Variant #0000610367 (NC_000006.11:g.43487842C>T, NM_203290.2:c.421C>T (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.43487842C>T
DNA change (hg38) g.43520104C>T
Published as POLR1C(NM_203290.2):c.421C>T (p.(Arg141Cys)), POLR1C(NM_203290.3):c.421C>T (p.R141C)
ISCN -
DB-ID POLR1C_000019 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) 0.00063 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 2019-12-04 15:24:38 +01:00 (CET)
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.-3297G>A r.(?) p.(=)
XPO5 NM_020750.2 ?/. - c.*3764G>A r.(=) p.(=)
POLR1C NM_203290.2 ?/. - c.421C>T r.(?) p.(Arg141Cys)


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