Variant #0000222241 (NC_000005.9:g.74009341_74009344del, NM_000521.3:c.782_785del (HEXB))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.74009341_74009344del
DNA change (hg38) g.74713516_74713519del
Published as 782_785delCTTT
ISCN -
DB-ID HEXB_000012
Variant remarks not in 200 control individuals
Reference Oller Ramirez, SAG2017, Cordoba
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 1/132 case chromosomes
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 2017-10-24 10:29:06 +02:00 (CEST)
Date last edited 2017-10-24 10:29:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HEXB NM_000521.3 +/. 7 c.782_785del r.(?) p.((Ser261Cysfs*12)


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