Variant #0000543741 (NC_000011.9:g.299286C>T, NC_000011.9(NM_001025295.2):c.186+19G>A (IFITM5))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.299286C>T
DNA change (hg38) g.299286C>T
Published as IFITM5(NM_001025295.3):c.186+19G>A
ISCN -
DB-ID IFITM5_000005
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) 0.01166 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFITM5 NM_001025295.2 -/. - c.186+19G>A r.(=) p.(=)
ATHL1 NM_025092.4 -/. - c.*4537C>T r.(=) p.(=)


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