Variant #0000526121 (NC_000005.9:g.7897217T>A, NM_002454.2:c.1809T>A (MTRR))

Chromosome 5
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.7897217T>A
DNA change (hg38) g.7897104T>A
Published as MTRR(NM_002454.3):c.1809T>A (p.T603=)
ISCN -
DB-ID MTRR_000066
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-09-27 18:50:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C5orf49 NM_001089584.2 -/. - c.-46083A>T r.(?) p.(=)
MTRR NM_002454.2 -/. - c.1809T>A r.(?) p.(Thr603=)
FASTKD3 NM_024091.3 -/. - c.-28239A>T r.(?) p.(=)


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