Variant #0000509165 (NC_000002.11:g.128615665C>A, NM_004805.3:c.10G>T (POLR2D))

Chromosome 2
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.128615665C>A
DNA change (hg38) g.127858091C>A
Published as POLR2D(NM_004805.4):c.10G>T (p.G4C)
ISCN -
DB-ID POLR2D_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
POLR2D NM_004805.3 ?/. - c.10G>T r.(?) p.(Gly4Cys)
AMMECR1L NM_031445.2 ?/. - c.*7003G>T r.(=) p.(=)


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