Variant #0000558418 (NC_000016.9:g.5127504C>T, NM_019109.4:c.598C>T (ALG1))

Chromosome 16
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.5127504C>T
DNA change (hg38) g.5077503C>T
Published as ALG1(NM_019109.4):c.598C>T (p.R200*)
ISCN -
DB-ID ALG1_000054
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) 1.0E-5 View details
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 2020-07-09 12:02:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG1 NM_019109.4 ?/. - c.598C>T r.(?) p.(Arg200Ter)
FAM86A NM_201400.2 ?/. - c.*8129G>A r.(=) p.(=)


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