SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3665567 | snp | C/T | 0.362812 | 0.2231 | utr-variant-3-prime, intron-variant | Rmnd5a | GRCm38.p3 | 6:71392213 | TCCACACACACAATG[C/T]TTGATGCTGGTGCAC | 68477 |
rs3723437 | snp | A/T | 0.429688 | 0.173817 | utr-variant-3-prime | Rmnd5a | GRCm38.p3 | 6:71391921 | GTAGTTAGTTCCTCA[A/T]ACAGAGAACAACTCT | 68477 |
rs13475613 | snp | A/G | | | utr-variant-3-prime | Rmnd5a | GRCm38.p3 | 6:71389153 | ATGTATCTCTTCACC[A/G]TGTCTTCTCTCACCT | 68477 |
rs29826345 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rmnd5a | Mm_Celera | 6:71410812 | GGTGAGATGGCTCAG[C/T]GGTTAAGAGCACTGA | 68477 |
rs29828421 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71424117 | GTACTGATTAGTTCA[C/T]ATAATATCCAAGATA | 68477 |
rs29833707 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71428240 | ACCCCATGGGAAAAA[C/T]AGCTTCAGTGCTAAA | 68477 |
rs29871158 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Rmnd5a | Mm_Celera | 6:71442267 | CAGACAAACCTTGTT[C/T]TTCCCCTTGAACCAA | 68477 |
rs29879970 | snp | A/T | 0.32 | 0.24 | intron-variant | Rmnd5a | Mm_Celera | 6:71415141 | AACATATTTTTTTTA[A/T]AAAAAATTGGGAAAC | 68477 |
rs29916826 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71397428 | AGCATTTAAAGGGGA[A/G]GAGACTCTTCTGGGC | 68477 |
rs29918143 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71432080 | TAGAGTTCTTTTTTC[C/T]TTTGAAACTGTTTAT | 68477 |
rs29962650 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71396782 | ACATGTTGAATAGCT[A/G]CAATAGCGTTTTCTG | 68477 |
rs29964448 | snp | A/C | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Rmnd5a | Mm_Celera | 6:71392978 | TCCCATCTGGAGCAC[A/C]CCCTCCGTGCACACG | 68477 |
rs29964495 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71429465 | TATGGGGCAGGTGAC[A/G]GCAGTGAAACAGCAG | 68477 |
rs29968945 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71413792 | ACTTTGTTTAAGCTG[C/T]TATCTTGAGTCTGTT | 68477 |
rs29970169 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Rmnd5a | GRCm38.p3 | 6:71389487 | GAAAATGAAGCATAC[A/G]CCTGCTACAGCTTTA | 68477 |
rs29970202 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Rmnd5a | GRCm38.p3 | 6:71441815 | CCGTTTTTATAATGT[A/G]GCAGCTAGTGGGCGG | 68477 |
rs29971221 | snp | A/C/T | 0.33241 | 0.236027 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71427979 | CTTGCGTTTCTCGGA[A/C/T]GGTCCAGATTACAGC | 68477 |
rs29979903 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71397210 | TCAAAAGATTGCGTT[C/T]TGATAGGACATTTAA | 68477 |
rs30007165 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71430830 | TAAACACTGGCTACT[A/G]AATTTACAGCATAGA | 68477 |
rs30016459 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71409807 | TCAGAATTAAGGCCA[A/G]TTAATTGGGTAAAAA | 68477 |
rs30017638 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71410104 | CCTGGACAAGAGATA[C/T]AGATGGTTGTGGGTC | 68477 |
rs30019932 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71425987 | AAAATGAGCCCTACC[A/G]CCAAGTACTTAAGTA | 68477 |
rs30021860 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71423149 | TGTAAGCTAAGCACG[A/G]GATTTAATTGCTGCA | 68477 |
rs30022028 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Rmnd5a | GRCm38.p3 | 6:71390237 | GAAAAAGTAAAACGA[A/G]AAATTTACTTAATAA | 68477 |
rs30068887 | snp | A/G | 0.33241 | 0.236027 | utr-variant-3-prime | Rmnd5a | GRCm38.p3 | 6:71390533 | TCCTAAGGCAGCCTT[A/G]TCCACAACCAGAAAA | 68477 |
rs30075015 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71406120 | TTGCCTTGGTCATGG[C/T]ATCCCCTCATAGCAG | 68477 |
rs30116237 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rmnd5a | GRCm38.p3 | 6:71442634 | GTGTGCGCCACCACG[C/T]CCGGCTGTAAGAGCT | 68477 |
rs30116855 | snp | C/T | 0.493827 | 0.0552116 | upstream-variant-2KB | Rmnd5a | GRCm38.p3 | 6:71441521 | TCATAGCATTCCTAC[C/T]TCCACCATGGTTGTA | 68477 |
rs30129556 | snp | A/G | 0.32 | 0.24 | intron-variant | Rmnd5a | Mm_Celera | 6:71411734 | AGCATGCTACCTTTC[A/G]TTATCTTGTTCTTTA | 68477 |
rs30162201 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Rmnd5a | GRCm38.p3 | 6:71389367 | GCCCACCCCTGCCTG[A/G]CAGTGAGGAGTTTAA | 68477 |
rs30167595 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71397495 | TGAATAAAACATTCC[A/C]AAGTTTTCCCACCAG | 68477 |
rs30173287 | snp | A/C | 0.32 | 0.24 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71425277 | GGCAAAACATTAATG[A/C]ACATAAAATAAAGGC | 68477 |
rs30174476 | snp | A/G | 0.32 | 0.24 | intron-variant | Rmnd5a | Mm_Celera | 6:71400067 | ACAGGAGAGCACTGG[A/G]GTCCCTTGCACTGGG | 68477 |
rs30209312 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71406708 | GTAGGAATATGGAAG[A/G]CTGTGTTCCTGAGAG | 68477 |
rs30213915 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71400435 | AAGCCTATCCTTTAA[C/T]TGACTTTTATTTGGA | 68477 |
rs30218971 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Rmnd5a | GRCm38.p3 | 6:71440951 | GTTGGCTTGAAGAGC[A/G]GAGCTTGGCGCTTCT | 68477 |
rs30226035 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71427673 | CCACAGCCATATTCA[C/T]CCATATCAAGTTACC | 68477 |
rs30254860 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rmnd5a | Mm_Celera | 6:71411770 | ACTTCATGTGATTTA[A/C]TATAAATATCCTAGT | 68477 |
rs30265639 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71411181 | CAGGTCCCAGGAAAT[C/T]ATTTTATGTTCTAAG | 68477 |
rs30314442 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71400554 | ATTCTGTGGTGGAGC[A/G]CTTGCCCAGCATGTA | 68477 |
rs30319824 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71429240 | TGACAGGAAGAAAAA[C/T]GAAGGAAAACCAGTA | 68477 |
rs30321532 | snp | C/T | 0.5 | 0 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71393519 | AGGTTTACATTGCAC[C/T]TGTCCCTAAATGAAT | 68477 |
rs30324548 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71405550 | CCGTCTCACAGACAA[C/T]AGCAACCTAAAGTGG | 68477 |
rs30365901 | snp | C/T | 0.32 | 0.24 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71411851 | TAAACAAATAACTTG[C/T]TCCCTATTTTATGTG | 68477 |
rs30366042 | snp | A/C | 0.444444 | 0.157135 | downstream-variant-500B | Rmnd5a | Mm_Celera | 6:71388459 | AAACAAACAAAAAAA[A/C]CCAAACCAAAACAAA | 68477 |
rs30366939 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rmnd5a | Mm_Celera | 6:71430779 | CAAAACAAAACAAAA[A/C]AAAAACTATGCTAAA | 68477 |
rs30366963 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71425798 | AAGTTCAAGTTAAAT[A/G]TGTAGGACTTAACAA | 68477 |
rs30368325 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rmnd5a | Mm_Celera | 6:71411624 | AAAAAAAAAAAAAAA[A/G]GAGTATCCTCTACCC | 68477 |
rs30404736 | snp | C/T | 0.32 | 0.24 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71404029 | CTGTAACTCCAGTTC[C/T]AGGAGATCCAACTCC | 68477 |
rs30407437 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71423359 | TTAAAACTTTTTTTC[C/T]TCATAATTTCATTGT | 68477 |
rs30409168 | snp | C/T | 0.33241 | 0.236027 | upstream-variant-2KB | Rmnd5a | GRCm38.p3 | 6:71441063 | TTTCTCCGCATGGAA[C/T]TTTGGCCGGAGTTTC | 68477 |
rs30418274 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71424910 | CATATGAAACACACA[A/C]TAGATGTAACACAGG | 68477 |
rs30418320 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71405535 | AAAGGCGGCTTCTAG[C/T]CGTCTCACAGACAAC | 68477 |
rs30461107 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71403866 | GCTCTCAAAAAGCAA[G/T]GCCCTCAATACCCCA | 68477 |
rs30467462 | snp | C/G | 0.33241 | 0.236027 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71396831 | AACATTCATCTTCAA[C/G]GATTGTCAAGTTGAA | 68477 |
rs30472216 | snp | A/G | 0.32 | 0.24 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71415250 | GCAATATTTTCAGAA[A/G]TATGCTATAGTAAGC | 68477 |
rs30508849 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Rmnd5a | Mm_Celera | 6:71394971 | GCCTAAATACCTTGT[A/C]ATTTCACCAGAACAT | 68477 |
rs30510593 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rmnd5a | Mm_Celera | 6:71410876 | GCAACCACATGGTGG[C/T]TCACAATCATCCGTA | 68477 |
rs30522348 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71393528 | TTGCACTTGTCCCTA[A/G]ATGAATTTCCAATGT | 68477 |
rs30523389 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71424961 | AACCTCAACTTCGAC[C/T]TTAAGCTACCATTCC | 68477 |
rs30543477 | snp | C/T | 0.5 | 0 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71397456 | GGCCTGTCTTCTCTT[C/T]AAGTATGATTATGCA | 68477 |
rs30550587 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71406618 | TGTGATATGCCTGAC[C/T]GTGCTTTTGTTTGGA | 68477 |
rs30559312 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71414244 | CATGGTGCTCCTGTC[C/T]AACAGAAACACGACG | 68477 |
rs30569747 | snp | A/G | 0.492188 | 0.0620098 | synonymous-codon | Rmnd5a | GRCm38.p3 | 6:71414791 | TGTGCTTACCTGGCA[A/G]AGCTCCTCAGCTACA | 68477 |
rs30570130 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71407864 | CCAAGAATCAGAGTC[C/T]TACACTGATAAAAAA | 68477 |
rs30572708 | snp | A/C | 0.32 | 0.24 | intron-variant | Rmnd5a | Mm_Celera | 6:71404118 | TGCAGGCAAACCCAA[A/C]AAAAAATAAGTTAAT | 68477 |
rs30601523 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71433606 | CTTCTTTCTCTACCA[A/G/T]GATCACCTCGATGGT | 68477 |
rs30612661 | snp | A/T | 0.32 | 0.24 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71403876 | AGCAATGCCCTCAAT[A/T]CCCCAAATAAAAAGA | 68477 |
rs30614917 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71409851 | CTCTAGGGGGAAAAT[C/T]CAACTTGTTTGATCT | 68477 |
rs30648644 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rmnd5a | Mm_Celera | 6:71393643 | CAAAGAGCGCTAGTT[C/G]CTTGTGGCCACAGTC | 68477 |
rs30648646 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rmnd5a | Mm_Celera | 6:71393797 | GACTAGCCTAACTAC[C/T]TAAGCCAGAACACCT | 68477 |
rs30648648 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rmnd5a | Mm_Celera | 6:71393835 | CTGTTTTGTTTTAAA[C/T]TGGGCTGTCTGTAAA | 68477 |
rs30648650 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rmnd5a | Mm_Celera | 6:71394566 | CACTCATTTATCCTT[A/G]TTACATCTTACTTCC | 68477 |
rs30648652 | snp | A/C | 0.124444 | 0.216185 | missense | Rmnd5a | Mm_Celera | 6:71394687 | ACCACAAACCAATTT[A/C]ATGGGTGGATTGTTA | 68477 |
rs30648654 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rmnd5a | Mm_Celera | 6:71411338 | TCCCATTGTAAGCAA[A/G]CAGTTCAAAATTTTC | 68477 |
rs30648656 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Rmnd5a | Mm_Celera | 6:71411639 | AGAGTATCCTCTACC[A/C]TAAACACAAAATTCA | 68477 |
rs30648659 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rmnd5a | Mm_Celera | 6:71412098 | AAAACCTAAAATAAT[C/T]ATTATTTGGCCTGTC | 68477 |
rs30648661 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rmnd5a | Mm_Celera | 6:71413557 | CTTCGCAAATCTTCG[C/T]ACCAGCCGTGGACTC | 68477 |
rs30648663 | snp | A/T | 0.495868 | 0.0452663 | intron-variant | Rmnd5a | Mm_Celera | 6:71414009 | TTTTTTTTAACAACA[A/T]AAAAATGCAACAGAA | 68477 |
rs30649494 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rmnd5a | Mm_Celera | 6:71394881 | TCTGAGAAAATCAAA[C/T]ATGATGCTTCAGAAG | 68477 |
rs30649497 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71395255 | TTTAGTCCAGCGCCC[C/T]ATCCTAGCTCCTGAC | 68477 |
rs30649499 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rmnd5a | Mm_Celera | 6:71396006 | GCTTTTCCAGTCAAG[A/T]GCATGCTGTTAGCTG | 68477 |
rs30649501 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rmnd5a | Mm_Celera | 6:71396402 | CGGCATCTGTGACAT[A/C]ATTTTCTCACAAATG | 68477 |
rs30649503 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rmnd5a | Mm_Celera | 6:71396424 | TCACAAATGGAAATT[A/G]CAGGTTAAAGTCCCT | 68477 |
rs30649745 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Rmnd5a | Mm_Celera | 6:71414432 | TGCCAATAAGTGTAG[C/G]ACTAGGGAGGCTGAA | 68477 |
rs30649746 | snp | A/G | 0.5 | 0 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71414552 | AGAAACAACAATTTG[A/G]ATGTTAACTCTGAGT | 68477 |
rs30649748 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Rmnd5a | Mm_Celera | 6:71414688 | ATTACAAATCTATCT[A/C]CAGTTTGAGGTACAC | 68477 |
rs30649750 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rmnd5a | Mm_Celera | 6:71414763 | TGTTTGTTTTCCCTA[C/T]GCCTCACTGGCATGT | 68477 |
rs30649753 | snp | C/G | 0.48 | 0.0979796 | missense | Rmnd5a | Mm_Celera | 6:71414866 | GAGAAGCCGTTGGCT[C/G]TCTGCCTGCCAGCAG | 68477 |
rs30650392 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Rmnd5a | GRCm38.p3 | 6:71393502 | CTAATCTCTGCCTAC[A/C]GAGGTTTACATTGCA | 68477 |
rs30650457 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Rmnd5a | GRCm38.p3 | 6:71396921 | AGCTTTGATGTTAAT[C/T]AGCGCAGGCAGCGCC | 68477 |
rs30650459 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rmnd5a | Mm_Celera | 6:71396973 | AGGGCAAAAGAGGAA[A/G]CATCAGTGCCAACCC | 68477 |
rs30650461 | snp | A/G | 0.32 | 0.24 | intron-variant | Rmnd5a | Mm_Celera | 6:71397041 | TTCCTCTAAAAAGAA[A/G]ACAACTCAACTTTTT | 68477 |
rs30650725 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Rmnd5a | Mm_Celera | 6:71415787 | AGAAATGTATTGTTG[A/T]TCTCTCTTTCTACCA | 68477 |
rs30650727 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rmnd5a | Mm_Celera | 6:71415827 | TAGTGACAGAACTCA[A/G]TTTGTCAAATTCTGA | 68477 |
rs30650729 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Rmnd5a | Mm_Celera | 6:71416210 | CCCACTTGAAAGCAT[A/C]AAAATGTTAACATCT | 68477 |
rs30650731 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rmnd5a | Mm_Celera | 6:71416467 | TACATATACAGCAGG[A/G]ACAAGAACACCTAAA | 68477 |
rs30650733 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rmnd5a | Mm_Celera | 6:71416966 | GAGGAAAGCAAATCT[A/G]TATCCTGGTTTCAAG | 68477 |
rs30651515 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Rmnd5a | Mm_Celera | 6:71417229 | CTTGAACTAGACCCT[A/C]ACCAGTGAAAAAAAC | 68477 |
rs30651517 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rmnd5a | Mm_Celera | 6:71417270 | CTAATGCTAAAATGA[C/T]GCACACATAAACTGA | 68477 |