View genomic variant #0000024565

Chromosome 12
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.32895600A>G
Published as -
GERP -
Segregation -
DB-ID DNM1L_000022
MSCV -
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 Lishuang Shen




Variant on transcripts

13 entries on 1 page. Showing entries 1 - 13.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
YARS2 00000367 NM_001040436.2 0000024565 ./. - - c.*4538T>C p.(=) - - - -
DNM1L 00000107 NM_001278463.1 0000024565 ./. - - c.2039A>G p.(Tyr680Cys) - - - -
DNM1L 00000103 NM_001278464.1 0000024565 ./. - - c.2111A>G p.(Tyr704Cys) - - - -
DNM1L 00000104 NM_001278465.1 0000024565 ./. - - c.2078A>G p.(Tyr693Cys) - - - -
DNM1L 00000105 NM_001278466.1 0000024565 ./. - - c.1463A>G p.(Tyr488Cys) - - - -
DNM1L 00000109 NM_005690.4 0000024565 ./. - - c.1961A>G p.(Tyr654Cys) - - - -
DNM1L 00000106 NM_012062.4 0000024565 ./. - - c.2072A>G p.(Tyr691Cys) - - - -
DNM1L 00000108 NM_012063.3 0000024565 ./. - - c.1994A>G p.(Tyr665Cys) - - - -
DNM1L 00000110 XM_005253282.1 0000024565 ./. - - c.2000A>G p.(Tyr667Cys) - - - -
DNM1L 00000111 XM_005253283.1 0000024565 ./. - - c.1625A>G p.(Tyr542Cys) - - - -
YARS2 00000366 XM_005253381.1 0000024565 ./. - - c.*4538T>C p.(=) - - - -
YARS2 00000365 XR_242891.1 0000024565 ./. - - n.*3116T>C - - - - -
YARS2 00000364 XR_242892.1 0000024565 ./. - - n.1649+4410T>C - - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000757997; RCV000850546;
Chromosome 12:32895600..32895600
ClinVar Allele ID 610426
Disease database name and identifier MONDO:MONDO:0012543, MedGen:C1853139, OMIM:610708, Orphanet:98673|MONDO:MONDO:0013726, MedGen:C3280660, OMIM:614388, Orphanet:330050
ClinVar preferred disease name Optic atrophy 5|Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1
HGVS variant names NC 000012.11:g.32895600A>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. DNM1L:10059
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 1565548029
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