Variant #0000726621 (NC_000017.10:g.62492991C>T, NM_007215.3:c.96G>A (POLG2))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.62492991C>T
DNA change (hg38) -
Published as POLG2(NM_007215.3):c.96G>A (p.L32=)
ISCN -
DB-ID DDX5_000002
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX5 NM_004396.3 -?/. - c.*3050G>A r.(=) p.(=)
POLG2 NM_007215.3 -?/. - c.96G>A r.(?) p.(Leu32=)


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