Variant #0000864830 (NC_000016.9:g.5129764C>T, NM_019109.4:c.917C>T (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.5129764C>T
DNA change (hg38) -
Published as ALG1(NM_019109.4):c.917C>T (p.T306I)
ISCN -
DB-ID ALG1_000073
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +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.917C>T r.(?) p.(Thr306Ile)
FAM86A NM_201400.2 -?/. - c.*5869G>A r.(=) p.(=)


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