Product Details

SNP ID

rs139406164

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:140335468 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCACGAGAGAGAATATTTCCCTCA[C/G]TATTAATGGCGAGATAAACACAATT

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC37A3 PubMed Links

Gene Details

Gene

SLC37A3

Gene Name

solute carrier family 37 member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001287498.1	1930	Missense Mutation	CTG,GTG	L461V	NP_001274427.1
NM_032295.3	1930	Missense Mutation	ACT,AGT	T376S	NP_115671.1
NM_207113.2	1930	Missense Mutation	CTG,GTG	L477V	NP_996996.1
XM_011516626.2	1930	Missense Mutation	ACT,AGT	T426S	XP_011514928.1
XM_011516627.2	1930	Missense Mutation	ACT,AGT	T410S	XP_011514929.1
XM_017012712.1	1930	Missense Mutation	CTG,GTG	L477V	XP_016868201.1
XM_017012713.1	1930	Missense Mutation	ACT,AGT	T376S	XP_016868202.1
XM_017012714.1	1930	Missense Mutation	CTG,GTG	L396V	XP_016868203.1
XM_017012715.1	1930	Missense Mutation	CTG,GTG	L389V	XP_016868204.1
XM_017012716.1	1930	Missense Mutation	ACT,AGT	T288S	XP_016868205.1
XM_017012717.1	1930	Missense Mutation	CTG,GTG	L329V	XP_016868206.1
XM_017012718.1	1930	Intron			XP_016868207.1

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