Variant #0000556472 (NC_000016.9:g.104021T>G, NM_022450.3:c.*4318A>C (RHBDF1))

Chromosome 16
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.104021T>G
DNA change (hg38) g.54021T>G
Published as SNRNP25(NM_024571.3):c.32T>G (p.V11G)
ISCN -
DB-ID POLR3K_000001
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) 0 View details
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     
POLR3K NM_016310.3 ?/. - c.-435A>C r.(?) p.(=)
RHBDF1 NM_022450.3 ?/. - c.*4318A>C r.(=) p.(=)
SNRNP25 NM_024571.3 ?/. - c.32T>G r.(?) p.(Val11Gly)


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