Variant #0000040019 (NC_000012.11:g.26275297G>C, NM_030762.2:c.1151C>G (BHLHE41))

Chromosome 12
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.26275297G>C
DNA change (hg38) g.26122364G>C
Published as Pro385Arg
ISCN -
DB-ID BHLHE41_000001 See all 3 reported entries
Variant remarks expression cloning HEK293 cells (luciferase assay) attenuated repressive activity of CLOCK/BMAL1-mediated transactivation (effect moderate compared to R57A/K variants); physical interaction with hSIRT1 not affected
Reference PubMed: He 2009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-08-14 22:48:19 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BHLHE41 NM_030762.2 +/. 5 c.1151C>G r.(?) p.Pro384Arg


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