Full data view for gene NDN

Information The variants shown are described using the NM_002487.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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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.263C>T benign r.(?) p.(Pro88Leu) Unknown g.23932102G>A - NDN(NM_002487.2):c.263C>T (p.P88L) - NDN_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-?/. - c.325G>T likely benign r.(?) p.(Val109Leu) Unknown g.23932040C>A - NDN(NM_002487.2):c.325G>T (p.(Val109Leu)) - NDN_000005 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.497C>A likely benign r.(?) p.(Ala166Glu) Unknown g.23931868G>T - NDN(NM_002487.2):c.497C>A (p.A166E) - NDN_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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