Product Details

SNP ID: rs199996471
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:91630225 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGAATGACAGGGGGTAAGTCAATG[A/G]CAAATGAGAAGGTATCACTATCTGT
Phenotype: MIM: 602999
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: PPP1R3C PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005398.5	788	Missense Mutation	GCC,GTC	A219V	NP_005389.1