Product Details

SNP ID

rs138124634

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:46352194 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGAGCAGCCCTGTGTCCTGGAAAC[A/G]GAAGATTTTCTCAGATGTGGACAAA

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	954	Missense Mutation	CGT,TGT	R118C	NP_001268386.1
NM_001281458.1	954	Missense Mutation	CGT,TGT	R261C	NP_001268387.1
NM_001281459.1	954	Missense Mutation	CGT,TGT	R97C	NP_001268388.1
NM_001281460.1	954	Missense Mutation	CGT,TGT	R232C	NP_001268389.1
NM_015945.11	954	Missense Mutation	CGT,TGT	R232C	NP_057029.8
NM_173073.3	954	Missense Mutation	CGT,TGT	R211C	NP_775096.1
NM_173179.3	954	Missense Mutation	CGT,TGT	R232C	NP_775271.1
XM_011528831.1	954	Missense Mutation	CGT,TGT	R232C	XP_011527133.1
XM_011528832.1	954	Missense Mutation	CGT,TGT	R232C	XP_011527134.1
XM_011528833.1	954	Missense Mutation	CGT,TGT	R232C	XP_011527135.1
XM_011528834.1	954	Intron			XP_011527136.1
XM_011528835.1	954	Intron			XP_011527137.1
XM_011528836.1	954	Missense Mutation	CGT,TGT	R118C	XP_011527138.1
XM_011528837.1	954	Missense Mutation	CGT,TGT	R118C	XP_011527139.1
XM_011528838.1	954	Missense Mutation	CGT,TGT	R80C	XP_011527140.1
XM_017027856.1	954	Missense Mutation	CGT,TGT	R232C	XP_016883345.1
XM_017027857.1	954	Missense Mutation	CGT,TGT	R232C	XP_016883346.1
XM_017027858.1	954	Missense Mutation	CGT,TGT	R232C	XP_016883347.1
XM_017027859.1	954	Missense Mutation	CGT,TGT	R232C	XP_016883348.1
XM_017027860.1	954	Missense Mutation	CGT,TGT	R232C	XP_016883349.1
XM_017027861.1	954	Missense Mutation	CGT,TGT	R211C	XP_016883350.1
XM_017027862.1	954	Silent Mutation	TCC,TCT	S244S	XP_016883351.1

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