Variant #0000863389 (NC_000013.10:g.41382672T>C, NM_014252.3:c.721T>C (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.41382672T>C
DNA change (hg38) -
Published as SLC25A15(NM_014252.3):c.721T>C (p.S241P)
ISCN -
DB-ID SLC25A15_000038
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A15 NM_014252.3 -?/. - c.721T>C r.(?) p.(Ser241Pro)
TPTE2P5 NR_038258.1 -?/. - n.623-7812A>G r.(?) -


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