ClinVar for Gene (Select 8648) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3358799	NM_003743.5(NCOA1):c.2145A>T (p.Ala715=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3358771	NM_003743.5(NCOA1):c.1902G>A (p.Val634=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3358717	NM_003743.5(NCOA1):c.2675C>T (p.Thr892Ile)	NCOA1 (T892I)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3358693	NM_003743.5(NCOA1):c.4278C>T (p.Thr1426=)	NCOA1	Single nucleotide variant (3 prime UTR variant +1 more)	NCOA1-related disorder	GLikely benign
Select item 3358673	NM_003743.5(NCOA1):c.1184C>G (p.Ser395Cys)	NCOA1 (S395C)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3358553	NM_003743.5(NCOA1):c.1724T>G (p.Ile575Arg)	NCOA1 (I575R)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3358462	NM_003743.5(NCOA1):c.3601C>T (p.Arg1201Cys)	NCOA1 (R1201C)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3358381	NM_003743.5(NCOA1):c.906T>G (p.Pro302=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3358376	NM_003743.5(NCOA1):c.3292A>T (p.Ile1098Phe)	NCOA1 (I1098F)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3358347	NM_003743.5(NCOA1):c.3996C>A (p.Asn1332Lys)	NCOA1 (N1332K)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3358307	NM_003743.5(NCOA1):c.713-4G>A	NCOA1	Single nucleotide variant (intron variant)	NCOA1-related disorder	GLikely benign
Select item 3358279	NM_003743.5(NCOA1):c.1292A>C (p.His431Pro)	NCOA1 (H431P)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3358209	NM_003743.5(NCOA1):c.1097+4C>T	NCOA1	Single nucleotide variant (intron variant)	NCOA1-related disorder	GLikely benign
Select item 3358201	NM_003743.5(NCOA1):c.2296C>G (p.Leu766Val)	NCOA1 (L766V)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3358200	NM_003743.5(NCOA1):c.3201+7G>A	NCOA1	Single nucleotide variant (intron variant)	NCOA1-related disorder	GLikely benign
Select item 3358140	NM_003743.5(NCOA1):c.202A>C (p.Lys68Gln)	NCOA1 (K68Q)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3358138	NM_003743.5(NCOA1):c.723A>G (p.Ser241=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3358137	NM_003743.5(NCOA1):c.1066C>A (p.Pro356Thr)	NCOA1 (P356T)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3358064	NM_003743.5(NCOA1):c.3914C>T (p.Thr1305Met)	NCOA1 (T1305M)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357961	NM_003743.5(NCOA1):c.3735T>C (p.Phe1245=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3357951	NM_003743.5(NCOA1):c.2039A>G (p.His680Arg)	NCOA1 (H680R)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357922	NM_003743.5(NCOA1):c.1799A>G (p.Asn600Ser)	NCOA1 (N600S)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357917	NM_003743.5(NCOA1):c.2991T>C (p.Ser997=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3357904	NM_003743.5(NCOA1):c.3947G>A (p.Ser1316Asn)	NCOA1 (S1316N)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357898	NM_003743.5(NCOA1):c.3825C>T (p.Ser1275=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3357893	NM_003743.5(NCOA1):c.3282G>C (p.Met1094Ile)	NCOA1 (M1094I)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357884	NM_003743.5(NCOA1):c.-7T>C	NCOA1	Single nucleotide variant (5 prime UTR variant)	NCOA1-related disorder	GLikely benign
Select item 3357714	NM_003743.5(NCOA1):c.1016G>C (p.Ser339Thr)	NCOA1 (S339T)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357636	NM_003743.5(NCOA1):c.2901T>G (p.Asp967Glu)	NCOA1 (D967E)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357598	NM_003743.5(NCOA1):c.2670A>G (p.Pro890=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3357561	NM_003743.5(NCOA1):c.986G>A (p.Arg329Lys)	NCOA1 (R329K)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357536	NM_003743.5(NCOA1):c.578A>G (p.His193Arg)	NCOA1 (H193R)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357532	NM_003743.5(NCOA1):c.649C>T (p.Arg217Cys)	NCOA1 (R217C)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357510	NM_003743.5(NCOA1):c.*3A>G	NCOA1	Single nucleotide variant (3 prime UTR variant)	NCOA1-related disorder	GLikely benign
Select item 3357445	NM_003743.5(NCOA1):c.4075C>T (p.Pro1359Ser)	NCOA1 (P1359S)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357382	NM_003743.5(NCOA1):c.1315G>A (p.Gly439Arg)	NCOA1 (G439R)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357323	NM_003743.5(NCOA1):c.2011T>G (p.Ser671Ala)	NCOA1 (S671A)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357234	NM_003743.5(NCOA1):c.1485T>C (p.Ser495=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3357173	NM_003743.5(NCOA1):c.31C>T (p.Pro11Ser)	NCOA1 (P11S)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3357090	NM_003743.5(NCOA1):c.*8del	NCOA1	Deletion (3 prime UTR variant)	NCOA1-related disorder	GLikely benign
Select item 3357074	NM_003743.5(NCOA1):c.1714A>C (p.Arg572=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3357004	NM_003743.5(NCOA1):c.3915G>A (p.Thr1305=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3356939	NM_003743.5(NCOA1):c.3888C>T (p.Phe1296=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3356842	NM_003743.5(NCOA1):c.1812T>C (p.Asp604=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3356653	NM_003743.5(NCOA1):c.2102A>G (p.Asp701Gly)	NCOA1 (D701G)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3356640	NM_003743.5(NCOA1):c.1485T>G (p.Ser495=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3356503	NM_003743.5(NCOA1):c.3912C>A (p.Pro1304=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3356478	NM_003743.5(NCOA1):c.4211G>C (p.Gly1404Ala)	NCOA1 (G1403A +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	NCOA1-related disorder	GUncertain significance
Select item 3356371	NM_003743.5(NCOA1):c.3673A>T (p.Met1225Leu)	NCOA1 (M1225L)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3356365	NM_003743.5(NCOA1):c.3294T>G (p.Ile1098Met)	NCOA1 (I1098M)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3356295	NM_003743.5(NCOA1):c.3304-3C>T	NCOA1	Single nucleotide variant (intron variant)	NCOA1-related disorder	GLikely benign
Select item 3356268	NM_003743.5(NCOA1):c.3977C>T (p.Thr1326Met)	NCOA1 (T1326M)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3356252	NM_003743.5(NCOA1):c.1791A>C (p.Gln597His)	NCOA1 (Q597H)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3356042	NM_003743.5(NCOA1):c.2018G>A (p.Gly673Glu)	NCOA1 (G673E)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3356025	NM_003743.5(NCOA1):c.28G>A (p.Asp10Asn)	NCOA1 (D10N)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3355859	NM_003743.5(NCOA1):c.3033G>T (p.Met1011Ile)	NCOA1 (M1011I)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3355823	NM_003743.5(NCOA1):c.1324G>A (p.Gly442Arg)	NCOA1 (G442R)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3355563	NM_003743.5(NCOA1):c.1868A>G (p.Asp623Gly)	NCOA1 (D623G)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3355502	NM_003743.5(NCOA1):c.2137G>T (p.Asp713Tyr)	NCOA1 (D713Y)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3355431	NM_003743.5(NCOA1):c.3828G>A (p.Gly1276=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3355421	NM_003743.5(NCOA1):c.2934A>C (p.Ala978=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3355161	NM_003743.5(NCOA1):c.3929G>C (p.Gly1310Ala)	NCOA1 (G1310A)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3355145	NM_003743.5(NCOA1):c.2936C>T (p.Thr979Met)	NCOA1 (T979M)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3355120	NM_003743.5(NCOA1):c.1394_1396dup (p.Ser465_Asn466insSer)	NCOA1	Duplication (inframe_insertion)	NCOA1-related disorder	GUncertain significance
Select item 3355063	NM_003743.5(NCOA1):c.1180A>G (p.Ile394Val)	NCOA1 (I394V)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3355011	NM_003743.5(NCOA1):c.3552C>T (p.Thr1184=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3354950	NM_003743.5(NCOA1):c.1948A>G (p.Ile650Val)	NCOA1 (I650V)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3354879	NM_003743.5(NCOA1):c.3488C>T (p.Ala1163Val)	NCOA1 (A1163V)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3354869	NM_003743.5(NCOA1):c.3557C>T (p.Pro1186Leu)	NCOA1 (P1186L)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3354844	NM_003743.5(NCOA1):c.1275C>A (p.Asp425Glu)	NCOA1 (D425E)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3354666	NM_003743.5(NCOA1):c.2398A>G (p.Lys800Glu)	NCOA1 (K800E)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3354557	NM_003743.5(NCOA1):c.924T>G (p.Ser308=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3354522	NM_003743.5(NCOA1):c.89+3A>G	NCOA1	Single nucleotide variant (intron variant)	NCOA1-related disorder	GLikely benign
Select item 3354367	NM_003743.5(NCOA1):c.2323G>A (p.Val775Met)	NCOA1 (V775M)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3354288	NM_003743.5(NCOA1):c.3660A>G (p.Gly1220=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3354043	NM_003743.5(NCOA1):c.1038T>C (p.Leu346=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3353912	NM_003743.5(NCOA1):c.4207G>T (p.Val1403Leu)	NCOA1 (V1402L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	NCOA1-related disorder	GUncertain significance
Select item 3353849	NM_003743.5(NCOA1):c.222C>T (p.Val74=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3353845	NM_003743.5(NCOA1):c.66G>A (p.Ser22=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3353837	NM_003743.5(NCOA1):c.2010C>T (p.Asn670=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3353797	NM_003743.5(NCOA1):c.6T>C (p.Ser2=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3353747	NM_003743.5(NCOA1):c.1670G>C (p.Ser557Thr)	NCOA1 (S557T)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3353730	NM_003743.5(NCOA1):c.4155+7A>G	NCOA1	Single nucleotide variant (intron variant)	NCOA1-related disorder	GLikely benign
Select item 3353540	NM_003743.5(NCOA1):c.1047T>C (p.Pro349=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3353236	NM_003743.5(NCOA1):c.3148G>A (p.Ala1050Thr)	NCOA1 (A1050T)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3353199	NM_003743.5(NCOA1):c.2922A>G (p.Pro974=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3352949	NM_003743.5(NCOA1):c.3143C>T (p.Pro1048Leu)	NCOA1 (P1048L)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3352721	NM_003743.5(NCOA1):c.2995_2997del (p.Ser999del)	NCOA1 (S999del)	Deletion (inframe_deletion)	NCOA1-related disorder	GUncertain significance
Select item 3352659	NM_003743.5(NCOA1):c.3822C>T (p.Ala1274=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3352258	NM_003743.5(NCOA1):c.3090T>G (p.Gly1030=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3352238	NM_003743.5(NCOA1):c.531A>G (p.Leu177=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3352229	NM_003743.5(NCOA1):c.4213G>A (p.Gly1405Arg)	NCOA1 (G1404R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	NCOA1-related disorder	GUncertain significance
Select item 3352166	NM_003743.5(NCOA1):c.3085C>T (p.Arg1029Ter)	NCOA1 (R1029*)	Single nucleotide variant (nonsense)	NCOA1-related disorder	GUncertain significance
Select item 3352047	NM_003743.5(NCOA1):c.651T>G (p.Arg217=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3351716	NM_003743.5(NCOA1):c.99G>A (p.Lys33=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3351673	NM_003743.5(NCOA1):c.2002T>A (p.Ser668Thr)	NCOA1 (S668T)	Single nucleotide variant (missense variant)	NCOA1-related disorder	GUncertain significance
Select item 3351572	NM_003743.5(NCOA1):c.1866A>G (p.Gly622=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3351505	NM_003743.5(NCOA1):c.1791A>G (p.Gln597=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3351387	NM_003743.5(NCOA1):c.297C>T (p.Ile99=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign
Select item 3351360	NM_003743.5(NCOA1):c.432A>G (p.Leu144=)	NCOA1	Single nucleotide variant (synonymous variant)	NCOA1-related disorder	GLikely benign

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