SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6153819 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Rchy1 | Mm_Celera | 5:91954877 | TAAACCAACTGAGAC[A/G]Ctgtactggctggtt | 68098 |
rs6153850 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rchy1 | Mm_Celera | 5:91954901 | gctggttcatgtcaa[C/T]gtggcacaagttaaa | 68098 |
rs13459347 | snp | A/C | | | stop-gained, nc-transcript-variant | Rchy1 | Mm_Celera | 5:91949784 | GCTTTGTGACTCCTA[A/C]AATACTGCCCAAGCT | 68098 |
rs29509498 | snp | A/G | 0.5 | 0 | intron-variant | Rchy1 | Mm_Celera | 5:91959176 | CTAGAGTCATCAGAG[A/G]GGAAGGTGCTTCAGT | 68098 |
rs29526204 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Rchy1 | Mm_Celera | 5:91957008 | TACAGGCAATAAATC[A/G]GATTATGACTTTCAG | 68098 |
rs29545223 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Rchy1 | Mm_Celera | 5:91952694 | AGTATATGTGGATGG[A/G]AAACAAGAGGGTTTG | 68098 |
rs29546658 | snp | A/G | 0.5 | 0 | intron-variant | Rchy1 | Mm_Celera | 5:91958053 | AGTTAATCACAAATA[A/G]AGGAAGTCCTAGCAG | 68098 |
rs29561766 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Rchy1 | Mm_Celera | 5:91950940 | ATGAGCTCCAATGTA[C/T]GTGAGGTATACCTTC | 68098 |
rs29581511 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rchy1 | Mm_Celera | 5:91957051 | TAGATGAATGATCTC[C/T]CTTAAAACAAAAGAA | 68098 |
rs29583878 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Rchy1 | Mm_Celera | 5:91954933 | TCATCAGAGAGGAAG[C/G]AGAATCAGTGAGGCA | 68098 |
rs29634000 | snp | C/G | 0.5 | 0 | intron-variant | Rchy1 | Mm_Celera | 5:91959662 | TTCATCTTTTATTCT[C/G]AAACATGTCATTGGC | 68098 |
rs29723069 | snp | A/C | 0.5 | 0 | intron-variant | Rchy1 | Mm_Celera | 5:91956727 | GTGTATGCTTTAATC[A/C]CAGTACTCAGGAAGC | 68098 |
rs29773567 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Rchy1 | Mm_Celera | 5:91952436 | CAAAGAAATGGTTTT[C/T]CTAAAACTTATCCCA | 68098 |
rs29773875 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Rchy1, Thap6 | Mm_Celera | 5:91965023 | GCCTAATATATGTAT[A/G]TATATATATATATAT | 68098 |
rs29774350 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rchy1 | Mm_Celera | 5:91953279 | AGGAGAATCTTACAT[C/T]AACAAAAGCATCAAA | 68098 |
rs29777602 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Rchy1 | Mm_Celera | 5:91957455 | CTAAGTTGCCTTGGT[A/C]ATAATGTTTTATCAC | 68098 |
rs29778734 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Rchy1 | Mm_Celera | 5:91951188 | TCCCTCCTACTGAGG[C/T]ACATATCCAATATTA | 68098 |
rs30671205 | snp | A/G | 0.277778 | 0.248452 | downstream-variant-500B | Rchy1 | Mm_Celera | 5:91948657 | TGCTTGCATTAATAA[A/G]ACAGAATATGTTGAC | 68098 |
rs31761862 | snp | A/G | 0.42 | 0.183303 | utr-variant-3-prime, nc-transcript-variant | Rchy1 | Mm_Celera | 5:91948976 | TAACAACCTAGAGGG[A/G]AAAAAAGTCTGTAAA | 68098 |
rs31761863 | snp | C/T | 0.473373 | 0.11227 | utr-variant-3-prime, nc-transcript-variant | Rchy1 | Mm_Celera | 5:91948998 | GTCTGTAAAACAGTA[C/T]TTCAGTACAATTTCA | 68098 |
rs31762474 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91955180 | CACTTCCTTGAATAA[C/T]GAACAGCAATATGGA | 68098 |
rs31762475 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91955241 | AAACCTCTCTTTCCC[C/T]AAGGTGCTTTTTGAT | 68098 |
rs31762476 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rchy1 | Mm_Celera | 5:91955439 | AGTTGAAGTTGGCAA[C/T]ATATGAAAAATAGCA | 68098 |
rs31762477 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91955963 | TAGGATGGGGTATAG[A/G]TGTACCATGTTCAAC | 68098 |
rs31762478 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rchy1 | Mm_Celera | 5:91956058 | TCAGATGGTACTGGA[C/T]CATCAACTGTAATAC | 68098 |
rs31762479 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91956133 | ACAGTGCACAATCCA[C/T]GTTCCTCACAACCTG | 68098 |
rs31762480 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rchy1 | Mm_Celera | 5:91956155 | CACAACCTGCACATC[A/G]GCACATGTATAACAG | 68098 |
rs31762481 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91956318 | TCAATTTAAAAGAAA[C/T]CTTTATACATCCTGG | 68098 |
rs31762482 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Rchy1 | Mm_Celera | 5:91956422 | AACCAAGGTTATAAA[C/G]AGAGAAACCTTGTCT | 68098 |
rs31762483 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91956520 | ATTTTGTTCTCATAT[A/G]ATAAAGACTATGATC | 68098 |
rs31762694 | snp | A/G | 0.359862 | 0.224567 | utr-variant-3-prime, nc-transcript-variant | Rchy1 | Mm_Celera | 5:91949289 | AGAAAAGAAAATTAA[A/G]AAGCACACGTAATTA | 68098 |
rs31762695 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Rchy1 | Mm_Celera | 5:91949522 | TTTCCAATCTACACA[C/G]GCTCAGAGGCTTCAC | 68098 |
rs31762696 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Rchy1 | Mm_Celera | 5:91949622 | GTGTTCACGCTGTGA[C/G]CCCCTGTTGTGACAG | 68098 |
rs31762697 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Rchy1 | Mm_Celera | 5:91949641 | CTGTTGTGACAGTGG[A/T]ATGAAACATCTCTGA | 68098 |
rs31762698 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Rchy1 | GRCm38.p3 | 5:91949672 | TGCAGATGAACGAAC[A/C]CTGGGATCTTTTACA | 68098 |
rs31762699 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Rchy1 | Mm_Celera | 5:91949715 | CATCACAGAGCTGTT[C/G]TCTAGCCAAGGACAG | 68098 |
rs31762700 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Rchy1 | Mm_Celera | 5:91949760 | ATCCACTGGCACTCT[A/G]CGGCCTCCAGCTTGG | 68098 |
rs31762701 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Rchy1 | Mm_Celera | 5:91949805 | GTCACAAAGCTTACA[C/T]TTCATGCCTAAGATA | 68098 |
rs31762702 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rchy1 | Mm_Celera | 5:91949877 | AATCTGAAAAATGAA[A/G]AGGAAAAGTTTTAAG | 68098 |
rs31762703 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rchy1 | Mm_Celera | 5:91949945 | ACTTGAAAGTCATAT[A/G]AAAGATGTGAAAATA | 68098 |
rs31763164 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Rchy1 | Mm_Celera | 5:91949954 | TCATATGAAAGATGT[C/G]AAAATACACGTATGT | 68098 |
rs31763165 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91950037 | TATTAGGATGGCTTT[A/G]AATTCATAAAATGAA | 68098 |
rs31763166 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91950274 | TCTACAAATTGGAAT[A/G]TTTTGCTTAATTTTT | 68098 |
rs31763167 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rchy1 | Mm_Celera | 5:91950391 | ATAACAAGGACTCAA[C/T]CTTTTCTGATGCTAA | 68098 |
rs31763168 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91950446 | CTGCAAATAGATCAA[C/T]ATATAACTATGCAGC | 68098 |
rs31763169 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91950893 | CACACTCCATAAATA[C/T]ACTAAGTCAGTGCCT | 68098 |
rs31763170 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rchy1 | Mm_Celera | 5:91950916 | CAGTGCCTTGTACAC[G/T]TTTAAGGAATGAGCT | 68098 |
rs31763171 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rchy1 | Mm_Celera | 5:91950925 | GTACACGTTTAAGGA[A/G]TGAGCTCCAATGTAT | 68098 |
rs31763172 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91950974 | AAGCTATTATTCAAA[C/G]CAAGCATCTACACGA | 68098 |
rs31763173 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rchy1 | Mm_Celera | 5:91950987 | AAGCAAGCATCTACA[C/T]GAACACAGTAAACTT | 68098 |
rs31763324 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rchy1 | Mm_Celera | 5:91956901 | GTTAGTTTATGAGAG[G/T]GTTCGGAGGGAAGAA | 68098 |
rs31763325 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rchy1 | Mm_Celera | 5:91957020 | ATCAGATTATGACTT[C/T]CAGATGACTCTATCT | 68098 |
rs31763326 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Rchy1 | Mm_Celera | 5:91957070 | AAAACAAAAGAAAGT[C/G]AAACTGGGCAATGGT | 68098 |
rs31763327 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91957142 | TGGCATGGAGTATAT[A/G]GTGAGCAGTGAGATG | 68098 |
rs31763328 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91957158 | GTGAGCAGTGAGATG[C/T]ACTTGTGTGAATGGA | 68098 |
rs31763329 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91957176 | TTGTGTGAATGGAAA[C/T]GTGCCCCTTGTGGGC | 68098 |
rs31763330 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91957302 | CTCTGAGACTCAGGT[A/G]ACTGCTAGTTCTCAT | 68098 |
rs31763331 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91957447 | ACTCTCTTCTAAGTT[A/G]CCTTGGTCATAATGT | 68098 |
rs31763332 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rchy1 | Mm_Celera | 5:91957458 | AGTTGCCTTGGTCAT[A/G]ATGTTTTATCACAGC | 68098 |
rs31763333 | snp | C/T | 0.142012 | 0.225474 | missense, nc-transcript-variant, intron-variant | Rchy1 | Mm_Celera | 5:91957598 | AACAGGTGGCAAATA[C/T]TGCAGTAATATTCTC | 68098 |
rs31764054 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rchy1 | Mm_Celera | 5:91951155 | TAGGATCAAATCTAG[A/G]CCCTTGCACTCACTA | 68098 |
rs31764055 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91951161 | CAAATCTAGACCCTT[A/G]CACTCACTACCTCCC | 68098 |
rs31764056 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91951299 | TTCAGACATCCAAAA[A/G]CTATTATTTTCCAAC | 68098 |
rs31764057 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Rchy1 | Mm_Celera | 5:91951354 | TGAAAATAAGCTACA[A/T]AGCAACCCTCTCATT | 68098 |
rs31764058 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Rchy1 | GRCm38.p3 | 5:91951833 | TACGTCAACAGTCAC[A/G]TTCTGGTATTCGGAT | 68098 |
rs31764059 | snp | C/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Rchy1 | Mm_Celera | 5:91951845 | CACGTTCTGGTATTC[C/G]GATGGCATGGGAGTC | 68098 |
rs31764060 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Rchy1 | GRCm38.p3 | 5:91951881 | TACCTCAGTATCTAG[C/T]TGTCTCCAGTACCGA | 68098 |
rs31764061 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Rchy1 | GRCm38.p3 | 5:91951920 | TAAGGCAGAATGCAT[A/G]CACAATGGGCATCTG | 68098 |
rs31764062 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91951966 | ATAGTAAGTGGGATC[C/T]GCATCAACTCAGGCT | 68098 |
rs31764063 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91951969 | GTAAGTGGGATCCGC[A/G]TCAACTCAGGCTCAC | 68098 |
rs31765024 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91952010 | CAGCTCACTAGCACG[A/T]AAATCTCCAGAGTAT | 68098 |
rs31765025 | snp | C/T | 0.255 | 0.24995 | intron-variant | Rchy1 | Mm_Celera | 5:91952017 | CTAGCACGTAAATCT[C/T]CAGAGTATTAGTCTA | 68098 |
rs31765026 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91952132 | ATCATATGTCTTTAT[C/T]CTTTTTTTCCCCCCT | 68098 |
rs31765027 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rchy1 | Mm_Celera | 5:91952537 | TTCATCAGTGGAATC[A/G]AAGCACCTTTCCACT | 68098 |
rs31765028 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rchy1 | Mm_Celera | 5:91952570 | TTCCTAGTTCTCATC[G/T]TACTGTAGTTCCAGT | 68098 |
rs31765029 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Rchy1 | Mm_Celera | 5:91952571 | TCCTAGTTCTCATCG[C/T]ACTGTAGTTCCAGTC | 68098 |
rs31765030 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91952916 | AATCTTAAACTGTAA[A/G]CTTTTAAATCCATCA | 68098 |
rs31765031 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91953040 | TCGAGCAGGAAGAAC[A/G]TCATCTGCTTACCTA | 68098 |
rs31765032 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91953211 | AAAATATTCCACACT[A/C]ACCTCCAAGCATATT | 68098 |
rs31765033 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Rchy1 | Mm_Celera | 5:91953316 | AAATGTCAACTATAA[C/T]AGCATTAATAAAATA | 68098 |
rs31766114 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91953489 | TCTGACTTCCACAGG[C/T]GAACAACTAAGTTAG | 68098 |
rs31766115 | snp | A/G | 0.32 | 0.24 | intron-variant | Rchy1 | Mm_Celera | 5:91953519 | GAATCCCGGCAGTGG[A/G]AGTTTTTATCGTGGC | 68098 |
rs31766116 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rchy1 | Mm_Celera | 5:91953765 | AGCCCTGCCATTTAT[A/G]AATCTTTAAGATTTT | 68098 |
rs31766117 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91953926 | ATGTTTCTGACAGTC[C/T]ACAGCATTGCTGAGT | 68098 |
rs31766118 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91954040 | CAGAACAGAGCCAGA[A/G]AAATATAATCCATGA | 68098 |
rs31766119 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91954106 | TTTTGAATTCTCATC[G/T]TAAGAGGCGTCTCTG | 68098 |
rs31766120 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91954266 | TCTTTAACAAAGTCA[C/T]ATTCTGCTCATCAGG | 68098 |
rs31766121 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Rchy1 | Mm_Celera | 5:91954362 | GTGTTCACTATTCAC[A/C]CTGACTTCTTTGCTA | 68098 |
rs31766122 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rchy1 | Mm_Celera | 5:91954763 | TCATGAAAGGAAATA[C/T]AAAGAATTATTCTTA | 68098 |
rs31766123 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rchy1 | Mm_Celera | 5:91954767 | GAAAGGAAATACAAA[A/G]AATTATTCTTAGGAC | 68098 |
rs31767064 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rchy1 | Mm_Celera | 5:91954951 | AATCAGTGAGGCAAA[C/G]CCTGCATGAGATCTA | 68098 |
rs33145255 | snp | A/G | 0.5 | 0 | intron-variant | Rchy1 | Mm_Celera | 5:91958191 | ACACAAAAATTTTAA[A/G]AGATAGAAATCGCTA | 68098 |
rs33147168 | snp | A/G | 0.5 | 0 | intron-variant | Rchy1 | Mm_Celera | 5:91958565 | TCAAGCGAAACCTTT[A/G]CATTACTGGGACTAT | 68098 |
rs33211951 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rchy1 | Mm_Celera | 5:91957054 | ATGAATGATCTCCCT[C/T]AAAACAAAAGAAAGT | 68098 |
rs33219267 | snp | A/G | 0.5 | 0 | intron-variant | Rchy1 | Mm_Celera | 5:91957683 | ATTAAAAACTCGAGT[A/G]AATTTATCAAAACGA | 68098 |
rs33423178 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | Rchy1, Thap6 | Mm_Celera | 5:91963211 | GCGCCCCCTTTAGAA[A/G]ATATTGTGCTGTCAC | 68098 |
rs33447003 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Rchy1, Thap6 | Mm_Celera | 5:91963624 | GGGAGGCAATTGTCC[A/G]GGAGGAGATGCCTTT | 68098 |
rs33510410 | snp | A/G | 0.5 | 0 | intron-variant | Rchy1 | Mm_Celera | 5:91958743 | CTTGGTAATGTGTAA[A/G]AGTCACCCAGGTGGT | 68098 |
rs33612901 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rchy1 | Mm_Celera | 5:91953994 | ATGTGCATGTGTGAA[A/C]TCAAATGTATTCTAT | 68098 |
rs33638042 | snp | A/G | 0.5 | 0 | intron-variant | Rchy1 | Mm_Celera | 5:91959635 | TCTTTTTTTTCCTAT[A/G]CTATAAGTGAGTTCA | 68098 |