Variant #0000860569 (NC_000007.13:g.102212959G>T, NM_001097615.2:c.10C>A (POLR2J3))

Chromosome 7
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.102212959G>T
DNA change (hg38) -
Published as POLR2J3(NM_001097615.2):c.10C>A (p.P4T)
ISCN -
DB-ID POLR2J3_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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPDYE2 NM_001031618.3 ?/. - c.*10502G>T r.(=) p.(=)
POLR2J3 NM_001097615.2 ?/. - c.10C>A r.(?) p.(Pro4Thr)


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