ClinVar Miner

List of variants in gene ARL13B reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_001174150.2(ARL13B):c.1043C>G (p.Thr348Ser) rs33944211 0.07857
NM_001174150.2(ARL13B):c.105C>T (p.Thr35=) rs146396078 0.00721
NM_001174150.2(ARL13B):c.1186C>G (p.Pro396Ala) rs11554412 0.00529
NM_001174150.2(ARL13B):c.1025-48G>A rs78946357 0.00270
NM_001174150.2(ARL13B):c.1151G>A (p.Gly384Glu) rs146264035 0.00143
NM_001174150.2(ARL13B):c.831C>A (p.Asn277Lys) rs139997243 0.00089
NM_001174150.2(ARL13B):c.59+8G>A rs183229189 0.00061
NM_001174150.2(ARL13B):c.1045A>G (p.Lys349Glu) rs139063474 0.00050
NM_001174150.2(ARL13B):c.*2C>T rs377420487 0.00013
NM_001174150.2(ARL13B):c.270T>C (p.Tyr90=) rs753336861 0.00006
NM_001174150.2(ARL13B):c.30C>T (p.Gly10=) rs375770842 0.00006
NM_001174150.2(ARL13B):c.487-9C>A rs1394028422 0.00001
NM_001174150.2(ARL13B):c.*8G>A
NM_001174150.2(ARL13B):c.1134T>A (p.Pro378=) rs1401884380
NM_001174150.2(ARL13B):c.1137T>A (p.Pro379=) rs1325555759
NM_001174150.2(ARL13B):c.1140T>A (p.Pro380=)
NM_001174150.2(ARL13B):c.1140T>G (p.Pro380=)
NM_001174150.2(ARL13B):c.130+726G>A
NM_001174150.2(ARL13B):c.380+10G>A
NM_001174150.2(ARL13B):c.380+36G>A rs147980419
NM_001174150.2(ARL13B):c.495T>C (p.Cys165=)

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