Variant #0000978263 (NC_000008.10:g.65494045_65494050dup, NM_152414.4:c.698_703dup (BHLHE22))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.65494045_65494050dup
DNA change (hg38) -
Published as BHLHE22(NM_152414.5):c.698_703dup (p.(Ser233_Ser234dup))
ISCN -
DB-ID BHLHE22_000005
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BHLHE22 NM_152414.4 -?/. - c.698_703dup r.(?) p.(Ser233_Ser234dup)


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