View genomic variant #0000002849

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.211469907G>T
Published as -
GERP 3.640
Segregation -
DB-ID CPS1_000008
MSCV MSCV_0002849
dbSNP ID rs142693704
Frequency -
Sources ;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00062 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 0000002849 ?/? - 18/39 c.1936G>T p.? benign(0.007) missense_variant - tolerated(0.14)
CPS1 00000659 NM_001122634.2 0000002849 ?/? - 7/28 c.565G>T p.(Ala189Ser) benign(0.012) missense_variant - tolerated(0.17)
CPS1 00000658 NM_001875.4 0000002849 ?/? - 17/38 c.1918G>T p.(Ala640Ser) benign(0.012) missense_variant - tolerated(0.14)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV001142901; RCV001806029;
Chromosome 2:211469907..211469907
Allele frequencies from ESP 0.00062
Allele frequencies from ExAC 0.00047
Allele frequencies from TGP 0.00020
ClinVar Allele ID 883645
Disease database name and identifier MONDO:MONDO:0009376, MedGen:C4082171, OMIM:237300, Orphanet:147|MedGen:CN169374
ClinVar preferred disease name Congenital hyperammonemia, type I|not specified
HGVS variant names NC 000002.11:g.211469907G>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Likely benign(1)
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 142693704
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