View genomic variant #0000019510

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.211456617A>G
Published as -
GERP -
Segregation -
DB-ID CPS1_000001 See all 2 reported entries
MSCV MSCV_0000857
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 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 0000019510 ./. - - c.1028A>G p.(His343Arg) - - - -
CPS1 00000659 NM_001122634.2 0000019510 ./. - - c.-1971A>G p.(=) - - - -
CPS1 00000658 NM_001875.4 0000019510 ./. - - c.1010A>G p.(His337Arg) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000002522;
Chromosome 2:211456617..211456617
ClinVar Allele ID 17460
Disease database name and identifier MONDO:MONDO:0009376, MedGen:C4082171, OMIM:237300, Orphanet:147
ClinVar preferred disease name Congenital hyperammonemia, type I
HGVS variant names NC 000002.11:g.211456617A>G
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA115530|OMIM:608307.0004|UniProtKB:P31327#VAR 014077
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 28940283
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