View genomic variant #0000000470

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.32884052C>A
Published as -
GERP 4.910
Segregation -
DB-ID chr12_000001
MSCV MSCV_0000470
dbSNP ID rs121908531
Frequency -
Sources ; clinVar; Ensembl;
Reference 17460227
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 0000000470 +/+ - 10/18 c.1184C>A p.(Ala395Asp) probably_damaging(1) missense_variant - deleterious(0)
DNM1L 00000103 NM_001278464.1 0000000470 +/+ - 11/20 c.1223C>A p.(Ala408Asp) probably_damaging(0.996) missense_variant - deleterious(0)
DNM1L 00000104 NM_001278465.1 0000000470 +/+ - 11/20 c.1223C>A p.(Ala408Asp) probably_damaging(0.996) missense_variant - deleterious(0)
DNM1L 00000105 NM_001278466.1 0000000470 +/+ - 7/17 c.575C>A p.(Ala192Asp) probably_damaging(0.999) missense_variant - deleterious(0)
DNM1L 00000109 NM_005690.4 0000000470 +/+ - 10/18 c.1184C>A p.(Ala395Asp) probably_damaging(1) missense_variant - deleterious(0)
DNM1L 00000106 NM_012062.4 0000000470 +/+ - 10/18 c.1184C>A p.(Ala395Asp) probably_damaging(1) missense_variant - deleterious(0)
DNM1L 00000108 NM_012063.3 0000000470 +/+ - 10/18 c.1184C>A p.(Ala395Asp) probably_damaging(1) missense_variant - deleterious(0)
DNM1L 00000110 XM_005253282.1 0000000470 +/+ - 11/20 c.1223C>A p.(Ala408Asp) probably_damaging(0.996) missense_variant - deleterious(0)
DNM1L 00000111 XM_005253283.1 0000000470 +/+ - 10/20 c.737C>A p.(Ala246Asp) - missense_variant - -
YARS2 00000364 XR_242892.1 0000000470 +/+ - - n.1650-5753G>T - - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000006386;
Chromosome 12:32884052..32884052
ClinVar Allele ID 21054
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.32884052C>A
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA117911|OMIM:603850.0001|UniProtKB:O00429#VAR 063704
Gene symbol:Gene id. DNM1L:10059
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121908531
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