Variant #0000925374 (NC_000011.9:g.299371C>A, NM_001025295.2:c.120G>T (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.299371C>A
DNA change (hg38) -
Published as IFITM5(NM_001025295.3):c.120G>T (p.S40=)
ISCN -
DB-ID ATHL1_000007
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) 0.00518 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.120G>T r.(?) p.(Ser40=)
ATHL1 NM_025092.4 -/. - c.*4622C>A r.(=) p.(=)


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