Product Details

SNP ID

rs7146118

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:92926489 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGTCCCTGAGCCAGGGATCATGGA[A/C]TCCCAAAGACAAAAGCAAATACCCT

Phenotype

MIM: 118910

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

CHGA PubMed Links

Gene Details

Gene

CHGA

Gene Name

chromogranin A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001275.3		Intron			NP_001266.1
NM_001301690.1		Intron			NP_001288619.1
XM_011536370.1		Intron			XP_011534672.1

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