Variant #0000999460 (NC_000011.9:g.72537832C>T, NM_033388.1:c.1330C>T (ATG16L2))

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.72537832C>T
DNA change (hg38) -
Published as ATG16L2(NM_033388.1):c.1330C>T (p.(Arg444Trp))
ISCN -
DB-ID ATG16L2_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
FCHSD2 NM_014824.2 ?/. - c.*12004G>A r.(=) p.(=)
ATG16L2 NM_033388.1 ?/. - c.1330C>T r.(?) p.(Arg444Trp)


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