Product Details

SNP ID

hCV25753893

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:46765578 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAAATTTAAATTATCCCCAGACAT[C/T]TGTAGACAGATACATATGAATGGAT

Phenotype

MIM: 608065

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC38A4 PubMed Links

Gene Details

Gene

SLC38A4

Gene Name

solute carrier family 38 member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001143824.1	3166	UTR 3			NP_001137296.1
NM_018018.4	3166	UTR 3			NP_060488.2

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