Product Details

SNP ID

rs11548772

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:25123969 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTTACCTTTGTTCTTATTGGCGG[C/G]TGTGTAAGAGTATCCAGGGGCCTGA

Phenotype

MIM: 123970

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CYCS PubMed Links

Gene Details

Gene

CYCS

Gene Name

cytochrome c, somatic

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018947.5	321	Missense Mutation	CCC,GCC	P51A	NP_061820.1

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