View genomic variant #0000002542

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.89876578G>C
Published as -
GERP 3.100
Segregation -
DB-ID POLG_000049 See all 2 reported entries
MSCV MSCV_0002542
dbSNP ID rs115109291
Frequency -
Sources ; POLG_MUT_DB;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00047 View details
Owner LOVD




Variant on transcripts

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

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
POLG 00000266 NM_001126131.1 0000002542 +?/+? - 2/23 c.408C>G p.(Asp136Glu) benign(0.063) missense_variant - tolerated(1)
POLG 00000267 NM_002693.2 0000002542 +?/+? - 2/23 c.408C>G p.(Asp136Glu) benign(0.063) missense_variant - tolerated(1)
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ClinVar @ MSeqDR

RCVaccession RCV000514076; RCV000758561; RCV002321762;
Chromosome 15:89876578..89876578
Allele frequencies from ESP 0.00047
Allele frequencies from ExAC 0.00052
Allele frequencies from TGP 0.00120
ClinVar Allele ID 203047
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0008758, MedGen:C0205710, OMIM:203700, Orphanet:726|MedGen:C3661900
ClinVar preferred disease name Inborn genetic diseases|Progressive sclerosing poliodystrophy|not provided
HGVS variant names NC 000015.9:g.89876578G>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(5)|Likely benign(3)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA316796
Gene symbol:Gene id. POLG:5428|POLGARF:125316803
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 115109291
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