Product Details

SNP ID
rs11039035
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:46945864 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAGACAGTATAATAAGTAAAGAGTA[G/T]GTGACCTATATGGTTCTAGAGCCAG
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 Intron NP_001003676.1
NM_001003677.2 Intron NP_001003677.1
NM_001003678.2 Intron NP_001003678.1
NM_001278222.1 Intron NP_001265151.1
NM_024113.4 Intron NP_077018.1
XM_006718315.1 Intron XP_006718378.1
XM_011520364.2 Intron XP_011518666.1
XM_011520365.2 Intron XP_011518667.1
XM_017018276.1 Intron XP_016873765.1
XM_017018277.1 Intron XP_016873766.1
XM_017018278.1 Intron XP_016873767.1
XM_017018279.1 Intron XP_016873768.1
XM_017018280.1 Intron XP_016873769.1
XM_017018281.1 Intron XP_016873770.1
XM_017018282.1 Intron XP_016873771.1

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