View genomic variant #0000003420

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.133346264G>A
Published as -
GERP 3.340
Segregation -
DB-ID ASS1_000015
MSCV MSCV_0003420
dbSNP ID rs121908638
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
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     
ASS1 00000477 NM_000050.4 0000003420 +/+ - 8/16 c.539G>A p.(Ser180Asn) benign(0.341) missense_variant - deleterious(0)
ASS1 00000478 NM_054012.3 0000003420 +/+ - 8/16 c.539G>A p.(Ser180Asn) benign(0.341) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000006698; RCV000185782; RCV001376618;
Chromosome 9:133346264..133346264
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 21365
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.133346264G>A
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:CA253831|OMIM:603470.0006|UniProtKB:P00966#VAR 000686
Gene symbol:Gene id. ASS1:445
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121908638
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000529881; RCV001376549; RCV002254300;
Chromosome 9:133346264..133346264
ClinVar Allele ID 458935
Disease database name and identifier MedGen:C3661900|Human Phenotype Ontology:HP:0032397, MONDO:MONDO:0015991, MedGen:C0175683, Orphanet:187|MONDO:MONDO:0008988, MedGen:C4721769, OMIM:215700, Orphanet:247525
ClinVar preferred disease name not provided|Citrullinuria|Citrullinemia type I
HGVS variant names NC 000009.11:g.133346264G>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA375227223
Gene symbol:Gene id. ASS1:445
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121908638
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