Variant #0000690819 (NC_000010.10:g.89621905_89621906del, NM_000314.4:c.-2322_-2321del (PTEN))

Chromosome 10
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.89621905_89621906del
DNA change (hg38) -
Published as KLLN(NM_001126049.1):c.339_340del (p.(Ala115SerfsTer58)), KLLN(NM_001126049.1):c.339_340delAG (p.A115Sfs*58)
ISCN -
DB-ID KLLN_000006 See all 3 reported entries
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) 0.00142 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTEN NM_000314.4 ?/. - c.-2322_-2321del r.(?) p.(=)
KLLN NM_001126049.1 ?/. - c.339_340del r.(?) p.(Ala115SerfsTer58)


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