Variant #0000979219 (NC_000010.10:g.89624218C>G, NM_000314.4:c.-9C>G (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.89624218C>G
DNA change (hg38) -
Published as PTEN(NM_000314.8):c.-9C>G, PTEN(NM_001304717.5):c.511C>G (p.(Leu171Val))
ISCN -
DB-ID PTEN_000023 See all 5 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) 0.00362 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTEN NM_000314.4 -?/. - c.-9C>G r.(?) p.(=)
KLLN NM_001126049.1 -?/. - c.-1974G>C r.(?) p.(=)


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