View genomic variant #0000018607

Chromosome 19
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.17452321_17452322insC
Published as -
GERP -
Segregation -
DB-ID GTPBP3_000003
MSCV MSCV_0018607
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 0000018607 ./. - - c.1225_1226insC p.(Arg410Profs*87) - - - -
GTPBP3 00002003 NM_001195422.1 0000018607 ./. - - c.1354_1355insC p.(Arg453Profs*87) - - - -
GTPBP3 00002005 NM_032620.3 0000018607 ./. - - c.1288_1289insC p.(Arg431Profs*87) - - - -
GTPBP3 00002004 NM_133644.3 0000018607 ./. - - c.1384_1385insC p.(Arg463Profs*87) - - - -
GTPBP3 00002000 XM_005260120.1 0000018607 ./. - - c.1450_1451insC p.(Arg485Profs*87) - - - -
GTPBP3 00002001 XM_005260121.1 0000018607 ./. - - c.1387_1388insC p.(Arg464Profs*87) - - - -
GTPBP3 00002002 XM_005260122.1 0000018607 ./. - - c.1291_1292insC p.(Arg432Profs*87) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000157590;
Chromosome 19:17452321..17452322
ClinVar Allele ID 178780
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.17452324dup
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA358281|OMIM:608536.0001
Gene symbol:Gene id. GTPBP3:84705
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 869320746
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