Variant #0000544680 (NC_000011.9:g.609714G>C, NM_020901.2:c.4255G>C (PHRF1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.609714G>C
DNA change (hg38) g.609714G>C
Published as PHRF1(NM_001286581.2):c.4258G>C (p.A1420P)
ISCN -
DB-ID IRF7_000014
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) 0.00019 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 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHRF1 NM_001286581.1 -?/. - c.4258G>C r.(?) p.(Ala1420Pro)
IRF7 NM_001572.3 -?/. - c.*2931C>G r.(=) p.(=)
PHRF1 NM_020901.2 -?/. - c.4255G>C r.(?) p.(Ala1419Pro)


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