Variant #0001039197 (NC_000012.11:g.32890847C>T, NM_001278464.1:c.1684C>T (DNM1L))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.32890847C>T
DNA change (hg38) -
Published as DNM1L(NM_012062.5):c.1645C>T (p.(Pro549Ser))
ISCN -
DB-ID YARS2_000032
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YARS2 NM_001040436.2 ?/. - c.*9291G>A r.(=) p.(=)
DNM1L NM_001278464.1 ?/. - c.1684C>T r.(?) p.(Pro562Ser)


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