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See other CBFA2T2 GT Assays ›
SNP ID:
rs9679764
Gene
CBFA2T2
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.20: 33614973 - 33614973 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

CCTACTATGTTAACTCTTTTTTGTA[C/T]AGAACCATTACAAATAATGTTCCTA

Assay ID C__30108021_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 603672

Literature Links:

 CBFA2T2 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.19)
(0.81)
Caucasian - Not Available CEPH (CEU)
T (0.16)
(0.84)
EAS
T (0.35)
(0.65)
African American - Not Available YRI (Yoruba)
T (0.01)
(0.99)
SAS
T (0.29)
(0.71)
Chinese - Not Available JPT (Japanese)
T (0.36)
(0.64)
AFR
T (0.03)
(0.97)
Japanese - Not Available CHB (Han Chinese)
T (0.45)
(0.55)
EUR
T (0.16)
(0.84)
AMR
T (0.14)
(0.86)
CBFA2T2 - CBFA2/RUNX1 translocation partner 2
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid 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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