Variant #0000889296 (NC_000010.10:g.89624302del, NM_000314.4:c.76del (PTEN))

Chromosome 10
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.89624302del
DNA change (hg38) -
Published as PTEN(NM_000314.8):c.76delA (p.T26Pfs*28)
ISCN -
DB-ID KLLN_000040
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 2022-11-01 13:01:21 +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     
PTEN NM_000314.4 +/. - c.76del r.(?) p.(Thr26Profs*28)
KLLN NM_001126049.1 +/. - c.-2058del r.(?) p.(=)


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