View genomic variant #0000019562

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.211540507C>A
Published as -
GERP -
Segregation -
DB-ID CPS1_000011 See all 3 reported entries
MSCV MSCV_0002856
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.32916 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 0000019562 ./. - - c.4235C>A p.(Thr1412Asn) - - - -
CPS1 00000659 NM_001122634.2 0000019562 ./. - - c.2864C>A p.(Thr955Asn) - - - -
CPS1 00000658 NM_001875.4 0000019562 ./. - - c.4217C>A p.(Thr1406Asn) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000116832; RCV000274786; RCV003334452; RCV003334453;
Chromosome 2:211540507..211540507
Allele frequencies from ESP 0.32916
Allele frequencies from ExAC 0.30339
Allele frequencies from TGP 0.28854
ClinVar Allele ID 134300
Disease database name and identifier .|MONDO:MONDO:0014151, MedGen:C3714958, OMIM:615371|MedGen:CN169374|MONDO:MONDO:0009376, MedGen:C4082171, OMIM:237300, Orphanet:147
ClinVar preferred disease name CARBAMOYL PHOSPHATE SYNTHETASE I POLYMORPHISM|Pulmonary hypertension, neonatal, susceptibility to|not specified|Congenital hyperammonemia, type I
HGVS variant names NC 000002.11:g.211540507C>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:CA288789|OMIM:608307.0006|UniProtKB:P31327#VAR 017569
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 1047891
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