Product Details

SNP ID

rs145406831

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:46352141 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCCCAAACCAAAGGCGAGAATCCC[A/G]CCAAGGAAGAGGCTCCCAAGTACCC

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	1007	Silent Mutation	GGC,GGT	G135G	NP_001268386.1
NM_001281458.1	1007	Silent Mutation	GGC,GGT	G278G	NP_001268387.1
NM_001281459.1	1007	Silent Mutation	GGC,GGT	G114G	NP_001268388.1
NM_001281460.1	1007	Silent Mutation	GGC,GGT	G249G	NP_001268389.1
NM_015945.11	1007	Silent Mutation	GGC,GGT	G249G	NP_057029.8
NM_173073.3	1007	Silent Mutation	GGC,GGT	G228G	NP_775096.1
NM_173179.3	1007	Silent Mutation	GGC,GGT	G249G	NP_775271.1
XM_011528831.1	1007	Silent Mutation	GGC,GGT	G249G	XP_011527133.1
XM_011528832.1	1007	Silent Mutation	GGC,GGT	G249G	XP_011527134.1
XM_011528833.1	1007	Silent Mutation	GGC,GGT	G249G	XP_011527135.1
XM_011528834.1	1007	Silent Mutation	GGC,GGT	G248G	XP_011527136.1
XM_011528835.1	1007	Silent Mutation	GGC,GGT	G211G	XP_011527137.1
XM_011528836.1	1007	Silent Mutation	GGC,GGT	G135G	XP_011527138.1
XM_011528837.1	1007	Silent Mutation	GGC,GGT	G135G	XP_011527139.1
XM_011528838.1	1007	Silent Mutation	GGC,GGT	G97G	XP_011527140.1
XM_017027856.1	1007	Silent Mutation	GGC,GGT	G249G	XP_016883345.1
XM_017027857.1	1007	Silent Mutation	GGC,GGT	G249G	XP_016883346.1
XM_017027858.1	1007	Silent Mutation	GGC,GGT	G249G	XP_016883347.1
XM_017027859.1	1007	Silent Mutation	GGC,GGT	G249G	XP_016883348.1
XM_017027860.1	1007	Silent Mutation	GGC,GGT	G249G	XP_016883349.1
XM_017027861.1	1007	Silent Mutation	GGC,GGT	G228G	XP_016883350.1
XM_017027862.1	1007	Missense Mutation	GCG,GTG	A262V	XP_016883351.1

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