Product Details

SNP ID

rs149036444

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:46350507 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGCTGGAGCCCAGCCCCTTCAAGG[A/C]CTTGGGGCCACCATCACCTTGGGAT

Phenotype

Polymorphism

A/C, 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	1245	Missense Mutation	GCC,TCC	A215S	NP_001268386.1
NM_001281458.1	1245	Missense Mutation	GCC,TCC	A358S	NP_001268387.1
NM_001281459.1	1245	Missense Mutation	GCC,TCC	A194S	NP_001268388.1
NM_001281460.1	1245	Missense Mutation	GCC,TCC	A329S	NP_001268389.1
NM_015945.11	1245	Missense Mutation	GCC,TCC	A329S	NP_057029.8
NM_173073.3	1245	Missense Mutation	GCC,TCC	A308S	NP_775096.1
NM_173179.3	1245	Missense Mutation	GCC,TCC	A329S	NP_775271.1
XM_011528831.1	1245	Missense Mutation	GCC,TCC	A329S	XP_011527133.1
XM_011528832.1	1245	Missense Mutation	GCC,TCC	A329S	XP_011527134.1
XM_011528833.1	1245	Missense Mutation	GCC,TCC	A329S	XP_011527135.1
XM_011528834.1	1245	Missense Mutation	GCC,TCC	A328S	XP_011527136.1
XM_011528835.1	1245	Missense Mutation	GCC,TCC	A291S	XP_011527137.1
XM_011528836.1	1245	Missense Mutation	GCC,TCC	A215S	XP_011527138.1
XM_011528837.1	1245	Missense Mutation	GCC,TCC	A215S	XP_011527139.1
XM_011528838.1	1245	Missense Mutation	GCC,TCC	A177S	XP_011527140.1
XM_017027856.1	1245	Missense Mutation	GCC,TCC	A329S	XP_016883345.1
XM_017027857.1	1245	Missense Mutation	GCC,TCC	A329S	XP_016883346.1
XM_017027858.1	1245	Missense Mutation	GCC,TCC	A329S	XP_016883347.1
XM_017027859.1	1245	Missense Mutation	GCC,TCC	A329S	XP_016883348.1
XM_017027860.1	1245	Missense Mutation	GCC,TCC	A329S	XP_016883349.1
XM_017027861.1	1245	Missense Mutation	GCC,TCC	A308S	XP_016883350.1
XM_017027862.1	1245	UTR 3			XP_016883351.1

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