Variant #0000948168 (NC_000003.11:g.39431961C>G, NM_017875.2:c.239C>G (SLC25A38))

Chromosome 3
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.39431961C>G
DNA change (hg38) -
Published as SLC25A38(NM_017875.2):c.239C>G (p.(Thr80Arg)), SLC25A38(NM_017875.4):c.239C>G (p.T80R)
ISCN -
DB-ID SLC25A38_000007 See all 2 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) 0.00477 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A38 NM_017875.2 -?/. - c.239C>G r.(?) p.(Thr80Arg)


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