SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3663747 | snp | A/C | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:42013619 | TACAGAGACTGAAAA[A/C]AAACAAGCAAAACAT | 226122 |
rs3696425 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ubtd1 | Mm_Celera | 19:42028662 | GCAGCCTCAGCCTCG[A/G]CTACTAGCATGACCA | 226122 |
rs3715391 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Ubtd1 | Mm_Celera | 19:42003253 | AGGGGTAAGTGGAGT[A/T]ATCCCACTGTCTGGC | 226122 |
rs3716702 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Ubtd1 | Mm_Celera | 19:42003476 | CCTGATAAAACTCCA[A/T]AAGATGAAAATATCA | 226122 |
rs3717192 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ubtd1 | GRCm38.p3 | 19:42003479 | GATAAAACTCCAAAA[A/G]ATGAAAATATCATTA | 226122 |
rs3717891 | snp | C/T | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:41997058 | ATTTAATCACTCATC[C/T]ACCTCATAAATGTCA | 226122 |
rs3720143 | snp | C/T | 0.32 | 0.24 | intron-variant | Ubtd1 | Mm_Celera | 19:42006813 | CCTGCCTTAACTCTT[C/T]GCTGCCCAGACACAT | 226122 |
rs3720214 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Ubtd1 | Mm_Celera | 19:42006851 | CCTTTCTGACCACAG[C/T]ATTCTTATTGCAGCA | 226122 |
rs3723698 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:42032323 | GGCACAGAACCAAGC[A/G]TAGTGGCACATGCCT | 226122 |
rs4139713 | snp | C/T | 0.5 | 0 | intron-variant | Ubtd1 | GRCm38.p3 | 19:42007091 | AACTCCTGGGGTctc[C/T]cctcccctcccctcc | 226122 |
rs6193914 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ubtd1 | Mm_Celera | 19:42021382 | ACATAGGCCAATTCT[C/T]CCTCAGGAAGTAGCC | 226122 |
rs6194453 | snp | A/G | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:42021481 | TTTCCAGGGGCCTGG[A/G]CCTGGGGTTCAGGCC | 226122 |
rs6250947 | snp | A/T | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:42024986 | CTGCTGAATAAAACC[A/T]TTTATCTTGGGGATA | 226122 |
rs6258693 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Mms19, Ubtd1 | Mm_Celera | 19:41980396 | gatccgatgtcctct[C/T]ctggtgtgtctgaca | 226122 |
rs6259235 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Mms19, Ubtd1 | Mm_Celera | 19:41980490 | TGAATCTTTAAAGAC[A/T]CTAGTCATCTACACG | 226122 |
rs6272669 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Mms19, Ubtd1 | Mm_Celera | 19:41980702 | ACCAGAACACCCGAG[G/T]CCAAGTCCCAGCTCC | 226122 |
rs13474358 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Ubtd1, Ankrd2 | Mm_Celera | 19:42033707 | GAGCCTGGAGCCTCC[C/T]GAGCCCACCCCTAGT | 226122 |
rs30307453 | snp | A/G | 0 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:42018160 | CAAGCTGTGCTGCAC[A/G]AGGAAGTGGGTGATG | 226122 |
rs30320874 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ubtd1 | Mm_Celera | 19:42015257 | AGTGGTCTGAGCACT[C/T]TCTCTCTCTGTCTCT | 226122 |
rs30321731 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ubtd1 | Mm_Celera | 19:42001200 | GTCTCGGGAACATGC[A/G]CACCATGGTTTTCTT | 226122 |
rs30323458 | snp | A/G | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:41999243 | AATGGGGGAAGCTCT[A/G]GGACCTGTGAACATT | 226122 |
rs30328648 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ubtd1 | Mm_Celera | 19:42015296 | TCTGTGTGTGTGCAC[A/G]TGTGCTTGTGTATGT | 226122 |
rs30351841 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Ubtd1 | Mm_Celera | 19:42019239 | GATGCTTTCTTCTAC[G/T]TGCGCCCCTTCCCTT | 226122 |
rs30353232 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubtd1 | Mm_Celera | 19:42026745 | TTGAACTCAGGTCCT[C/T]ACAGTTGCACAACAG | 226122 |
rs30354630 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Ubtd1 | Mm_Celera | 19:41997657 | TCTACGAAGGGCACA[A/T]TTTGAAAACGAGTTG | 226122 |
rs30362984 | snp | A/G | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:41988824 | TCATAGGATTTCAGA[A/G]CTGAAAAGAAACCTA | 226122 |
rs30364832 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:41985244 | AGTTTCATGTTGTCA[A/G]ACTGATGCCTCGAAC | 226122 |
rs30371622 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Ubtd1 | Mm_Celera | 19:42005036 | AAAGTCAGACTATGC[A/G]GGATGCATGAACCCT | 226122 |
rs30403669 | snp | A/G | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:42021558 | CCTGTGAATGTGTAC[A/G]TTGTGTCAGAGTAGT | 226122 |
rs30404469 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ubtd1 | Mm_Celera | 19:42032744 | CGAACTCAGAAATCC[A/G]CCTGCCTCTGCCTCC | 226122 |
rs30408964 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubtd1 | Mm_Celera | 19:42019174 | GACAGCACTCACAAG[C/T]CTTGCTGAGAGGAGG | 226122 |
rs30413098 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:42006614 | TTATTGCCCAGGGCT[A/G]CTGTGTCCTTTCGCG | 226122 |
rs30414684 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ubtd1 | Mm_Celera | 19:42015491 | AGGTCCAGAGTTTAA[A/G]TCCCAGCAACCACAT | 226122 |
rs30416681 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB, downstream-variant-500B | Ankrd2, Ubtd1 | Mm_Celera | 19:42034952 | TTGGGGGGCGGTCCA[C/G]ATAGGAAAAGTGAAG | 226122 |
rs30417446 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubtd1 | GRCm38.p3 | 19:42003687 | GTGTTAATACCTATT[A/G]TATATTTATTGAGCC | 226122 |
rs30417849 | snp | A/G | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:41992985 | AGCATAGCTCATCCT[A/G]TAACCTGGGAGGGGC | 226122 |
rs30419209 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ubtd1 | Mm_Celera | 19:41998577 | TAATAAATAAATCTT[A/T]AAAAAAAAAAAAAAG | 226122 |
rs30452609 | snp | A/C | 0.265928 | 0.249492 | intron-variant, upstream-variant-2KB | Ubtd1 | Mm_Celera | 19:42015396 | TACGAACAGTAGTGC[A/C]GAGGAGCTCAGCTAA | 226122 |
rs30501385 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubtd1 | Mm_Celera | 19:42002134 | AGCTATCTGATATGC[A/G]ACCCCCCCAAGGGGG | 226122 |
rs30521156 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:41990332 | GGGATTCCGGGATTG[G/T]GGCACCAGGCCTATG | 226122 |
rs30542547 | snp | A/G | 0.465374 | 0.126941 | intron-variant, utr-variant-5-prime | Ubtd1 | Mm_Celera | 19:42017166 | GAGTCTTTTCTATGC[A/G]CACAACCACATCTTG | 226122 |
rs30559242 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubtd1 | Mm_Celera | 19:42003100 | CAGACATACAGAGAT[C/T]CTCCTGCCTCTGCCT | 226122 |
rs30616259 | snp | C/T | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:42033333 | GATGCTTCTTGGTTT[C/T]TTTGCTGTTTTTACG | 226122 |
rs30623080 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Ubtd1 | Mm_Celera | 19:42018494 | GAACAAAATGCCAGT[A/T]AAACTAACCGAGGGC | 226122 |
rs30643300 | snp | A/G | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:42030526 | TTTTATGCTGAACAT[A/G]TACTTCTTTATAATC | 226122 |
rs30664214 | snp | G/T | 0.265928 | 0.249492 | intron-variant, upstream-variant-2KB | Ubtd1 | Mm_Celera | 19:42015343 | CTTACAGACTTTCCA[G/T]TGAGTGGATTGGAGC | 226122 |
rs30700959 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubtd1 | Mm_Celera | 19:41998478 | AAATCCCAGAAACCA[C/T]ATGGTGGCTCACAAT | 226122 |
rs30704245 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:42025689 | TTGATTTTTGTTTCT[C/T]TGAGACAGGGTTTCT | 226122 |
rs30707492 | snp | C/G | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:42031538 | CTTATAGAGGACCCT[C/G]GTTTAGTTTCAGCTC | 226122 |
rs30750330 | snp | C/T | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:41996345 | CAGGGGTTCAGGGTT[C/T]ATCTCCAAAGGAAGC | 226122 |
rs30761055 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubtd1 | Mm_Celera | 19:42027623 | CCTACCAGCAGTGTT[C/T]TTTCTTGCTGGAGGA | 226122 |
rs30787946 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:41985437 | GGCACCAAACCTGAC[A/T]ACCTGCGTTTAATCC | 226122 |
rs30797424 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:42002842 | TTTACTTAATGACTG[C/T]ATTGCTTAACTTTGT | 226122 |
rs30809073 | snp | C/T | 0.290657 | 0.246672 | intron-variant, upstream-variant-2KB | Ubtd1 | Mm_Celera | 19:42016390 | TTACGACTCATGTGA[C/T]GGCAGAGGACATGGT | 226122 |
rs30844549 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Ubtd1 | Mm_Celera | 19:42003593 | TTGAGCCCAGAACTT[C/G]TAGACCATCCTGGGA | 226122 |
rs30845299 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubtd1 | Mm_Celera | 19:42030703 | AACAGCAAAGGTTGT[A/G]CAAACAGTCCCTAAC | 226122 |
rs30848674 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Ubtd1 | Mm_Celera | 19:42005506 | TGTCCGAGCTGTGCA[C/T]GCCCTCCTGCAGATC | 226122 |
rs30851621 | snp | C/T | 0.455 | 0.143091 | intron-variant, upstream-variant-2KB | Mms19, Ubtd1 | Mm_Celera | 19:41980581 | CAGCTGGAGCGCACG[C/T]TACTTCCAGGAAGGC | 226122 |
rs30867784 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ubtd1 | Mm_Celera | 19:42002051 | CCCAACATAAAATTA[G/T]TTTGTTGTTACTTCA | 226122 |
rs30941655 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ubtd1 | Mm_Celera | 19:42031034 | TAAGACGCCCATACA[A/C]ATCACAGAAAGTTTA | 226122 |
rs30944618 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubtd1 | Mm_Celera | 19:42001074 | TCTTCCACCTCCCTA[A/G]ATTCAGTGGGCCCCA | 226122 |
rs30946613 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:42002853 | ACTGCATTGCTTAAC[C/T]TTGTGTTATTGTAAT | 226122 |
rs30947860 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Ubtd1 | Mm_Celera | 19:42005552 | CATATAGTGGATTCT[C/T]ATCCCCCTTCAATAA | 226122 |
rs30950892 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:42018662 | ATGGTCCTGAACTCC[A/T]GATCTTCCTGCCCCC | 226122 |
rs30951032 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Ubtd1 | Mm_Celera | 19:42029019 | AAAAGTTCATTATAT[C/T]GACATGGTAGAGTAA | 226122 |
rs30968062 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:42030258 | CCATAGCCACAGTTC[A/G]AACGTTCTGTAATGA | 226122 |
rs30980279 | snp | C/G/T | 0.5 | 0 | intron-variant | Ubtd1 | GRCm38.p3 | 19:41985588 | GTGTGTGTGTGTGTG[C/G/T]GCGCGTGTGCGCGCG | 226122 |
rs31002184 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ubtd1 | Mm_Celera | 19:41986496 | TGCTGGGATTAAAGG[C/T]GTGTACACCACCACC | 226122 |
rs31012916 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ubtd1 | Mm_Celera | 19:42015809 | CAGGGAAGGCAGTGG[A/G]AGCTGAGGCTCTGAT | 226122 |
rs31017024 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Mms19, Ubtd1 | Mm_Celera | 19:41982522 | GAAATCTTTATTTCC[C/T]CCCACCTCTCCACAC | 226122 |
rs31040227 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ubtd1 | Mm_Celera | 19:41989042 | GGAGGAGCATTTAGT[C/T]TCTGTTATGTTCATG | 226122 |
rs31052224 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubtd1 | Mm_Celera | 19:42020968 | CACACTTAGCCCTTA[A/G]CATAGCCCCATGAAA | 226122 |
rs31054612 | snp | A/G | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:42030520 | GATTTCTTTTATGCT[A/G]AACATATACTTCTTT | 226122 |
rs31057171 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubtd1 | Mm_Celera | 19:42019150 | CTGTCAGCCCACTCC[C/T]GAGACCCTGACAGCA | 226122 |
rs31087960 | snp | A/T | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:41986228 | CCTGAGTTGGTTCTC[A/T]CTGTCTACCATGTAG | 226122 |
rs31094635 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ubtd1 | Mm_Celera | 19:41999309 | TTGGTAGTCACATCC[C/T]TCTTAGTCATCAGCT | 226122 |
rs31096020 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:42017678 | TGTGGTGCTGGGAGC[C/G]AGGAGCAGACTCTAG | 226122 |
rs31145148 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:42004180 | CCATGTTTATCTCCC[G/T]GTGGCCCCATCCCTG | 226122 |
rs31146468 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:42010272 | AAAGCCACCACCTGG[A/G]GGGAGCCAAGGTGTT | 226122 |
rs31150643 | snp | A/C/T | 0.5 | 0 | intron-variant | Ubtd1 | GRCm38.p3 | 19:42031072 | ATACCCATACCCACA[A/C/T]GGAAGTCAGAGGGCA | 226122 |
rs31152484 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:41990297 | TTTGTTGAATGCCTT[A/G]CCTCTGCCTTCTGAG | 226122 |
rs31162900 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ubtd1 | Mm_Celera | 19:42015892 | CACCCTTCCCCAAAC[C/T]GCCTCCCTTTGCCTG | 226122 |
rs31186936 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:41999373 | AACATCCCAAACTCC[A/G]CAGCATCCCAGGGGA | 226122 |
rs31189725 | snp | G/T | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:42021799 | CTCAGGCCCTCCTCT[G/T]TTCCCCCTCCCTGTC | 226122 |
rs31191892 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ubtd1 | Mm_Celera | 19:41986814 | TGTGCATCTATGGTA[C/T]TCTTCATTGTTTAGT | 226122 |
rs31196755 | snp | C/G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ubtd1 | GRCm38.p3 | 19:42016617 | TCCCAAGTGCTTGGG[C/G/T]TATAGGCCTGTACCG | 226122 |
rs31212577 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Mms19, Ubtd1 | Mm_Celera | 19:41980420 | TCTGACAGCGTACTC[A/G]CATACTATATATATA | 226122 |
rs31217719 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:42025648 | CACAGGGTTGGGGGG[G/T]TTGAACTTAACCTTT | 226122 |
rs31223633 | snp | A/G | 0.5 | 0 | intron-variant | Ubtd1 | Mm_Celera | 19:41986509 | GGCGTGTACACCACC[A/G]CCGCCCAGCTCCATA | 226122 |
rs31234102 | snp | A/G/T | 0.465374 | 0.126941 | intron-variant | Ubtd1 | GRCm38.p3 | 19:42020899 | CTGCTGACCTCTGTC[A/G/T]AAGTGCACTGTGGTA | 226122 |
rs31246872 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ubtd1 | Mm_Celera | 19:41999008 | CCAACTTTGTGGGGA[A/G]CATGTCATAGCCACA | 226122 |
rs31248457 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ubtd1 | Mm_Celera | 19:42009035 | ACTCTGTCCACAGTC[A/G]CAGGCCTAGGGCTTC | 226122 |
rs31257610 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd1 | Mm_Celera | 19:42014831 | GGTCAGGTTTGGAGG[C/T]CTCCGCTGAGCAGCC | 226122 |
rs31281392 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ubtd1 | Mm_Celera | 19:42019989 | GCTCCTATTCTGGTT[A/T]TTTTGTTTGTTTGTT | 226122 |
rs31284025 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubtd1 | Mm_Celera | 19:42001169 | GCAGCAACGTTTCAC[A/G]TCCCCCCTTCCCTGT | 226122 |
rs31290338 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ubtd1 | Mm_Celera | 19:42001832 | CTGTCGTAAACTGTT[C/G]CTAGCACAGTTGAGG | 226122 |
rs31304090 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ubtd1 | Mm_Celera | 19:42014297 | TTAAACTGTCAACTT[C/T]ACTTCCTCAGGCCCT | 226122 |
rs36246598 | snp | C/T | 0.18 | 0.24 | intron-variant | Ubtd1 | Mm_Celera | 19:41996730 | TTGTGTGCAAGGGGA[C/T]AGACGTATGAAATGA | 226122 |
rs36263309 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Ubtd1 | Mm_Celera | 19:41994446 | GGCGCCCTGTCTTCT[C/T]GCAATAGGTGCACAC | 226122 |
rs36272180 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubtd1 | Mm_Celera | 19:42033476 | TCCTGTCATTTACCC[A/G]TGTAATCTTATTCCT | 226122 |