Variant #0000145982 (NC_000016.9:g.30100437G>A, NM_004608.3:c.448C>T (TBX6))

Chromosome 16
Allele Paternal (confirmed)
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.30100437G>A
DNA change (hg38) g.30089116G>A
Published as -
ISCN -
DB-ID TBX6_000003
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation no
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Kazuki Takeda
Database submission license No license selected
Created by Kazuki Takeda
Date created 2016-11-24 08:06:59 +01:00 (CET)
Date last edited 2016-11-24 08:36:02 +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 -/. 4 c.448C>T r.(?) p.(Arg150Cys)



Screenings

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