View genomic variant #0000019511

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.211456628T>G
Published as -
GERP -
Segregation -
DB-ID CPS1_000069
MSCV MSCV_0019511
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00069 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 0000019511 ./. - - c.1039T>G p.(Leu347Val) - - - -
CPS1 00000659 NM_001122634.2 0000019511 ./. - - c.-1960T>G p.(=) - - - -
CPS1 00000658 NM_001875.4 0000019511 ./. - - c.1021T>G p.(Leu341Val) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000309973; RCV000731747; RCV002487483; RCV002521381;
Chromosome 2:211456628..211456628
Allele frequencies from ESP 0.00069
Allele frequencies from ExAC 0.00037
ClinVar Allele ID 284542
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0009376, MedGen:C4082171, OMIM:237300, Orphanet:147|MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0014151, MedGen:C3714958, OMIM:615371
ClinVar preferred disease name not provided|Congenital hyperammonemia, type I|Inborn genetic diseases|Pulmonary hypertension, neonatal, susceptibility to
HGVS variant names NC 000002.11:g.211456628T>G
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(5)|Benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA2086220
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 138424013
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