Variant #0000274614 (NC_000016.9:g.88772985C>A, NM_001142864.2:c.*9028G>T (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.88772985C>A
DNA change (hg38) g.88706577C>A
Published as CTU2(NM_001012759.3):c.47C>A (p.P16Q)
ISCN -
DB-ID CTU2_000001
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.47C>A r.(?) p.(Pro16Gln)
PIEZO1 NM_001142864.2 -?/. - c.*9028G>T r.(=) p.(=)
RNF166 NM_178841.3 -?/. - c.-252G>T r.(?) p.(=)


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