:126940636 | CGAACCCCCCCCCCC[A/C]AAAAAAAAAAAAAAC | 233877 |
rs31185476 | snp | G/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Kctd13, Tmem219 | Mm_Celera | 7:126929875 | GATGCGTCAGTTACT[G/T]CTAGAGAAAGTTTGG | 233877 |
rs31195484 | snp | A/C | 0.5 | 0 | intron-variant | Kctd13 | GRCm38.p3 | 7:126940637 | GAACCCCCCCCCCCC[A/C]AAAAAAAAAAAAACT | 233877 |
rs31202715 | snp | C/T | 0.375 | 0.216506 | utr-variant-5-prime, upstream-variant-2KB | Kctd13, Tmem219 | Mm_Celera | 7:126929026 | GCGCAGAGAGGGCCT[C/T]CGACTGCCACCCGCG | 233877 |
rs31231934 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Asphd1, Kctd13 | Mm_Celera | 7:126947582 | TGAGTTCAATTCCCA[A/G]CAACCACACGGTGGC | 233877 |
rs31233585 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Kctd13 | Mm_Celera | 7:126940834 | GAACAGACGCAGGCA[C/T]AGACTTAAGTGCTGT | 233877 |
rs31307942 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd13 | Mm_Celera | 7:126943116 | AGCAGGCTTTGATTC[C/T]GCAGGATTGCAGAAG | 233877 |
rs31317332 | snp | A/G | 0.277778 | 0.248452 | downstream-variant-500B, intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126945967 | TTGGTAACTGGGAAG[A/G]AAAGAATCAGGACTT | 233877 |
rs31381935 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126946621 | TGTGGCTCGCCCAAG[C/G]CTGTGCAGTCCCAAA | 233877 |
rs31430274 | snp | C/T | 0.415225 | 0.187619 | utr-variant-3-prime, intron-variant | Kctd13 | Mm_Celera | 7:126945436 | TAGAAAGGACAGTGC[C/T]ATCAGCCACACTCCA | 233877 |
rs31481394 | snp | C/T | 0.5 | 0 | intron-variant | Kctd13 | Mm_Celera | 7:126940472 | TGGGTGGTGGTAGCG[C/T]ACACCTTTAATCCCA | 233877 |
rs31590194 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Kctd13 | Mm_Celera | 7:126942613 | TGTTAGTGGCTTTTT[A/T]AAAAAGCTGTATTTA | 233877 |
rs31621833 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd13 | Mm_Celera | 7:126936985 | CTGGCCAGCATCTTA[C/T]ATTGTTTTCAGTTTT | 233877 |
rs31648622 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kctd13 | Mm_Celera | 7:126933424 | GTTTTCTCGCCATAT[C/T]TTACTCATTTATCCT | 233877 |
rs31670576 | snp | C/G | 0.32 | 0.24 | utr-variant-5-prime, upstream-variant-2KB | Kctd13, Tmem219 | Mm_Celera | 7:126928927 | GCTGGTGGACGTCGC[C/G]GAGTAGCTGTGGAGA | 233877 |
rs31670908 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kctd13 | Mm_Celera | 7:126940251 | GGATTGTTTTTTGTT[C/T]TGTTTGTTTTTGAGA | 233877 |
rs31690635 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Kctd13 | Mm_Celera | 7:126942865 | GTGGAGAGGGCTCAG[C/T]GTTGTCTGCGGTGCC | 233877 |
rs31763635 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kctd13 | Mm_Celera | 7:126937527 | TTTCTTTTTATTTTT[A/G]TGTTTGTTTGTTTGT | 233877 |
rs31798227 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB, utr-variant-5-prime | Kctd13, Tmem219 | Mm_Celera | 7:126928846 | CCGAGACGCGGCCCT[A/C]GGCCTGGCCGCGCCT | 233877 |
rs31883652 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Kctd13 | Mm_Celera | 7:126940871 | AAGCAACCAATACTC[C/T]GAACCCAAGGAAGCT | 233877 |
rs32002455 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126946613 | GGAGGAGCTGTGGCT[C/T]GCCCAAGGCTGTGCA | 233877 |
rs32070651 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B, intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126945804 | CGAGGCCAGCCTAGT[C/T]TACAGAATGAGCTTC | 233877 |
rs32102209 | snp | G/T | 0.375 | 0.216506 | intron-variant | Kctd13 | Mm_Celera | 7:126942841 | AAAGCAGGATTCTTA[G/T]TGTAGGCAGTGGAGA | 233877 |
rs32103269 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Kctd13 | Mm_Celera | 7:126945136 | ACCTTGGCCTTCCCC[C/T]GCTGTCCTCTTGCTT | 233877 |
rs32141104 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kctd13 | Mm_Celera | 7:126936416 | CCTGAGCCGTCTTCC[A/G]CCCTCAGATGTGGAC | 233877 |
rs32226398 | snp | A/C | 0.32 | 0.24 | intron-variant | Kctd13 | Mm_Celera | 7:126933865 | AGTTCAAAGCTAGCA[A/C]GAGTTACATAGGAGC | 233877 |
rs32228431 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Kctd13 | Mm_Celera | 7:126943754 | CCGTGCAGAGCTTCC[G/T]TAGTGGTGTCTGATG | 233877 |
rs32330346 | snp | C/G | 0.375 | 0.216506 | intron-variant | Kctd13 | Mm_Celera | 7:126934538 | GCCTCCCAAGTGCTG[C/G]GATTAAAGGCGTGCA | 233877 |
rs32345221 | snp | C/T | 0.5 | 0 | intron-variant | Kctd13 | Mm_Celera | 7:126940618 | TAAGAGAAACCCTGT[C/T]TCGAACCCCCCCCCC | 233877 |
rs32359193 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Kctd13, Tmem219 | Mm_Celera | 7:126928549 | AGGTGTGTGCCACCA[C/G]GCGCGGTGAACTTTC | 233877 |
rs32449023 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Kctd13 | Mm_Celera | 7:126943916 | AAGTGCTGTTGTCTT[C/G]GGTAGAACACTGGCT | 233877 |
rs32456610 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kctd13 | Mm_Celera | 7:126934499 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCAC | 233877 |
rs32481888 | snp | C/T | 0.345679 | 0.230967 | utr-variant-3-prime, intron-variant | Kctd13 | Mm_Celera | 7:126945393 | ATCTGATTCCCTTTC[C/T]GTTTTGTTAATACAT | 233877 |
rs33110941 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Kctd13, Tmem219 | Mm_Celera | 7:126927634 | GAGCAGGCTTGGCAA[C/T]CCCTCTTGGCAGAAC | 233877 |
rs33110943 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Kctd13, Tmem219 | Mm_Celera | 7:126927680 | GCCGGACACATTTCT[C/T]GATAACATCTTCTAA | 233877 |
rs33111218 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126946009 | GAGAATTTGTATTCA[A/G]TGCTGGCTGAGGAGG | 233877 |
rs33111221 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime, downstream-variant-500B, intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126946100 | GTGCCAGAAGCGTCT[C/T]TCAAGGGTCTGGAGC | 233877 |
rs33111875 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Kctd13 | Mm_Celera | 7:126939910 | GTAGTTGGGCCTTAC[A/G]GTTCCATTTAAATTC | 233877 |
rs33111878 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd13 | Mm_Celera | 7:126940774 | CATTCAGCAAAGTGT[A/G]CTTACACTGGTCATC | 233877 |
rs33111883 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd13 | Mm_Celera | 7:126940848 | ACAGACTTAAGTGCT[A/G]TGAAGAGAAGCAACC | 233877 |
rs33112044 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon, downstream-variant-500B, intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126946102 | GCCAGAAGCGTCTCT[C/T]AAGGGTCTGGAGCGA | 233877 |
rs33112047 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126946254 | CTGATACCAGAACTC[A/C]TGTGCTAGGATTCAT | 233877 |
rs33112050 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126946270 | TGTGCTAGGATTCAT[A/G]GTATAGACTGAGGAA | 233877 |
rs33112053 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126946296 | AGGAAAGCAAAGTCA[A/G]CACCAGGCCCTCACC | 233877 |
rs33112796 | snp | A/G | 0.32 | 0.24 | intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126946427 | GCATTTACAGTGGTA[A/G]CTCTGTGTGCCCAAA | 233877 |
rs33112801 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asphd1, Kctd13 | Mm_Celera | 7:126946710 | ACCAGAATGTGAGTC[C/T]TATTACCATTATGAG | 233877 |
rs33112808 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Kctd13 | Mm_Celera | 7:126940877 | CCAATACTCCGAACC[A/C]AAGGAAGCTATGTAA | 233877 |
rs33112811 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Kctd13 | Mm_Celera | 7:126940964 | AGCACACCCCTAGCA[C/G]GCTGACCCATGCAGT | 233877 |
rs33113634 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B, upstream-variant-2KB | Asphd1, Kctd13, Sez6l2 | Mm_Celera | 7:126948247 | GTAGGAAAGATGGAA[A/G]GTTTGTAGACAGGCT | 233877 |
rs33113674 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd13 | Mm_Celera | 7:126940988 | ATGCAGTGTGTGCCT[A/G]CAGAACAGCAGGTTG | 233877 |
rs33113677 | snp | A/C | 0.32 | 0.24 | intron-variant | Kctd13 | Mm_Celera | 7:126941208 | GCGTGGAGTGGTCAC[A/C]TCCTAGTGAGCCTTG | 233877 |
rs33113680 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kctd13 | Mm_Celera | 7:126941277 | ACACAGCCTTTATTT[A/G]AGTGGTGTGAGTCAA | 233877 |
rs33113683 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Kctd13 | Mm_Celera | 7:126941669 | CTCTACTATTATATT[A/C]CATGGAGGACTGTGG | 233877 |
rs33114496 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Kctd13 | Mm_Celera | 7:126942324 | CATAGTCTATGCTAC[A/G]GAGAAGAAGCAGACC | 233877 |
rs33114498 | snp | A/G | 0.32 | 0.24 | intron-variant | Kctd13 | Mm_Celera | 7:126942421 | ATCTGGCAAAGGAAA[A/G]CTCTTTGGTGGTTAT | 233877 |
rs33114500 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd13 | Mm_Celera | 7:126942484 | GTTTGGGAAGGTCAC[C/T]TCATTACCAATGAAA | 233877 |
rs33114502 | snp | A/G | 0.32 | 0.24 | intron-variant | Kctd13 | Mm_Celera | 7:126942516 | GAGGCTACTAGATTA[A/G]AGAAGATTCTGTTTT | 233877 |
rs33115465 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd13 | Mm_Celera | 7:126942843 | AGCAGGATTCTTAGT[A/G]TAGGCAGTGGAGAGG | 233877 |
rs33115470 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Kctd13 | Mm_Celera | 7:126943083 | TCACTTTAGAACCTC[A/C]GAAGGTCCACTAGCA | 233877 |
rs33115473 | snp | C/T | 0.32 | 0.24 | intron-variant | Kctd13 | Mm_Celera | 7:126943325 | GACCTTCAGCTTCAA[C/T]ACTCTGAGGCAGTTC | 233877 |
rs33116405 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd13 | Mm_Celera | 7:126943741 | GGCAGCCTGTTGACC[A/G]TGCAGAGCTTCCTTA | 233877 |
rs33116410 | snp | A/C | 0.32 | 0.24 | intron-variant | Kctd13 | Mm_Celera | 7:126943764 | CTTCCTTAGTGGTGT[A/C]TGATGAGCAGTCAAT | 233877 |
rs33116413 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd13 | Mm_Celera | 7:126943786 | GCAGTCAATCCCTGT[C/T]GCCTGTCGCCTAATG | 233877 |
rs33117376 | snp | A/G | 0.32 | 0.24 | intron-variant | Kctd13 | Mm_Celera | 7:126943846 | ACACATTTGCTCATG[A/G]AATCTCAATGCAACT | 233877 |
rs33117379 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Kctd13 | Mm_Celera | 7:126944367 | GCCCCTTTTCCTGTG[C/T]CTTCCTCTGTTTGTC | 233877 |
rs33117382 | snp | A/G | 0.32 | 0.24 | intron-variant | Kctd13 | Mm_Celera | 7:126944823 | GCCCACAGAGGAGCC[A/G]CTGGGGAAGCGCTGT | 233877 |
rs33118135 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Kctd13 | Mm_Celera | 7:126945285 | TCACTGCTAACCACA[C/T]GGTACATTCCAGCAT | 233877 |
rs45718259 | snp | C/T | | | intron-variant | Kctd13 | Mm_Celera | 7:126943638 | CATGGAGACAAAACA[C/T]CCACACATATAAAAA | 233877 |
rs48208626 | snp | A/G | | | intron-variant | Kctd13 | Mm_Celera | 7:126944566 | CACATCCCCTTTCCA[A/G]CTTTCTTCATAAGAT | 233877 |
rs49781899 | snp | A/T | | | intron-variant | Kctd13 | Mm_Celera | 7:126940118 | ATCTGTCTTTTAAAA[A/T]AAAAATAAGTCTCAA | 233877 |
rs49883562 | snp | A/G | | | intron-variant | Kctd13 | Mm_Celera | 7:126932444 | TTAAACTTATTTTAT[A/G]ACCCATTAAAGAGTC | 233877 |
rs50363598 | snp | C/T | | | intron-variant | Kctd13 | Mm_Celera | 7:126944680 | TTGTTTATAATACTA[C/T]GTTCCTGATGCTTGG | 233877 |
rs51403667 | snp | A/T | | | intron-variant | Kctd13 | Mm_Celera | 7:126940121 | TGTCTTTTAAAAAAA[A/T]AATAAGTCTCAAAAC | 233877 |
rs52456222 | snp | C/T | | | intron-variant | Kctd13 | Mm_Celera | 7:126934914 | CTTCTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 233877 |
rs211939223 | snp | A/G | | | intron-variant | Kctd13 | Mm_Celera | 7:126932538 | ATGTGCCACATGTAT[A/G]TGTGGAGGCCAGAGG | 233877 |
rs212004692 | snp | A/C | | | synonymous-codon | Kctd13 | Mm_Celera | 7:126941387 | ACAGTGACATCACCC[A/C]GGGAAGAGCAGCAGC | 233877 |
rs212217544 | in-del | -/CAGCCTGCTCTCA | | | intron-variant | Kctd13 | Mm_Celera | 7:126931477 | ACTGAGCCATCTTAG[-/CAGCCTGCTCTCA]CTTCATCTCAGTTTC | 233877 |
rs212279647 | snp | C/T | | | intron-variant | Kctd13 | Mm_Celera | 7:126933251 | TATCCTTGGATTATA[C/T]CTCTTCCCTGGAAGA | 233877 |
rs212571981 | snp | A/G | | | upstream-variant-2KB, intron-variant | Kctd13, Tmem219 | Mm_Celera | 7:126927965 | GAGCCAACACTGCCT[A/G]GTTTGACTTTGCTTA | 233877 |
rs212682215 | snp | C/T | | | intron-variant | Kctd13 | Mm_Celera | 7:126937657 | CAGTCCCAAGCTTTC[C/T]AATAATGCATACAAT | 233877 |
rs212964241 | snp | A/G | | | intron-variant | Kctd13 | Mm_Celera | 7:126940015 | AACCCTAGTACTTAG[A/G]AATCAGAGGCAGGTA | 233877 |
rs213029785 | snp | G/T | | | intron-variant | Kctd13 | Mm_Celera | 7:126939330 | CCGTAAAGACCTTAC[G/T]TTAAGTGAGGCTGTG | 233877 |
rs213094196 | in-del | -/T | | | intron-variant | Kctd13 | Mm_Celera | 7:126938676 | GGGCACTGGAACTCC[-/T]GTGTGGATCATACCT | 233877 |
rs213293572 | snp | A/G | | | intron-variant, upstream-variant-2KB | Kctd13, Tmem219 | Mm_Celera | 7:126930426 | TTTCATGTCACCTTG[A/G]CTGCTGGAACTCACT | 233877 |
rs213338390 | snp | A/G | | | intron-variant | Kctd13 | GRCm38.p3 | 7:126933508 | TTGTTTTGTTTTTTC[A/G]AGACAGGGTTTCTCT | 233877 |
rs213339795 | snp | C/T | | | intron-variant | Kctd13 | Mm_Celera | 7:126943350 | CAGTTCTGGACCTGC[C/T]AGGGCAGCATAGTAA | 233877 |
rs213398850 | snp | A/G | | | intron-variant | Kctd13 | Mm_Celera | 7:126942809 | GCTCTTAACCATTGA[A/G]GCAACTGGCCAGCCT | 233877 |
rs213913849 | snp | C/G | | | intron-variant | Kctd13 | Mm_Celera | 7:126936851 | CCCAAATAGTTCTTG[C/G]GAAGTCTCCCTGGTA | 233877 |
rs214015921 | snp | C/T | | | utr-variant-3-prime, intron-variant | Kctd13 | Mm_Celera | 7:126945349 | ACCGCCCCTCCTCTA[C/T]ATCCTTGTTCTGCCA | 233877 |
rs214218547 | in-del | -/GCCTGGTGACA | | | intron-variant | Kctd13 | Mm_Celera | 7:126941963 | TGGCAGTGCTGGGGT[-/GCCTGGTGACA]GCCTGGTGACAGCCT | 233877 |
rs214268909 | snp | C/T | | | intron-variant | Kctd13 | Mm_Celera | 7:126940826 | ACATGTCAGAACAGA[C/T]GCAGGCACAGACTTA | 233877 |
rs214591799 | snp | C/G | | | intron-variant | Kctd13 | Mm_Celera | 7:126941290 | TTAAGTGGTGTGAGT[C/G]AACACCAGTTGTACT | 233877 |
rs214987133 | snp | A/G | | | intron-variant | Kctd13 | Mm_Celera | 7:126931512 | TCAGTTTCAGCTGGA[A/G]TGTAATAACCTTGAC | 233877 |
rs215309679 | snp | A/C | | | intron-variant, utr-variant-3-prime | Asphd1, Kctd13 | Mm_Celera | 7:126947467 | AAGTCATAATATTTA[A/C]TTTCCCAATTTTCTT | 233877 |
rs215320136 | snp | A/G | | | intron-variant | Kctd13 | Mm_Celera | 7:126932294 | TCAAATTTTTTACCC[A/G]TAGCCCATGGGGGGA | 233877 |