View genomic variant #0000017206

Chromosome 13
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.41367296A>T
Published as -
GERP -
Segregation -
DB-ID SLC25A15_000073
MSCV MSCV_0017206
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00657 View details
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

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Variant ID     

Affects function     

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DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SLC25A15 00001152 NM_014252.3 0000017206 ./. - - c.-67A>T p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000400406; RCV001718637;
Chromosome 13:41367296..41367296
Allele frequencies from ESP 0.00657
Allele frequencies from TGP 0.00300
ClinVar Allele ID 328357
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0009393, MedGen:C0268540, OMIM:238970, Orphanet:415
ClinVar preferred disease name not provided|Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
HGVS variant names NC 000013.10:g.41367296A>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10639581
Gene symbol:Gene id. SLC25A15:10166
Molecular consequence SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 112276566
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