Product Details

SNP ID
rs17028290
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:60456238 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCTTTTGTTTTGGTTTTTTACAAAA[A/G]TAAGAACAATGTCGTATTCATTCAT
Phenotype
MIM: 606557
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
BCL11A PubMed Links

Gene Details

Gene
BCL11A
Gene Name
B-cell CLL/lymphoma 11A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018014.3 Intron NP_060484.2
NM_022893.3 Intron NP_075044.2
NM_138559.1 Intron NP_612569.1
XM_011532909.1 Intron XP_011531211.1
XM_011532910.1 Intron XP_011531212.1
XM_011532912.1 Intron XP_011531214.1
XM_017004333.1 Intron XP_016859822.1
XM_017004334.1 Intron XP_016859823.1
XM_017004335.1 Intron XP_016859824.1
XM_017004336.1 Intron XP_016859825.1
XM_017004337.1 Intron XP_016859826.1
XM_017004338.1 Intron XP_016859827.1

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