Variant #0000555193 (NC_000015.9:g.66995675_66995680del, NM_005585.4:c.79_84del (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.66995675_66995680del
DNA change (hg38) g.66703337_66703342del
Published as SMAD6(NM_005585.4):c.79_84delAGCGGC (p.S27_G28del), SMAD6(NM_005585.5):c.79_84delAGCGGC (p.S27_G28del)
ISCN -
DB-ID SMAD6_000008 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_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 2022-05-09 15:51:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMAD6 NM_005585.4 -?/. - c.79_84del r.(?) p.(Ser27_Gly28del)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.