Variant #0000562989 (NC_000017.10:g.73269592G>A, NM_021734.4:c.903C>T (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.73269592G>A
DNA change (hg38) g.75273511G>A
Published as SLC25A19(NM_001126121.2):c.903C>T (p.F301=)
ISCN -
DB-ID MIF4GD_000002
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 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-14 12:34:01 +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.*7588G>A r.(=) p.(=)
MIF4GD NM_020679.3 -?/. - c.-2418C>T r.(?) p.(=)
SLC25A19 NM_021734.4 -?/. - c.903C>T r.(?) p.(Phe301=)


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