Product Details

SNP ID

rs202041610

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:46350462 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCACCTTCCTCCCGCTGGCTGCTCC[C/G]GAGCAGCAGCTCCAGGTCGGGGCTG

Phenotype

Polymorphism

C/G, Transversion 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	1290	Missense Mutation	CGG,GGG	R230G	NP_001268386.1
NM_001281458.1	1290	Missense Mutation	CGG,GGG	R373G	NP_001268387.1
NM_001281459.1	1290	Missense Mutation	CGG,GGG	R209G	NP_001268388.1
NM_001281460.1	1290	Missense Mutation	CGG,GGG	R344G	NP_001268389.1
NM_015945.11	1290	Missense Mutation	CGG,GGG	R344G	NP_057029.8
NM_173073.3	1290	Missense Mutation	CGG,GGG	R323G	NP_775096.1
NM_173179.3	1290	Missense Mutation	CGG,GGG	R344G	NP_775271.1
XM_011528831.1	1290	Missense Mutation	CGG,GGG	R344G	XP_011527133.1
XM_011528832.1	1290	Missense Mutation	CGG,GGG	R344G	XP_011527134.1
XM_011528833.1	1290	Missense Mutation	CGG,GGG	R344G	XP_011527135.1
XM_011528834.1	1290	Missense Mutation	CGG,GGG	R343G	XP_011527136.1
XM_011528835.1	1290	Missense Mutation	CGG,GGG	R306G	XP_011527137.1
XM_011528836.1	1290	Missense Mutation	CGG,GGG	R230G	XP_011527138.1
XM_011528837.1	1290	Missense Mutation	CGG,GGG	R230G	XP_011527139.1
XM_011528838.1	1290	Missense Mutation	CGG,GGG	R192G	XP_011527140.1
XM_017027856.1	1290	Missense Mutation	CGG,GGG	R344G	XP_016883345.1
XM_017027857.1	1290	Missense Mutation	CGG,GGG	R344G	XP_016883346.1
XM_017027858.1	1290	Missense Mutation	CGG,GGG	R344G	XP_016883347.1
XM_017027859.1	1290	Missense Mutation	CGG,GGG	R344G	XP_016883348.1
XM_017027860.1	1290	Missense Mutation	CGG,GGG	R344G	XP_016883349.1
XM_017027861.1	1290	Missense Mutation	CGG,GGG	R323G	XP_016883350.1
XM_017027862.1	1290	UTR 3			XP_016883351.1

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