Variant #0000679496 (NC_000012.11:g.32875577A>G, NC_000012.11(NM_001278464.1):c.1118+10A>G (DNM1L))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32875577A>G
DNA change (hg38) -
Published as DNM1L(NM_001278464.1):c.1118+10A>G
ISCN -
DB-ID DNM1L_000033
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) 0.0006 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2025-10-06 12:05:34 +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.*24561T>C r.(=) p.(=)
DNM1L NM_001278464.1 -?/. - c.1118+10A>G r.(=) p.(=)


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