Variant #0000321663 (NC_000010.10:g.89621810del, NM_000314.4:c.-2417del (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.89621810del
DNA change (hg38) g.87862053del
Published as KLLN(NM_001126049.1):c.438del (p.(Ala147ProfsTer35))
ISCN -
DB-ID KLLN_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-28 14:30:01 +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.-2417del r.(?) p.(=)
KLLN NM_001126049.1 ?/. - c.438del r.(?) p.(Ala147ProfsTer35)


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