Variant #0000807440 (NC_000016.9:g.5132576T>G, NM_019109.4:c.1089T>G (ALG1))

Chromosome 16
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.5132576T>G
DNA change (hg38) -
Published as ALG1(NM_019109.4):c.1089T>G (p.G363=)
ISCN -
DB-ID ALG1_000070
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) 0.0001 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +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     
ALG1 NM_019109.4 -?/. - c.1089T>G r.(?) p.(Gly363=)
FAM86A NM_201400.2 -?/. - c.*3057A>C r.(=) p.(=)


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