Variant #0000547834 (NC_000012.11:g.32884296C>T, NM_001278464.1:c.1246C>T (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.32884296C>T
DNA change (hg38) g.32731362C>T
Published as DNM1L(NM_001278464.2):c.1246C>T (p.R416C)
ISCN -
DB-ID DNM1L_000009 See all 5 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YARS2 NM_001040436.2 +?/. - c.*15842G>A r.(=) p.(=)
DNM1L NM_001278464.1 +?/. - c.1246C>T r.(?) p.(Arg416Cys)


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