Variant #0001051910 (NC_000005.9:g.7875364T>A, NC_000005.9(NM_002454.2):c.284-7T>A (MTRR))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.7875364T>A
DNA change (hg38) -
Published as MTRR(NM_002454.3):c.284-7T>A
ISCN -
DB-ID C5orf49_000048
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C5orf49 NM_001089584.2 ?/. - c.-24230A>T r.(?) p.(=)
MTRR NM_002454.2 ?/. - c.284-7T>A r.(=) p.(=)
FASTKD3 NM_024091.3 ?/. - c.-6386A>T r.(?) p.(=)


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