View genomic variant #0000019514

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.211456639C>T
Published as -
GERP -
Segregation -
DB-ID CPS1_000072
MSCV MSCV_0019514
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.59757 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 0000019514 ./. - - c.1050C>T p.(=) - - - -
CPS1 00000659 NM_001122634.2 0000019514 ./. - - c.-1949C>T p.(=) - - - -
CPS1 00000658 NM_001875.4 0000019514 ./. - - c.1032C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000116830; RCV000302372;
Chromosome 2:211456639..211456639
Allele frequencies from ESP 0.59757
Allele frequencies from ExAC 0.57363
Allele frequencies from TGP 0.59125
ClinVar Allele ID 134298
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0009376, MedGen:C4082171, OMIM:237300, Orphanet:147
ClinVar preferred disease name not specified|Congenital hyperammonemia, type I
HGVS variant names NC 000002.11:g.211456639C>T
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:CA288781
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001619|non-coding transcript variant, SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 2229589
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