Variant #0000316514 (NC_000014.8:g.76447141G>A, NM_003239.2:c.96C>T (TGFB3))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.76447141G>A
DNA change (hg38) g.75980798G>A
Published as TGFB3(NM_003239.2):c.96C>T (p.F32=)
ISCN -
DB-ID TGFB3_000047
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-05 16:16:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
TGFB3 NM_003239.2 -?/. - c.96C>T r.(?) p.(Phe32=) -
IFT43 NM_052873.2 -?/. - c.-4989G>A r.(?) p.(=) -


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