Product Details

SNP ID
rs11548798
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:25124043 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGGAGATTTGGCCCAGTCTTGTGC[A/T]TGCCTCCCTTTTCAACGGTGTGGCA
Phenotype
MIM: 123970
Polymorphism
A/T, 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_018947.5 247 Missense Mutation AAG,ATG K26M NP_061820.1

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