Variant #0000308311 (NC_000017.10:g.73273488del, NM_021734.4:c.720del (SLC25A19))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.73273488del
DNA change (hg38) g.75277407del
Published as SLC25A19(NM_001126121.2):c.720del (p.(Phe240Leufs*51)), SLC25A19(NM_021734.4):c.720delC (p.F240Lfs*51)
ISCN -
DB-ID SLC25A19_000003 See all 3 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) 1.0E-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 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A19 NM_021734.4 +/. - c.720del r.(?) p.(Phe240LeufsTer51)


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