Variant #0000294557 (NC_000010.10:g.89623861T>C, NM_000314.4:c.-366dup (PTEN))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.89623861T>C
DNA change (hg38) g.87864104T>C
Published as PTEN(NM_000314.8):c.-366T>C, PTEN(NM_001304717.5):c.154+1T>C
ISCN -
DB-ID PTEN_000605 See all 2 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) 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 2024-04-19 20:27:30 +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.-366dup r.(?) p.(=)
KLLN NM_001126049.1 -/. - c.-1617A>G r.(?) p.(=)


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