All variants in the ARL13B gene

Information The variants shown are described using the NM_182896.2 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.896A>C r.(?) p.(Glu299Ala) - VUS g.93761956A>C g.94043112A>C ARL13B(NM_001174150.1):c.896A>C (p.E299A, p.(Glu299Ala)) - ARL13B_000011 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Rotterdam
-?/. - c.896A>C r.(?) p.(Glu299Ala) - likely benign g.93761956A>C g.94043112A>C ARL13B(NM_001174150.1):c.896A>C (p.E299A, p.(Glu299Ala)) - ARL13B_000011 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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