Variant #0000335208 (NC_000023.10:g.111003127A>T, ALG13(NM_001099922.2):c.3314A>T)

Chromosome X
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.111003127A>T
DNA change (hg38) g.111759899A>T
Published as ALG13(NM_001099922.2):c.3314A>T (p.(Tyr1105Phe)), ALG13(NM_001257231.1):c.3080A>T (p.Y1027F)
ISCN -
DB-ID ALG13_000029 See all 2 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG13 NM_001099922.2 ?/. - c.3314A>T r.(?) p.(Tyr1105Phe)