Variant #0000949936 (NC_000012.11:g.32884329G>A, NM_001278464.1:c.1279G>A (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.32884329G>A
DNA change (hg38) -
Published as DNM1L(NM_012062.5):c.1240G>A (p.E414K)
ISCN -
DB-ID DNM1L_000044
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2025-10-06 12:06:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YARS2 NM_001040436.2 +?/. - c.*15809C>T r.(=) p.(=)
DNM1L NM_001278464.1 +?/. - c.1279G>A r.(?) p.(Glu427Lys)


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