Variant #0000288916 (NC_000007.13:g.65440006_65440007del, NM_000181.3:c.965_966del (GUSB))

Chromosome 7
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.65440006_65440007del
DNA change (hg38) g.65975019_65975020del
Published as GUSB(NM_000181.3):c.965_966delTC (p.L322Pfs*30)
ISCN -
DB-ID GUSB_000012
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-22 17:34:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GUSB NM_000181.3 +/. - c.965_966del r.(?) p.(Leu322ProfsTer30)


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