Product Details

SNP ID

rs77662163

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:66744899 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGTTCCCTGCGCGGCATGGAGGGG[A/G]CGGCCGTGGCCGTGTTCGAGGTGAT

Phenotype

MIM: 616109

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C11orf80 PubMed Links

Gene Details

Gene

C11orf80

Gene Name

chromosome 11 open reading frame 80

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001302084.1	164	UTR 5			NP_001289013.1
NM_024650.3	164	Missense Mutation	ACG,GCG	T53A	NP_078926.3

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