Product Details

SNP ID

rs201404860

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:164908670 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTCTAGAACTATCCCGAGGCAATC[A/G]ATCAGCAATGACACAAGCGTGGCTA

Phenotype

MIM: 616526

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC38A11 PubMed Links

Gene Details

Gene

SLC38A11

Gene Name

solute carrier family 38 member 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199148.1	1542	Silent Mutation	ATC,ATT	I299I	NP_001186077.1
NM_173512.2	1542	Silent Mutation	ATC,ATT	I277I	NP_775783.1
XM_005246350.4	1542	Silent Mutation	ATC,ATT	I355I	XP_005246407.1
XM_006712337.3	1542	Silent Mutation	ATC,ATT	I301I	XP_006712400.1
XM_011510737.2	1542	Silent Mutation	ATC,ATT	I333I	XP_011509039.1
XM_011510742.2	1542	Silent Mutation	ATC,ATT	I160I	XP_011509044.1
XM_017003455.1	1542	Silent Mutation	ATC,ATT	I381I	XP_016858944.1
XM_017003456.1	1542	Silent Mutation	ATC,ATT	I359I	XP_016858945.1
XM_017003457.1	1542	Silent Mutation	ATC,ATT	I356I	XP_016858946.1
XM_017003458.1	1542	Silent Mutation	ATC,ATT	I325I	XP_016858947.1
XM_017003459.1	1542	Silent Mutation	ATC,ATT	I303I	XP_016858948.1
XM_017003460.1	1542	Silent Mutation	ATC,ATT	I381I	XP_016858949.1
XM_017003461.1	1542	Silent Mutation	ATC,ATT	I381I	XP_016858950.1
XM_017003462.1	1542	Silent Mutation	ATC,ATT	I381I	XP_016858951.1
XM_017003463.1	1542	Silent Mutation	ATC,ATT	I233I	XP_016858952.1
XM_017003464.1	1542	Silent Mutation	ATC,ATT	I186I	XP_016858953.1
XM_017003465.1	1542	Silent Mutation	ATC,ATT	I186I	XP_016858954.1

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