Product Details

SNP ID

rs111565436

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:38674206 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCGGCGGCGGTGTTAGGAACGCCG[A/G]GCCGCCCGGTCGGTGCCCAGAGGTG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C17orf96 PubMed Links

Gene Details

Gene

C17orf96

Gene Name

chromosome 17 open reading frame 96

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130677.1	729	Missense Mutation	CCC,CTC	P97L	NP_001124149.1

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