Variant #0001042980 (NC_000019.9:g.41858694C>A, NM_000660.4:c.256G>T (TGFB1))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.41858694C>A
DNA change (hg38) -
Published as TGFB1(NM_000660.7):c.256G>T (p.(Asp86Tyr))
ISCN -
DB-ID B9D2_000024
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) 3.0E-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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TGFB1 NM_000660.4 ?/. - c.256G>T r.(?) p.(Asp86Tyr)
TMEM91 NM_001042595.2 ?/. - c.-24564C>A r.(?) p.(=)
B9D2 NM_030578.3 ?/. - c.*1911G>T r.(=) p.(=)


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