Product Details

SNP ID
rs138489782
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:63813813 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCGCGGCCCGAGCCGATGCTCAGA[A/G]GTGAGGATGGAGGGGATTCCACTTC
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_138471.2 440 Missense Mutation ATG,GTG M43V NP_612480.1
XM_005273782.2 440 Missense Mutation ATG,GTG M43V XP_005273839.1
XM_005273783.2 440 Missense Mutation ATG,GTG M43V XP_005273840.1
XM_006718437.1 440 Missense Mutation ATG,GTG M43V XP_006718500.1
XM_011544770.1 440 Missense Mutation ATG,GTG M43V XP_011543072.1
XM_011544771.1 440 Missense Mutation ATG,GTG M43V XP_011543073.1
XM_011544772.1 440 Missense Mutation ATG,GTG M43V XP_011543074.1

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