Variant #0000559591 (NC_000016.9:g.88782676A>G, NM_001142864.2:c.7059T>C (PIEZO1))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.88782676A>G
DNA change (hg38) g.88716268A>G
Published as PIEZO1(NM_001142864.4):c.7059T>C (p.P2353=)
ISCN -
DB-ID PIEZO1_000065
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) 0.88213 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-10 15:13:49 +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.*1048A>G r.(=) p.(=)
PIEZO1 NM_001142864.2 -/. - c.7059T>C r.(?) p.(Pro2353=)


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