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.106G>A r.(?) p.(Ala36Thr) - likely benign g.93714764G>A g.93995920G>A ARL13B(NM_001174150.1):c.106G>A (p.A36T, p.(Ala36Thr)) - ARL13B_000019 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
?/. - c.106G>A r.(?) p.(Ala36Thr) - VUS g.93714764G>A - ARL13B(NM_001174150.1):c.106G>A (p.A36T, p.(Ala36Thr)) - ARL13B_000019 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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