Related gene-specific medical variations for Gene (Select 55811) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3344930	NM_018417.6(ADCY10):c.1572del (p.Ile525fs)	ADCY10, DCAF6 (I372fs +2 more)	Deletion (frameshift variant)	ADCY10-related disorder	GLikely pathogenic
Select item 3269257	NM_018417.6(ADCY10):c.520G>A (p.Asp174Asn)	ADCY10, DCAF6 (D21N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3269247	NM_018417.6(ADCY10):c.526C>T (p.Arg176Cys)	ADCY10, DCAF6 (R176C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3248012	NC_000001.10:g.(?_167798485)_(167798681_?)del	ADCY10	Deletion	not provided	GPathogenic
Select item 3248011	NC_000001.10:g.(?_167823571)_(167823747_?)del	ADCY10	Deletion	not provided	GPathogenic
Select item 3081347	NM_018417.6(ADCY10):c.878C>T (p.Thr293Met)	ADCY10, DCAF6 (T201M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081342	NM_018417.6(ADCY10):c.767A>G (p.Lys256Arg)	ADCY10, DCAF6 (K256R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081340	NM_018417.6(ADCY10):c.761C>T (p.Thr254Met)	ADCY10, DCAF6 (T101M +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3081150	NM_018417.6(ADCY10):c.163A>T (p.Thr55Ser)	ADCY10, DCAF6 (T55S)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3081135	NM_018417.6(ADCY10):c.1489A>T (p.Met497Leu)	ADCY10, DCAF6 (M344L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3058198	NM_018417.6(ADCY10):c.293-20C>T	ADCY10, DCAF6	Single nucleotide variant (5 prime UTR variant +1 more)	ADCY10-related disorder	GLikely benign
Select item 3045832	NM_018417.6(ADCY10):c.213G>A (p.Leu71=)	ADCY10, DCAF6	Single nucleotide variant (5 prime UTR variant +2 more)	ADCY10-related disorder	GLikely benign
Select item 3023936	NM_018417.6(ADCY10):c.595C>T (p.Arg199Trp)	ADCY10, DCAF6 (R199W +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3000070	NM_018417.6(ADCY10):c.1023C>T (p.Gly341=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2972942	NM_018417.6(ADCY10):c.27G>A (p.Gln9=)	ADCY10, DCAF6	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 2972525	NM_018417.6(ADCY10):c.705C>T (p.Thr235=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2972334	NM_018417.6(ADCY10):c.702G>A (p.Thr234=)	DCAF6, ADCY10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2963510	NM_018417.6(ADCY10):c.292+6G>A	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2895388	NM_018417.6(ADCY10):c.369C>G (p.Ser123Arg)	ADCY10, DCAF6 (S31R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2894612	NM_018417.6(ADCY10):c.1362A>T (p.Ala454=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2891680	NM_018417.6(ADCY10):c.1206C>T (p.His402=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2891547	NM_018417.6(ADCY10):c.1071C>T (p.Asp357=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2891098	NM_018417.6(ADCY10):c.1490T>A (p.Met497Lys)	ADCY10, DCAF6 (M344K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2863448	NM_018417.6(ADCY10):c.28G>C (p.Asp10His)	ADCY10, DCAF6 (D10H)	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GUncertain significance
Select item 2834689	NM_018417.6(ADCY10):c.1217-20C>A	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2834688	NM_018417.6(ADCY10):c.1217-12T>A	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2796200	NM_018417.6(ADCY10):c.1378T>C (p.Tyr460His)	ADCY10, DCAF6 (Y368H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2787037	NM_018417.6(ADCY10):c.149-11A>G	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2776642	NM_018417.6(ADCY10):c.1196C>T (p.Thr399Ile)	ADCY10, DCAF6 (T399I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2770834	NM_018417.6(ADCY10):c.331C>G (p.Gln111Glu)	ADCY10, DCAF6 (Q111E +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2756741	NM_018417.6(ADCY10):c.697dup (p.Cys233fs)	ADCY10, DCAF6 (C233fs +2 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 2756237	NM_018417.6(ADCY10):c.402G>A (p.Glu134=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2756222	NM_018417.6(ADCY10):c.82C>G (p.His28Asp)	ADCY10, DCAF6 (H28D)	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GUncertain significance
Select item 2755580	NM_018417.6(ADCY10):c.889G>A (p.Val297Met)	ADCY10, DCAF6 (V144M +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2718650	NM_018417.6(ADCY10):c.1119C>T (p.Cys373=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2696979	NM_018417.6(ADCY10):c.253+13A>G	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2690844	NM_018417.6(ADCY10):c.2971G>T (p.Ala991Ser)	ADCY10 (A838S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2690843	NM_018417.6(ADCY10):c.4483-12_4484del	ADCY10	Deletion (splice acceptor variant)	not provided	GUncertain significance
Select item 2690842	NM_018417.6(ADCY10):c.710T>C (p.Met237Thr)	ADCY10, DCAF6 (M145T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2690841	NM_018417.6(ADCY10):c.1787T>C (p.Leu596Pro)	ADCY10 (L443P +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2639530	NM_018417.6(ADCY10):c.1021-8C>T	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2627674	NM_018417.6(ADCY10):c.386T>C (p.Leu129Ser)	ADCY10, DCAF6 (L129S +1 more)	Single nucleotide variant (missense variant +1 more)	Familial idiopathic hypercalciuria	GUncertain significance
Select item 2592146	NM_018417.6(ADCY10):c.1385A>G (p.Tyr462Cys)	ADCY10, DCAF6 (Y370C +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2585314	NM_018417.6(ADCY10):c.257T>C (p.Val86Ala)	ADCY10, DCAF6 (V86A)	Single nucleotide variant (5 prime UTR variant +1 more)	Familial idiopathic hypercalciuria	GUncertain significance
Select item 2561081	NM_018417.6(ADCY10):c.512C>G (p.Ala171Gly)	ADCY10, DCAF6 (A79G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553976	NM_018417.6(ADCY10):c.709A>T (p.Met237Leu)	ADCY10, DCAF6 (M84L +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2540528	NM_018417.6(ADCY10):c.315G>C (p.Trp105Cys)	ADCY10, DCAF6 (W105C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531151	NM_018417.6(ADCY10):c.1336C>T (p.Pro446Ser)	ADCY10, DCAF6 (P354S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523191	NM_018417.6(ADCY10):c.1421C>T (p.Ala474Val)	ADCY10, DCAF6 (A321V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516393	NM_018417.6(ADCY10):c.1580T>C (p.Met527Thr)	ADCY10, DCAF6 (M435T +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2377830	NM_018417.6(ADCY10):c.586C>T (p.Leu196Phe)	ADCY10, DCAF6 (L104F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367996	NM_018417.6(ADCY10):c.1207G>A (p.Glu403Lys)	ADCY10, DCAF6 (E250K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367890	NM_018417.6(ADCY10):c.1199T>C (p.Val400Ala)	ADCY10, DCAF6 (V247A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343775	NM_018417.6(ADCY10):c.1372C>T (p.Pro458Ser)	ADCY10, DCAF6 (P305S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314945	NM_018417.6(ADCY10):c.448G>A (p.Gly150Ser)	ADCY10, DCAF6 (G58S +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2296104	NM_018417.6(ADCY10):c.801G>T (p.Lys267Asn)	ADCY10, DCAF6 (K175N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259165	NM_018417.6(ADCY10):c.1604G>T (p.Gly535Val)	ADCY10, DCAF6 (G535V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256365	NM_018417.6(ADCY10):c.1052C>G (p.Pro351Arg)	ADCY10, DCAF6 (P351R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242706	NM_018417.6(ADCY10):c.959A>C (p.His320Pro)	ADCY10, DCAF6 (H167P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227969	NM_018417.6(ADCY10):c.230A>G (p.Tyr77Cys)	ADCY10, DCAF6 (Y77C)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2206571	NM_018417.6(ADCY10):c.1283A>G (p.Asp428Gly)	ADCY10, DCAF6 (D428G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2196677	NM_018417.6(ADCY10):c.1311A>T (p.Leu437=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2130659	NM_018417.6(ADCY10):c.105T>C (p.Phe35=)	ADCY10, DCAF6	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 2130325	NM_018417.6(ADCY10):c.1355G>T (p.Gly452Val)	ADCY10, DCAF6 (G360V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2128967	NM_018417.6(ADCY10):c.497T>A (p.Leu166Gln)	ADCY10, DCAF6 (L166Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2114368	NM_018417.6(ADCY10):c.1307A>G (p.Asn436Ser)	ADCY10, DCAF6 (N436S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2106928	NM_018417.6(ADCY10):c.1090G>A (p.Glu364Lys)	ADCY10, DCAF6 (E211K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2071226	NM_018417.6(ADCY10):c.945G>A (p.Gln315=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2070996	NM_018417.6(ADCY10):c.325C>T (p.Arg109Ter)	ADCY10, DCAF6 (R109* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 2069420	NM_018417.6(ADCY10):c.423C>T (p.Ile141=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2061074	NM_018417.6(ADCY10):c.1373C>G (p.Pro458Arg)	ADCY10, DCAF6 (P366R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2060624	NM_018417.6(ADCY10):c.828G>A (p.Gln276=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2054527	NM_018417.6(ADCY10):c.1153G>A (p.Gly385Ser)	ADCY10, DCAF6 (G232S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2044664	NM_018417.6(ADCY10):c.1415G>T (p.Gly472Val)	ADCY10, DCAF6 (G380V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2001177	NM_018417.6(ADCY10):c.253+1G>A	ADCY10, DCAF6	Single nucleotide variant (intron variant +1 more)	not provided	GLikely pathogenic
Select item 1974734	NM_018417.6(ADCY10):c.534C>A (p.Ala178=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1947780	NM_018417.6(ADCY10):c.739+18A>G	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1924335	NM_018417.6(ADCY10):c.1164T>C (p.Ser388=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1902874	NM_018417.6(ADCY10):c.1275G>A (p.Val425=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1902102	NM_018417.6(ADCY10):c.1216+15C>T	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1901853	NM_018417.6(ADCY10):c.437-8C>G	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1899822	NM_018417.6(ADCY10):c.1021-13C>G	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1898043	NM_018417.6(ADCY10):c.829-15C>T	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1722186	NM_018417.6(ADCY10):c.849G>C (p.Gln283His)	ADCY10, DCAF6 (Q130H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1715876	NM_018417.6(ADCY10):c.1202G>A (p.Arg401Lys)	ADCY10, DCAF6 (R248K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1714660	NM_018417.6(ADCY10):c.1451A>G (p.Tyr484Cys)	ADCY10, DCAF6 (Y331C +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1706798	NM_018417.6(ADCY10):c.1407-140G>A	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1660785	NM_018417.6(ADCY10):c.254-20A>T	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1623973	NM_018417.6(ADCY10):c.643-8T>G	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1618519	NM_018417.6(ADCY10):c.1021-11C>T	ADCY10, DCAF6	Single nucleotide variant (intron variant)	Familial idiopathic hypercalciuria +1 more	GBenign/Likely benign
Select item 1561964	NM_018417.6(ADCY10):c.426A>G (p.Arg142=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1521167	NM_018417.6(ADCY10):c.20A>C (p.Glu7Ala)	ADCY10, DCAF6 (E7A)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified +1 more	GUncertain significance
Select item 1517696	NM_018417.6(ADCY10):c.1415G>A (p.Gly472Asp)	ADCY10, DCAF6 (G380D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1500675	NM_018417.6(ADCY10):c.878C>G (p.Thr293Arg)	ADCY10, DCAF6 (T140R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1478066	NM_018417.6(ADCY10):c.1185C>A (p.Ile395=)	ADCY10, DCAF6	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1454870	NM_018417.6(ADCY10):c.952dup (p.Tyr318fs)	ADCY10, DCAF6 (Y226fs +2 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 1453952	NM_018417.6(ADCY10):c.651C>A (p.Phe217Leu)	ADCY10, DCAF6 (F217L +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1426702	NM_018417.6(ADCY10):c.229T>C (p.Tyr77His)	ADCY10, DCAF6 (Y77H)	Single nucleotide variant (5 prime UTR variant +2 more)	not provided +1 more	GUncertain significance
Select item 1416848	NM_018417.6(ADCY10):c.147A>C (p.Ser49=)	ADCY10, DCAF6	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GUncertain significance
Select item 1403077	NM_018417.6(ADCY10):c.1025G>T (p.Cys342Phe)	ADCY10, DCAF6 (C189F +2 more)	Single nucleotide variant (missense variant)	Familial idiopathic hypercalciuria +1 more	GUncertain significance

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