SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs213999964 | in-del | -/G | | | intron-variant | Trim7 | Mm_Celera | 11:48826979 | CCCTACCTGGACTGC[-/G]GGGGTTGGGCCTCAG | 94089 |
rs215121658 | in-del | -/TC | | | intron-variant | Trim7 | Mm_Celera | 11:48844996 | TTTCATTTTTTTTTT[-/TC]CCAAGACGGGGTTTT | 94089 |
rs215828266 | in-del | -/TTTTC | | | intron-variant | Trim7 | Mm_Celera | 11:48844936 | AACTTATCTCTCTCA[-/TTTTC]TTTTCTTTTCTTTTC | 94089 |
rs220428933 | in-del | -/T | | | intron-variant | Trim7 | Mm_Celera | 11:48826776 | CTTTTTCTTTTTTTC[-/T]TTTTTTTTTAGCAGA | 94089 |
rs220653351 | in-del | -/AAAA | | | intron-variant | Trim7 | Mm_Celera | 11:48827173 | GGATGTAAAGTGAGT[-/AAAA]AAAAAAAAATTGGGG | 94089 |
rs220716856 | in-del | -/TC | | | upstream-variant-2KB | Trim7 | Mm_Celera | 11:48825347 | CTTACACTCTTTCTT[-/TC]TTTTTTTTTTTAATG | 94089 |
rs221280044 | in-del | -/AAAA | | | intron-variant | Trim7 | Mm_Celera | 11:48834388 | TAAATTTAGAATGTC[-/AAAA]AAAAAAAAAAGACTA | 94089 |
rs223030590 | in-del | -/AGGCTCCCCACGC | | | intron-variant | Trim7 | Mm_Celera | 11:48827604 | AGTGTGTGGAGCTGA[-/AGGCTCCCCACGC]AGCATCTCCACGTAG | 94089 |
rs227333653 | in-del | -/T | | | intron-variant | Trim7 | Mm_Celera | 11:48831784 | CAAACTCAGGTTTTC[-/T]TTTTTTTTTTTCCAT | 94089 |
rs230846220 | in-del | -/GTTGGAATCCGAG | | | intron-variant, upstream-variant-2KB | Trim7 | Mm_Celera | 11:48835793 | CCCAGGGACTGGCTC[-/GTTGGAATCCGAG]GCTGGTAAAGAGCTA | 94089 |
rs231307405 | in-del | -/AAAT | | | intron-variant | Trim7 | Mm_Celera | 11:48833330 | AACTCTGAAATACCA[-/AAAT]AAATAAATAAATAAA | 94089 |
rs232264777 | in-del | -/CCC | | | intron-variant | Trim7 | Mm_Celera | 11:48832423 | GGAACATTCCCTTTT[-/CCC]CTTTTCTTTTCTTTT | 94089 |
rs235667704 | in-del | -/GGAGGAGGAGGAGGA | | | intron-variant | Trim7 | Mm_Celera | 11:48833438 | AGGGGGAAAGGAGGT[-/GGAGGAGGAGGAGGA]GGAGGAGGAGGAGGA | 94089 |
rs240966369 | snp | A/G | | | intron-variant | Trim7 | Mm_Celera | 11:48829430 | ggaggaggaggagga[A/G]aaggaggaggaggag | 94089 |
rs249100317 | in-del | -/AC | | | upstream-variant-2KB | Trim7 | Mm_Celera | 11:48825349 | TACACTCTTTCTTTT[-/AC]TTTTTTTTTAATGAA | 94089 |
rs249978054 | in-del | -/TTTGTTTG | | | intron-variant | Trim7 | Mm_Celera | 11:48831287 | ACCCAACTAGGCTTT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 94089 |
rs252927414 | in-del | -/TTG | | | intron-variant | Trim7 | Mm_Celera | 11:48845189 | AGGAGTTGAAGATGC[-/TTG]TCAAAGATAGAAGAG | 94089 |
rs253033734 | in-del | -/AGAGAGAGAGAGAGAGAG | | | intron-variant, upstream-variant-2KB | Trim7 | Mm_Celera | 11:48838977 | GTGGATGACCAAGGC[-/AGAGAGAGAGAGAGAGAG]AGAGAGAGAGAGAGA | 94089 |
rs253163007 | in-del | -/TTTTT | | | intron-variant, upstream-variant-2KB | Trim7 | Mm_Celera | 11:48836031 | TCCACAGAAAAAAAC[-/TTTTT]TTTTTTTTTTTTTTT | 94089 |
rs255106723 | in-del | -/GTCGCT | | | intron-variant | Trim7 | Mm_Celera | 11:48848409 | ACACTTGGGGGGGGG[-/GTCGCT]TCGCTTCCATATGTT | 94089 |
rs255167189 | snp | A/G | | | intron-variant, upstream-variant-2KB | Trim7 | Mm_Celera | 11:48838984 | ACCAAGGCagagaga[A/G]agagagagagagaga | 94089 |
rs255493991 | in-del | -/TG | | | intron-variant | Trim7 | Mm_Celera | 11:48831349 | TTGTGTAGCCCTGGC[-/TG]TCCTGGAACTCACTC | 94089 |
rs255724134 | in-del | -/TTT | | | intron-variant, upstream-variant-2KB | Trim7 | Mm_Celera | 11:48836032 | TCCACAGAAAAAAAC[-/TTT]TTTTTTTTTTTTTTT | 94089 |
rs256785212 | snp | A/G | | | intron-variant | Trim7 | Mm_Celera | 11:48829431 | gaggaggaggaggaa[A/G]aggaggaggaggagg | 94089 |
rs259895264 | in-del | -/A | | | intron-variant | Trim7 | Mm_Celera | 11:48844506 | TAAAAAGAGAGAAAG[-/A]AAAAAAAAATCTGGG | 94089 |
rs578756814 | snp | C/T | | | intron-variant | Trim7 | GRCm38.p3 | 11:48828676 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 94089 |
rs579151373 | snp | A/G | | | upstream-variant-2KB | Trim7 | GRCm38.p3 | 11:48825996 | ATGGGCCTTCAGACC[A/G]GCCAGGGGCTAGGAC | 94089 |
rs579784382 | snp | C/T | | | intron-variant | Trim7 | GRCm38.p3 | 11:48828706 | TTTCTTTCTTTCTTC[C/T]TTTCTTTCTTTCTTT | 94089 |
rs580343810 | snp | C/G | | | intron-variant | Trim7 | GRCm38.p3 | 11:48826442 | GCCGGGCGGCCCCAC[C/G]TCCCCGCAGCCGTCC | 94089 |
rs580474634 | snp | C/T | | | intron-variant | Trim7 | GRCm38.p3 | 11:48826402 | AGGCCGCGAGCGCGC[C/T]GGCGAGGCCGAGGCC | 94089 |
rs581955916 | snp | G/T | | | utr-variant-5-prime | Trim7 | GRCm38.p3 | 11:48826261 | CGATATTGGGAGGAG[G/T]TCGCCATGCTAGTAG | 94089 |
rs582159356 | snp | C/T | | | intron-variant | Trim7 | GRCm38.p3 | 11:48828680 | TCTTTCTTTCTCTCT[C/T]TCTTTCTTTCTTTCT | 94089 |
rs582231963 | snp | A/G | | | upstream-variant-2KB | Trim7 | GRCm38.p3 | 11:48826002 | CTTCAGACCAGCCAG[A/G]GGCTAGGACCTGGCA | 94089 |
rs583074745 | snp | A/T | | | intron-variant | Trim7 | GRCm38.p3 | 11:48826450 | GCCCCACGTCCCCGC[A/T]GCCGTCCGAGCGCCC | 94089 |
rs584120175 | snp | C/T | | | intron-variant | Trim7 | GRCm38.p3 | 11:48826405 | CCGCGAGCGCGCCGG[C/T]GAGGCCGAGGCCGAG | 94089 |
rs585364914 | snp | C/T | | | intron-variant | Trim7 | GRCm38.p3 | 11:48828705 | CTTTCTTTCTTTCTT[C/T]TTTTCTTTCTTTCTT | 94089 |
rs585765624 | snp | A/G | | | utr-variant-5-prime | Trim7 | GRCm38.p3 | 11:48826258 | TGGCGATATTGGGAG[A/G]AGGTCGCCATGCTAG | 94089 |
rs585879067 | snp | A/C | | | intron-variant | Trim7 | GRCm38.p3 | 11:48826385 | CCGGGCAGAGCCGGG[A/C]CAGGCCGCGAGCGCG | 94089 |
rs587011648 | snp | C/T | | | intron-variant | Trim7 | GRCm38.p3 | 11:48826468 | CGTCCGAGCGCCCGC[C/T]GGGAGCCCGCGCACT | 94089 |
rs587200439 | snp | C/T | | | intron-variant | Trim7 | GRCm38.p3 | 11:48826424 | GCCGAGGCCGAGGCC[C/T]GGGCCGGGCGGCCCC | 94089 |
rs864292652 | snp | G/T | | | upstream-variant-2KB | Trim7 | GRCm38.p3 | 11:48825356 | CTTTCTTTTTTTTTT[G/T]TTAATGAAAATAAGC | 94089 |