Product Details

SNP ID
rs148481778
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:46936827 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGGATGCTGAGTCCGGAGCGCCTA[G/T]CCCTACCGGACTACGAGTATCTGGG
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
C11orf49 PubMed Links

Gene Details

Gene
C11orf49
Gene Name
chromosome 11 open reading frame 49
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001003676.2 130 Missense Mutation GCC,TCC A8S NP_001003676.1
NM_001003677.2 130 Missense Mutation GCC,TCC A8S NP_001003677.1
NM_001003678.2 130 Missense Mutation GCC,TCC A8S NP_001003678.1
NM_001278222.1 130 Missense Mutation AGC,ATC S33I NP_001265151.1
NM_024113.4 130 Missense Mutation GCC,TCC A8S NP_077018.1
XM_006718315.1 130 Missense Mutation GCC,TCC A8S XP_006718378.1
XM_011520364.2 130 Missense Mutation AGC,ATC S33I XP_011518666.1
XM_011520365.2 130 Missense Mutation GCC,TCC A8S XP_011518667.1
XM_017018276.1 130 Missense Mutation GCC,TCC A8S XP_016873765.1
XM_017018277.1 130 UTR 5 XP_016873766.1
XM_017018278.1 130 UTR 5 XP_016873767.1
XM_017018279.1 130 UTR 5 XP_016873768.1
XM_017018280.1 130 UTR 5 XP_016873769.1
XM_017018281.1 130 UTR 5 XP_016873770.1
XM_017018282.1 130 UTR 5 XP_016873771.1

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