Full data view for gene PBX2

Information The variants shown are described using the NM_002586.4 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Allele     

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/Death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. - c.-2239C>G VUS r.(?) p.(=) Unknown g.32159931G>C - GPSM3(NM_022107.1):c.139C>G (p.(His47Asp)) - GPSM3_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-?/. - c.*2701C>T likely benign r.(=) p.(=) Unknown g.32151458G>A - AGER(NM_001136.4):c.229C>T (p.(Arg77Cys), p.(Arg63Cys)) - AGER_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.*3457C>T likely benign r.(=) p.(=) Unknown g.32150702G>A - AGER(NM_001136.4):c.607C>T (p.R203C) - AGER_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-?/. - c.*5019G>A likely benign r.(=) p.(=) Unknown g.32149140C>T - AGER(NM_001136.4):c.1106G>A (p.(Arg369Gln), p.(Arg385Gln), p.(Arg355Gln), p.(=)) - AGER_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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