Variant #0000854696 (NC_000016.9:g.88779260G>C, NM_001142864.2:c.*2753C>G (PIEZO1))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.88779260G>C
DNA change (hg38) -
Published as CTU2(NM_001318507.1):c.897G>C (p.L299=)
ISCN -
DB-ID PIEZO1_000283
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) 0.00017 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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.684G>C r.(?) p.(Leu228=)
PIEZO1 NM_001142864.2 -?/. - c.*2753C>G r.(=) p.(=)


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