View genomic variant #0000002550

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.89876841G>C
Published as -
GERP 0.355
Segregation -
DB-ID POLG_000154
MSCV MSCV_0002550
dbSNP ID rs200132079
Frequency -
Sources ; POLG_MUT_DB;
Reference -
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 0000002550 +?/+? - 2/23 c.145C>G p.(Gln49Glu) benign(0) missense_variant - tolerated(1)
POLG 00000267 NM_002693.2 0000002550 +?/+? - 2/23 c.145C>G p.(Gln49Glu) benign(0) missense_variant - tolerated(1)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV001523583;
Chromosome 15:89876841..89876841
Allele frequencies from ExAC 0.00056
ClinVar Allele ID 1157566
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.89876841G>C
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. POLG:5428|POLGARF:125316803
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 200132079
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