All variants in the MTRR gene

Information The variants shown are described using the NM_002454.2 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. - c.1677-3_1677-2insTTTT r.spl? p.? - likely benign g.7896974_7896975insTTTT g.7896861_7896862insTTTT MTRR(NM_002454.2):c.1677-5_1677-4insTTTT (p.?) - C5orf49_000033 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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