All transcript variants in gene VPS35

Information The variants shown are described using the NM_018206.4 transcript reference sequence.

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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.1905T>G likely benign r.(?) p.(Phe635Leu) g.46696317A>C - VPS35(NM_018206.5):c.1905T>G (p.F635L) - VPS35_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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