Variant #0000680704 (NC_000016.9:g.88782650dup, NM_001142864.2:c.7089dup (PIEZO1))

Chromosome 16
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.88782650dup
DNA change (hg38) -
Published as PIEZO1(NM_001142864.4):c.7089dupC (p.N2364Qfs*15)
ISCN -
DB-ID PIEZO1_000228
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
CTU2 NM_001012762.1 +?/. - c.*1022dup r.(?) p.(=)
PIEZO1 NM_001142864.2 +?/. - c.7089dup r.(?) p.(Asn2364GlnfsTer15)


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