Product Details

SNP ID

rs201705812

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:46352167 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAAGGAAGAGGCTCCCAAGTACCC[A/G]CAGGAGCAGCCCTGTGTCCTGGAAA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC35C2 PubMed Links

Gene Details

Gene

SLC35C2

Gene Name

solute carrier family 35 member C2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001281457.1	981	Missense Mutation	CGG,TGG	R127W	NP_001268386.1
NM_001281458.1	981	Missense Mutation	CGG,TGG	R270W	NP_001268387.1
NM_001281459.1	981	Missense Mutation	CGG,TGG	R106W	NP_001268388.1
NM_001281460.1	981	Missense Mutation	CGG,TGG	R241W	NP_001268389.1
NM_015945.11	981	Missense Mutation	CGG,TGG	R241W	NP_057029.8
NM_173073.3	981	Missense Mutation	CGG,TGG	R220W	NP_775096.1
NM_173179.3	981	Missense Mutation	CGG,TGG	R241W	NP_775271.1
XM_011528831.1	981	Missense Mutation	CGG,TGG	R241W	XP_011527133.1
XM_011528832.1	981	Missense Mutation	CGG,TGG	R241W	XP_011527134.1
XM_011528833.1	981	Missense Mutation	CGG,TGG	R241W	XP_011527135.1
XM_011528834.1	981	Missense Mutation	CGG,TGG	R240W	XP_011527136.1
XM_011528835.1	981	Missense Mutation	CGG,TGG	R203W	XP_011527137.1
XM_011528836.1	981	Missense Mutation	CGG,TGG	R127W	XP_011527138.1
XM_011528837.1	981	Missense Mutation	CGG,TGG	R127W	XP_011527139.1
XM_011528838.1	981	Missense Mutation	CGG,TGG	R89W	XP_011527140.1
XM_017027856.1	981	Missense Mutation	CGG,TGG	R241W	XP_016883345.1
XM_017027857.1	981	Missense Mutation	CGG,TGG	R241W	XP_016883346.1
XM_017027858.1	981	Missense Mutation	CGG,TGG	R241W	XP_016883347.1
XM_017027859.1	981	Missense Mutation	CGG,TGG	R241W	XP_016883348.1
XM_017027860.1	981	Missense Mutation	CGG,TGG	R241W	XP_016883349.1
XM_017027861.1	981	Missense Mutation	CGG,TGG	R220W	XP_016883350.1
XM_017027862.1	981	Silent Mutation	TGC,TGT	C253C	XP_016883351.1

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