View genomic variant #0000002541

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.89876559C>A
Published as -
GERP 4.150
Segregation -
DB-ID POLG_000048
MSCV MSCV_0002541
dbSNP ID -
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 0000002541 +?/+? - 2/23 c.427G>T p.(Ala143Ser) probably_damaging(0.999) missense_variant - deleterious(0.02)
POLG 00000267 NM_002693.2 0000002541 +?/+? - 2/23 c.427G>T p.(Ala143Ser) probably_damaging(0.999) missense_variant - deleterious(0.02)
Legend  


MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None