Product Details

SNP ID
rs144369518
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:35075476 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACCCCGGGCTCACCTGCTAAATTC[A/G]CTAATTGCCACTTTTTGGGCACCCA
Phenotype
MIM: 602956 MIM: 601023
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
FANCG PubMed Links

Gene Details

Gene
FANCG
Gene Name
Fanconi anemia complementation group G
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004629.1 1914 Silent Mutation AGC,AGT S474S NP_004620.1
Gene
VCP
Gene Name
valosin containing protein
There are no transcripts associated with this gene.

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