Product Details

SNP ID

rs149564251

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:74216825 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTAATCCTGGCCTTTTCTTGCAG[G/T]TGCAAAGAGGTCAGAGAAAATCTAC

Phenotype

MIM: 605719

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

LAT2 PubMed Links

Gene Details

Gene

LAT2

Gene Name

linker for activation of T-cells family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014146.3	485	Missense Mutation	GGT,GTT	G32V	NP_054865.2
NM_032463.2	485	Missense Mutation	GGT,GTT	G32V	NP_115852.1
NM_032464.2	485	Missense Mutation	GGT,GTT	G32V	NP_115853.2
XM_011516558.2	485	Missense Mutation	GGT,GTT	G32V	XP_011514860.1

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