SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs265585515 | snp | C/T | | | intron-variant | Dtx4 | Mm_Celera | 19:12488990 | TATAAAAGGCAGAGT[C/T]GAAAGCCTGGCAGAG | 207521 |
rs265608867 | snp | A/T | | | intron-variant | Dtx4 | Mm_Celera | 19:12481224 | AGAAGCCTTATCTCA[A/T]CCCCCTACAATGGAT | 207521 |
rs265735561 | in-del | -/CAA | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Dtx4 | Mm_Celera | 19:12501294 | CCGGCGCCGCCGCCT[-/CAA]CCGGGTCTCAACCGC | 207521 |
rs265797936 | snp | A/G | | | intron-variant | Dtx4 | Mm_Celera | 19:12477976 | AGTACTACAAGGGAT[A/G]CTGGAAAGACACAGA | 207521 |
rs265835985 | snp | C/T | | | intron-variant | Dtx4 | Mm_Celera | 19:12499367 | ACCATGCATCACTTC[C/T]AGATCCTCCACCAAA | 207521 |
rs265846116 | snp | A/T | | | intron-variant | Dtx4 | Mm_Celera | 19:12490417 | GGAAACAAAACTTAT[A/T]CCAAGTGGCACAGCA | 207521 |
rs265886763 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Dtx4 | Mm_Celera | 19:12467728 | CAGCACCAGGGAAGT[A/G]GGTTAGGGACACTTG | 207521 |
rs265931892 | in-del | -/AATCAGAACAAAATGA | | | intron-variant | Dtx4 | Mm_Celera | 19:12486527 | TATTATGGCTCTGAC[-/AATCAGAACAAAATGA]ATCAGAACAAAATGA | 207521 |
rs265932100 | in-del | -/T | | | intron-variant | Dtx4 | Mm_Celera | 19:12488883 | GGCAACTGTTTACAC[-/T]TTTATTTTTCCAATT | 207521 |
rs266015690 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Dtx4 | Mm_Celera | 19:12469465 | CCTGTGGTCCCCAGT[A/G]CCCTCCCTCCTCAGT | 207521 |
rs266038541 | snp | A/T | | | intron-variant | Dtx4 | Mm_Celera | 19:12485556 | GCATTCTGTATGCAC[A/T]CATATGCAGTCGCAT | 207521 |
rs266136979 | snp | C/T | | | intron-variant | Dtx4 | Mm_Celera | 19:12495057 | ACTCATGTCCTAAAA[C/T]TTCCCTCTCTTTTAC | 207521 |
rs266192888 | snp | A/G | | | intron-variant | Dtx4 | Mm_Celera | 19:12487448 | TTTAATGCTGGAGAT[A/G]CAGCTGTGAGCATGA | 207521 |
rs266242387 | in-del | -/A | | | intron-variant | Dtx4 | Mm_Celera | 19:12473714 | AAGTCAACTGGCTGC[-/A]AAAAATGTTAACTGA | 207521 |
rs386837328 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12500574 | GGGGGTGGGGGGTGG[A/G]GGCAAGTGTATGTTA | 207521 |
rs386846010 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12493377 | AAATAAACGTTAAAA[A/G]AAAATTAAAGACAAA | 207521 |
rs386872358 | in-del | -/ACATCCCCGCACACACAT | | | downstream-variant-500B | Dtx4 | Mm_Celera | 19:12466009 | TCCCCGCACACACAT[-/ACATCCCCGCACACACAT]GCATCCCCCAACATG | 207521 |
rs386907677 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12470064 | TGGAGACCACTGGCT[A/G]ACCACTGGCTCCACC | 207521 |
rs386907855 | snp | C/G | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12501364 | CTGCGGCCCATGGGG[C/G]AGTCCGCAGCCGCGT | 207521 |
rs386959313 | in-del | -/TGTCAGAAGGGATGAATGC | | | intron-variant | Dtx4 | Mm_Celera | 19:12474138 | AAGAGGCGATGAGGC[-/TGTCAGAAGGGATGAATGC]CTTCTCCTGAGAGCT | 207521 |
rs386959964 | in-del | -/ACCCCC | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12495024 | CCCACCCCCACCCCC[-/ACCCCC]CACCTCCGTCACACT | 207521 |
rs387047645 | in-del | -/T | | | intron-variant | Dtx4 | Mm_Celera | 19:12479442 | TTGCTACCACGGTTT[-/T]GCCTCATCATAAGCA | 207521 |
rs387053560 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12496115 | CAAGTTTGAGCCAGG[A/G]CATGGAAAGTCTAGA | 207521 |
rs387075535 | in-del | -/GNN | | | intron-variant | Dtx4 | Mm_Celera | 19:12482051 | TGACCTCACACTGCT[-/GNN]CGCCCTCATGGCTGA | 207521 |
rs387086258 | snp | G/T | | | upstream-variant-2KB | Dtx4 | GRCm38.p3 | 19:12502726 | GAGCAATCTTATATT[G/T]GTAATGAGATTGTTA | 207521 |
rs387096037 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12479930 | ATAATAGTTTGCATT[C/T]ATGGTCACTGCTTTC | 207521 |
rs387105327 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12498346 | CAGCTTTAAAGTATC[A/G]CTTGGGGACAATGGG | 207521 |
rs387119116 | in-del | -/TCTA | | | intron-variant | Dtx4 | Mm_Celera | 19:12470260 | ACTAATAATGGCATA[-/TCTA]AGGGAATTGGTGAGA | 207521 |
rs387120527 | snp | A/C | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12475598 | ACGACTCTGCCTCAG[A/C]CTGGCCCAGAGCTCC | 207521 |
rs387146499 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12477512 | CACTGTGTGAGGGAA[A/G]AGCTACATTGCGTTT | 207521 |
rs387149131 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12478059 | GGAAGGAGGCTTCTC[C/T]TAGCACAACATTTTA | 207521 |
rs387163398 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12466926 | AATCTCATTGAAATG[A/G]ATTCTGTATATTTGG | 207521 |
rs387163663 | in-del | -/TTAGAG | | | intron-variant | Dtx4 | Mm_Celera | 19:12494568 | GTATAAGGGAGAGAG[-/TTAGAG]CTGGAGAATATAAAA | 207521 |
rs387178230 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12487107 | AGCCGAGACTCCTCC[C/T]CTTGCTGACCTCCCC | 207521 |
rs387187110 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12471412 | GTTGCTCACACAGAG[C/G]TATTTCTTTTATGTG | 207521 |
rs387199876 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12500113 | TATGGAGTTTAGTGC[C/T]TTGGGAGGTCAGAGT | 207521 |
rs387224030 | in-del | -/CAAAA | | | intron-variant | Dtx4 | Mm_Celera | 19:12483459 | CAAAACAAAACAAAA[-/CAAAA]ACAACAACATACCCA | 207521 |
rs387264620 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12480276 | GTGAAAGAACATGGA[A/G]TCTTTCACCAAGTCT | 207521 |
rs387277423 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12474501 | AGAAGAACCGAAAGG[C/G]AAAGGAGTTTATTTG | 207521 |
rs387283514 | snp | A/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12478569 | AAGCCAGCACAGGGA[A/T]TTGTGGTTTAGCCAA | 207521 |
rs387301944 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12480914 | TGCTTCCCGCCATGC[C/T]GCCTCCGTTCTTCCC | 207521 |
rs387319088 | in-del | -/CCC | | | intron-variant | Dtx4 | Mm_Celera | 19:12499787 | CTCTTCTCCCCCCCC[-/CCC]TCCCCCCCACACCTG | 207521 |
rs387332494 | in-del | -/TT | | | intron-variant | Dtx4 | Mm_Celera | 19:12470323 | GGGTTTTCTTTTTTT[-/TT]CTTCCTTTTTTTTTT | 207521 |
rs387341875 | in-del | -/CCCC | | | downstream-variant-500B | Dtx4 | Mm_Celera | 19:12466085 | TGACCCTTTCCCCCC[-/CCCC]AAGTTCACATATTCA | 207521 |
rs387409840 | in-del | -/G | | | intron-variant | Dtx4 | Mm_Celera | 19:12479755 | GAAAAGGAAAGGGGG[-/G]TAGGGAAGAAAGCGC | 207521 |
rs387428249 | in-del | -/GCTTTCTTGCTT | | | intron-variant | Dtx4 | Mm_Celera | 19:12475998 | CTTGCTTTCTTGCTT[-/GCTTTCTTGCTT]TCTCTTTCATTTTTA | 207521 |
rs387429423 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12478354 | CCTTCCCCTCAACCC[A/G]CCTAAAGCACCAGAG | 207521 |
rs387433243 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12479908 | ATTCATGGTTGGTTC[C/T]TTTCAAATAATAGTT | 207521 |
rs387487370 | in-del | -/CC | | | intron-variant | Dtx4 | Mm_Celera | 19:12499323 | GCTGCTCCCCCCGCA[-/CC]CCCCCCCACACCCAC | 207521 |
rs387493193 | snp | G/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12479358 | AGAAGGACACAAGCA[G/T]AGGCTACATGATATA | 207521 |
rs387516418 | in-del | -/CCT | | | intron-variant | Dtx4 | Mm_Celera | 19:12500236 | CCTCCTCCTCCTCCT[-/CCT]TCTCTATGGACAAAG | 207521 |
rs387519627 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12473035 | ACACAGAGAGAGAGA[C/G]AGAGAGAGAGAGAGA | 207521 |
rs387588436 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12470062 | CTTGGAGACCACTGG[C/T]TGACCACTGGCTCCA | 207521 |
rs387596852 | snp | A/C | | | downstream-variant-500B | Dtx4 | GRCm38.p3 | 19:12465866 | ATAACTAATGTCAAC[A/C]TTTAGCTTCAGCAGA | 207521 |
rs387599599 | snp | A/C | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12480890 | TAAGCCAAGGTTTCA[A/C]TTCAGGCGTGCTTCC | 207521 |
rs387610285 | snp | G/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12495112 | CTTGAAATGTTCTAC[G/T]CTGAGCCCCACCCCT | 207521 |
rs387615938 | in-del | -/CAA | | | intron-variant | Dtx4 | Mm_Celera | 19:12487541 | CTAACTCTTCAACAA[-/CAA]TAAGCCTACTCAGTC | 207521 |
rs387631397 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12484556 | CTCTCTCTCTCTCTC[C/T]CTCTCTCTCTCTCTC | 207521 |
rs387653345 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12499385 | ATCCTCCACCAAATA[C/T]ACAATGGGCATCTCC | 207521 |
rs387682173 | in-del | -/C | | | intron-variant | Dtx4 | Mm_Celera | 19:12479410 | GTGATGTACTCCCTC[-/C]GTCACACCTCACATG | 207521 |
rs387692765 | in-del | -/AAAA | | | utr-variant-3-prime, nc-transcript-variant | Dtx4 | Mm_Celera | 19:12469079 | AAAAAAAAAAAAAAA[-/AAAA]GCAGAAACTCCACTC | 207521 |
rs387699830 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12497159 | TGCTCCAGGCACGGG[C/T]TGAGGTCACTAAGAC | 207521 |
rs387719782 | snp | A/C | | | missense, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12492029 | CTGTCTTCCCTGGGC[A/C]TCGAATGGTGCCAGT | 207521 |
rs387729858 | snp | C/G | | | intron-variant | Dtx4 | Mm_Celera | 19:12494412 | TCTCTCTCTCTCTCT[C/G]TCTCTCTCTGTCTCT | 207521 |
rs387743568 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12491325 | CCAACAGCACCAGCA[C/T]GTCATGAGAATGCTA | 207521 |
rs387764413 | in-del | -/AAA | | | intron-variant | Dtx4 | Mm_Celera | 19:12473932 | GACAAAAAAAAAAAA[-/AAA]TCTCGTGACACATCA | 207521 |
rs387784778 | in-del | -/CCT | | | intron-variant | Dtx4 | Mm_Celera | 19:12482045 | CAGTCATGACCTCAC[-/CCT]ACTGCTCGCCCTCAT | 207521 |
rs387789069 | in-del | -/AGAG | | | intron-variant | Dtx4 | Mm_Celera | 19:12473024 | GTGAGAGAGAGACAC[-/AGAG]AGAGAGAGAGAGAGA | 207521 |
rs387808693 | in-del | -/A | | | intron-variant | Dtx4 | Mm_Celera | 19:12480390 | AGCCATAGCCAAAAA[-/A]GAGATATAATTTTGA | 207521 |
rs387816758 | in-del | -/C | | | intron-variant | Dtx4 | Mm_Celera | 19:12475548 | CCCAGTAAGGCTGCT[-/C]GTTTGTTCTGGGCCT | 207521 |
rs387830370 | in-del | -/NN | | | intron-variant | Dtx4 | Mm_Celera | 19:12489439 | AGAGAGAGAGAGAGA[-/NN]GAGAGAGAGAGATCC | 207521 |
rs387835421 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12471027 | CTTACATGGCAGGCA[C/T]GTGTTCTACCAATGG | 207521 |
rs387837150 | snp | C/T | | | upstream-variant-2KB | Dtx4 | GRCm38.p3 | 19:12502521 | GGTACATCACACGGG[C/T]AACTTCCACACTTGA | 207521 |
rs387842191 | snp | G/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12471409 | AACGTTGCTCACACA[G/T]AGCTATTTCTTTTAT | 207521 |
rs387844152 | in-del | -/G | | | intron-variant | Dtx4 | Mm_Celera | 19:12493793 | TGCTGGGGTAGGGGG[-/G]TCCCTGTATCTGCCA | 207521 |
rs578283513 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12481785 | TGGATAGACATGACC[A/G]CCCCTTAACTATGAA | 207521 |
rs578293878 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12494516 | TCTGTCTCTCTCTGT[C/T]TCTCTCTGTCTCTCT | 207521 |
rs578652722 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12494422 | TCTCTCTCTCTCTCT[C/G]TCTCTCTCTGTCTGT | 207521 |
rs578691102 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12471723 | CACACCCCCCCCCAA[A/G]TTCATGGGAACTTCT | 207521 |
rs578737419 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12476800 | CTCCTCCTCCTCCTC[C/T]TCCTCCTCCTCCTCC | 207521 |
rs578762308 | snp | A/C | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12486983 | AATCCATATCACCCC[A/C]CCCCCATGTTCCCCG | 207521 |
rs578854618 | snp | C/T | | | downstream-variant-500B | Dtx4 | GRCm38.p3 | 19:12465920 | ACACACACACACACA[C/T]ACTGCACCCCCCACA | 207521 |
rs578898467 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12476779 | CTCCTCCTCCTCCTC[C/T]TCCTCCTCCTCCTCC | 207521 |
rs579334449 | snp | A/C | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12494650 | ACCAGCTCTGTACAA[A/C]TTCCATGGCAATCTT | 207521 |
rs579458624 | snp | G/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12472972 | GAGACAGAGAGTGAG[G/T]GAGGGAGAGAGACAG | 207521 |
rs579495274 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12484206 | TGAAACCTTGGGCCA[C/T]TCCTCTAGCTTTCCC | 207521 |
rs579890270 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12479738 | TAATTCTCAGGTTCG[C/T]AGAAAAGGAAAGGGG | 207521 |
rs580392399 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12494402 | TAGAGGACTCTCTCT[C/G]TCTCTCTCTCTCTCT | 207521 |
rs580418721 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12481812 | TGAATAGACATGACT[A/G]CCCCTAACTATGGGT | 207521 |
rs580458826 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12476829 | CCTCCTCCTCCTCCT[C/T]CTCCTTACCACACCT | 207521 |
rs580571635 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12473045 | AGAGAGAGAGAGAGA[C/G]AGAGAGACAGACAGA | 207521 |
rs580735103 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12494534 | TCTCTGTCTCTCTCT[C/G]TCTCTCTCTCTCTCT | 207521 |
rs580916084 | snp | A/C | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12473451 | AAAAAAAAAAAAAGC[A/C]AGAAAACCACAGTCT | 207521 |
rs581208696 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12480773 | CGTGCGCACGCGCGC[A/G]CGCGCACACACACAC | 207521 |
rs581211377 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12494450 | TGTCTGTCTCTCTGT[C/G]TGTCTGTCTCTCTCT | 207521 |
rs581381622 | snp | A/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12486970 | CATGCACCACAGGAA[A/T]CCATATCACCCCACC | 207521 |
rs581580351 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12486275 | GCTCGGTGTTTAGCA[C/T]CACCCACTGAGCTTT | 207521 |
rs581911888 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12476815 | CTCCTCCTCCTCCTC[C/T]TCCTCCTCCTCCTCC | 207521 |
rs581961307 | snp | G/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12481801 | CCCCTTAACTATGAA[G/T]AGACATGACTGCCCC | 207521 |
rs582356942 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12476781 | CCTCCTCCTCCTCCT[C/T]CTCCTCCTCCTCCTC | 207521 |
rs582437769 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12481826 | TGCCCCTAACTATGG[A/G]TAAACATGACCAGCT | 207521 |
rs583070759 | snp | A/C | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12500834 | TCTTTAAACTACTTG[A/C]AAGGACATTTACTTG | 207521 |
rs583140673 | snp | A/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12498751 | GGTGAACATCTGTAA[A/T]CCTAGCACTGGGGGT | 207521 |
rs583251243 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12473701 | AGTGCACTCCACCAA[A/G]GTCAACTGGCTGCAA | 207521 |
rs583646807 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12494408 | ACTCTCTCTCTCTCT[C/G]TCTCTCTCTCTCTGT | 207521 |
rs583658297 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12486544 | TCAGAACAAAATGAA[C/G]CAGTGTTTAAACCTA | 207521 |
rs583683015 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12499390 | CCACCAAATACACAA[C/T]GGGCATCTCCTTCTT | 207521 |
rs583692776 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12473049 | AGAGAGAGAGAGAGA[C/G]AGACAGACAGACAGA | 207521 |
rs583804780 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12494436 | TGTCTCTCTCTGTCT[C/G]TCTGTCTCTCTGTCT | 207521 |
rs584226336 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12494452 | TCTGTCTCTCTGTCT[C/G]TCTGTCTCTCTCTGT | 207521 |
rs584318383 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12481784 | ATGGATAGACATGAC[C/T]ACCCCTTAACTATGA | 207521 |
rs584345225 | snp | A/C | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12502025 | ACATCCACACCCACA[A/C]ACGCACGCAACACCC | 207521 |
rs584441838 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12486990 | ATCACCCCACCCCCA[C/T]GTTCCCCGGAGAGCA | 207521 |
rs584456126 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12476790 | CCTCCTCCTCCTCCT[C/T]CTCCTCCTCCTCCTC | 207521 |
rs584498285 | snp | G/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12486976 | CCACAGGAATCCATA[G/T]CACCCCACCCCCATG | 207521 |
rs584692616 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12480777 | CGCACGCGCGCGCGC[A/G]CACACACACACACAC | 207521 |
rs584802255 | snp | C/G/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12494550 | TCTCTCTCTCTCTCT[C/G/T]TGTGTATAAGGGAGA | 207521 |
rs585446764 | snp | A/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12472958 | GAGACAGAGACAGAG[A/T]GACAGAGAGTGAGTG | 207521 |
rs585649749 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12476827 | CTCCTCCTCCTCCTC[C/T]TCCTCCTTACCACAC | 207521 |
rs586174818 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12495587 | ACATATTTCTTGTAT[A/G]CTGGCCTCTAGTCTT | 207521 |
rs586178916 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12471695 | ATGAGGAGTCTGCAG[A/G]TGAATGCTTATGCAC | 207521 |
rs586240450 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12481811 | ATGAATAGACATGAC[C/T]GCCCCTAACTATGGG | 207521 |
rs586348639 | snp | G/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12498771 | GCACTGGGGGTGAGG[G/T]GCTGAGACAGGTAGC | 207521 |
rs586352838 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12473041 | AGAGAGAGAGAGAGA[C/G]AGAGAGAGAGACAGA | 207521 |
rs586549613 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12474131 | AGAAATGTAAGAGGC[A/G]ATGAGGCCTTCTCCT | 207521 |
rs586929297 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12486963 | CCAAATCCATGCACC[A/G]CAGGAATCCATATCA | 207521 |
rs586947908 | snp | A/C | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12484177 | AAAAAAAAACCACAG[A/C]GCAAGGAGAGCCATG | 207521 |
rs587007251 | snp | A/G | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12501259 | CTGCCCACCTCCCGG[A/G]CCCGGCCTTCTGCGC | 207521 |
rs587008661 | snp | G/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12494448 | TCTGTCTGTCTCTCT[G/T]TCTGTCTGTCTCTCT | 207521 |
rs587172649 | snp | A/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12480771 | CGCGTGCGCACGCGC[A/G]CGCGCGCACACACAC | 207521 |
rs587439433 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12473053 | AGAGAGAGAGAGAGA[C/G]AGACAGACAGACAAA | 207521 |
rs587552131 | snp | C/G | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12494416 | TCTCTCTCTCTCTCT[C/G]TCTCTGTCTCTCTCT | 207521 |
rs864256726 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12466890 | AGCACTCTGGGTCAA[A/C]GTCGCTTGTGTCCAG | 207521 |
rs864293473 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12467545 | TAGCAGGAGTTTTCC[C/T]CGAGGTGCAGTGAAT | 207521 |
rs864298675 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12467259 | GTGAAAACATCCCCC[A/G]CTGGCCATTCCCACA | 207521 |
rs864314032 | in-del | -/CCT | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12500217 | CTGCCTCCCTCCGTC[-/CCT]CCTCCTCCTCCTCCT | 207521 |
rs864315795 | in-del | -/CCT | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12500215 | CTGCCTCCCTCCGTC[-/CCT]CCTCCTCCTCCTCCT | 207521 |