Product Details

SNP ID

rs149748302

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:190429701 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGGGTTTGAGTTTGAAGGTGAATT[C/T]CAACAGTTGGACTCACAGCTGCTTC

Phenotype

MIM: 614786

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TMEM207 PubMed Links

Gene Details

Gene

TMEM207

Gene Name

transmembrane protein 207

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207316.2	402	Missense Mutation	GAA,GGA	E112G	NP_997199.1

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