Variant #0000692088 (NC_000016.9:g.5131021C>A, NM_019109.4:c.1036C>A (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.5131021C>A
DNA change (hg38) -
Published as ALG1(NM_019109.4):c.1036C>A (p.P346T)
ISCN -
DB-ID ALG1_000068
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) 3.0E-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 2020-09-15 15:50:26 +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.1036C>A r.(?) p.(Pro346Thr)
FAM86A NM_201400.2 ?/. - c.*4612G>T r.(=) p.(=)


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