Full data view for gene TOP2B

Information The variants shown are described using the NM_001068.2 transcript reference sequence.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

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     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. - c.221C>T r.(?) p.(Thr74Met) Unknown - VUS g.25686795G>A g.25645304G>A TOP2B(NM_001068.3):c.221C>T (p.(Thr74Met)) - TOP2B_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-?/. - c.614G>A r.(?) p.(Ser205Asn) Unknown - likely benign g.25678716C>T g.25637225C>T TOP2B(NM_001068.3):c.614G>A (p.(Ser205Asn)) - RARB_000011 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.2886A>T r.(?) p.(Gly962=) Unknown - likely benign g.25661515T>A - TOP2B(NM_001068.3):c.2886A>T (p.G962=) - RARB_000015 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.3937C>T r.(?) p.(Pro1313Ser) Unknown - VUS g.25650815G>A - TOP2B(NM_001068.3):c.3937C>T (p.P1313S) - RARB_000017 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.4482G>A r.(?) p.(Pro1494=) Unknown - likely benign g.25642709C>T - TOP2B(NM_001068.3):c.4482G>A (p.P1494=) - RARB_000014 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.4843G>A r.(?) p.(Val1615Ile) Unknown - VUS g.25639821C>T g.25598330C>T TOP2B(NM_001068.3):c.4843G>A (p.(Val1615Ile)), TOP2B(NM_001330700.1):c.4858G>A (p.V1620I) - TOP2B_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-?/. - c.4843G>A r.(?) p.(Val1615Ile) Unknown - likely benign g.25639821C>T g.25598330C>T TOP2B(NM_001068.3):c.4843G>A (p.(Val1615Ile)), TOP2B(NM_001330700.1):c.4858G>A (p.V1620I) - TOP2B_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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