View genomic variant #0000003505

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type ins
DNA change (genomic) (Relative to hg19 / GRCh37) g.153641544_153641545insC
Published as -
GERP -
Segregation -
DB-ID TAZ_000039 See all 2 reported entries
MSCV MSCV_0003505
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 0000003505 +?/+? - 3/10 c.239_240insC p.(Ile81Aspfs*53) - frameshift_variant,splice_region_variant - -
TAZ 00000323 NM_181311.2 0000003505 +?/+? - 3/10 c.239_240insC p.(Ile81Aspfs*92) - frameshift_variant,splice_region_variant - -
TAZ 00000322 NM_181312.2 0000003505 +?/+? - 3/10 c.239_240insC p.(Ile81Aspfs*53) - frameshift_variant,splice_region_variant - -
TAZ 00000324 NM_181313.2 0000003505 +?/+? - 3/10 c.239_240insC p.(Ile81Aspfs*78) - frameshift_variant,splice_region_variant - -
TAZ 00000320 NR_024048.1 0000003505 +?/+? - 3/10 n.543_544insC - - splice_region_variant,non_coding_transcript_exon_variant,non_coding_transcript_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000011849;
Chromosome X:153641543..153641543
ClinVar Allele ID 26139
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.153641543G>A
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported OMIM:300394.0001
Gene symbol:Gene id. TAFAZZIN:6901
Molecular consequence SO:0001574|splice acceptor variant
Allele origin germline
dbSNP ID 1603377590
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000011851;
Chromosome X:153641543..153641543
ClinVar Allele ID 26141
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.153641543G>C
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported OMIM:300394.0003
Gene symbol:Gene id. TAFAZZIN:6901
Molecular consequence SO:0001574|splice acceptor variant
Allele origin germline
dbSNP ID 1603377590
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