Variant #0001017894 (NC_000016.9:g.88815867C>T, NM_001142864.2:c.85G>A (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.88815867C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID PIEZO1_000409
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs987409464
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 2024-12-03 15:41:01 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIEZO1 NM_001142864.2 ?/. - c.85G>A r.(?) p.(Gly29Arg)


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