Variant #0000289729 (NC_000011.9:g.614243C>T, NM_020901.2:c.*2466C>T (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.614243C>T
DNA change (hg38) g.614243C>T
Published as IRF7(NM_004031.3):c.649G>A (p.D217N), IRF7(NM_004031.4):c.649G>A (p.D217N)
ISCN -
DB-ID IRF7_000001 See all 2 reported entries
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) 0.00246 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 2018-01-15 20:58:59 +01:00 (CET)
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.*2466C>T r.(=) p.(=)
IRF7 NM_001572.3 -?/. - c.610G>A r.(?) p.(Asp204Asn)
PHRF1 NM_020901.2 -?/. - c.*2466C>T r.(=) p.(=)
CDHR5 NM_021924.4 -?/. - c.*3108G>A r.(=) p.(=)


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