Variant #0000251121 (NC_000006.11:g.43488144A>G, NM_203290.2:c.634A>G (POLR1C))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.43488144A>G
DNA change (hg38) g.43520406A>G
Published as POLR1C(NM_203290.2):c.634A>G (p.(Met212Val)), POLR1C(NM_203290.4):c.634A>G (p.M212V)
ISCN -
DB-ID POLR1C_000005 See all 3 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) 0.00865 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.-3599T>C r.(?) p.(=)
XPO5 NM_020750.2 -/. - c.*3462T>C r.(=) p.(=)
POLR1C NM_203290.2 -/. - c.634A>G r.(?) p.(Met212Val)


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