Variant #0001015617 (NC_000017.10:g.7416512_7416532del, NM_000937.4:c.4929_4949del (POLR2A))

Chromosome 17
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.7416512_7416532del
DNA change (hg38) -
Published as POLR2A(NM_000937.4):c.4929_4949delTTCGCCAACGTCACCCAGCTA (p.(Ser1644_Tyr1650del)), POLR2A(NM_000937.5):c.4929_4949delTTCGCCAACGTCACCCAGCTA (p.S1740...)
ISCN -
DB-ID POLR2A_000040 See all 2 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 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLR2A NM_000937.4 ?/. - c.4929_4949del r.(?) p.(Ser1740_Pro1746del)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.