Variant #0001002414 (NC_000016.9:g.5129080C>G, NM_019109.4:c.878C>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.5129080C>G
DNA change (hg38) -
Published as ALG1(NM_019109.4):c.878C>G (p.(Ser293Cys))
ISCN -
DB-ID ALG1_000086
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 2024-08-28 13:16:32 +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.878C>G r.(?) p.(Ser293Cys)
FAM86A NM_201400.2 -?/. - c.*6553G>C r.(=) p.(=)


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