View genomic variant #0000025819

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.211459268G>C
Published as -
GERP -
Segregation -
DB-ID CPS1_000132
MSCV -
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 Lishuang Shen




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 0000025819 ./. - - c.1219G>C p.(Gly407Arg) - - - -
CPS1 00000659 NM_001122634.2 0000025819 ./. - - c.-153G>C p.(=) - - - -
CPS1 00000658 NM_001875.4 0000025819 ./. - - c.1201G>C p.(Gly401Arg) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000673871; RCV001267424; RCV003465530; RCV003317334;
Chromosome 2:211459268..211459268
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 541828
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0009376, MedGen:C4082171, OMIM:237300, Orphanet:147|MONDO:MONDO:0014151, MedGen:C3714958, OMIM:615371|MedGen:CN169374
ClinVar preferred disease name Inborn genetic diseases|Congenital hyperammonemia, type I|Pulmonary hypertension, neonatal, susceptibility to|not specified
HGVS variant names NC 000002.11:g.211459268G>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Uncertain significance(4)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 760895692
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