Variant #0000145980 (NC_000016.9:g.30097995_30097996dup, NM_004608.3:c.934_935dup (TBX6))

Chromosome 16
Allele Maternal (confirmed)
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.30097995_30097996dup
DNA change (hg38) g.30086674_30086675dup
Published as 935_936insGA
ISCN -
DB-ID TBX6_000005
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
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 07:58:57 +01:00 (CET)
Date last edited 2016-11-24 08:39:17 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBX6 NM_004608.3 +/. 8 c.934_935dup r.(?) p.(Asp312Glufs*187)



Screenings

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