View genomic variant #0000003428

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.133374932G>A
Published as -
GERP 3.560
Segregation -
DB-ID ASS1_000002
MSCV MSCV_0003428
dbSNP ID rs121908641
Frequency -
Sources ; clinvar;
Reference 23757202;19006241
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00023 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 0000003428 +/+ - 15/16 c.1168G>A p.(Gly390Arg) probably_damaging(0.938) missense_variant - deleterious(0.03)
ASS1 00000478 NM_054012.3 0000003428 +/+ - 15/16 c.1168G>A p.(Gly390Arg) probably_damaging(0.938) missense_variant - deleterious(0.03)
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ClinVar @ MSeqDR

RCVaccession RCV000006701; RCV000185789; RCV001376575; RCV002512846;
Chromosome 9:133374932..133374932
ClinVar Allele ID 21368
Disease database name and identifier Human Phenotype Ontology:HP:0032397, MONDO:MONDO:0015991, MedGen:C0175683, Orphanet:187|MeSH:D030342, MedGen:C0950123|MedGen:C3661900|MONDO:MONDO:0008988, MedGen:C4721769, OMIM:215700, Orphanet:247525
ClinVar preferred disease name Citrullinuria|Inborn genetic diseases|not provided|Citrullinemia type I
HGVS variant names NC 000009.11:g.133374932G>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:CA253834|OMIM:603470.0009|UniProtKB:P00966#VAR 000694
Gene symbol:Gene id. ASS1:445
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 121908641
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