Product Details

SNP ID

rs142686850

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:109424213 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCTGGCGAGGGCCTTTTGCAAACG[A/G]TGGTACTGTCCTGATCGTCTAGCCC

Phenotype

Polymorphism

A/G, Transition 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	1087	Missense Mutation	ATG,GTG	M194V	NP_997528.2
XM_011542817.2	1087	Missense Mutation	ATG,GTG	M341V	XP_011541119.1
XM_011542818.2	1087	Missense Mutation	ATG,GTG	M194V	XP_011541120.1

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