Product Details

SNP ID

rs11166387

Assay Type

Functionally tested

NCBI dbSNP Submissions

38

Location

Chr.1:99984241 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATATTTAGAAGCCGGATAATTGATT[A/C]CCCTGGAGGGAAGAGGAAAGGAATA

Phenotype

MIM: 605632

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC35A3 PubMed Links

Gene Details

Gene

SLC35A3

Gene Name

solute carrier family 35 member A3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271684.1		Intron			NP_001258613.1
NM_001271685.1		Intron			NP_001258614.1
NM_012243.2		Intron			NP_036375.1
XM_005270691.4		Intron			XP_005270748.1
XM_011541135.2		Intron			XP_011539437.1
XM_011541136.2		Intron			XP_011539438.1
XM_011541137.2		Intron			XP_011539439.1
XM_011541138.2		Intron			XP_011539440.1
XM_017000869.1		Intron			XP_016856358.1
XM_017000870.1		Intron			XP_016856359.1
XM_017000871.1		Intron			XP_016856360.1
XM_017000872.1		Intron			XP_016856361.1

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