Variant #0000831839 (NC_000018.9:g.45371828T>C, NM_005901.5:c.1163A>G (SMAD2))

Chromosome 18
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45371828T>C
DNA change (hg38) g.47845457T>C
Published as -
ISCN -
DB-ID SMAD2_000003 See all 3 reported entries
Variant remarks ACMG PP3, PS3, PP2
Reference PubMed: Schepers 2018
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-01-01 13:58:51 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMAD2 NM_005901.5 +?/. - c.1163A>G r.(?) p.(Gln388Arg)


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