Variant #0000528930 (NC_000006.11:g.43488006C>T, NC_000006.11(NM_203290.2):c.503-7C>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.43488006C>T
DNA change (hg38) g.43520268C>T
Published as POLR1C(NM_203290.2):c.503-7C>T (p.(=))
ISCN -
DB-ID POLR1C_000016
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) 0.0002 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YIPF3 NM_015388.3 -?/. - c.-3461G>A r.(?) p.(=)
XPO5 NM_020750.2 -?/. - c.*3600G>A r.(=) p.(=)
POLR1C NM_203290.2 -?/. - c.503-7C>T r.(=) p.(=)


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