Product Details

SNP ID

rs111543981

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:233905711 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACGTCCATCGAGGAGCGGATCCTGC[C/G]CATCACTGGCTACTATGGCTACCAG

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC35F3 PubMed Links

Gene Details

Gene

SLC35F3

Gene Name

solute carrier family 35 member F3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001300845.1	602	Intron			NP_001287774.1
NM_173508.3	602	Missense Mutation	CCC,CGC	P79R	NP_775779.1

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