Variant #0000872937 (NC_000018.9:g.10689744G>A, NM_001378183.1:c.7406C>T (PIEZO2))

Chromosome 18
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.10689744G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID PIEZO2_000012 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs878853137
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-07-25 14:17:01 +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     
PIEZO2 NM_001378183.1 +?/. - c.7406C>T r.(?) p.(Thr2469Met)


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