Variant #0000323434 (NC_000013.10:g.72440684_72440689del, NM_004392.5:c.244_249del (DACH1))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.72440684_72440689del
DNA change (hg38) -
Published as DACH1(NM_004392.5):c.235_240del (p.(Gly82_Gly83del)), DACH1(NM_080759.5):c.244_249delGGCGGC (p.S82_G83del)
ISCN -
DB-ID DACH1_000006
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DACH1 NM_004392.5 ?/. - c.244_249del r.(?) p.(Gly82_Gly83del)


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