Variant #0001001604 (NC_000015.9:g.66995828_66995846del, NM_005585.4:c.232_250del (SMAD6))

Chromosome 15
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.66995828_66995846del
DNA change (hg38) -
Published as SMAD6(NM_005585.4):c.232_250delCAGGGCGCGGGGAGGCGCC (p.(Gln78fs))
ISCN -
DB-ID SMAD6_000063 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMAD6 NM_005585.4 +/. - c.232_250del r.(?) p.(Gln78Glyfs*41)


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