Variant #0001054116 (NC_000011.9:g.111742173C>G, NM_024740.2:c.34G>C (ALG9))

Chromosome 11
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.111742173C>G
DNA change (hg38) -
Published as ALG9(NM_024740.2):c.34G>C (p.(Gly12Arg))
ISCN -
DB-ID ALG9_000049
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) 1.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C11orf1 NM_022761.2 ?/. - c.-8112C>G r.(?) p.(=)
ALG9 NM_024740.2 ?/. - c.34G>C r.(?) p.(Gly12Arg)
FDXACB1 NM_138378.2 ?/. - c.*3473G>C r.(=) p.(=)


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