Variant #0000569961 (NC_000020.10:g.49571802del, NM_003859.1:c.182del (DPM1))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49571802del
DNA change (hg38) g.50955265del
Published as DPM1(NM_003859.1):c.182delT (p.(Ile61LysfsTer3))
ISCN -
DB-ID DPM1_000010
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DPM1 NM_003859.1 +?/. - c.182del r.(?) p.(Ile61LysfsTer3)
MOCS3 NM_014484.3 +?/. - c.-3578del r.(?) p.(=)


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