Product Details

SNP ID

hCV11896232

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:55396542 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTCCCGGGGTGGAGGGCGGTCGG[C/G]TGCGCTGTTTTCCGGTGAGGCCTGG

Phenotype

MIM: 614726

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

TMEM165 PubMed Links

Gene Details

Gene

TMEM165

Gene Name

transmembrane protein 165

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018475.4		Intron			NP_060945.2

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