Variant #0000857578 (NC_000001.10:g.63902565A>T, NM_013339.3:c.1398A>T (ALG6))

Chromosome 1
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.63902565A>T
DNA change (hg38) -
Published as ALG6(NM_013339.4):c.1398A>T (p.L466=)
ISCN -
DB-ID ALG6_000032
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) 0.00035 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 2022-05-09 15:51:19 +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     
ALG6 NM_013339.3 -?/. - c.1398A>T r.(?) p.(Leu466=)
ITGB3BP NM_014288.4 -?/. - c.*4211T>A r.(=) p.(=)


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