Variant #0000805209 (NC_000011.9:g.608695G>C, NM_020901.2:c.3236G>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.608695G>C
DNA change (hg38) -
Published as PHRF1(NM_020901.3):c.3236G>C (p.G1079A)
ISCN -
DB-ID IRF7_000025
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHRF1 NM_001286581.1 -?/. - c.3239G>C r.(?) p.(Gly1080Ala)
IRF7 NM_001572.3 -?/. - c.*3950C>G r.(=) p.(=)
PHRF1 NM_020901.2 -?/. - c.3236G>C r.(?) p.(Gly1079Ala)


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