View genomic variant #0000018602

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.17449476C>T
Published as -
GERP -
Segregation -
DB-ID GTPBP3_000009
MSCV MSCV_0018602
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

7 entries on 1 page. Showing entries 1 - 7.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
GTPBP3 00002006 NM_001128855.2 0000018602 ./. - - c.517C>T p.(Arg173Trp) - - - -
GTPBP3 00002003 NM_001195422.1 0000018602 ./. - - c.583C>T p.(Arg195Trp) - - - -
GTPBP3 00002005 NM_032620.3 0000018602 ./. - - c.517C>T p.(Arg173Trp) - - - -
GTPBP3 00002004 NM_133644.3 0000018602 ./. - - c.517C>T p.(Arg173Trp) - - - -
GTPBP3 00002000 XM_005260120.1 0000018602 ./. - - c.583C>T p.(Arg195Trp) - - - -
GTPBP3 00002001 XM_005260121.1 0000018602 ./. - - c.583C>T p.(Arg195Trp) - - - -
GTPBP3 00002002 XM_005260122.1 0000018602 ./. - - c.583C>T p.(Arg195Trp) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000578243;
Chromosome 19:17449476..17449476
ClinVar Allele ID 481394
Disease database name and identifier MONDO:MONDO:0014525, MedGen:C5567743, OMIM:616198, Orphanet:444013
ClinVar preferred disease name Combined oxidative phosphorylation defect type 23
HGVS variant names NC 000019.9:g.17449476C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA404733340
Gene symbol:Gene id. GTPBP3:84705
Molecular consequence SO:0001583|missense variant
Allele origin paternal
dbSNP ID 1274363168
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001389269;
Chromosome 19:17449477..17449483
ClinVar Allele ID 1064671
Disease database name and identifier MedGen:C3661900
ClinVar preferred disease name not provided
HGVS variant names NC 000019.9:g.17449480 17449486del
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Gene symbol:Gene id. GTPBP3:84705
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 2145701171
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