Variant #0000802609 (NC_000006.11:g.43487911G>A, NM_203290.2:c.490G>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.43487911G>A
DNA change (hg38) -
Published as POLR1C(NM_001363658.1):c.490G>A (p.V164M), POLR1C(NM_203290.2):c.490G>A (p.(Val164Met))
ISCN -
DB-ID POLR1C_000036 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) 0.00021 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +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.-3366C>T r.(?) p.(=)
XPO5 NM_020750.2 -?/. - c.*3695C>T r.(=) p.(=)
POLR1C NM_203290.2 -?/. - c.490G>A r.(?) p.(Val164Met)


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