| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs258328160 | in-del | -/A | | | downstream-variant-500B | Dtx2 | Mm_Celera | 5:136033331 | TATTTTTTTCCCTAT[-/A]TTTTGGTCATTTTCA | 74198 |
| rs258388193 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136025176 | TAGAAAGGCATGAGG[C/T]GTAGGAGGGCTGTGC | 74198 |
| rs258400339 | snp | A/C | | | intron-variant, upstream-variant-2KB | Dtx2 | Mm_Celera | 5:136014386 | ACAGGTGCCACAGTG[A/C]CCCGTGTGAGCTAGT | 74198 |
| rs258407157 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:135999224 | GGCTCACAAAGCCTG[C/T]AACTCCTCGGGGTCC | 74198 |
| rs258529572 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dtx2 | Mm_Celera | 5:136013803 | TCATGCAAAGCCAGG[C/T]GGAGTTTTGCTGTTG | 74198 |
| rs258547611 | snp | G/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136021622 | AGGTTGAACACCTTG[G/T]CTTCAGAGTTTGGGA | 74198 |
| rs258630637 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136005199 | AGCCCACAGTTGCCT[A/G]TAATTCCAGCTCCAG | 74198 |
| rs258632306 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:135995863 | GCCCTAAGCTATATA[C/T]TGTGGCCCCTGCTTA | 74198 |
| rs258663169 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136023765 | AGGCCCCTATAGTTG[C/T]ACTTGGGTAGTTAGA | 74198 |
| rs258676676 | snp | G/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136019213 | CCTCTTGAGGGGTGG[G/T]GGAGAGGCACAGGAA | 74198 |
| rs258759029 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136004398 | GTATGTGCACTGTGT[A/G]CATGCCCAGTGCCCT | 74198 |
| rs258782026 | snp | C/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136031123 | ATAGGAGTGGACCTA[C/G]CTTGGAAGGTGAGGC | 74198 |
| rs258848066 | snp | A/C | | | intron-variant | Dtx2 | Mm_Celera | 5:136023535 | TTTTAAAAAATATTT[A/C]TTTTTGAAGCAGGGT | 74198 |
| rs258894427 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136025510 | TCAACATCAGTGCCT[A/G]GTGTGGCCACAGCCG | 74198 |
| rs258931521 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136007185 | TTTGCATAGGCTCTG[A/G]AGGTCTGAACTCAGG | 74198 |
| rs258990661 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136006558 | AGATTCTGAGGTGAA[C/T]CAGCTTTGCCCAGGA | 74198 |
| rs259098027 | snp | G/T | | | intron-variant, utr-variant-5-prime | Dtx2 | Mm_Celera | 5:136015140 | GGCATGCGTACGTCC[G/T]CTGGGACACGTGGGT | 74198 |
| rs259099444 | snp | A/C | | | intron-variant | Dtx2 | Mm_Celera | 5:136005744 | ATTTGGGTCTCCCCC[A/C]TATTTTTATTACATT | 74198 |
| rs259196886 | snp | C/T | | | upstream-variant-2KB | Dtx2 | Mm_Celera | 5:135994258 | GACTGTGCTTGTAAG[C/T]TCAGCAATTAGGAAG | 74198 |
| rs259330001 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136030217 | GTCACACAGTAGTCA[C/T]TGGGGCCCACTTCCT | 74198 |
| rs259451085 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136031946 | TAGCCCACTGTGCCA[C/T]CTTGCTAGCCGCCTT | 74198 |
| rs259583397 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136010720 | TGGGGGCTGAAGGGT[C/T]AGGAGTTCAAGGCTT | 74198 |
| rs259604719 | in-del | -/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136019565 | GAAGAGGTAGAAACA[-/G]GCTTAGGGAAGGGTG | 74198 |
| rs259612238 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136017414 | GATCCTCAGGCTTGG[C/T]AGCGCATCCCCACCC | 74198 |
| rs259688778 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dtx2 | Mm_Celera | 5:136013409 | TCTCAGGGTCCTAGG[A/G]TGCGGCAGACCTTTG | 74198 |
| rs259864090 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:135999300 | TAGTCTTTACCAAGA[C/T]AACAAGGTGGAGAGT | 74198 |
| rs259877604 | in-del | -/CTG | | | utr-variant-3-prime | Dtx2 | Mm_Celera | 5:136032662 | TGTCTGCGCCGGGGT[-/CTG]CTGCCTGGAAAATGG | 74198 |
| rs259951069 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136019031 | AGGTCTTAACTGTGC[A/G]ACCCTGCCTGACTTG | 74198 |
| rs259958768 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136001534 | GCAGTTGTAGGTGCT[A/G]CGGTGCATGCAGAGG | 74198 |
| rs259993466 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136027711 | GTGGCTGTCACCTGC[C/T]TTTCTAGCTGGAGGG | 74198 |
| rs260002614 | in-del | -/CTTAC | | | intron-variant | Dtx2 | Mm_Celera | 5:136009105 | CCTGTTCTTTCACAT[-/CTTAC]CATCTGACCTTGCAA | 74198 |
| rs260084888 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136022902 | TTTTTAGTTTTCAAG[A/G]CAGTGTTTCTCTGTG | 74198 |
| rs260136342 | in-del | -/GGCA | | | intron-variant | Dtx2 | Mm_Celera | 5:136016007 | TCGTATGTGTGGGCG[-/GGCA]GGCGTGTGTGTGTGT | 74198 |
| rs260148312 | snp | A/G/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136003230 | CTTAGGGATAGGAGC[A/G/T]GCTGTGCACAGCAGT | 74198 |
| rs260209767 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136002284 | AGTGCAGTATTGGGG[C/T]ATATCCTCAGCTTCT | 74198 |
| rs260283843 | in-del | -/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136023317 | TGAAGTCCTGTCCTC[-/T]CTCCCTCTCCCTCTC | 74198 |
| rs260315056 | snp | G/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136011512 | ATGTGAGGTCCCTGG[G/T]GTCCATGTCCAGCAA | 74198 |
| rs260448522 | in-del | -/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136028278 | CATGCTGGTCTGTTA[-/T]GCATCCTTCGCTTCT | 74198 |
| rs260584309 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136028356 | CAGGTGTCCTGTGCT[A/G]ACTCTCTTGTCTCAG | 74198 |
| rs260826457 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136020851 | TTTTTGAGATGGGGT[C/T]TCTCATTGAACCTGG | 74198 |
| rs260887461 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136017199 | GTTTCTCTGTGTAGC[C/T]CTGACTGTCCTGGAA | 74198 |
| rs260906573 | snp | C/T | | | synonymous-codon | Dtx2 | Mm_Celera | 5:136012306 | TTCAGACATCGCTGT[C/T]CCACGCCAAATGGGA | 74198 |
| rs261014912 | snp | C/T | | | synonymous-codon | Dtx2 | Mm_Celera | 5:136032415 | CGGCTATCCGGACCC[C/T]AACTACCTGCAGAAT | 74198 |
| rs261014984 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136024897 | TGGCAACTGCATTTG[A/G]GCCCAGAAGTGTCCT | 74198 |
| rs261043199 | snp | A/C | | | intron-variant | Dtx2 | Mm_Celera | 5:136031991 | TGAGGTGGAATTCCC[A/C]GATAAGTGTTCCACC | 74198 |
| rs261126454 | snp | A/C/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136004040 | TGTATGTCTATGTGA[A/C/G]GGTTTCAGTCCACTC | 74198 |
| rs261138343 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:135999252 | TCCATCTTGTGGCGG[C/T]TATGGATACTGGCAC | 74198 |
| rs261185081 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:135998667 | ACTGCTACAGGCTTG[C/T]GGTCCTAGCGTGCAG | 74198 |
| rs261218041 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dtx2 | Mm_Celera | 5:136013569 | GGTAAGTGGGAAAGA[C/T]GGAAGGCGTGGGATA | 74198 |
| rs261239080 | snp | G/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136007686 | ATCAGGAGACTGAAG[G/T]GGGCAAGAACTGGTC | 74198 |
| rs261356546 | in-del | -/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136022658 | TAGTTGCCACAGTGA[-/T]TTTTTTACCAGCTGT | 74198 |
| rs261433423 | in-del | -/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136008536 | GCCCAGCTTTTCTGT[-/G]GGTTCTGTAGGTCTA | 74198 |
| rs261444950 | snp | A/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136005512 | TTGAGGCTTTTCCCC[A/T]CATCCAATTAGTGTA | 74198 |
| rs261449118 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136030695 | TTCTTCCTGCCCAGC[A/G]CTCTCTCAGCATCTG | 74198 |
| rs261533088 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136025659 | GAAGGATCAGGTTGA[C/T]TTGTCTCGGTTTAAA | 74198 |
| rs261579681 | in-del | -/TAG | | | intron-variant | Dtx2 | Mm_Celera | 5:136004129 | CTCAGGAAAAACAGC[-/TAG]TAGTGCTTTTAACCA | 74198 |
| rs261600262 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:135997827 | TGGCAACTCCTTGGG[C/T]GGAAAGACAGGTGCA | 74198 |
| rs261683676 | in-del | -/ACAT | | | intron-variant | Dtx2 | Mm_Celera | 5:136017932 | TTTATGTGTGTCTCC[-/ACAT]ACACACATGCACAAA | 74198 |
| rs261743936 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136003373 | AAAAATTTTTTTTTG[C/T]TTTTGTTTTTGTTTT | 74198 |
| rs261795148 | snp | C/G | | | intron-variant | Dtx2 | Mm_Celera | 5:135999166 | GAAAGCACTGCTGCT[C/G]TCTTAAAGGACTGGA | 74198 |
| rs261832400 | in-del | -/TATT | | | intron-variant | Dtx2 | Mm_Celera | 5:136001073 | AGTCCAGTGCTCTGC[-/TATT]TATTTATTTATTTAT | 74198 |
| rs261860311 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136005525 | CCACATCCAATTAGT[A/G]TAATTTCCGTAATTA | 74198 |
| rs261893323 | snp | A/T | | | intron-variant, upstream-variant-2KB | Dtx2 | Mm_Celera | 5:136014336 | GTGTGAGAGTGTGAG[A/T]GAGTGAGAGAGAGAG | 74198 |
| rs261929084 | snp | A/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136001211 | TTTAGCTAGTTAAAA[A/T]TTTTAAATTATATTT | 74198 |
| rs261993525 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136007492 | GAGCAAGGGCTTCTA[A/G]AGACTTTGGAGCCTG | 74198 |
| rs261994251 | snp | A/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136009689 | CCCCGGGGCTGGCTC[A/T]CCCTCTCCAAGAATG | 74198 |
| rs262012120 | snp | A/C/T | | | utr-variant-3-prime | Dtx2 | Mm_Celera | 5:136032506 | CGGGCCTGCCTCTGC[A/C/T]GACCCCACAGCCCTG | 74198 |
| rs262044344 | snp | A/G | | | upstream-variant-2KB | Dtx2 | Mm_Celera | 5:135994538 | CCTTGAGTTCGATCC[A/G]TGGAACCCACGTGAA | 74198 |
| rs262126230 | snp | A/C | | | intron-variant | Dtx2 | Mm_Celera | 5:136030369 | GTGTACTTTGTCTAG[A/C]GTACACCACTGAGGT | 74198 |
| rs262248264 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136022807 | GTAGGTTCAGTTTTT[C/T]CTGTCATCTCCCAGG | 74198 |
| rs262303290 | snp | G/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136032013 | TGTTCCACCACTGAC[G/T]TCCACTCCTTGCCCC | 74198 |
| rs262315025 | in-del | -/CACAGCAGTGCTTTTGAGC | | | intron-variant | Dtx2 | Mm_Celera | 5:136003237 | ATAGGAGCTGCTGTG[-/CACAGCAGTGCTTTTGAGC]CACAGCAGTGGCACT | 74198 |
| rs262455382 | snp | C/G | | | upstream-variant-2KB | Dtx2 | Mm_Celera | 5:135993714 | CAGACTGTCCCTCTG[C/G]AGTGTCAGATGGAGA | 74198 |
| rs262487400 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136002168 | GTGCTAGCACCTTGT[A/G]TGTGCTAGGCAAGTC | 74198 |
| rs262555650 | snp | G/T | | | intron-variant | Dtx2 | Mm_Celera | 5:135998245 | ACAGGGTGGACTTTA[G/T]GGGTAGGGAGATGGT | 74198 |
| rs262593363 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136004183 | AGAGTTATTTTAAAG[A/G]GAGAAACTAATACTT | 74198 |
| rs262651776 | snp | A/C | | | intron-variant | Dtx2 | Mm_Celera | 5:135996597 | TTTGCTCTCCAGAAC[A/C]AAGGTAAAAAGCCTG | 74198 |
| rs262699844 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:135999765 | GCCTGTGCTTATGAA[C/T]ATGGGAGATGGAAGA | 74198 |
| rs262724500 | snp | A/C | | | intron-variant | Dtx2 | Mm_Celera | 5:136027638 | GTGGTCGAATTTGGT[A/C]ATAACACATGAACTA | 74198 |
| rs262756975 | in-del | -/AGTTT | | | intron-variant | Dtx2 | Mm_Celera | 5:136007258 | TCAACAGCCCTCAAC[-/AGTTT]AGTTTGTTTGTTTCT | 74198 |
| rs262808694 | in-del | -/TTAT | | | intron-variant | Dtx2 | Mm_Celera | 5:135998552 | GGGCTGTCTCCATAA[-/TTAT]ATGAGCGCCAATTCA | 74198 |
| rs262840432 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136029384 | AAGAGACATTGTCTC[A/G]AGAAAAACGAAGAAT | 74198 |
| rs262937623 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136032140 | TGGGTCAGCTGGTGG[A/G]ACGTGCTCCCGGAGG | 74198 |
| rs262953572 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136018460 | CTCTTGGTTATTCAG[C/T]GTAAAGATGGAAGCT | 74198 |
| rs262984957 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:135995750 | ACTATATTACATCCC[C/T]CTCACTCCCCAAAAG | 74198 |
| rs263021184 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136025955 | AGGCCAGATGATCAC[A/G]AGCCAAGAGGGCACA | 74198 |
| rs263093707 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:135998013 | AAAGTCAGAGGAGCA[A/G]GAGAAAGCGGGAAGG | 74198 |
| rs263258352 | snp | C/T | | | upstream-variant-2KB | Dtx2 | Mm_Celera | 5:135993294 | GGCTGGGGATATGCC[C/T]GAGTCAGCAGAGAGC | 74198 |
| rs263278000 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136029430 | GGCTGAAGGGCAGGT[A/G]CTAAGCCATGGGTGA | 74198 |
| rs263281375 | snp | G/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136017981 | GGCACAAGTGTGGAG[G/T]TCAGAGGGCAACTCG | 74198 |
| rs263283276 | in-del | -/G | | | intron-variant | Dtx2 | Mm_Celera | 5:135998480 | ATATATGTGTTTAAA[-/G]AGGTCATTAGCTTTG | 74198 |
| rs263342086 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136023969 | GCTATTGGATAGTGT[C/T]ATGGCCATGACAGTG | 74198 |
| rs263402979 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136019465 | CTCTATCTCGGAGGC[C/T]GGAGTTGAGGGTGAT | 74198 |
| rs263418446 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136026674 | TGCTGCCTGGACTCT[C/T]TTCTTTGCCCACCGT | 74198 |
| rs263641577 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136024427 | GCATTTTTATCCTGT[A/G]GGGCTCATGCTGAGG | 74198 |
| rs263686437 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136022134 | GGGCCTTCAGGGGAG[C/T]CAGGGGACCTTTTTA | 74198 |
| rs263739165 | snp | A/T | | | upstream-variant-2KB | Dtx2 | Mm_Celera | 5:135994669 | TTAAAAATCAAATGC[A/T]TCAGTGATTAGCGAG | 74198 |
| rs263758094 | in-del | -/C | | | intron-variant | Dtx2 | Mm_Celera | 5:136002252 | ATCCCTAGCCCCTTA[-/C]GGGGTGATTCTAGGC | 74198 |
| rs263954455 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dtx2 | Mm_Celera | 5:136013638 | CCAACCAGGCAGTAC[A/G]CTTTTAGTTCTGAGC | 74198 |
| rs263959085 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136021230 | ATCCCAAGAGATTTC[C/T]TGTTTCATTTCTATT | 74198 |
| rs264060340 | snp | C/T | | | intron-variant, utr-variant-5-prime | Dtx2 | Mm_Celera | 5:136015260 | CGTCCCTCTCTCTCT[C/T]GCTACTTAGGCTTAG | 74198 |
| rs264066642 | in-del | -/AGAG | | | intron-variant | Dtx2 | Mm_Celera | 5:136005709 | TCTAGGCACCAACTC[-/AGAG]AGCCCAGGTCCCCTG | 74198 |
| rs264089195 | snp | C/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136023388 | TTTTTCTGGTCCTGT[C/G]CATGCATACTGGGCA | 74198 |
| rs264121452 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136008891 | CCCACATGTGAAGGA[A/G]GGAGGGAAAGACGGA | 74198 |
| rs264155186 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136017798 | CTGGCTGTCTCAGAG[C/T]TCACTGTGTAGTCTA | 74198 |
| rs264270055 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136011424 | TGTCTACCAACAGTG[A/G]TGATGGTGAATTGTT | 74198 |
| rs264330379 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136019365 | GGGGCTGTAGCTAAG[C/T]TAGCAGAGACTTACT | 74198 |
| rs264377055 | in-del | -/TGACAGTGACAAAAGGCGTGGTCCT | | | intron-variant | Dtx2 | Mm_Celera | 5:136023977 | ATAGTGTCATGGCCA[-/TGACAGTGACAAAAGGCGTGGTCCT]TGGTGTTCCTGTTTC | 74198 |
| rs264463945 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136002491 | GCAGGGGCTCTACCA[C/T]TGAGCCACGCCCCCA | 74198 |
| rs264502073 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136011674 | TGACATGGACACATC[A/G]CTGACAAACACATAT | 74198 |
| rs264586109 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136017533 | CTGCTGGGATTACAG[A/G]CATGAGCCACCACAC | 74198 |
| rs264815695 | snp | C/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136006397 | AGAGCTCTGGAAGTT[C/G]GTTTATCTGAGAATG | 74198 |
| rs264828781 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136029965 | GAACAAGTCTAATCG[C/T]CCGAGTCCATGTAAA | 74198 |
| rs264864114 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dtx2 | Mm_Celera | 5:136013663 | CTGAGCGTCTGGGCT[C/T]TGCGCTTGCCCACTG | 74198 |
| rs264886296 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | Dtx2 | Mm_Celera | 5:136014122 | GACTCCGTTTTAGAT[-/GG]GTTTTTTTTGTTTTT | 74198 |
| rs264936745 | snp | G/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136031003 | AAGGCAAGTGAGCAT[G/T]CAGCATGAGTGCCCA | 74198 |
| rs264955336 | in-del | -/TG | | | intron-variant | Dtx2 | Mm_Celera | 5:135999815 | GTGGCCGCTGTTGAC[-/TG]TGTAGGCTTGAGGCA | 74198 |
| rs264989834 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136025677 | GTCTCGGTTTAAAGA[C/T]GTGCTACAGAAGGCA | 74198 |
| rs265129885 | snp | C/T | | | upstream-variant-2KB | Dtx2 | Mm_Celera | 5:135992804 | GATATTTGTCTGGGA[C/T]GTGAATTCAGTTGAC | 74198 |
| rs265133375 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136001599 | CATGTTCTGAGGCTC[A/G]AACTCAGGCTGTTAG | 74198 |
| rs265186593 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Dtx2 | Mm_Celera | 5:135994906 | TTCCCAGGCCGAGCC[A/G]GAGCTGAGCCCGGAG | 74198 |
| rs265201608 | in-del | -/GTGTTGGG | | | intron-variant | Dtx2 | Mm_Celera | 5:135999997 | TGCATGAGTGTGTGT[-/GTGTTGGG]GTGTGTTGGGGTGTG | 74198 |
| rs265203728 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136003431 | TAGCCCAGCTGTCCT[A/G]GATCTCTTTCTAGAT | 74198 |
| rs265267349 | snp | A/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136026901 | TCCCACCACGTCCGG[A/T]TCATGTAGCGTTGAG | 74198 |
| rs265360525 | snp | C/T | | | synonymous-codon | Dtx2 | Mm_Celera | 5:136028545 | GATCAGAAAGTACAC[C/T]GAGGAGCTGAAAGTG | 74198 |
| rs265398254 | in-del | -/CT | | | intron-variant | Dtx2 | Mm_Celera | 5:136021199 | GGCCAGCCTGCTGAG[-/CT]CTGTCTGTGTAGGTA | 74198 |
| rs265456134 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:135998564 | ATAAATGAGCGCCAA[C/T]TCAATTGTTTTAGGG | 74198 |
| rs265530545 | in-del | -/T | | | intron-variant | Dtx2 | Mm_Celera | 5:135996039 | AATTTTTATCCTCTC[-/T]GGTGTGTTGATTTCC | 74198 |
| rs265574635 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136017360 | ATAAGAGAACTGTTC[A/G]TGAAGTTGCTTCTCC | 74198 |
| rs265581873 | snp | C/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136024701 | TTTATTTCGATTTAC[C/G]GTTCCACAGGGTACA | 74198 |
| rs265630570 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136018837 | AGTAGCCAGGGACCC[C/T]GTCTCTGTGGGGCCA | 74198 |
| rs265644745 | snp | A/C | | | intron-variant | Dtx2 | Mm_Celera | 5:136026177 | GCCACCATCCTTGTC[A/C]CTTACTCTGTCCCCG | 74198 |
| rs265649356 | in-del | -/TG | | | intron-variant | Dtx2 | Mm_Celera | 5:136001238 | ATTTTATCTATCTAC[-/TG]TGTGTGTGTGTGTGT | 74198 |
| rs265716811 | in-del | -/TTT | | | upstream-variant-2KB | Dtx2 | Mm_Celera | 5:135994007 | AAGCCAAGGTTTAAC[-/TTT]TTTTTTTTTTGTTTT | 74198 |
| rs265872662 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dtx2 | Mm_Celera | 5:136014139 | TTTTTTTTGTTTTTT[G/T]TTTCTCCCCGAGACA | 74198 |
| rs265891661 | in-del | -/GT | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136027474 | GAGAGGTAGTGGTAC[-/GT]GTGTGTGTGTGTCTC | 74198 |
| rs265942075 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136016380 | AGTCTGAACAGCGCA[A/G]CTTGGGGGAGCTGGG | 74198 |
| rs266049554 | snp | A/G | | | downstream-variant-500B | Dtx2 | Mm_Celera | 5:136033044 | ACACACATGCTCCGT[A/G]CCCTGTGGTCCCCAG | 74198 |
| rs266139776 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136007246 | CACTGGGCTATCTCA[A/G]CAGCCCTCAACAGTT | 74198 |
| rs266174500 | snp | A/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136025335 | GTGGGTGGGTGGGTG[A/G]GGTGTTGTACAGTGT | 74198 |
| rs266212027 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136009358 | GATCTGCAGGACCTG[C/T]CCCTTCACATGCTCA | 74198 |
| rs266215629 | snp | C/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136018041 | CCAGGGATCCAGCTC[C/T]GGTCATCAGGCCTGG | 74198 |
| rs386898729 | in-del | -/TGTAA | | | intron-variant | Dtx2 | Mm_Celera | 5:136019410 | AATCTTTAGCACTGT[-/TGTAA]TGGGATGTGGTAGTG | 74198 |
| rs386974657 | in-del | -/G | | | intron-variant | Dtx2 | Mm_Celera | 5:136023000 | GTACCAAGGCTGGTG[-/G]CAGAAGGCCTTCAAC | 74198 |
| rs387020147 | in-del | -/AAAAA | | | upstream-variant-2KB | Dtx2 | Mm_Celera | 5:135993189 | ACAAAAAAAAAAAAA[-/AAAAA]TGAGAATAATAAAAA | 74198 |
| rs387030465 | in-del | -/A | | | intron-variant | Dtx2 | Mm_Celera | 5:136003540 | GAGGCTAAAAAAAAA[-/A]TGTTTATTCTGTGTG | 74198 |
| rs387055490 | in-del | -/CA | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136027069 | GTATGGGGAAGCATA[-/CA]GACACGTGGCCTTCT | 74198 |
| rs387147705 | in-del | -/GTGTGT | | | intron-variant | Dtx2 | Mm_Celera | 5:136006961 | TGTGTGTGTGTGTGT[-/GTGTGT]TACTCTCCTGGGGAA | 74198 |
| rs387236056 | in-del | -/GTGTGT | | | intron-variant | Dtx2 | Mm_Celera | 5:136016044 | TGTGTGTGTGTGTGT[-/GTGTGT]AGGTCAGAGGACAGC | 74198 |
| rs387247068 | in-del | -/GT | | | intron-variant | Dtx2 | Mm_Celera | 5:136027486 | TACGTGTGTGTGTGT[-/GT]CTCTCTGTGTGTGTC | 74198 |
| rs387287459 | in-del | -/ACAGTGACAAAAGGCGTGGTCCTTG | | | intron-variant | Dtx2 | Mm_Celera | 5:136023979 | AGTGTCATGGCCATG[-/ACAGTGACAAAAGGCGTGGTCCTTG]GTGTTCCTGTTTCAT | 74198 |
| rs387313647 | in-del | -/TGTTTT | | | intron-variant | Dtx2 | Mm_Celera | 5:136017135 | ATTTGTTGGTGGTGG[-/TGTTTT]TGTTTTTGTTTTTGT | 74198 |
| rs387322880 | in-del | -/TGTGTGTGCG | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136021556 | GTGTGTGTGTGTGTG[-/TGTGTGTGCG]CGTGTGCGTGTGCGT | 74198 |
| rs387329884 | in-del | -/GG | | | intron-variant | Dtx2 | Mm_Celera | 5:136003581 | GAGAGAGAGAGAGAG[-/GG]AGGGAGAGAGAGAGA | 74198 |
| rs387449847 | in-del | -/GTGT | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136027474 | AGAGGTAGTGGTACG[-/GTGT]TGTGTGTGTCTCTCT | 74198 |
| rs387541585 | in-del | -/T | | | intron-variant | Dtx2 | Mm_Celera | 5:136022664 | CCACAGTGATTTTTT[-/T]ACCAGCTGTTCTATC | 74198 |
| rs387637870 | in-del | -/CC | | | intron-variant | Dtx2 | Mm_Celera | 5:136023313 | GGCTTGAAGTCCTGT[-/CC]TCTCTCCCTCTCCCT | 74198 |
| rs387684751 | in-del | -/TT | | | intron-variant | Dtx2 | Mm_Celera | 5:136011181 | CTTTTTTTTTTTTTT[-/TT]GTTTTGTTTTTGTTT | 74198 |
| rs387695548 | in-del | -/TCACTTAGA | | | intron-variant | Dtx2 | Mm_Celera | 5:136005324 | CATGCCCATAACAGA[-/TCACTTAGA]GGCTGAAGCAAGAGA | 74198 |
| rs387706535 | in-del | -/GTTTTT | | | intron-variant | Dtx2 | Mm_Celera | 5:136017160 | TTTGTTTTTGTTTTT[-/GTTTTT]TGAGTTTTTCGAGAC | 74198 |
| rs387750422 | in-del | -/C | | | intron-variant | Dtx2 | Mm_Celera | 5:136027965 | GCTCCCCTAAGCCCC[-/C]ACACACAGCCAGCCA | 74198 |
| rs387860703 | in-del | -/TCTTTAAGCTTGTGACAT | | | intron-variant, cds-indel | Dtx2 | Mm_Celera | 5:136014760 | CTTGGCAAGCTTTAT[-/TCTTTAAGCTTGTGACAT]GGGCAGGGATGGCCA | 74198 |
| rs387884222 | in-del | -/GT | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136001239 | TTTTATCTATCTACT[-/GT]GTGTGTGTGTGTGTG | 74198 |
| rs578356036 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136003572 | GTGTGATTTTGAGAG[A/G]GAGAGAGAGAGGGAG | 74198 |
| rs578363466 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136023361 | CTCCCCCTCCCCCTC[C/T]CCCTCTCCTGGTTTT | 74198 |
| rs578525163 | snp | A/G | | | utr-variant-3-prime | Dtx2 | GRCm38.p3 | 5:136032658 | CATCCTGTCTGCGCC[A/G]GGGTCTGCCTGGAAA | 74198 |
| rs578531572 | snp | A/T | | | intron-variant, upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:136014330 | GTGAGTGTGTGAGAG[A/T]GTGAGTGAGTGAGAG | 74198 |
| rs578542440 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:136013212 | GCTGGGATTAAAGGC[A/G]TGTGCCATCACTGCC | 74198 |
| rs578546367 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:135999399 | AGATCCATGCACACA[C/T]AGAGTTCAGGCTGGG | 74198 |
| rs578587358 | snp | A/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:135999986 | TGTGTGTGCATGTGC[A/T]TGAGTGTGTGTGTGT | 74198 |
| rs578931726 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:136014161 | CCCGAGACAGGGTTT[C/T]TCTGTGTAGCCCTGG | 74198 |
| rs579094517 | snp | C/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136004250 | GTTAGGTGGGCTCCC[C/G]GGTAGATGTGTGCTT | 74198 |
| rs579169714 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136022866 | GAAGAACCTTGTCCT[A/G]CCGCCATCTCCGCAG | 74198 |
| rs579478678 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136007460 | CTCTTTTCTCGATGA[A/G]ACCAGGCAAGCTGAG | 74198 |
| rs579553838 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136001084 | CTGCTATTTATTTAT[C/T]TATTTATTTATTTAT | 74198 |
| rs579574454 | snp | C/T | | | upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:135994050 | TGTTTGTTTGTTTTT[C/T]GAGACAGGGTTTCTC | 74198 |
| rs579650958 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136028306 | TCTGTGATCTCCCCT[A/G]GTGGCCCAGCCCCCT | 74198 |
| rs579752146 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136001452 | AGCCCCAACTATCTT[C/T]AACCCGCCCCCCACC | 74198 |
| rs579792389 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136017418 | CTCAGGCTTGGCAGC[A/G]CATCCCCACCCCACC | 74198 |
| rs580085605 | snp | C/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136017928 | TACATTTATGTGTGT[C/G]TCCACATACACACAT | 74198 |
| rs580162538 | snp | A/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136001074 | GTCCAGTGCTCTGCT[A/T]TTTATTTATTTATTT | 74198 |
| rs580211033 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136011277 | CTCGAACTCAGAAAT[C/T]CACCTGCCTCCCGAG | 74198 |
| rs580334588 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136005723 | TCAGCCCAGGTCCCC[C/T]GGTATATTTGGGTCT | 74198 |
| rs580412980 | snp | C/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136025347 | GTGAGGTGTTGTACA[C/G]TGTGGTGGGGCAAGG | 74198 |
| rs580787655 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:136013098 | TTTTGTTTTTTTTTC[A/G]AAACAGGGTTTCTCT | 74198 |
| rs581206129 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136021563 | GTGTGTGTGCGTGTG[C/T]GTGTGCGTGTGTGTA | 74198 |
| rs581229691 | snp | A/G | | | upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:135994182 | TGCGCCACCACGCCC[A/G]GCTTAACATTTTTTA | 74198 |
| rs581318028 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136029678 | GACAGTACATGACTC[C/T]TCCAGCTTGCCTGCA | 74198 |
| rs581355093 | snp | A/C | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136002502 | ACCATTGAGCCACGC[A/C]CCCAGCCCCTCACTG | 74198 |
| rs581473891 | snp | C/G | | | intron-variant, upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:136013246 | CTGTTTTTTGTTTTT[C/G]TTTTTGTTTTTTTTA | 74198 |
| rs581665651 | snp | A/T | | | downstream-variant-500B | Dtx2 | GRCm38.p3 | 5:136033322 | GGCAGGGTCTTATTT[A/T]TTTCCCTATTTTTGG | 74198 |
| rs581765991 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136032151 | GTGGGACGTGCTCCC[A/G]GAGGCCCCCCCCACC | 74198 |
| rs581770187 | snp | G/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:135997234 | CTGGCCCCTCCCAAT[G/T]CTATTTAATTTTTTA | 74198 |
| rs581816803 | snp | A/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136007241 | TCTCCCACTGGGCTA[A/T]CTCAACAGCCCTCAA | 74198 |
| rs581842435 | snp | A/C | | | intron-variant, utr-variant-5-prime | Dtx2 | GRCm38.p3 | 5:136014631 | GTTAGAGCACTAAGC[A/C]GTCACTCCATCATCC | 74198 |
| rs581870485 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:135999979 | GCCTGAGTGTGTGTG[C/T]ATGTGCATGAGTGTG | 74198 |
| rs582026683 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136023319 | AAGTCCTGTCCTCTC[C/T]CCCTCTCCCTCTCCC | 74198 |
| rs582209618 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136024477 | AAGCCTGAGGGATTT[C/T]AGATAGCTAGGTGGA | 74198 |
| rs582332935 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136023362 | TCCCCCTCCCCCTCC[C/T]CCTCTCCTGGTTTTT | 74198 |
| rs582363611 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136003691 | TTTCCATTTTCCTCT[A/G]TTGCTCCCTGCCCCA | 74198 |
| rs582407837 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136000006 | TGTGTGTGTGTGTTG[A/G]GGTGTGTGTGTGTAC | 74198 |
| rs582445014 | snp | A/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136005305 | AAGAGCTGGGTATAG[A/T]GGCTCATGCCCATAA | 74198 |
| rs582869931 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:136014229 | CAAACTCAGAAATCC[G/T]CCTGCCTCTGCCTCC | 74198 |
| rs582929553 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136001163 | TATGCTGTACCCATA[C/T]CTGCTTTGTGTGTGT | 74198 |
| rs582996746 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136001076 | CCAGTGCTCTGCTAT[C/T]TATTTATTTATTTAT | 74198 |
| rs583064720 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136019575 | GAAACAGCTTAGGGA[A/G]GGGTGGAGCTTGCAA | 74198 |
| rs583307821 | snp | A/G | | | upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:135994087 | GCCCTGGCTGTCCTG[A/G]AACTCACTTTGTAGA | 74198 |
| rs583501865 | snp | A/C | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136028311 | GATCTCCCCTGGTGG[A/C]CCAGCCCCCTCTAAG | 74198 |
| rs583604634 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136008546 | TCTGTGGGTTCTGTA[A/G]GTCTAAACTTGGATC | 74198 |
| rs583697959 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:136013005 | TCCAGGCAAGCACTT[G/T]ACCACCAAGCACAGC | 74198 |
| rs583815578 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136017726 | CCAGGGTTCTTTTTA[C/T]CAAATTTTAGTTCGT | 74198 |
| rs583978081 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136025765 | TTCCTTCCCCCTCTG[C/T]CAGTCCAGACAGTAG | 74198 |
| rs583982442 | snp | C/T | | | upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:135993478 | CAGGTGCTAAGACAC[C/T]CTGTCTCCAAAACAA | 74198 |
| rs584161271 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136003518 | TAAAGGTGTGTGCCA[C/T]CAGCGTGAGGCTAAA | 74198 |
| rs584263469 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136021557 | GTGTGTGTGTGTGTG[C/T]GTGTGCGTGTGCGTG | 74198 |
| rs584354740 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:135999980 | CCTGAGTGTGTGTGC[A/G]TGTGCATGAGTGTGT | 74198 |
| rs584529138 | snp | C/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136029922 | CCACCACCACCACCA[C/G]CAGGGAAAGCATGCA | 74198 |
| rs584615246 | snp | A/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136004127 | GACCTCAGGAAAAAC[A/T]GCTAGTGCTTTTAAC | 74198 |
| rs584653964 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:136013148 | GGAACTCACTCTGTA[A/G]ACCACACTGGCCTCG | 74198 |
| rs584858710 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:135995612 | AACTCTCTTTTCTCC[A/G]TGCCGTCTTAGCCCC | 74198 |
| rs585174645 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136021569 | GTGCGTGTGCGTGTG[C/T]GTGTGTGTATGTGTC | 74198 |
| rs585379861 | snp | A/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136002506 | TTGAGCCACGCCCCC[A/T]GCCCCTCACTGAAGG | 74198 |
| rs585391911 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136023363 | CCCCCTCCCCCTCCC[C/T]CTCTCCTGGTTTTTC | 74198 |
| rs585460603 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136023325 | TGTCCTCTCTCCCTC[C/T]CCCTCTCCCTCTCCC | 74198 |
| rs585549672 | snp | A/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136007270 | AACAGTTTAGTTTGT[A/T]TGTTTCTCTGAGACA | 74198 |
| rs585875388 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136016010 | GTATGTGTGGGCGGG[C/T]GTGTGTGTGTGTGTG | 74198 |
| rs585973122 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:136014243 | CGCCTGCCTCTGCCT[C/T]CCAAGAGCTAGGATT | 74198 |
| rs585980707 | snp | A/C | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136005333 | TAACAGAGGCTGAAG[A/C]AAGAGAATTGCCTGG | 74198 |
| rs586116704 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136017921 | TTTTCATTACATTTA[C/T]GTGTGTCTCCACATA | 74198 |
| rs586191028 | snp | A/C | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136000431 | TCAGTGGCTAAGAGC[A/C]CTGACTGCTCTTCCA | 74198 |
| rs586341978 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136001080 | TGCTCTGCTATTTAT[C/T]TATTTATTTATTTAT | 74198 |
| rs586424090 | snp | A/C | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136024484 | AGGGATTTCAGATAG[A/C]TAGGTGGAAAAAAAA | 74198 |
| rs586442945 | snp | C/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136028316 | CCCCTGGTGGCCCAG[C/G]CCCCTCTAAGCAGCT | 74198 |
| rs586721926 | snp | G/T | | | upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:135994014 | AGGTTTAACTTTTTT[G/T]TTTGTTTTTTGTTTT | 74198 |
| rs586732023 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136027975 | GCCCCCACACACAGC[C/T]AGCCATTTCCAGGAT | 74198 |
| rs586783565 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:136013057 | TGTTTTTTGGTTTTT[G/T]GGTTTGTTTGTTTGT | 74198 |
| rs586812386 | snp | A/T | | | upstream-variant-2KB | Dtx2 | GRCm38.p3 | 5:135994150 | CCTCTGCCTCCTGAG[A/T]GCTGGGATTAAAGGC | 74198 |
| rs586970379 | snp | C/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136021330 | GCCCCTTGAGTGCTG[C/G]GTTACAGGCGTGTGC | 74198 |
| rs586981616 | snp | A/G | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136019459 | CTAACACTCTATCTC[A/G]GAGGCCGGAGTTGAG | 74198 |
| rs587172431 | snp | A/C | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136011850 | TCATGCATACAAAAC[A/C]CAAAAGCACACAGAC | 74198 |
| rs587568528 | snp | C/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:136031770 | GAGCTGGACTTGCTT[C/T]TTGGTTTTTGTTTGT | 74198 |
| rs587570730 | snp | G/T | | | intron-variant | Dtx2 | GRCm38.p3 | 5:135996027 | TGACTTTGGTCAAAT[G/T]TTTATCCTCTCTGGT | 74198 |