Variant #0000692197 (NC_000016.9:g.88804349G>T, NM_001142864.2:c.1013C>A (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.88804349G>T
DNA change (hg38) -
Published as LOC100289580(NR_103774.1):n.390G>T (-), PIEZO1(NM_001142864.4):c.1013C>A (p.S338Y)
ISCN -
DB-ID PIEZO1_000165 See all 2 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) 0.03953 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.*22721G>T r.(=) p.(=)
PIEZO1 NM_001142864.2 -/. - c.1013C>A r.(?) p.(Ser338Tyr)


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