Variant #0000977263 (NC_000006.11:g.43488793A>G, NC_000006.11(NM_203290.2):c.922+7A>G (POLR1C))

Chromosome 6
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.43488793A>G
DNA change (hg38) -
Published as POLR1C(NM_203290.2):c.922+7A>G (p.?)
ISCN -
DB-ID POLR1C_000045
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) 1.0E-5 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.-4248T>C r.(?) p.(=)
XPO5 NM_020750.2 ?/. - c.*2813T>C r.(=) p.(=)
POLR1C NM_203290.2 ?/. - c.922+7A>G r.(=) p.(=)


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