Variant #0000342096 (NC_000013.10:g.41381512C>T, NM_014252.3:c.535C>T (SLC25A15))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.41381512C>T
DNA change (hg38) g.40807376C>T
Published as -
ISCN -
DB-ID SLC25A15_000009 See all 7 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) 6.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-03 16:50:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A15 NM_014252.3 +/. - c.535C>T r.(?) p.(Arg179Ter)
TPTE2P5 NR_038258.1 +/. - n.623-6652G>A r.(?) -


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