View genomic variant #0000023508

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.100603537del
Published as -
GERP -
Segregation -
DB-ID TIMM8A_000007
MSCV MSCV_0023508
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

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 0000023508 ./. - - c.116del p.(Met39Argfs*17) - - - -
TIMM8A 00000327 NM_004085.3 0000023508 ./. - - c.116del p.(Met39Argfs*26) - - - -
TIMM8A 00000326 XM_005262092.1 0000023508 ./. - - c.116del p.(Met39Argfs*11) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000012070;
Chromosome X:100603537..100603537
ClinVar Allele ID 26357
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.100603537del
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA358813|OMIM:300356.0001
Gene symbol:Gene id. TIMM8A:1678
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 869320664
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