Product Details

SNP ID

rs1045967

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:10730653 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCAAAGTTGGAGTTAGTATGTTCA[A/T]CAGACCCCATTAGCAGAAGTCATGT

Phenotype

MIM: 615318

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

TMEM14C PubMed Links

Gene Details

Gene

TMEM14C

Gene Name

transmembrane protein 14C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001165258.1	697	Missense Mutation	AAC,ATC	N109I	NP_001158730.1
NM_016462.3	697	Missense Mutation	AAC,ATC	N109I	NP_057546.1

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