Rnf123
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs8145267snpA/Tintron-variant, missense, nc-transcript-variantGmppb, Rnf123Rn_Celera8:116841732GTGGCTGCCTGGAGC[A/T]CCAGGGGATCAATCA100190936
rs8153241snpA/Gutr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantGmppb, Rnf123, Amigo3Rn_Celera8:116829153GGGTGGGAGTGGTAA[A/G]AGCGAGGGTGTTGGG100190936
rs8162084snpA/T00intron-variant, utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantGmppb, Rnf123, Amigo3Rn_Celera8:116829164TTGGCCCTGTCCCCA[A/T]CACCCTCGCTCTTAC100190936
rs8165668snpC/Tintron-variant, synonymous-codon, nc-transcript-variantGmppb, Rnf123Rn_Celera8:116844960GAGAGCTTACGAGCG[C/T]GGCTGCCAAAGACTC100190936
rs13450146snpA/G00synonymous-codon, downstream-variant-500B, upstream-variant-2KBGmppb, Rnf123, Amigo3Rn_Celera8:116828778CTTGTGGGGCAGCAC[A/G]CTGGCTCCGTTGAGG100190936
rs105118600snpA/G00intron-variantGmppb, Rnf123Rn_Celera8:116849424CACCCTCTTCCTTGC[A/G]CATTGGCGGGCGGCT100190936
rs105139278snpA/G00intron-variantGmppb, Rnf123Rn_Celera8:116847770CCCTTGGTCTCCTGA[A/G]CTTGACCTGCATCCC100190936
rs105171802snpC/T00intron-variant, synonymous-codon, upstream-variant-2KB, downstream-variant-500B, nc-transcript-variantGmppb, Rnf123, Amigo3Rn_Celera8:116829702AGCACTGATGTAATC[C/T]GCATCTGGATTAGTA100190936
rs105239038snpC/G00intron-variantGmppb, Rnf123Rn_Celera8:116839135AGGTGAAAGAGAGTT[C/G]AGAAGCGGCCAGAGA100190936
rs105391751snpA/G00intron-variantGmppb, Rnf123Rn_Celera8:116845498CTCATGATGGTGAAC[A/G]TTAAGAAAGATCTAC100190936
rs105933846snpC/T00intron-variantGmppb, Rnf123Rn_Celera8:116837473GTGTGAGCAGTGAAC[C/T]GAAGGTGGAGGAATG100190936
rs106010336snpA/G00intron-variantGmppb, Rnf123Rn_Celera8:116835481TGGAGAAGACTCAAG[A/G]GCAGTGAGAGTAGCA100190936
rs106021387snpA/G00intron-variantGmppb, Rnf123Rn_Celera8:116854207AAGAAATCACAGTAG[A/G]CTAAGTCACATTTAA100190936
rs106204625snpC/T00intron-variantGmppb, Rnf123Rn_Celera8:116842996CACTGAGCTAAATCC[C/T]CAACCCCTGTGTGTT100190936
rs106349553snpC/T00intron-variantGmppb, Rnf123Rn_Celera8:116845670CTCTTGGTCAGCTAG[C/T]CTCTTTCTCTTTCTC100190936
rs106433849snpC/T00intron-variant, synonymous-codon, nc-transcript-variantGmppb, Rnf123Rn_Celera8:116833797ACCAGGTAGCCGCAG[C/T]GTGACTACACGGTCA100190936
rs106597793snpC/T00intron-variantGmppb, Rnf123Rn_Celera8:116848835AACTATATCCATGCC[C/T]AGAGCTTCTGGGACA100190936
rs107320111snpC/T00intron-variantGmppb, Rnf123Rn_Celera8:116854037CTTCAGTCCTCTCGC[C/T]TTTTCCAGCCCCAAG100190936
rs107518953snpC/T00intron-variantGmppb, Rnf123Rn_Celera8:116840469AAATCGGGGCCTTTT[C/T]CTACAAATGCATTTC100190936
rs107560192snpA/G00intron-variantGmppb, Rnf123Rn_Celera8:116838551GAAATACAAATTTAA[A/G]GCATCCAAATTGGGA100190936
rs196996015snpA/C00intron-variantGmppb, Rnf123Rnor_6.08:116852060CTGCAGGCAAAAAAA[A/C]CCCTATGTGATCCCA100190936
rs197197892snpC/T00upstream-variant-2KB, intron-variantRnf123, Mst1Rn_Celera8:116858253CAGACTAGTAATAAT[C/T]TCCCTACTGGGTATG100190936
rs197364327snpC/T00intron-variantGmppb, Rnf123Rn_Celera8:116839090GATAGCACCTGGATA[C/T]ACGCGTCAGCCTTTA100190936
rs197421092snpA/G00intron-variantGmppb, Rnf123Rn_Celera8:116844768TGGGGCAAGGAATAT[A/G]GCCCTTAGGCTCCCA100190936
rs197516986snpA/G00intron-variantGmppb, Rnf123Rn_Celera8:116842937TTTTTTTCGGAGCTG[A/G]GGACTGAACCCAGGG100190936
rs197648269snpC/T00intron-variantGmppb, Rnf123Rn_Celera8:116846254AGTCCTGGGAAGAGA[C/T]CCTAGGGCAGCCATG100190936
rs198101403snpA/G00intron-variantGmppb, Rnf123Rn_Celera8:116837627CTGTGAGGGAGGCAC[A/G]ACACTGTCCAGGCCT100190936
rs198102971snpC/G00intron-variantGmppb, Rnf123Rn_Celera8:116844898ATACACACACAAACC[C/G]TTCCCTACCCACGGC100190936
rs198229567snpA/G00intron-variantGmppb, Rnf123Rn_Celera8:116844118GAGGCAACCCCAGGC[A/G]TTTCAATCTGGCGTT100190936
rs198601022snpC/T00intron-variantGmppb, Rnf123Rn_Celera8:116839379AAGAAGGCAGGGGTC[C/T]GTAAGGGTCCCGGTG100190936
rs198775803snpC/T00intron-variantGmppb, Rnf123Rn_Celera8:116844434CCCCTGCAACACAGC[C/T]GGGAGCCCACAGTCG100190936
rs198817744snpC/T00intron-variantGmppb, Rnf123Rn_Celera8:116846569TGAAGAAGCAGGCCT[C/T]AGACACCAAGTCTTG100190936
rs199008675snpC/T00intron-variantGmppb, Rnf123Rn_Celera8:116854831GAAGAGCAACCATTC[C/T]AAGTGCACTTTTCTA100190936
rs199051596snpA/T00intron-variantGmppb, Rnf123Rn_Celera8:116850249CACCATCTGAGGATG[A/T]TAGACAACGTTTCCT100190936
rs199069548snpA/G00intron-variantGmppb, Rnf123Rn_Celera8:116836553GGGGAGGGAGTGAGC[A/G]GATCTACATCAGAGT100190936
rs199106298snpC/G00intron-variantGmppb, Rnf123Rn_Celera8:116846255GTCCTGGGAAGAGAC[C/G]CTAGGGCAGCCATGA100190936
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