Product Details

SNP ID

rs150609476

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:5916883 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCTTGTCGAAGTCCAGCGCTCCA[C/T]CCATCACCCCTGAGTGCCGCCAAGT

Phenotype

MIM: 118920

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CHGB PubMed Links

Gene Details

Gene

CHGB

Gene Name

chromogranin B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001819.2	460	Missense Mutation	CCC,TCC	P52S	NP_001810.2

View Full Product Details