Product Details

SNP ID

rs6053789

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:5917854 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTTTCACCTTTAAAAATCTTTCA[G/T]GTGGGCATAGTGGCTCACACCTGTA

Phenotype

MIM: 118920

Polymorphism

G/T, Transversion 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		Intron			NP_001810.2

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