Product Details

SNP ID

rs184942906

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:2817265 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGAGACACCAGCGGGAAGGTGTCT[A/G]TGTATAAAAATGATGACAGTCGGCC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ITFG2 PubMed Links

Gene Details

Gene

ITFG2

Gene Name

integrin alpha FG-GAP repeat containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018463.3	279	Missense Mutation	ATG,GTG	M47V	NP_060933.3
XM_005253707.4	279	Missense Mutation	ATG,GTG	M47V	XP_005253764.1
XM_005253709.4	279	Intron			XP_005253766.1
XM_017019641.1	279	Intron			XP_016875130.1

Gene

NRIP2

Gene Name

nuclear receptor interacting protein 2

There are no transcripts associated with this gene.

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