Variant #0000726663 (NC_000017.10:g.73269653A>C, NM_021734.4:c.842T>G (SLC25A19))

Chromosome 17
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.73269653A>C
DNA change (hg38) -
Published as SLC25A19(NM_001126121.2):c.842T>G (p.(Phe281Cys)), SLC25A19(NM_021734.4):c.842T>G (p.F281C)
ISCN -
DB-ID MIF4GD_000004 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) 0.00014 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPS7 NM_015971.3 -?/. - c.*7649A>C r.(=) p.(=)
MIF4GD NM_020679.3 -?/. - c.-2479T>G r.(?) p.(=)
SLC25A19 NM_021734.4 -?/. - c.842T>G r.(?) p.(Phe281Cys)


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