Product Details

SNP ID
rs2909000
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:12055075 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAGTCATAAACAGTTAGAGAATGAG[C/G]CATTTTTCACAAAATATTGAGGGCT
Phenotype
MIM: 606126
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
BCL2L14 PubMed Links

Gene Details

Gene
BCL2L14
Gene Name
BCL2 like 14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change 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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