Variant #0000541392 (NC_000010.10:g.89623200C>A, NM_000314.4:c.-1026C>A (PTEN))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.89623200C>A
DNA change (hg38) g.87863443C>A
Published as KLLN(NM_001126049.2):c.-956G>T, PTEN(NM_000314.8):c.-1027C>A
ISCN -
DB-ID PTEN_000322 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 2019-07-18 18:22:55 +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.-1026C>A r.(?) p.(=)
KLLN NM_001126049.1 -?/. - c.-956G>T r.(?) p.(=)


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