SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3677910 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Btk | GRCm38.p3 | X:134566098 | CTTTTATTCATTTTT[G/T]GGGGGCTTGAATAAG | 12229 |
rs6370789 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Btk | Mm_Celera | X:134566322 | ATAAAATATAAAAAA[A/T]TTGGTTTTAAAGTCA | 12229 |
rs8251039 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Btk | Mm_Celera | X:134574192 | ACACAAATATACAAC[A/G]CTAGCAGGGAATCTT | 12229 |
rs8251040 | in-del | -/C | 0.21875 | 0.248039 | intron-variant | Btk | Mm_Celera | X:134574245 | TCTTCCACAGTCCCC[-/C]NATCTTGGTCAAATT | 12229 |
rs8251041 | in-del | -/C | 0.21875 | 0.248039 | intron-variant | Btk | Mm_Celera | X:134574246 | CTTCCACAGTCCCCN[-/C]ATCTTGGTCAAATTT | 12229 |
rs8251042 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134574283 | CAGTGAACGCATACt[A/T]ttttttttaaaaaag | 12229 |
rs8251052 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134574377 | ngatccctttacaga[G/T]ggntgtgagncncca | 12229 |
rs8251053 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Btk | Mm_Celera | X:134574380 | tccctttacagangg[C/T]tgtgagncnccatgt | 12229 |
rs8251054 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Btk | Mm_Celera | X:134574387 | ACAGATGGCTGTGAG[C/T]CACCATGTGGTTGCT | 12229 |
rs8251055 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Btk | Mm_Celera | X:134574389 | aganggntgtgagnc[A/G]ccatgtggttgctgg | 12229 |
rs8251056 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134574414 | tgctgggaattgaac[G/T]nnggacctntggaag | 12229 |
rs8251057 | in-del | -/C | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134574415 | gctgggaattgaacn[-/C]nggacctntggaaga | 12229 |
rs8251058 | in-del | -/A | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134574416 | ctgggaattgaacnn[-/A]ggacctntggaagag | 12229 |
rs8251059 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134574423 | ttgaacnnnggacct[C/G]tggaagagcagtcag | 12229 |
rs8251060 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134574458 | cttaaccactgagcc[A/T]tctctccagcccAAA | 12229 |
rs8251061 | in-del | -/T | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134574485 | cAAACTCATACTATT[-/T]AACCAGGGGATTGAT | 12229 |
rs8251062 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Btk | GRCm38.p3 | X:134558789 | GCCCCCACCTAAAGT[G/T]CATTTTACACTACCA | 12229 |
rs8251063 | in-del | -/A | 0.244898 | 0.249948 | frameshift-variant | Btk | Mm_Celera | X:134558750 | TTGTTTTACAGGCTT[-/A]AAACCTGGGAGTTCT | 12229 |
rs8251064 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Btk | GRCm38.p3 | X:134558729 | TGGGAGTTCTCATCG[A/G]AAAACGAAAAAGCCT | 12229 |
rs8251065 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Btk | GRCm38.p3 | X:134558605 | CACACCTTTAGTCCC[A/G]GCATTTGGCAGAGGA | 12229 |
rs8251066 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Btk | GRCm38.p3 | X:134558546 | AGAGGCAGAGGGAGA[A/G]GCAGAGGCAGGTGGA | 12229 |
rs8251067 | in-del | -/A | 0.408163 | 0.193609 | intron-variant | Btk | Mm_Celera | X:134552523 | cagtatgtgctctta[-/A]ccactgagccacttc | 12229 |
rs8251068 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Btk | Mm_Celera | X:134552485 | GAGGACTAACTTCTT[A/T]CTTGGTGCTAAGTGA | 12229 |
rs8251069 | snp | A/G | 0.393491 | 0.20472 | intron-variant | Btk | GRCm38.p3 | X:134552435 | CTAATGAGTCAGAGC[A/G]TGTTCACTAGCAACT | 12229 |
rs8251070 | in-del | -/C | 0.197531 | 0.244432 | intron-variant | Btk | Mm_Celera | X:134552379 | AACTATTCAGTGTTC[-/C]TACCACGTACCCTTG | 12229 |
rs8251071 | in-del | -/G | 0.197531 | 0.244432 | intron-variant | Btk | Mm_Celera | X:134552356 | TACCCTTGCAATTCA[-/G]NNNNNCTNNNNNNNN | 12229 |
rs8251072 | in-del | -/G | 0.70321 | 0.0938324 | intron-variant | Btk | Mm_Celera | X:134552357 | CCCTTGCAATTCANN[-/G]NNNCTNNNNNNNNNN | 12229 |
rs8251077 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Btk | GRCm38.p3 | X:134552245 | ATTGAACCTGTTCCT[A/G]NACCTTCACCAGCAG | 12229 |
rs8251078 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Btk | Mm_Celera | X:134552245 | TTGAACCTGTTCCTN[C/T]ACCTTCACCAGCAGC | 12229 |
rs8251079 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Btk | GRCm38.p3 | X:134552223 | ACCAGCAGCTGGGGC[A/G]TCTCCACCCCTTGTG | 12229 |
rs8251080 | snp | C/G | 0.4608 | 0.1344 | intron-variant | Btk | Mm_Celera | X:134546838 | AACAAGTCTTGAATC[C/G]CTTGCAGGTATGTCC | 12229 |
rs8251081 | in-del | -/T | 0.21875 | 0.248039 | intron-variant | Btk | GRCm38.p3 | X:134544052 | CACAGAAAGTGTATT[-/T]GGGACCTGGCCTTTA | 12229 |
rs8251082 | snp | C/T | 0.32 | 0.24 | intron-variant | Btk | GRCm38.p3 | X:134543979 | TTTCAATTGAAGCTC[C/T]GTTATTTCGAAGAGT | 12229 |
rs8251086 | snp | A/G | 0.42 | 0.183303 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543531 | gcggtggtggtgcac[A/G]cctttaatcccagca | 12229 |
rs8251087 | snp | C/T | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543547 | cctttaatcccagca[C/T]ttgggaggcagangc | 12229 |
rs8251088 | snp | A/G | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543560 | canttgggaggcaga[A/G]gcaggcngatttctg | 12229 |
rs8251089 | snp | A/G | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543567 | gaggcagangcaggc[A/G]gatttctgagttnga | 12229 |
rs8251090 | snp | C/G | 0.42 | 0.183303 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543580 | gcngatttctgagtt[C/G]gaggccagcctggtc | 12229 |
rs8251091 | snp | A/G | 0.42 | 0.183303 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543600 | ccagcctggtctaca[A/G]agtgantnccagnan | 12229 |
rs8251092 | snp | A/G | 0.46281 | 0.131194 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543606 | tggtctacanagtga[A/G]tnccagnanagccag | 12229 |
rs8251093 | snp | G/T | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543608 | gtctacanagtgant[G/T]ccagnanagccaggg | 12229 |
rs8251094 | snp | A/G | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543613 | canagtgantnccag[A/G]anagccagggntnna | 12229 |
rs8251095 | snp | C/T | 0.42 | 0.183303 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543615 | nagtgantnccagna[C/T]agccagggntnnaca | 12229 |
rs8251096 | snp | C/G | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543624 | ccagnanagccaggg[C/G]tnnacagngaaaccc | 12229 |
rs8251097 | snp | A/G | 0.42 | 0.183303 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543626 | agnanagccagggnt[A/G]nacagngaaaccctg | 12229 |
rs8251099 | snp | A/G | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543632 | gccagggntnnacag[A/G]gaaaccctgtntcna | 12229 |
rs8251100 | snp | A/C | 0.46281 | 0.131194 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543643 | acagngaaaccctgt[A/C]tcnaaaanaaanaaa | 12229 |
rs8251101 | snp | A/G | 0.46281 | 0.131194 | intron-variant, upstream-variant-2KB | Btk, Timm8a1 | Mm_Celera | X:134543646 | gngaaaccctgtntc[A/G]aaaanaaanaaaCAA | 12229 |
rs29266644 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134556776 | GACTTAGGAGGGGCT[G/T]CGGGAACTCACCCAT | 12229 |
rs29266645 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134556745 | ATTTTGTGTGCAGGT[A/G]GAGCGGGCAGGCAAA | 12229 |
rs29266646 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134556693 | TGAGGAGAACAAACT[C/T]TGATCCAAACACGGG | 12229 |
rs29266647 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134556018 | GGATTTGCGGGTGGG[G/T]ATCCCAGCAAGATAG | 12229 |
rs29266648 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134555923 | TGTTTTCAGATGTTT[C/T]CTCTGAGAGTCTCAG | 12229 |
rs29266649 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134555887 | AGAAGAAAGGACACT[C/G]GTTCAGTTTTGGCGT | 12229 |
rs29266650 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Btk | Mm_Celera | X:134555470 | AGCTCAAACTGGGAG[C/T]GCAGTTTAAAGTTGG | 12229 |
rs29266651 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134555392 | AGAGAAAATAGAATA[C/G]CCCTGACTTTCTGCT | 12229 |
rs29266652 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Btk | Mm_Celera | X:134554269 | ATCTTGACTCGAACC[C/T]TGTTCAGCGTCACAG | 12229 |
rs29266653 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Btk | Mm_Celera | X:134554223 | GAAAAAGAAAATAAA[A/T]AAATAAGTCAATGTG | 12229 |
rs29266985 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134552186 | GCTGGTTTCAAAGCA[A/C]AGAGCCCATTTACAC | 12229 |
rs29266986 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Btk | Mm_Celera | X:134551894 | GTGCCCAAGGATGAC[A/C]AGAAGAAGAAAGATG | 12229 |
rs29266987 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Btk | Mm_Celera | X:134551373 | GTATGAACCTTTCTA[A/G]TTCATTTTGAATTCC | 12229 |
rs29266988 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Btk | Mm_Celera | X:134551313 | GTCAGCATCGGGGCT[A/G]GGATTCCTTGCACAT | 12229 |
rs29266989 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Btk | Mm_Celera | X:134551230 | TGCAGTAGAAGGCGC[A/G]TTTTTGTTTTGTTTA | 12229 |
rs29266990 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Btk | Mm_Celera | X:134551054 | CCACTAGAGGGAGAC[A/G]TTTTCTAAATATCTT | 12229 |
rs29266991 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134550740 | TCCAAAATTCATTTA[A/C]GACTAGGTTAATAAT | 12229 |
rs29266992 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btk | Mm_Celera | X:134549906 | AATATTGTACATGTC[A/G]CTCAAAATGCTACTG | 12229 |
rs29266993 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134549789 | AAGTGCCTCAAATGT[G/T]GGGGTGCGCAGGGCT | 12229 |
rs29267374 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Btk | Mm_Celera | X:134549439 | GTGAAGGAACTGCTT[C/T]GACTCCAAGTATTCC | 12229 |
rs29267375 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Btk | Mm_Celera | X:134549353 | CTCAGCGGTGGACGC[A/T]CTATCTCCCAGCGTT | 12229 |
rs29267376 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134549268 | ATGATGGGTTCAACT[C/G]TGGGGTAGATGCACA | 12229 |
rs29267377 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134549124 | CCAAATAGTGGCTTC[A/G]TATCAGAAGTCCCAC | 12229 |
rs29267378 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btk | Mm_Celera | X:134547704 | CATCAGCATGGAGTT[A/G]CATATGCACATGTAT | 12229 |
rs29269233 | snp | C/T | 0.497041 | 0.0383476 | intron-variant, upstream-variant-2KB | Btk | Mm_Celera | X:134582546 | TTTCCTCAGCACTGC[C/T]GTTGGGTACACAGGA | 12229 |
rs29269584 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Btk | Mm_Celera | X:134581637 | AAGGAACAGAGCTAA[A/G]GCATATACCTACCTA | 12229 |
rs29269585 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134580642 | TTCCAGGTTTATAAC[G/T]TTCTAAGACGATGCT | 12229 |
rs29269586 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Btk | Mm_Celera | X:134580609 | TGGGCAGTGGGGAAG[A/G]ATGCCCGTGTTTAGA | 12229 |
rs29269587 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Btk | Mm_Celera | X:134580391 | TCATTTTTTTTTAAA[A/C]TCTGGCTTTATTCTA | 12229 |
rs29269588 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134579467 | ATATATCCATTCATC[A/C]ATCCATGCACCATAC | 12229 |
rs29269589 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134578574 | CCTTGTCCACCTTCA[C/T]CCATCTCTAGCTCCT | 12229 |
rs29269590 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134578371 | GTGTCGTCTACCTGT[C/G]AGGCACTTTATATTA | 12229 |
rs29269591 | snp | A/C/T | 0.497778 | 0.0332592 | intron-variant | Btk | GRCm38.p3 | X:134578134 | TAGAAACCACACTGG[A/C/T]GCAATATGCAGTAAA | 12229 |
rs29269592 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134577896 | ATATAGTGTTGTCAC[A/G]TTATTACAATCCAAA | 12229 |
rs29269593 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134577405 | CATGGCCCTCTGAGC[A/G]AGAAGTGAGATGGTC | 12229 |
rs29269884 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134577371 | TTCAGTGCTGGTCTA[A/C]ATATGAGGAAGTAGC | 12229 |
rs29269885 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134577019 | CAATTATGCTGAGTG[C/G]TCTAAGTGGACACAT | 12229 |
rs29269886 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134576637 | GTAGCATGGCAAACC[C/T]TATACTCGTCTTATT | 12229 |
rs29269887 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Btk | Mm_Celera | X:134575872 | TATAATCAGAGGCTC[A/G]TTCCCTGCAAGGAGT | 12229 |
rs29269888 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Btk | Mm_Celera | X:134575787 | CTAGAAACATATGTG[A/G]AAAGATGATAGTCAT | 12229 |
rs29269889 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134575547 | TTTCTGTGGTGCTGA[A/G]GATTGATGCCCCAGC | 12229 |
rs29269890 | snp | A/C/G | 0.142012 | 0.225474 | intron-variant | Btk | GRCm38.p3 | X:134575505 | GCTTAGAATACTCCA[A/C/G]AACATTCCACAAAAC | 12229 |
rs29269891 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Btk | Mm_Celera | X:134575447 | AGTGACATAACTATG[A/T]TGCTGTTAAGGATGC | 12229 |
rs29269892 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Btk | Mm_Celera | X:134575399 | GCAAAACACTCATAA[C/T]CATACACTAAAATAA | 12229 |
rs29269893 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134574935 | AGCTTTCCTACAGTA[A/G]TTTAGCACTTTGGCC | 12229 |
rs29270164 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134574870 | TGATTTAGCCCATTG[C/T]CAGCTAACCAGGGTA | 12229 |
rs29270165 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134574475 | CTCTCCAGCCCAAAC[G/T]CATACTATTTAACCA | 12229 |
rs29270166 | snp | A/G | 0.277778 | 0.248452 | utr-variant-5-prime | Btk | Mm_Celera | X:134574087 | GGAACTTGTTTGTGT[A/G]CTGTGGATAAGGAAA | 12229 |
rs29270167 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Btk | Mm_Celera | X:134573964 | GTTTGTGTACAGTCA[A/G]GAGAAACAGGCGCTT | 12229 |
rs29270168 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134573691 | TTCTCAAGAAGCATA[G/T]AGTGAGTTCTTACTA | 12229 |
rs29270169 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Btk | Mm_Celera | X:134573420 | GTACTGGCAGCCTAA[A/C]AGAACCTGGTTTTTT | 12229 |
rs29270170 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Btk | Mm_Celera | X:134573350 | GAGAAAGGTTACGAG[C/T]GATCGAGCCACCAGA | 12229 |