View genomic variant #0000019565

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.211541721A>G
Published as -
GERP -
Segregation -
DB-ID CPS1_000049
MSCV MSCV_0019565
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.03737 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 0000019565 ./. - - c.4293-10A>G p.(=) - - - -
CPS1 00000659 NM_001122634.2 0000019565 ./. - - c.2922-10A>G p.(=) - - - -
CPS1 00000658 NM_001875.4 0000019565 ./. - - c.4275-10A>G p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000185815; RCV000276425;
Chromosome 2:211541721..211541721
Allele frequencies from ESP 0.03737
Allele frequencies from TGP 0.01937
ClinVar Allele ID 199993
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.211541721A>G
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:CA312387
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 41272673
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