View genomic variant #0000019317

Chromosome 2
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.172650245T>G
Published as -
GERP -
Segregation -
DB-ID SLC25A12_000027
MSCV MSCV_0019317
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00584 View details
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SLC25A12 00001148 NM_003705.4 0000019317 ./. - - c.1338A>C p.(=) - - - -
SLC25A12 00001147 NR_047549.1 0000019317 ./. - - n.1314A>C p.(Arg438Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV002201626;
Chromosome 2:172650245..172650245
ClinVar Allele ID 1616581
Disease database name and identifier MedGen:C3661900
ClinVar preferred disease name not provided
HGVS variant names NC 000002.11:g.172650245T>C
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SLC25A12:8604
Molecular consequence SO:0001619|non-coding transcript variant, SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 149278617
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000676743;
Chromosome 2:172650245..172650245
Allele frequencies from ESP 0.00584
Allele frequencies from ExAC 0.00204
Allele frequencies from TGP 0.00639
ClinVar Allele ID 282888
Disease database name and identifier MedGen:C3661900
ClinVar preferred disease name not provided
HGVS variant names NC 000002.11:g.172650245T>G
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1966134
Gene symbol:Gene id. SLC25A12:8604
Molecular consequence SO:0001619|non-coding transcript variant, SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 149278617
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