Variant #0000981369 (NC_000015.9:g.67457630C>T, NM_005902.3:c.440C>T (SMAD3))

Chromosome 15
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.67457630C>T
DNA change (hg38) -
Published as SMAD3(NM_005902.3):c.440C>T (p.P147L, p.(Pro147Leu)), SMAD3(NM_005902.4):c.440C>T (p.P147L)
ISCN -
DB-ID SMAD3_000018 See all 3 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) 3.0E-5 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMAD3 NM_005902.3 ?/. - c.440C>T r.(?) p.(Pro147Leu)


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