Variant #0000543742 (NC_000011.9:g.299372G>A, NM_001025295.2:c.119C>T (IFITM5))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.299372G>A
DNA change (hg38) g.299372G>A
Published as IFITM5(NM_001025295.3):c.119C>T (p.S40L)
ISCN -
DB-ID IFITM5_000002 See all 11 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFITM5 NM_001025295.2 +/. - c.119C>T r.(?) p.(Ser40Leu)
ATHL1 NM_025092.4 +/. - c.*4623G>A r.(=) p.(=)


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