Variant #0000520599 (NC_000003.11:g.66463388C>T, NM_001164796.1:c.*35157C>T (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.66463388C>T
DNA change (hg38) g.66412964C>T
Published as LRIG1(NM_015541.2):c.698G>A (p.(Gly233Glu))
ISCN -
DB-ID SLC25A26_000012
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) 0.00027 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A26 NM_001164796.1 ?/. - c.*35157C>T r.(=) p.(=)
LRIG1 NM_015541.2 ?/. - c.698G>A r.(?) p.(Gly233Glu)


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