Variant #0000282679 (NC_000005.9:g.7885793_7885794dup, MTRR(NM_002454.2):c.904-21_904-20dup)

Chromosome 5
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.7885793_7885794dup
DNA change (hg38) g.7885680_7885681dup
Published as MTRR(NM_002454.3):c.904-19_904-18insTT
ISCN -
DB-ID MTRR_000023
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) Variant not found in online data sets
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C5orf49 NM_001089584.2 -?/. - c.-34650_-34649dup r.(?) p.(=)
MTRR NM_002454.2 -?/. - c.904-21_904-20dup r.(=) p.(=)
FASTKD3 NM_024091.3 -?/. - c.-16806_-16805dup r.(?) p.(=)