Product Details

SNP ID
rs141345077
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:32937195 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCGAGTCCTCCGTGCTGCTTCCAC[C/T]CACCAGCTGATAGTGGCTTGGTTTG
Phenotype
MIM: 610872
Polymorphism
C/T, 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 2441 UTR 3 NP_001120833.1
NM_001300826.1 2441 Missense Mutation AGT,GGT S603G NP_001287755.1
NM_153341.3 2441 Missense Mutation AGT,GGT S604G NP_699172.2
XM_006710356.2 2441 Missense Mutation AGT,GGT S604G XP_006710419.1
XM_006710357.3 2441 Missense Mutation AGT,GGT S560G XP_006710420.1
XM_006710358.3 2441 UTR 3 XP_006710421.1

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