Variant #0000805212 (NC_000011.9:g.613358dup, NM_020901.2:c.*1581dup (PHRF1))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.613358dup
DNA change (hg38) -
Published as IRF7(NM_004031.3):c.1128dupG (p.P377Afs*38)
ISCN -
DB-ID CDHR5_000023
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 2021-09-17 14:40:49 +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.*1581dup r.(?) p.(=)
IRF7 NM_001572.3 +/. - c.1089dup r.(?) p.(Pro364Alafs*38)
PHRF1 NM_020901.2 +/. - c.*1581dup r.(?) p.(=)
CDHR5 NM_021924.4 +/. - c.*3997dup r.(?) p.(=)


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