Variant #0000951299 (NC_000019.9:g.41889499G>A, NM_000660.4:c.-30550C>T (TGFB1))

Chromosome 19
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.41889499G>A
DNA change (hg38) -
Published as TMEM91(NM_001042595.2):c.394G>A (p.(Val132Ile))
ISCN -
DB-ID B9D2_000021
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TGFB1 NM_000660.4 -?/. - c.-30550C>T r.(?) p.(=)
TMEM91 NM_001042595.2 -?/. - c.394G>A r.(?) p.(Val132Ile)
EXOSC5 NM_020158.3 -?/. - c.*3039C>T r.(=) p.(=)
B9D2 NM_030578.3 -?/. - c.-19641C>T r.(?) p.(=)


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