Variant #0000979682 (NC_000011.9:g.615103G>A, NM_020901.2:c.*3326G>A (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.615103G>A
DNA change (hg38) -
Published as IRF7(NM_001572.5):c.177C>T (p.(Ile59=))
ISCN -
DB-ID CDHR5_000028
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) 0.04093 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.*3326G>A r.(=) p.(=)
IRF7 NM_001572.3 -?/. - c.177C>T r.(?) p.(=)
PHRF1 NM_020901.2 -?/. - c.*3326G>A r.(=) p.(=)
CDHR5 NM_021924.4 -?/. - c.*2248C>T r.(=) p.(=)


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