Product Details

SNP ID
rs114534916
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:33512740 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATTCTTCTGTGTATGTGGGTGCAC[A/G]TATGTATGTCTTTTTTTTTTTTTTT
Phenotype
MIM: 603672
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CBFA2T2 PubMed Links

Gene Details

Gene
CBFA2T2
Gene Name
CBFA2/RUNX1 translocation partner 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001032999.2 Intron NP_001028171.1
NM_001039709.1 Intron NP_001034798.1
NM_005093.3 Intron NP_005084.1
XM_011529101.2 Intron XP_011527403.1
XM_011529102.2 Intron XP_011527404.1
XM_011529103.2 Intron XP_011527405.1
XM_011529107.2 Intron XP_011527409.1
XM_017028121.1 Intron XP_016883610.1
XM_017028122.1 Intron XP_016883611.1
XM_017028123.1 Intron XP_016883612.1
XM_017028124.1 Intron XP_016883613.1
XM_017028125.1 Intron XP_016883614.1

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