Variant #0000877506 (NC_000016.9:g.88793220G>A, NM_001142864.2:c.3602C>T (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.88793220G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID PIEZO1_000280 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs372935580
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00079 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-09-01 14:12:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIEZO1 NM_001142864.2 ?/. - c.3602C>T r.(?) p.(Thr1201Met)


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