Variant #0000975528 (NC_000003.11:g.125650591C>T, NM_001015050.2:c.165G>A (ALG1L))

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.125650591C>T
DNA change (hg38) -
Published as ALG1L(NM_001385064.1):c.228G>A (p.(Ser76=))
ISCN -
DB-ID ALG1L_000003
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 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 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     
ROPN1B NM_001012337.1 ?/. - c.-37665C>T r.(?) p.(=)
ALG1L NM_001015050.2 ?/. - c.165G>A r.(?) p.(=)


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