Product Details

SNP ID

rs199919922

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:46350511 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGAGCCCAGCCCCTTCAAGGCCTT[A/G]GGGCCACCATCACCTTGGGATAGAG

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	1241	Silent Mutation	CCC,CCT	P213P	NP_001268386.1
NM_001281458.1	1241	Silent Mutation	CCC,CCT	P356P	NP_001268387.1
NM_001281459.1	1241	Silent Mutation	CCC,CCT	P192P	NP_001268388.1
NM_001281460.1	1241	Silent Mutation	CCC,CCT	P327P	NP_001268389.1
NM_015945.11	1241	Silent Mutation	CCC,CCT	P327P	NP_057029.8
NM_173073.3	1241	Silent Mutation	CCC,CCT	P306P	NP_775096.1
NM_173179.3	1241	Silent Mutation	CCC,CCT	P327P	NP_775271.1
XM_011528831.1	1241	Silent Mutation	CCC,CCT	P327P	XP_011527133.1
XM_011528832.1	1241	Silent Mutation	CCC,CCT	P327P	XP_011527134.1
XM_011528833.1	1241	Silent Mutation	CCC,CCT	P327P	XP_011527135.1
XM_011528834.1	1241	Silent Mutation	CCC,CCT	P326P	XP_011527136.1
XM_011528835.1	1241	Silent Mutation	CCC,CCT	P289P	XP_011527137.1
XM_011528836.1	1241	Silent Mutation	CCC,CCT	P213P	XP_011527138.1
XM_011528837.1	1241	Silent Mutation	CCC,CCT	P213P	XP_011527139.1
XM_011528838.1	1241	Silent Mutation	CCC,CCT	P175P	XP_011527140.1
XM_017027856.1	1241	Silent Mutation	CCC,CCT	P327P	XP_016883345.1
XM_017027857.1	1241	Silent Mutation	CCC,CCT	P327P	XP_016883346.1
XM_017027858.1	1241	Silent Mutation	CCC,CCT	P327P	XP_016883347.1
XM_017027859.1	1241	Silent Mutation	CCC,CCT	P327P	XP_016883348.1
XM_017027860.1	1241	Silent Mutation	CCC,CCT	P327P	XP_016883349.1
XM_017027861.1	1241	Silent Mutation	CCC,CCT	P306P	XP_016883350.1
XM_017027862.1	1241	UTR 3			XP_016883351.1

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