Product Details

SNP ID
rs193292809
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:92924204 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACTCTCTTCTTCTTCCCAGTCACT[A/G]CGCTCCCTGTGAACAGCCCTATGAA
Phenotype
MIM: 118910
Polymorphism
A/G, Transition 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_001275.3 664 Missense Mutation ACG,GCG T18A NP_001266.1
NM_001301690.1 664 Missense Mutation ACG,GCG T18A NP_001288619.1
XM_011536370.1 664 Missense Mutation ACG,GCG T18A XP_011534672.1

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