Variant #0000145981 (NC_000016.9:g.30102099C>A, NM_004608.3:c.333G>T (TBX6))

Chromosome 16
Allele Unknown
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.30102099C>A
DNA change (hg38) g.30090778C>A
Published as -
ISCN -
DB-ID TBX6_000002
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 08:03:25 +01:00 (CET)
Date last edited 2016-11-24 08:35:29 +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 +/. 3 c.333G>T r.(?) p.(Met111Ile)



Screenings

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