ClinVar for Gene (Select 6389) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3369953	NM_004168.4(SDHA):c.1952A>T (p.Glu651Val)	SDHA (E570V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368154	NM_004168.4(SDHA):c.574G>T (p.Val192Leu)	SDHA (V144L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367475	NM_004168.4(SDHA):c.1552-3C>A	SDHA	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3367268	NM_004168.4(SDHA):c.908C>T (p.Ala303Val)	SDHA (A255V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367234	NM_004168.4(SDHA):c.1823A>G (p.Lys608Arg)	SDHA (K527R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3340185	NM_004168.4(SDHA):c.-6G>A	SDHA	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 3338849	NM_004168.4(SDHA):c.117del (p.Asn40fs)	SDHA (N40fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 3338666	NM_004168.4(SDHA):c.964C>T (p.Gln322Ter)	SDHA (Q274* +1 more)	Single nucleotide variant (nonsense)	Paragangliomas 5	GLikely pathogenic
Select item 3316862	NM_004168.4(SDHA):c.55G>T (p.Ala19Ser)	SDHA (A19S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316861	NM_004168.4(SDHA):c.1279G>A (p.Gly427Ser)	SDHA (G379S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316860	NM_004168.4(SDHA):c.351C>G (p.Asp117Glu)	SDHA (D117E)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316859	NM_004168.4(SDHA):c.1577T>C (p.Phe526Ser)	SDHA (F478S +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316857	NM_004168.4(SDHA):c.896-5T>C	SDHA	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316856	NM_004168.4(SDHA):c.158C>T (p.Ala53Val)	SDHA (A53V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316855	NM_004168.4(SDHA):c.806C>T (p.Ala269Val)	SDHA (A221V +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316854	NM_004168.4(SDHA):c.864G>A (p.Gln288=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3316853	NM_004168.4(SDHA):c.1200C>G (p.Ile400Met)	SDHA (I352M +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316851	NM_004168.4(SDHA):c.118A>T (p.Asn40Tyr)	SDHA (N40Y)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316850	NM_004168.4(SDHA):c.1909-4C>T	SDHA	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3316849	NM_004168.4(SDHA):c.138del (p.Val47fs)	SDHA (V47fs)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3316848	NM_004168.4(SDHA):c.457-3dup	SDHA	Duplication (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316847	NM_004168.4(SDHA):c.827del (p.Gly276fs)	SDHA (G276fs +1 more)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3316846	NM_004168.4(SDHA):c.310_311del (p.Gln104fs)	SDHA (Q104fs)	Microsatellite (frameshift variant)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3316845	NM_004168.4(SDHA):c.277C>T (p.Leu93=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3316843	NM_004168.4(SDHA):c.1046T>G (p.Leu349Arg)	SDHA (L349R +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316842	NM_004168.4(SDHA):c.778G>T (p.Gly260Trp)	SDHA (G212W +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316841	NM_004168.4(SDHA):c.661G>A (p.Ala221Thr)	SDHA (A173T +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316840	NM_004168.4(SDHA):c.234T>C (p.Phe78=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3316839	NM_004168.4(SDHA):c.907G>C (p.Ala303Pro)	SDHA (A303P +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316838	NM_004168.4(SDHA):c.706G>T (p.Ala236Ser)	SDHA (A188S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316837	NM_004168.4(SDHA):c.1058A>T (p.Glu353Val)	SDHA (E305V +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316835	NM_004168.4(SDHA):c.660T>C (p.Phe220=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3316834	NM_004168.4(SDHA):c.634G>T (p.Asp212Tyr)	SDHA (D164Y +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316833	NM_004168.4(SDHA):c.1174G>T (p.Gly392Cys)	SDHA (G344C +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316832	NM_004168.4(SDHA):c.1794+1dup	SDHA	Duplication (splice donor variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely pathogenic
Select item 3316831	NM_004168.4(SDHA):c.1794+5G>T	SDHA	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316830	NM_004168.4(SDHA):c.1836del (p.Gln613fs)	SDHA (Q532fs +2 more)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome	GLikely pathogenic
Select item 3316827	NM_004168.4(SDHA):c.1988C>G (p.Ser663Cys)	SDHA (S582C +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316826	NM_004168.4(SDHA):c.803C>G (p.Ser268Cys)	SDHA (S268C +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3316824	NM_004168.4(SDHA):c.1206C>A (p.Val402=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3316822	NM_004168.4(SDHA):c.1003A>G (p.Lys335Glu)	SDHA (K335E +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3256421	NM_004168.4(SDHA):c.1319del (p.Glu440fs)	SDHA (E392fs +1 more)	Deletion (frameshift variant)	not provided	GLikely pathogenic
Select item 3254407	NM_004168.4(SDHA):c.9_10dup (p.Val4fs)	SDHA (V4fs)	Duplication (frameshift variant)	Paragangliomas 5 +1 more	GPathogenic
Select item 3254392	NM_004168.4(SDHA):c.1192del (p.Glu398fs)	SDHA (E350fs +1 more)	Deletion (frameshift variant)	Paragangliomas 5	GPathogenic
Select item 3240437	NM_004168.4(SDHA):c.1226A>T (p.Asn409Ile)	SDHA (N361I +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1GG	GUncertain significance
Select item 3240436	NM_004168.4(SDHA):c.52C>A (p.Leu18Met)	SDHA (L18M)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1GG	GUncertain significance
Select item 3240435	NM_004168.4(SDHA):c.761T>C (p.Val254Ala)	SDHA (V206A +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1GG	GUncertain significance
Select item 3240433	NM_004168.4(SDHA):c.1591G>C (p.Val531Leu)	SDHA (V483L +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 3240430	NM_004168.4(SDHA):c.1197_1199dup (p.Pro399_Ile400insMet)	SDHA	Duplication (inframe_insertion)	Dilated cardiomyopathy 1GG	GUncertain significance
Select item 3223763	NM_004168.4(SDHA):c.995C>G (p.Pro332Arg)	SDHA (P284R +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223762	NM_004168.4(SDHA):c.931T>C (p.Cys311Arg)	SDHA (C263R +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223761	NM_004168.4(SDHA):c.890C>T (p.Pro297Leu)	SDHA (P249L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223760	NM_004168.4(SDHA):c.870A>G (p.Leu290=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3223759	NM_004168.4(SDHA):c.825C>G (p.Asp275Glu)	SDHA (D227E +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223758	NM_004168.4(SDHA):c.80A>G (p.Gln27Arg)	SDHA (Q27R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223757	NM_004168.4(SDHA):c.771-5T>G	SDHA	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223756	NM_004168.4(SDHA):c.770+2T>A	SDHA	Single nucleotide variant (splice donor variant)	Hereditary cancer-predisposing syndrome	GLikely pathogenic
Select item 3223755	NM_004168.4(SDHA):c.756T>C (p.Thr252=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3223754	NM_004168.4(SDHA):c.721G>A (p.Asp241Asn)	SDHA (D193N +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223753	NM_004168.4(SDHA):c.710T>G (p.Leu237Arg)	SDHA (L189R +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223752	NM_004168.4(SDHA):c.692G>T (p.Cys231Phe)	SDHA (C183F +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223751	NM_004168.4(SDHA):c.-5C>G	SDHA	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GUncertain significance
Select item 3223750	NM_004168.4(SDHA):c.554A>G (p.Gln185Arg)	SDHA (Q137R +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223749	NM_004168.4(SDHA):c.540T>A (p.Phe180Leu)	SDHA (F132L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223748	NM_004168.4(SDHA):c.473T>A (p.Met158Lys)	SDHA (M110K +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223747	NM_004168.4(SDHA):c.470del (p.Gly157fs)	SDHA (G109fs +1 more)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3223746	NM_004168.4(SDHA):c.45C>A (p.Arg15=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3223745	NM_004168.4(SDHA):c.405C>A (p.Asp135Glu)	SDHA (D135E)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223744	NM_004168.4(SDHA):c.383A>G (p.Lys128Arg)	SDHA (K128R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223743	NM_004168.4(SDHA):c.310C>G (p.Gln104Glu)	SDHA (Q104E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223742	NM_004168.4(SDHA):c.298A>G (p.Thr100Ala)	SDHA (T100A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223741	NM_004168.4(SDHA):c.268G>C (p.Val90Leu)	SDHA (V90L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223740	NM_004168.4(SDHA):c.247G>T (p.Ala83Ser)	SDHA (A83S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223739	NM_004168.4(SDHA):c.21G>A (p.Leu7=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3223738	NM_004168.4(SDHA):c.203G>C (p.Gly68Ala)	SDHA (G68A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223737	NM_004168.4(SDHA):c.1965C>T (p.Ala655=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3223736	NM_004168.4(SDHA):c.1957G>T (p.Asp653Tyr)	SDHA (D572Y +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223735	NM_004168.4(SDHA):c.1905G>A (p.Gly635=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3223734	NM_004168.4(SDHA):c.1877C>G (p.Thr626Ser)	SDHA (T626S +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223733	NM_004168.4(SDHA):c.1874A>G (p.His625Arg)	SDHA (H544R +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223732	NM_004168.4(SDHA):c.1831C>T (p.Gln611Ter)	SDHA (Q530* +2 more)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3223731	NM_004168.4(SDHA):c.1815T>A (p.Asp605Glu)	SDHA (D524E +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223730	NM_004168.4(SDHA):c.180T>C (p.His60=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3223729	NM_004168.4(SDHA):c.1795-36G>C	SDHA	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223728	NM_004168.4(SDHA):c.1764A>T (p.Ser588=)	SDHA	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3223727	NM_004168.4(SDHA):c.1752A>T (p.Ala584=)	SDHA	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3223726	NM_004168.4(SDHA):c.1701G>A (p.Glu567=)	SDHA	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3223725	NM_004168.4(SDHA):c.167_178del (p.Pro56_Asp59del)	SDHA	Deletion (inframe_deletion)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223724	NM_004168.4(SDHA):c.1664-3C>G	SDHA	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223723	NM_004168.4(SDHA):c.1636C>G (p.Leu546Val)	SDHA (L498V +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223722	NM_004168.4(SDHA):c.1598A>G (p.Gln533Arg)	SDHA (Q485R +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223721	NM_004168.4(SDHA):c.1516A>T (p.Ile506Leu)	SDHA (I458L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223720	NM_004168.4(SDHA):c.1388_1389del (p.Phe463fs)	SDHA (F415fs +1 more)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3223719	NM_004168.4(SDHA):c.1352G>C (p.Arg451Pro)	SDHA (R403P +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223718	NM_004168.4(SDHA):c.1348A>T (p.Asn450Tyr)	SDHA (N402Y +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223717	NM_004168.4(SDHA):c.1316_1330del (p.Gly439_Cys443del)	SDHA	Deletion (inframe_deletion)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223715	NM_004168.4(SDHA):c.1251C>T (p.Tyr417=)	SDHA	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3223714	NM_004168.4(SDHA):c.124A>G (p.Arg42Gly)	SDHA (R42G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223713	NM_004168.4(SDHA):c.1202C>T (p.Pro401Leu)	SDHA (P353L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3223712	NM_004168.4(SDHA):c.1192G>A (p.Glu398Lys)	SDHA (E350K +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance

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