Product Details

SNP ID
rs201189917
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:63817976 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGGTGTGTGGCGCTGAGATCCGGG[C/T]ACCCTCGGCCGACACAGCTCGCTCG
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C11orf84 PubMed Links

Gene Details

Gene
C11orf84
Gene Name
chromosome 11 open reading frame 84
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_138471.2 612 Missense Mutation GCA,GTA A100V NP_612480.1
XM_005273782.2 612 Missense Mutation GCA,GTA A100V XP_005273839.1
XM_005273783.2 612 Missense Mutation GCA,GTA A100V XP_005273840.1
XM_006718437.1 612 Missense Mutation GCA,GTA A100V XP_006718500.1
XM_011544770.1 612 Missense Mutation GCA,GTA A100V XP_011543072.1
XM_011544771.1 612 Missense Mutation GCA,GTA A100V XP_011543073.1
XM_011544772.1 612 Missense Mutation GCA,GTA A100V XP_011543074.1

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