All variants in the MTRR gene

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

2 entries on 1 page. Showing entries 1 - 2.
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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.1761T>C r.(?) p.(Tyr587=) - benign g.7897061T>C g.7896948T>C MTRR(NM_002454.2):c.1761T>C (p.Y587=) - C5orf49_000035 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_AMC
?/. - c.1761T>C r.(=) p.(=) - VUS g.7897061T>C g.7896948T>C - - C5orf49_000035 conflicting interpretations of pathogenicity; 17 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs6874544 Germline - 17/2792 individuals - 0 - Mohammed Faruq
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