Variant #0000808882 (NC_000019.9:g.41858590C>T, NC_000019.9(NM_000660.4):c.355+5G>A (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.41858590C>T
DNA change (hg38) -
Published as TGFB1(NM_000660.4):c.355+5G>A (p.?)
ISCN -
DB-ID B9D2_000011
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) 0.00213 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 2021-09-17 14:40:49 +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.355+5G>A r.spl? p.?
TMEM91 NM_001042595.2 -?/. - c.-24668C>T r.(?) p.(=)
B9D2 NM_030578.3 -?/. - c.*2015G>A r.(=) p.(=)


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