Variant #0000926365 (NC_000016.9:g.88782477C>T, NM_001142864.2:c.7180G>A (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.88782477C>T
DNA change (hg38) -
Published as PIEZO1(NM_001142864.2):c.7180G>A (p.(Gly2394Ser)), PIEZO1(NM_001142864.4):c.7180G>A (p.G2394S)
ISCN -
DB-ID PIEZO1_000259 See all 3 reported entries
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) 0.0011 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.*849C>T r.(=) p.(=)
PIEZO1 NM_001142864.2 -?/. - c.7180G>A r.(?) p.(Gly2394Ser)


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