Variant #0001041432 (NC_000016.9:g.88773596C>G, NM_001142864.2:c.*8417G>C (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.88773596C>G
DNA change (hg38) -
Published as CTU2(NM_001012759.3):c.121C>G (p.(Arg41Gly))
ISCN -
DB-ID PIEZO1_000415
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTU2 NM_001012762.1 ?/. - c.121C>G r.(?) p.(Arg41Gly)
PIEZO1 NM_001142864.2 ?/. - c.*8417G>C r.(=) p.(=)
RNF166 NM_178841.3 ?/. - c.-863G>C r.(?) p.(=)


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