Product Details

SNP ID

hCV25761992

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:30475462 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGGGGAAACTGAGGCTGGCCCCA[G/C]CCCACCTAGACTGCCTGAGCTCCTC

Phenotype

MIM: 153370

Polymorphism

G/C, Transversion substitution

Allele Nomenclature

Literature Links

ITGAL PubMed Links

Gene Details

Gene

ITGAL

Gene Name

integrin subunit alpha L

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001114380.1		Intron			NP_001107852.1
NM_002209.2		Intron			NP_002200.2

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