Variant #0000720521 (NC_000005.9:g.89783821C>T, NM_006467.2:c.122C>T (POLR3G))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.89783821C>T
DNA change (hg38) -
Published as POLR3G(NM_006467.3):c.122C>T (p.T41I)
ISCN -
DB-ID MBLAC2_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) 5.0E-5 View details
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     
POLR3G NM_006467.2 ?/. - c.122C>T r.(?) p.(Thr41Ile)
MBLAC2 NM_203406.1 ?/. - c.-13712G>A r.(?) p.(=)


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