SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6214220 | snp | C/T | 0.5 | 0 | intron-variant | Ankrd13b | Mm_Celera | 11:77472422 | TGCCTGCCCTCGCTG[C/T]AGCTTGGAGTGGCAT | 268445 |
rs6214697 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | Ankrd13b | Mm_Celera | 11:77472528 | TCTTCATCACGAGGC[A/G]CAGCCTCTCGCTGGC | 268445 |
rs6214783 | snp | A/G | 0.207612 | 0.24638 | synonymous-codon, missense, nc-transcript-variant | Ankrd13b | Mm_Celera | 11:77472575 | GCCACGTGGGGCCTC[A/G]AACAGTGCAGGGGAG | 268445 |
rs6229024 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon, missense, nc-transcript-variant | Ankrd13b | GRCm38.p3 | 11:77472801 | GGGGCTACCTCGCAC[C/T]GAGGGCACTGGCTCA | 268445 |
rs28211648 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ankrd13b | Mm_Celera | 11:77481816 | AAGTATCCCTGCAGC[A/C]ACATGGGACTAGCCA | 268445 |
rs28211649 | snp | A/G | 0.32 | 0.24 | intron-variant | Ankrd13b | Mm_Celera | 11:77481069 | GGGACAAAGAAAAGC[A/G]CCTCTCTCTTGCCTC | 268445 |
rs28211650 | snp | C/G | 0.5 | 0 | intron-variant | Ankrd13b | Mm_Celera | 11:77479947 | GGATGCGGTGGCTCA[C/G]ACCTGTAATCCCAAC | 268445 |
rs28211651 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ankrd13b | Mm_Celera | 11:77478901 | CAACTGGCAACAGGT[A/G]TCTCTGACTGGGACC | 268445 |
rs28211652 | snp | G/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77478205 | GTTGGCATGACCACT[G/T]AGTATCAGTTGGCAA | 268445 |
rs28211653 | snp | G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77478081 | AGCAGGGCAGAAACT[G/T]AATGGCGGTCCATCC | 268445 |
rs28211654 | snp | A/G | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77478063 | CGTGGGCCTCCTGTG[A/G]AAAGCAGGGCAGAAA | 268445 |
rs28211655 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77477907 | CTCACAAGGCCACGA[A/G]AGAGACCGACATGAT | 268445 |
rs28211656 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77477783 | TCAATGTCCACCTGT[A/G]GAAGAAGTTGAGATG | 268445 |
rs28211657 | snp | G/T | 0.244898 | 0.249948 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Ankrd13b | GRCm38.p3 | 11:77477754 | GAGGAGTCCGGCCTC[G/T]GGGATCTAGTTGTTC | 268445 |
rs28211658 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77477407 | CAGTCGGCAGGTGGA[A/G]ATCCGGTCTCACCTT | 268445 |
rs28211659 | snp | A/G | 0.297521 | 0.245442 | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77477340 | GAAATCCTGGGCCTG[A/G]AGGAGGACAGAGACA | 268445 |
rs28211660 | snp | C/T | 0.396694 | 0.202437 | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77477223 | GAGCCCCAGGAAGAG[C/T]ATGGAACCACACTCC | 268445 |
rs28211661 | snp | C/T | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77476800 | GGCCAGCTCGGGGCA[C/T]AGGCGTTGGAGCTGG | 268445 |
rs28211662 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Ankrd13b | GRCm38.p3 | 11:77476457 | GCCCGGCCAGCGCCA[A/G]GGTCTCCATGTACAC | 268445 |
rs28211663 | snp | C/T | 0.260355 | 0.249785 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Ankrd13b | GRCm38.p3 | 11:77476356 | GTTCTTGGTGTCGAG[C/T]TGTGTGGTGACAACG | 268445 |
rs28211664 | snp | C/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77476290 | AAAGAATGGCCCATC[C/G]GGCTGGCTCCTGGCC | 268445 |
rs28211665 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ankrd13b | Mm_Celera | 11:77476084 | AAGGATTCTGCAAAC[G/T]GCCTTCTCCTGGGGA | 268445 |
rs28211666 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ankrd13b | Mm_Celera | 11:77475644 | TCTTCTCTGAGCATA[C/G]AGACCAGGGAGGAAA | 268445 |
rs28211667 | snp | C/T | 0.32 | 0.24 | intron-variant | Ankrd13b | Mm_Celera | 11:77475613 | GATGCATGCAATAGC[C/T]GAGACACCTGAGACC | 268445 |
rs28211668 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ankrd13b | Mm_Celera | 11:77474279 | ATGACTAGATTAGCC[C/T]CTGAATGGTATGCAT | 268445 |
rs28211669 | snp | A/G | 0.32 | 0.24 | synonymous-codon, missense, nc-transcript-variant | Ankrd13b | GRCm38.p3 | 11:77473039 | GAAGCCAGGAGGCAG[A/G]CGCAACGTGATGAAG | 268445 |
rs28211670 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ankrd13b | Mm_Celera | 11:77472956 | TGCCTCTAAACCGCA[C/T]CCTCTCCAAGCGGCT | 268445 |
rs29461860 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ankrd13b | Mm_Celera | 11:77484934 | TTGTTTGTTTTTTTT[G/T]GGGGGGGGGGGTAAC | 268445 |
rs47592882 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77485456 | TGTTTGTTTAATTGC[C/T]GCAATGAAAAGGTTT | 268445 |
rs50047254 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77485085 | CTCCCTGGGTTGCGG[A/G]TGAGCTACTGGGCAT | 268445 |
rs50090492 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77485611 | CCTGCCCCCACCCAC[A/G]AGCAGCACCCCCGTG | 268445 |
rs50894700 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77483818 | TCAATGTCTTCCCAG[A/G]CCCTGGACAGCATCT | 268445 |
rs51724020 | snp | G/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77484935 | TGTTTGTTTTTTTTG[G/T]GGGGGGGGGGTAACT | 268445 |
rs211743558 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ankrd13b, 2210008F06Rik | Mm_Celera | 11:77487886 | CAGCCAGAGAAAACA[A/G]GATTGGATCTTTACG | 268445 |
rs211783465 | snp | G/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77487239 | GGTCACTCACCCCCA[G/T]GTTTGTCCCCTGAGA | 268445 |
rs211878546 | snp | A/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77478883 | AAAGAAATTGTTTTC[A/T]GACAACTGGCAACAG | 268445 |
rs212433099 | snp | C/G | | | upstream-variant-2KB, intron-variant | Ankrd13b, 2210008F06Rik | GRCm38.p3 | 11:77489746 | GCGGCGGGCGTCCTC[C/G]GGAGGCGGCGGCGGG | 268445 |
rs212784473 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77475341 | GAACAACCCAGCAGT[C/T]CCTGCCCCTTTGAGA | 268445 |
rs212820309 | in-del | -/GGGGGGTGGGGAGA | | | intron-variant | Ankrd13b | Mm_Celera | 11:77480365 | GTTATTGGGGGGGGG[-/GGGGGGTGGGGAGA]GGTTAAGACACCGCC | 268445 |
rs212964809 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77477397 | CACAGGGCCACAGTC[A/G]GCAGGTGGAAATCCG | 268445 |
rs213169445 | snp | A/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77484380 | GCTCACGAATGCCTG[A/T]AAGTCCAGCTCCAAG | 268445 |
rs213270753 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77476891 | CCCTAACGGAGATTT[A/G]AACAATCTGAGGCTG | 268445 |
rs213410556 | in-del | -/A | | | intron-variant | Ankrd13b | Mm_Celera | 11:77486671 | CAGAGGCAACCCCAG[-/A]AAAAAAACAAACAAA | 268445 |
rs213434492 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77482612 | AACACAGGGAAAGCA[A/G]AGAGGCGGCTCAGTG | 268445 |
rs213444316 | in-del | -/GGTACTG | | | intron-variant | Ankrd13b | Mm_Celera | 11:77484859 | AGACGGCCAGAAAAA[-/GGTACTG]GGTCCCTGGAACTGC | 268445 |
rs213446842 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77485233 | GACCTGCAAGGTGGA[C/T]GCCTTTCCCTATCCA | 268445 |
rs214110023 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77473933 | GGATTTGAGACCAGG[A/G]TTACATAGTGAGAAT | 268445 |
rs214155141 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77476922 | GGCATGGGGATGGCT[C/T]GCTCACGCTGTCTCT | 268445 |
rs214290693 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77479948 | GATGCGGTGGCTCAG[A/G]CCTGTAATCCCAACA | 268445 |
rs214405157 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77472965 | ACCGCATCCTCTCCA[A/G]GCGGCTGAGGAGAAA | 268445 |
rs214477889 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77475444 | AGTAGTTAAGAGCAC[C/T]GACTGCTCTTCCAGA | 268445 |
rs214523384 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77477549 | CTCCTGCAGCACTGG[G/T]GGGAGGGGAATGATA | 268445 |
rs214531784 | snp | A/C | | | intron-variant | Ankrd13b | Mm_Celera | 11:77486162 | GGAAGAGGGGTGGGG[A/C]GGGGGCTGACTGTCC | 268445 |
rs214608165 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77475934 | GATTAAGTGGGGTCT[A/G]TGGGGAAAGCTCAGT | 268445 |
rs214624414 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77480517 | ATGGCCCCAGAATCC[A/G]TTGACTAATATGTCT | 268445 |
rs214639681 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Git1, Ankrd13b, 2210008F06Rik | Mm_Celera | 11:77491562 | CTGTGTGAGCCAGGG[C/T]CCCTCCCAGGCAGTC | 268445 |
rs214853306 | snp | A/C | | | intron-variant | Ankrd13b | Mm_Celera | 11:77483016 | ATGATCCCTTGGATA[A/C]CCCAATATTATGATT | 268445 |
rs215043038 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ankrd13b, 2210008F06Rik | Mm_Celera | 11:77490134 | AGAACCGTGCGTTTC[A/G]GATGACCAGAGATGG | 268445 |
rs215238400 | snp | G/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77483997 | GCCCAGTGAGTACAC[G/T]CGGTGAGTAGTTGAA | 268445 |
rs215274143 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77484975 | TCTTCTGCAAGAGCA[A/G]CAAGTACTCTTAAGC | 268445 |
rs215472582 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77474084 | TCTTCTCTTTGGGAA[C/T]GTGTGTATGCTTTCC | 268445 |
rs215555237 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77484159 | ACCTGCACTCAAGGC[A/G]CATACCCACATGCAG | 268445 |
rs215567674 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77481685 | CTCCACCCAGGTAAG[A/G]TAGAGTTCTTCCTTG | 268445 |
rs215613610 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ankrd13b, 2210008F06Rik | Mm_Celera | 11:77488910 | GGCTCCGAAGCCAGG[A/G]CTGGCATCTGAAGCA | 268445 |
rs215840859 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77476023 | GGTACAAGTTTCTCT[A/G]CACCCATACAGCGTG | 268445 |
rs215856970 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ankrd13b, 2210008F06Rik | Mm_Celera | 11:77488080 | AGTGAACCCCTAGGC[C/T]GGCCCGGAGGCTTGC | 268445 |
rs216068450 | in-del | -/G | | | splice-acceptor-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77477546 | GCCTCCTGCAGCACT[-/G]GGTGGGAGGGGAATG | 268445 |
rs216179886 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77475147 | AATATGGTAAACTAT[C/T]CATCCACTTATTTAT | 268445 |
rs216199896 | snp | C/T | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Ankrd13b | Mm_Celera | 11:77476744 | CTTGGATACCAGAGG[C/T]ACTGGGTGGAAGGGA | 268445 |
rs216288304 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77479694 | GCGTTGCATATCAGA[C/T]ATCCTGCATATCAGA | 268445 |
rs216395683 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77480400 | CTGGCCTTGAACTCA[A/G]GAGGTAGCTAGGGCT | 268445 |
rs216454842 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Ankrd13b, Coro6 | GRCm38.p3 | 11:77470947 | CCTTGCCCAAACTAG[A/G]GGGCACCTTAGGCAC | 268445 |
rs216559687 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ankrd13b, 2210008F06Rik | Mm_Celera | 11:77489113 | TGTCGCGTCTAGATC[A/G]AGTGGGGTGGACTCT | 268445 |
rs216571438 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ankrd13b, 2210008F06Rik | Mm_Celera | 11:77488128 | TTATTAAACGGGATG[A/C]AATGCAGAGTCAAGT | 268445 |
rs216688998 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77479924 | CTTGGAAGACGGAAT[A/G]TGATGCAGGATGCGG | 268445 |
rs216729935 | snp | G/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77481777 | TTGTCCTATATGTCA[G/T]TGAGCTCTAGGCCCC | 268445 |
rs216790688 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77478988 | AGAGAGGGGGGGAGC[A/G]GCAGACTTTGTGGAA | 268445 |
rs216854349 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77482936 | ACTCATTTACCTCGC[C/T]CACCCTCCACCCTTC | 268445 |
rs216857793 | snp | A/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77474160 | TAGGAGTTACTTGTA[A/T]CCACTTGAGACAGGT | 268445 |
rs217090683 | snp | A/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77486221 | TTCTTCCATCCCAGA[A/T]CTCACTGATTTGCAT | 268445 |
rs217184632 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77486980 | GAAAGCTCTCTGTTC[A/G]GCCCTACTCAGCCAG | 268445 |
rs217406796 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77480865 | ACTCCTACACTCAAC[C/T]GTAAGTTTTCGTTTT | 268445 |
rs217437501 | snp | G/T | | | intron-variant, missense | Ankrd13b | Mm_Celera | 11:77472663 | GCTCGCCCCTTAGTG[G/T]CTGGGGGGGAAATGG | 268445 |
rs217685296 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77477837 | CCTGACATGGACCTA[G/T]GCTGGCCATGGACCT | 268445 |
rs217732594 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Ankrd13b | GRCm38.p3 | 11:77471081 | ACTGGGGGGGCTGGG[C/T]ACCCCGCTAAGTGCA | 268445 |
rs217913671 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | Ankrd13b | GRCm38.p3 | 11:77477056 | ACAAGGTAAGTCCCC[C/G/T]GCCTGTTGGACTTTA | 268445 |
rs218208705 | snp | C/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77478358 | CCCTCTTTCAACACT[C/G]GTAGTGCTGAAGGAG | 268445 |
rs218283000 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77479338 | TCTGTGACCCTCCCG[A/G]GTAGGGATAAACCGT | 268445 |
rs218566325 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77482381 | CCTTGAAAAATAAAA[A/G]CCTGTATGTCCTCTC | 268445 |
rs218639562 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77483266 | TGCCCCATCCCACCC[C/T]GGGGTTCCTTCTGTG | 268445 |
rs218820005 | in-del | -/A | | | intron-variant | Ankrd13b | Mm_Celera | 11:77478977 | GGTTGCTACTCAGAG[-/A]GGGGGGGAGCGGCAG | 268445 |
rs219107980 | snp | C/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77476055 | CTGAACAGAGCCTTG[C/G]ATGTGACTACCCTAA | 268445 |
rs219117739 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77475581 | TACATAAAATAAATA[A/G]TTTTTTTTTAAAGTG | 268445 |
rs219274321 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77475697 | GTGTCAGCTCCTTCA[C/T]CCATCATGTGCTGGG | 268445 |
rs219450398 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ankrd13b | Mm_Celera | 11:77478134 | TTGCATGCCTATGGC[A/G]AAACCCTCCTAGTGG | 268445 |
rs220102848 | snp | A/G | | | intron-variant | Ankrd13b | Mm_Celera | 11:77474328 | GCAATACAGACATTA[A/G]TAATCAATTCCGGAG | 268445 |
rs220160042 | snp | C/G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Ankrd13b | GRCm38.p3 | 11:77471421 | GCAGGGAGACCAGCA[C/G/T]CCCTCTAGGGCTCTG | 268445 |
rs220258097 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ankrd13b, 2210008F06Rik | Mm_Celera | 11:77487642 | GTCTAAACAGCCCTG[A/G]CTACCATGACCTCAG | 268445 |
rs220341820 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77473709 | TGCCTGGGGTAGGAG[C/T]GTGGGTAGCTCCTGC | 268445 |
rs220345905 | snp | C/T | | | intron-variant | Ankrd13b | Mm_Celera | 11:77486266 | GAGGTTTGTGGCTCT[C/T]GCTGCTGACCTTCCT | 268445 |