Variant #0000286701 (NC_000005.9:g.7885907C>G, MTRR(NM_002454.2):c.997C>G)

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.7885907C>G
DNA change (hg38) g.7885794C>G
Published as MTRR(NM_002454.2):c.997C>G (p.L333V), MTRR(NM_002454.3):c.997C>G (p.L333V)
ISCN -
DB-ID MTRR_000007 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 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01021 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C5orf49 NM_001089584.2 -/. - c.-34773G>C r.(?) p.(=)
MTRR NM_002454.2 -/. - c.997C>G r.(?) p.(Leu333Val)
FASTKD3 NM_024091.3 -/. - c.-16929G>C r.(?) p.(=)