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SNP ID:
rs888152
Gene
BCL2L14
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.12: 12087731 - 12087731 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

ACCAGTGACCCTGGGCCAATTTGCA[C/T]CAGGTACAGTTGGAGCGTCAAGCCA

Assay ID C___8904460_20
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 606126

Literature Links:

 BCL2L14 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.20)
(0.80)
Caucasian - Not Available CEPH (CEU)
T (0.23)
(0.77)
EAS
T (0.18)
(0.82)
African American - Not Available YRI (Yoruba)
T (0.15)
(0.85)
SAS
T (0.29)
(0.71)
Chinese - Not Available JPT (Japanese)
T (0.13)
(0.87)
AFR
T (0.14)
(0.86)
Japanese - Not Available CHB (Han Chinese)
T (0.14)
(0.86)
EUR
T (0.20)
(0.80)
AMR
T (0.22)
(0.78)
BCL2L14 - BCL2 like 14
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_030766.1 Intron NP_110393.1
NM_138722.1 Intron NP_620048.1
NM_138723.1 Intron NP_620049.1
XM_006719151.3 Intron XP_006719214.1
XM_011520848.1 Intron XP_011519150.1
XM_011520849.1 Intron XP_011519151.1
XM_017019963.1 Intron XP_016875452.1

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