Product Details

SNP ID
rs201963756
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:63817997 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGGCACCCTCGGCCGACACAGCTC[A/G]CTCGCACATCTTGGAGCAGCACCCT
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_138471.2 633 Missense Mutation CAC,CGC H107R NP_612480.1
XM_005273782.2 633 Missense Mutation CAC,CGC H107R XP_005273839.1
XM_005273783.2 633 Missense Mutation CAC,CGC H107R XP_005273840.1
XM_006718437.1 633 Missense Mutation CAC,CGC H107R XP_006718500.1
XM_011544770.1 633 Missense Mutation CAC,CGC H107R XP_011543072.1
XM_011544771.1 633 Missense Mutation CAC,CGC H107R XP_011543073.1
XM_011544772.1 633 Missense Mutation CAC,CGC H107R XP_011543074.1

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