Variant #0000308306 (NC_000013.10:g.41382628C>T, NM_014252.3:c.677C>T (SLC25A15))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.41382628C>T
DNA change (hg38) g.40808492C>T
Published as SLC25A15(NM_014252.3):c.677C>T (p.A226V)
ISCN -
DB-ID SLC25A15_000027
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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.677C>T r.(?) p.(Ala226Val)
TPTE2P5 NR_038258.1 -?/. - n.623-7768G>A r.(?) -


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