Variant #0000808885 (NC_000019.9:g.41863821G>A, NM_000660.4:c.-4872C>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.41863821G>A
DNA change (hg38) -
Published as B9D2(NM_030578.3):c.195C>T (p.F65=), B9D2(NM_030578.4):c.195C>T (p.F65=)
ISCN -
DB-ID B9D2_000001 See all 2 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) 0.00203 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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.-4872C>T r.(?) p.(=)
TMEM91 NM_001042595.2 -?/. - c.-19437G>A r.(?) p.(=)
B9D2 NM_030578.3 -?/. - c.195C>T r.(?) p.(Phe65=)


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