Variant #0000274612 (NC_000016.9:g.88780649_88780658del, NM_001142864.2:c.*1368_*1377del (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.88780649_88780658del
DNA change (hg38) g.88714241_88714250del
Published as CTU2(NM_001012759.1):c.1097+1_1097+10del (p.?), CTU2(NM_001012759.3):c.1097+14_1097+23delTGGGTGTGTG
ISCN -
DB-ID CTU2_000007 See all 2 reported entries
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 2019-12-04 15:24:38 +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.1097+14_1097+23del r.(=) p.(=)
PIEZO1 NM_001142864.2 -/. - c.*1368_*1377del r.(=) p.(=)


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