Product Details

SNP ID

rs10882362

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:93895733 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCAACAAAGCTTTTTTCAAGTTCTG[C/G]TTGGAACTGTTACCCATATGTCTTA

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC35G1 PubMed Links

Gene Details

Gene

SLC35G1

Gene Name

solute carrier family 35 member G1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001134658.1		Intron			NP_001128130.1
NM_153226.2		Intron			NP_694958.1
XM_011539371.2		Intron			XP_011537673.1
XM_011539373.2		Intron			XP_011537675.1

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