View genomic variant #0000019500

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.211444452T>C
Published as -
GERP -
Segregation -
DB-ID CPS1_000097
MSCV MSCV_0019500
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00331 View details
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
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 0000019500 ./. - - c.504T>C p.(=) - - - -
CPS1 00000658 NM_001875.4 0000019500 ./. - - c.486T>C p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV002310304;
Chromosome 2:211444452..211444452
ClinVar Allele ID 1784147
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.211444452T>A
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001587|nonsense, SO:0001619|non-coding transcript variant
Allele origin unknown
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000185813; RCV000374734; RCV001531951;
Chromosome 2:211444452..211444452
Allele frequencies from ESP 0.00331
Allele frequencies from ExAC 0.00412
Allele frequencies from TGP 0.00060
ClinVar Allele ID 199988
Disease database name and identifier MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0009376, MedGen:C4082171, OMIM:237300, Orphanet:147
ClinVar preferred disease name not specified|not provided|Congenital hyperammonemia, type I
HGVS variant names NC 000002.11:g.211444452T>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA312379
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001619|non-coding transcript variant, SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 138779023
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