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.1043C>G r.(?) p.(Thr348Ser) - benign g.93768268C>G g.94049424C>G ARL13B(NM_001174150.2):c.1043C>G (p.T348S), ARL13B(NM_182896.2):c.1043C>G (p.T348S) - ARL13B_000013 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Groningen
-/. - c.1043C>G r.(?) p.(Thr348Ser) - benign g.93768268C>G g.94049424C>G ARL13B(NM_001174150.2):c.1043C>G (p.T348S), ARL13B(NM_182896.2):c.1043C>G (p.T348S) - ARL13B_000013 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Rotterdam
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