Variant #0000280095 (NC_000005.9:g.7897191C>T, MTRR(NM_002454.2):c.1783C>T)

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.7897191C>T
DNA change (hg38) g.7897078C>T
Published as MTRR(NM_002454.2):c.1783C>T (p.H595Y)
ISCN -
DB-ID MTRR_000014
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.15587 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C5orf49 NM_001089584.2 -/. - c.-46057G>A r.(?) p.(=)
MTRR NM_002454.2 -/. - c.1783C>T r.(?) p.(His595Tyr)
FASTKD3 NM_024091.3 -/. - c.-28213G>A r.(?) p.(=)