Variant #0001014898 (NC_000012.11:g.106821117T>C, NM_018082.5:c.1244T>C (POLR3B))

Chromosome 12
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.106821117T>C
DNA change (hg38) -
Published as POLR3B(NM_018082.5):c.1244T>C (p.M415T), POLR3B(NM_018082.6):c.1244T>C (p.(Met415Thr), p.M415T)
ISCN -
DB-ID POLR3B_000032 See all 8 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) 0.00056 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +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     
POLR3B NM_018082.5 ?/. - c.1244T>C r.(?) p.(Met415Thr)


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