ClinVar for Gene (Select 23309) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3368355	NM_001297595.2(SIN3B):c.1906C>G (p.Leu636Val)	SIN3B (L226V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368129	NM_001297595.2(SIN3B):c.2027C>T (p.Ala676Val)	SIN3B (A266V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3365848	NM_001297595.2(SIN3B):c.3001del (p.Ala1001fs)	SIN3B (A1001fs +2 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 3365698	NM_001297595.2(SIN3B):c.908G>A (p.Gly303Glu)	SIN3B (G303E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3365068	NM_001297595.2(SIN3B):c.2845C>T (p.Pro949Ser)	SIN3B (P539S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3364875	NM_001297595.2(SIN3B):c.1381G>A (p.Glu461Lys)	SIN3B (E461K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3364786	NM_001297595.2(SIN3B):c.2063C>T (p.Pro688Leu)	SIN3B (P278L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3364774	NM_001297595.2(SIN3B):c.2727G>T (p.Trp909Cys)	SIN3B (W499C +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3363655	NM_001297595.2(SIN3B):c.2069G>A (p.Gly690Glu)	SIN3B (G280E +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361651	NM_001297595.2(SIN3B):c.676G>A (p.Asp226Asn)	SIN3B (D226N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361513	NM_001297595.2(SIN3B):c.2635G>A (p.Glu879Lys)	SIN3B (E469K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3360684	NM_001297595.2(SIN3B):c.3129G>A (p.Met1043Ile)	SIN3B (M1043I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3360333	NM_001297595.2(SIN3B):c.2240A>G (p.Asn747Ser)	SIN3B (N337S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3357517	NM_001297595.2(SIN3B):c.1122G>A (p.Ala374=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3355798	NM_001297595.2(SIN3B):c.3162+5C>T	SIN3B	Single nucleotide variant (intron variant)	SIN3B-related disorder	GLikely benign
Select item 3353091	NM_001297595.2(SIN3B):c.984C>T (p.Leu328=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3352868	NM_001297595.2(SIN3B):c.1807-8C>A	SIN3B	Single nucleotide variant (intron variant)	SIN3B-related disorder	GLikely benign
Select item 3343801	NM_001297595.2(SIN3B):c.1481T>A (p.Phe494Tyr)	SIN3B (F494Y +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3342777	NM_001297595.2(SIN3B):c.25G>T (p.Gly9Cys)	SIN3B (G9C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3341018	NM_001297595.2(SIN3B):c.1376G>A (p.Arg459His)	SIN3B (R459H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3318562	NM_001297595.2(SIN3B):c.2875G>C (p.Val959Leu)	SIN3B (V991L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318561	NM_001297595.2(SIN3B):c.2996C>T (p.Ala999Val)	SIN3B (A1031V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3318560	NM_001297595.2(SIN3B):c.2684C>T (p.Ser895Phe)	SIN3B (S895F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318559	NM_001297595.2(SIN3B):c.2177C>T (p.Pro726Leu)	SIN3B (P316L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318558	NM_001297595.2(SIN3B):c.478G>A (p.Val160Met)	SIN3B (V160M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318557	NM_001297595.2(SIN3B):c.1838C>T (p.Ala613Val)	SIN3B (A613V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3251109	NM_001297595.2(SIN3B):c.43G>C (p.Gly15Arg)	SIN3B (G15R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3162340	NM_001297595.2(SIN3B):c.965A>G (p.Glu322Gly)	SIN3B (E322G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162339	NM_001297595.2(SIN3B):c.844G>A (p.Ala282Thr)	SIN3B (A282T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162338	NM_001297595.2(SIN3B):c.832G>A (p.Val278Met)	SIN3B (V278M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162337	NM_001297595.2(SIN3B):c.764A>C (p.Gln255Pro)	SIN3B (Q255P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162336	NM_001297595.2(SIN3B):c.756C>G (p.His252Gln)	SIN3B (H252Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162335	NM_001297595.2(SIN3B):c.421A>C (p.Lys141Gln)	SIN3B (K141Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162334	NM_001297595.2(SIN3B):c.3350C>T (p.Thr1117Ile)	SIN3B (T1149I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162333	NM_001297595.2(SIN3B):c.31A>C (p.Ser11Arg)	SIN3B (S11R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162332	NM_001297595.2(SIN3B):c.3046G>A (p.Val1016Met)	SIN3B (V1016M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162331	NM_001297595.2(SIN3B):c.3017C>T (p.Ala1006Val)	SIN3B (A1006V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162330	NM_001297595.2(SIN3B):c.3007C>T (p.Arg1003Cys)	SIN3B (R1035C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162329	NM_001297595.2(SIN3B):c.2912C>T (p.Ser971Leu)	SIN3B (S561L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162328	NM_001297595.2(SIN3B):c.2870G>A (p.Arg957Gln)	SIN3B (R547Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162327	NM_001297595.2(SIN3B):c.271C>T (p.His91Tyr)	SIN3B (H91Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162326	NM_001297595.2(SIN3B):c.2372G>A (p.Arg791His)	SIN3B (R823H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162325	NM_001297595.2(SIN3B):c.2195C>T (p.Pro732Leu)	SIN3B (P322L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162324	NM_001297595.2(SIN3B):c.2144C>A (p.Ala715Asp)	SIN3B (A305D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162323	NM_001297595.2(SIN3B):c.1664G>C (p.Gly555Ala)	SIN3B (G587A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162322	NM_001297595.2(SIN3B):c.16G>A (p.Gly6Ser)	SIN3B (G6S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162321	NM_001297595.2(SIN3B):c.1496C>A (p.Ser499Tyr)	SIN3B (S499Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162320	NM_001297595.2(SIN3B):c.1403C>T (p.Thr468Met)	SIN3B (T468M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162319	NM_001297595.2(SIN3B):c.1340C>T (p.Pro447Leu)	SIN3B (P37L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162318	NM_001297595.2(SIN3B):c.1160G>A (p.Arg387Gln)	SIN3B (R387Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062393	GRCh37/hg19 19p13.13-13.11(chr19:13970692-18139376)x3	CYP4F8, DCAF15 +109 more	Copy number gain	not specified	GUncertain significance
Select item 3062387	GRCh37/hg19 19p13.11(chr19:16857649-17423590)x3	NR2F6, NWD1 +13 more	Copy number gain	not specified	GUncertain significance
Select item 3055351	NM_001297595.2(SIN3B):c.1452T>C (p.Ser484=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GBenign
Select item 3053118	NM_001297595.2(SIN3B):c.2423-4G>A	SIN3B	Single nucleotide variant (intron variant)	SIN3B-related disorder	GLikely benign
Select item 3052153	NM_001297595.2(SIN3B):c.759C>T (p.Ser253=)	SIN3B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3049595	NM_001297595.2(SIN3B):c.1389C>T (p.Asp463=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3044602	NM_001297595.2(SIN3B):c.1120G>A (p.Ala374Thr)	SIN3B (A374T)	Single nucleotide variant (missense variant)	SIN3B-related disorder	GLikely benign
Select item 3044305	NM_001297595.2(SIN3B):c.2184G>A (p.Pro728=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3042916	NM_001297595.2(SIN3B):c.2031C>T (p.Ser677=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3042581	NM_001297595.2(SIN3B):c.2955-7C>T	SIN3B	Single nucleotide variant (intron variant)	SIN3B-related disorder	GLikely benign
Select item 3041466	NM_001297595.2(SIN3B):c.2204C>T (p.Pro735Leu)	SIN3B (P325L +2 more)	Single nucleotide variant (missense variant)	SIN3B-related disorder	GBenign
Select item 3041154	NM_001297595.2(SIN3B):c.2523C>T (p.Arg841=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3040879	NM_001297595.2(SIN3B):c.365C>T (p.Ser122Leu)	SIN3B (S122L)	Single nucleotide variant (missense variant)	SIN3B-related disorder	GLikely benign
Select item 3040221	NM_001297595.2(SIN3B):c.1509G>A (p.Thr503=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3040128	NM_001297595.2(SIN3B):c.1599C>T (p.Thr533=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3036137	NM_001297595.2(SIN3B):c.1848C>T (p.Ser616=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3034782	NM_001297595.2(SIN3B):c.576G>A (p.Thr192=)	SIN3B	Single nucleotide variant (synonymous variant)	SIN3B-related disorder	GLikely benign
Select item 3034407	NM_001297595.2(SIN3B):c.2102C>T (p.Pro701Leu)	SIN3B (P291L +2 more)	Single nucleotide variant (missense variant)	SIN3B-related disorder	GLikely benign
Select item 2827167	NM_001297595.2(SIN3B):c.771C>A (p.Asn257Lys)	SIN3B (N257K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2752222	NM_001297595.2(SIN3B):c.92C>T (p.Ser31Phe)	SIN3B (S31F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2684887	GRCh37/hg19 19p13.12-13.11(chr19:14888106-17360864)x3	ADGRE2, AKAP8 +55 more	Copy number gain	not provided	GUncertain significance
Select item 2663145	NM_001297595.2(SIN3B):c.203T>C (p.Ile68Thr)	SIN3B (I68T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2662332	NM_001297595.2(SIN3B):c.2408G>C (p.Arg803Pro)	SIN3B (R393P +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2649522	NM_001297595.2(SIN3B):c.3218G>A (p.Arg1073His)	SIN3B (R1073H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2649521	NM_001297595.2(SIN3B):c.1941C>T (p.Ile647=)	SIN3B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2637120	NM_001297595.2(SIN3B):c.731C>G (p.Thr244Arg)	SIN3B (T244R)	Single nucleotide variant (missense variant)	SIN3B-related disorder	GUncertain significance
Select item 2631283	NM_001297595.2(SIN3B):c.2340G>T (p.Glu780Asp)	SIN3B (E370D +2 more)	Single nucleotide variant (missense variant)	SIN3B-related disorder	GUncertain significance
Select item 2609043	NM_001297595.2(SIN3B):c.2794G>T (p.Val932Leu)	SIN3B (V522L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604751	NM_001297595.2(SIN3B):c.137C>G (p.Thr46Ser)	SIN3B (T46S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595827	NM_001297595.2(SIN3B):c.1562C>T (p.Pro521Leu)	SIN3B (P521L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2580026	NM_001297595.2(SIN3B):c.841C>G (p.Pro281Ala)	SIN3B (P281A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2578318	NM_001297595.2(SIN3B):c.2785_2786delinsTC (p.Lys929Ser)	SIN3B (K519S +2 more)	Indel (missense variant)	not provided	GUncertain significance
Select item 2562079	NM_001297595.2(SIN3B):c.2910C>G (p.Ser970Arg)	SIN3B (S970R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548728	NM_001297595.2(SIN3B):c.742C>T (p.Pro248Ser)	SIN3B (P248S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514908	NM_001297595.2(SIN3B):c.3008G>A (p.Arg1003His)	SIN3B (R1003H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514525	NM_001297595.2(SIN3B):c.291T>G (p.Ile97Met)	SIN3B (I97M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510263	NM_001297595.2(SIN3B):c.1880G>A (p.Arg627Gln)	SIN3B (R217Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2504803	NM_001297595.2(SIN3B):c.1412C>G (p.Ala471Gly)	SIN3B (A471G +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2504758	NM_001297595.2(SIN3B):c.3178C>A (p.Leu1060Met)	SIN3B (L1060M +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2504747	NM_001297595.2(SIN3B):c.3089C>G (p.Thr1030Ser)	SIN3B (T1030S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2504442	NM_001297595.2(SIN3B):c.286C>T (p.Leu96Phe)	SIN3B (L96F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2504384	NM_001297595.2(SIN3B):c.2467G>T (p.Val823Leu)	SIN3B (V413L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2497827	NM_001297595.2(SIN3B):c.1954C>G (p.Gln652Glu)	SIN3B (Q242E +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2495028	NM_001297595.2(SIN3B):c.1219A>G (p.Thr407Ala)	SIN3B (T407A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485879	NM_001297595.2(SIN3B):c.788C>T (p.Pro263Leu)	SIN3B (P263L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2471707	NM_001297595.2(SIN3B):c.1492G>A (p.Asp498Asn)	SIN3B (D88N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469610	NM_001297595.2(SIN3B):c.3289G>A (p.Glu1097Lys)	SIN3B (E1129K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2442605	NM_001297595.2(SIN3B):c.599C>A (p.Thr200Lys)	SIN3B (T200K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2442439	NM_001297595.2(SIN3B):c.823C>T (p.Leu275Phe)	SIN3B (L275F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2425869	NC_000019.9:g.(?_14847048)_(17394124_?)del	ADGRE2, AKAP8 +57 more	Deletion	not provided	GUncertain significance

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