Variant #0000724548 (NC_000013.10:g.41382583C>T, NM_014252.3:c.632C>T (SLC25A15))

Chromosome 13
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.41382583C>T
DNA change (hg38) -
Published as SLC25A15(NM_014252.4):c.632C>T (p.P211L)
ISCN -
DB-ID SLC25A15_000035
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) 0.0003 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +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     
SLC25A15 NM_014252.3 ?/. - c.632C>T r.(?) p.(Pro211Leu)
TPTE2P5 NR_038258.1 ?/. - n.623-7723G>A r.(?) -


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