View genomic variant #0000001541

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.100603541G>A
Published as -
GERP 5.110
Segregation -
DB-ID TIMM8A_000002 See all 2 reported entries
MSCV MSCV_0001541
dbSNP ID rs80356559
Frequency -
Sources ; clinVar; Ensembl;
Reference 20301395;17999202
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 0000001541 +/+ - 1/2 c.112C>T p.(Gln38*) - stop_gained - -
TIMM8A 00000327 NM_004085.3 0000001541 +/+ - 1/2 c.112C>T p.(Gln38*) - stop_gained - -
TIMM8A 00000326 XM_005262092.1 0000001541 +/+ - 1/2 c.112C>T p.(Gln38*) - stop_gained - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000020579;
Chromosome X:100603541..100603541
ClinVar Allele ID 34245
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.100603541G>A
ClinVar review status no assertion provided
Clinical Significance not provided
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA342010
Gene symbol:Gene id. TIMM8A:1678
Molecular consequence SO:0001587|nonsense
Allele origin unknown
dbSNP ID 80356559
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