Product Details

SNP ID
rs115732479
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:49665280 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCACAGTCCCCCTACAGAAGATCTC[C/T]CAAAACATTTCCAACACAGAACTTC
Phenotype
MIM: 610837 MIM: 603734
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
BCL2L12 PubMed Links

Gene Details

Gene
BCL2L12
Gene Name
BCL2 like 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040668.1 139 UTR 5 NP_001035758.1
NM_001282516.1 139 UTR 5 NP_001269445.1
NM_001282517.1 139 UTR 5 NP_001269446.1
NM_001282519.1 139 UTR 5 NP_001269448.1
NM_001282520.1 139 UTR 5 NP_001269449.1
NM_001282521.1 139 UTR 5 NP_001269450.1
NM_138639.1 139 UTR 5 NP_619580.1
XM_017027345.1 139 UTR 5 XP_016882834.1
XM_017027346.1 139 UTR 5 XP_016882835.1
Gene
IRF3
Gene Name
interferon regulatory factor 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001197122.1 139 Intron NP_001184051.1
NM_001197123.1 139 Intron NP_001184052.1
NM_001197124.1 139 Intron NP_001184053.1
NM_001197125.1 139 Intron NP_001184054.1
NM_001197126.1 139 Intron NP_001184055.1
NM_001197127.1 139 Intron NP_001184056.1
NM_001197128.1 139 Intron NP_001184057.1
NM_001571.5 139 Intron NP_001562.1
XM_006723197.1 139 Intron XP_006723260.1
XM_006723198.1 139 Intron XP_006723261.1
XM_006723200.1 139 Intron XP_006723263.1
XM_006723201.1 139 Intron XP_006723264.1
XM_006723202.2 139 Intron XP_006723265.1
XM_017026766.1 139 Intron XP_016882255.1
XM_017026767.1 139 Intron XP_016882256.1
Gene
SCAF1
Gene Name
SR-related CTD associated factor 1
There are no transcripts associated with this gene.

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