Product Details

SNP ID

rs201703215

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:5916876 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTCAAATGCCTTGTCGAAGTCCAG[C/T]GCTCCACCCATCACCCCTGAGTGCC

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	453	Silent Mutation	AGC,AGT	S49S	NP_001810.2

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