All transcript variants in gene CUBN

Information The variants shown are described using the NM_001081.3 transcript reference sequence.

1 entry on 1 page. Showing entry 1.
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Effect     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

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.7331G>A likely benign r.(?) p.(Arg2444Gln) g.16957051C>T - CUBN(NM_001081.3):c.7331G>A (p.R2444Q) - CUBN_000114 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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Genomic reference sequence: hg19 (GRCh37)