List of variants in gene ANO5 reported as likely benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_213599.3(ANO5):c.1898+29G>T	rs76084798	0.02917
NM_213599.3(ANO5):c.2259A>G (p.Ser753=)	rs61746201	0.01772
NM_213599.3(ANO5):c.1181-21T>A	rs114582774	0.01015
NM_213599.3(ANO5):c.1029C>T (p.Asp343=)	rs78899595	0.00992
NM_213599.3(ANO5):c.616A>G (p.Thr206Ala)	rs78266558	0.00922
NM_213599.3(ANO5):c.2387C>T (p.Ser796Leu)	rs61910685	0.00804
NM_213599.3(ANO5):c.1181-48T>A	rs150412089	0.00767
NM_213599.3(ANO5):c.1545A>G (p.Ser515=)	rs35843353	0.00699
NM_213599.3(ANO5):c.2354T>G (p.Leu785Arg)	rs146136277	0.00524
NM_213599.3(ANO5):c.1631-35G>A	rs72982041	0.00334
NM_213599.3(ANO5):c.680G>C (p.Gly227Ala)	rs140903276	0.00320
NM_213599.3(ANO5):c.259G>A (p.Val87Ile)	rs34994927	0.00293
NM_213599.3(ANO5):c.155A>G (p.Asn52Ser)	rs143777403	0.00238
NM_213599.3(ANO5):c.1095A>G (p.Leu365=)	rs35804601	0.00183
NM_213599.3(ANO5):c.2698A>C (p.Met900Leu)	rs148293985	0.00169
NM_213599.3(ANO5):c.2521-7C>T	rs201438159	0.00109
NM_213599.3(ANO5):c.1013+29G>C	rs371272245	0.00039
NM_213599.3(ANO5):c.1227A>G (p.Glu409=)	rs781554633	0.00003
NM_213599.3(ANO5):c.276A>G (p.Lys92=)	rs201678262	0.00003
NM_213599.3(ANO5):c.181-16T>C	rs762760550	0.00001
NM_213599.3(ANO5):c.2139C>T (p.Thr713=)	rs767479331	0.00001
NM_213599.3(ANO5):c.2175T>C (p.His725=)	rs1057522538	0.00001
NM_213599.3(ANO5):c.1222C>T (p.Leu408=)	rs997655691
NM_213599.3(ANO5):c.181-18C>T	rs1350082012
NM_213599.3(ANO5):c.1962A>G (p.Arg654=)	rs1057521970
NM_213599.3(ANO5):c.2236-13_2236-10del	rs72105710
NM_213599.3(ANO5):c.2415-7T>C	rs1554935084
NM_213599.3(ANO5):c.2646C>G (p.Asn882Lys)	rs34969327
NM_213599.3(ANO5):c.2688C>G (p.Ala896=)	rs377549896
NM_213599.3(ANO5):c.295-16T>A	rs746448319
NM_213599.3(ANO5):c.878+17G>A	rs749031281

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