Variant #0000831871 (NC_000015.9:g.67473662T>C, NM_005902.3:c.742T>C (SMAD3))

Chromosome 15
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.67473662T>C
DNA change (hg38) g.67181324T>C
Published as -
ISCN -
DB-ID SMAD3_000122 See all 2 reported entries
Variant remarks ACMG PM2, PP3, PP2, PP4, PP5
Reference PubMed: Schepers 2018
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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     
SMAD3 NM_005902.3 +?/. - c.742T>C r.(?) p.(Phe248Leu)


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