View genomic variant #0000000858

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.211465360C>T
Published as -
GERP 5.090
Segregation -
DB-ID CPS1_000002 See all 2 reported entries
MSCV MSCV_0000858
dbSNP ID rs121912592
Frequency -
Sources ; clinVar; Ensembl;
Reference 9711878
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 0000000858 +/+ - 16/39 c.1649C>T p.? possibly_damaging(0.755) missense_variant - deleterious(0)
CPS1 00000659 NM_001122634.2 0000000858 +/+ - 5/28 c.278C>T p.(Thr93Met) possibly_damaging(0.573) missense_variant - deleterious(0)
CPS1 00000658 NM_001875.4 0000000858 +/+ - 15/38 c.1631C>T p.(Thr544Met) possibly_damaging(0.573) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000002520; RCV003466784;
Chromosome 2:211465360..211465360
ClinVar Allele ID 17458
Disease database name and identifier MONDO:MONDO:0014151, MedGen:C3714958, OMIM:615371|MONDO:MONDO:0009376, MedGen:C4082171, OMIM:237300, Orphanet:147
ClinVar preferred disease name Pulmonary hypertension, neonatal, susceptibility to|Congenital hyperammonemia, type I
HGVS variant names NC 000002.11:g.211465360C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA115525|OMIM:608307.0002|UniProtKB:P31327#VAR 006835
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 121912592
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