Variant #0001039630 (NC_000013.10:g.28195935G>A, NM_015972.3:c.-186G>A (POLR1D))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.28195935G>A
DNA change (hg38) -
Published as POLR1D(NM_001374407.1):c.-186G>A
ISCN -
DB-ID LNX2_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLR1D NM_015972.3 ?/. - c.-186G>A r.(?) p.(=)
LNX2 NM_153371.3 ?/. - c.-1524C>T r.(?) p.(=)


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