Variant #0000541044 (NC_000010.10:g.79741937C>T, NM_007055.3:c.3734G>A (POLR3A))

Chromosome 10
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.79741937C>T
DNA change (hg38) g.77982179C>T
Published as POLR3A(NM_007055.3):c.3734G>A (p.R1245Q), POLR3A(NM_007055.4):c.3734G>A (p.(Arg1245Gln))
ISCN -
DB-ID POLR3A_000047 See all 7 reported entries
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) 0.00152 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLR3A NM_007055.3 -?/. - c.3734G>A r.(?) p.(Arg1245Gln)


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