SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs27099817 | snp | A/G | 0.345679 | 0.230967 | downstream-variant-500B | Trim25 | GRCm38.p3 | 11:89020526 | GCTGCTGGGACAGAG[A/G]GACCTGCAAGGATGA | 217069 |
rs48529381 | snp | A/C | | | utr-variant-3-prime | Trim25 | GRCm38.p3 | 11:89017899 | CTGAAGCGAGAGACG[A/C]GCGGGAGATAGCTGG | 217069 |
rs49057844 | snp | C/G | | | intron-variant | Trim25 | GRCm38.p3 | 11:89007375 | AATACATTTAACAGG[C/G]TTTTTTTTTTTTCAT | 217069 |
rs52478466 | snp | A/G | | | intron-variant | Trim25 | GRCm38.p3 | 11:89006985 | GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTCGA | 217069 |
rs211795756 | in-del | -/TCTCTTTTTT | | | upstream-variant-2KB, intron-variant | Trim25, LOC102637854 | Mm_Celera | 11:88997828 | GAGTAAAAATTTCTC[-/TCTCTTTTTT]TTTTTTTTTTTTTCA | 217069 |
rs213255414 | in-del | -/CCCCC | | | intron-variant, upstream-variant-2KB | Trim25, LOC102637854 | Mm_Celera | 11:89001278 | AGTGGCTTTAGAGGT[-/CCCCC]CCCCCCCCCATTACA | 217069 |
rs213398230 | in-del | -/GG | | | intron-variant | Trim25 | GRCm38.p3 | 11:89016172 | TTGTCAAAATTCCCT[-/GG]GGGGGGGGAATGTCT | 217069 |
rs213509595 | in-del | -/GG | | | downstream-variant-500B | Trim25 | GRCm38.p3 | 11:89020525 | TGCTGCTGGGACAGA[-/GG]GACCTGCAAGGATGA | 217069 |
rs214011668 | in-del | -/C | | | intron-variant | Trim25 | GRCm38.p3 | 11:89009871 | CTTGAAGGCCTCTTA[-/C]CCCGTTGAGTCTGGT | 217069 |
rs214875305 | snp | A/C | | | utr-variant-3-prime | Trim25 | Mm_Celera | 11:89018894 | TAAGACCTTACCTTA[A/C]CCATAAGCATTTCTG | 217069 |
rs216585592 | snp | G/T | | | intron-variant | Trim25 | GRCm38.p3 | 11:89016019 | tgggagggtaggtgg[G/T]tagatggatgggtag | 217069 |
rs218860277 | snp | A/T | | | intron-variant | Trim25 | GRCm38.p3 | 11:89007404 | Atttgtttttatttt[A/T]tgtgcattattgttt | 217069 |
rs219523550 | in-del | -/TGTT | | | intron-variant | Trim25 | GRCm38.p3 | 11:89013667 | TTTTTCACACGTGTG[-/TGTT]TGTGTGTGTGTGTGT | 217069 |
rs219579245 | in-del | -/CCCCTG | | | intron-variant | Trim25 | GRCm38.p3 | 11:89012599 | TTGAGGACCCCCCCC[-/CCCCTG]CCAAGATGTGCTTTA | 217069 |
rs219594560 | snp | A/C/G | | | intron-variant | Trim25 | GRCm38.p3 | 11:89007003 | TTTCTGAGTTCGAGG[A/C/G]CAGCCTGGTCTACAA | 217069 |
rs219900744 | in-del | -/CCAGCCC | | | upstream-variant-2KB, intron-variant | Trim25, LOC102637854 | GRCm38.p3 | 11:88999173 | GAGGGTGGGAATATT[-/CCAGCCC]CTGCGACAATTCATC | 217069 |
rs220891103 | in-del | -/AGCCCCT | | | upstream-variant-2KB, intron-variant | Trim25, LOC102637854 | GRCm38.p3 | 11:88999175 | GGGTGGGAATATTCC[-/AGCCCCT]GCGACAATTCATCTG | 217069 |
rs221551664 | in-del | -/GTGTGG | | | intron-variant | Trim25 | GRCm38.p3 | 11:89010720 | AGGAACCATCAGTGT[-/GTGTGG]GGGGGGGGGTCTATG | 217069 |
rs221884110 | in-del | -/GTGTGTG | | | intron-variant | Trim25 | GRCm38.p3 | 11:89010718 | ATAGGAACCATCAGT[-/GTGTGTG]GGGGGGGGGGTCTAT | 217069 |
rs224013662 | in-del | -/CCCCTGC | | | upstream-variant-2KB, intron-variant | Trim25, LOC102637854 | GRCm38.p3 | 11:88999177 | GTGGGAATATTCCAG[-/CCCCTGC]GACAATTCATCTGCA | 217069 |
rs224528351 | snp | A/C/G | | | intron-variant | Trim25 | Mm_Celera | 11:89014188 | GGCAGGTGGATCTCT[A/C/G]TGGGTTTGAGGCCAG | 217069 |
rs224755891 | in-del | -/TTTATTTATTTA | | | intron-variant | Trim25 | GRCm38.p3 | 11:89012013 | AGCCCCCTTGAACAT[-/TTTATTTATTTA]TTTATTTATTTATTT | 217069 |
rs224859845 | in-del | -/C | | | intron-variant | Trim25 | GRCm38.p3 | 11:89013546 | ACCATTCGTAAGTAG[-/C]CCCCCCGTTTTTTTT | 217069 |
rs225113591 | snp | A/C/G/T | | | intron-variant | Trim25 | GRCm38.p3 | 11:89012603 | GGACCCCCCCCCCCC[A/C/G/T]GCCAAGATGTGCTTT | 217069 |
rs226703844 | in-del | -/TCCTAAA | | | utr-variant-3-prime | Trim25 | GRCm38.p3 | 11:89017891 | CTGTGGCCTGAAGCG[-/TCCTAAA]AGAGACGAGCGGGAG | 217069 |
rs226960788 | in-del | -/T | | | intron-variant | Trim25 | GRCm38.p3 | 11:89013268 | GCTGATGGAGGAGAC[-/T]TTTTCCCATCTGTAT | 217069 |
rs228116989 | in-del | -/GTGTGAA | | | intron-variant | Trim25 | GRCm38.p3 | 11:89010723 | ACCATCAGTGTGTGT[-/GTGTGAA]GGGGGGGGGGGTCTA | 217069 |
rs228142699 | snp | A/G | | | upstream-variant-2KB, intron-variant | Trim25, LOC102637854 | GRCm38.p3 | 11:88999176 | GGTGGGAATATTCCA[A/G]CCCCTGCGACAATTC | 217069 |
rs232293712 | in-del | -/GTA | | | intron-variant | Trim25 | GRCm38.p3 | 11:89012070 | GGGTCTCTCTACTTG[-/GTA]TAGCTCTGGCTGTTC | 217069 |
rs232321641 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | Trim25, LOC102637854 | Mm_Celera | 11:89001118 | CTGTCTCGAAAAACC[-/AAA]AAAAAAAAAAAAAGA | 217069 |
rs233179283 | in-del | -/TTTT | | | intron-variant | Trim25 | GRCm38.p3 | 11:89003483 | AATGCTATTATAATA[-/TTTT]TTTTTTTGTAGAAAT | 217069 |
rs233718003 | in-del | -/GTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | Trim25 | GRCm38.p3 | 11:89002435 | CGTATGCATGTGATC[-/GTGTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 217069 |
rs233743722 | in-del | -/AG | | | intron-variant | Trim25 | GRCm38.p3 | 11:89013215 | CCCTGATGTATGGCC[-/AG]AGAGAGAGAGCAACC | 217069 |
rs233898006 | in-del | -/TTTTTCATTTGTTTTTATTTTA | | | intron-variant | Trim25 | GRCm38.p3 | 11:89007383 | TAACAGGGTTTTTTT[-/TTTTTCATTTGTTTTTATTTTA]TGTGCATTATTGTTT | 217069 |
rs236635222 | in-del | -/TTTTTTTTTT | | | intron-variant | Trim25 | Mm_Celera | 11:89004433 | TTTTGGTTCCAAGTC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 217069 |
rs236924711 | in-del | -/C | | | intron-variant | Trim25 | GRCm38.p3 | 11:89003960 | TCACCCAGCTTCCTT[-/C]CCCCTCCTGGAAGTC | 217069 |
rs237737822 | in-del | -/AA/AC | | | intron-variant | Trim25 | Mm_Celera | 11:89007078 | CGAAAAACCAAAAAA[-/AA/AC]AAACAAAAAGAAAAA | 217069 |
rs239143132 | snp | A/C | | | upstream-variant-2KB, intron-variant | Trim25, LOC102637854 | GRCm38.p3 | 11:88999174 | AGGGTGGGAATATTC[A/C]AGCCCCTGCGACAAT | 217069 |
rs241312742 | snp | A/C/G | | | upstream-variant-2KB, intron-variant | Trim25, LOC102637854 | GRCm38.p3 | 11:88999177 | GTGGGAATATTCCAG[A/C/G]CCCTGCGACAATTCA | 217069 |
rs242991022 | in-del | -/AGG | | | intron-variant, upstream-variant-2KB | Trim25, LOC102637854 | GRCm38.p3 | 11:89001163 | AAAAAGAAATTGAGC[-/AGG]AGGAATTGGGCCTCT | 217069 |
rs243036955 | snp | A/T | | | intron-variant | Trim25 | GRCm38.p3 | 11:89015999 | tagatgaatggttag[A/T]tggatgggagggtag | 217069 |
rs243162364 | in-del | -/CCC | | | intron-variant, upstream-variant-2KB | Trim25, LOC102637854 | Mm_Celera | 11:89001279 | AGTGGCTTTAGAGGT[-/CCC]CCCCCCATTACAGAC | 217069 |
rs246243655 | snp | G/T | | | intron-variant | Trim25 | GRCm38.p3 | 11:89008936 | GCTGGGTCTTGGGGT[G/T]TGTTCACCTCCAAGC | 217069 |
rs248117111 | in-del | -/CTCAGT | | | intron-variant | Trim25 | GRCm38.p3 | 11:89008415 | AGTGACCCTCCTGCC[-/CTCAGT]TCTGGAGGAACTGGA | 217069 |
rs249417802 | snp | A/C | | | intron-variant | Trim25 | GRCm38.p3 | 11:89012597 | TCTTGAGGACCCCCC[A/C]CCCCCTGCCAAGATG | 217069 |
rs249542854 | in-del | -/TGTGTT | | | intron-variant | Trim25 | GRCm38.p3 | 11:89013665 | AGTTTTTCACACGTG[-/TGTGTT]TGTGTGTGTGTGTGT | 217069 |
rs250713224 | in-del | -/TTC | | | intron-variant | Trim25 | GRCm38.p3 | 11:89007386 | CAGGGTTTTTTTTTT[-/TTC]ATTTGTTTTTATTTT | 217069 |
rs250789668 | in-del | -/CGC | | | intron-variant | Trim25 | GRCm38.p3 | 11:89004058 | TTCTTAGTTCTCCAG[-/CGC]CACCTTTGATATTTT | 217069 |
rs251721105 | in-del | -/TA | | | intron-variant | Trim25 | Mm_Celera | 11:89014187 | AGGCAGGTGGATCTC[-/TA]TGGGTTTGAGGCCAG | 217069 |
rs254466493 | in-del | -/ATATATAT/TT | | | utr-variant-3-prime | Trim25 | Mm_Celera | 11:89017344 | ATATATATATATATA[-/ATATATAT/TT]ATCATCTCTTTGGTG | 217069 |
rs255135401 | in-del | -/CTG | | | intron-variant | Trim25 | GRCm38.p3 | 11:89012602 | AGGACCCCCCCCCCC[-/CTG]CCAAGATGTGCTTTA | 217069 |
rs255473983 | in-del | -/TTTT | | | intron-variant | Trim25 | GRCm38.p3 | 11:89014685 | CTGGTGACCTTGTGC[-/TTTT]TTTTTGGATGGAGAA | 217069 |
rs255538225 | in-del | -/TGGA | | | intron-variant | Trim25 | GRCm38.p3 | 11:89015860 | TCATGCATACCTGGG[-/TGGA]TGGATGGATGGATGG | 217069 |
rs255906388 | in-del | -/A | | | intron-variant | Trim25 | GRCm38.p3 | 11:89015148 | AAATATCCTAATCTG[-/A]AAAATCTTTCCTTTT | 217069 |
rs256334920 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Trim25, LOC102637854 | GRCm38.p3 | 11:89000796 | ACTGTGGTATAGCCC[-/T]TTTTTTGGTTGTTTT | 217069 |
rs257705038 | in-del | -/ACACACAC | | | intron-variant | Trim25 | Mm_Celera | 11:89009017 | TTCCTGGTGCTCCAT[-/ACACACAC]ACACACATACACACA | 217069 |
rs257914452 | snp | A/G | | | upstream-variant-2KB, intron-variant | Trim25, LOC102637854 | GRCm38.p3 | 11:88999175 | GGGTGGGAATATTCC[A/G]GCCCCTGCGACAATT | 217069 |
rs258567621 | in-del | -/TGTA | | | intron-variant | Trim25 | Mm_Celera | 11:89013864 | AGCCATCGTCTTGCT[-/TGTA]GTAAGACTTCTGGGA | 217069 |
rs261395372 | in-del | -/GTGT | | | intron-variant | Trim25 | GRCm38.p3 | 11:89008934 | TTGCTGGGTCTTGGG[-/GTGT]GTTCACCTCCAAGCA | 217069 |
rs263224544 | in-del | -/AAAAAA | | | intron-variant | Trim25 | GRCm38.p3 | 11:89002093 | AAATAAATAAATCTT[-/AAAAAA]AAAAAAAAAAAAAGG | 217069 |
rs263659388 | in-del | -/TG | | | intron-variant | Trim25 | Mm_Celera | 11:89010332 | TGTTTTGTTTTGTTT[-/TG]TTTTTAAGATTTATT | 217069 |
rs263757593 | snp | A/G | | | intron-variant | Trim25 | GRCm38.p3 | 11:89015986 | GTAAGTGTTCTGATA[A/G]ATGAATGGTTAGTTG | 217069 |
rs263984151 | in-del | -/TCT | | | upstream-variant-2KB, intron-variant | Trim25, LOC102637854 | Mm_Celera | 11:88997827 | GTGAGTAAAAATTTC[-/TCT]TTTTTTTTTTTTCAG | 217069 |
rs264617101 | in-del | -/CCAT | | | intron-variant | Trim25 | GRCm38.p3 | 11:89015932 | GGTGGTCAATGCACC[-/CCAT]GGGGAGTAGGTAGCT | 217069 |
rs386858484 | in-del | -/C | | | intron-variant | Trim25 | Mm_Celera | 11:89005808 | TGGGCTAGCCAGGCC[-/C]TACATAGTGAGACCT | 217069 |
rs386888240 | in-del | -/AT | | | intron-variant | Trim25 | Mm_Celera | 11:89014188 | GGCAGGTGGATCTCT[-/AT]GGGTTTGAGGCCAGC | 217069 |
rs386901887 | in-del | -/TTTTCATTTGTTTTTATTTTAT | | | intron-variant | Trim25 | GRCm38.p3 | 11:89007384 | AACAGGGTTTTTTTT[-/TTTTCATTTGTTTTTATTTTAT]GTGCATTATTGTTTT | 217069 |
rs386943270 | in-del | -/CC | | | intron-variant, upstream-variant-2KB | Trim25, LOC102637854 | Mm_Celera | 11:89001279 | AGTGGCTTTAGAGGT[-/CC]CCCCCCCATTACAGA | 217069 |
rs386990351 | in-del | -/C | | | intron-variant | Trim25 | GRCm38.p3 | 11:89009434 | GTGTGTGTGTGTGTG[-/C]TTTGTGTGTGTGTGT | 217069 |
rs387068089 | in-del | -/A | | | downstream-variant-500B | Trim25 | Mm_Celera | 11:89020476 | ACACTTAACTCTAAA[-/A]TGGCTGGCGTATTCT | 217069 |
rs387079732 | in-del | -/CC | | | intron-variant | Trim25 | Mm_Celera | 11:89008815 | CCTGCCTCTGCCTCC[-/CC]AAGGGTTAGGAAAGG | 217069 |
rs387215720 | in-del | -/T | | | intron-variant | Trim25 | Mm_Celera | 11:89006894 | ACAGTGTACTCATAT[-/T]AAATAAATAAATCTT | 217069 |
rs387227370 | in-del | -/CCTGCC | | | intron-variant | Trim25 | GRCm38.p3 | 11:89012601 | GAGGACCCCCCCCCC[-/CCTGCC]AAGATGTGCTTTAAC | 217069 |
rs387265889 | in-del | -/T | | | intron-variant | Trim25 | GRCm38.p3 | 11:89003483 | AATGCTATTATAATA[-/T]TTTTTTTTTTGTAGA | 217069 |
rs387271592 | in-del | -/TTGT | | | intron-variant | Trim25 | Mm_Celera | 11:89007634 | TTTTTGTTTGTTTGT[-/TTGT]CGTGTTTGATTCTGA | 217069 |
rs387277642 | in-del | -/GG | | | downstream-variant-500B | Trim25 | GRCm38.p3 | 11:89020526 | GCTGCTGGGACAGAG[-/GG]ACCTGCAAGGATGAG | 217069 |
rs387337867 | in-del | -/A | | | utr-variant-3-prime | Trim25 | GRCm38.p3 | 11:89018894 | TAAGACCTTACCTTA[-/A]CCATAAGCATTTCTG | 217069 |
rs387357785 | in-del | -/CC | | | intron-variant | Trim25 | GRCm38.p3 | 11:89008814 | GCCTGCCTCTGCCTC[-/CC]CAAGGGTTAGGAAAG | 217069 |
rs387463229 | in-del | -/GTGT | | | intron-variant | Trim25 | GRCm38.p3 | 11:89008936 | GCTGGGTCTTGGGGT[-/GTGT]TCACCTCCAAGCAGG | 217069 |
rs387630585 | in-del | -/AGTCTC | | | intron-variant | Trim25 | GRCm38.p3 | 11:89008418 | TGACCCTCCTGCCTC[-/AGTCTC]TGGAGGAACTGGAGT | 217069 |
rs387673928 | in-del | -/CAAA | | | intron-variant | Trim25 | Mm_Celera | 11:89005153 | AAACAAACAAACAAA[-/CAAA]ACTGTGGTAGAGTGG | 217069 |
rs387781418 | in-del | -/A | | | downstream-variant-500B | Trim25 | Mm_Celera | 11:89020318 | CCTGCCTTTTGCAAA[-/A]CGACCAAAATGGGAG | 217069 |
rs387793031 | in-del | -/TTTT | | | intron-variant | Trim25 | GRCm38.p3 | 11:89014686 | TGGTGACCTTGTGCT[-/TTTT]TTTTGGATGGAGAAG | 217069 |
rs580910513 | snp | G/T | | | intron-variant | Trim25 | GRCm38.p3 | 11:89013670 | TTCACACGTGTGTGT[G/T]TGTGTGTGTGTGTGT | 217069 |
rs582288470 | snp | A/T | | | intron-variant | Trim25 | GRCm38.p3 | 11:89007009 | AGTTCGAGGCCAGCC[A/T]GGTCTACAAAGTGAG | 217069 |
rs584773570 | snp | G/T | | | intron-variant | Trim25 | GRCm38.p3 | 11:89007012 | TCGAGGCCAGCCTGG[G/T]CTACAAAGTGAGTTC | 217069 |