Variant #0000925373 (NC_000011.9:g.298622G>A, NM_001025295.2:c.278C>T (IFITM5))

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.298622G>A
DNA change (hg38) -
Published as IFITM5(NM_001025295.3):c.278C>T (p.T93M)
ISCN -
DB-ID ATHL1_000006
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) 0.00086 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-04-16 21:50:28 +02:00 (CEST)
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.278C>T r.(?) p.(Thr93Met)
ATHL1 NM_025092.4 -?/. - c.*3873G>A r.(=) p.(=)


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