Variant #0000249230 (NC_000017.10:g.73269530A>G, NM_021734.4:c.*2T>C (SLC25A19))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73269530A>G
DNA change (hg38) g.75273449A>G
Published as MIF4GD-DT(NR_036520.1):n.2151A>G, SLC25A19(NM_001126121.2):c.*2T>C
ISCN -
DB-ID SLC25A19_000001 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) 0.93064 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPS7 NM_015971.3 -/. - c.*7526A>G r.(=) p.(=)
MIF4GD NM_020679.3 -/. - c.-2356T>C r.(?) p.(=)
SLC25A19 NM_021734.4 -/. - c.*2T>C r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.