Variant #0000891897 (NC_000014.8:g.76447198G>A, NM_003239.2:c.39C>T (TGFB3))

Chromosome 14
Allele Unknown
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.76447198G>A
DNA change (hg38) -
Published as TGFB3(NM_001329939.1):c.39C>T (p.A13=), TGFB3(NM_003239.5):c.39C>T (p.A13=)
ISCN -
DB-ID TGFB3_000003 See all 3 reported entries
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) 0.00095 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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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.39C>T r.(?) p.(Ala13=) -
IFT43 NM_052873.2 -/. - c.-4932G>A r.(?) p.(=) -


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