Variant #0000925619 (NC_000012.11:g.32861135_32861136del, NM_001278464.1:c.385_386del (DNM1L))

Chromosome 12
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.32861135_32861136del
DNA change (hg38) -
Published as DNM1L(NM_001278464.2):c.385_386delGA (p.E129Kfs*6)
ISCN -
DB-ID DNM1L_000003 See all 4 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) 4.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNM1L NM_001278464.1 +?/. - c.385_386del r.(?) p.(Glu129Lysfs*6)
DNM1L NM_012062.3 +?/. - c.346_347del r.(?) p.(Glu116Lysfs*6)


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