Product Details

SNP ID

rs201417604

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:122932612 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTTTCTTTTCCATCAGTTCCATAT[C/T]TTTAGAAAGAATCTTTTCCAAGTAG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C10orf88 PubMed Links

Gene Details

Gene

C10orf88

Gene Name

chromosome 10 open reading frame 88

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024942.3	1378	Missense Mutation	AAT,GAT	N385D	NP_079218.2

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