View genomic variant #0000016921

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.32884296C>T
Published as -
GERP -
Segregation -
DB-ID DNM1L_000005
MSCV MSCV_0016921
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 0000016921 ./. - - c.1207C>T p.(Arg403Cys) - - - -
DNM1L 00000103 NM_001278464.1 0000016921 ./. - - c.1246C>T p.(Arg416Cys) - - - -
DNM1L 00000104 NM_001278465.1 0000016921 ./. - - c.1246C>T p.(Arg416Cys) - - - -
DNM1L 00000105 NM_001278466.1 0000016921 ./. - - c.598C>T p.(Arg200Cys) - - - -
DNM1L 00000109 NM_005690.4 0000016921 ./. - - c.1207C>T p.(Arg403Cys) - - - -
DNM1L 00000106 NM_012062.4 0000016921 ./. - - c.1207C>T p.(Arg403Cys) - - - -
DNM1L 00000108 NM_012063.3 0000016921 ./. - - c.1207C>T p.(Arg403Cys) - - - -
DNM1L 00000110 XM_005253282.1 0000016921 ./. - - c.1246C>T p.(Arg416Cys) - - - -
DNM1L 00000111 XM_005253283.1 0000016921 ./. - - c.760C>T p.(Arg254Cys) - - - -
YARS2 00000364 XR_242892.1 0000016921 ./. - - n.1650-5997G>A - - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000200196; RCV000239677; RCV000622584; RCV000850522;
Chromosome 12:32884296..32884296
ClinVar Allele ID 211619
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0013726, MedGen:C3280660, OMIM:614388, Orphanet:330050|MONDO:MONDO:0012543, MedGen:C1853139, OMIM:610708, Orphanet:98673|MeSH:D030342, MedGen:C0950123
ClinVar preferred disease name not provided|Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1|Optic atrophy 5|Inborn genetic diseases
HGVS variant names NC 000012.11:g.32884296C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA324758|OMIM:603850.0006|UniProtKB:O00429#VAR 076318
Gene symbol:Gene id. DNM1L:10059
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 863223953
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