Variant #0000441424 (NC_000014.8:g.76447058G>A, NM_003239.2:c.179C>T (TGFB3))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.76447058G>A
DNA change (hg38) g.75980715G>A
Published as -
ISCN -
DB-ID TGFB3_000006 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs4252315
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00016 View details
Owner Paul van der Zwaag
Database submission license No license selected
Created by Paul van der Zwaag
Date created 2009-02-25 10:09:40 +01:00 (CET)
Date last edited 2009-06-17 15:06:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
TGFB3 NM_003239.2 -/- 1 c.179C>T r.(?) p.(Thr60Met) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.