View genomic variant #0000019516

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.211457596C>T
Published as -
GERP -
Segregation -
DB-ID CPS1_000074
MSCV MSCV_0019516
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00015 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 0000019516 ./. - - c.1105-7C>T p.(=) - - - -
CPS1 00000659 NM_001122634.2 0000019516 ./. - - c.-992C>T p.(=) - - - -
CPS1 00000658 NM_001875.4 0000019516 ./. - - c.1087-7C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000267073; RCV000601231;
Chromosome 2:211457596..211457596
Allele frequencies from ESP 0.00015
Allele frequencies from ExAC 0.00007
ClinVar Allele ID 287393
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.211457596C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Likely benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA2086247
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 202117044
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