Variant #0001031621 (NC_000001.10:g.207075354G>A, NM_005449.4:c.*3010C>T (FAIM3))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.207075354G>A
DNA change (hg38) -
Published as IL24(NM_001185158.1):c.119G>A (p.(Arg40Lys))
ISCN -
DB-ID FAIM3_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAIM3 NM_005449.4 ?/. - c.*3010C>T r.(=) p.(=)
IL24 NM_006850.3 ?/. - c.474G>A r.(?) p.(Glu158=)


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