View genomic variant #0000019560

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.211539650G>A
Published as -
GERP -
Segregation -
DB-ID CPS1_000046
MSCV MSCV_0019560
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.01238 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 0000019560 ./. - - c.4144G>A p.(Gly1382Ser) - - - -
CPS1 00000659 NM_001122634.2 0000019560 ./. - - c.2773G>A p.(Gly925Ser) - - - -
CPS1 00000658 NM_001875.4 0000019560 ./. - - c.4126G>A p.(Gly1376Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000253072; RCV000560165;
Chromosome 2:211539650..211539650
Allele frequencies from ESP 0.01238
Allele frequencies from ExAC 0.01178
Allele frequencies from TGP 0.00859
ClinVar Allele ID 250541
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.211539650G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Benign(3)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA2087194|UniProtKB:P31327#VAR 017568
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 140578009
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