Variant #0000550741 (NC_000013.10:g.37453680_37453683del, NM_001127217.2:c.145_148del (SMAD9))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.37453680_37453683del
DNA change (hg38) g.36879543_36879546del
Published as SMAD9(NM_001127217.3):c.145_148delAAGG (p.K49Efs*41)
ISCN -
DB-ID SMAD9_000009
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +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     
SMAD9 NM_001127217.2 +/. - c.145_148del r.(?) p.(Lys49GlufsTer41)


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