Variant #0000621959 (NC_000007.13:g.95818685_95818688del, NM_014251.2:c.852_855del (SLC25A13))

Chromosome 7
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.95818685_95818688del
DNA change (hg38) g.96189373_96189376del
Published as SLC25A13(NM_001160210.2):c.852_855delTATG (p.M285Pfs*2)
ISCN -
DB-ID SLC25A13_000007 See all 60 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A13 NM_014251.2 +/. - c.852_855del r.(?) p.(Met285ProfsTer2)


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