View genomic variant #0000001539

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.100601543G>A
Published as -
GERP 5.330
Segregation -
DB-ID TIMM8A_000005 See all 2 reported entries
MSCV MSCV_0001539
dbSNP ID rs1054894
Frequency -
Sources ; clinVar; Ensembl;
Reference 11405816
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
TIMM8A 00000328 NM_001145951.1 0000001539 +/+ - - c.*1832C>T p.(=) - - - -
TIMM8A 00000327 NM_004085.3 0000001539 +/+ - 2/2 c.238C>T p.(Arg80*) - stop_gained - -
TIMM8A 00000326 XM_005262092.1 0000001539 +/+ - - c.132+1978C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000012076;
Chromosome X:100601543..100601543
ClinVar Allele ID 26363
Disease database name and identifier MONDO:MONDO:0010578, MedGen:C0796074, OMIM:304700, Orphanet:52368
ClinVar preferred disease name Deafness dystonia syndrome
HGVS variant names NC 000023.10:g.100601543G>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:CA255782|OMIM:300356.0007
Gene symbol:Gene id. TIMM8A:1678
Molecular consequence SO:0001587|nonsense, SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 1054894
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