View genomic variant #0000016919

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.32884003G>A
Published as -
GERP -
Segregation -
DB-ID DNM1L_000003
MSCV MSCV_0016919
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

10 entries on 1 page. Showing entries 1 - 10.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
DNM1L 00000107 NM_001278463.1 0000016919 ./. - - c.1135G>A p.(Glu379Lys) - - - -
DNM1L 00000103 NM_001278464.1 0000016919 ./. - - c.1174G>A p.(Glu392Lys) - - - -
DNM1L 00000104 NM_001278465.1 0000016919 ./. - - c.1174G>A p.(Glu392Lys) - - - -
DNM1L 00000105 NM_001278466.1 0000016919 ./. - - c.526G>A p.(Glu176Lys) - - - -
DNM1L 00000109 NM_005690.4 0000016919 ./. - - c.1135G>A p.(Glu379Lys) - - - -
DNM1L 00000106 NM_012062.4 0000016919 ./. - - c.1135G>A p.(Glu379Lys) - - - -
DNM1L 00000108 NM_012063.3 0000016919 ./. - - c.1135G>A p.(Glu379Lys) - - - -
DNM1L 00000110 XM_005253282.1 0000016919 ./. - - c.1174G>A p.(Glu392Lys) - - - -
DNM1L 00000111 XM_005253283.1 0000016919 ./. - - c.688G>A p.(Glu230Lys) - - - -
YARS2 00000364 XR_242892.1 0000016919 ./. - - n.1650-5704C>T - - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000414839;
Chromosome 12:32884003..32884003
ClinVar Allele ID 361204
Disease database name and identifier MONDO:MONDO:0013726, MedGen:C3280660, OMIM:614388, Orphanet:330050
ClinVar preferred disease name Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1
HGVS variant names NC 000012.11:g.32884003G>A
ClinVar review status no assertion criteria provided
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA16043679
Gene symbol:Gene id. DNM1L:10059
Molecular consequence SO:0001583|missense variant
Allele origin de-novo
dbSNP ID 1057518694
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None