Variant #0000555195 (NC_000015.9:g.66995716C>T, NM_005585.4:c.120C>T (SMAD6))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66995716C>T
DNA change (hg38) g.66703378C>T
Published as SMAD6(NM_005585.4):c.120C>T (p.G40=), SMAD6(NM_005585.5):c.120C>T (p.(Gly40=))
ISCN -
DB-ID SMAD6_000022 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) 0.03639 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMAD6 NM_005585.4 -?/. - c.120C>T r.(?) p.(Gly40=)


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