ClinVar Miner

List of variants in gene ANO5 reported as uncertain significance by GeneDx

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Total variants: 20
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HGVS dbSNP
GRCh38/hg38 11p14.3(chr11:22162150-22321563)x3
GRCh38/hg38 11p15.1-14.3(chr11:21948209-22239692)x3
NM_213599.2(ANO5):c.1036A>C (p.Ile346Leu) rs146233625
NM_213599.2(ANO5):c.1081G>C (p.Asp361His) rs1554929295
NM_213599.2(ANO5):c.11C>A (p.Pro4Gln) rs376116831
NM_213599.2(ANO5):c.1630+5del rs1064795273
NM_213599.2(ANO5):c.1664G>T (p.Ser555Ile) rs375014127
NM_213599.2(ANO5):c.170G>A (p.Arg57Gln) rs781702630
NM_213599.2(ANO5):c.1981C>T (p.Leu661Phe) rs944857212
NM_213599.2(ANO5):c.2141C>G (p.Thr714Ser) rs200631556
NM_213599.2(ANO5):c.2623A>C (p.Ile875Leu) rs1131691364
NM_213599.2(ANO5):c.2639A>G (p.Glu880Gly) rs1554935957
NM_213599.2(ANO5):c.294G>A (p.Ala98=) rs142858990
NM_213599.2(ANO5):c.385T>C (p.Tyr129His) rs370952911
NM_213599.2(ANO5):c.584G>A (p.Arg195Gln) rs143078257
NM_213599.2(ANO5):c.637A>G (p.Arg213Gly) rs1490746741
NM_213599.2(ANO5):c.650T>C (p.Val217Ala) rs749876289
NM_213599.2(ANO5):c.736T>C (p.Tyr246His) rs1219063834
NM_213599.2(ANO5):c.817C>T (p.Leu273Phe) rs772929002
NM_213599.2(ANO5):c.845A>G (p.Tyr282Cys) rs561417561

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