Product Details

SNP ID
rs116749570
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:63817973 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCATGGTGTGTGGCGCTGAGATCC[A/G]GGCACCCTCGGCCGACACAGCTCGC
Phenotype
Polymorphism
A/G, 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_138471.2 609 Missense Mutation CAG,CGG Q99R NP_612480.1
XM_005273782.2 609 Missense Mutation CAG,CGG Q99R XP_005273839.1
XM_005273783.2 609 Missense Mutation CAG,CGG Q99R XP_005273840.1
XM_006718437.1 609 Missense Mutation CAG,CGG Q99R XP_006718500.1
XM_011544770.1 609 Missense Mutation CAG,CGG Q99R XP_011543072.1
XM_011544771.1 609 Missense Mutation CAG,CGG Q99R XP_011543073.1
XM_011544772.1 609 Missense Mutation CAG,CGG Q99R XP_011543074.1

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