Variant #0001004796 (NC_000019.9:g.41892591del, NM_000660.4:c.-33642del (TGFB1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.41892591del
DNA change (hg38) -
Published as EXOSC5(NM_020158.3):c.655delC (p.(His219fs))
ISCN -
DB-ID B9D2_000023
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 2024-08-28 13:16:32 +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     
TGFB1 NM_000660.4 +?/. - c.-33642del r.(?) p.(=)
TMEM91 NM_001042595.2 +?/. - c.*3066del r.(?) p.(=)
EXOSC5 NM_020158.3 +?/. - c.655del r.(?) p.(His219Thrfs*59)
B9D2 NM_030578.3 +?/. - c.-22733del r.(?) p.(=)


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