Variant #0000145977 (NC_000016.9:g.29567295_30226930del, NM_004608.3:c.-123785_*530251del (TBX6))

Chromosome 16
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.29567295_30226930del
DNA change (hg38) g.29555974_30215609del
Published as -
ISCN -
DB-ID TBX6_000006
Variant remarks NOTE: unclear whether breakpoint was sequenced or whether description represents the minimal or maximal extent of the deletion
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency 5/94 cases
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Kazuki Takeda
Database submission license No license selected
Created by Kazuki Takeda
Date created 2016-11-24 07:43:58 +01:00 (CET)
Date last edited 2020-07-09 15:07:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBX6 NM_004608.3 +/. _1_9_ c.-123785_*530251del r.0 p.0



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