SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6230677 | snp | A/C | 0.5 | 0 | intron-variant | Dtx4 | GRCm38.p3 | 19:12487585 | AGGTAAGGAGTGTTA[A/C]AGTCAATCTTGCTGC | 207521 |
rs6230690 | snp | C/T | 0.5 | 0 | intron-variant | Dtx4 | Mm_Celera | 19:12487595 | TGTTANAGTCAATCT[C/T]NCTGCATAAGTAACA | 207521 |
rs6230692 | snp | A/G | 0.5 | 0 | intron-variant | Dtx4 | GRCm38.p3 | 19:12487595 | GTTANAGTCAATCTN[A/G]CTGCATAAGTAACAA | 207521 |
rs6231195 | snp | A/G | 0.5 | 0 | intron-variant | Dtx4 | GRCm38.p3 | 19:12487662 | CTAGACGCAACAAGA[A/G]TCCAACACACACTAT | 207521 |
rs6232844 | snp | A/C | 0.5 | 0 | intron-variant | Dtx4 | Mm_Celera | 19:12487961 | ACTGGATGTGGGGAG[A/C]TGAGGGAAAAGCTGA | 207521 |
rs30312539 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dtx4 | GRCm38.p3 | 19:12470970 | ATTACAGGCATGTGC[A/T]AGTTGCTTGGTTATA | 207521 |
rs30318488 | snp | C/T | | | intron-variant | Dtx4 | GRCm38.p3 | 19:12496345 | AACAAGATTTCAAGG[C/T]TACTTGTTCATAATC | 207521 |
rs30318801 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Dtx4 | GRCm38.p3 | 19:12488133 | CACCTTCCCATTACA[C/T]TATTTGAGAGAAAGG | 207521 |
rs30322749 | snp | A/G | 0.5 | 0 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12492519 | GGCTGAGGATGGGTC[A/G]TAGTAGTTTCGTCGA | 207521 |
rs30324348 | snp | A/G | 0.5 | 0 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12492498 | CCACACGACACCCTT[A/G]CCAGGGGCTGAGGAT | 207521 |
rs30325098 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dtx4 | GRCm38.p3 | 19:12482997 | GGGACAGAGGACATG[C/T]ACTTGGTGATGGAGA | 207521 |
rs30327181 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Dtx4 | GRCm38.p3 | 19:12474224 | AGCAAGGTTGCTTGT[A/T]GTGTTCTCTCTCTTC | 207521 |
rs30327779 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Dtx4 | Mm_Celera | 19:12492927 | GGTGATTCGTTTATA[C/T]AATCAATGAATATAC | 207521 |
rs30349937 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Dtx4 | GRCm38.p3 | 19:12486529 | ATTATGGCTCTGACA[A/T]CAGAACAAAATGAAC | 207521 |
rs30355442 | snp | A/G | 0.48 | 0.0979796 | downstream-variant-500B | Dtx4 | GRCm38.p3 | 19:12466268 | AAGGAAGTAATCCTC[A/G]TGCTTCTGAGCCAGC | 207521 |
rs30367191 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dtx4 | GRCm38.p3 | 19:12477921 | TGCCTAAATGTGGCT[C/T]TTTGTGCAAAACTGG | 207521 |
rs30397381 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dtx4 | GRCm38.p3 | 19:12478025 | GTGAAGGGGGAGGCA[C/T]AGTCTGGGGACAAAG | 207521 |
rs30401182 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Dtx4 | GRCm38.p3 | 19:12493064 | CCAAGGCTATGGAAG[A/G]AAAGAACACAGAGCT | 207521 |
rs30416678 | snp | C/T | 0.5 | 0 | intron-variant | Dtx4 | Mm_Celera | 19:12496510 | TAAGAGAAAGAATCC[C/T]GAGGCTGACCGTGAG | 207521 |
rs30424026 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dtx4 | GRCm38.p3 | 19:12469895 | CTCACCTCTGTCATT[A/G]AATAACTGGGTAACT | 207521 |
rs30447240 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dtx4 | GRCm38.p3 | 19:12471610 | TGTCAGATGTCCCTT[A/G]GGACCACCCTAAAGT | 207521 |
rs30452329 | snp | C/G | 0.32 | 0.24 | intron-variant | Dtx4 | GRCm38.p3 | 19:12497707 | GGCTAGTACTAAACA[C/G]TTAGAGCTGGAAAGA | 207521 |
rs30452472 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dtx4 | GRCm38.p3 | 19:12470099 | TGCTTTGTTTTGTTT[C/T]TGAAACAGGATCTCT | 207521 |
rs30454058 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Dtx4 | GRCm38.p3 | 19:12492963 | CACATGCCAGGATTT[C/T]TTATGAATGGATTTC | 207521 |
rs30455877 | snp | C/G | 0.375 | 0.216506 | intron-variant | Dtx4 | GRCm38.p3 | 19:12478567 | GGAAGCCAGCACAGG[C/G]AATTGTGGTTTAGCC | 207521 |
rs30498997 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dtx4 | GRCm38.p3 | 19:12470110 | GTTTTTGAAACAGGA[A/T]CTCTCACTAAACCAT | 207521 |
rs30511663 | snp | A/G | 0.5 | 0 | intron-variant | Dtx4 | GRCm38.p3 | 19:12487601 | AGTCAATCTTGCTGC[A/G]TAAGTAACAAAATTG | 207521 |
rs30521664 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Dtx4 | GRCm38.p3 | 19:12471012 | TGGAAGCCACGGTTG[C/G]TTACATGGCAGGCAC | 207521 |
rs30523292 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dtx4 | GRCm38.p3 | 19:12481841 | GTAAACATGACCAGC[C/T]ACTTCACCTACCCAT | 207521 |
rs30524256 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Dtx4 | GRCm38.p3 | 19:12471297 | AAAATAGGGTGTATT[A/T]TGAGATACAGGGAGG | 207521 |
rs30547149 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dtx4 | GRCm38.p3 | 19:12473699 | AGAGTGCACTCCACC[A/G]AAGTCAACTGGCTGC | 207521 |
rs30548837 | snp | C/G | 0.5 | 0 | intron-variant | Dtx4 | Mm_Celera | 19:12494096 | TATCAGGATGGGAGG[C/G]GGGTGTTCCCGGTTT | 207521 |
rs30565705 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dtx4 | Mm_Celera | 19:12496414 | TGGCCTGGGAATCCA[A/G]TTGTGTTCATGCACA | 207521 |
rs30643297 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dtx4 | GRCm38.p3 | 19:12477866 | ACATAGAACAAAAAA[A/C]CCCTAAGGTTCATAT | 207521 |
rs30647810 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dtx4 | Mm_Celera | 19:12499278 | CTGGAACTCTGTCAG[A/G]TGGTCTGTTGATCCC | 207521 |
rs30649838 | snp | A/G | 0.5 | 0 | intron-variant | Dtx4 | Mm_Celera | 19:12496718 | CTTCCTAATGCTGTG[A/G]CCCTTTAATACAGTT | 207521 |
rs30656185 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dtx4 | GRCm38.p3 | 19:12470913 | CAGCCTGGCCTCAAA[C/T]GTAACAGGTAGCAAA | 207521 |
rs30662339 | snp | A/G | 0.375 | 0.216506 | synonymous-codon, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12482095 | CCCATTGTTGTACAT[A/G]GCCACCAGGCAGTAG | 207521 |
rs30689625 | snp | A/T | 0.5 | 0 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Dtx4 | Mm_Celera | 19:12492492 | CCATTCCCACACGAC[A/T]CCCTTGCCAGGGGCT | 207521 |
rs30706664 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dtx4 | GRCm38.p3 | 19:12478439 | CTAGCTACTTAAGCC[A/T]TTTTGGCTTTCTCTA | 207521 |
rs30714493 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Dtx4 | GRCm38.p3 | 19:12487855 | TTCCGTGAAGACAGA[A/C]GCAGTGAAGCTAATC | 207521 |
rs30716618 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Dtx4 | GRCm38.p3 | 19:12471286 | AAGCAGGACAGAAAA[C/T]AGGGTGTATTATGAG | 207521 |
rs30763383 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Dtx4 | GRCm38.p3 | 19:12478612 | TGCAACACATGGTAA[C/T]GGCTCAAGAGCAGCA | 207521 |
rs30768260 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12466619 | ACAAGTACTTTTGAC[C/T]GAAGTATAAAATCAC | 207521 |
rs30799883 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dtx4 | Mm_Celera | 19:12499791 | TCTTCTCCCCCCCCT[C/T]CCCCCCACACCTGCT | 207521 |
rs30801297 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Dtx4 | GRCm38.p3 | 19:12466205 | AGAAAATAAAGAAAG[A/G]AGAGTTTCCCTTTAT | 207521 |
rs30803557 | snp | G/T | 0.487535 | 0.077957 | downstream-variant-500B | Dtx4 | GRCm38.p3 | 19:12466054 | ATGCAAGAAGCCAGT[G/T]TCCATGTTTTTAAAG | 207521 |
rs30821816 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dtx4 | Mm_Celera | 19:12493251 | CCGATGGCCTGGATT[C/T]GGTCCCCAGGACCCA | 207521 |
rs30843164 | snp | C/T | 0.432133 | 0.171253 | utr-variant-3-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12466918 | CAGGGCCTAATCTCA[C/T]TGAAATGAATTCTGT | 207521 |
rs30862917 | snp | C/G | 0.401235 | 0.199068 | utr-variant-3-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12466620 | CAAGTACTTTTGACT[C/G]AAGTATAAAATCACA | 207521 |
rs30876899 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Dtx4 | GRCm38.p3 | 19:12470622 | CTCCTTTGGTTAAAA[C/G]AAATTAAAATTAAAG | 207521 |
rs30884597 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dtx4 | GRCm38.p3 | 19:12470121 | AGGATCTCTCACTAA[A/G]CCATCATTAATAAGT | 207521 |
rs30886154 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Dtx4 | GRCm38.p3 | 19:12470145 | AATAAGTGGCAGAAA[C/T]AAAAGTATGACCCAG | 207521 |
rs30898611 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dtx4 | Mm_Celera | 19:12495943 | CAATAGCTGAAGTAA[C/T]GGTGGTTTGCAGAAC | 207521 |
rs30902280 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12466844 | GGCTCCCTGCTTGGC[C/T]CAGTAGAGCACACCA | 207521 |
rs30907144 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12466845 | GCTCCCTGCTTGGCC[A/C]AGTAGAGCACACCAG | 207521 |
rs30908130 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dtx4 | GRCm38.p3 | 19:12496032 | GTATCCCTTCAAGGG[A/G]AACCCATGTGAAGAG | 207521 |
rs30918152 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dtx4 | GRCm38.p3 | 19:12488086 | CAACTGCTTGAGCCT[C/T]AGGGATCTGGGGTTA | 207521 |
rs30931569 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Dtx4 | GRCm38.p3 | 19:12471198 | GAATCTTTCTTGATA[C/T]TGCTGTTTCTTTGTT | 207521 |
rs30945717 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dtx4 | Mm_Celera | 19:12481669 | CTCCACTCTATTGGC[A/T]GAAGCCCTGACTGAA | 207521 |
rs30948254 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dtx4 | GRCm38.p3 | 19:12473703 | TGCACTCCACCAAAG[C/T]CAACTGGCTGCAAAA | 207521 |
rs30953932 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dtx4 | GRCm38.p3 | 19:12493369 | GCCAAAATAAATAAA[C/T]GTTAAAAAAAAATTA | 207521 |
rs30995653 | snp | C/T | 0.5 | 0 | intron-variant | Dtx4 | Mm_Celera | 19:12494272 | GACTTGAAAATTAAA[C/T]GAAGAAACAAGTACA | 207521 |
rs30999014 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Dtx4 | GRCm38.p3 | 19:12486880 | GACCCTGCCCGTTTC[C/T]GCTTACATTCCCTTA | 207521 |
rs31000149 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Dtx4 | GRCm38.p3 | 19:12473676 | TTCTACTCTTTTATG[A/G]ACGATGAAGAGTGCA | 207521 |
rs31011111 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dtx4 | GRCm38.p3 | 19:12477913 | AAACAATGTGCCTAA[A/T]TGTGGCTTTTTGTGC | 207521 |
rs31013692 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dtx4 | Mm_Celera | 19:12493431 | ATCTTCTTAAGAAAA[C/T]TTTCACCCGTTTCCC | 207521 |
rs31021899 | snp | C/T | 0.5 | 0 | intron-variant | Dtx4 | GRCm38.p3 | 19:12470677 | CTCCAGAAGGCCCGA[C/T]ACCATGTCAGTTATC | 207521 |
rs31042233 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Dtx4 | GRCm38.p3 | 19:12466206 | GAAAATAAAGAAAGA[A/G]GAGTTTCCCTTTATC | 207521 |
rs31049849 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Dtx4 | GRCm38.p3 | 19:12482046 | CAGTCATGACCTCAC[A/C]CTGCTCGCCCTCATG | 207521 |
rs31049921 | snp | G/T | 0.484429 | 0.0868505 | synonymous-codon, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12492302 | GGTCTAGTCGTCGTC[G/T]GACACGGCGCTGGCG | 207521 |
rs31053177 | snp | A/G | 0.32 | 0.24 | intron-variant | Dtx4 | Mm_Celera | 19:12477834 | CACAGACATAAGAAT[A/G]AGGACATTCTCTATT | 207521 |
rs31054408 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Dtx4 | GRCm38.p3 | 19:12487447 | GTTTAATGCTGGAGA[C/T]GCAGCTGTGAGCATG | 207521 |
rs31077116 | snp | C/G | 0.375 | 0.216506 | intron-variant | Dtx4 | GRCm38.p3 | 19:12497694 | GATAAAAGAGATAGG[C/G]TAGTACTAAACACTT | 207521 |
rs31132705 | snp | A/T | 0.5 | 0 | intron-variant | Dtx4 | Mm_Celera | 19:12494033 | AACATTCAGAGAAGC[A/T]GAACAATCCTCTATT | 207521 |
rs31137531 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dtx4 | GRCm38.p3 | 19:12478528 | AGTCACCTCTGTCCT[G/T]GAGGGGAAGAGCTGA | 207521 |
rs31147464 | snp | A/G | 0.5 | 0 | intron-variant | Dtx4 | GRCm38.p3 | 19:12487681 | AACACACACTATCTG[A/G]CTCCAGAGTCCTTTC | 207521 |
rs31152964 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Dtx4 | Mm_Celera | 19:12471576 | TGGTCTAGGGTTTTC[C/T]TTATCAATTTGAATC | 207521 |
rs31186240 | snp | C/G | 0.387812 | 0.208586 | utr-variant-3-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12467021 | CAAGCTTCCATCAGA[C/G]CAGAAAGCTGAAAGA | 207521 |
rs31206457 | snp | C/T | 0.487535 | 0.077957 | downstream-variant-500B | Dtx4 | GRCm38.p3 | 19:12466105 | TCACATATTCATTTC[C/T]GTTGCTTTATGGCCC | 207521 |
rs31223620 | snp | C/T | 0.5 | 0 | intron-variant | Dtx4 | Mm_Celera | 19:12496346 | ACAAGATTTCAAGGT[C/T]ACTTGTTCATAATCC | 207521 |
rs31242269 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Dtx4 | GRCm38.p3 | 19:12484818 | TTGTGAAGGAAGGTT[G/T]ATGGAGAGGCTCCAG | 207521 |
rs31254985 | snp | C/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12466512 | ATATAAGTGACCAAC[C/G]AACAAGCAAGGGGGG | 207521 |
rs31265497 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Dtx4 | GRCm38.p3 | 19:12471562 | TTCTTGTATCCCTGT[A/G]GTCTAGGGTTTTCTT | 207521 |
rs31269504 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Dtx4 | Mm_Celera | 19:12492827 | CAGACAAATCAATTC[A/G]CTTTCCAGCTAATTC | 207521 |
rs31290686 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dtx4 | GRCm38.p3 | 19:12495982 | AAATAGATGACAAAT[A/G]TCGTAAGTCTTGAGT | 207521 |
rs31302276 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dtx4 | Mm_Celera | 19:12491709 | TTCTACCTGCCAGGG[A/G]CAGCTCAGCCTGAGA | 207521 |
rs36252145 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Dtx4 | GRCm38.p3 | 19:12474843 | CAAGGGGTGAATGGT[G/T]TATGAAGACTGATGT | 207521 |
rs36261685 | snp | C/T | 0.497778 | 0.0332592 | utr-variant-3-prime, nc-transcript-variant | Dtx4 | GRCm38.p3 | 19:12468762 | TAGTGCAGATGCTCA[C/T]TGGGATGCAGGCTCT | 207521 |
rs36287400 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Dtx4 | Mm_Celera | 19:12468402 | TAAGAAGGAGAAGGG[C/T]CAATCTAGCTCTTGA | 207521 |
rs36306725 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dtx4 | Mm_Celera | 19:12484099 | AGAGTAAGGCTCTTC[A/G]GGAGCTGGGTCCTCA | 207521 |
rs36318213 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Dtx4 | Mm_Celera | 19:12480104 | AGTGGCTTGGGAAAC[A/G]TGCTCGGAGCCCTAC | 207521 |
rs36333835 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime, nc-transcript-variant | Dtx4 | Mm_Celera | 19:12468079 | GATTCTCCATTCTCT[C/T]TTACCTGACACCTAA | 207521 |
rs36337294 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Dtx4 | GRCm38.p3 | 19:12490211 | GATTGGCTCAGCTTA[A/G]CCTTGAGTTCACTAA | 207521 |
rs36337679 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dtx4 | Mm_Celera | 19:12489199 | ATCTTCCAGGCAACC[A/G]AGCCAAAGCCCTTTG | 207521 |
rs36346671 | snp | C/G/T | 0.152778 | 0.230321 | intron-variant | Dtx4 | GRCm38.p3 | 19:12487747 | CCATACTGTAATGCA[C/G/T]GAAGGCACCATCAGG | 207521 |
rs36362322 | snp | C/T | 0.5 | 0 | intron-variant | Dtx4 | GRCm38.p3 | 19:12479410 | GTGATGTACTCCCTC[C/T]GTCACACCTCACATG | 207521 |
rs36371381 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Dtx4 | Mm_Celera | 19:12475494 | CTTGCTGATGCCCTG[A/G]GCTGCTGGCTGTTTC | 207521 |
rs36392837 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dtx4 | Mm_Celera | 19:12471647 | CAGGCTTCTTGGAAA[C/T]CTATCAGCTTGACTT | 207521 |
rs36408078 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Dtx4 | Mm_Celera | 19:12486351 | TTCTCCCCTCTTTAT[A/T]AATATGTGTTCACTA | 207521 |