View genomic variant #0000019549

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.211518742G>A
Published as -
GERP -
Segregation -
DB-ID CPS1_000081
MSCV MSCV_0019549
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
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 0000019549 ./. - - c.3499-7G>A p.(=) - - - -
CPS1 00000659 NM_001122634.2 0000019549 ./. - - c.2128-7G>A p.(=) - - - -
CPS1 00000658 NM_001875.4 0000019549 ./. - - c.3481-7G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000354131; RCV000606745; RCV003221931;
Chromosome 2:211518742..211518742
Allele frequencies from TGP 0.00280
ClinVar Allele ID 284559
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0009376, MedGen:C4082171, OMIM:237300, Orphanet:147|MedGen:CN169374
ClinVar preferred disease name not provided|Congenital hyperammonemia, type I|not specified
HGVS variant names NC 000002.11:g.211518742G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA2086967
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 368909569
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001143010;
Chromosome 2:211518742..211518742
ClinVar Allele ID 887259
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.211518742G>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Likely benign(1)
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
dbSNP ID 368909569
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