Variant #0000691100 (NC_000011.9:g.615254dup, NM_020901.2:c.*3477dup (PHRF1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.615254dup
DNA change (hg38) -
Published as IRF7(NM_004031.3):c.68dupC (p.R24Tfs*18)
ISCN -
DB-ID CDHR5_000018
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHRF1 NM_001286581.1 +?/. - c.*3477dup r.(?) p.(=)
IRF7 NM_001572.3 +?/. - c.29dup r.(?) p.(Arg11ThrfsTer18)
PHRF1 NM_020901.2 +?/. - c.*3477dup r.(?) p.(=)
CDHR5 NM_021924.4 +?/. - c.*2100dup r.(?) p.(=)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.