SCN3B[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 303125	NM_001040151.2(SCN3B):c.*4588T>C	SCN3B	Single nucleotide variant (3 prime UTR variant)	Brugada syndrome	GUncertain significance
Select item 303146	NM_001040151.2(SCN3B):c.*2795GAA[1]	SCN3B	Microsatellite (3 prime UTR variant)	Brugada syndrome	GUncertain significance
Select item 303154	NM_001040151.2(SCN3B):c.*2366G>A	SCN3B	Single nucleotide variant (3 prime UTR variant)	Brugada syndrome	GUncertain significance
Select item 303161	NM_001040151.2(SCN3B):c.*1948TATT[2]	SCN3B	Microsatellite (3 prime UTR variant)	Brugada syndrome	GUncertain significance
Select item 303178	NM_001040151.2(SCN3B):c.*1007dup	SCN3B	Duplication (3 prime UTR variant)	Brugada syndrome	GUncertain significance
Select item 303187	NM_001040151.2(SCN3B):c.*509G>A	SCN3B	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 303188	NM_001040151.2(SCN3B):c.*447C>A	SCN3B	Single nucleotide variant (3 prime UTR variant)	Brugada syndrome	GUncertain significance
Select item 1235607	NM_001040151.2(SCN3B):c.*153C>T	SCN3B	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1273376	NM_001040151.2(SCN3B):c.*26G>A	SCN3B	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 392040	NM_001040151.2(SCN3B):c.*23-15T>A	SCN3B	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 671838	NM_001040151.2(SCN3B):c.*22+156G>C	SCN3B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 139035	NM_001040151.2(SCN3B):c.*22+16A>C	SCN3B	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 574131	NM_001040151.2(SCN3B):c.632T>G (p.Val211Gly)	SCN3B (V211G)	Single nucleotide variant (missense variant)	Brugada syndrome 7	GUncertain significance
Select item 2563488	NM_001040151.2(SCN3B):c.631G>A (p.Val211Ile)	SCN3B (V211I)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1086381	NM_001040151.2(SCN3B):c.630G>A (p.Ala210=)	SCN3B	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 190884	NM_001040151.2(SCN3B):c.629C>T (p.Ala210Val)	SCN3B (A210V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 1752650	NM_001040151.2(SCN3B):c.628G>A (p.Ala210Thr)	SCN3B (A210T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2964160	NM_001040151.2(SCN3B):c.624C>T (p.Asn208=)	SCN3B	Single nucleotide variant (synonymous variant)	Brugada syndrome 7	GLikely benign
Select item 3227135	NM_001040151.2(SCN3B):c.621G>A (p.Glu207=)	SCN3B	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1956227	NM_001040151.2(SCN3B):c.618G>C (p.Lys206Asn)	SCN3B (K206N)	Single nucleotide variant (missense variant)	Brugada syndrome 7	GUncertain significance
Select item 426980	NM_001040151.2(SCN3B):c.614A>G (p.Asn205Ser)	SCN3B (N205S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 2497037	NM_001040151.2(SCN3B):c.608C>T (p.Ser203Phe)	SCN3B (S203F)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2153493	NM_001040151.2(SCN3B):c.601A>G (p.Ile201Val)	SCN3B (I201V)	Single nucleotide variant (missense variant)	Brugada syndrome 7	GUncertain significance
Select item 3227134	NM_001040151.2(SCN3B):c.597T>C (p.Leu199=)	SCN3B	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 519417	NM_001040151.2(SCN3B):c.591dup (p.Tyr198fs)	SCN3B (Y198fs)	Duplication (frameshift variant)	Cardiovascular phenotype	GUncertain significance
Select item 222800	NM_001040151.2(SCN3B):c.587C>G (p.Ser196Cys)	SCN3B (S196C)	Single nucleotide variant (missense variant)	Sudden cardiac death	GUncertain significance
Select item 2184067	NM_001040151.2(SCN3B):c.585-1G>C	SCN3B	Single nucleotide variant (splice acceptor variant)	Brugada syndrome 7	GUncertain significance
Select item 1677762	NM_001040151.2(SCN3B):c.585-2A>G	SCN3B	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 519377	NM_001040151.2(SCN3B):c.585-4A>G	SCN3B	Single nucleotide variant (intron variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 1613444	NM_001040151.2(SCN3B):c.585-16C>T	SCN3B	Single nucleotide variant (intron variant)	Brugada syndrome 7	GLikely benign
Select item 670950	NM_001040151.2(SCN3B):c.585-45G>C	SCN3B	Single nucleotide variant (intron variant)	Brugada syndrome 7 +1 more	GBenign
Select item 672213	NM_001040151.2(SCN3B):c.585-130T>C	SCN3B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1210765	NM_001040151.2(SCN3B):c.585-156A>G	SCN3B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 671837	NM_001040151.2(SCN3B):c.585-185G>A	SCN3B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1193693	NM_001040151.2(SCN3B):c.585-190T>A	SCN3B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 675388	NM_001040151.2(SCN3B):c.584+206C>A	SCN3B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 670949	NM_001040151.2(SCN3B):c.584+130C>T	SCN3B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 670948	NM_001040151.2(SCN3B):c.584+91C>T	SCN3B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 675387	NM_001040151.2(SCN3B):c.584+52T>C	SCN3B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 380685	NM_001040151.2(SCN3B):c.584+12G>A	SCN3B	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 1640661	NM_001040151.2(SCN3B):c.584+9A>C	SCN3B	Single nucleotide variant (intron variant)	Brugada syndrome 7	GLikely benign
Select item 1484460	NM_001040151.2(SCN3B):c.584+2dup	SCN3B	Duplication (splice donor variant)	Brugada syndrome 7	GUncertain significance
Select item 3227133	NM_001040151.2(SCN3B):c.584+1G>A	SCN3B	Single nucleotide variant (splice donor variant)	Cardiovascular phenotype	GUncertain significance
Select item 1931405	NM_001040151.2(SCN3B):c.584C>T (p.Ala195Val)	SCN3B (A195V)	Single nucleotide variant (missense variant)	Brugada syndrome 7	GUncertain significance
Select item 642346	NM_001040151.2(SCN3B):c.583G>A (p.Ala195Thr)	SCN3B (A195T)	Single nucleotide variant (missense variant)	Brugada syndrome 7 +3 more	GConflicting classifications of pathogenicity
Select item 190883	NM_001040151.2(SCN3B):c.582C>T (p.Asn194=)	SCN3B	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 1749428	NM_001040151.2(SCN3B):c.574C>G (p.Gln192Glu)	SCN3B (Q192E)	Single nucleotide variant (missense variant)	Brugada syndrome 7 +1 more	GUncertain significance
Select item 1129101	NM_001040151.2(SCN3B):c.570A>G (p.Ala190=)	SCN3B	Single nucleotide variant (synonymous variant)	Brugada syndrome 7 +1 more	GLikely benign
Select item 994414	NM_001040151.2(SCN3B):c.568G>A (p.Ala190Thr)	SCN3B (A190T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2448565	NM_001040151.2(SCN3B):c.565G>A (p.Glu189Lys)	SCN3B (E189K)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1748746	NM_001040151.2(SCN3B):c.562G>A (p.Glu188Lys)	SCN3B (E188K)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1152790	NM_001040151.2(SCN3B):c.561C>T (p.Ala187=)	SCN3B	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1937416	NM_001040151.2(SCN3B):c.541T>A (p.Tyr181Asn)	SCN3B (Y181N)	Single nucleotide variant (missense variant)	Brugada syndrome 7	GUncertain significance
Select item 519216	NM_001040151.2(SCN3B):c.537T>C (p.Tyr179=)	SCN3B	Single nucleotide variant (synonymous variant)	Brugada syndrome 7 +1 more	GBenign/Likely benign
Select item 1747068	NM_001040151.2(SCN3B):c.535T>C (p.Tyr179His)	SCN3B (Y179H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 2714526	NM_001040151.2(SCN3B):c.525C>T (p.Ile175=)	SCN3B	Single nucleotide variant (synonymous variant)	Brugada syndrome 7	GLikely benign
Select item 2064572	NM_001040151.2(SCN3B):c.519G>T (p.Leu173=)	SCN3B	Single nucleotide variant (synonymous variant)	Brugada syndrome 7	GLikely benign
Select item 1745840	NM_001040151.2(SCN3B):c.517C>G (p.Leu173Val)	SCN3B (L173V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 389585	NM_001040151.2(SCN3B):c.489C>T (p.Tyr163=)	SCN3B	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 1743697	NM_001040151.2(SCN3B):c.486G>A (p.Met162Ile)	SCN3B (M162I)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1743547	NM_001040151.2(SCN3B):c.484A>G (p.Met162Val)	SCN3B (M162V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 140598	NM_001040151.2(SCN3B):c.482T>C (p.Met161Thr)	SCN3B (M161T)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 16	GPathogenic
Select item 1741428	NM_001040151.2(SCN3B):c.454G>A (p.Asp152Asn)	SCN3B (D152N)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1056663	NM_001040151.2(SCN3B):c.446C>G (p.Ala149Gly)	SCN3B (A149G)	Single nucleotide variant (missense variant)	Brugada syndrome 7	GUncertain significance
Select item 752463	NM_001040151.2(SCN3B):c.446-4T>G	SCN3B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1107382	NM_001040151.2(SCN3B):c.446-7C>G	SCN3B	Single nucleotide variant (intron variant)	Brugada syndrome 7	GLikely benign
Select item 675386	NM_001040151.2(SCN3B):c.446-204C>T	SCN3B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275417	NM_001040151.2(SCN3B):c.445+197T>C	SCN3B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3000956	NM_001040151.2(SCN3B):c.445+20T>G	SCN3B	Single nucleotide variant (intron variant)	Brugada syndrome 7	GLikely benign
Select item 741757	NM_001040151.2(SCN3B):c.445+8T>C	SCN3B	Single nucleotide variant (intron variant)	Brugada syndrome 7	GLikely benign
Select item 378923	NM_001040151.2(SCN3B):c.445+3G>A	SCN3B	Single nucleotide variant (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2563486	NM_001040151.2(SCN3B):c.441G>T (p.Glu147Asp)	SCN3B (E147D)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1740287	NM_001040151.2(SCN3B):c.439G>A (p.Glu147Lys)	SCN3B (E147K)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1740156	NM_001040151.2(SCN3B):c.438_439delinsTA (p.Glu147Lys)	SCN3B (E147K)	Indel (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 261028	NM_001040151.2(SCN3B):c.438C>T (p.Thr146=)	SCN3B	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 139034	NM_001040151.2(SCN3B):c.438C>A (p.Thr146=)	SCN3B	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 1899279	NM_001040151.2(SCN3B):c.436A>G (p.Thr146Ala)	SCN3B (T146A)	Single nucleotide variant (missense variant)	Brugada syndrome 7	GUncertain significance
Select item 1116932	NM_001040151.2(SCN3B):c.423C>T (p.Ile141=)	SCN3B	Single nucleotide variant (synonymous variant)	Brugada syndrome 7	GLikely benign
Select item 224720	NM_001040151.2(SCN3B):c.423C>G (p.Ile141Met)	SCN3B (I141M)	Single nucleotide variant (missense variant)	Brugada syndrome 7	GUncertain significance
Select item 1738740	NM_001040151.2(SCN3B):c.420G>T (p.Leu140=)	SCN3B	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 190888	NM_001040151.2(SCN3B):c.416G>A (p.Arg139Gln)	SCN3B (R139Q)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 519233	NM_001040151.2(SCN3B):c.415C>T (p.Arg139Trp)	SCN3B (R139W)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 986187	NM_001040151.2(SCN3B):c.409ACG[1] (p.Thr138del)	SCN3B (T138del)	Microsatellite (inframe_deletion)	Brugada syndrome 7 +1 more	GUncertain significance
Select item 519456	NM_001040151.2(SCN3B):c.414G>A (p.Thr138=)	SCN3B	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 806755	NM_001040151.2(SCN3B):c.413C>T (p.Thr138Met)	SCN3B (T138M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2062002	NM_001040151.2(SCN3B):c.411G>A (p.Thr137=)	SCN3B	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 950266	NM_001040151.2(SCN3B):c.410C>T (p.Thr137Met)	SCN3B (T137M)	Single nucleotide variant (missense variant)	Brugada syndrome 7	GUncertain significance
Select item 2196926	NM_001040151.2(SCN3B):c.407A>G (p.Lys136Arg)	SCN3B (K136R)	Single nucleotide variant (missense variant)	Brugada syndrome 7	GUncertain significance
Select item 3227132	NM_001040151.2(SCN3B):c.404T>C (p.Val135Ala)	SCN3B (V135A)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2448564	NM_001040151.2(SCN3B):c.399C>A (p.Pro133=)	SCN3B	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1486045	NM_001040151.2(SCN3B):c.392_397del (p.His131_Arg132del)	SCN3B	Deletion (inframe_deletion)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 695598	NM_001040151.2(SCN3B):c.396G>T (p.Arg132=)	SCN3B	Single nucleotide variant (synonymous variant)	Brugada syndrome 7 +1 more	GLikely benign
Select item 644208	NM_001040151.2(SCN3B):c.395G>A (p.Arg132Gln)	SCN3B (R132Q)	Single nucleotide variant (missense variant)	Brugada syndrome 7 +1 more	GUncertain significance
Select item 646266	NM_001040151.2(SCN3B):c.394C>T (p.Arg132Trp)	SCN3B (R132W)	Single nucleotide variant (missense variant)	Brugada syndrome 7 +2 more	GUncertain significance
Select item 1474456	NM_001040151.2(SCN3B):c.392A>G (p.His131Arg)	SCN3B (H131R)	Single nucleotide variant (missense variant)	Brugada syndrome 7	GUncertain significance
Select item 3227131	NM_001040151.2(SCN3B):c.391C>A (p.His131Asn)	SCN3B (H131N)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 264285	NM_001040151.2(SCN3B):c.390G>T (p.Ala130=)	SCN3B	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 139033	NM_001040151.2(SCN3B):c.390G>A (p.Ala130=)	SCN3B	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 1328589	NM_001040151.2(SCN3B):c.389C>A (p.Ala130Glu)	SCN3B (A130E)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 140597	NM_001040151.2(SCN3B):c.389C>T (p.Ala130Val)	SCN3B (A130V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

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