Product Details

SNP ID
rs2416987
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:12051811 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGCTCTTTAGGCAAACAGGGTGAAG[A/G]CAAGAGGCATAGGTGATGGACACTA
Phenotype
MIM: 606126
Polymorphism
A/G, Transition 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_030766.1 107 Intron NP_110393.1
NM_138722.1 107 Intron NP_620048.1
NM_138723.1 107 Intron NP_620049.1
XM_006719151.3 107 UTR 5 XP_006719214.1
XM_011520848.1 107 Intron XP_011519150.1
XM_011520849.1 107 Intron XP_011519151.1
XM_017019963.1 107 UTR 5 XP_016875452.1

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