View genomic variant #0000000506

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.41367406C>A
Published as -
GERP 5.190
Segregation -
DB-ID SLC25A15_000020 See all 2 reported entries
MSCV MSCV_0000506
dbSNP ID rs202247806
Frequency -
Sources ; clinVar; Ensembl;
Reference 22649802
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     
SLC25A15 00001152 NM_014252.3 0000000506 +/+ - 2/7 c.44C>A p.(Ala15Glu) possibly_damaging(0.588) missense_variant - deleterious(0)
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ClinVar @ MSeqDR

RCVaccession RCV001250167;
Chromosome 13:41367406..41367406
ClinVar Allele ID 961871
Disease database name and identifier MONDO:MONDO:0009393, MedGen:C0268540, OMIM:238970, Orphanet:415
ClinVar preferred disease name Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
HGVS variant names NC 000013.10:g.41367406C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SLC25A15:10166
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 202247806
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