Product Details

SNP ID: rs20571
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.8:85439768 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: TGCCAAGGGGGAAAACCAGTCGCCC[G/A]TTGAGCTGCATACTAAAGACATCAG
Phenotype: MIM: 114750
Polymorphism: G/A, Transition substitution
Allele Nomenclature
Literature Links: CA3 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005181.3	174	Missense Mutation	ATT,GTT	I31V	NP_005172.1

There are no transcripts associated with this gene.