View genomic variant #0000017198

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.41363549G>C
Published as -
GERP -
Segregation -
DB-ID SLC25A15_000065
MSCV MSCV_0017198
dbSNP ID -
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

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 0000017198 ./. - - c.-320G>C p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000296364;
Chromosome 13:41363549..41363549
ClinVar Allele ID 334805
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.41363549G>C
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10643496
Gene symbol:Gene id. SLC25A15:10166|LOC130009616:130009616
Allele origin germline
dbSNP ID 12372842
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