Variant #0000505412 (NC_000001.10:g.218520315G>A, NM_003238.3:c.272G>A (TGFB2))

Chromosome 1
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.218520315G>A
DNA change (hg38) g.218346973G>A
Published as TGFB2(NM_001135599.2):c.272G>A (p.(Arg91His)), TGFB2(NM_001135599.3):c.272G>A (p.R91H), TGFB2(NM_001135599.4):c.272G>A (p.R91H), TGFB2(NM_003238.4)...
ISCN -
DB-ID TGFB2_000031 See all 5 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) 0.00398 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TGFB2 NM_003238.3 ?/. - c.272G>A r.(?) p.(Arg91His)


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