Product Details

SNP ID

rs200271005

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:42105293 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTGTCAGAGCTGGCCTCGGCTTG[C/G]TGGCTGTGGTCACGGAGACTTCCTG

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C6orf132 PubMed Links

Gene Details

Gene

C6orf132

Gene Name

chromosome 6 open reading frame 132

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001164446.2	3152	Missense Mutation	CAC,CAG	H873Q	NP_001157918.1

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