SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3668791 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31125090 | CAGTGGGAGAGAGAC[A/G]CACATGCATCGTTGG | 68867 |
rs3669445 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31125258 | CTTAGAGCATCTTTC[C/T]TCAGCTCTTCATTCG | 68867 |
rs3669964 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31125299 | AAACTCTTGTAGTCC[C/T]GGCTTTCTGAGAACC | 68867 |
rs3670650 | snp | A/G | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31125438 | CAGGAATCTGTTAAG[A/G]GTGTGGATGGCTTTA | 68867 |
rs3670672 | snp | C/T | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31125442 | AATCTGTTAAGAGTG[C/T]GGATGGCTTTATGCC | 68867 |
rs3685409 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf122 | Mm_Celera | 8:31125490 | CAGAATCTGCAACTC[A/G]CCATCACAAGAATGC | 68867 |
rs3685411 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Rnf122 | Mm_Celera | 8:31125491 | AGAATCTGCAACTCG[C/T]CATCACAAGAATGCT | 68867 |
rs3685460 | snp | A/G | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31125523 | TGTAGAATCTGTAAG[A/G]GCATCACAGGCTCTA | 68867 |
rs3685462 | snp | A/G | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31125526 | AGAATCTGTAAGAGC[A/G]TCACAGGCTCTATGC | 68867 |
rs3696314 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf122 | Mm_Celera | 8:31112780 | CCTAGGTGGTGACGG[C/T]ACCTTCCAGCACAGC | 68867 |
rs4140245 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf122 | Mm_Celera | 8:31125557 | CATGGGCAATCTGCT[A/G]TATTGACTCTTGGGG | 68867 |
rs13461458 | snp | G/T | 0.444444 | 0.157135 | utr-variant-5-prime | Rnf122 | Mm_Celera | 8:31111998 | CTTCCTCCTCTGCCC[G/T]CTTTGTTGCTCTGCA | 68867 |
rs32579105 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Rnf122 | Mm_Celera | 8:31132240 | AGCTATCTCTCCAGC[C/T]CCCAATGAATGACTT | 68867 |
rs32594245 | snp | A/G | 0.429688 | 0.173817 | upstream-variant-2KB | Rnf122 | Mm_Celera | 8:31110751 | GACTCAGTTCCAACA[A/G]ATCAATAGTGGGATG | 68867 |
rs32598394 | snp | C/T | 0.426035 | 0.177515 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31131102 | AGAACACCTGCTGCC[C/T]GGTTTGGCCACTTGA | 68867 |
rs32619185 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31121161 | AGGGCACAGGCACAC[A/C]AGCCACTTCCTCTAC | 68867 |
rs32639940 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf122 | Mm_Celera | 8:31125034 | GTGTCCCCAGGTTGG[G/T]TTTGCCATTCGCTTT | 68867 |
rs32670742 | snp | C/T | 0.415225 | 0.187619 | downstream-variant-500B, utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31131521 | TAAGCAAATTATTCT[C/T]TCCTCTGGGTCCTAT | 68867 |
rs32670797 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf122 | Mm_Celera | 8:31119468 | ACGTGAATGCACATG[C/T]ATCATGTATACATTC | 68867 |
rs32683827 | snp | C/T | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31122855 | GATATGCTGATGTCA[C/T]TTTTTAATTTTTTTA | 68867 |
rs32683830 | snp | A/T | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31126256 | AGGCATTTCTTCAAC[A/T]GAGGCTCCTTTCTCT | 68867 |
rs32687282 | snp | C/T | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31120357 | CTCCCGCTAAACTCT[C/T]CTTATTCACTGATCT | 68867 |
rs32736132 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B | Rnf122 | Mm_Celera | 8:31132086 | ATTTATTATTTATAT[A/G]TATGTATACTGTACC | 68867 |
rs32756486 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf122 | Mm_Celera | 8:31121813 | GGGAAGGCAATTGAA[C/T]CTTTAAAAAAATGTG | 68867 |
rs32780484 | snp | A/C | 0.375 | 0.216506 | downstream-variant-500B | Rnf122 | Mm_Celera | 8:31132231 | ACCTCGCTGAGCTAT[A/C]TCTCCAGCCCCCAAT | 68867 |
rs32791054 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Rnf122 | Mm_Celera | 8:31124546 | CAGCAGCCTAACTCC[C/G]TCTGCACACAGGAAG | 68867 |
rs32811241 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf122 | Mm_Celera | 8:31121006 | ACTGTGGTGTGCCAC[A/C]GTGCCATCTGTCCTT | 68867 |
rs32824561 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31129078 | CACTCCTGCCAGAGC[C/T]TTCCATGGGATGGTT | 68867 |
rs32842167 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31121097 | GCCCCCTGGGTCTCA[C/T]GCTTCCAAAGGTGTT | 68867 |
rs32869694 | snp | G/T | 0.375 | 0.216506 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31131055 | ATTCACACAGTCACC[G/T]GTGAAGTCTTGTGAC | 68867 |
rs32880767 | snp | A/C | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31120355 | TCCTCCCGCTAAACT[A/C]TTCTTATTCACTGAT | 68867 |
rs32897695 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31121262 | GCCAAGGACGCCTCC[A/G]CTGCCAGCTGCCCCC | 68867 |
rs32923263 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31119689 | TGTTTATAAGTCAGC[A/G]TCTCTCTAGGTAGCC | 68867 |
rs32929252 | snp | C/T | 0.345679 | 0.230967 | downstream-variant-500B | Rnf122 | Mm_Celera | 8:31131952 | TAGGCCTGTGAGCTG[C/T]ACCCTAGCCACTGTT | 68867 |
rs32948366 | snp | C/T | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31119797 | TGGGATTAAAGGCGG[C/T]GTGTACCACTGCCCC | 68867 |
rs32976125 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B | Rnf122 | Mm_Celera | 8:31131777 | GTGCTCACATAATTA[A/G]ACACTAAGTGTCAGC | 68867 |
rs32988528 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31121599 | CAACCCTTCGACGAT[C/T]CCACCCCCCACCCCC | 68867 |
rs33024077 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Rnf122 | Mm_Celera | 8:31124723 | AGCGGTGCCCCGTTG[A/G]TATCTATGAAACAAG | 68867 |
rs33080882 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31119517 | ATTGGATGTGCGTGA[C/T]GCTTAGAGCAGAGTT | 68867 |
rs33087908 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf122 | Mm_Celera | 8:31119464 | AGGGACGTGAATGCA[C/T]ATGCATCATGTATAC | 68867 |
rs33102604 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31121667 | ATGCAGGCTAACGAA[A/G]GAGCTGTGAGGGTTC | 68867 |
rs33103883 | snp | C/T | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31125007 | CATCCCAGAGGCCTA[C/T]CACTCCTGTTAGTGT | 68867 |
rs33112106 | snp | C/T | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31120788 | CCAGACAGTCAAGGA[C/T]TTGCTCAAAGTCATA | 68867 |
rs33122028 | snp | A/C | 0.401235 | 0.199068 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31128713 | TCCTGGCACATGGAC[A/C]CTGGGAAAGACTGCC | 68867 |
rs33157772 | snp | A/T | 0.401235 | 0.199068 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31129109 | TCCAAGGGAAAGGAG[A/T]GAAAGATCAAGAAAC | 68867 |
rs33167104 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Rnf122 | Mm_Celera | 8:31132220 | CGGTGCTCTTAACCT[C/T]GCTGAGCTATCTCTC | 68867 |
rs33178918 | snp | A/C | 0.429688 | 0.173817 | upstream-variant-2KB | Rnf122 | Mm_Celera | 8:31110840 | ACACACTGCTTCTGA[A/C]CGTGGCTGTGGCGCC | 68867 |
rs33187843 | snp | A/G | 0.401235 | 0.199068 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31129000 | GTGACTGTGACCATG[A/G]ACGCCTCCCTTTGGA | 68867 |
rs33201658 | snp | C/T | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31124068 | ATGACACAGAATCTG[C/T]GTATAATTATGGTTC | 68867 |
rs33201864 | snp | C/T | 0.429688 | 0.173817 | intron-variant, upstream-variant-2KB | Rnf122 | Mm_Celera | 8:31113609 | CACTGACCTGCTCAG[C/T]ACCCTTTATCTTGCA | 68867 |
rs33250944 | snp | A/G | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31123319 | GTCAGGTCATGAAAT[A/G]CAAGTTTTTGTATTA | 68867 |
rs33267706 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Rnf122 | Mm_Celera | 8:31121740 | AGAGGGCATCTGGCA[A/C]TAGGGCCCAGTGGTC | 68867 |
rs33278501 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf122 | Mm_Celera | 8:31119455 | TATACACATAGGGAC[A/G]TGAATGCACATGCAT | 68867 |
rs33285690 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf122 | Mm_Celera | 8:31110774 | GTGGGATGATAAGTC[C/G]TGACAAAGGAAGAGC | 68867 |
rs33291640 | snp | A/C/T | 0.444444 | 0.157135 | downstream-variant-500B, utr-variant-3-prime | Rnf122 | GRCm38.p3 | 8:31131693 | TGTTCTTTTCCCCCC[A/C/T]ACAGAAGACATTTTT | 68867 |
rs33314880 | snp | C/G | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31120347 | CTATAATTTCCTCCC[C/G]CTAAACTCTTCTTAT | 68867 |
rs33333515 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Rnf122 | Mm_Celera | 8:31124902 | GCTACAAGGAGGTGA[A/C]GTAGCATCTCTTTAT | 68867 |
rs33342149 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf122 | Mm_Celera | 8:31124647 | AATGGCCCATAATAT[A/G]GCTGACATCTAGTCA | 68867 |
rs33352831 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf122 | Mm_Celera | 8:31111074 | AACATATAAAATAAA[A/C]TATGCAATGTCATCC | 68867 |
rs33368467 | snp | A/C | 0.375 | 0.216506 | downstream-variant-500B | Rnf122 | Mm_Celera | 8:31131807 | CTAACTAACACAACC[A/C]CAGGCAGTGTGGATC | 68867 |
rs33370256 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf122 | Mm_Celera | 8:31119541 | CAGAGTTCTAGTGGG[A/G]CGTTCTGTTGGTGCT | 68867 |
rs33405783 | snp | C/T | 0.429688 | 0.173817 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31131091 | TAAGCCTTTTTAGAA[C/T]ACCTGCTGCCCGGTT | 68867 |
rs33458560 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf122 | Mm_Celera | 8:31120757 | GGGTTATCAAACTGC[A/C]TAAATGAAGACAGGG | 68867 |
rs33460674 | snp | C/G | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31122633 | AGGATGGAGGAGATG[C/G]ATAGCCAGATCTTCC | 68867 |
rs33470477 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31122324 | TTCTTTTTCTAGAGG[A/G]AAACCACACACAGGC | 68867 |
rs33498671 | snp | C/T | 0.345679 | 0.230967 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31128917 | ACTGCTCTATCCTGG[C/T]ACTGGACTGACCGTC | 68867 |
rs33501964 | snp | A/T | 0.375 | 0.216506 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31129083 | CTGCCAGAGCCTTCC[A/T]TGGGATGGTTTCCAA | 68867 |
rs33523891 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31121098 | CCCCCTGGGTCTCAC[A/G]CTTCCAAAGGTGTTC | 68867 |
rs33569543 | snp | A/G | 0.42 | 0.183303 | intron-variant | Rnf122 | Mm_Celera | 8:31121701 | ATCCTTCTTTTAAAG[A/G]GAACCTGGCATATAC | 68867 |
rs33586731 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31128707 | AAGCGCTCCTGGCAC[A/G]TGGACACTGGGAAAG | 68867 |
rs33598592 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31126328 | CAGGGCCATTTCCTG[A/G]TCACTCCCCCTAGCC | 68867 |
rs36241362 | snp | A/G | 0.260355 | 0.249785 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31129771 | CTAATCCTTAACAAA[A/G]CCTGAGGGCTGGACA | 68867 |
rs36250519 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf122 | Mm_Celera | 8:31116467 | TGAGGTTTCCATCTC[G/T]CGGGCAGGAGAAATG | 68867 |
rs36272496 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rnf122 | Mm_Celera | 8:31112382 | GAGCCGAGTCTTCCC[G/T]GCCTTTGTATGGCGG | 68867 |
rs36281552 | snp | G/T | 0.473373 | 0.11227 | intron-variant | Rnf122 | Mm_Celera | 8:31115688 | TTAGCTCAGGGCCCT[G/T]CGAGGGGTTCCAAGC | 68867 |
rs36284716 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf122 | Mm_Celera | 8:31120435 | AGGGCAAAGATATGC[A/G]GGTTCAGATATCGCA | 68867 |
rs36300803 | snp | C/T | 0.197531 | 0.244432 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31130922 | ATACCTTTTATTCCC[C/T]GTGCTTCTATTGAAC | 68867 |
rs36310478 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Rnf122 | Mm_Celera | 8:31126563 | CTCTTACGACACCTT[C/G]TGCAGTAGTTCAGCT | 68867 |
rs36325740 | snp | A/G | 0.408163 | 0.193609 | upstream-variant-2KB | Rnf122 | Mm_Celera | 8:31109925 | CTGGAGCACTTTTTC[A/G]CCCCCAAGACAGGGT | 68867 |
rs36327361 | snp | C/G | 0.297521 | 0.245442 | upstream-variant-2KB | Rnf122 | Mm_Celera | 8:31110964 | GAGTATGGTGGCACA[C/G]GCCTTTCATCCTAGC | 68867 |
rs36332267 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Rnf122 | Mm_Celera | 8:31119051 | TTGCCCTGGTGTGAA[A/T]TTGCCAAGGTGCAAA | 68867 |
rs36381658 | snp | A/G | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31117354 | AGCTTCAGTGTGCGC[A/G]GGAATCTCCAAGCAT | 68867 |
rs36381666 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rnf122 | Mm_Celera | 8:31115515 | ACCCACAACAATACC[C/T]GTTGGCTGACTGGTG | 68867 |
rs36444417 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf122 | Mm_Celera | 8:31127830 | CGAGCAGTCATCACC[A/G]TAAACTCTTTAATGG | 68867 |
rs36459522 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Rnf122 | Mm_Celera | 8:31115917 | ATGAGGCAAATGAAG[G/T]TGGTACTAGCAACAA | 68867 |
rs36466370 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Rnf122 | Mm_Celera | 8:31115792 | TTATCTCATCGAAGG[C/T]TGCTAGTGACGGCGT | 68867 |
rs36467414 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Rnf122 | Mm_Celera | 8:31119993 | AGAAGCTTCCTGGAC[A/T]GGTCTTTCTTTCTTT | 68867 |
rs36473547 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31128752 | GTACCTGGGTTTCTC[C/T]ACACAATGAACAAGA | 68867 |
rs36482632 | snp | A/C | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Rnf122 | Mm_Celera | 8:31114907 | GGAAAGCATTTTAGA[A/C]GACTGGTGATAAACT | 68867 |
rs36501489 | snp | C/T | 0.18 | 0.24 | intron-variant | Rnf122 | Mm_Celera | 8:31124034 | AATTCATAATAAAGA[C/T]TTCCCTCACAGATGT | 68867 |
rs36517516 | snp | A/G | 0.5 | 0 | intron-variant | Rnf122 | Mm_Celera | 8:31122698 | CTCTGCTTCATCTTC[A/G]TTCTGGGAGGAACCT | 68867 |
rs36523322 | snp | G/T | 0.46875 | 0.121031 | intron-variant | Rnf122 | Mm_Celera | 8:31120458 | ATATCGCAGACTTAC[G/T]TAGGATATGGTTGGA | 68867 |
rs36545031 | snp | A/G | 0.42 | 0.183303 | utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31130179 | CCTGCGTGCATCCAG[A/G]TCCTCCACCCACAGC | 68867 |
rs36546094 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Rnf122 | Mm_Celera | 8:31120432 | TGAAGGGCAAAGATA[G/T]GCAGGTTCAGATATC | 68867 |
rs36556030 | snp | A/T | 0.132653 | 0.220748 | downstream-variant-500B, utr-variant-3-prime | Rnf122 | Mm_Celera | 8:31131749 | TAGGATTAGTTTGTT[A/T]AAAAAAAAATCGGTG | 68867 |
rs36560791 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf122 | Mm_Celera | 8:31116311 | TGGTCCTAGATTTTG[A/G]TTGAAGGCTTAGGTC | 68867 |
rs36573824 | snp | G/T | 0.46281 | 0.131194 | intron-variant, upstream-variant-2KB | Rnf122 | Mm_Celera | 8:31114095 | TACATGAAACAGGAT[G/T]AATTTCATGTTTAGA | 68867 |
rs36581869 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Rnf122 | Mm_Celera | 8:31115275 | GTAGGAAGTTGCTTT[G/T]CAAAAGGCCCACAGA | 68867 |
rs36600183 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf122 | Mm_Celera | 8:31124090 | TTATGGTTCTAGCCA[C/T]CTGCACAGTAGGCCA | 68867 |
rs36604225 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rnf122 | Mm_Celera | 8:31113831 | ATTAAACTTGGCTTC[A/G]TGACTGGGTGTGGTG | 68867 |