Variant #0000720491 (NC_000005.9:g.74018233dup, NM_000521.3:c.*1233dup (HEXB))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.74018233dup
DNA change (hg38) -
Published as GFM2(NM_032380.5):c.2182dupA (p.I728Nfs*66)
ISCN -
DB-ID HEXB_000047
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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 ?/. - c.*1233dup r.(?) p.(=)
ENC1 NM_003633.3 ?/. - c.-82115dup r.(?) p.(=)
GFM2 NM_032380.3 ?/. - c.2182dup r.(?) p.(Ile728Asnfs*66)


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