Variant #0000541389 (NC_000010.10:g.89622196C>T, NM_000314.4:c.-2031C>T (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.89622196C>T
DNA change (hg38) g.87862439C>T
Published as KLLN(NM_001126049.1):c.49G>A (p.(Val17Ile))
ISCN -
DB-ID KLLN_000016
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) 0.00048 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTEN NM_000314.4 ?/. - c.-2031C>T r.(?) p.(=)
KLLN NM_001126049.1 ?/. - c.49G>A r.(?) p.(Val17Ile)


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