Variant #0000924516 (NC_000006.11:g.43484912G>A, NM_203290.2:c.65G>A (POLR1C))

Chromosome 6
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.43484912G>A
DNA change (hg38) -
Published as POLR1C(NM_001318876.1):c.65G>A (p.(Arg22His)), POLR1C(NM_203290.3):c.65G>A (p.R22H)
ISCN -
DB-ID POLR1C_000013 See all 2 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) 0.00016 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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YIPF3 NM_015388.3 -?/. - c.-367C>T r.(?) p.(=)
XPO5 NM_020750.2 -?/. - c.*6694C>T r.(=) p.(=)
POLR1C NM_203290.2 -?/. - c.65G>A r.(?) p.(Arg22His)


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