Product Details

SNP ID

rs146805332

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:140337327 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAAACCCACATCCATCCTAGCTTG[C/T]CCCGGATCAGAGACACTAAATACTG

Phenotype

Polymorphism

C/T, Transition 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	1850	Missense Mutation	GAC,GGC	D434G	NP_001274427.1
NM_032295.3	1850	Silent Mutation	GGA,GGG	G349G	NP_115671.1
NM_207113.2	1850	Missense Mutation	GAC,GGC	D450G	NP_996996.1
XM_011516626.2	1850	Silent Mutation	GGA,GGG	G399G	XP_011514928.1
XM_011516627.2	1850	Silent Mutation	GGA,GGG	G383G	XP_011514929.1
XM_017012712.1	1850	Missense Mutation	GAC,GGC	D450G	XP_016868201.1
XM_017012713.1	1850	Silent Mutation	GGA,GGG	G349G	XP_016868202.1
XM_017012714.1	1850	Missense Mutation	GAC,GGC	D369G	XP_016868203.1
XM_017012715.1	1850	Missense Mutation	GAC,GGC	D362G	XP_016868204.1
XM_017012716.1	1850	Silent Mutation	GGA,GGG	G261G	XP_016868205.1
XM_017012717.1	1850	Missense Mutation	GAC,GGC	D302G	XP_016868206.1
XM_017012718.1	1850	Intron			XP_016868207.1

View Full Product Details