Variant #0000616033 (NC_000016.9:g.5121858C>A, NM_019109.4:c.8C>A (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.5121858C>A
DNA change (hg38) g.5071857C>A
Published as ALG1(NM_019109.4):c.8C>A (p.(Ala3Asp))
ISCN -
DB-ID ALG1_000060
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) 0.00097 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG1 NM_019109.4 -?/. - c.8C>A r.(?) p.(Ala3Asp)
FAM86A NM_201400.2 -?/. - c.*13775G>T r.(=) p.(=)


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