View genomic variant #0000019496

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.211438136G>A
Published as -
GERP -
Segregation -
DB-ID CPS1_000093
MSCV MSCV_0019496
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

2 entries on 1 page. Showing entries 1 - 2.
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 0000019496 ./. - - c.254+5G>A p.? - - - -
CPS1 00000658 NM_001875.4 0000019496 ./. - - c.236+5G>A p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000540344;
Chromosome 2:211438136..211438136
ClinVar Allele ID 450313
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.211438136G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA658657202
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 1553509024
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