View genomic variant #0000000991

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.17493951T>C
Published as -
GERP 5.260
Segregation -
DB-ID QDPR_000005
MSCV MSCV_0000991
dbSNP ID rs104893866
Frequency -
Sources ;
Reference 9744478
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
QDPR 00002711 NM_000320.2 0000000991 ?/? - 5/7 c.449A>G p.(Tyr150Cys) probably_damaging(0.998) missense_variant - deleterious(0)
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ClinVar @ MSeqDR

RCVaccession RCV000000523; RCV001558625;
Chromosome 4:17493951..17493951
ClinVar Allele ID 15533
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0009862, MedGen:C0268465, OMIM:261630, Orphanet:226, Orphanet:238583
ClinVar preferred disease name not provided|Dihydropteridine reductase deficiency
HGVS variant names NC 000004.11:g.17493951T>C
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA114327|OMIM:612676.0006|UniProtKB:P09417#VAR 006966
Gene symbol:Gene id. QDPR:5860
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 104893866
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