Variant #0001053746 (NC_000011.9:g.299391G>A, NM_001025295.2:c.100C>T (IFITM5))

Chromosome 11
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.299391G>A
DNA change (hg38) -
Published as IFITM5(NM_001025295.3):c.100C>T (p.(Arg34*))
ISCN -
DB-ID ATHL1_000016
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) 4.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFITM5 NM_001025295.2 ?/. - c.100C>T r.(?) p.(Arg34*)
ATHL1 NM_025092.4 ?/. - c.*4642G>A r.(=) p.(=)


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