Variant #0000720490 (NC_000005.9:g.74016509_74016512dup, NM_000521.3:c.1550_1553dup (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.74016509_74016512dup
DNA change (hg38) -
Published as HEXB(NM_001292004.2):c.875_878dupAAGA (p.D293Efs*8)
ISCN -
DB-ID HEXB_000039
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HEXB NM_000521.3 +/. - c.1550_1553dup r.(?) p.(Asp518GlufsTer8)
ENC1 NM_003633.3 +/. - c.-80393_-80390dup r.(?) p.(=)
GFM2 NM_032380.3 +/. - c.*969_*972dup r.(=) p.(=)


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