View genomic variant #0000005307

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.153640551G>A
Published as -
GERP -
Segregation -
DB-ID TAZ_000104 See all 3 reported entries
MSCV MSCV_0005307
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 0000005307 ./. - - c.238G>A p.(Gly80Arg) - - - -
TAZ 00000323 NM_181311.2 0000005307 ./. - - c.238G>A p.(Gly80Arg) - - - -
TAZ 00000322 NM_181312.2 0000005307 ./. - - c.238G>A p.(Gly80Arg) - - - -
TAZ 00000324 NM_181313.2 0000005307 ./. - - c.238G>A p.(Gly80Arg) - - - -
TAZ 00000320 NR_024048.1 0000005307 ./. - - n.542G>A - - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000637296;
Chromosome X:153640551..153640551
ClinVar Allele ID 534659
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.153640551G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA415180284
Gene symbol:Gene id. TAFAZZIN:6901
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin
dbSNP ID 1557191170
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000995886;
Chromosome X:153640551..153640551
ClinVar Allele ID 798809
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.153640551G>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. TAFAZZIN:6901
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin
dbSNP ID 1557191170
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