Product Details

SNP ID

rs201877771

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:46350800 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTTTGAGGGCAACGTGGAGGGATA[G/T]TCCCGAGAGGCAGAGGGCGAAGCCC

Phenotype

Polymorphism

G/T, 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	1188	Missense Mutation	ATA,CTA	I196L	NP_001268386.1
NM_001281458.1	1188	Missense Mutation	ATA,CTA	I339L	NP_001268387.1
NM_001281459.1	1188	Missense Mutation	ATA,CTA	I175L	NP_001268388.1
NM_001281460.1	1188	Missense Mutation	ATA,CTA	I310L	NP_001268389.1
NM_015945.11	1188	Missense Mutation	ATA,CTA	I310L	NP_057029.8
NM_173073.3	1188	Missense Mutation	ATA,CTA	I289L	NP_775096.1
NM_173179.3	1188	Missense Mutation	ATA,CTA	I310L	NP_775271.1
XM_011528831.1	1188	Missense Mutation	ATA,CTA	I310L	XP_011527133.1
XM_011528832.1	1188	Missense Mutation	ATA,CTA	I310L	XP_011527134.1
XM_011528833.1	1188	Missense Mutation	ATA,CTA	I310L	XP_011527135.1
XM_011528834.1	1188	Missense Mutation	ATA,CTA	I309L	XP_011527136.1
XM_011528835.1	1188	Missense Mutation	ATA,CTA	I272L	XP_011527137.1
XM_011528836.1	1188	Missense Mutation	ATA,CTA	I196L	XP_011527138.1
XM_011528837.1	1188	Missense Mutation	ATA,CTA	I196L	XP_011527139.1
XM_011528838.1	1188	Missense Mutation	ATA,CTA	I158L	XP_011527140.1
XM_017027856.1	1188	Missense Mutation	ATA,CTA	I310L	XP_016883345.1
XM_017027857.1	1188	Missense Mutation	ATA,CTA	I310L	XP_016883346.1
XM_017027858.1	1188	Missense Mutation	ATA,CTA	I310L	XP_016883347.1
XM_017027859.1	1188	Missense Mutation	ATA,CTA	I310L	XP_016883348.1
XM_017027860.1	1188	Missense Mutation	ATA,CTA	I310L	XP_016883349.1
XM_017027861.1	1188	Missense Mutation	ATA,CTA	I289L	XP_016883350.1
XM_017027862.1	1188	UTR 3			XP_016883351.1

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