Product Details

SNP ID

rs7935096

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:62868700 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCATTCTATAGGCGGTTGCAAATTG[C/T]TCTCCTAGAACGGATGTACCAACTA

Phenotype

MIM: 158070

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC3A2 PubMed Links

Gene Details

Gene

SLC3A2

Gene Name

solute carrier family 3 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012662.2		Intron			NP_001012680.1
NM_001012664.2		Intron			NP_001012682.1
NM_001013251.2		Intron			NP_001013269.1
NM_002394.5		Intron			NP_002385.3

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