Product Details

SNP ID

rs138645125

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:5832204 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCTGCCCCTGCCGCCTCGGGGAGC[A/G]TGGGAGCTGGGCACTGGGGTTGTAC

Phenotype

MIM: 136836 MIM: 602018

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FUT6 PubMed Links

Additional Information

For this assay, SNP(s) [rs778805] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

FUT6

Gene Name

fucosyltransferase 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000150.2	1698	Missense Mutation	CGC,TGC	R122C	NP_000141.1
NM_001040701.1	1698	Missense Mutation	CGC,TGC	R122C	NP_001035791.1
XM_005259526.4	1698	Missense Mutation	CGC,TGC	R122C	XP_005259583.1
XM_005259527.3	1698	Missense Mutation	CGC,TGC	R122C	XP_005259584.1
XM_011527868.2	1698	Missense Mutation	CGC,TGC	R122C	XP_011526170.1
XM_011527869.2	1698	Missense Mutation	CGC,TGC	R122C	XP_011526171.1
XM_011527870.2	1698	Missense Mutation	CGC,TGC	R122C	XP_011526172.1
XM_011527872.2	1698	Missense Mutation	CGC,TGC	R122C	XP_011526174.1
XM_011527873.2	1698	Missense Mutation	CGC,TGC	R122C	XP_011526175.1
XM_011527874.2	1698	Missense Mutation	CGC,TGC	R122C	XP_011526176.1
XM_011527875.2	1698	Missense Mutation	CGC,TGC	R122C	XP_011526177.1
XM_011527876.2	1698	Missense Mutation	CGC,TGC	R122C	XP_011526178.1
XM_011527878.2	1698	Missense Mutation	CGC,TGC	R122C	XP_011526180.1
XM_011527879.2	1698	Missense Mutation	CGC,TGC	R122C	XP_011526181.1

Gene

NRTN

Gene Name

neurturin

There are no transcripts associated with this gene.

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