Variant #0000573049 (NC_000023.10:g.110987996_110987998dup, ALG13(NM_001099922.2):c.2796_2798dup)

Chromosome X
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.110987996_110987998dup
DNA change (hg38) g.111744768_111744770dup
Published as ALG13(NM_001099922.2):c.2753_2754insACC (p.(Pro945dup)), ALG13(NM_001257231.1):c.2562_2564dupACC (p.P867dup), ALG13(NM_001257231.2):c.2562_2564dupA...
ISCN -
DB-ID ALG13_000020 See all 3 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG13 NM_001099922.2 -?/. - c.2796_2798dup r.(?) p.(Pro945dup)