Variant #0000528926 (NC_000006.11:g.43484855C>T, NM_203290.2:c.8C>T (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.43484855C>T
DNA change (hg38) g.43517117C>T
Published as POLR1C(NM_203290.3):c.8C>T (p.A3V)
ISCN -
DB-ID POLR1C_000012
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) 0.00057 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YIPF3 NM_015388.3 -?/. - c.-310G>A r.(?) p.(=)
XPO5 NM_020750.2 -?/. - c.*6751G>A r.(=) p.(=)
POLR1C NM_203290.2 -?/. - c.8C>T r.(?) p.(Ala3Val)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.