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SNP ID

rs61740898

Assay Type

Functionally tested

NCBI dbSNP Submissions

14

Location

Chr.1:209675694 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGCCCAGAGCCGAGATGGAAACG[A/G]TCCAGGAGCTGATCCCCCTGGCCAA

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	267	Missense Mutation	ATC,GTC	I4V	NP_056529.1

Gene

LOC101930114

Gene Name

uncharacterized LOC101930114

There are no transcripts associated with this gene.

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