Variant #0000541403 (NC_000010.10:g.89624270G>C, NM_000314.4:c.44G>C (PTEN))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.89624270G>C
DNA change (hg38) g.87864513G>C
Published as PTEN(NM_001304717.5):c.564G>C (p.R188S)
ISCN -
DB-ID KLLN_000028
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.44G>C r.(?) p.(Arg15Thr)
KLLN NM_001126049.1 +?/. - c.-2026C>G r.(?) p.(=)


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