Variant #0000278604 (NC_000010.10:g.89623031_89623042del, NM_000314.4:c.-1196_-1185del (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.89623031_89623042del
DNA change (hg38) g.87863274_87863285del
Published as KLLN(NM_001126049.2):c.-794_-783delTGCGGCTTTTGC
ISCN -
DB-ID KLLN_000011
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +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.-1196_-1185del r.(?) p.(=)
KLLN NM_001126049.1 ?/. - c.-794_-783del r.(?) p.(=)


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