Product Details

SNP ID: rs4765998
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:2827847 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CTGGGAACTCCTCGTGCTGCAGGGA[C/G]TGAAAGTCTCAGCCTTTGCCCCACC
Phenotype
Polymorphism: C/G, Transversion 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	851	Intron			NP_060933.3
XM_005253707.4	851	Intron			XP_005253764.1
XM_005253709.4	851	Intron			XP_005253766.1
XM_017019641.1	851	Intron			XP_016875130.1

Gene: LOC100507424
Gene Name: uncharacterized LOC100507424

There are no transcripts associated with this gene.

Gene: NRIP2
Gene Name: nuclear receptor interacting protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031474.2	851	Intron			NP_113662.1
XM_005253797.3	851	Intron			XP_005253854.1
XM_005253798.3	851	Intron			XP_005253855.1
XM_011521031.2	851	Intron			XP_011519333.1
XM_017020000.1	851	Missense Mutation	ACT,AGT	T260S	XP_016875489.1
XM_017020001.1	851	Intron			XP_016875490.1

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