Variant #0000678949 (NC_000010.10:g.89624312A>T, NC_000010.10(NM_000314.4):c.79+7A>T (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.89624312A>T
DNA change (hg38) -
Published as PTEN(NM_000314.4):c.79+7A>T (p.(=)), PTEN(NM_001304718.2):c.-627+7A>T
ISCN -
DB-ID PTEN_000330 See all 4 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.79+7A>T r.(=) p.(=)
KLLN NM_001126049.1 -?/. - c.-2068T>A r.(?) p.(=)


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