Variant #0000559707 (NC_000016.9:g.88804734A>G, NM_001142864.2:c.749T>C (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.88804734A>G
DNA change (hg38) g.88738326A>G
Published as PIEZO1(NM_001142864.4):c.749T>C (p.V250A)
ISCN -
DB-ID PIEZO1_000171
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) 0.82793 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTU2 NM_001012762.1 -/. - c.*23106A>G r.(=) p.(=)
PIEZO1 NM_001142864.2 -/. - c.749T>C r.(?) p.(Val250Ala)


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