Variant #0000805693 (NC_000012.11:g.32875481T>C, NM_001278464.1:c.1032T>C (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.32875481T>C
DNA change (hg38) -
Published as DNM1L(NM_001278464.1):c.1032T>C (p.A344=)
ISCN -
DB-ID DNM1L_000038
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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     
YARS2 NM_001040436.2 -?/. - c.*24657A>G r.(=) p.(=)
DNM1L NM_001278464.1 -?/. - c.1032T>C r.(?) p.(Ala344=)
DNM1L NM_012062.3 -?/. - c.993T>C r.(?) p.(Ala331=)


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