Product Details

SNP ID

rs2310958

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:406497 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGTCAGGGCACCCTCGCCTGGCCCC[G/A]CTCCCCACCGGAGCCTGGGAAGCTG

Phenotype

MIM: 610336

Polymorphism

G/A, Transition substitution

Allele Nomenclature

Literature Links

C2CD4C PubMed Links

Gene Details

Gene

C2CD4C

Gene Name

C2 calcium dependent domain containing 4C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136263.1	1481	UTR 3			NP_001129735.1
XM_011527694.1	1481	Missense Mutation	CGG,TGG	R440W	XP_011525996.1

View Full Product Details