View genomic variant #0000019490

Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.211421452_211421453insTCT
Published as -
GERP -
Segregation -
DB-ID CPS1_000088
MSCV MSCV_0019490
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.46149 View details
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 0000019490 ./. - - c.13_14insTCT p.(Ile5_Lys6insPhe) - - - -
CPS1 00000658 NM_001875.4 0000019490 ./. - - c.-6_-5insTCT p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000185816; RCV000377067; RCV000509330;
Chromosome 2:211421452..211421453
ClinVar Allele ID 199986
Disease database name and identifier MONDO:MONDO:0009376, MedGen:C4082171, OMIM:237300, Orphanet:147|MedGen:CN169374|MedGen:C3661900
ClinVar preferred disease name Congenital hyperammonemia, type I|not specified|not provided
HGVS variant names NC 000002.11:g.211421454 211421455insTTC
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type Insertion
Sequence Ontology for variant type SO:0000667
Variant clinical sources reported ClinGen:CA312388
Gene symbol:Gene id. CPS1:1373
Molecular consequence SO:0001619|non-coding transcript variant, SO:0001623|5 prime UTR variant, SO:0001821|inframe insertion
Allele origin germline
dbSNP ID 61509952
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