Variant #0001034467 (NC_000004.11:g.186068118_186068119del, NM_001151.3:c.890_891del (SLC25A4))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.186068118_186068119del
DNA change (hg38) -
Published as SLC25A4(NM_001151.4):c.890_891del (p.(Tyr297Cysfs*4))
ISCN -
DB-ID SLC25A4_000013
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
SLC25A4 NM_001151.3 +?/. - c.890_891del r.(?) p.(Tyr297Cysfs*4)


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