Product Details

SNP ID

rs201040223

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:48459733 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGACTGGGGTGAGGTTTACTGACC[A/G]ATAACTCCAAAGATATCCCGGATGG

Phenotype

MIM: 300649

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC38A5 PubMed Links

Gene Details

Gene

SLC38A5

Gene Name

solute carrier family 38 member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033518.3	1390	Silent Mutation	ATC,ATT	I404I	NP_277053.2
XM_005272694.3	1390	Silent Mutation	ATC,ATT	I451I	XP_005272751.2
XM_005272695.4	1390	Silent Mutation	ATC,ATT	I451I	XP_005272752.3
XM_005272697.2	1390	Silent Mutation	ATC,ATT	I410I	XP_005272754.2
XM_005272698.4	1390	Silent Mutation	ATC,ATT	I404I	XP_005272755.2
XM_006724569.3	1390	Silent Mutation	ATC,ATT	I404I	XP_006724632.1
XM_017029960.1	1390	Silent Mutation	ATC,ATT	I410I	XP_016885449.1
XM_017029961.1	1390	Silent Mutation	ATC,ATT	I404I	XP_016885450.1

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