Product Details

SNP ID
rs10462013
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:40912122 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TATGTCTATCACTGTCATTCACATG[A/G]TTTATTTGTGTTTGTTCTATCTCTC
Phenotype
MIM: 217070
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
C7 PubMed Links

Gene Details

Gene
C7
Gene Name
complement component 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000587.2 Intron NP_000578.2

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