Product Details

SNP ID

rs1143679

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.16:31265490 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

AGCACAGGCTCATGCGAGCCCATCC[G/A]CCTGCAGGGTGAGTCACTGCCCCGC

Phenotype

MIM: 120980

Polymorphism

G/A, Transition substitution

Allele Nomenclature

Literature Links

ITGAM PubMed Links

Gene Details

Gene

ITGAM

Gene Name

integrin subunit alpha M

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000632.3	95	Missense Mutation	CAC,CGC	H77R	NP_000623.2
NM_001145808.1	95	Missense Mutation	CAC,CGC	H77R	NP_001139280.1
XM_006721045.1	95	Missense Mutation	CAC,CGC	H77R	XP_006721108.1
XM_011545850.2	95	Silent Mutation	CCA,CCG	P5P	XP_011544152.1
XM_011545851.2	95	Missense Mutation	CAC,CGC	H77R	XP_011544153.1
XM_017023216.1	95	Missense Mutation	CAC,CGC	H77R	XP_016878705.1

View Full Product Details