Variant #0000567433 (NC_000019.9:g.41854250G>A, NM_000660.4:c.466C>T (TGFB1))

Chromosome 19
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.41854250G>A
DNA change (hg38) g.41348345G>A
Published as TGFB1(NM_000660.7):c.466C>T (p.R156C)
ISCN -
DB-ID B9D2_000004
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
TGFB1 NM_000660.4 +/. - c.466C>T r.(?) p.(Arg156Cys)
TMEM91 NM_001042595.2 +/. - c.-29008G>A r.(?) p.(=)
B9D2 NM_030578.3 +/. - c.*6355C>T r.(=) p.(=)


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