Product Details

SNP ID
rs199961427
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:32936850 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTCTGGCTTCAAGACAGTTTGTC[A/C]CTCGGCTAGGGCAGAGAGGTTCATA
Phenotype
MIM: 610872
Polymorphism
A/C, Transversion 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 2786 UTR 3 NP_001120833.1
NM_001300826.1 2786 Nonsense Mutation GGA,TGA G718* NP_001287755.1
NM_153341.3 2786 Nonsense Mutation GGA,TGA G719* NP_699172.2
XM_006710356.2 2786 Nonsense Mutation GGA,TGA G719* XP_006710419.1
XM_006710357.3 2786 Nonsense Mutation GGA,TGA G675* XP_006710420.1
XM_006710358.3 2786 UTR 3 XP_006710421.1

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