View genomic variant #0000019545

Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.211507400del
Published as -
GERP -
Segregation -
DB-ID CPS1_000036
MSCV MSCV_0019545
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00655 View details
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     
CPS1 00000657 NM_001122633.2 0000019545 ./. - - c.3159+11del p.(=) - - - -
CPS1 00000659 NM_001122634.2 0000019545 ./. - - c.1788+11del p.(=) - - - -
CPS1 00000658 NM_001875.4 0000019545 ./. - - c.3141+11del p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV002576867;
Chromosome 2:211507399..211507399
ClinVar Allele ID 1960682
Disease database name and identifier MONDO:MONDO:0009376, MedGen:C4082171, OMIM:237300, Orphanet:147
ClinVar preferred disease name Congenital hyperammonemia, type I
HGVS variant names NC 000002.11:g.211507399G>C
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001627|intron variant
Allele origin germline
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000339021; RCV000513937;
Chromosome 2:211507400..211507400
ClinVar Allele ID 284558
Disease database name and identifier MONDO:MONDO:0009376, MedGen:C4082171, OMIM:237300, Orphanet:147|MedGen:C3661900
ClinVar preferred disease name Congenital hyperammonemia, type I|not provided
HGVS variant names NC 000002.11:g.211507404del
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Benign(2)|Likely benign(3)
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA2086838
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 577707531
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