Product Details

SNP ID

rs199739977

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:181458197 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCACGTGCACGTGTCTCGCTTTAGG[C/G]TCCTAGTGGGTGCGCCCACTGCCAA

Phenotype

MIM: 192975

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

ITGA4 PubMed Links

Additional Information

For this assay, SNP(s) [rs539227893] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

ITGA4

Gene Name

integrin subunit alpha 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000885.5	962	Missense Mutation	CTC,GTC	L67V	NP_000876.3
NM_001316312.1	962	Missense Mutation	CTC,GTC	L67V	NP_001303241.1

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