Product Details

SNP ID

rs200039068

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:50215440 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGCTACTCCATCCACCTGCTACT[C/G]AAGTCCTCAGGGGTCGTGGGTGAGC

Phenotype

MIM: 604437

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC38A3 PubMed Links

Gene Details

Gene

SLC38A3

Gene Name

solute carrier family 38 member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006841.5	508	Silent Mutation	CTC,CTG	L118L	NP_006832.1
XM_006712954.2	508	Silent Mutation	CTC,CTG	L118L	XP_006713017.1

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