View genomic variant #0000000610

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.89876934G>A
Published as -
GERP 1.840
Segregation -
DB-ID POLG_000019 See all 2 reported entries
MSCV MSCV_0000610
dbSNP ID rs3087373
Frequency -
Sources ; clinVar; ensembl; POLG_MUT_DB;
Reference 20301791
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
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     
POLG 00000266 NM_001126131.1 0000000610 -/- - 2/23 c.52C>T p.(Pro18Ser) benign(0.003) missense_variant - tolerated(0.59)
POLG 00000267 NM_002693.2 0000000610 -/- - 2/23 c.52C>T p.(Pro18Ser) benign(0.003) missense_variant - tolerated(0.59)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV001851970;
Chromosome 15:89876934..89876934
ClinVar Allele ID 34169
Disease database name and identifier MONDO:MONDO:0008758, MedGen:C0205710, OMIM:203700, Orphanet:726
ClinVar preferred disease name Progressive sclerosing poliodystrophy
HGVS variant names NC 000015.9:g.89876934G>A
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:CA341889|UniProtKB:P54098#VAR 014904
Gene symbol:Gene id. POLG:5428|POLGARF:125316803
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 3087373
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