Product Details

SNP ID
rs13229466
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:135149405 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTTCTAAAAGATGCATAGTATTTTA[C/T]CCTTGATACATCATAGTTTACTTCT
Phenotype
MIM: 616980
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
C7orf49 PubMed Links

Gene Details

Gene
C7orf49
Gene Name
chromosome 7 open reading frame 49
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001243749.1 Intron NP_001230678.1
NM_001243751.1 Intron NP_001230680.1
NM_001243752.1 Intron NP_001230681.1
NM_001243753.1 Intron NP_001230682.1
NM_001243754.1 Intron NP_001230683.1
NM_001243755.1 Intron NP_001230684.1
NM_001305629.1 Intron NP_001292558.1
NM_001305630.1 Intron NP_001292559.1
NM_024033.3 Intron NP_076938.2
XM_017012589.1 Intron XP_016868078.1
XM_017012590.1 Intron XP_016868079.1
XM_017012591.1 Intron XP_016868080.1
XM_017012592.1 Intron XP_016868081.1
XM_017012593.1 Intron XP_016868082.1
XM_017012594.1 Intron XP_016868083.1
XM_017012595.1 Intron XP_016868084.1
Gene
TMEM140
Gene Name
transmembrane protein 140
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018295.4 Intron NP_060765.4

View Full Product Details