Variant #0000854144 (NC_000015.9:g.67394601_67394606dup, NC_000015.9(NM_005902.3):c.206+35903_206+35908dup (SMAD3))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.67394601_67394606dup
DNA change (hg38) -
Published as SMAD3(NM_005902.4):c.206+35900_206+35905dupGTGTGT
ISCN -
DB-ID SMAD3_000150
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMAD3 NM_005902.3 -/. - c.206+35903_206+35908dup r.(=) p.(=)


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