Variant #0000982151 (NC_000016.9:g.88776624C>T, NM_001142864.2:c.*5389G>A (PIEZO1))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.88776624C>T
DNA change (hg38) -
Published as CTU2(NM_001012759.3):c.223-7C>T
ISCN -
DB-ID PIEZO1_000341
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) 0.00048 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.223-7C>T r.(=) p.(=)
PIEZO1 NM_001142864.2 -?/. - c.*5389G>A r.(=) p.(=)
RNF166 NM_178841.3 -?/. - c.-3891G>A r.(?) p.(=)


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