Product Details

SNP ID

rs199977178

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:56795128 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAGTGAGGGTTCAGCCAGTGCTCC[A/G]GGAACTGCTCCTCAGCGCGATGCTC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C17orf67 PubMed Links

Gene Details

Gene

C17orf67

Gene Name

chromosome 17 open reading frame 67

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001085430.2	1488	Missense Mutation	CCG,CTG	P70L	NP_001078899.2
XM_011524735.2	1488	Intron			XP_011523037.1

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