Variant #0000550132 (NC_000013.10:g.28197244C>T, NM_015972.3:c.259C>T (POLR1D))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.28197244C>T
DNA change (hg38) g.27623107C>T
Published as POLR1D(NM_015972.4):c.259C>T (p.R87*)
ISCN -
DB-ID POLR1D_000026 See all 5 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-12-13 12:08:34 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLR1D NM_015972.3 +/. - c.259C>T r.(?) p.(Arg87Ter)
LNX2 NM_153371.3 +/. - c.-2833G>A r.(?) p.(=)


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