View genomic variant #0000024567

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.32896366A>T
Published as -
GERP -
Segregation -
DB-ID DNM1L_000020
MSCV -
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.03437 View details
Owner Lishuang Shen




Variant on transcripts

13 entries on 1 page. Showing entries 1 - 13.
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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 0000024567 ./. - - c.*3772T>A p.(=) - - - -
DNM1L 00000107 NM_001278463.1 0000024567 ./. - - c.*22A>T p.(=) - - - -
DNM1L 00000103 NM_001278464.1 0000024567 ./. - - c.*22A>T p.(=) - - - -
DNM1L 00000104 NM_001278465.1 0000024567 ./. - - c.*22A>T p.(=) - - - -
DNM1L 00000105 NM_001278466.1 0000024567 ./. - - c.*22A>T p.(=) - - - -
DNM1L 00000109 NM_005690.4 0000024567 ./. - - c.*22A>T p.(=) - - - -
DNM1L 00000106 NM_012062.4 0000024567 ./. - - c.*22A>T p.(=) - - - -
DNM1L 00000108 NM_012063.3 0000024567 ./. - - c.*22A>T p.(=) - - - -
DNM1L 00000110 XM_005253282.1 0000024567 ./. - - c.*22A>T p.(=) - - - -
DNM1L 00000111 XM_005253283.1 0000024567 ./. - - c.*22A>T p.(=) - - - -
YARS2 00000366 XM_005253381.1 0000024567 ./. - - c.*3772T>A p.(=) - - - -
YARS2 00000365 XR_242891.1 0000024567 ./. - - n.*2350T>A - - - - -
YARS2 00000364 XR_242892.1 0000024567 ./. - - n.1649+3644T>A - - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000275050; RCV000313747; RCV001660612; RCV001660611; RCV001683241;
Chromosome 12:32896366..32896366
Allele frequencies from ESP 0.03437
Allele frequencies from ExAC 0.13261
Allele frequencies from TGP 0.14357
ClinVar Allele ID 332011
Disease database name and identifier MONDO:MONDO:0000863, MedGen:C1838103, OMIM:PS600462, Orphanet:2598|MedGen:C3661900|MONDO:MONDO:0013726, MedGen:C3280660, OMIM:614388, Orphanet:330050|MONDO:MONDO:0012543, MedGen:C1853139, OMIM:610708, Orphanet:98673|MedGen:CN239187
ClinVar preferred disease name Myopathy, lactic acidosis, and sideroblastic anemia|not provided|Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1|Optic atrophy 5|Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis
HGVS variant names NC 000012.11:g.32896366A>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA6507817
Gene symbol:Gene id. DNM1L:10059|YARS2:51067
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 3200103
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