View genomic variant #0000024569

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.32896737A>C
Published as -
GERP -
Segregation -
DB-ID DNM1L_000011
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 0000024569 ./. - - c.*3401T>G p.(=) - - - -
DNM1L 00000107 NM_001278463.1 0000024569 ./. - - c.*393A>C p.(=) - - - -
DNM1L 00000103 NM_001278464.1 0000024569 ./. - - c.*393A>C p.(=) - - - -
DNM1L 00000104 NM_001278465.1 0000024569 ./. - - c.*393A>C p.(=) - - - -
DNM1L 00000105 NM_001278466.1 0000024569 ./. - - c.*393A>C p.(=) - - - -
DNM1L 00000109 NM_005690.4 0000024569 ./. - - c.*393A>C p.(=) - - - -
DNM1L 00000106 NM_012062.4 0000024569 ./. - - c.*393A>C p.(=) - - - -
DNM1L 00000108 NM_012063.3 0000024569 ./. - - c.*393A>C p.(=) - - - -
DNM1L 00000110 XM_005253282.1 0000024569 ./. - - c.*393A>C p.(=) - - - -
DNM1L 00000111 XM_005253283.1 0000024569 ./. - - c.*393A>C p.(=) - - - -
YARS2 00000366 XM_005253381.1 0000024569 ./. - - c.*3401T>G p.(=) - - - -
YARS2 00000365 XR_242891.1 0000024569 ./. - - n.*1979T>G - - - - -
YARS2 00000364 XR_242892.1 0000024569 ./. - - n.1649+3273T>G - - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000326445; RCV000364831; RCV000407287;
Chromosome 12:32896737..32896737
Allele frequencies from TGP 0.00978
ClinVar Allele ID 332012
Disease database name and identifier MONDO:MONDO:0000863, MedGen:C1838103, OMIM:PS600462, Orphanet:2598|MedGen:CN239368|MedGen:CN239187
ClinVar preferred disease name Myopathy, lactic acidosis, and sideroblastic anemia|Lethal Encephalopathy|Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis
HGVS variant names NC 000012.11:g.32896737A>C
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10641930
Gene symbol:Gene id. DNM1L:10059|YARS2:51067
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 77298476
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