SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3022930 | snp | C/T | 0.473373 | 0.11227 | downstream-variant-500B | Cpne1 | Mm_Celera | 2:156071586 | GGAGCTAGTTCTCTC[C/T]TCCTGCCTTTACATG | 266692 |
rs3022931 | snp | A/G | 0.473373 | 0.11227 | downstream-variant-500B | Cpne1 | Mm_Celera | 2:156071668 | AGGCTTATACAGCAA[A/G]CATTGTACCCAGTGA | 266692 |
rs3089031 | snp | C/T | 0.46875 | 0.121031 | downstream-variant-500B | Cpne1 | Mm_Celera | 2:156071633 | TTTACATGGCTCCTA[C/T]GGGTAGAACTCAGGC | 266692 |
rs3089032 | snp | A/G | 0.46875 | 0.121031 | downstream-variant-500B | Cpne1 | Mm_Celera | 2:156071635 | TACATGGCTCCTATG[A/G]GTAGAACTCAGGCTG | 266692 |
rs3653461 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156099662 | TTAATTCCTGTTGAA[C/T]CTGGTTGCTTATCTC | 266692 |
rs3655350 | snp | A/G | 0.5 | 0 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156099943 | TGAGGCTGAGCTCAC[A/G]ACCACTCTCAGCTCC | 266692 |
rs3677398 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Cpne1 | Mm_Celera | 2:156093291 | TTTCTTTTTAGCATT[C/T]ATCTAAGATGTAGAA | 266692 |
rs3678176 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Cpne1 | Mm_Celera | 2:156093468 | ATAAACCTGCAGTTG[G/T]AATAAGAAGCCCAAA | 266692 |
rs3678721 | snp | A/G | 0.5 | 0 | intron-variant | Cpne1 | Mm_Celera | 2:156093514 | TCACACTATGTCTTC[A/G]AACGAGAAATGATTC | 266692 |
rs3684423 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156103853 | GACACTCACAGACAT[C/T]ACCGCAATGACTCTT | 266692 |
rs3692630 | snp | A/G | 0.5 | 0 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156100050 | ACTCATGTATGTAAA[A/G]TTATTATTATTATTA | 266692 |
rs3718312 | snp | C/T | 0.5 | 0 | intron-variant | Cpne1 | Mm_Celera | 2:156085927 | GCTATATGGAACAGA[C/T]TGGCCTAAAACTTGC | 266692 |
rs4221932 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Cpne1 | GRCm38.p3 | 2:156072207 | ACACATTTTTGAAGA[A/G]TTGGTTTTTCAGTAT | 266692 |
rs4221933 | snp | A/G | 0.578512 | 0.104538 | utr-variant-3-prime | Cpne1 | GRCm38.p3 | 2:156072121 | TTCTGTAGAGGGGTG[A/G]TCTGACCTCTGATAA | 266692 |
rs4221934 | snp | C/T | 0.21875 | 0.248039 | utr-variant-3-prime | Cpne1 | GRCm38.p3 | 2:156072089 | CTGTGGGTCACCTTC[C/T]TTCCCCAGATCTCAT | 266692 |
rs4221935 | snp | C/G | 0.40625 | 0.270633 | utr-variant-3-prime | Cpne1 | Mm_Celera | 2:156072052 | TTTCCATTTATTTCT[C/G]TATATTATTTCATAC | 266692 |
rs4221936 | snp | C/T | 0.46281 | 0.131194 | utr-variant-3-prime | Cpne1 | GRCm38.p3 | 2:156072037 | CTATATTATTTCATA[C/T]ACATTTCCTTCTCAG | 266692 |
rs4221937 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Cpne1 | GRCm38.p3 | 2:156072004 | ACCTGTTCACAAACT[A/G]TATGTTAGAGCTTTT | 266692 |
rs4221938 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Cpne1 | GRCm38.p3 | 2:156072002 | CTGTTCACAAACTGT[A/G]TGTTAGAGCTTTTAT | 266692 |
rs4221939 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Cpne1 | GRCm38.p3 | 2:156071994 | AAACTGTATGTTAGA[A/G]CTTTTATTTTGTTCT | 266692 |
rs4221940 | snp | C/T | 0.21875 | 0.248039 | utr-variant-3-prime | Cpne1 | GRCm38.p3 | 2:156071980 | AGCTTTTATTTTGTT[C/T]TTGACATGTTGAAAG | 266692 |
rs6304038 | snp | A/C | 0.5 | 0 | intron-variant | Cpne1 | Mm_Celera | 2:156083880 | GATTCAAAGACACCC[A/C]ATAAACATGAGTAAG | 266692 |
rs6304464 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Cpne1 | Mm_Celera | 2:156083927 | TGACCCACAGCATAA[A/G]TGACAAGAGAAAGGC | 266692 |
rs13472930 | snp | A/G | | | utr-variant-3-prime, intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156095200 | ACTCACAGAATAAAC[A/G]TTGCAATTTGTTACA | 266692 |
rs13472931 | snp | C/T | | | synonymous-codon | Cpne1 | Mm_Celera | 2:156073626 | ACAGACCGTACTCGC[C/T]GAAGTGCCCACTCAG | 266692 |
rs13472932 | snp | A/G | | | utr-variant-3-prime | Cpne1 | Mm_Celera | 2:156072559 | GTTTGCAGACTGGGG[A/G]GAGGGGAGCTCCTAA | 266692 |
rs13472933 | snp | A/G | | | utr-variant-3-prime | Cpne1 | Mm_Celera | 2:156072420 | tgatgtgaatttgag[A/G]tacacgaggagtttc | 266692 |
rs27308536 | snp | A/G | 0.18 | 0.24 | upstream-variant-2KB | Rbm12, Cpne1 | Mm_Celera | 2:156113239 | TCAATATTTCCTATA[A/G]TCCCCAGTATTTGAT | 266692 |
rs27308537 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156111350 | TCCCTAGTGTAGTCC[A/C]CTTTTGCAGGTCATA | 266692 |
rs27308538 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156111026 | TCCTTCTATTTTACG[C/T]GGCTGCAAAGTGGCG | 266692 |
rs27308539 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156108844 | GTTCGCCTCAAAGAT[C/T]AGCAACAAAGCCTCT | 266692 |
rs27308540 | snp | A/G | 0.5 | 0 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156108450 | GAGAAAGTTAGCCAC[A/G]AGTCCACACAGTTCA | 266692 |
rs27308541 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156107265 | AGCCCAGCTGATCTG[C/T]GTAAACGTGTAGTTT | 266692 |
rs27308542 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156106549 | TTTTTGTGTTAAACA[C/T]CTGACACCTATTAGA | 266692 |
rs27308543 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156103627 | TTTCGAGTCTGAAAA[C/T]CATTCTATCAAGAAA | 266692 |
rs27308544 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156101759 | GTAAGCAAGAATGAC[A/G]GACTGGCGCTAGAAT | 266692 |
rs27308545 | snp | A/G | 0.32 | 0.24 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156101203 | AAGAAATTCTTCAAT[A/G]TCAAATACTGTATGA | 266692 |
rs27308546 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156101159 | CAAGGCTTCCTGCTA[C/T]AAGCTCTAAGACTTA | 266692 |
rs27308547 | snp | A/G | 0.5 | 0 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156100943 | CCATTCCAGTACCTG[A/G]CAGGATTTCCATTTC | 266692 |
rs27308548 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156099646 | GGGCCTCCAACCCAA[C/T]TTAATTCCTGTTGAA | 266692 |
rs27308549 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156098944 | AAAAAATCTCAAATG[A/G]TAACAGATTCCATAT | 266692 |
rs27308550 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156098680 | TAAATGTGCAAAAAC[A/T]CTATAGGGGAATCAT | 266692 |
rs27308551 | snp | C/T | 0.487535 | 0.077957 | synonymous-codon, intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156098099 | ACGCCTACGACTCAG[C/T]TCAATCATATTTTGC | 266692 |
rs27308552 | snp | A/G | 0.493827 | 0.0552116 | missense, intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156097986 | TTAAAGTTGGGTACT[A/G]TTGCTGGCAAGTTCA | 266692 |
rs27308553 | snp | C/T | 0.498615 | 0.0262793 | synonymous-codon, intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156097823 | TGGAGAAGCTGTACT[C/T]GGAATGGTTGAACTG | 266692 |
rs27308554 | snp | A/C | 0.444444 | 0.157135 | synonymous-codon, intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156097799 | CGGTGGCGGTGGGAC[A/C]GTGTTCATTGGAGAA | 266692 |
rs27308555 | snp | A/G | 0.498615 | 0.0262793 | synonymous-codon, intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156097364 | CAAATGCACTGCATC[A/G]ACTCGGAGCCCATGG | 266692 |
rs27308556 | snp | C/T | 0.48 | 0.0979796 | missense, intron-variant | Rbm12, Cpne1 | Mm_Celera | 2:156096636 | AGAACATGCACAGCA[C/T]TCTCATCCACTGGGA | 266692 |
rs27308557 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156094329 | ACACACATCAACCTA[C/T]GATCCAACTTAAGGA | 266692 |
rs27308558 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Cpne1 | Mm_Celera | 2:156094227 | TCTCTTCTGACATTG[A/G]TACTTAAGACTCTGC | 266692 |
rs27308559 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156093707 | GACCATCGCAGTATT[A/G]GAGAGGCTTTCCACA | 266692 |
rs27308560 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156093649 | TTTTCAAAGCCTGCA[A/C]AACCCTTTCCCTGAA | 266692 |
rs27308561 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156093436 | TTCTAAAATATAGTC[A/G]GTTTCCAATGGGGAA | 266692 |
rs27308562 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156093005 | AAAAAAATTGTCTGA[C/T]GAGAGGTATGAATAG | 266692 |
rs27308563 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Cpne1 | Mm_Celera | 2:156092808 | AACAAATTAAGCCTA[A/G]TGAAATATTCTTTTC | 266692 |
rs27308564 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156092455 | GATTTTCATCAAGCA[A/G]ATCAAGACTGACCTA | 266692 |
rs27308565 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Cpne1 | GRCm38.p3 | 2:156092383 | TTTGTGCAAGGTGAG[A/C/T]ATTTCCACCTAAAAA | 266692 |
rs27308566 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156092176 | TAACTTACACATGGC[A/G]ATTGTGAGTGGGAAA | 266692 |
rs27308567 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Cpne1 | Mm_Celera | 2:156091287 | GGATATTTAAATACA[A/G]GCTAAACTCTTACAT | 266692 |
rs27324768 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Cpne1 | Mm_Celera | 2:156091255 | CAGACTGCCTGCTTG[A/G]ACTTGCTAACACAAT | 266692 |
rs27324769 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156091185 | GAAGTCTCTCAGTTG[C/T]TGTCTGGAATTAGTC | 266692 |
rs27324770 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Cpne1 | Mm_Celera | 2:156091176 | ACAATCAATGAAGTC[A/T]CTCAGTTGCTGTCTG | 266692 |
rs27324771 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Cpne1 | Mm_Celera | 2:156091022 | AGCTGCTGATGTCAC[G/T]CCATCATTTTGCAAA | 266692 |
rs27324772 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156090778 | CTATTATACAGGAAC[C/T]TTTCATGCCCTATCA | 266692 |
rs27324773 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Cpne1 | Mm_Celera | 2:156090753 | ACGTGCTAGCACAGC[A/G]CTCTTCAAGCTATTA | 266692 |
rs27324774 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Cpne1 | Mm_Celera | 2:156090567 | GGTTGCTTATTGTTA[C/T]TGTTGATCCAGAAAA | 266692 |
rs27324775 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Cpne1 | GRCm38.p3 | 2:156090372 | CTAACCTTTAACGAA[C/G]CCCCAGAGTCCCAAC | 266692 |
rs27324776 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Cpne1 | Mm_Celera | 2:156090066 | CCAAGACATTCATCA[C/T]CCTGGTTTCCAGCAG | 266692 |
rs27324777 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cpne1 | Mm_Celera | 2:156089832 | CTCAGCTCCTTCAGC[C/T]TTTCTTTTCCCTCTT | 266692 |
rs27324778 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Cpne1 | Mm_Celera | 2:156089810 | GGTATTCTGGCTATT[C/G]AAGTGGCTCAGCTCC | 266692 |
rs27324779 | snp | A/G | 0.5 | 0 | intron-variant | Cpne1 | Mm_Celera | 2:156089700 | AATTACAGATGCAGT[A/G]CCTCCATTTGCAACC | 266692 |
rs27324780 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156089301 | TTTGCTTTGCCATCA[G/T]TAAATCCTGTTGTGC | 266692 |
rs27324781 | snp | A/C/G | 0.475309 | 0.108333 | intron-variant | Cpne1 | GRCm38.p3 | 2:156088849 | GGATTTCATCAAACA[A/C/G]GTGTATGGTAAAATT | 266692 |
rs27324782 | snp | C/T | 0.5 | 0 | intron-variant | Cpne1 | Mm_Celera | 2:156088659 | CTCCCATTTTATAGT[C/T]CAGTCCAGTCTCAGA | 266692 |
rs27324783 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cpne1 | Mm_Celera | 2:156088513 | CTCATACCAATTTCC[A/G]AAAGAAATGGAATAG | 266692 |
rs27324784 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Cpne1 | Mm_Celera | 2:156088492 | AAGTTTCTCTTCGGG[A/G]CCAAACTCATACCAA | 266692 |
rs27324785 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Cpne1 | Mm_Celera | 2:156087954 | ACTCCATGTTTACCT[C/T]AGTTAGTTCATGGAG | 266692 |
rs27324786 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Cpne1 | Mm_Celera | 2:156087370 | AGGTCACAAACTGAC[C/T]CAAATAATTCTTTTG | 266692 |
rs27324787 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Cpne1 | Mm_Celera | 2:156087189 | GGCTCCCAAGTGAAG[A/C]CCGGCCACCCATAGA | 266692 |
rs27324788 | snp | A/C | 0.255 | 0.24995 | intron-variant | Cpne1 | Mm_Celera | 2:156086981 | ACCCTGCAATCCCTA[A/C]CTCCCTTTATCTATC | 266692 |
rs27324789 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cpne1 | Mm_Celera | 2:156086960 | ACTCAAGAGCTTAAT[C/T]AGGTAACCCTGCAAT | 266692 |
rs27324790 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Cpne1 | Mm_Celera | 2:156086834 | CAGGCTCTAACTGCC[C/T]TTCTTAAGTCCAAGG | 266692 |
rs27324791 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cpne1 | Mm_Celera | 2:156086827 | GCATTAGCAGGCTCT[A/G]ACTGCCTTTCTTAAG | 266692 |
rs27324792 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Cpne1 | Mm_Celera | 2:156086668 | GTGAACAAGTAGCCT[C/T]GGTACATTCAAGATT | 266692 |
rs27324793 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Cpne1 | Mm_Celera | 2:156086641 | CAGACTTAAACGAAT[A/C]TAAAGGGTCGTGTGA | 266692 |
rs27324794 | snp | A/G | 0.255 | 0.24995 | intron-variant | Cpne1 | Mm_Celera | 2:156086290 | CTAGGACCTGTGCTG[A/G]AATTAACAGCATGTT | 266692 |
rs27324795 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Cpne1 | Mm_Celera | 2:156086255 | CTGATGTAACAAATA[C/T]GTGCAGGACTCTTAG | 266692 |
rs27324796 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156086139 | ATTTCTTCCTGGCCA[C/T]AAGACGCTACTGTAC | 266692 |
rs27324797 | snp | C/T | 0.32 | 0.24 | intron-variant | Cpne1 | Mm_Celera | 2:156086097 | AAAGGATGGACTTCC[C/T]AACAGTGAGCAGACA | 266692 |
rs27324798 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156085716 | CCAAATGAAAAACCC[A/C/G]ATCTCAGTTTCATAG | 266692 |
rs27324799 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Cpne1 | Mm_Celera | 2:156085423 | GATGATAATGTCTAG[C/G]TTGAGTTCTAACCTC | 266692 |
rs27324800 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Cpne1 | Mm_Celera | 2:156085364 | GTGAGCTTTCTGGCA[C/T]ATTCTATTATCTCCT | 266692 |
rs27324801 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156085111 | ACAGACTTTACCCAG[A/G]CGCACTGCTCATATA | 266692 |
rs27324802 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cpne1 | Mm_Celera | 2:156084840 | GCAGCTGAAAACCAT[C/T]ATACCTATCTACAGC | 266692 |
rs27324803 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Cpne1 | Mm_Celera | 2:156084806 | TTGCTGTCCTGATCC[A/G]TCTTCAAGTGCTGGG | 266692 |
rs27324804 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156084133 | AAGACCTTATAGCCA[C/T]CAAACTTTACAGAAT | 266692 |
rs27324805 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cpne1 | Mm_Celera | 2:156083601 | GAAGCTGGTGCTCAT[A/G]GCTATTTGATGAACT | 266692 |
rs27324806 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cpne1 | Mm_Celera | 2:156083434 | CCATGGACAGCAAGC[C/T]ACCCTACTTATAACA | 266692 |
rs27324807 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Cpne1 | Mm_Celera | 2:156083376 | ATTCACCCACAGGAT[C/T]GAGCCCATTCTCCAG | 266692 |
rs27324808 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cpne1 | Mm_Celera | 2:156083308 | AAAATCTAACCCATG[C/T]GTAAAGAGTCACCCA | 266692 |