SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3663313 | snp | C/G | 0.492188 | 0.0620098 | intron-variant | Herc2 | GRCm38.p3 | 7:56132741 | GTTGCCTGTGAACTA[C/G]ACTGTATTACTTGTA | 15204 |
rs3666280 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Herc2 | GRCm38.p3 | 7:56133240 | CCTGATCCTGCATCT[C/T]ACATGCTACAGTACA | 15204 |
rs3671005 | snp | C/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56143439 | AGAAGAATGTATATT[C/T]TTCTGTGTTTGGGTA | 15204 |
rs3681702 | snp | C/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56052720 | GTTGTCAGGTTTTGT[C/T]GGCAATGACTTACCT | 15204 |
rs3682975 | snp | G/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56052909 | GTGATACTGGTATTT[G/T]GCCCTTTTTAGATAT | 15204 |
rs3691306 | snp | G/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56127016 | ATTTATGCTGCCCAT[G/T]ATAGATGCACTAAAA | 15204 |
rs3714163 | snp | A/T | 0.495 | 0.0497494 | intron-variant | Herc2 | Mm_Celera | 7:56137887 | GTGAGCTAAACAAAA[A/T]GTGATAATTAGAAGG | 15204 |
rs6216458 | snp | G/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56145542 | acacttaaccactgt[G/T]gtgaagatctgagtt | 15204 |
rs6216914 | snp | C/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56145578 | agttttcagcaccca[C/T]atttggtggcttaca | 15204 |
rs6217008 | snp | C/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56145632 | GACATCAGAGGCCGT[C/T]TTTCAGGCTCATGTT | 15204 |
rs6217446 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56145689 | acaTTTAGACATAGA[A/G]TTTACACATAAGTAG | 15204 |
rs6217487 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56145710 | ACATAAGTAGTGACA[C/T]aattttaaaaaaata | 15204 |
rs6218021 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Herc2 | Mm_Celera | 7:56145801 | GGACGACATGAATGC[A/G]TCTGCCCGGGGAGCC | 15204 |
rs6218560 | snp | A/G | 0.42 | 0.183303 | synonymous-codon | Herc2 | Mm_Celera | 7:56145879 | GCTCCCTGTTTCAGG[A/G]CCAGAACTGGCTGCT | 15204 |
rs6218623 | snp | C/T | 0.408163 | 0.193609 | synonymous-codon | Herc2 | Mm_Celera | 7:56145912 | GATGAAGATTGGAAC[C/T]AGGGTCATGAGAGGG | 15204 |
rs6219128 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Herc2 | GRCm38.p3 | 7:56145990 | CTTAGCACATCTTAC[A/G]TATCAGTGGAAGATA | 15204 |
rs6252440 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | GRCm38.p3 | 7:56049389 | gacccttgggagtga[A/G]tttgaagatacatac | 15204 |
rs6252479 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | GRCm38.p3 | 7:56049425 | atgacaaaagacagg[C/T]attttaacgttgcaa | 15204 |
rs6253472 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | GRCm38.p3 | 7:56049599 | AAAgtttaatttcca[A/C]atgcttgaagattnt | 15204 |
rs6253491 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | GRCm38.p3 | 7:56049613 | anatgcttgaagatt[A/G]tgttatgttttattt | 15204 |
rs6254034 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | GRCm38.p3 | 7:56049705 | TTTCTTACTCCCGCA[C/T]CCCCATNCCCCCAGg | 15204 |
rs6254045 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | GRCm38.p3 | 7:56049712 | CTCCCGCANCCCCAT[C/T]CCCCCAGggtctctt | 15204 |
rs6254095 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | GRCm38.p3 | 7:56049738 | ctcttaacccagaat[C/T]cacctgcttctgcct | 15204 |
rs6254545 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, nc-transcript-variant | Herc2, Gm34121 | GRCm38.p3 | 7:56049794 | tactaccaggcccgg[A/C]TCAATTACTTTTTCT | 15204 |
rs6254602 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, nc-transcript-variant | Herc2, Gm34121 | Mm_Celera | 7:56049825 | TAAATTTCCTCTTCT[A/G]TCCACTGACTCAAAG | 15204 |
rs6255098 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, nc-transcript-variant | Herc2, Gm34121 | Mm_Celera | 7:56049874 | TTAAAGCACAGGGAG[A/C]CTCGAGAACNTCGTC | 15204 |
rs6255113 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, nc-transcript-variant | Herc2, Gm34121 | Mm_Celera | 7:56049884 | GGGAGNCTCGAGAAC[C/T]TCGTCCCGCTGCAAA | 15204 |
rs6270685 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56128373 | tctctggagtgtaca[A/G]ccacacattggatat | 15204 |
rs6270757 | snp | G/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56128414 | ccctacccactccag[G/T]gcttatggaccatca | 15204 |
rs6270791 | snp | G/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56128434 | atggaccatcatgga[G/T]agggtgtagacatat | 15204 |
rs6284320 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56128647 | AGCTAGGGAGAGTCA[A/G]TGGTGtcacttttct | 15204 |
rs6284710 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56128675 | TCTTTGTGGGTGTGG[C/T]TCCTGGACTCAAGTA | 15204 |
rs6305806 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56097112 | tgtacatgagtagct[A/G]cagctgtcttcagac | 15204 |
rs6306262 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56097186 | accatgtggttgctg[A/G]gaantgaactcagga | 15204 |
rs6306282 | snp | C/G | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56097190 | tgtggttgctgngaa[C/G]tgaactcaggatgtc | 15204 |
rs6341883 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Herc2 | Mm_Celera | 7:56099180 | ATGGAACCATTTTAT[A/G]TTGTGTTGTTTTAAG | 15204 |
rs6341971 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Herc2 | Mm_Celera | 7:56099226 | AGACTTGGCAGTAGG[A/T]GGGTGTGCTATTCCC | 15204 |
rs6369437 | snp | G/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56172509 | tttattatttaccag[G/T]tgctgcatttaggtt | 15204 |
rs6369481 | snp | A/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56172533 | ttaggtttagtttgt[A/T]tttatttttattttt | 15204 |
rs6370480 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56172680 | acagtctgcagccca[A/G]ttcccaacaatggtt | 15204 |
rs6370630 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Herc2 | Mm_Celera | 7:56172764 | tacTAGAGGCTTATC[C/T]TGTCTGATACATTGT | 15204 |
rs6371055 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Herc2 | Mm_Celera | 7:56172812 | TTGGCATTTTTCTCC[A/C]TCATTTCTTCAGTGA | 15204 |
rs6371074 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | GRCm38.p3 | 7:56172828 | TCATTTCTTCAGTGA[A/G]TCAATCAAACTAATT | 15204 |
rs6371108 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Herc2 | Mm_Celera | 7:56172847 | ATCAAACTAATTGTT[A/T]AATCATCAAGTATTT | 15204 |
rs6371628 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56172944 | TCAGGGATTATTtct[A/G]tatctttgtttctgt | 15204 |
rs6372060 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Herc2 | Mm_Celera | 7:56172997 | CTTGATTGCTTTGTG[C/G]CCTGTAACATGATCA | 15204 |
rs6372134 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Herc2 | Mm_Celera | 7:56173052 | ctatagatacctatt[A/G]agtccatttgatcta | 15204 |
rs31009431 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56222081 | GCAACCAGGGATTCA[G/T]AGTCGGAAAATGCTC | 15204 |
rs31011246 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Herc2 | Mm_Celera | 7:56231235 | AGAATACCACTCCTT[A/G]AAATGTGTGGAAGAG | 15204 |
rs31018590 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56130782 | ATCTGGGTTTTAGGC[C/G]AGCCAAGGCTATATA | 15204 |
rs31040538 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Herc2 | Mm_Celera | 7:56090701 | AATCCTACACACTGA[A/G]GGAAGCACCCCCCAA | 15204 |
rs31040960 | snp | A/C | 0.429688 | 0.173817 | intron-variant | Herc2 | Mm_Celera | 7:56132185 | AATTTAGAATCTTTC[A/C]CCCAGGGTTCTCCTC | 15204 |
rs31042396 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56114095 | TTAAGTTCGTCAGGG[A/G]GAAAGTGGGTGCTAA | 15204 |
rs31042399 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56158076 | CAGTTACCTTGGAAG[C/G]TGAAAGCAGGAAGAT | 15204 |
rs31047956 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56195499 | AGTCTTGTTTTATTT[A/G]AAATGATTTCTTTAA | 15204 |
rs31048166 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Herc2 | Mm_Celera | 7:56159799 | TCAGTTATTGGGTAC[C/G]TACTCATCTTGCTTG | 15204 |
rs31048758 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56170541 | CTTACTTTTAGTAAC[A/G]ATTATTTGATTTCTT | 15204 |
rs31052877 | snp | G/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56186877 | AGTCATGGAGGGTGG[G/T]TCATAGGACTACATA | 15204 |
rs31053275 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56136287 | AAACAGAAGCAGTGG[A/G]AGAGTGCTGATTGCT | 15204 |
rs31056130 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56141293 | AGATTAAGCTGCACA[A/G]CTGTAACATATGTGT | 15204 |
rs31056488 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56195461 | CTACTCTTAAATTCT[A/T]ATATGCATTTGGATT | 15204 |
rs31056822 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Herc2 | GRCm38.p3 | 7:56147164 | GATTGATTGATTGAA[A/C]GTTGAAATACAGAGA | 15204 |
rs31058101 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Herc2 | GRCm38.p3 | 7:56069128 | CGACTGCATATATGG[G/T]CTGGCCGACTGCATA | 15204 |
rs31059180 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56108064 | TGACTTCAGTGTTTT[C/T]CCTGATTACAGGTTT | 15204 |
rs31060442 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56122211 | AGAGCCAAAGGCTGA[G/T]GGTAAATTGTTCTTT | 15204 |
rs31063374 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56149352 | CCTCACTGAGCTCTA[C/T]AGGAAGGTCCCCTTT | 15204 |
rs31064930 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56061042 | TCTTCCTTTCTGGAT[A/G]GAAAGTTTGAGTTCT | 15204 |
rs31086909 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56189060 | AACATGCACAAAATG[A/G]GAACTAATGAAGGTA | 15204 |
rs31097086 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Herc2 | Mm_Celera | 7:56147531 | TTTGGAAGTGGATCC[A/G]AGCTATAGAGTGTGC | 15204 |
rs31100194 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56092203 | AGTCATCTAAGAGCT[C/T]TTCTTTTAACATGTT | 15204 |
rs31133992 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56058530 | GCTTATAGAAGATAG[A/G]GGTTCCAGGACAGCC | 15204 |
rs31134213 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Herc2 | Mm_Celera | 7:56063636 | ATCAATAATATTTCC[A/G]TGATGTCTATAGGAC | 15204 |
rs31135402 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Herc2 | GRCm38.p3 | 7:56068502 | GAGTGAATAGCTTTT[A/G]GTTTAAACTGAAACA | 15204 |
rs31137392 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56182299 | CTGTGGCTAAGGTAA[A/T]TAGAAACTAACAGCT | 15204 |
rs31143061 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56167821 | TGCATGCCTGATACC[C/T]GTGGAAGCCAGAAAA | 15204 |
rs31146126 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56193376 | TCCTTGCAAGGCTCC[C/T]GGTGTGGACCAGACA | 15204 |
rs31160201 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56122517 | TTTTTTTTTTTTAAT[C/T]TTTCTTTTACTTTGA | 15204 |
rs31160626 | snp | A/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | Mm_Celera | 7:56048408 | CAAACCAGCGAGTTT[A/T]GAGAGAGAGAACTAC | 15204 |
rs31163338 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Herc2 | Mm_Celera | 7:56219094 | AAGAGATACCTAGTG[A/G]CTGAATGATCTCCCT | 15204 |
rs31180182 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Herc2 | Mm_Celera | 7:56158159 | CTGGTTAAAATACAA[A/G]TAAACATTCTGGGCC | 15204 |
rs31182047 | snp | C/T | 0.487535 | 0.077957 | synonymous-codon | Herc2 | GRCm38.p3 | 7:56153423 | TAACTCCCAGCTTTG[C/T]TCTGTCACACAAAGC | 15204 |
rs31182052 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Herc2 | GRCm38.p3 | 7:56205865 | ATTTTTTGCTGACTG[C/T]AGGTGCTAGTAGCTC | 15204 |
rs31186208 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56210405 | AGGGATGGCTCAGCC[G/T]TTAAAATCACTGGCT | 15204 |
rs31192953 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56213264 | GATTTACATTTTCAT[A/T]TAAATATAAATTTAT | 15204 |
rs31217635 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56190918 | AAGTCATAGTTTAAT[A/G]TATATAATCCATTGT | 15204 |
rs31228772 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Herc2 | Mm_Celera | 7:56188418 | AACTGTATGTACTCA[A/T]GTTCTCTGGATACAT | 15204 |
rs31229024 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Herc2 | Mm_Celera | 7:56159896 | AATGCTTTTGGATTT[A/T]TCAGCTCAGGTTTTC | 15204 |
rs31230505 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56222079 | GGGCAACCAGGGATT[C/G]ATAGTCGGAAAATGC | 15204 |
rs31231358 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Herc2 | Mm_Celera | 7:56206054 | GTGTGTGTTAATTAA[C/T]TAATTTTTGGAATTC | 15204 |
rs31231830 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56138643 | ATAGATCTGCCCTAA[C/T]CACATTATGTGGAAA | 15204 |
rs31232190 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56116346 | CATACACACACACAC[C/T]CCAATAGATTTTTCC | 15204 |
rs31233452 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56182746 | ACATCGTGAGCAGTT[C/T]CTCATAAGCTTTTGC | 15204 |
rs31234093 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56171438 | TTCTATTATGATTTT[A/G]TATACTATGTCTTTA | 15204 |
rs31235454 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56220106 | ATAGAATGCTTACTT[A/G]CTTGGCATGCACAAA | 15204 |
rs31239156 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56225358 | TGCTCTCCTCTGGGA[C/G]CACGAATCCTTTCAA | 15204 |
rs31240501 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Herc2 | Mm_Celera | 7:56223399 | TCCAGTTTAATAACC[C/T]AGTATTGCTAACATT | 15204 |
rs31240749 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Herc2 | Mm_Celera | 7:56157090 | TGAAGCAGTCAGCAG[C/T]GTTATTTGACTATCA | 15204 |
rs31246933 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56228018 | AGAGCAGAGAAAAGT[A/G]TGCATCTGAGAGAGT | 15204 |
rs31247625 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Herc2 | GRCm38.p3 | 7:56148445 | ACTGAGTTCAGGTAG[C/T]CACCTATTCTAAGTT | 15204 |
rs31249357 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Herc2 | Mm_Celera | 7:56109783 | TTTCTCCCTTCAGGG[C/T]ATGTGAGATTAAAGT | 15204 |
rs31259016 | snp | C/T | 0.432133 | 0.171253 | synonymous-codon | Herc2 | Mm_Celera | 7:56131827 | GGAAGATCCAGTGGT[C/T]GCTCTGGAGGCAGCT | 15204 |
rs31264725 | snp | G/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56147591 | TCAGCTATATCTGGG[G/T]TATTCCTCATTGTAG | 15204 |
rs31269202 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56226077 | CCTAGGGTGGAGTTG[C/T]CTAAATAGCTTTGTT | 15204 |
rs31269992 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56205521 | ATGGGAGGTGTTGTG[C/T]CATAGACCTATTTGG | 15204 |
rs31275489 | snp | A/T | 0.487535 | 0.077957 | intron-variant | Herc2 | GRCm38.p3 | 7:56146761 | GTCTTGGAGTTCAAG[A/T]GAGCAGGGCAAATTG | 15204 |
rs31277618 | snp | A/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56107948 | ACTTCCCTTTGAGAT[A/T]GATCCCAATTTGGGC | 15204 |
rs31283804 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Herc2 | Mm_Celera | 7:56181690 | AGTTCCAAGGAAAAG[C/T]CGTATGACAGCTCCC | 15204 |
rs31284598 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Herc2 | Mm_Celera | 7:56224922 | ATGGTGCTGTTTGGT[A/G]TGTGGAAAATCTGAA | 15204 |
rs31288269 | snp | C/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56052781 | GCTTCAAGATTTGCT[C/G]TTTGGAGTTAACATA | 15204 |
rs31292651 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56109935 | CTCTACCAGGAGCCA[C/T]AGACATTTATTTAAT | 15204 |
rs31294211 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56195853 | AGGGAAATAGAGGAG[A/G]ATAATCCTGGAAAAC | 15204 |
rs31296271 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56068766 | CTGTTTTAGAACTTA[C/T]TCTGTACACCAGGCT | 15204 |
rs31302073 | snp | G/T | 0.387812 | 0.208586 | utr-variant-3-prime | Herc2 | Mm_Celera | 7:56231208 | ATTGTAAATGTCGAG[G/T]GCACTTGATGAAGAA | 15204 |
rs31305625 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56139698 | TAAAAGGAGTAGAAT[A/G]CTGAGGTCATGTGGT | 15204 |
rs31308783 | snp | A/C | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56165968 | AATCAGTAATTAAGA[A/C]AATGCACCATGAACT | 15204 |
rs31314561 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56136573 | ATAAATGATTTTTAT[A/G]TTTTTAATTATAGTT | 15204 |
rs31322717 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56086728 | AATAGTTAAGAAAAG[A/G]GGCTGTTATTTTGAG | 15204 |
rs31323594 | snp | G/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56065459 | GAGATGGCTCAGCAG[G/T]TAAAAGCACTTACTA | 15204 |
rs31327239 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Herc2 | GRCm38.p3 | 7:56154023 | GTATATAGCTTGTGC[A/T]TAGTATTAGGGGTGA | 15204 |
rs31339545 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56114397 | GATTCCCAGGACTCA[C/T]GTGCTGGCTTACAAT | 15204 |
rs31340527 | snp | A/G | 0.387812 | 0.208586 | synonymous-codon | Herc2 | Mm_Celera | 7:56177923 | CCGCATCCGTGCTGA[A/G]GAGGAGGACCTGGCT | 15204 |
rs31341694 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56085926 | GAACCTTGAAGAACT[A/G]TAGTCTCCCTGGAAA | 15204 |
rs31344054 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56205087 | TGGATTTGTACGCCA[A/G]AGAGGGAAGTTCCCT | 15204 |
rs31344299 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Herc2 | GRCm38.p3 | 7:56205035 | TGTTATAATGAGAAC[A/G]TTCCATTCCAGTTTT | 15204 |
rs31345139 | snp | A/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56060876 | CATGAAAACTAACCC[A/T]GGAGCTCTGTGGATG | 15204 |
rs31353200 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Herc2 | Mm_Celera | 7:56179965 | ACTATGAGACTTTTA[G/T]CAAGTTGAGAACTAA | 15204 |
rs31358875 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Herc2 | Mm_Celera | 7:56087219 | AAAAATGACACTAAA[A/G]CCCACAAAGGACCCT | 15204 |
rs31364344 | snp | A/C | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56200292 | AGAGTCAGGTAGATT[A/C]TGTGAATTTGAGGCC | 15204 |
rs31370355 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56205510 | TGAGAGCTGTTATGG[G/T]AGGTGTTGTGCCATA | 15204 |
rs31374816 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Herc2 | Mm_Celera | 7:56159865 | GCCCGCATGATGGTG[A/G]TTTTCTGACTTACTC | 15204 |
rs31376033 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56141364 | GCTGTTCAGTCTCTC[C/T]GAGCCACTGTGGGCT | 15204 |
rs31386215 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Herc2 | Mm_Celera | 7:56121668 | GTTGCTGCGCTTTCA[A/G]CGCCTGCTCATTAGT | 15204 |
rs31387615 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Herc2 | Mm_Celera | 7:56170843 | TTACATTTTTACTGG[C/T]TTTTTGGTAGTAAGC | 15204 |
rs31387911 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56095846 | TAGGTGGAAGTATTC[C/T]TGTCAAGATTATGCA | 15204 |
rs31393993 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Herc2 | GRCm38.p3 | 7:56135827 | GTCATAGTATTTATG[C/T]ATATTTGTGATTGAA | 15204 |
rs31398281 | snp | A/C | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56128759 | TTATTAAAAACAACA[A/C]CCCCCCCCCCATAAA | 15204 |
rs31403415 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56219383 | TCGGGAGCTGTCTAG[A/G]TTGTTAGGAATATTT | 15204 |
rs31422546 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Herc2 | Mm_Celera | 7:56090822 | GTGCTTGCCTCTTTA[C/T]ATGGGAAAGTAAATA | 15204 |
rs31423901 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56141387 | TGTGGGCTCAGGTTT[A/G]TTGATTCTGTAGGTT | 15204 |
rs31428766 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56159856 | TCATTGTAGGCCCGC[A/G]TGATGGTGGTTTTCT | 15204 |
rs31429745 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Herc2 | GRCm38.p3 | 7:56106305 | CCTTACAGCCATAGG[C/T]TTAATGGTGTAACTG | 15204 |
rs31429819 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Herc2 | GRCm38.p3 | 7:56148462 | ACCTATTCTAAGTTT[A/T]AAAAAACCAGTTTGT | 15204 |
rs31431484 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon | Herc2 | Mm_Celera | 7:56114773 | CAGTGCCTCCACATT[C/T]CATAGAAGTAGGACT | 15204 |
rs31433604 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56057999 | AATACCCAATAGACA[C/T]GTCCACAGGCATTTT | 15204 |
rs31434417 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56191000 | TATTTTAGCTTAGAG[C/T]GGTTGGCTACCTGGT | 15204 |
rs31441588 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56205843 | TCTAAGACTCCCCAT[A/G]TTTCCAATTTTTTGC | 15204 |
rs31444846 | snp | A/C | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56128761 | ATTAAAAACAACACC[A/C]CCCCCCCCATAAATC | 15204 |
rs31445864 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Herc2 | Mm_Celera | 7:56061608 | AGAACTGTTGATGGT[A/G]AGTAATTTACTCTTT | 15204 |
rs31448535 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Herc2 | Mm_Celera | 7:56120047 | AGATTACCTATGGTT[G/T]CTGGGAACCAAACTT | 15204 |
rs31453671 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Herc2 | GRCm38.p3 | 7:56170232 | TATGTGTGTTTGTAC[C/T]GTGTGGATTCAGGTC | 15204 |
rs31453713 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Herc2 | GRCm38.p3 | 7:56086507 | AACTTAAGATACAGA[A/C]TTGTCTTAATGCTCT | 15204 |
rs31459218 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56103676 | ATTTAAAGCTTCCAC[C/T]ATGATGTGCAATGAT | 15204 |
rs31468593 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56180579 | AAAAGATAACATGTT[A/G]CTGGGTATGGCAATG | 15204 |
rs31468821 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Herc2 | GRCm38.p3 | 7:56058739 | ATAGTGAGACAGCAT[A/G]AGTTCCTTTGTGGAG | 15204 |
rs31478049 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Herc2 | Mm_Celera | 7:56159826 | CTTGTTCTACAGTAA[A/G]TACCAAGCCTAGACT | 15204 |
rs31480075 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56065797 | GGTGTCTGTCAGTGG[A/G]AGAATAAGTAAAGAA | 15204 |
rs31484378 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56099242 | GGGTGTGCTATTCCC[C/T]GTGCAAGCTTACTTC | 15204 |
rs31486621 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Herc2 | Mm_Celera | 7:56114623 | GGCATGGTCAGCTGT[G/T]TGCATCAGCAGCTGA | 15204 |
rs31491113 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56107225 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAGAA | 15204 |
rs31492489 | snp | A/C | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56220162 | CAGCAAAACCAAAAC[A/C]AAACCAAAACAAAGG | 15204 |
rs31495307 | snp | A/G | 0.49827 | 0.0293608 | synonymous-codon | Herc2 | GRCm38.p3 | 7:56134609 | AGAGTGGCTGCAGTC[A/G]TCGATTTTTTCTGGG | 15204 |
rs31502021 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Herc2 | Mm_Celera | 7:56206299 | TTTGTACTAAGTATA[A/G]AATCATGTTGATGTT | 15204 |
rs31509750 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Herc2 | Mm_Celera | 7:56058185 | ATATTTTTTGAAAAA[A/T]GTTGAAAAATTGACT | 15204 |
rs31513355 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Herc2 | Mm_Celera | 7:56087098 | GCACAAAGCCTCCCC[G/T]GTACTATTGAGACCC | 15204 |
rs31523859 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56096609 | AGGGTTCTGCCTATC[C/T]TTGTCTCTGGAGTGC | 15204 |
rs31525472 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56124440 | ACTTTTGTGTGCTAT[A/G]ACCTAGTCCTTCCTT | 15204 |
rs31525494 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56130138 | TTACTGTAAAATGAC[A/T]CTTTTTTTGTAGCTA | 15204 |
rs31531110 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56210049 | CAAGTTTCAAGTCAG[A/T]GAGAGATGCTGTCTC | 15204 |
rs31542511 | snp | C/G | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56185372 | TCTCTCTCTCTCTCT[C/G]TGTCGTGTGTGTGTG | 15204 |
rs31548008 | snp | A/C | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56131553 | TTATTTTTTGAGATA[A/C]GAGTTTTCTCCGTGT | 15204 |
rs31553525 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56130115 | TTCTTTTCATTTGCA[A/G]ATGATAGTTACTGTA | 15204 |
rs31566524 | snp | G/T | 0.265928 | 0.249492 | intron-variant | Herc2 | Mm_Celera | 7:56192005 | AAGTTAGGAGTCATA[G/T]TTAGAGCTAGAACAT | 15204 |
rs31567741 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56225596 | TTACATCGAGCAGCT[A/G]AGGCTACAAACTGTA | 15204 |
rs31569471 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Herc2 | GRCm38.p3 | 7:56219502 | TTTGGCTAACAGGTG[G/T]TGTAGAGAGTCCTGG | 15204 |
rs31572036 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Herc2 | Mm_Celera | 7:56103671 | CAGTCATTTAAAGCT[C/T]CCACCATGATGTGCA | 15204 |
rs31573964 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56219959 | AACTAACTATCATGC[A/G]GGTACAGCCAAAGAT | 15204 |
rs31574146 | snp | A/G | 0.42 | 0.183303 | intron-variant | Herc2 | Mm_Celera | 7:56066301 | AAGACTGGAGTTGGA[A/G]CTGGCCTAGGCTACT | 15204 |
rs31574335 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56205055 | ATTCCAGTTTTTTGT[A/G]ACCACTGGAGATGAG | 15204 |
rs31581226 | snp | C/G | 0.387812 | 0.208586 | utr-variant-3-prime | Herc2 | Mm_Celera | 7:56231272 | AGAGACTGACTGACT[C/G]AGAGAACTGTGTGGT | 15204 |
rs31590070 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56072454 | CTTTCTGACAGCAGT[A/G]GGTCAAGTTGTCATT | 15204 |
rs31590815 | snp | C/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56190993 | GGGTATATATTTTAG[C/G]TTAGAGCGGTTGGCT | 15204 |
rs31610039 | snp | C/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56145074 | AGGTAGAGAGTGCCT[C/T]TGCATATTGGAGGCT | 15204 |
rs31611084 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Herc2 | Mm_Celera | 7:56191194 | TGGAGCCTTGATGCC[A/G]GCCGGCATGCTCGCC | 15204 |
rs31612339 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Herc2 | GRCm38.p3 | 7:56165460 | TTTTAGAGTAGTAAG[A/G]TTTGCTTGTCTGCAT | 15204 |
rs31612706 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56059309 | AGCTCCCAGGTATCC[A/G]GGTTTGTTAATTCTA | 15204 |
rs31628302 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56192399 | TACTCAGTGCCCTCT[C/T]GCAGATGTGTGGATG | 15204 |
rs31628444 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56220433 | GTTTTTTGGCTTTCT[A/G]TGCTTTGCTACTTAG | 15204 |
rs31630117 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56060420 | TCTTGGGCATATATA[A/T]AAATTGCTTTAGATC | 15204 |
rs31637425 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56090365 | TGACCATGAACTTCT[G/T]TTCCTTCTGCTTCCC | 15204 |
rs31641863 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56110286 | GGGAGCGACAGATAC[A/G]GGAAAGCAAACACAG | 15204 |
rs31643285 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Herc2 | Mm_Celera | 7:56147429 | TCCATCAGCGTCAAG[C/T]TGCAATGTATGGCCC | 15204 |
rs31646250 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56153217 | GTGCCTTTACTCATT[A/T]CTTCTGTTCAGTGAG | 15204 |
rs31650673 | snp | C/G | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56185374 | TCTCTCTCTCTCTGT[C/G]TCGTGTGTGTGTGTA | 15204 |
rs31655939 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56178533 | AGACTTCTCGTTAGT[C/T]CTGACTTTATGTGTA | 15204 |
rs31656321 | snp | A/C | 0.197531 | 0.244432 | synonymous-codon | Herc2 | GRCm38.p3 | 7:56090993 | GGCTTTGGCCATTCT[A/C]CTGGAGTTGGCTGTC | 15204 |
rs31657585 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56121428 | GCAGATCCATCTCAT[A/G]CATTTGGTGGGTAAC | 15204 |
rs31659996 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56211905 | CTTTTTGTTTTGGGA[G/T]ACAGGATTTTGCTAT | 15204 |
rs31662504 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | GRCm38.p3 | 7:56048855 | TATTCTTGCCACACA[C/T]GGGTTCTCTTGCCTC | 15204 |
rs31663135 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56130668 | GCTATGCAAGTTTGA[A/G]GATGGAGTTTGTATC | 15204 |
rs31670332 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Herc2 | Mm_Celera | 7:56087669 | TTAAGACTGTTCATT[C/T]ATTACAACCCGATCT | 15204 |
rs31676771 | snp | G/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56073286 | TTGCCGTGGAACCAT[G/T]GATGGGCCGTGGTAA | 15204 |
rs31684728 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Herc2 | Mm_Celera | 7:56088045 | GCACCCAACATTTCA[C/T]GTAAGAGACACTCAG | 15204 |
rs31684868 | snp | C/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56063184 | TTTGCTGACATGACC[C/T]TGATATAGCTGTCTC | 15204 |
rs31684869 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56131424 | GTTTATGAATAAGTT[C/G]TTAAATTTAGCCCCA | 15204 |
rs31687883 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56054796 | GTCTCTGTCAGTAAA[G/T]AAAGGATGGAAAAGG | 15204 |
rs31693760 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Herc2 | GRCm38.p3 | 7:56067318 | CTAGAAGAGGACATC[A/G]GATCTCATTATGGGT | 15204 |
rs31695231 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56151451 | AAAGTGAGCACATGT[A/C]TGTGCATAGGTGGAT | 15204 |
rs31704974 | snp | G/T | 0.375 | 0.216506 | synonymous-codon | Herc2 | Mm_Celera | 7:56103927 | CAATCAGAGGCTTGG[G/T]CATGGAACAGAAGAA | 15204 |
rs31711476 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56195646 | GGGTCCTAGGAATTT[A/G]ACTCAGTTGCTCAGG | 15204 |
rs31712394 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Herc2 | GRCm38.p3 | 7:56181346 | GTGAGAAGTCTCTAT[C/T]GTTTAGATATAGTTG | 15204 |
rs31723912 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56090450 | GGGTATGGAAACCAG[G/T]GGCTTGTGCATGCAG | 15204 |
rs31733671 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Herc2 | GRCm38.p3 | 7:56140650 | AGTTGCAATCTTTGT[C/T]TTTTTGTTACTGGTA | 15204 |
rs31734455 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56064982 | TTTGACATTTTGGTG[A/G]GTGAGGAGTCTGTAG | 15204 |
rs31744237 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56126395 | CTCAAGCTGGTACTG[G/T]TCTAGAATCTCTATC | 15204 |
rs31747509 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Herc2 | GRCm38.p3 | 7:56069113 | CGGGTATGGTCTGGC[C/G]GACTGCATATATGGT | 15204 |
rs31748521 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56107774 | TCTTCCAGCCTTTCC[C/T]TAATTCAACCACTGG | 15204 |
rs31752547 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Herc2 | Mm_Celera | 7:56211551 | AACCAAGTGTGATTG[C/T]GTTTTTCTGTAATAA | 15204 |
rs31758373 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56182134 | ATTGAACTCAAATCC[C/T]TGTGCCTGTGTGGCA | 15204 |
rs31761394 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Herc2 | Mm_Celera | 7:56231048 | TGGAGAGCCCGCTGC[C/T]GATGACAGCAGTGAG | 15204 |
rs31765982 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56222085 | CCAGGGATTCATAGT[A/C]GGAAAATGCTCTGAG | 15204 |
rs31771223 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56189316 | AAGTACATGCCTGAT[A/G]CTGCAACCCAATCCA | 15204 |
rs31771789 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56144656 | CTGTACTGCCTGAGA[G/T]TCTCTCTTCTATATC | 15204 |
rs31774441 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Herc2 | Mm_Celera | 7:56124375 | GCTGGCCTGGCCTGG[A/G]ATTATGGGTATGCTA | 15204 |
rs31778805 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Herc2 | Mm_Celera | 7:56147401 | GTATTGTTTTGGACC[A/G]TTTGCTTTTTTGTCC | 15204 |
rs31779596 | snp | A/G | 0.32 | 0.24 | missense | Herc2 | Mm_Celera | 7:56194346 | GCAGGGCTGGAGACA[A/G]GGGCAGGGAAGTGCT | 15204 |
rs31791628 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Herc2 | GRCm38.p3 | 7:56181368 | ATATAGTTGTATTCT[A/G]CCTACCTAAAAGGCT | 15204 |
rs31793666 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Herc2 | Mm_Celera | 7:56182260 | TAAAATGCTTTAGCA[C/T]GTATATGTAAGAGGT | 15204 |
rs31796574 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56092962 | AATATGGCAGCTTTT[A/G]GATTTGGACTTAGGA | 15204 |
rs31799043 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56151351 | ACAGTGATTTCTGTG[C/G]TTGCACTATTTTAAA | 15204 |
rs31803742 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Herc2 | Mm_Celera | 7:56133994 | GGTTCTAGTATCATG[C/T]ATTTTAGTTCTATCC | 15204 |
rs31804585 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56120829 | CAAACAAACAAACAA[A/G]CAAGCAAAGCCTCAG | 15204 |
rs31807287 | snp | C/T | 0.484429 | 0.0868505 | synonymous-codon | Herc2 | GRCm38.p3 | 7:56157730 | AGAAACACTATCTGA[C/T]GAGTATTCAGACGAG | 15204 |
rs31807524 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56182142 | CAAATCCTTGTGCCT[A/G]TGTGGCAAGCCCTGG | 15204 |
rs31807649 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56193214 | ACCCAGATGAGGCAC[A/G]TTCACAGACTAGGGC | 15204 |
rs31811115 | snp | A/C | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56065499 | AAGACCTGGATTAGT[A/C]CTCAGGACCTACCTA | 15204 |
rs31811118 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56141342 | TCCCATGTAGGCTTC[C/T]TGGTTGGCTGTTCAG | 15204 |
rs31813285 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56182561 | TGAAAAGTGACACTT[C/G]TTTTGACTGTTCTTG | 15204 |
rs31814631 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Herc2 | GRCm38.p3 | 7:56194973 | TTTTCTTTCTCCTAC[C/G]ATATAGTCCATATAG | 15204 |
rs31823260 | snp | A/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56122514 | TTTTTTTTTTTTTTT[A/T]ATCTTTCTTTTACTT | 15204 |
rs31834768 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56165426 | ACCCATCTCCTCCCC[C/T]TTCCCCCTACTTCTT | 15204 |
rs31836116 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56107933 | GTGTCAGGCCTTGGA[A/G]CTTCCCTTTGAGATT | 15204 |
rs31836225 | snp | A/C | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56124397 | GGTATGCTATCTTCA[A/C]CTAAAGCACCTTCAC | 15204 |
rs31837409 | snp | C/T | 0.401235 | 0.199068 | synonymous-codon | Herc2 | Mm_Celera | 7:56205422 | CAAACAGCTGCTCCA[C/T]AGTCCATTCTTTAAG | 15204 |
rs31842512 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Herc2 | GRCm38.p3 | 7:56136919 | GAAAAGTATTTCCTT[C/T]TGTTTTTGGCTCAGT | 15204 |
rs31848452 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56184527 | AATAATATATAGCAA[A/G]GATAAGCCTTAAGTC | 15204 |
rs31859524 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56106034 | GTATCTTATTCTGTA[C/T]GAATAAGACTAGGGA | 15204 |
rs31870427 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Herc2 | Mm_Celera | 7:56089412 | TGTACTCTGCTCTAG[C/T]TACTAAGTGTTCTGC | 15204 |
rs31871145 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Herc2 | GRCm38.p3 | 7:56166133 | GTCAAATATTTACTC[A/G]TTGATTGTGGCTTAG | 15204 |
rs31872080 | snp | G/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56111393 | CTTCTTTTTTTTTTT[G/T]TTTTTGTTTTTTGAG | 15204 |
rs31882006 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56179054 | ACTTTGCTCCGAGTT[A/G]CTTTCAGTGATGTAA | 15204 |
rs31882009 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56093177 | TGTTTTGTGTAAATG[C/T]AAACAAATCCTAGTG | 15204 |
rs31883313 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Herc2 | Mm_Celera | 7:56066046 | ATAAGCCAGATTCAG[A/G]AAGGCAAAACTTGTT | 15204 |
rs31885336 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | GRCm38.p3 | 7:56165350 | TGGAGTTAGCTCTTA[A/G]GTTCAGATGTGTACA | 15204 |
rs31894633 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56225609 | CTGAGGCTACAAACT[A/G]TAGGAGGAGCCAAGT | 15204 |
rs31896526 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Herc2 | GRCm38.p3 | 7:56227564 | AGGGACAAGAGTTGG[C/T]TTACTGTGGTTTAAT | 15204 |
rs31901381 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56089410 | TTTGTACTCTGCTCT[A/G]GTTACTAAGTGTTCT | 15204 |
rs31903189 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56114076 | ACTGTGATCACTAGG[A/G]TTATTAAGTTCGTCA | 15204 |
rs31904746 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56065125 | TTTCTGCTGGCTTTA[A/G]TTTGGTCAAGTAAGC | 15204 |
rs31904826 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Herc2 | Mm_Celera | 7:56193156 | AATGACTTACCTGGC[A/G]TCTGTAGCTGCCTGA | 15204 |
rs31924116 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56186036 | GCTCATTGGGCTACA[C/T]CCCTTATCTTGTCAA | 15204 |
rs31925475 | snp | A/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56196176 | GATGGGCCTGAGAGG[A/T]TTGGTTGTTCCTGGT | 15204 |
rs31932527 | snp | A/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56123690 | GTTTTTTATTTATTT[A/T]TTTTTTTGTTTTTTT | 15204 |
rs31937044 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Herc2 | GRCm38.p3 | 7:56181508 | AATGCCATAGTGGTA[C/T]AAAGATGAATTAGTT | 15204 |
rs31939443 | snp | G/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56106618 | ATGTAGAAATACCCG[G/T]GTTTGTGTGTCATCC | 15204 |
rs31945895 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56064116 | CTTTAATTTCTAAAC[G/T]GAACTAATTCTTATT | 15204 |
rs31963703 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56220031 | ATAACAGTTCAGTTT[A/C]TAGTACCATGAAACG | 15204 |
rs31964645 | snp | C/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56197467 | CTCCATGTCACAATC[C/T]ATATTGAGGGAAGTT | 15204 |
rs31965788 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56193143 | GTGCCACTGATAAAA[C/T]GACTTACCTGGCGTC | 15204 |
rs31965792 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Herc2 | Mm_Celera | 7:56096752 | GTTGTGTGATTTGGT[A/G]CATATTTCTCTGTTT | 15204 |
rs31969897 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56138423 | ACTAAGAGTCAGGGT[C/T]TTACTATGTATTCTT | 15204 |
rs31972430 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Herc2 | GRCm38.p3 | 7:56110467 | GAGTTCAAATCAATA[C/T]GTTGGGTGCCATTTT | 15204 |
rs31972657 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56225384 | TTCAAGGGTTGCTGT[A/G]CAGTTGAAAGAAAAT | 15204 |
rs31974830 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56186183 | CCAGCCTGGGCCATA[C/T]TTTTGCATGCTACAC | 15204 |
rs31981270 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56195980 | TGAAAGGCAGCATGA[C/T]ATGTATATGTGTGGA | 15204 |
rs31993392 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Herc2 | Mm_Celera | 7:56096870 | CCCTCACCAATAAAA[A/G]CATTTTCGCCCATCC | 15204 |
rs31994043 | snp | C/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56060621 | ATCCTTCACATTTTC[C/T]TCAAGCTGTCCAGTC | 15204 |
rs31994470 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Herc2 | GRCm38.p3 | 7:56178916 | AATCTGTGCATGTGG[A/T]ATTGTTGTGGCAAAC | 15204 |
rs31995480 | snp | A/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56186533 | ATCACTTTAATGCAC[A/T]TTTCTCAATATGTGG | 15204 |
rs31997459 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56084270 | TCACTTGTCAGTCCT[A/G]GCACTAAGGAGGAAG | 15204 |
rs32001967 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56103693 | TGATGTGCAATGATT[C/T]TTACTTAAATGTTTT | 15204 |
rs32010213 | snp | G/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56196073 | AAACTCAGTTTGTCA[G/T]GCTTACATGGCAAGT | 15204 |
rs32013840 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Herc2 | Mm_Celera | 7:56159489 | TGGGCATTGCTCAGG[C/G]TGAACCGTATTCATG | 15204 |
rs32015281 | snp | C/G | 0.33241 | 0.236027 | intron-variant | Herc2 | Mm_Celera | 7:56087629 | AAGAGGCTCCAGAGT[C/G]TTTTTGAGTTTCCAG | 15204 |
rs32016175 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56093199 | ATCCTAGTGAAATCT[C/G]AGGACTTTGGCTCTT | 15204 |
rs32017854 | snp | A/G | 0.432133 | 0.171253 | synonymous-codon | Herc2 | Mm_Celera | 7:56229308 | ATTTGATGAACAAGT[A/G]GCTGCTGTCCGGGAA | 15204 |
rs32018689 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56122682 | CATCCAACCCACTCC[C/T]ACCTTCCTGCCCTCG | 15204 |
rs32023922 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56146369 | AGGAACATGAACATG[C/T]GATTTCATGGCATTT | 15204 |
rs32024291 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56084842 | GACATACAGTACTAC[A/C]AGCTAATATGTGCAC | 15204 |
rs32026539 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Herc2 | Mm_Celera | 7:56115048 | TTTAAACATGGCTAA[A/G]AGGAGAGGCTATGGA | 15204 |
rs32030552 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56181470 | GCCTTCAGTACAATA[A/C]AATACTTAGACAATA | 15204 |
rs32030670 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Herc2 | GRCm38.p3 | 7:56225997 | TGGCGTACATCATTG[C/T]TTGCAAGTGTGTTTG | 15204 |
rs32039774 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56065791 | AGCTTTGGTGTCTGT[C/T]AGTGGGAGAATAAGT | 15204 |
rs32046017 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Herc2 | Mm_Celera | 7:56207656 | ATGCTTATTCTTTGC[G/T]GTAACTACAGGAATA | 15204 |
rs32049615 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56114067 | TTTAAGTCTACTGTG[A/G]TCACTAGGGTTATTA | 15204 |
rs32057697 | snp | A/C | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56089159 | GAAAAAGAAAACAAA[A/C]CAAACCTATGAACCT | 15204 |
rs32067366 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56146266 | AGGTCACTGGGGAGA[C/T]CACTTGCATTGCTCG | 15204 |
rs32069972 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56114227 | TCTTACAATTGAACA[C/T]GTATGTAAGAGCTGC | 15204 |
rs32070799 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Herc2 | Mm_Celera | 7:56098039 | ACACACCAGAAGAGG[G/T]CGTCAGATCTCGTTA | 15204 |
rs32073201 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Herc2 | Mm_Celera | 7:56181227 | TGCTTACTGTTGCTT[C/T]TGTCTGAGTCCCAGC | 15204 |
rs32076907 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56123238 | TGTATGTTCTCTTAC[A/G]GAGGCCAGACCAGAC | 15204 |
rs32078526 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Herc2 | Mm_Celera | 7:56167721 | GTAGTCTTTATGTAC[C/T]TTTGTGTTCTTGGTT | 15204 |
rs32079976 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56120559 | CCATGGTAGGTGTTG[A/G]TAGCTTAAATATATT | 15204 |
rs32092629 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56141070 | TCCCCTCCCTCCTCT[C/T]CTCATTTCAGCCCTC | 15204 |
rs32093255 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Herc2 | Mm_Celera | 7:56058654 | ATTGAAAAAGGTAAC[A/G]GAAAGCAGCCTTGCC | 15204 |
rs32095680 | snp | C/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56225450 | AGAAAAGTTCATTCT[C/G]TAGGGATCTATAGTT | 15204 |
rs32098341 | snp | C/G | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56064960 | ACTTCAAACAACTCA[C/G]TTCTCTTTTGACATT | 15204 |
rs32104319 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Herc2 | Mm_Celera | 7:56170791 | TTATTCAGCGCCTTA[C/T]TTTATACAACTCTTC | 15204 |
rs32109127 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Herc2 | Mm_Celera | 7:56181740 | TAAATAATTCTGTTG[A/G]AGGCTAATTTGTATT | 15204 |
rs32110330 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Herc2 | GRCm38.p3 | 7:56227445 | CCTGTCACTCTTTGT[C/T]TAGGTCTGTGCAGAG | 15204 |
rs32112405 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56179946 | TCTTAACACTGTCCC[A/G]TGCACTATGAGACTT | 15204 |
rs32115796 | snp | C/G | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56178436 | TAAGTTTATAGTTCG[C/G]TGGCATTAAATACAT | 15204 |
rs32119712 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56054637 | TTATATATCTCTGCA[A/C]ACACAAATTCTGATT | 15204 |
rs32124811 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Herc2 | Mm_Celera | 7:56232259 | AGGACACAGGACAAC[C/T]AACTTTTAACTTTTT | 15204 |
rs32127046 | snp | A/G | 0.401235 | 0.199068 | synonymous-codon | Herc2 | Mm_Celera | 7:56113077 | TCACCAGGTTGACCC[A/G]GAATTCCTTGGTTTA | 15204 |
rs32134691 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56178417 | TCTTCCATTTCGACA[A/G]TTTTAAGTTTATAGT | 15204 |
rs32135002 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Herc2 | Mm_Celera | 7:56087860 | ACACTAAAGATACTG[C/T]GTAAGATTTCCTCCA | 15204 |
rs32136175 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Herc2 | Mm_Celera | 7:56170259 | GGTCATCAGGTTTAG[A/C]AGCAAATACCTTTAT | 15204 |
rs32152233 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56136903 | GCTAGTTACACTGCT[A/G]GAAAAGTATTTCCTT | 15204 |
rs32153665 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Herc2 | GRCm38.p3 | 7:56059869 | CTGTAGGTCCATATA[C/G]CACTAGTGGCCCAGT | 15204 |
rs32159302 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56173815 | TTTGCTTGGTAGCTT[A/G]ATTTCCAACTTTTGG | 15204 |
rs32161528 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56226663 | GTCAAGTTTGTGGGT[A/G]AGTTTCTGTGCATAT | 15204 |
rs32163531 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Herc2 | GRCm38.p3 | 7:56169504 | AGTGAGATCTTACTC[A/T]AATTAGGTCGTGATA | 15204 |
rs32178139 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56222069 | GAGGGGAGCTGGGCA[A/G]CCAGGGATTCATAGT | 15204 |
rs32192698 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56128755 | GATTATTAAAAACAA[A/C/T]ACCCCCCCCCCCATA | 15204 |
rs32193809 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56178100 | GCATCGTGCCTACTA[C/G]AGTGCTTGATACAGC | 15204 |
rs32197009 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56059161 | TCTTGACCAGGTTAG[A/G]TGCATCCTCTCCCAC | 15204 |
rs32201306 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56179087 | AGACAGAGAAAATAG[C/T]TCCATCTGCATTACT | 15204 |
rs32202803 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56171170 | TCCTTGCAATTCCAT[C/T]TGTTAACTCTTGGGC | 15204 |
rs32209126 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56180708 | TATGCCAGACAGGAT[G/T]ACATACTGAGATCCT | 15204 |
rs32214929 | snp | A/G | 0.42 | 0.183303 | intron-variant | Herc2 | Mm_Celera | 7:56191018 | TTGGCTACCTGGTTA[A/G]TAATGCACAGTAGTT | 15204 |
rs32224852 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56205083 | GAGCTGGATTTGTAC[A/G]CCAGAGAGGGAAGTT | 15204 |
rs32226605 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Herc2 | GRCm38.p3 | 7:56134394 | TTTGTTCAAACTAAC[C/T]GTCACATCATCCTTA | 15204 |
rs32231302 | snp | C/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56123225 | CTTCAGAGTTAGGTG[C/T]ATGTTCTCTTACGGA | 15204 |
rs32245696 | snp | A/C | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56085933 | GAAGAACTATAGTCT[A/C]CCTGGAAAGTCTGCA | 15204 |
rs32249563 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Herc2 | Mm_Celera | 7:56193207 | GCAGCCGACCCAGAT[A/G]AGGCACATTCACAGA | 15204 |
rs32251744 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56109932 | GCTCTCTACCAGGAG[C/T]CATAGACATTTATTT | 15204 |
rs32262316 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56089162 | AAAGAAAACAAAACA[A/G]ACCTATGAACCTGTT | 15204 |
rs32268766 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Herc2 | GRCm38.p3 | 7:56178985 | CCATGCTGAATTCCT[A/C]GTAGAGCCAGAGCCT | 15204 |
rs32272607 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56136731 | CCAAGGTGAAGTATG[C/T]TCTGTGTTTCTTAGA | 15204 |
rs32276415 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56123341 | TGAGAGATCTCGGGG[A/G]TGGGGGTCCAGGTCA | 15204 |
rs32277260 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56131674 | TTGAGTTGCCCGAGG[C/T]AAGCGTGGGAGAGTG | 15204 |
rs32283210 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56167534 | TCATTCTTTTTTTGT[A/G]AACTGTTGCTTCTCA | 15204 |
rs32289330 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56092210 | TAAGAGCTCTTCTTT[C/T]AACATGTTTTCCCCT | 15204 |
rs32298421 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56138323 | GTATAATATGGAGTG[C/T]CACACTTTGGGGTGC | 15204 |
rs32302846 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56134078 | TGGCTTACAATTGCA[A/G]GTTACAGTCCATCAT | 15204 |
rs32310202 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56224839 | CAAGTAACCATTAAC[C/T]CTATCAAAAGACTCT | 15204 |
rs32313452 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56123301 | TATCAGCTGGTGTAT[A/G]CTACCTGGTTGGTGG | 15204 |
rs32327248 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56110036 | AGAGCAGGCAATTAT[C/T]ACTGCTCTCTCTACT | 15204 |
rs32327873 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56068825 | AATAAAGACATGCAC[C/T]GACACCACCCAGCTT | 15204 |
rs32328305 | snp | G/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56124439 | TACTTTTGTGTGCTA[G/T]GACCTAGTCCTTCCT | 15204 |
rs32330844 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | Mm_Celera | 7:56048415 | GCGAGTTTTGAGAGA[G/T]AGAACTACTTATTGG | 15204 |
rs32330852 | snp | C/T | 0.387812 | 0.208586 | synonymous-codon | Herc2 | Mm_Celera | 7:56177951 | GCTGCAGTTCCTTTT[C/T]TGGCTTCAGACAATG | 15204 |
rs32330925 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Herc2 | Mm_Celera | 7:56193221 | TGAGGCACATTCACA[A/G]ACTAGGGCCTTGAGA | 15204 |
rs32335638 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56110598 | TCTACAATAGGTAAA[C/G]CTTTTTAAAATGTAA | 15204 |
rs32337051 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56204893 | CATCTAGACCTTTTT[C/T]TTTTTTCCTTGCTGC | 15204 |
rs32339537 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56219303 | AACTAGGGAAGGGTA[C/T]ATGTCTTTAAAACGT | 15204 |
rs32340074 | snp | C/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56085975 | GTGAGAGCTTGCAGC[C/T]GCACAAACCTCGGTC | 15204 |
rs32342078 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Herc2 | Mm_Celera | 7:56087754 | TATAATCTGAAAATA[G/T]GCAGTCTGACATGCT | 15204 |
rs32350416 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56108092 | TTTAATTTTATTGAT[C/T]TTTAAAAATAATTAC | 15204 |
rs32351265 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56147061 | GTTCTCCTTTCATCA[A/G]CCATGTCTCAGGGGA | 15204 |
rs32358191 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56220331 | CTAATATTTGTACAT[C/T]CTTTGATGCTTATTT | 15204 |
rs32360153 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Herc2 | GRCm38.p3 | 7:56212050 | TTGTTTGGAGGCCTT[A/T]AGGATGTTGAGCAAA | 15204 |
rs32362224 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56170821 | CTTGGTAAAGAAACA[A/G]AATTGATTACATTTT | 15204 |
rs32365668 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56091806 | GCCTTAGGTGGTATC[A/G]CCAGCTACTCAGATC | 15204 |
rs32369147 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56117598 | CCGGATCCTCTGGTA[C/G]TACTATGTCCAATTT | 15204 |
rs32370069 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56062278 | TAAAGAACTGAAGAA[C/G]GTGGACTCCAGAAAA | 15204 |
rs32374405 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Herc2 | GRCm38.p3 | 7:56200541 | AATAAGTGGGCCCAC[C/G]GGGCTCGAGCCAGTG | 15204 |
rs32382854 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56065276 | GTTTGTCAAGAGAGA[A/T]CACAAGTTGAATGTA | 15204 |
rs32389706 | snp | A/C | 0.32 | 0.24 | intron-variant | Herc2 | GRCm38.p3 | 7:56197954 | TTCTTCTACACTAAT[A/C]CTGTTCTTACATCTT | 15204 |
rs32390540 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Herc2 | Mm_Celera | 7:56098179 | TTCTTAATGTTCTCT[C/T]GGTGCTGGAATGGAG | 15204 |
rs32394156 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56054698 | TGATGGCCCTTCTGT[A/G]ATCTCTGTGACTAAA | 15204 |
rs32396965 | snp | C/G | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56196713 | GTTTTGAGACACTAC[C/G]TCTTACTCAGCCTAG | 15204 |
rs32398652 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56090436 | GTTTATGGAGTAATG[G/T]GTATGGAAACCAGGG | 15204 |
rs32398891 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Herc2 | GRCm38.p3 | 7:56070128 | ATTCATCGCGCTCTC[A/G]AGGGACTTACCTTGT | 15204 |
rs32401987 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56205503 | GAGCCACTGAGAGCT[C/G]TTATGGGAGGTGTTG | 15204 |
rs32405108 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Herc2 | Mm_Celera | 7:56090792 | TGTATGCAGTGCTGT[A/C]TGCATGTTCCAGCAG | 15204 |
rs32406853 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56209690 | TTCGAAAGGAGTCGG[A/G]GCGGGTCACATTAAA | 15204 |
rs32415370 | snp | C/G | 0.401235 | 0.199068 | intron-variant | Herc2 | Mm_Celera | 7:56179137 | TCATGAGTGGGCCAG[C/G]AACTGTGGGTGAGCC | 15204 |
rs32417180 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Herc2 | GRCm38.p3 | 7:56179514 | AAGCAGTTTGTCTTA[A/G]AGCCAGCTCCCAAGT | 15204 |
rs32418198 | snp | A/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56055277 | GAAATTAGATATGCA[A/T]GAAGCATTTGTAAAC | 15204 |
rs32421084 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Herc2 | GRCm38.p3 | 7:56060475 | TCCATATAGCCTTTT[C/T]CTTAGATAATTTGTC | 15204 |
rs32423297 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56072021 | CATTGAGTGACTGAC[A/G]TGTGCGGTAGCTCTC | 15204 |
rs32425017 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Herc2 | GRCm38.p3 | 7:56180164 | AAGTAGCAAATTGCC[C/T]GATGTGTGTCTATAT | 15204 |
rs32427281 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56147269 | GGAACAAATTTAGGT[A/G]GTAGCAAGTAGCTAT | 15204 |
rs32427583 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Herc2 | Mm_Celera | 7:56157951 | TAATTAGCTTTTCTC[C/T]GTTAAAATTTCTCTC | 15204 |
rs32432343 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Herc2 | Mm_Celera | 7:56219401 | GTTAGGAATATTTCC[C/T]TAAGTTTTATCTTAC | 15204 |
rs32433897 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56225793 | GTACAGCTGGTCTTA[A/G]CCTTTAGAGAACCTT | 15204 |
rs32441178 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56121758 | AGACATGAAGATGTC[A/G/T]TATACATTTGGAGCT | 15204 |
rs32444007 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Herc2 | Mm_Celera | 7:56122086 | CCATGTGGGTGCTCT[C/T]TCCAGTGGTGGAGCA | 15204 |
rs32444395 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56186107 | ATCCCAGCATTTGGA[A/G]GTCTGGAGCAGGAGG | 15204 |
rs32445950 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Herc2 | Mm_Celera | 7:56054852 | CTCCAGACACATTTG[C/T]ATGTATGTGTACCTG | 15204 |
rs32457398 | snp | C/T | 0.387812 | 0.208586 | synonymous-codon | Herc2 | GRCm38.p3 | 7:56177983 | GGAGGAGGAGGATGA[C/T]AAGGGCAGCACTGGG | 15204 |
rs32458396 | snp | C/G/T | 0.498615 | 0.0262793 | intron-variant | Herc2 | GRCm38.p3 | 7:56226834 | TGATTCTCCTTTCTT[C/G/T]CAGGTGAATCCGTGG | 15204 |
rs32460420 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56193577 | GAGTAATTGCATACC[A/G]CTGGATCAGGGGGAC | 15204 |
rs32462633 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Herc2 | Mm_Celera | 7:56072042 | GGTAGCTCTCGCATG[C/T]TTGGGAAGAGCATTT | 15204 |
rs32463829 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56189293 | CAAACCCAGGGCCCT[A/G]TGCACTGAAGTACAT | 15204 |
rs32464459 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56109979 | TCTGTCTGTTATGCT[C/T]TCTACCTAGAGCCAG | 15204 |
rs32474054 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56061205 | ACAACTACTTCCAGG[A/G]GTGGGCTTTGTGAGT | 15204 |
rs32479194 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56091242 | CATGGACCCCAATCC[C/T]GCTCATCTCTTTGTC | 15204 |
rs32488211 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Herc2 | Mm_Celera | 7:56146312 | ATTTGTTCAGAGTAC[C/T]CTAGTTGAGAGAGTT | 15204 |
rs32490787 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Herc2 | Mm_Celera | 7:56196173 | ATAGATGGGCCTGAG[A/T]GGATTGGTTGTTCCT | 15204 |
rs32497211 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56116327 | CTACACACACACACA[C/T]GCACATACACACACA | 15204 |
rs32497507 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56125883 | GTCAGTGCTCTTAAC[C/T]GCTGAGCCATCTCTC | 15204 |
rs32498139 | snp | A/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56184509 | ACATTTTTATTGCTT[A/T]TAAATAATATATAGC | 15204 |
rs32503873 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56061502 | CTGTAATCTGTTATC[A/T]ATAAATCACTTGCTG | 15204 |
rs32509797 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56060627 | CACATTTTCCTCAAG[C/T]TGTCCAGTCTGTGCC | 15204 |
rs32511633 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56149187 | TCCATTTCCACACAA[A/G]ACCACATTTTGAGAT | 15204 |
rs32514601 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56210465 | TCCCTAGCATTCGCA[C/T]AGTGCCTCACAACCA | 15204 |
rs32518089 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56063507 | GAGTGGGGGGGGAGG[G/T]TATGGGGGACTTTTG | 15204 |
rs32527232 | snp | A/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56225457 | TTCATTCTGTAGGGA[A/T]CTATAGTTTTGACCT | 15204 |
rs32968644 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56094948 | AAAGACTGAGCTTCA[A/T]CCAGTTTAGTATTAT | 15204 |
rs32968645 | snp | C/G/T | 0.142012 | 0.225474 | intron-variant | Herc2 | GRCm38.p3 | 7:56095193 | TGAAACTAATCAAAT[C/G/T]TATTGTGTAGGTATA | 15204 |
rs32968646 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56096786 | AGATGTGCCTTTGCA[A/G]CATTAGTGAGATAAC | 15204 |
rs32968647 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56097873 | TCACTTAAGGAAAGT[A/G]CTTGAGTTGTGCGTC | 15204 |
rs32968648 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Herc2 | Mm_Celera | 7:56098235 | CTAGTCTGTCTATTT[C/G]AGTATGTTTGCTCAG | 15204 |
rs32968649 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56098860 | CCATTCTTGATGAAT[A/G]ACTCCTTGAGAACTT | 15204 |
rs32968650 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56098968 | ACCCCACATATTGTC[C/T]TGTTGTTCACATTGT | 15204 |
rs32968651 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56099998 | AGAAAGGCAAAAAGT[C/T]CTGTGCTCTGATTAC | 15204 |
rs32968652 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56100023 | GATTACCTCTTTCCT[C/T]TTTTGTATCTCTTAT | 15204 |
rs32968653 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Herc2 | GRCm38.p3 | 7:56100073 | TTGTTGTCTTCCTTC[C/T]TGCAGGCCTCTGGAG | 15204 |
rs32968964 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | GRCm38.p3 | 7:56060211 | TGAGATGTAGTAACA[C/T]TCTGTTTCATCCAAC | 15204 |
rs32968965 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56061486 | GGGATGTTGACATTT[A/C]CTGTAATCTGTTATC | 15204 |
rs32968966 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Herc2 | GRCm38.p3 | 7:56061638 | TGAGAAAAAAATTTG[A/G]CTAAGTGAGGATCAC | 15204 |
rs32968967 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56064381 | CATAATACTTTCCTT[A/G]TCTTGATTAATCAAC | 15204 |
rs32968968 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Herc2 | Mm_Celera | 7:56065423 | AACTGGAGTGAAAGT[A/C]TAGAAGAGTTCAGGG | 15204 |
rs32968969 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Herc2 | Mm_Celera | 7:56065955 | ACAAACACACAAAGA[C/T]TGTTTCTCAACTATT | 15204 |
rs32968970 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Herc2 | GRCm38.p3 | 7:56068278 | CTGTTATGTGGTTTC[C/G]TGATGAGTAACTTTG | 15204 |
rs32968971 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Herc2 | GRCm38.p3 | 7:56068951 | GGTTGCATTATCTAG[C/T]AGAGTGAGCTCTGTT | 15204 |
rs32968972 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56070091 | TTCTTTCCTGTGAGC[C/T]GGTGTTGCTAATTAT | 15204 |
rs32968973 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56070151 | TACCTTGTTCTTGCT[C/T]TGGTATTCTGATTTG | 15204 |
rs32969324 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56110925 | ATAAGATGGTGATTC[C/T]AGCACATTTTCCTAG | 15204 |
rs32969325 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56110961 | TGCAACTGGAGCCTC[A/T]GTGTATGCAAACCAA | 15204 |
rs32969326 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56111058 | CACTTCTGTCTCAAC[A/G]CTTCTGTTTTTGGAA | 15204 |
rs32969327 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56111129 | TTGTTTTTAATCTCA[A/G]TATTTTTGTTTTCTG | 15204 |
rs32969328 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Herc2 | GRCm38.p3 | 7:56111890 | ACCCTAGAAGCCAGT[A/T]TTGATTTTGTTTCCG | 15204 |
rs32969329 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56111904 | TATTGATTTTGTTTC[C/T]GTTGTGTTGTAGGGT | 15204 |
rs32969330 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56111990 | GATGGGCAGTAGACT[A/G]TTATCTTGTAGCTAC | 15204 |
rs32969331 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56112020 | CTCAGAAGGTAGGCT[A/G]GCTCCCTGGTTTCTT | 15204 |
rs32969332 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56112060 | AAACTTTGCATATGA[A/G]TAGTGCAGCACTCTG | 15204 |
rs32969333 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56112089 | TGTCACACTAGGCTG[G/T]CAGATTTCTAGGGAA | 15204 |
rs32969994 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56100261 | CTGTACCTGAGTACA[A/G]TCACGAGGTAGGAGG | 15204 |
rs32969995 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56100480 | GGGCAGTTTCTTAGG[A/G]ATGTAGCCTGGATGA | 15204 |
rs32969996 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56101224 | GAATTTTGATTCCAG[G/T]ATCTAAGTACTCTAT | 15204 |
rs32969997 | snp | A/C/T | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56101483 | GAGGGAGAGAGATAT[A/C/T]ATGTAGTGGTTCAGA | 15204 |
rs32969998 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56102004 | TTATACATAGACATG[C/T]TCAGAAGCTCTGTGC | 15204 |
rs32969999 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56102304 | ATTCTTTGTAAAATT[C/T]CTGAGGAAACTTTTA | 15204 |
rs32970000 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56102361 | CTAAGGCTATAAATA[C/T]TGCTCACCTCACACT | 15204 |
rs32970001 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56102406 | GCAGCTCTTTGAGAG[A/G]AACGTTTCTGCTGCA | 15204 |
rs32970002 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56102471 | CACCTGCCTGCCTGT[C/G]CCGTCTGCTCTGGGT | 15204 |
rs32970003 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56102490 | TCTGCTCTGGGTGAT[A/G]GGCTCACTGGAAACA | 15204 |
rs32970064 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Herc2 | Mm_Celera | 7:56112214 | AAGGCAGACTCCTGC[C/T]TTGTCAGTGTACTTG | 15204 |
rs32970065 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56112229 | CTTGTCAGTGTACTT[A/G]TTTTTCTCTGAGGAC | 15204 |
rs32970066 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56112301 | CGGTTGGTTCCAGGC[A/G]TTTTTCTGTTGGATA | 15204 |
rs32970067 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56112446 | GTACTTTCACAGTGA[G/T]ATTTCCCAGCTATAG | 15204 |
rs32970068 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56112471 | CTATAGTGGTTAAAA[A/T]TTTTTAGTAGTTTTA | 15204 |
rs32970069 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | GRCm38.p3 | 7:56112508 | CATGTAAGGATCAAT[A/C/G]TTTGTCATCTGAAAA | 15204 |
rs32970070 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56112554 | GTCCCAATTTGAAAC[G/T]TTTTCAGTGTTAATG | 15204 |
rs32970071 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56112797 | TATATAAGGTATATG[A/G]TATAAGGTATATGGA | 15204 |
rs32970072 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56112845 | GTAATACACAAGTCC[C/T]TTAAGTTACCTCCTA | 15204 |
rs32970073 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56112917 | GTGTAAGGGATGTCA[A/G]CTTGAACTGAAAAGT | 15204 |
rs32970654 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56181957 | TAGTCATGCCCCTCT[C/T]TCACCGTTATCTTTG | 15204 |
rs32970655 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56182261 | AAAATGCTTTAGCAC[A/G]TATATGTAAGAGGTA | 15204 |
rs32970656 | snp | C/G | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56182629 | AGCCACAAATGGCCG[C/G]CTAGGTCTGGGTATG | 15204 |
rs32970657 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56182747 | ATCAGTGAGCAGTTC[C/T]TCATAAGCTTTTGCT | 15204 |
rs32970658 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56182825 | TGAATCTTCAGTGAT[A/G]AGAAAGATATTTTTC | 15204 |
rs32970659 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56182909 | CTGAAGTACTATGCT[A/G]GGTTCCTAAGGAATG | 15204 |
rs32970660 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56183028 | AAACAAGAATTTACT[C/T]TTCTACTCTGTTAAC | 15204 |
rs32970661 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56183271 | TGGGCCCATCTATAA[C/G]GCATCTACCTGTGAA | 15204 |
rs32970662 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56183323 | CTCTGTGGGAAGGTG[C/G]CTATAATACTCTAGC | 15204 |
rs32970663 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56183361 | GCACCTCTCTAGAGT[A/G]GAAGTTGTTGTCCCT | 15204 |
rs32970674 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56102513 | TGGAAACATTGGCTT[A/C]AGTGTAAGCGGTAGG | 15204 |
rs32970675 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56102626 | CAGATGACGGATTAG[C/T]CTGGCCTGATAGCTA | 15204 |
rs32970676 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56102712 | TTAGTAGTATGGCAT[A/G]GTTGGGTCATTATTA | 15204 |
rs32970677 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56102764 | ACTAAAGAAAAGGAT[C/T]ATTTTATTTTTCAGA | 15204 |
rs32970678 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56102939 | CAGTTTTTTCCCCCG[A/G]TTTATTGAGGTTTTG | 15204 |
rs32970679 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Herc2 | Mm_Celera | 7:56103021 | TTTATGTCATATTTA[A/G]TTAAATTACATTGCA | 15204 |
rs32970680 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56103084 | GTGGGGACACCACAG[G/T]GCACAGTGCAGGCAG | 15204 |
rs32970681 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56103103 | CAGTGCAGGCAGACT[C/G]GAGGGTGGTCAGTCA | 15204 |
rs32970682 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56103136 | GACAGCATTGCCACA[C/T]ACCTCAGTGCTCATG | 15204 |
rs32970683 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56103208 | TTGAAGCAGCAGCAT[C/T]GGTCCCAAAAAGTAA | 15204 |
rs32970714 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56070486 | CTTTGTGCCATTTGG[C/T]GTTTGTTCCAGAAAA | 15204 |
rs32970715 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56070818 | GTGTATTATGGTTTG[C/T]TGTTAAATGAAGCAG | 15204 |
rs32970716 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56072250 | AGCTTGACCGTTGCA[A/T]TTTGAAAAACAATTA | 15204 |
rs32970717 | snp | A/G | 0.336735 | 0.234472 | synonymous-codon | Herc2 | Mm_Celera | 7:56072363 | GAAGAAGGAAGAAGA[A/G]GAGACACCTGCACCT | 15204 |
rs32970718 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56072405 | CAAGTCAATCCTGGA[A/G]AGCTGGGTGTGGGGC | 15204 |
rs32970719 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56072467 | GTGGGTCAAGTTGTC[A/G]TTTGTTAATGGAATT | 15204 |
rs32970720 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56072950 | AAGCTCATCTTATAC[A/G]AGTTTCCAAGTAGTT | 15204 |
rs32970721 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Herc2 | Mm_Celera | 7:56073677 | TTCTTCTTTGGTCTC[C/T]CATTATTATATTTAC | 15204 |
rs32970722 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Herc2 | GRCm38.p3 | 7:56081834 | CTATATATTTTTGTT[C/T]TCTGTGGATTTTTTT | 15204 |
rs32970723 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56082956 | CCTACTTTCTGCCTT[C/T]GTGCATGAGGTGAGG | 15204 |
rs32970824 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Herc2 | Mm_Celera | 7:56113248 | GGAGCGGGCCAGGGC[A/G]CTCTCAGCACTCTTG | 15204 |
rs32970825 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56113390 | AGAGCAAAACCTTCT[C/T]TTTTCAGTTTCAGGC | 15204 |
rs32970826 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56113555 | CAGAGGAGTCAATGA[G/T]TGCTTTTACTTAGTG | 15204 |
rs32970827 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56113629 | ATCGTGACTATAATC[A/G]TTGAAGAACCCAAAA | 15204 |
rs32970828 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56113653 | CCCAAAATGTAAAAA[A/T]TTTAAAGAACCCAAA | 15204 |
rs32970829 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Herc2 | Mm_Celera | 7:56113717 | AATTTAAAACTCTTG[C/T]TTTTATTTGTGATAA | 15204 |
rs32970830 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56114300 | TGTCAGAATTGCTGG[C/T]AAAGATTTCAGTGTC | 15204 |
rs32970831 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56114594 | GGTGGAGTTTCTGAC[A/G]GGGTATACAGGTAGG | 15204 |
rs32970832 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56114973 | TGAAGAATGGGTTTA[A/G]CTGTGGAAGACTTAC | 15204 |
rs32970833 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56115539 | GTTCTTTGGAAAGTC[A/G]GTTTCAGGTGTAGTA | 15204 |
rs32971284 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56103626 | ATATAGGTAAGATTG[A/T]TTTATGTGTTTTATG | 15204 |
rs32971285 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56103685 | TTCCACCATGATGTG[C/T]AATGATTTTTACTTA | 15204 |
rs32971286 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56103720 | TTTTTTTAATTTGTG[A/T]TTTCTAGGCCAAGTG | 15204 |
rs32971287 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56103873 | GTTTTCTATTGCCTT[A/G]ACAAAAGATGGCCAA | 15204 |
rs32971288 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56104073 | AGTGAATGGAGTGTC[A/G]TTAGAAATATCTTGA | 15204 |
rs32971289 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56104152 | AAATTATTCTCATCA[A/G]ATTTAACTTTTAATT | 15204 |
rs32971290 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56104243 | CGACTTAGTCTGCTG[A/T]GACCTTGTTTTTGGT | 15204 |
rs32971291 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Herc2 | GRCm38.p3 | 7:56104575 | CGAGCTGACAAGAAA[G/T]CGAGAAAGGTGAGGT | 15204 |
rs32971292 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56104630 | TGGATGCCCATTGGA[C/T]CCTTTGGTATTTTAT | 15204 |
rs32971293 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56104681 | CTCTTCTTAAGGGGC[C/T]AGCTTATTAATTGTT | 15204 |
rs32971604 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56083005 | TCTTCTCATACAGTG[A/G]GGGCATTTAGGATGT | 15204 |
rs32971605 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56083137 | GCATGGAGCACTGCT[A/T]GTTTATTAGCACATG | 15204 |
rs32971606 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56083233 | TTTGTTTTTCTAGTG[A/G]CTCTGTTGTGGTGAG | 15204 |
rs32971607 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56083341 | CTTTGAGTTCTTTAG[A/G]CTTTACTTCATGTAC | 15204 |
rs32971608 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56083402 | TTTTATGATTTTTTT[A/T]AAACTGGCAGAAGAG | 15204 |
rs32971609 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56083847 | TGAGTCTTGAAGTCT[G/T]GACTGTTGTAGTAAA | 15204 |
rs32971610 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56084686 | TATGGCTCTTCACTT[C/T]TGTATTAGCAACTTG | 15204 |
rs32971611 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56084895 | ATTGTATACTTAAGT[C/G]TTTCCTATTGTCGTT | 15204 |
rs32971612 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56084944 | TTTGACAACCATGCC[C/T]AAGATACTAACAAAT | 15204 |
rs32971613 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Herc2 | Mm_Celera | 7:56085383 | AGTATCTACTAAAAT[A/G]TTTAAGGCTCATGTA | 15204 |
rs32971644 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56153481 | TGTTTCATGTTTTCA[A/C]ATAAGCACGGTGGGA | 15204 |
rs32971645 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56153697 | AGTAAGTGAGATAAA[A/G]TGACTCGTAAGGCCA | 15204 |
rs32971646 | snp | A/C | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56153779 | CCTCCTGCACTAGGC[A/C]CAGCTAGAAGATTAC | 15204 |
rs32971647 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56154036 | GCATAGTATTAGGGG[C/T]GAAACTGGCTTGTGA | 15204 |
rs32971648 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56154197 | CAGGGAACTTTCAAC[A/G]TCCTAGACATAAAAA | 15204 |
rs32971649 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56154470 | AACTTTAGCAGTTTA[A/G]GAGTTTCTAAAACAT | 15204 |
rs32971650 | snp | C/T | 0.5 | 0 | intron-variant | Herc2 | Mm_Celera | 7:56154500 | TTTTTATTGAATAAA[C/T]TTCTAAAAAATGACT | 15204 |
rs32971651 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56154588 | ATATCTTAACTAGCT[A/G]CTGTAGCATAAGCTT | 15204 |
rs32971652 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56154711 | ATTAAAGGAATAAAT[A/G]CATGTAGAAAATTTC | 15204 |
rs32971653 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56154992 | CACCAGCAACTCTGA[A/C]GGTTTCTGTGCTCTC | 15204 |
rs32971674 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | GRCm38.p3 | 7:56183431 | GTGAATGCTGGGTGT[C/T]AGGAGCCTCATTTGC | 15204 |
rs32971675 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | GRCm38.p3 | 7:56183443 | TGTTAGGAGCCTCAT[C/T]TGCTGCAATGCCCTG | 15204 |
rs32971676 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Herc2 | GRCm38.p3 | 7:56183522 | CTATAACCTGAGGCA[A/G]ATCATTGGGCTCAGT | 15204 |
rs32971677 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Herc2 | GRCm38.p3 | 7:56183532 | AGGCAGATCATTGGG[A/C]TCAGTGCCTGGGAAG | 15204 |
rs32971678 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | GRCm38.p3 | 7:56183557 | GGGAAGAGCATAAGC[C/T]GTGTGTGCTTTCAAA | 15204 |
rs32971679 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56183728 | AGTCACTATTATTTT[A/G]CTGCTTCTTTGTAGG | 15204 |
rs32971680 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56183786 | CTAAAAGTCCATTTA[C/T]TTTACATATATGTCA | 15204 |
rs32971681 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56183902 | AAGCAGAATGGGTAG[C/G]AAAAACCTTTGACAG | 15204 |
rs32971682 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Herc2 | Mm_Celera | 7:56184102 | AATAGTGTATTTTCA[A/G]TTATTTTGCAGAAAA | 15204 |
rs32971683 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Herc2 | Mm_Celera | 7:56184664 | AGTAATCCAGGTTGC[A/G]TGTGGAAGCAGAGAT | 15204 |
rs32971784 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56115873 | CTTTGTTTATTATGC[C/T]TTCAGTTTTGGGAGA | 15204 |
rs32971785 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Herc2 | Mm_Celera | 7:56115876 | TGTTTATTATGCTTT[C/T]AGTTTTGGGAGAGGA | 15204 |
rs32971786 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56116061 | TTAACATCAGGAGCC[A/G]AGGTTCTGACAGCAG | 15204 |
rs32971787 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56116490 | AGTTGGCTCTGTTGC[A/G]TTTGGGACTGTGTTG | 15204 |
rs32971788 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Herc2 | Mm_Celera | 7:56116497 | TCTGTTGCATTTGGG[A/C]CTGTGTTGCATCATG | 15204 |
rs32971789 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56118952 | TAAATATATTAAATT[A/G/T]TGAGTGCTTCCTTTT | 15204 |
rs32971790 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Herc2 | GRCm38.p3 | 7:56119034 | CGTCTTTTTATTTAG[G/T]GAGTGTGTTTTCCAT | 15204 |
rs32971791 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | GRCm38.p3 | 7:56119069 | ATGGCAGGTAGGTTC[C/T]CACATATGCCACACA | 15204 |
rs32971792 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Herc2 | GRCm38.p3 | 7:56119147 | TTTGAGTGCCTCTAA[A/G]TCTAGGCTGTTAAGA | 15204 |
rs32971793 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56119560 | TTGATATAATGTGCC[A/C]TTTTTATATGAATAG | 15204 |
rs32971984 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56137617 | TAGGGTAAAGCTTTA[C/T]AAATTTTTTCTCAAT | 15204 |
rs32971985 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56138006 | TTTGCTTTAGAAACC[C/T]GTTTATCAGATCAAT | 15204 |
rs32971986 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56138406 | TTGAGTTTTTGGATC[C/T]TACTAAGAGTCAGGG | 15204 |
rs32971987 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56138600 | AGCAGTGTGTGGAAT[A/G]TAGATAATGGGAATA | 15204 |
rs32971988 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Herc2 | Mm_Celera | 7:56138969 | AGCCCTAAGGCTGAT[C/T]GGTAGGTTGGAATTG | 15204 |
rs32971989 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56139005 | GGGCCCTTTAGGAAA[A/C]TGTGACTTACTTTCT | 15204 |
rs32971990 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56139019 | ACTGTGACTTACTTT[C/T]TCTCCTTAAAATAAA | 15204 |
rs32971991 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56139049 | AATTGTAGTAAAGTA[C/T]GCATAACGTAAAAGC | 15204 |
rs32971992 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56139752 | TTTGGAGGCCACCTA[C/T]TGGTGTTTCCAGGTT | 15204 |
rs32971993 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56139784 | TTTTGTACTGGAACA[A/G]GAATCAGAGTAGAAA | 15204 |
rs32972124 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Herc2 | Mm_Celera | 7:56104858 | GCTTTCCAGTTTTTG[C/T]CCATGAGTTTTATTT | 15204 |
rs32972125 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56104898 | TACTACTTTAGTCAG[A/T]GGCAGTCTTCTGTGT | 15204 |
rs32972126 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56104904 | TTTAGTCAGAGGCAG[C/T]CTTCTGTGTTCATCG | 15204 |
rs32972127 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56104924 | TGTGTTCATCGGGTG[C/T]TTAATCCCCAGGCTT | 15204 |
rs32972128 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Herc2 | Mm_Celera | 7:56105066 | TAAGTAAAATTTGTC[A/G]AATTACTTTACTATA | 15204 |
rs32972129 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56105132 | TAACTCAGACTTATA[A/G]GGTAACGCTTTTTTT | 15204 |
rs32972130 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56105259 | TTTCTTTCACAACCA[A/G]AAATGTTTACATCAT | 15204 |
rs32972131 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56105339 | ATCTGGGATACTGAA[A/G]AAAAAAGTCATTAAC | 15204 |
rs32972132 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56105353 | AGAAAAAAGTCATTA[A/C]CTGAAAATACCATTT | 15204 |
rs32972133 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56105390 | TAACATAATTAAATG[C/T]CAGAATTAGTGGGAA | 15204 |
rs32972294 | snp | A/G | 0.336735 | 0.234472 | synonymous-codon | Herc2 | Mm_Celera | 7:56184899 | AAATGGCCAGGGGGT[A/G]TGCCAGATTGAGTGT | 15204 |
rs32972295 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56185180 | TTTTAAACCAGTTTC[C/T]ATGAGGTTTAAATAG | 15204 |
rs32972296 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Herc2 | Mm_Celera | 7:56185262 | AAACATTTGGCCCTC[A/G]GAAAATTTCTCTCTG | 15204 |
rs32972297 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56185599 | TGTCTATTCTTTTTT[A/G]TTTGTTTTAAACAAT | 15204 |
rs32972298 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56185713 | TGGCATGTAGAGTTA[C/G]AGGACCTTGAGTACT | 15204 |
rs32972299 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56185774 | ATGTATGGCAGTGAA[A/T]GTCTCCTTGTATAGC | 15204 |
rs32972300 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Herc2 | Mm_Celera | 7:56186008 | GGCCTGTGGTAAGGT[A/G]CCCTCTTGGAGTGCT | 15204 |
rs32972301 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56187843 | ACCTTGTTTACTGAT[A/G]TATTGTCAGCACAAG | 15204 |
rs32972302 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Herc2 | GRCm38.p3 | 7:56187857 | TATATTGTCAGCACA[A/G]GTTGGGTTGGGGCCT | 15204 |
rs32972303 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56187912 | GTCCATGCTGGAGTA[C/T]AAAAATTATCATTGA | 15204 |
rs32972322 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | Mm_Celera | 7:56048266 | CAAGATAAAGACTTA[G/T]TGGGTTTTTCCTATC | 15204 |
rs32972323 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | Mm_Celera | 7:56048286 | TTTTTCCTATCAGAG[A/G]GACTGTTCAGTGAGA | 15204 |
rs32972374 | snp | A/C | 0.408163 | 0.193609 | missense | Herc2 | Mm_Celera | 7:56155142 | AGAAGTCAGCAAAAC[A/C]GGCCTTTGCAGGTGA | 15204 |
rs32972375 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56155156 | CCGGCCTTTGCAGGT[C/G]AGTATATAGTGCTCC | 15204 |
rs32972376 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56155352 | AGTGCTTCTGACTGT[C/T]AGTGTTTAATTTAAT | 15204 |
rs32972377 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56155419 | TCTATCTCTGGCTTA[G/T]GACACCATGGGTGTC | 15204 |
rs32972378 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56155695 | TCCAGCTTTTAGGAT[G/T]GTAAACACCTTTAAT | 15204 |
rs32972379 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56155742 | CTGAATGGCAGGCTC[C/G]TGGATATAAACAACT | 15204 |
rs32972380 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56155856 | ATTTAGGTGTTTTCA[C/T]TCTCTCAACCTACAC | 15204 |
rs32972381 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56155896 | TGCCTCCTGGGCCTC[C/T]TGCATATCCTGCTGG | 15204 |
rs32972382 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56156038 | ATGGCTCCAGTTATA[C/T]TAGATGCATTTGAGA | 15204 |
rs32972383 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Herc2 | Mm_Celera | 7:56156059 | GCATTTGAGAGAATC[C/T]CTCATAGGATTATTG | 15204 |
rs32972394 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Herc2 | Mm_Celera | 7:56085592 | CATCTTGCAGACAAG[C/T]GTTAATTGTAGCTTC | 15204 |
rs32972395 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56085997 | ACCTCGGTCCTAAGA[C/T]GCTCCAGGCAGACCT | 15204 |
rs32972397 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56086165 | TGAATAAAAGTAACT[G/T]GAATGAGCTAGTCAG | 15204 |
rs32972398 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Herc2 | Mm_Celera | 7:56086195 | GAGACAGTCTTTTTT[A/C]AATAAAACTGAACCC | 15204 |
rs32972399 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56086395 | GTTTTTCATTTTCTA[A/G]CCACATAGGCTGCAG | 15204 |
rs32972401 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Herc2 | Mm_Celera | 7:56086719 | ACACGAAGCAATAGT[A/T]AAGAAAAGAGGCTGT | 15204 |
rs32972402 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56086754 | TTGAGAGTGGTTTTA[C/T]CCTGGCTTAGGGCTC | 15204 |
rs32972403 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Herc2 | Mm_Celera | 7:56086778 | AGGGCTCTAGCTTCT[C/T]TCTTGGGGTCAAGAG | 15204 |
rs32972464 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Herc2 | Mm_Celera | 7:56119695 | TGTCATTTATTTCTT[A/T]AAAAATGGGAGTTGA | 15204 |
rs32972465 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Herc2 | Mm_Celera | 7:56119868 | ATTCTGATTATGGAT[C/T]TGAACTTTGTAATAA | 15204 |
rs32972466 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56120068 | AACCAAACTTGGGTC[C/G]TTGTAACTTCTGAGA | 15204 |
rs32972467 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56120173 | TGTCAGGGCTACTTA[C/T]CAGGTAGTGAGCTTG | 15204 |
rs32972468 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56120327 | ATTTTTTCTTACTGT[C/T]CTGTCTTCATTCACA | 15204 |
rs32972469 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56120339 | TGTCCTGTCTTCATT[C/T]ACATTGTTCAAAGTT | 15204 |
rs32972470 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Herc2 | Mm_Celera | 7:56120383 | AGTATAGAAACTATC[A/C]ATATTTTTTTCAATA | 15204 |
rs32972471 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56120531 | GAGTAGGTCCCAGGA[A/G]GTCTTCTGGGGACCA | 15204 |
rs32972472 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Herc2 | Mm_Celera | 7:56121381 | GATCTTTGGCATCTG[A/G]TCAGTTTGGAATGAG | 15204 |
rs32972473 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56121413 | GTGTCCTTGCTGCCT[G/T]CAGATCCATCTCATA | 15204 |
rs32972844 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56140370 | TTCTGCTTCACTCCT[G/T]CCCAGGAATATGGGT | 15204 |
rs32972845 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56140398 | GGTGCTCCATTTTGA[A/G]TGATTAGTGCAGCAG | 15204 |
rs32972846 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56140581 | ACAAATGACTTTAGG[A/G]TCTGTTTACATCTTT | 15204 |
rs32972847 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56140664 | TTTTTTTGTTACTGG[G/T]ATATAGGAGTACTAG | 15204 |
rs32972848 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56140747 | TAAGCTCTTCACAAA[A/T]TATGTTGGGTGATAG | 15204 |
rs32972849 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56140766 | GTTGGGTGATAGACC[C/T]TTGCACATCTGTAGA | 15204 |
rs32972850 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56145295 | ATCTTTGTGTCTGTC[C/T]TTCCTCCCTTCCCTT | 15204 |
rs32972851 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56145443 | TTTGAACTTGCAGTT[C/T]TCTTGAGTGCTGCCA | 15204 |
rs32972852 | snp | A/G | 0.42 | 0.183303 | intron-variant | Herc2 | GRCm38.p3 | 7:56145472 | CACATCTGCTGATGT[A/G]TCTATTAAAAACAGG | 15204 |
rs32972853 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | GRCm38.p3 | 7:56145653 | GGCTCATGTTACCAC[C/T]GTGCCCCCATGTACA | 15204 |
rs32972884 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Herc2 | Mm_Celera | 7:56105881 | CTGCTTTAAGTTTGT[A/T]GGTTTTTTGGGACAG | 15204 |
rs32972885 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56105891 | TTTGTAGGTTTTTTG[A/G]GACAGGGTTTAAAGC | 15204 |
rs32972886 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56105932 | TCTTGAACAGTGCAG[A/G]TGAATAAGTTATCAG | 15204 |
rs32972887 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Herc2 | Mm_Celera | 7:56106161 | ACTAACAAATCAGAG[G/T]TGACAAGACATGGTA | 15204 |
rs32972888 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56106175 | GGTGACAAGACATGG[C/T]ATATATTTTAATAGC | 15204 |
rs32972889 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56106256 | GAAGTTAATATTGAA[C/G]GATTTATGTTCTTCT | 15204 |
rs32972890 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56106379 | AGGCTCCACGCACTG[C/T]CTTGCTCTGACAGAA | 15204 |
rs32972891 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56106460 | CACTTTGCGTGTGAC[C/T]AAGCCAGAACCGACT | 15204 |
rs32972892 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56106633 | GGTTTGTGTGTCATC[C/G]TTCTATCTTGCAGTC | 15204 |
rs32972893 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56106662 | TCGTTCCACAACAAA[C/T]TACTACATTTAGTTC | 15204 |
rs32972924 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Herc2 | Mm_Celera | 7:56168989 | TGGCAGTGAGCCCTG[C/T]TGGCAGTCATCTGGG | 15204 |
rs32972925 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56169031 | GGTAATGTTTGGTGG[C/G]ATGTGTCAGGAAATA | 15204 |
rs32972926 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56169050 | TGTCAGGAAATACTC[A/T]GATTTGGAAGGTGGA | 15204 |
rs32972927 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56169113 | CAGCTTTCCTAATAC[G/T]CTCTCAAAATTCACT | 15204 |
rs32972928 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56169184 | GTATGTTGTGTATTG[C/T]TAGATTTTAAACAGA | 15204 |
rs32972929 | snp | G/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56169240 | CCAATTGATAAAAGG[G/T]TCACTGTTTTTTGTT | 15204 |
rs32972930 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56169297 | CTTATTATACTTCTG[A/G]CTAGAAATTTTTCTA | 15204 |
rs32972931 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56169525 | GGTCGTGATAAGGAG[A/G]GATGTGTTCCGGTAA | 15204 |
rs32972932 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56170067 | TCCCATGTAAGCATA[A/C]ATCAATTTCCCTACA | 15204 |
rs32972933 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56170139 | TTACATTTTGTATTT[A/T]AAAAAAATCTTATAG | 15204 |
rs32972974 | snp | C/G | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant | Herc2, Gm34121 | Mm_Celera | 7:56048321 | CAAATCTCCCACTAA[C/G]AGGGTGTCCAGTATG | 15204 |
rs32972975 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56052904 | TCAGTGTGATACTGG[C/T]ATTTTGCCCTTTTTA | 15204 |
rs32972976 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56053231 | TTCCTTGATTGAGAA[C/G]TTCCTCATTTCTTAC | 15204 |
rs32972977 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56053351 | TGGTAAGCTTATTTT[G/T]TTGGAAATACCCAAG | 15204 |
rs32972978 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56053579 | GCCACTGTTGTCCAG[C/T]AAAGTCTGAAAACTT | 15204 |
rs32972979 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56053637 | CTTGACTACTTTTTA[A/T]AGATATTAACATGCC | 15204 |
rs32972980 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56053701 | GCAGTGCCTGTTGCA[A/T]GCCAGTTACCTGTCT | 15204 |
rs32972981 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56054091 | CACTTATATATACAG[A/G]CATTGTGAACTGGGG | 15204 |
rs32972982 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Herc2 | Mm_Celera | 7:56054210 | CTAAGATGCTAAGCT[C/T]TCATTTCCTGAAGGA | 15204 |
rs32972983 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56054277 | CTGACTAGCTCATTC[A/C]AGTTACTTTTATTCA | 15204 |
rs32973004 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Herc2 | Mm_Celera | 7:56086857 | GTTTTCCTCAAGGGA[A/G]AATGTTGGTAGTAGT | 15204 |
rs32973005 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56086901 | CTGATCAGATATGAC[A/G]TAAGTACATAGCTTT | 15204 |
rs32973006 | snp | C/G | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56087133 | AGATGAGTGCACAGA[C/G]TGTCCCTGAAGTATT | 15204 |
rs32973007 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Herc2 | GRCm38.p3 | 7:56087316 | TGGCTGACCAGTTGT[C/T]ATAGCCCATGTGTTT | 15204 |
rs32973008 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56087640 | GAGTGTTTTTGAGTT[C/T]CCAGATCTTTGTTTT | 15204 |
rs32973009 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56087716 | GAATGAAAGCCTTAG[G/T]AAGAAGTTACCAGTT | 15204 |
rs32973010 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56087786 | TAAAGTCTCTTTATC[C/T]TTGATTTCACAAATG | 15204 |
rs32973011 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56087814 | ATGGAAAATCCCTTA[C/T]TCAGGGATACTTTGC | 15204 |
rs32973012 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Herc2 | Mm_Celera | 7:56087896 | TCTGTGTAAGATATA[C/T]ACGAAACAGAACTGA | 15204 |
rs32973013 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc2 | GRCm38.p3 | 7:56088042 | CTGGCACCCAACATT[C/T]CATGTAAGAGACACT | 15204 |
rs32973094 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56187917 | TGCTGGAGTATAAAA[A/G]TTATCATTGAAAGTT | 15204 |
rs32973095 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56187946 | TTACTCCTGCCTCTA[A/G]GCTATTAGCAGTTTC | 15204 |
rs32973096 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56188018 | ACAACGGGAGGCTGT[A/G]CCTTCATGAGAGAAG | 15204 |
rs32973097 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56188261 | ATTTTTATTTTTCCT[G/T]TATAATTTATGGTGT | 15204 |
rs32973098 | snp | C/T | 0.408163 | 0.193609 | synonymous-codon | Herc2 | Mm_Celera | 7:56188719 | AACAGTGGATGTAGC[C/T]ACACCATCTGTCCAT | 15204 |
rs32973099 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56189001 | TATACATTAAAAAAG[A/G]AAGACTTTATTGCAT | 15204 |
rs32973100 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56189135 | GGCTGAATGTAGTTA[A/C]AAACGCTACTCTACA | 15204 |
rs32973101 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56189743 | CATAAATGCTCAAAC[C/T]AGAGAAAAAGAGCAA | 15204 |
rs32973102 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Herc2 | Mm_Celera | 7:56189901 | TGCCAAGATCCTCCT[A/G]TCACTGGAAGGAAAC | 15204 |
rs32973103 | snp | C/G | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56189981 | TGTATGCCAGGTAGG[C/G]TGCTGTGTTGGCTTG | 15204 |
rs32973154 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56156100 | AGAAAATGTTTTACT[G/T]GTGTCTGGTTAGAGT | 15204 |
rs32973155 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Herc2 | GRCm38.p3 | 7:56156153 | AATGATGACACTGTA[A/T]GTTTATGTGGTTCGC | 15204 |
rs32973156 | snp | A/C | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56156168 | TGTTTATGTGGTTCG[A/C]GTTTCCTGCTCAGCT | 15204 |
rs32973157 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56156185 | TTTCCTGCTCAGCTC[A/G]TTAGGACGGCTAGCT | 15204 |
rs32973158 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56156282 | TGGGTGATCAGTTCA[C/T]TCCTGAAGGTCATGG | 15204 |
rs32973159 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56156297 | CTCCTGAAGGTCATG[G/T]CACTGCCTTCATGTT | 15204 |
rs32973160 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56156326 | TTGCAGAGATGACAT[G/T]GTCGGTGAAGAAGAG | 15204 |
rs32973161 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56156342 | GTCGGTGAAGAAGAG[C/T]CTGAGCTGGATCTGA | 15204 |
rs32973162 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Herc2 | Mm_Celera | 7:56156475 | TTCCCACCAAGACAA[A/G]CTGAGGCAGATACTA | 15204 |
rs32973163 | snp | A/C | 0.46281 | 0.131194 | intron-variant | Herc2 | Mm_Celera | 7:56156568 | GAAATGTTTTAAATA[A/C]ATTTGAGAGAAAGGA | 15204 |
rs32973234 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Herc2 | Mm_Celera | 7:56121525 | ATCCTTCATTTTTTA[C/T]TTTCTCTTCCCTTAC | 15204 |
rs32973235 | snp | A/C/G | 0.48 | 0.0979796 | intron-variant | Herc2 | GRCm38.p3 | 7:56125502 | AGGATGTCAAATCAA[A/C/G]TTTTTTACATTTTTA | 15204 |
rs32973236 | snp | G/T | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56126890 | TACATTTGAAAACAA[G/T]CTAGAAATTTGTAGA | 15204 |
rs32973237 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56127965 | AGATACGCCCTGTGA[A/G]CTACAGTAACAATTA | 15204 |
rs32973238 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56130091 | GTGTTCCTTGGTGGA[A/C]GTGCTGGTTTCTTTT | 15204 |
rs32973239 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56131257 | CCATAATAAAGATGG[C/T]GGCTTCTGGACTGTA | 15204 |
rs32973240 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Herc2 | Mm_Celera | 7:56131359 | GGCTTTTTTACTTTT[C/T]ATTCCATTGTTAAAA | 15204 |
rs32973241 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56131956 | TGCCCTTCTTAAGTG[C/G]CTGTTATGGTATGAC | 15204 |
rs32973242 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56132712 | GACAGCAAGCTGGCC[A/T]CCATGCCTGCTAAGT | 15204 |
rs32973243 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56132722 | TGGCCTCCATGCCTG[C/T]TAAGTTGCCTGTGAA | 15204 |
rs32973344 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56199237 | TCTTTGTTTGAACTC[C/T]TTTATCCACTGCAGT | 15204 |
rs32973345 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56199303 | GCCTTAGTTCTACTG[C/T]ATTAAATGTTCTCTC | 15204 |
rs32973346 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56199456 | TACTCATATGTAGTA[A/G]TGTGAGCAAGCTATT | 15204 |
rs32973347 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56199476 | AGCAAGCTATTGTTT[A/C]CTTTTTTTAAGTTAT | 15204 |
rs32973348 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56199514 | TTCTGCAGTAAAAAA[A/T]TGTATTAGAATATAT | 15204 |
rs32973349 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Herc2 | Mm_Celera | 7:56199543 | ATGTTTACTTTAGTC[A/G]CTCTAGGTACTATTT | 15204 |
rs32973350 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Herc2 | Mm_Celera | 7:56199547 | TTACTTTAGTCACTC[C/T]AGGTACTATTTACAG | 15204 |
rs32973351 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56199568 | CTATTTACAGATACA[A/G]GGTGTTCTTTCAGAG | 15204 |
rs32973352 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56199613 | AGTTTGTGATGCTCT[C/T]CCCCTAACTTAGTTT | 15204 |
rs32973353 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56199683 | TGGGTTCAGTGCTGG[C/T]TATTTCCTTCCTTGG | 15204 |
rs32973404 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56211836 | GTGATTTGTGATGTA[A/T]TGTAACCTAATTTTT | 15204 |
rs32973405 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56211865 | TTTCAAAACCTTCAA[A/G]AGAAAGGAGAAGTCT | 15204 |
rs32973406 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56211883 | AAAGGAGAAGTCTCC[A/C]TGATACCTTTTTGTT | 15204 |
rs32973407 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Herc2 | Mm_Celera | 7:56212452 | GCTCATAGGCCTTGT[A/G]AAAACATATCATATG | 15204 |
rs32973408 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56212465 | GTAAAAACATATCAT[A/G]TGTCTGGTTTGAAAC | 15204 |
rs32973409 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56212626 | AGATAGATAGATAGA[A/T]GTGATTAAATTTTGA | 15204 |
rs32973410 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56212669 | TAAGTGATTCTTCTT[C/T]ATTGACTTTATAATC | 15204 |
rs32973411 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56212695 | TAATCACCTAACTGA[C/G]AGAACATTTAGAGCC | 15204 |
rs32973412 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56212706 | CTGAGAGAACATTTA[G/T]AGCCACATGCTGAAT | 15204 |
rs32973413 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Herc2 | Mm_Celera | 7:56212818 | TGTTGTATTCTTTTA[C/T]AGTCCATGTGACCGC | 15204 |
rs32973644 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56156710 | ACTGTTAATGCAGTT[A/G]TCATCTTAAAAGATT | 15204 |
rs32973645 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Herc2 | GRCm38.p3 | 7:56156773 | GCCTAGCTGTGTAAG[C/G]TATGGTACAGGAAGC | 15204 |
rs32973646 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56156820 | GTAGAGATGTTGGTT[G/T]TTGAAAAGTAGAGTG | 15204 |
rs32973647 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Herc2 | Mm_Celera | 7:56157103 | AGCGTTATTTGACTA[C/T]CAATTCTCTTACCTA | 15204 |
rs32973648 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56157521 | GTTTGCTCTGAAGTC[A/G]CTCACCGGCACCTCT | 15204 |
rs32973649 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56157624 | CTATTGGTCTTGATG[C/G]CAGCTGAGTGTTTTT | 15204 |
rs32973650 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Herc2 | Mm_Celera | 7:56157754 | AGACGAGGAGGTGGT[A/G]GAAGATGTGGATGAT | 15204 |
rs32973651 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56158505 | TTGAGAACTGTTAAA[A/G]TTCATTTAGTCTAGA | 15204 |
rs32973652 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56159139 | TTATACTATAGATTT[A/C]GTGAGTTTTTTGTTT | 15204 |
rs32973653 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Herc2 | Mm_Celera | 7:56159365 | TTTGAATATGTTTAT[C/G]TCATTTAGGCTGCGG | 15204 |
rs32973684 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56106694 | TTCAGCCTTTTCTTC[C/T]GTACATTGTAGAGAC | 15204 |
rs32973685 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56108427 | ACTCCCAGCCATTAG[A/T]ATAGATTAGTAATTT | 15204 |
rs32973686 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56108428 | CTCCCAGCCATTAGT[A/G]TAGATTAGTAATTTT | 15204 |
rs32973687 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Herc2 | Mm_Celera | 7:56108488 | ATTTTTTTTAGGTGT[A/G]GAAGTGAGGTGGGAT | 15204 |
rs32973688 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Herc2 | Mm_Celera | 7:56108492 | TTTTTAGGTGTGGAA[A/G]TGAGGTGGGATGGTG | 15204 |
rs32973689 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56108661 | CCTACAGATTTCATG[C/T]TAGGTTCCTTTTTTC | 15204 |
rs32973690 | snp | C/G | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56108664 | ACAGATTTCATGTTA[C/G]GTTCCTTTTTTCCTT | 15204 |
rs32973691 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56108676 | TTAGGTTCCTTTTTT[C/T]CTTGCACAGAGCTTT | 15204 |
rs32973692 | snp | G/T | 0.444444 | 0.157135 | synonymous-codon | Herc2 | Mm_Celera | 7:56108787 | GCTGGATCTCCTGCT[G/T]CGTCAGGTCAGTGAG | 15204 |
rs32973693 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56108980 | TGTGAACTTCACCCT[A/C]TTCACTGAATTGATA | 15204 |
rs32973785 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56054445 | AGGTCTGCCTGGAGC[A/G]TCTTAGGACCGAGGT | 15204 |
rs32973786 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56054788 | AAGTGAGAGTCTCTG[C/T]CAGTAAAGAAAGGAT | 15204 |
rs32973787 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56054902 | ACACACACATGCACA[C/T]AAACATGTCAAAAGT | 15204 |
rs32973788 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56055160 | TGATGAAAGGCTAAG[A/T]GTATGTTTTTGAGCA | 15204 |
rs32973789 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56055195 | TCCAGAATAGAAATT[G/T]GTTGCTCTTTCTTAC | 15204 |
rs32973790 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Herc2 | Mm_Celera | 7:56055330 | TAGACTCAGGAAGTT[A/G]CCAACAAAATAATGA | 15204 |
rs32973791 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56055448 | CACAGTTCTGTGCCT[G/T]TCTGTTGTAATGTCA | 15204 |
rs32973792 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56055803 | ATCAAAAGGTGTATA[A/T]GCATGGACATTTAAT | 15204 |
rs32973793 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56055884 | CTTAAATAAAAGAAT[A/T]TGGTCAATGGTAAAT | 15204 |
rs32973874 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56170265 | CAGGTTTAGCAGCAA[A/G]TACCTTTATCTTCTA | 15204 |
rs32973875 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56170276 | GCAAATACCTTTATC[C/T]TCTACGAGTTCTAGT | 15204 |
rs32973876 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56170336 | TAAATTTTGGTTACT[A/G]AGAATGTTTTGTTTT | 15204 |
rs32973877 | snp | A/C | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56170475 | TAGCTACATGCCATC[A/C]CTGGTCGTGGTGTCA | 15204 |
rs32973878 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56170947 | CACTTAGTATCCTTT[C/T]CTAAGTGGTAGATGT | 15204 |
rs32973879 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56171158 | GGTTTCTTTAACTCC[A/T]TGCAATTCCATTTGT | 15204 |
rs32973880 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56171194 | CTTGGGCTATTCTAC[C/T]ATTGGTGCTCTATGC | 15204 |
rs32973881 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56171328 | ATGGATCTCTTCCTT[C/T]TTCTATAGTGTACAG | 15204 |
rs32973882 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56171397 | CAAGTTCTTTATTGC[A/C]ATATTAAGGAAAAGC | 15204 |
rs32973883 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56172778 | CCTGTCTGATACATT[A/G]TACTCTCATTGTAGG | 15204 |
rs32973884 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56145885 | TGTTTCAGGGCCAGA[A/G]CTGGCTGCTATGATG | 15204 |
rs32973885 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56146517 | ACTCTCTTACCTGGT[C/T]TGTATTTTTACTCTT | 15204 |
rs32973886 | snp | A/C | 0.444444 | 0.157135 | synonymous-codon | Herc2 | Mm_Celera | 7:56146581 | AATTGGTGAGCTGGG[A/C]GAGGATGGCTGGATC | 15204 |
rs32973887 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56146725 | AGACACAGAGGATGA[C/T]TCCGGTGGGTGACTC | 15204 |
rs32973888 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56146752 | ACTCACAAAGTCTTG[G/T]AGTTCAAGAGAGCAG | 15204 |
rs32973889 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56147341 | TGGTTTGTGTGGTTG[C/T]CCAAAGCCTGATAGT | 15204 |
rs32973890 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56147446 | GCAATGTATGGCCCC[A/G]CCTGCTTCCTTTAAG | 15204 |
rs32973891 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Herc2 | Mm_Celera | 7:56147887 | GTCTCATTTTTTTTT[A/T]AAAGGGTGGAATAGA | 15204 |
rs32973892 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Herc2 | GRCm38.p3 | 7:56147896 | TTTTTTAAAAGGGTG[A/G]AATAGATGGCTCAGT | 15204 |
rs32973893 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc2 | Mm_Celera | 7:56148216 | AAGGTAGGGACAGAA[A/G]TGATTGGGGTAGCTA | 15204 |
rs32973904 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56199762 | TTTGGACTTTTTTTA[A/C]ATTGTAAGTTGTTTG | 15204 |
rs32973905 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56199996 | TCATTTTAAATGTGT[A/C]GAACATAGTATTGAA | 15204 |
rs32973906 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56200035 | ATGAGGTAGGGCTTG[A/C]AAAAGTATTATTTTT | 15204 |
rs32973907 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56200458 | AACTTAAAAACTAAA[A/G]TGGCAGCTGGAAAAG | 15204 |
rs32973908 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56200548 | GGGCCCACCGGGCTC[G/T]AGCCAGTGGGGACAG | 15204 |
rs32973909 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56200593 | TAGGAACTCATTGGC[C/T]AACCAGCCGAGCTGA | 15204 |
rs32973910 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56200601 | CATTGGCCAACCAGC[C/T]GAGCTGAATTGATGA | 15204 |
rs32973911 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56200630 | GAGGCCAGGGAAACC[A/G]TAGTAGACAGTGCCT | 15204 |
rs32973912 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56200682 | CCTCTATACAGACAA[G/T]TAACTACACATGCAT | 15204 |
rs32973913 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56200709 | GCATACAAATAATGC[A/T]CACACACATGCAATA | 15204 |
rs32973944 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56190041 | CTTTGTAATATTTTA[A/G]TTGTCCAGATGTTTA | 15204 |
rs32973945 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56190100 | ATGAGTTGCAAGTCA[C/T]ATACCTTCACTGGGG | 15204 |
rs32973946 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56190156 | ATAAAATCCAACTGA[C/G]TATTGAAATATGAAT | 15204 |
rs32973947 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56190235 | CAGTATGAAAGAAGA[A/G]AAAGAATGAGTTGAT | 15204 |
rs32973948 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56190374 | CTCTGGTATCATGGT[A/G]GGATGCTGAGGCAGA | 15204 |
rs32973949 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56190435 | ACATGTTCTGCTGAC[A/G]CAGGGACACCCACTA | 15204 |
rs32973950 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56190528 | CACATGGTCTTTTGG[A/G]GAAGGTCCAAACCAT | 15204 |
rs32973951 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56190604 | GTGGATCTGATAGTT[A/G]TGCTTATATAGCGTA | 15204 |
rs32973952 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56190612 | GATAGTTGTGCTTAT[A/G]TAGCGTAAGAGCGAT | 15204 |
rs32973953 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56190627 | ATAGCGTAAGAGCGA[C/T]ACCTAAAACAGACAT | 15204 |
rs32974104 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56088072 | TCAGTCTTTATTGTT[C/T]ATGTGAGAGACATCA | 15204 |
rs32974105 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Herc2 | Mm_Celera | 7:56088200 | GAGTGACTGGAACTC[A/G]ACTTGTCACCAGTCC | 15204 |
rs32974106 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56088210 | AACTCGACTTGTCAC[C/T]AGTCCCTAAGGGTGG | 15204 |
rs32974107 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56088628 | TCTGTGTGCGTGAGA[G/T]AGAGAGTGTGTATTC | 15204 |
rs32974108 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56088809 | GATCTAATTCATGAT[G/T]ATTGTGACTTGACCC | 15204 |
rs32974109 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Herc2 | Mm_Celera | 7:56088861 | TGATAGAAAATATCA[C/G]CTGTTTTTTGTTATT | 15204 |
rs32974110 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56088949 | ATCCATCTGAACTGA[A/G]CACTTCTTGTGAGCC | 15204 |
rs32974111 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56089201 | TTACTAGTGCTATAA[C/G]AAAAACCTTGGACAG | 15204 |
rs32974112 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56089275 | TCTGCTACTTTGGAA[G/T]TGTGTCAACACAGTT | 15204 |
rs32974113 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56089386 | AGAATGCACCAGCAA[C/T]GATTCACTTTTGTAC | 15204 |
rs32974114 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56132768 | TGTATTCCTCCCTGA[A/G]ACTTGTCATACATAG | 15204 |
rs32974115 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Herc2 | Mm_Celera | 7:56132805 | AGGATGAGTTTCACA[G/T]AAGTCAGCAAAGGAG | 15204 |
rs32974116 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56132919 | TTGCTAATTCTTTCT[A/G]TAGCACAAGGTGATT | 15204 |
rs32974117 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56132976 | GAATTGATACAGCCA[C/T]TTGTGAAAGTTCCCT | 15204 |
rs32974118 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56133002 | TCCCTAGCACTTCAA[A/G]TCTAGATATCCAATA | 15204 |
rs32974119 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56133057 | TGATTGCTGGAGTGA[C/T]TAGCAGATTAGATTA | 15204 |
rs32974120 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56133103 | TAGGTCCTCAGTGAA[A/C]GCCTGCAGTAATGTT | 15204 |
rs32974121 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56133420 | GCTGTCTCTTGTCCG[C/T]ATGCTCAGTATCTTT | 15204 |
rs32974122 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56133586 | AGGGGAGCTTTTGTT[G/T]TGGTACCCGAGTCTT | 15204 |
rs32974123 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56133594 | TTTTGTTGTGGTACC[C/G]GAGTCTTCAGATGGT | 15204 |
rs32974184 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Herc2 | Mm_Celera | 7:56212926 | AGCAGCTGGAGACCT[C/T]TACACATGGGGCAAA | 15204 |
rs32974185 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56213062 | AGTGTTGACACGGGA[A/T]AGGGGCAGCTTGTCT | 15204 |
rs32974186 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Herc2 | Mm_Celera | 7:56213409 | TGATCATTAGTTACT[A/G]TCAGCTGAACCCTGC | 15204 |
rs32974187 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56213620 | TATTTTCGATTTATG[C/T]GTCCCAGATCTCCAG | 15204 |
rs32974188 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56213777 | TGTAATCCAGATGCG[G/T]TTCAAAGAGCCTGTG | 15204 |
rs32974189 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56213836 | CATGCCGAACTAACA[C/T]GGGTCCCACTTACTT | 15204 |
rs32974190 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56214017 | TAATTTCTTAAAGCT[A/G]TCAGGTGATCTGACT | 15204 |
rs32974191 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56214033 | TCAGGTGATCTGACT[A/G]TCTTTGGGAAGTGGC | 15204 |
rs32974192 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Herc2 | Mm_Celera | 7:56214196 | CTTACTGTACAGATG[C/T]GGAACAGAGTCTTGC | 15204 |
rs32974193 | snp | A/G | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56214212 | GGAACAGAGTCTTGC[A/G]ACACAGGCATCCTGG | 15204 |
rs32974314 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56109069 | CTTGTTTTGTTTTTC[C/T]GAGAAGTCAGTCATT | 15204 |
rs32974315 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56109070 | TTGTTTTGTTTTTCC[A/G]AGAAGTCAGTCATTG | 15204 |
rs32974316 | snp | A/C/T | 0.408163 | 0.193609 | intron-variant | Herc2 | GRCm38.p3 | 7:56109177 | GTATGGAGAAATGCC[A/C/T]GAGACAGTAGAAGAA | 15204 |
rs32974317 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56109211 | GAGGGGTAAACTCCA[G/T]TTGACAGACCATTGT | 15204 |
rs32974318 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56109227 | TTGACAGACCATTGT[C/T]CCCTGGATTGTTTTT | 15204 |
rs32974319 | snp | C/G/T | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56109311 | TTCCTCACATGGGTA[C/G/T]GAAAATCACCCAGCC | 15204 |
rs32974320 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Herc2 | Mm_Celera | 7:56109321 | GGGTATGAAAATCAC[C/T]CAGCCTTTCTACTAG | 15204 |
rs32974321 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56109553 | TTAGGAAATGGTATG[A/G]TTTTATGATTATAAA | 15204 |
rs32974322 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56109617 | AGTATAATTATTTTT[A/T]AATTTTTCTCTAGTA | 15204 |
rs32974323 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56109684 | TTGTTTTCCCAGTAG[C/T]CAGTTGACTTTGTGA | 15204 |
rs32974474 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56200776 | ATAAAAATCATGTGA[C/T]TATCTTCCTCTTCTG | 15204 |
rs32974475 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56200820 | TACCCATCTACTAAT[A/C]AAATATATGTTCCAA | 15204 |
rs32974476 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56201103 | AGTCTGTCCCTAGTT[A/T]TAATGTCAACCCACA | 15204 |
rs32974477 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56201159 | CAAAAGTTCATACAA[C/T]GCGATTGTGTTACCC | 15204 |
rs32974478 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56201458 | TGTAAGTTACAGTTC[A/G]TCTTGGGGTTTTACT | 15204 |
rs32974479 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56201888 | AACAGCTCAGCCCCG[G/T]GGGGTGGTTCTCTGG | 15204 |
rs32974480 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56201907 | GTGGTTCTCTGGCCG[G/T]TTAGTCCATGGGCAG | 15204 |
rs32974481 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56201959 | GCTGGGCAAGATGGC[C/G]AGCCTCAGGCTGTGA | 15204 |
rs32974482 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56202044 | TGCTTTGCTGAACGG[C/G/T]GACTTTCACTTGCTC | 15204 |
rs32974483 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, intron-variant | Herc2 | GRCm38.p3 | 7:56202156 | CACAGAGAGGCGCCA[C/T]GATCCTCTCACTGTC | 15204 |
rs32974504 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56222834 | TTTCAGAAATAGACT[A/G]TATAAAACAGCGGCA | 15204 |
rs32974505 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56223011 | AGCTCGCGCTCTCTC[G/T]ATCTGACAGTTGTAC | 15204 |
rs32974506 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Herc2 | Mm_Celera | 7:56223012 | GCTCGCGCTCTCTCT[A/C]TCTGACAGTTGTACA | 15204 |
rs32974507 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56223075 | GCAGTCTTGGGGGAT[A/G]GCAGCACTCATGGGC | 15204 |
rs32974508 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56223276 | TTCTATGTGGCCTTT[G/T]TATATTTGTTATACA | 15204 |
rs32974509 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56223342 | TTACATGTAACAGTT[C/T]ACATTCCTGTGAGCC | 15204 |
rs32974510 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56223684 | TCCTGATGGTGATTA[C/G]ATGACGAGAGTTTTT | 15204 |
rs32974511 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Herc2 | Mm_Celera | 7:56223943 | GTTTACAAGACAAGG[A/G]AAACTGTACATTCCT | 15204 |
rs32974512 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56223989 | CTTAGACAGACCTAC[A/G]GGCTCCTTGGAGCCA | 15204 |
rs32974513 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56224195 | AAAATGGCCAATATG[C/T]ATGAGAAAAAACTGA | 15204 |
rs32974524 | snp | C/T | 0.486111 | 0.0821678 | synonymous-codon | Herc2 | GRCm38.p3 | 7:56191197 | AGCCTTGATGCCAGC[C/T]GGCATGCTCGCCCCA | 15204 |
rs32974525 | snp | A/G | 0.142012 | 0.225474 | missense | Herc2 | Mm_Celera | 7:56191207 | CCAGCCGGCATGCTC[A/G]CCCCAGTGGAATGCC | 15204 |
rs32974526 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Herc2 | GRCm38.p3 | 7:56191421 | TTTATCTAGGGAACC[C/G]TACTTCTTCTGTCAC | 15204 |
rs32974527 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56191450 | ACCTCATTTTGTGTC[C/T]GCTATCTGATTTTGA | 15204 |
rs32974528 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56191451 | CCTCATTTTGTGTCC[C/G]CTATCTGATTTTGAG | 15204 |
rs32974529 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56192277 | AGGTGGCCATAAAAG[C/T]CTTTTTCATTGAGAT | 15204 |
rs32974530 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56192447 | CAGGGTTGTCAGTGA[A/G]CTTGCTATGTGAGTA | 15204 |
rs32974531 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56192566 | CTTGGATATTTTGTA[C/G]TATTGGTTCTTCCCA | 15204 |
rs32974532 | snp | A/C | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56193048 | CAGGATCTCTTTGTG[A/C]GCAGAGCAGCCACTC | 15204 |
rs32974533 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56194003 | GCTTCACGTGGCATG[A/G]CGTCCTTCTCACTCA | 15204 |
rs32974714 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc2 | GRCm38.p3 | 7:56159493 | CATTGCTCAGGGTGA[A/G]CCGTATTCATGCTTT | 15204 |
rs32974715 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Herc2 | GRCm38.p3 | 7:56159567 | TGAGTTGATAGATGC[C/G]CCTGTCCTCTGGGAG | 15204 |
rs32974716 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56159629 | GGCTTAGTAAGATCT[C/G]CTTATTAGAGACCAG | 15204 |
rs32974717 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56159704 | AAGTGCAGATAGAGC[A/G]TGAGCTAGGATTGGA | 15204 |
rs32974720 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Herc2 | GRCm38.p3 | 7:56159979 | GGAAAGACAGGACAA[A/G]CACCATAATTATTTT | 15204 |
rs32974721 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Herc2 | GRCm38.p3 | 7:56160035 | TTTCACAATGAATTG[A/G]TGGTCTGCTGCTTAT | 15204 |
rs32974722 | snp | G/T | 0.32 | 0.24 | intron-variant | Herc2 | GRCm38.p3 | 7:56160082 | CTTTGGTTTGCTTAT[G/T]ATCACCATGATGAAT | 15204 |
rs32974723 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Herc2 | Mm_Celera | 7:56160127 | GATATGTTTCCACTG[C/T]TCCTCTTTTTGATGA | 15204 |
rs32974764 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56214234 | GCATCCTGGGGCAGA[A/C]TCAGACCAGGTGGTT | 15204 |
rs32974765 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56214453 | ACAGCTTAACTTGGG[C/T]TATATAATGAGACTC | 15204 |
rs32974766 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Herc2 | Mm_Celera | 7:56214505 | AAAATCCACTGCTTC[A/C]CTCACACAGAGTGCT | 15204 |
rs32974767 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56214547 | TCAGGGTGGCACCCA[C/T]TTCTGTCACCTGTAG | 15204 |
rs32974768 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56214573 | TGTAGCCCTTTCCAT[C/T]TTCTAGTACAGGTAT | 15204 |
rs32974769 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56214753 | ACTAGTTAAGGGAAT[C/T]GGGTTTTAGTTAATG | 15204 |
rs32974770 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56214808 | GTAGGAAAGCATACA[C/T]AGATACCACACGAAG | 15204 |
rs32974771 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56214870 | TGACCAGATAAGTGA[G/T]GCCTGACAGGATCCT | 15204 |
rs32974772 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56214973 | GTGTGTTAATTCTGT[A/T]GACCTGATCAGAGGA | 15204 |
rs32974773 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56215054 | TCCTTGTGAGTCTCC[A/G]GGTCTGTGAGGAAAA | 15204 |
rs32974804 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56055986 | TTGCTATTTTTGTAT[A/G]TAATATTTTGTGGGG | 15204 |
rs32974805 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56056118 | TCAAGTTTAAGGAAC[A/G]CACCCAAAGGACAGT | 15204 |
rs32974806 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56056171 | ACTGATAATCTCATT[C/T]TTAAACAGACAAAAC | 15204 |
rs32974807 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56056488 | CCTATTTTTTTTTTT[C/T]CCAAAACTCTTTTTT | 15204 |
rs32974808 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56059824 | CCAGGAGGAATGAGC[A/G]GAGAAAGGAAGTTCT | 15204 |
rs32974834 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56089841 | TACAAAATTTAGTAC[A/C]AAGACACATAGAAAG | 15204 |
rs32974835 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | Mm_Celera | 7:56092274 | TATTCTTAATTTGTT[A/G]ACTTAAGATTCTAAA | 15204 |
rs32974836 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56092283 | TTTGTTAACTTAAGA[G/T]TCTAAAAGTTTTATG | 15204 |
rs32974837 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56093308 | ATGAGACTGTTTTTA[C/G]AAGAGTTAGAAATAT | 15204 |
rs32974838 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56093520 | GGTTTAATACCTGGG[A/G]CTGCAAAGATAAATA | 15204 |
rs32974839 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56094020 | GTTTGGCTGTCTTAA[C/G]AGTTCATAAAGTACT | 15204 |
rs32974840 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56094138 | TGTATAATCAACACT[A/G]TTCTTTGATGGCTAA | 15204 |
rs32974864 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56133627 | GTTCCCTTAACAGAT[C/T]CTAAGTAAATCCAAG | 15204 |
rs32974865 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56133660 | GCGTGACTCACAGGC[C/T]CATTCGGCTACATTA | 15204 |
rs32974866 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56133836 | ACCTACCTCTGAGGG[C/T]CTCCCACTGGGCTCA | 15204 |
rs32974867 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56133958 | CCAAATCAGACCACA[C/G]AGACTTGTGAGCCTG | 15204 |
rs32974868 | snp | A/G | 0.408163 | 0.193609 | synonymous-codon | Herc2 | Mm_Celera | 7:56134612 | GTGGCTGCAGTCATC[A/G]ATTTTTTCTGGGGGT | 15204 |
rs32974869 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56134618 | GCAGTCATCGATTTT[C/T]TCTGGGGGTCTGCAG | 15204 |
rs32974870 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56134765 | TCATTCTCAGGCTTT[C/T]CTGCAAGCCATTGCA | 15204 |
rs32974871 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56134850 | CATTCTGTATCTTCA[A/G]CATAGCACAGCTTTG | 15204 |
rs32974872 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | GRCm38.p3 | 7:56135174 | TTTAGGTACAGACCT[C/T]AGTATTCATGTGTTT | 15204 |
rs32974873 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56135415 | GAGTGGACTTTAATT[C/T]TTTTTCTGTGTTGTG | 15204 |
rs32974924 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56109698 | GTCAGTTGACTTTGT[C/G]ACCATTGCTAATTTA | 15204 |
rs32974925 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56109728 | ACACTGTCTTCTGAT[C/G]AGATCACTTCCTCAG | 15204 |
rs32974926 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56110147 | TCTCTCTTTATATCA[A/G]TGAATTACCTGGTCT | 15204 |
rs32974927 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Herc2 | GRCm38.p3 | 7:56110291 | CGACAGATACGGGAA[A/G]GCAAACACAGAAAGG | 15204 |
rs32974928 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56110457 | CAGGTTAGTTGAGTT[C/T]AAATCAATATGTTGG | 15204 |
rs32974929 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Herc2 | Mm_Celera | 7:56110619 | TAAAATGTAACTTGA[A/G]TTTATGGATGTTACT | 15204 |
rs32974930 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56110761 | TTCATGACTTCTTTG[A/G]TAGTTTTAAATCTTT | 15204 |
rs32975034 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Herc2 | Mm_Celera | 7:56202259 | CACTTGTGCTCCATA[A/G]AAGGAGTTGTTAGCA | 15204 |
rs32975035 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56202411 | TGTGATGTGTGCTTC[C/G]TACTATCAGAGAGGG | 15204 |
rs32975036 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Herc2 | Mm_Celera | 7:56202466 | TGCCCTGGTAGTTGG[A/G]GAACCATAGGTGTGT | 15204 |
rs32975037 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56202583 | TGGACTGCTGTGTCT[A/G]GAGGGTGGACAGAAT | 15204 |
rs32975038 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56202646 | AGTGTGTGGTCTTGT[A/G]TACTCTGCCTCGCTC | 15204 |
rs32975039 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56202656 | CTTGTGTACTCTGCC[G/T]CGCTCCATGAGGTCA | 15204 |
rs32975040 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56202676 | CCATGAGGTCAGGAA[A/G]AGTGGTCTAATAAAC | 15204 |
rs32975041 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56202713 | AAAACTTTGAACATT[A/G]TAGAGTTGTTAATGC | 15204 |
rs32975042 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56202840 | TATGTATGTGTGTAT[A/T]TGTTACTCGCCCTCC | 15204 |
rs32975043 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56203146 | GATAAATGTCTGTCA[A/G]AAGAGTTCTAGTAGT | 15204 |
rs32975154 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56224544 | AGTCCTATACACAGC[A/T]CATTTTCCTGGGGAG | 15204 |
rs32975155 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Herc2 | Mm_Celera | 7:56224942 | GAAAATCTGAAAAAT[A/G]GGTGTCTATAAAATC | 15204 |
rs32975156 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56225506 | GCTACAGATGGTAAA[A/G]TTTTGCTGGAGGACT | 15204 |
rs32975157 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56225812 | TTAGAGAACCTTGGT[A/T]TAGGTATAAGTTCTG | 15204 |
rs32975158 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56225847 | TCTGTCTCAGACCGT[A/T]AGAAGGACCATGTAG | 15204 |
rs32975159 | snp | A/G/T | 0.391111 | 0.206368 | intron-variant | Herc2 | GRCm38.p3 | 7:56227349 | ATGCTATATGCTTTC[A/G/T]TTGACATGCCTCATG | 15204 |
rs32975160 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc2 | GRCm38.p3 | 7:56227395 | ACATACCTGAAACTC[A/G]GGAGTGCATGGAGAG | 15204 |
rs32975161 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Herc2 | Mm_Celera | 7:56227412 | GAGTGCATGGAGAGA[A/G]ATGGCATTGGCAGTA | 15204 |
rs32975162 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56228195 | CTTGCTTTTTATGCC[C/G]TTTAGGGTTTAGGGT | 15204 |
rs32975163 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56228890 | GGATATCAGGCCTTC[A/G]TGCCCCTATATACTT | 15204 |
rs32975224 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Herc2 | GRCm38.p3 | 7:56173023 | GATCAGATTTTAGAG[A/G]TGGGTGGAGTATTCT | 15204 |
rs32975225 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Herc2 | Mm_Celera | 7:56174343 | GTGGTAGTGTTCTAG[A/T]TGGCTGGCTTAGTGA | 15204 |
rs32975226 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Herc2 | Mm_Celera | 7:56174355 | TAGATGGCTGGCTTA[G/T]TGATACTTTTTTCTT | 15204 |
rs32975227 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Herc2 | Mm_Celera | 7:56174376 | CTTTTTTCTTTCTCT[C/T]CTGGTAGTTTTGGAT | 15204 |
rs32975228 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56174449 | CATGTGTTGTTGTTC[C/T]TCTCCCTTTCTTCTT | 15204 |
rs32975229 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56174513 | TCTGGGGTGAAACTT[C/T]CTTCTTCCTCTGTGT | 15204 |
rs32975230 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56174559 | CTTTTTTTTGCACTA[C/T]TGGCCTAATTATCAT | 15204 |
rs32975231 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56174570 | ACTATTGGCCTAATT[A/G]TCATTGAATTGTTAT | 15204 |
rs32975232 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Herc2 | GRCm38.p3 | 7:56175609 | AATGTCTTGACTGTG[A/G]TATACTCTGCAGATT | 15204 |
rs32975233 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56175712 | TCTCACACTAAGTTT[A/G]GATCCTTCTTAGCTA | 15204 |
rs32975264 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56215101 | TGGACACTGGTAGTG[A/T]CATGTCAGTCCCAGG | 15204 |
rs32975265 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56215210 | TTAACGTTGGTTAGA[C/T]TAGATGTTAATATTG | 15204 |
rs32975266 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56215415 | TCAGTTTTCTGTCGC[C/T]CTTACCAAGTCTGGA | 15204 |
rs32975267 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56215476 | AATCCCACGAATACC[A/G]TATTTAAAAGGTGTA | 15204 |
rs32975268 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Herc2 | GRCm38.p3 | 7:56215690 | GCCCCTAAGACCATC[A/G]ACACTATTTTAATTG | 15204 |
rs32975269 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56215723 | GTCTTGTTAACTCTG[A/T]GACAGGCTGTGATTT | 15204 |
rs32975270 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Herc2 | GRCm38.p3 | 7:56216007 | TTCAAGGCTGATGTT[A/C]CAGAGCTGAGGCCTG | 15204 |
rs32975271 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56216031 | AGGCCTGTAACTCTA[A/G]GTTTCTCTCACATAA | 15204 |
rs32975272 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56216125 | ACCCTCAGGAATATG[C/T]TGTGTTGTATGGCTT | 15204 |
rs32975273 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Herc2 | Mm_Celera | 7:56216463 | CAAGGGACAAAATGT[C/T]CATGGGAGCTTACCA | 15204 |
rs32975284 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Herc2 | Mm_Celera | 7:56148549 | TCTAATTTTTTAAAA[G/T]AAAAAAGAATGTGAT | 15204 |
rs32975285 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Herc2 | Mm_Celera | 7:56148745 | AGTCCATGCTGACAT[C/T]ATGCAGAGCGAGGCC | 15204 |
rs32975286 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56148851 | ATTATGGGACACAGA[A/G]CCTCAGCATGGATAT | 15204 |
rs32975287 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56148889 | AAATCTCTCATGTTT[C/G]TGTGTTGGTGGGCTG | 15204 |
rs32975288 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56148994 | TAGAAACAAGGTATG[A/G]TAAACAACAGGAAGT | 15204 |
rs32975289 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56149332 | GGTCCACAGAGCCGT[G/T]TGCTCCTCACTGAGC | 15204 |
rs32975290 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56149421 | TCTCTGCATCTCTCT[A/G]CTTGTAGTCTGCGTG | 15204 |
rs32975291 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56149492 | AGCTCACCCAGCCCA[G/T]CATCTCATCTCAGCT | 15204 |
rs32975292 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56149664 | CATACGTAACTGTTA[A/G]CATGTTTGCGAATGT | 15204 |
rs32975293 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56149787 | GATATGTTTGTCATT[A/G]CTGAGTGTTCTAGTC | 15204 |
rs32975324 | snp | A/C/G | 0.497778 | 0.0332592 | intron-variant | Herc2 | GRCm38.p3 | 7:56160129 | TATGTTTCCACTGCT[A/C/G]CTCTTTTTGATGATC | 15204 |
rs32975325 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56160164 | GGTCCTCTTGTGTGA[A/G]CATTATAATCTGTAG | 15204 |
rs32975326 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Herc2 | GRCm38.p3 | 7:56160204 | GTGTCTTGTGTGAGC[A/G]TTATAATCTGTAGGT | 15204 |
rs32975327 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Herc2 | GRCm38.p3 | 7:56160280 | GTGTCTTGTGTGAGC[A/G]TTATAATCTGTAGGC | 15204 |
rs32975328 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Herc2 | GRCm38.p3 | 7:56160622 | GTGTCTTGTGTGAGC[A/G]TTATAATCTGTAGGC | 15204 |
rs32975329 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56160582 | CAGTGTCTTGTGTGA[A/G]CATTATAATCTGTAG | 15204 |
rs32975330 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Herc2 | Mm_Celera | 7:56163165 | ACAGTGTCTTGTGGA[C/G]AAAGATGATACAGGC | 15204 |
rs32975331 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Herc2 | GRCm38.p3 | 7:56163197 | CATGTATGTATGTAT[C/T]CCCAGAGACGTTTGC | 15204 |
rs32975332 | snp | C/T | 0.5 | 0 | intron-variant | Herc2 | GRCm38.p3 | 7:56163232 | CCTTAGTCTAAATAC[C/T]ACTTACCTTAATTTC | 15204 |
rs32975333 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56163676 | ACATTTTTTTCTGAA[A/G]AATAGAGAATGCTAT | 15204 |
rs32975624 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc2 | GRCm38.p3 | 7:56203169 | CTAGTAGTAGTAGTA[G/T]TTGTGCTGGTCTCAC | 15204 |
rs32975625 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56203206 | GAGATGGAAGTCCAG[C/T]GGGCTGCGTGTATGC | 15204 |
rs32975626 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56203257 | TCATTAAGTTGCTCC[A/G]TCTCCTGCTCTTTTA | 15204 |
rs32975627 | snp | G/T | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56203295 | GTTATGCAGCTCCAC[G/T]GATCCTTGGGTGTGA | 15204 |
rs32975628 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56203317 | TGGGTGTGACCAGGT[C/T]GCTCCATTGCTTCCT | 15204 |
rs32975629 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56203365 | GGTCATGCTGAATTG[C/T]TTACAAATGCCCCTG | 15204 |
rs32975630 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56203414 | TCTGCCATTGCCTAA[C/T]TACCTGCCATACTCA | 15204 |
rs32975631 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56203502 | GCATCCCAGTTGTGT[A/G]CATAATCATTTCCCC | 15204 |
rs32975632 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56203546 | TTCTTTTGGGGAAGT[A/G]TGTATGTGTGTGCCT | 15204 |
rs32975633 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56203646 | TGTGAATGTAAGCTT[C/G]AGAGGTCTTGGGCTG | 15204 |
rs32975744 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56194550 | ATCCCAGTTCTCCCC[A/G]TAGTTTCTTTTATCC | 15204 |
rs32975745 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56195260 | TAAAGAAATTTTCCT[A/G]ATTTTTCTCCTGAGC | 15204 |
rs32975746 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56195728 | TTGATGTCTTATCCT[C/T]ATGTAATATTTGGGA | 15204 |
rs32975747 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56195751 | ATTTGGGATTCGTAA[A/G]TTAATTTATATAACT | 15204 |
rs32975748 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56195858 | AATAGAGGAGAATAA[C/T]CCTGGAAAACAGAAA | 15204 |
rs32975749 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56195893 | GATTTTTCTTTGTAT[A/G]TTAAATTTGGGGACT | 15204 |
rs32975750 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56196495 | AGGTCTAAAATAAAA[C/T]CTTTGTTTCTTAACT | 15204 |
rs32975751 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Herc2 | Mm_Celera | 7:56197068 | TAGGTGGCAGACATG[C/T]TGTTGGAGCTCTGTG | 15204 |
rs32975752 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56197251 | TGCAAGGTCCGCTGT[C/G]TGTAGAAGGGCTGTT | 15204 |
rs32975753 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56197283 | TGTAGCCACTTCCAT[A/G]GGAATAGTCATTTCC | 15204 |
rs32975774 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56135875 | TTTTAGTAAGTTGAT[A/T]GGAAAAATTTATAAC | 15204 |
rs32975775 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56136008 | TTTCCCTCTATCTTA[C/T]TTATTGTGCTGGGTA | 15204 |
rs32975776 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc2 | Mm_Celera | 7:56136116 | TGAGATGATTGTAGT[A/G]ATAAAGCAGGAGAGT | 15204 |
rs32975844 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56216528 | TGAGCAGTTTGCCAT[C/T]AGGCCCCAGCTTCTT | 15204 |
rs32975845 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56216692 | TGATCTCTGTCTCTG[C/T]GTACAGATGAGGTAG | 15204 |
rs32975846 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56216768 | TCCTCACAAGATCTA[A/G]GAAGGAATCTAGCAC | 15204 |
rs32975847 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Herc2 | Mm_Celera | 7:56216877 | ACATACAGAAAAAGA[A/G]CAGTACCCATGCACC | 15204 |
rs32975848 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc2 | Mm_Celera | 7:56216898 | CCCATGCACCCAAGG[A/G]CTCTCATGTCCAGGC | 15204 |
rs32975849 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc2 | GRCm38.p3 | 7:56216920 | TGTCCAGGCTAGTGA[C/T]ACCTCCAATCAGGCT | 15204 |
rs32975850 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc2 | Mm_Celera | 7:56216972 | CTCTCTGGAGAAGGT[A/G]GAGGATAGTGAAGGT | 15204 |
rs32975851 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Herc2 | Mm_Celera | 7:56217052 | TAGGCACCATCTGCC[A/G]CCAAGACCACCAGCA | 15204 |
rs32975852 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Herc2 | Mm_Celera | 7:56217084 | CAGCACCACTTTGAG[C/T]AGCACTAGCAGTTGG | 15204 |
rs32975853 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56217109 | AGTTGGGCTTGAATG[C/T]AGTGGTGTACCTGGT | 15204 |
rs32975954 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Herc2 | Mm_Celera | 7:56175790 | ATATGAGTTACATGT[A/G]CAAGTATGATGTCTT | 15204 |
rs32975955 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Herc2 | Mm_Celera | 7:56175806 | CAAGTATGATGTCTT[C/G]AATTAGTCTTACATT | 15204 |
rs32975956 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Herc2 | GRCm38.p3 | 7:56175817 | TCTTGAATTAGTCTT[A/T]CATTTTGGTAGTTTT | 15204 |
rs32975957 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Herc2 | Mm_Celera | 7:56175844 | TTTTGGTTAAGCTCA[C/T]TGACCCTCATGTTGA | 15204 |
rs32975958 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Herc2 | GRCm38.p3 | 7:56176010 | CCATTTTGGAGTCTT[A/G]GTTTTCTTTCCAAAT | 15204 |
rs32975959 | snp | C/G | 0.375 | 0.216506 | intron-variant | Herc2 | GRCm38.p3 | 7:56176197 | TAGAATCTTTTCCTA[C/G]CATTTCATCTCATTG | 15204 |
rs32975960 | snp | A/C/G | 0.152778 | 0.230321 | intron-variant | Herc2 | GRCm38.p3 | 7:56176250 | AATGTTAGCTTGTGG[A/C/G]GAAGTCATGTTGTAC | 15204 |
rs32975961 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Herc2 | GRCm38.p3 | 7:56176260 | TGTGGAGAAGTCATG[C/T]TGTACTGCTGTGTTA | 15204 |
rs32975962 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Herc2 | Mm_Celera | 7:56176279 | ACTGCTGTGTTATGG[G/T]GTTTGAATTTGTTTT | 15204 |
rs32975963 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Herc2 | GRCm38.p3 | 7:56176477 | TTGGATTTACGTTCA[A/G]GGAAAAGTGACTGAA | 15204 |
rs32976074 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc2 | Mm_Celera | 7:56163719 | TTAGGTGTACTTGAC[C/T]TGACTTTGCATTTCA | 15204 |