Full data view for gene MAPT

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

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

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.307+9A>G benign r.(=) p.(=) Unknown g.44051846A>G - MAPT(NM_001123066.3):c.307+9A>G, MAPT(NM_005910.5):c.307+9A>G - MAPT_000112 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-/. - c.307+9A>G benign r.(=) p.(=) Unknown g.44051846A>G - MAPT(NM_001123066.3):c.307+9A>G, MAPT(NM_005910.5):c.307+9A>G - MAPT_000112 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-/. - c.307+9A>G benign r.(=) p.(=) Unknown g.44051846A>G - MAPT(NM_001123066.3):c.307+9A>G, MAPT(NM_005910.5):c.307+9A>G - MAPT_000112 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-/. - c.307+9A>G benign r.(=) p.(=) Unknown g.44051846A>G - MAPT(NM_001123066.3):c.307+9A>G, MAPT(NM_005910.5):c.307+9A>G - MAPT_000112 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
Legend