ANO7[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3127147	NM_001001666.3(ANO7):c.64G>A (p.Ala22Thr)	ANO7 (A22T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 715796	NM_001370694.2(ANO7):c.-75C>T	ANO7	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 2411607	NM_001370694.2(ANO7):c.-74G>A	ANO7 (R30Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2276524	NM_001370694.2(ANO7):c.-60G>A	ANO7 (A35T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3127122	NM_001370694.2(ANO7):c.-36G>A	ANO7 (E43K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1182034	NM_001370694.2(ANO7):c.-8+235G>A	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247216	NM_001370694.2(ANO7):c.-8+266G>A	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279620	NM_001370694.2(ANO7):c.-7-206C>T	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273665	NM_001370694.2(ANO7):c.-7-27A>G	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182026	NM_001370694.2(ANO7):c.9G>T (p.Arg3=)	ANO7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1246662	NM_001370694.2(ANO7):c.37G>A (p.Val13Ile)	ANO7 (V13I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 767880	NM_001370694.2(ANO7):c.75G>C (p.Arg25Ser)	ANO7 (R25S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2210319	NM_001370694.2(ANO7):c.85G>A (p.Gly29Arg)	ANO7 (G83R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 709659	NM_001370694.2(ANO7):c.105G>A (p.Ser35=)	ANO7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2525197	NM_001370694.2(ANO7):c.106G>A (p.Glu36Lys)	ANO7 (E36K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1264627	NM_001370694.2(ANO7):c.108+183T>G	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260208	NM_001370694.2(ANO7):c.108+245A>G	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3127141	NM_001370694.2(ANO7):c.119A>C (p.Gln40Pro)	ANO7 (Q40P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266777	NM_001370694.2(ANO7):c.124G>A (p.Ala42Thr)	ANO7 (A42T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608250	NM_001370694.2(ANO7):c.131C>T (p.Ala44Val)	ANO7 (A44V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305582	NM_001370694.2(ANO7):c.140C>G (p.Ala47Gly)	ANO7 (A47G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127142	NM_001370694.2(ANO7):c.160C>T (p.Arg54Trp)	ANO7 (R54W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456723	NM_001370694.2(ANO7):c.161G>A (p.Arg54Gln)	ANO7 (R108Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1267835	NM_001370694.2(ANO7):c.166+273T>A	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229920	NM_001370694.2(ANO7):c.167-261A>G	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290506	NM_001370694.2(ANO7):c.167-101A>C	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3299058	NM_001370694.2(ANO7):c.175G>A (p.Val59Ile)	ANO7 (V59I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127143	NM_001370694.2(ANO7):c.256T>C (p.Trp86Arg)	ANO7 (W85R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344316	NM_001370694.2(ANO7):c.284G>A (p.Arg95His)	ANO7 (R149H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275860	NM_001370694.2(ANO7):c.296T>C (p.Leu99Pro)	ANO7 (L98P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 767881	NM_001370694.2(ANO7):c.306C>A (p.Asp102Glu)	ANO7 (D101E +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1181621	NM_001370694.2(ANO7):c.310-241A>G	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2241425	NM_001370694.2(ANO7):c.325G>A (p.Gly109Arg)	ANO7 (G163R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127144	NM_001370694.2(ANO7):c.346G>A (p.Ala116Thr)	ANO7 (A116T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468269	NM_001370694.2(ANO7):c.385G>T (p.Ala129Ser)	ANO7 (A183S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127145	NM_001370694.2(ANO7):c.409C>T (p.Pro137Ser)	ANO7 (P137S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1253244	NM_001370694.2(ANO7):c.417+74C>T	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1296609	NM_001370694.2(ANO7):c.417+214G>A	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236639	NM_001370694.2(ANO7):c.418-13C>T	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2376361	NM_001370694.2(ANO7):c.446C>T (p.Ser149Leu)	ANO7 (S149L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127146	NM_001370694.2(ANO7):c.451G>A (p.Gly151Ser)	ANO7 (G151S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 713296	NM_001370694.2(ANO7):c.486G>T (p.Leu162=)	ANO7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2209980	NM_001370694.2(ANO7):c.505G>A (p.Val169Ile)	ANO7 (V169I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 780027	NM_001370694.2(ANO7):c.514G>A (p.Glu172Lys)	ANO7 (E172K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3299044	NM_001370694.2(ANO7):c.530G>A (p.Arg177Gln)	ANO7 (R177Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1220951	NM_001370694.2(ANO7):c.554+213C>A	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1246779	NM_001370694.2(ANO7):c.554+239C>T	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232356	NM_001370694.2(ANO7):c.555-286C>A	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275340	NM_001370694.2(ANO7):c.555-55_555-18del	ANO7	Deletion (intron variant)	not provided	GBenign
Select item 3299075	NM_001370694.2(ANO7):c.577G>A (p.Asp193Asn)	ANO7 (D193N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535099	NM_001370694.2(ANO7):c.606C>A (p.His202Gln)	ANO7 (H256Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1273466	NM_001370694.2(ANO7):c.612+15C>G	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264798	NM_001370694.2(ANO7):c.613-297C>T	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236659	NM_001370694.2(ANO7):c.613-96C>T	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2518250	NM_001370694.2(ANO7):c.617T>C (p.Phe206Ser)	ANO7 (F206S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213706	NM_001370694.2(ANO7):c.641A>T (p.Tyr214Phe)	ANO7 (Y214F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 730537	NM_001370694.2(ANO7):c.645C>G (p.Gly215=)	ANO7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2396911	NM_001370694.2(ANO7):c.649G>A (p.Glu217Lys)	ANO7 (E217K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127148	NM_001370694.2(ANO7):c.676C>G (p.Gln226Glu)	ANO7 (Q226E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511071	NM_001370694.2(ANO7):c.706G>A (p.Ala236Thr)	ANO7 (A236T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1242235	NM_001370694.2(ANO7):c.723C>T (p.Asp241=)	ANO7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1276517	NM_001370694.2(ANO7):c.723+207C>T	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267492	NM_001370694.2(ANO7):c.724-240G>A	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1246822	NM_001370694.2(ANO7):c.724-11=	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2591882	NM_001370694.2(ANO7):c.737C>T (p.Thr246Met)	ANO7 (T246M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488932	NM_001370694.2(ANO7):c.739C>A (p.Pro247Thr)	ANO7 (P247T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204358	NM_001370694.2(ANO7):c.776G>A (p.Arg259His)	ANO7 (R259H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353161	NM_001370694.2(ANO7):c.784C>A (p.Leu262Ile)	ANO7 (L316I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2652110	NM_001370694.2(ANO7):c.840C>T (p.His280=)	ANO7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2409737	NM_001370694.2(ANO7):c.841G>A (p.Val281Met)	ANO7 (V335M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468821	NM_001370694.2(ANO7):c.845G>A (p.Arg282His)	ANO7 (R336H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127121	NM_001370694.2(ANO7):c.880G>A (p.Ala294Thr)	ANO7 (A348T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1243963	NM_001370694.2(ANO7):c.889+8C>T	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258346	NM_001370694.2(ANO7):c.889+137C>T	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1285998	NM_001370694.2(ANO7):c.889+256G>A	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266118	NM_001370694.2(ANO7):c.890-271G>A	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2262239	NM_001370694.2(ANO7):c.893T>G (p.Phe298Cys)	ANO7 (F298C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 720027	NM_001370694.2(ANO7):c.917C>T (p.Ala306Val)	ANO7 (A306V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 736008	NM_001370694.2(ANO7):c.961dup (p.Val321fs)	ANO7 (V321fs)	Duplication (frameshift variant)	not provided	GLikely benign
Select item 2376031	NM_001370694.2(ANO7):c.989T>C (p.Leu330Pro)	ANO7 (L330P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232097	NM_001370694.2(ANO7):c.1012G>A (p.Glu338Lys)	ANO7 (E338K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 711876	NM_001370694.2(ANO7):c.1028G>A (p.Cys343Tyr)	ANO7 (C343Y)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2328774	NM_001370694.2(ANO7):c.1060G>A (p.Ala354Thr)	ANO7 (A408T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 727251	NM_001370694.2(ANO7):c.1077+10G>A	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258375	NM_001370694.2(ANO7):c.1077+73C>A	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235766	NM_001370694.2(ANO7):c.1077+179C>A	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286881	NM_001370694.2(ANO7):c.1078-320C>T	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253440	NM_001370694.2(ANO7):c.1078-310T>C	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178748	NM_001370694.2(ANO7):c.1078-309C>T	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1296526	NM_001370694.2(ANO7):c.1078-296A>G	ANO7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2487498	NM_001370694.2(ANO7):c.1081G>T (p.Gly361Cys)	ANO7 (G361C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369022	NM_001370694.2(ANO7):c.1081G>A (p.Gly361Ser)	ANO7 (G415S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395075	NM_001370694.2(ANO7):c.1099G>A (p.Gly367Ser)	ANO7 (G367S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508343	NM_001370694.2(ANO7):c.1108G>A (p.Val370Met)	ANO7 (V424M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597701	NM_001370694.2(ANO7):c.1130C>T (p.Ala377Val)	ANO7 (A377V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1255346	NM_001370694.2(ANO7):c.1142T>A (p.Val381Glu)	ANO7 (V381E)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2559420	NM_001370694.2(ANO7):c.1181T>C (p.Leu394Pro)	ANO7 (L448P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520704	NM_001370694.2(ANO7):c.1189C>T (p.Arg397Cys)	ANO7 (R397C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299078	NM_001370694.2(ANO7):c.1243G>A (p.Ala415Thr)	ANO7 (A415T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127123	NM_001370694.2(ANO7):c.1268C>T (p.Pro423Leu)	ANO7 (P423L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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