Product Details

SNP ID
rs199959013
Assay Type
Functionally Tested
NCBI dbSNP Submissions
13
Location
Chr.1:209675958 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCAAGCAGCAGGACACGGTCCTC[A/G]GCGGCCGGGCCCTGTCCAACCGGCA
Phenotype
MIM: 614447
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
G0S2 PubMed Links

Gene Details

Gene
G0S2
Gene Name
G0/G1 switch 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015714.3 531 Missense Mutation AGC,GGC S92G NP_056529.1
Gene
LOC101930114
Gene Name
uncharacterized LOC101930114
There are no transcripts associated with this gene.

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