ClinVar for Gene (Select 57690) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3327773	NM_001142640.2(TNRC6C):c.1258A>G (p.Met420Val)	TNRC6C (M210V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327772	NM_001142640.2(TNRC6C):c.908A>G (p.Asn303Ser)	TNRC6C (N303S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327771	NM_001142640.2(TNRC6C):c.2128A>G (p.Ser710Gly)	TNRC6C (S710G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327770	NM_001142640.2(TNRC6C):c.4201A>C (p.Asn1401His)	TNRC6C (N1401H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327769	NM_001142640.2(TNRC6C):c.4396C>G (p.Pro1466Ala)	TNRC6C (P1264A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327768	NM_001142640.2(TNRC6C):c.4906C>T (p.Arg1636Cys)	TNRC6C (R1429C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327767	NM_001142640.2(TNRC6C):c.4401C>A (p.Asn1467Lys)	TNRC6C (N1257K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327766	NM_001142640.2(TNRC6C):c.2531C>T (p.Thr844Met)	TNRC6C (T634M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327765	NM_001142640.2(TNRC6C):c.1517A>G (p.Asn506Ser)	TNRC6C (N296S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327764	NM_001142640.2(TNRC6C):c.1514G>C (p.Gly505Ala)	TNRC6C (G295A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327762	NM_001142640.2(TNRC6C):c.1508G>A (p.Ser503Asn)	TNRC6C (S293N +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3327761	NM_001142640.2(TNRC6C):c.1321T>A (p.Ser441Thr)	TNRC6C (S231T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327760	NM_001142640.2(TNRC6C):c.5038G>A (p.Val1680Ile)	TNRC6C (V1478I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3327759	NM_001142640.2(TNRC6C):c.4939C>A (p.Pro1647Thr)	TNRC6C (P1437T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3327758	NM_001142640.2(TNRC6C):c.2725G>A (p.Val909Ile)	TNRC6C (V699I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327757	NM_001142640.2(TNRC6C):c.1877C>T (p.Thr626Met)	TNRC6C (T416M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327756	NM_001142640.2(TNRC6C):c.5566G>A (p.Ala1856Thr)	TNRC6C (A1610T +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327755	NM_001142640.2(TNRC6C):c.2717C>T (p.Pro906Leu)	TNRC6C (P696L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327752	NM_001142640.2(TNRC6C):c.4303C>G (p.Pro1435Ala)	TNRC6C (P1233A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327751	NM_001142640.2(TNRC6C):c.1753G>A (p.Val585Ile)	TNRC6C (V585I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180777	NM_001142640.2(TNRC6C):c.1621C>G (p.Pro541Ala)	TNRC6C (P541A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180776	NM_001142640.2(TNRC6C):c.712G>A (p.Val238Ile)	TNRC6C (V238I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180775	NM_001142640.2(TNRC6C):c.701A>G (p.Asn234Ser)	TNRC6C (N234S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180773	NM_001142640.2(TNRC6C):c.1175A>G (p.Asp392Gly)	TNRC6C (D182G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180772	NM_001142640.2(TNRC6C):c.1150G>A (p.Ala384Thr)	TNRC6C (A174T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180771	NM_001142640.2(TNRC6C):c.5734G>A (p.Asp1912Asn)	TNRC6C (D1663N +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180770	NM_001142640.2(TNRC6C):c.5531C>G (p.Ala1844Gly)	TNRC6C (A1595G +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180768	NM_001142640.2(TNRC6C):c.5529G>T (p.Gln1843His)	TNRC6C (Q1594H +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180767	NM_001142640.2(TNRC6C):c.5029G>A (p.Ala1677Thr)	TNRC6C (A1475T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3180766	NM_001142640.2(TNRC6C):c.1055G>T (p.Gly352Val)	TNRC6C (G352V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180765	NM_001142640.2(TNRC6C):c.1054G>A (p.Gly352Arg)	TNRC6C (G142R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180764	NM_001142640.2(TNRC6C):c.4727G>A (p.Arg1576His)	TNRC6C (R1374H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180763	NM_001142640.2(TNRC6C):c.4702G>A (p.Val1568Ile)	TNRC6C (V1361I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180761	NM_001142640.2(TNRC6C):c.4532A>G (p.Asn1511Ser)	TNRC6C (N1304S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180760	NM_001142640.2(TNRC6C):c.1018G>A (p.Val340Ile)	TNRC6C (V340I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180759	NM_001142640.2(TNRC6C):c.4490C>T (p.Pro1497Leu)	TNRC6C (P1497L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180758	NM_001142640.2(TNRC6C):c.4433A>G (p.Asn1478Ser)	TNRC6C (N1271S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180756	NM_001142640.2(TNRC6C):c.4192A>T (p.Thr1398Ser)	TNRC6C (T1398S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180755	NM_001142640.2(TNRC6C):c.982G>A (p.Val328Met)	TNRC6C (V328M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180754	NM_001142640.2(TNRC6C):c.976G>A (p.Gly326Arg)	TNRC6C (G326R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180753	NM_001142640.2(TNRC6C):c.4072T>A (p.Leu1358Met)	TNRC6C (L1358M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180751	NM_001142640.2(TNRC6C):c.3574C>T (p.Arg1192Cys)	TNRC6C (R982C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180750	NM_001142640.2(TNRC6C):c.3515A>G (p.Asn1172Ser)	TNRC6C (N965S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180749	NM_001142640.2(TNRC6C):c.3346A>G (p.Ser1116Gly)	TNRC6C (S1116G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180748	NM_001142640.2(TNRC6C):c.3250G>A (p.Glu1084Lys)	TNRC6C (E1084K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180747	NM_001142640.2(TNRC6C):c.3133C>G (p.Pro1045Ala)	TNRC6C (P838A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180745	NM_001142640.2(TNRC6C):c.3113C>T (p.Thr1038Ile)	TNRC6C (T1038I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180744	NM_001142640.2(TNRC6C):c.2960C>T (p.Thr987Met)	TNRC6C (T777M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180743	NM_001142640.2(TNRC6C):c.2933C>T (p.Thr978Met)	TNRC6C (T768M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180742	NM_001142640.2(TNRC6C):c.2879C>A (p.Pro960Gln)	TNRC6C (P750Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180740	NM_001142640.2(TNRC6C):c.2798A>G (p.Glu933Gly)	TNRC6C (E723G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180739	NM_001142640.2(TNRC6C):c.2735A>G (p.Lys912Arg)	TNRC6C (K912R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180738	NM_001142640.2(TNRC6C):c.2699C>T (p.Thr900Ile)	TNRC6C (T900I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180737	NM_001142640.2(TNRC6C):c.2595G>C (p.Trp865Cys)	TNRC6C (W655C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180736	NM_001142640.2(TNRC6C):c.2236G>C (p.Val746Leu)	TNRC6C (V536L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180735	NM_001142640.2(TNRC6C):c.2192C>A (p.Thr731Lys)	TNRC6C (T731K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180734	NM_001142640.2(TNRC6C):c.2099G>A (p.Gly700Glu)	TNRC6C (G490E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180733	NM_001142640.2(TNRC6C):c.775G>T (p.Ala259Ser)	TNRC6C (A49S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180732	NM_001142640.2(TNRC6C):c.2042A>T (p.Lys681Ile)	TNRC6C (K681I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180731	NM_001142640.2(TNRC6C):c.1984A>G (p.Thr662Ala)	TNRC6C (T452A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180730	NM_001142640.2(TNRC6C):c.1873G>C (p.Gly625Arg)	TNRC6C (G415R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180729	NM_001142640.2(TNRC6C):c.1856G>T (p.Gly619Val)	TNRC6C (G409V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3025162	NM_001142640.2(TNRC6C):c.1367A>G (p.Asn456Ser)	TNRC6C (N246S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2648335	NM_001142640.2(TNRC6C):c.3249A>G (p.Gln1083=)	TNRC6C	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2648334	NM_001142640.2(TNRC6C):c.2996G>T (p.Arg999Leu)	TNRC6C (R789L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2648333	NM_001142640.2(TNRC6C):c.875G>A (p.Arg292Lys)	TNRC6C (R292K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2621395	NM_001142640.2(TNRC6C):c.2681C>T (p.Ser894Phe)	TNRC6C (S684F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618817	NM_001142640.2(TNRC6C):c.5507A>G (p.Asn1836Ser)	TNRC6C (N1626S +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611907	NM_001142640.2(TNRC6C):c.1758G>T (p.Gln586His)	TNRC6C (Q376H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593465	NM_001142640.2(TNRC6C):c.5257G>A (p.Asp1753Asn)	TNRC6C (D1504N +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570011	NM_001142640.2(TNRC6C):c.2723C>T (p.Pro908Leu)	TNRC6C (P698L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558107	NM_001142640.2(TNRC6C):c.4841C>T (p.Pro1614Leu)	TNRC6C (P1404L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549682	NM_001142640.2(TNRC6C):c.4928G>C (p.Gly1643Ala)	TNRC6C (G1643A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541362	NM_001142640.2(TNRC6C):c.3941G>T (p.Ser1314Ile)	TNRC6C (S1314I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539143	NM_001142640.2(TNRC6C):c.1063A>T (p.Thr355Ser)	TNRC6C (T145S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524496	NM_001142640.2(TNRC6C):c.4714C>T (p.His1572Tyr)	TNRC6C (H1365Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518262	NM_001142640.2(TNRC6C):c.3345A>C (p.Glu1115Asp)	TNRC6C (E908D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516952	NM_001142640.2(TNRC6C):c.4970C>T (p.Ser1657Leu)	TNRC6C (S1657L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495752	NM_001142640.2(TNRC6C):c.4405T>C (p.Phe1469Leu)	TNRC6C (F1259L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493516	NM_001142640.2(TNRC6C):c.5600G>A (p.Ser1867Asn)	TNRC6C (S1618N +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488139	NM_001142640.2(TNRC6C):c.1735A>G (p.Thr579Ala)	TNRC6C (T579A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488005	NM_001142640.2(TNRC6C):c.5101G>A (p.Ala1701Thr)	TNRC6C (A1499T +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487487	NM_001142640.2(TNRC6C):c.2823G>C (p.Trp941Cys)	TNRC6C (W941C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485106	NM_001142640.2(TNRC6C):c.5280C>G (p.Ser1760Arg)	TNRC6C (S1721R +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481011	NM_001142640.2(TNRC6C):c.2602A>C (p.Thr868Pro)	TNRC6C (T658P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479141	NM_001142640.2(TNRC6C):c.4064T>C (p.Met1355Thr)	TNRC6C (M1145T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468185	NM_001142640.2(TNRC6C):c.2099G>T (p.Gly700Val)	TNRC6C (G490V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468060	NM_001142640.2(TNRC6C):c.2339C>T (p.Thr780Ile)	TNRC6C (T570I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467360	NM_001142640.2(TNRC6C):c.851T>C (p.Met284Thr)	TNRC6C (M284T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466295	NM_001142640.2(TNRC6C):c.5720C>T (p.Pro1907Leu)	TNRC6C (P1661L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457101	NM_001142640.2(TNRC6C):c.1214A>G (p.Asn405Ser)	TNRC6C (N195S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456959	NM_001142640.2(TNRC6C):c.4255G>A (p.Val1419Met)	TNRC6C (V1209M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407859	NM_001142640.2(TNRC6C):c.865G>A (p.Gly289Arg)	TNRC6C (G289R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401200	NM_001142640.2(TNRC6C):c.5762C>T (p.Pro1921Leu)	TNRC6C (P1675L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396754	NM_001142640.2(TNRC6C):c.3341A>G (p.Gln1114Arg)	TNRC6C (Q1114R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394101	NM_001142640.2(TNRC6C):c.3162C>A (p.His1054Gln)	TNRC6C (H844Q +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2391606	NM_001142640.2(TNRC6C):c.2092A>G (p.Asn698Asp)	TNRC6C (N488D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388590	NM_001142640.2(TNRC6C):c.5623G>A (p.Asp1875Asn)	TNRC6C (D1844N +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383184	NM_001142640.2(TNRC6C):c.4640T>C (p.Ile1547Thr)	TNRC6C (I1337T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379951	NM_001142640.2(TNRC6C):c.1537C>T (p.Pro513Ser)	TNRC6C (P513S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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