Variant #0000975692 (NC_000003.11:g.183963313del, NM_005787.5:c.387del (ALG3))

Chromosome 3
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.183963313del
DNA change (hg38) -
Published as ALG3(NM_001006941.2):c.243delT (p.V82Cfs*12), ALG3(NM_005787.6):c.387del (p.(Val130CysfsTer12))
ISCN -
DB-ID ALG3_000017 See all 2 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
ALG3 NM_005787.5 ?/. - c.387del r.(?) p.(Val130CysfsTer12)
ECE2 NM_014693.3 ?/. - c.-4170del r.(?) p.(=)
CAMK2N2 NM_033259.2 ?/. - c.*14632del r.(?) p.(=)
VWA5B2 NM_138345.1 ?/. - c.*3487del r.(?) p.(=)


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