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SNP ID

rs200466062

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:35074413 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGACCCCTTAGTTTGGGCCTCCAGC[A/C]TCCACCAGAGTGCAGTGGCCTCATC

Phenotype

MIM: 602956 MIM: 601023

Polymorphism

A/C, Transversion 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	2210	Missense Mutation			NP_004620.1

Gene

VCP

Gene Name

valosin containing protein

There are no transcripts associated with this gene.

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