Variant #0000001399 (NC_000002.12:g.233260305C>T, NC_000002.12(NM_030803.6):c.210-2825C>T (ATG16L1))

Individual ID 00000283
Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.233260305C>T
Published as -
Reference Boon Pin Kee et al. (2020), dbSNP
DB-ID ATG16L1_000003 See all 5 reported entries
dbSNP ID rs6758317
Frequency 7/20
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2020-12-22 11:18:16 +08:00 (CST)
Date last edited 2021-08-29 17:26:59 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
ATG16L1 NM_030803.6 +/. - c.210-2825C>T - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000298 DNA TaqMan ATG16L1 6 Nuur Athirah Binti Mohd Daud