View genomic variant #0000003489

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type del
DNA change (genomic) (Relative to hg19 / GRCh37) g.153640484del
Published as -
GERP -1.230
Segregation -
DB-ID TAZ_000154 See all 2 reported entries
MSCV MSCV_0003489
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 0000003489 +?/+? - - c.171del p.(Gly58Alafs*25) - - - -
TAZ 00000323 NM_181311.2 0000003489 +?/+? - - c.171del p.(Gly58Alafs*25) - - - -
TAZ 00000322 NM_181312.2 0000003489 +?/+? - - c.171del p.(Gly58Alafs*25) - - - -
TAZ 00000324 NM_181313.2 0000003489 +?/+? - - c.171del p.(Gly58Alafs*25) - - - -
TAZ 00000320 NR_024048.1 0000003489 +?/+? - - n.475del - - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV003237283;
Chromosome X:153640484..153640484
ClinVar Allele ID 2671886
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.153640484del
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:0001589|frameshift variant, SO:0001619|non-coding transcript variant
Allele origin maternal
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