Variant #0000893224 (NC_000016.9:g.88803111G>A, NM_001142864.2:c.1232C>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.88803111G>A
DNA change (hg38) -
Published as PIEZO1(NM_001142864.4):c.1232C>T (p.P411L)
ISCN -
DB-ID PIEZO1_000316
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) 0.00025 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTU2 NM_001012762.1 ?/. - c.*21483G>A r.(=) p.(=)
PIEZO1 NM_001142864.2 ?/. - c.1232C>T r.(?) p.(Pro411Leu)


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