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SNP ID

rs140516625

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:116511890 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTCCTGCCTGGGTGTTACTGATCC[C/T]GGGATTCTTTCTGAACAATAGGTCG

Phenotype

MIM: 614137

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM26E PubMed Links

Gene Details

Gene

FAM26E

Gene Name

family with sequence similarity 26 member E

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153711.3	246	Missense Mutation	CCG,CTG	P65L	NP_714922.1

Gene

TRAPPC3L

Gene Name

trafficking protein particle complex 3 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001139444.2	246	Intron			NP_001132916.1

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