All variants in the SNX14 gene

Information The variants shown are described using the NM_153816.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     

Owner     
?/. - c.2670del r.(?) p.(Cys890Ter) - VUS g.86217761del g.85508043del SNX14(NM_001350532.1):c.2733delT (p.C911*), SNX14(NM_153816.3):c.2670del (p.?) - SNX14_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
+/. - c.2670del r.(?) p.(Cys890Ter) - pathogenic g.86217761del - SNX14(NM_001350532.1):c.2733delT (p.C911*), SNX14(NM_153816.3):c.2670del (p.?) - SNX14_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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