Product Details

SNP ID

rs200179923

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:109424052 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGAGGCAGCCCCGGGACTCTCCCT[G/T]CTGCGCCCCTTCCAACGCCTCGTCG

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

C11orf87 PubMed Links

Gene Details

Gene

C11orf87

Gene Name

chromosome 11 open reading frame 87

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207645.3	926	Missense Mutation	TGC,TTC	C140F	NP_997528.2
XM_011542817.2	926	Missense Mutation	TGC,TTC	C287F	XP_011541119.1
XM_011542818.2	926	Missense Mutation	TGC,TTC	C140F	XP_011541120.1

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