Product Details

SNP ID

rs72837329

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:56795078 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTGATCCCCTTACACAGGATGAA[C/T]CCTGTTCCTGTCACAGTGGGGTTTG

Phenotype

Polymorphism

C/T, 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	1538	Missense Mutation	ATT,GTT	I87V	NP_001078899.2
XM_011524735.2	1538	Intron			XP_011523037.1

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