Product Details

SNP ID
rs75240537
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:32937182 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCATGAACATGGAGCGAGTCCTCC[A/G]TGCTGCTTCCACTCACCAGCTGATA
Phenotype
MIM: 610872
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RNF19B PubMed Links

Gene Details

Gene
RNF19B
Gene Name
ring finger protein 19B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001127361.2 2454 UTR 3 NP_001120833.1
NM_001300826.1 2454 Missense Mutation ACG,ATG T607M NP_001287755.1
NM_153341.3 2454 Missense Mutation ACG,ATG T608M NP_699172.2
XM_006710356.2 2454 Missense Mutation ACG,ATG T608M XP_006710419.1
XM_006710357.3 2454 Missense Mutation ACG,ATG T564M XP_006710420.1
XM_006710358.3 2454 UTR 3 XP_006710421.1

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