Variant #0001051393 (NC_000003.11:g.66287103_66287105del, NC_000003.11(NM_001164796.1):c.-74-6524_-74-6522del (SLC25A26))

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.66287103_66287105del
DNA change (hg38) -
Published as SLC25A26(NM_001379210.1):c.169_171del (p.(Ala57del))
ISCN -
DB-ID SLC25A26_000019
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 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     
SLC25A26 NM_001164796.1 ?/. - c.-74-6524_-74-6522del r.(=) p.(=)
LRIG1 NM_015541.2 ?/. - c.*143587_*143589del r.(=) p.(=)


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