Product Details

SNP ID

rs149081467

Assay Type

Functionally tested

NCBI dbSNP Submissions

6

Location

Chr.1:196793486 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATTTCAAGCAGTGTGTCGGGAAGG[C/G]ATAGTGGAATACCCCAGATGCGAAT

Phenotype

MIM: 605336

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CFHR3 PubMed Links

Gene Details

Gene

CFHR3

Gene Name

complement factor H related 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001166624.1	870	Silent Mutation	GGC,GGG	G261G	NP_001160096.1
NM_021023.5	870	Silent Mutation	GGC,GGG	G322G	NP_066303.2

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