View genomic variant #0000003498

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.153640549G>A
Published as -
GERP 4.140
Segregation -
DB-ID TAZ_000102 See all 2 reported entries
MSCV MSCV_0003498
dbSNP ID -
Frequency -
Sources ; BSF_TAZ;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
TAZ 00000321 NM_000116.3 0000003498 ?/? - 2/10 c.236G>A p.(Trp79*) - stop_gained,splice_region_variant - -
TAZ 00000323 NM_181311.2 0000003498 ?/? - 2/10 c.236G>A p.(Trp79*) - stop_gained,splice_region_variant - -
TAZ 00000322 NM_181312.2 0000003498 ?/? - 2/10 c.236G>A p.(Trp79*) - stop_gained,splice_region_variant - -
TAZ 00000324 NM_181313.2 0000003498 ?/? - 2/10 c.236G>A p.(Trp79*) - stop_gained,splice_region_variant - -
TAZ 00000320 NR_024048.1 0000003498 ?/? - 2/10 n.540G>A - - splice_region_variant,non_coding_transcript_exon_variant,non_coding_transcript_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV003237290; RCV003396971;
Chromosome X:153640549..153640549
ClinVar Allele ID 2671893
Disease database name and identifier .|MONDO:MONDO:0010543, MedGen:C0574083, OMIM:302060, Orphanet:111
ClinVar preferred disease name TAFAZZIN-related condition|3-Methylglutaconic aciduria type 2
HGVS variant names NC 000023.10:g.153640549G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. TAFAZZIN:6901
Molecular consequence SO:0001587|nonsense, SO:0001619|non-coding transcript variant
Allele origin
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000818455;
Chromosome X:153640550..153640557
ClinVar Allele ID 653507
Disease database name and identifier MONDO:MONDO:0010543, MedGen:C0574083, OMIM:302060, Orphanet:111
ClinVar preferred disease name 3-Methylglutaconic aciduria type 2
HGVS variant names NC 000023.10:g.153640553 153640560del
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Gene symbol:Gene id. TAFAZZIN:6901
Molecular consequence SO:0001575|splice donor variant
Allele origin germline
dbSNP ID 1603376938
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