Variant #0001041431 (NC_000016.9:g.88773594T>A, NM_001142864.2:c.*8419A>T (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.88773594T>A
DNA change (hg38) -
Published as CTU2(NM_001012759.3):c.119T>A (p.(Ile40Lys))
ISCN -
DB-ID PIEZO1_000414
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) 0.00018 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTU2 NM_001012762.1 ?/. - c.119T>A r.(?) p.(Ile40Lys)
PIEZO1 NM_001142864.2 ?/. - c.*8419A>T r.(=) p.(=)
RNF166 NM_178841.3 ?/. - c.-861A>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.