Variant #0001034160 (NC_000003.11:g.66428118T>C, NM_001164796.1:c.448T>C (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.66428118T>C
DNA change (hg38) -
Published as SLC25A26(NM_001379210.1):c.712T>C (p.(Phe238Leu))
ISCN -
DB-ID SLC25A26_000018
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 2025-05-05 21:14:00 +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     
SLC25A26 NM_001164796.1 ?/. - c.448T>C r.(?) p.(Phe150Leu)
LRIG1 NM_015541.2 ?/. - c.*2569A>G r.(=) p.(=)


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