View genomic variant #0000003418

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.133342161G>A
Published as -
GERP 4.790
Segregation -
DB-ID ASS1_000013
MSCV MSCV_0003418
dbSNP ID rs121908637
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 View details
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
ASS1 00000477 NM_000050.4 0000003418 +/+ - 7/16 c.470G>A p.(Arg157His) benign(0.047) missense_variant - deleterious(0)
ASS1 00000478 NM_054012.3 0000003418 +/+ - 7/16 c.470G>A p.(Arg157His) benign(0.047) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000006697; RCV000259104; RCV001376613;
Chromosome 9:133342161..133342161
Allele frequencies from ExAC 0.00010
Allele frequencies from TGP 0.00020
ClinVar Allele ID 21364
Disease database name and identifier Human Phenotype Ontology:HP:0032397, MONDO:MONDO:0015991, MedGen:C0175683, Orphanet:187|MedGen:C3661900|MONDO:MONDO:0008988, MedGen:C4721769, OMIM:215700, Orphanet:247525
ClinVar preferred disease name Citrullinuria|not provided|Citrullinemia type I
HGVS variant names NC 000009.11:g.133342161G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(4)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA253830|OMIM:603470.0005|UniProtKB:P00966#VAR 000685
Gene symbol:Gene id. ASS1:445
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121908637
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