Product Details

SNP ID
rs16949453
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:48546228 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCTCTTCCTGCCATACTTCATTTTT[A/G]TAGAGCTGATGTGTTTTAGGCAAAC
Phenotype
MIM: 613178
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CTIF PubMed Links

Gene Details

Gene
CTIF
Gene Name
cap binding complex dependent translation initiation factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142397.1 Intron NP_001135869.1
NM_014772.2 Intron NP_055587.1
XM_005258392.4 Intron XP_005258449.1
XM_006722583.3 Intron XP_006722646.1
XM_006722586.3 Intron XP_006722649.1
XM_006722587.3 Intron XP_006722650.1
XM_006722588.3 Intron XP_006722651.1
XM_006722589.3 Intron XP_006722652.1
XM_011526278.2 Intron XP_011524580.1
XM_011526279.2 Intron XP_011524581.1
XM_017026100.1 Intron XP_016881589.1
XM_017026101.1 Intron XP_016881590.1
XM_017026102.1 Intron XP_016881591.1

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