View genomic variant #0000001537

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type ins
DNA change (genomic) (Relative to hg19 / GRCh37) g.100600982_100600983insATC
Published as -
GERP -
Segregation -
DB-ID TIMM8A_000003
MSCV MSCV_0001537
dbSNP ID rs80356558
Frequency -
Sources ; clinVar;
Reference 20301395
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 0000001537 -/- - - c.*2392_*2393insGAT p.(=) - - - -
TIMM8A 00000327 NM_004085.3 0000001537 -/- - - c.*504_*505insGAT p.(=) - - - -
TIMM8A 00000326 XM_005262092.1 0000001537 -/- - - c.132+2538_132+2539insGAT p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000020580;
Chromosome X:100600981..100600982
ClinVar Allele ID 34246
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.100600983 100600985dup
ClinVar review status no assertion criteria provided
Clinical Significance Benign
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA342012
Gene symbol:Gene id. TIMM8A:1678
Molecular consequence SO:0001624|3 prime UTR variant
dbSNP ID 4024308
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