Variant #0001002724 (NC_000016.9:g.88805016_88805025del, NM_001142864.2:c.590_599del (PIEZO1))

Chromosome 16
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.88805016_88805025del
DNA change (hg38) -
Published as PIEZO1(NM_001142864.2):c.590_599delTGGCGGCTGG (p.(Val197fs))
ISCN -
DB-ID PIEZO1_000403
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 2024-08-28 13:16:32 +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     
CTU2 NM_001012762.1 ?/. - c.*23388_*23397del r.(=) p.(=)
PIEZO1 NM_001142864.2 ?/. - c.590_599del r.(?) p.(Val197Glyfs*6)


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