ClinVar for Gene (Select 3827) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3289216	NM_001102416.3(KNG1):c.32C>G (p.Ser11Cys)	KNG1 (S11C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289215	NM_001102416.3(KNG1):c.1915C>T (p.Leu639Phe)	KNG1 (L639F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289214	NM_001102416.3(KNG1):c.515A>C (p.Gln172Pro)	KNG1 (Q172P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289213	NM_001102416.3(KNG1):c.373A>G (p.Thr125Ala)	KNG1 (T125A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289211	NM_001102416.3(KNG1):c.618T>G (p.Cys206Trp)	KNG1 (C206W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3148910	GRCh37/hg19 3q26.33-29(chr3:179313373-197851444)x3	ABCC5, ABCF3 +136 more	Copy number gain	See cases	GPathogenic
Select item 3116128	NM_001102416.3(KNG1):c.911T>A (p.Val304Glu)	KNG1 (V304E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116127	NM_001102416.3(KNG1):c.70G>A (p.Glu24Lys)	KNG1 (E24K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116126	NM_001102416.3(KNG1):c.703A>G (p.Ile235Val)	KNG1 (I235V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3116125	NM_001102416.3(KNG1):c.646C>G (p.Pro216Ala)	KNG1 (P216A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116124	NM_001102416.3(KNG1):c.587G>A (p.Arg196Gln)	KNG1 (R196Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116123	NM_001102416.3(KNG1):c.488G>A (p.Gly163Asp)	KNG1 (G163D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116122	NM_001102416.3(KNG1):c.383T>G (p.Ile128Ser)	KNG1 (I128S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116121	NM_001102416.3(KNG1):c.310A>T (p.Thr104Ser)	KNG1 (T104S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116120	NM_001102416.3(KNG1):c.1810T>A (p.Ser604Thr)	KNG1 (S604T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116118	NM_001102416.3(KNG1):c.131A>G (p.Tyr44Cys)	KNG1 (Y44C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116117	NM_001102416.3(KNG1):c.1204G>A (p.Val402Ile)	KNG1 (V402I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3059701	NM_001102416.3(KNG1):c.246T>C (p.Asp82=)	KNG1	Single nucleotide variant (synonymous variant)	KNG1-related disorder	GBenign
Select item 3059276	NM_001102416.3(KNG1):c.324G>A (p.Thr108=)	KNG1	Single nucleotide variant (synonymous variant)	KNG1-related disorder	GBenign
Select item 3058543	NM_001102416.3(KNG1):c.1254T>C (p.Asp418=)	KNG1	Single nucleotide variant (synonymous variant +1 more)	KNG1-related disorder	GLikely benign
Select item 3057213	NM_001102416.3(KNG1):c.1461G>A (p.Gly487=)	KNG1	Single nucleotide variant (synonymous variant +1 more)	KNG1-related disorder	GLikely benign
Select item 3056243	NM_001102416.3(KNG1):c.1590C>T (p.Asp530=)	KNG1	Single nucleotide variant (synonymous variant +1 more)	KNG1-related disorder	GLikely benign
Select item 3052145	NM_001102416.3(KNG1):c.159G>A (p.Gln53=)	KNG1	Single nucleotide variant (synonymous variant)	KNG1-related disorder	GLikely benign
Select item 3041593	NM_001102416.3(KNG1):c.1053C>T (p.Cys351=)	KNG1	Single nucleotide variant (synonymous variant)	KNG1-related disorder	GLikely benign
Select item 3038288	NM_001102416.3(KNG1):c.591T>G (p.Ile197Met)	KNG1 (I197M)	Single nucleotide variant (missense variant +1 more)	KNG1-related disorder	GBenign
Select item 3030394	NM_001102416.3(KNG1):c.1106A>G (p.Asn369Ser)	KNG1 (N333S +1 more)	Single nucleotide variant (missense variant)	KNG1-related disorder	GUncertain significance
Select item 2671619	Single allele	ABCC5, ABCF3 +145 more	Duplication	not provided	GPathogenic
Select item 2671595	Single allele	MUC20, MUC4 +286 more	Duplication	not provided	GPathogenic
Select item 2654340	NM_001102416.3(KNG1):c.1431C>T (p.Phe477=)	KNG1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2654339	NM_001102416.3(KNG1):c.350C>T (p.Thr117Met)	KNG1 (T117M)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2599908	NM_001102416.3(KNG1):c.1171T>C (p.Ser391Pro)	KNG1 (S391P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2581707	NM_001102416.3(KNG1):c.727T>G (p.Ser243Ala)	KNG1 (S207A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2578037	NM_001102416.3(KNG1):c.718C>T (p.Arg240Ter)	KNG1 (R204* +1 more)	Single nucleotide variant (nonsense)	High molecular weight kininogen deficiency	GPathogenic
Select item 2578036	NM_001102416.3(KNG1):c.1038+1G>A	KNG1	Single nucleotide variant (splice donor variant)	High molecular weight kininogen deficiency	GPathogenic
Select item 2578035	NM_001102416.3(KNG1):c.306+2T>A	KNG1	Single nucleotide variant (splice donor variant)	High molecular weight kininogen deficiency	GPathogenic
Select item 2559798	NM_001102416.3(KNG1):c.1618G>A (p.Glu540Lys)	KNG1 (E540K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2553220	NM_001102416.3(KNG1):c.1280G>A (p.Arg427His)	KNG1 (R427H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2553091	NM_001102416.3(KNG1):c.935T>G (p.Val312Gly)	KNG1 (V276G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544825	NM_001102416.3(KNG1):c.127A>C (p.Lys43Gln)	KNG1 (K43Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542521	NM_001102416.3(KNG1):c.460C>G (p.Pro154Ala)	KNG1 (P154A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489644	NM_001102416.3(KNG1):c.679G>A (p.Gly227Ser)	KNG1 (G191S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486552	NM_001102416.3(KNG1):c.1070T>A (p.Val357Glu)	KNG1 (V321E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480671	NM_001102416.3(KNG1):c.896T>G (p.Phe299Cys)	KNG1 (F263C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474720	NM_001102416.3(KNG1):c.1189A>G (p.Lys397Glu)	KNG1 (K397E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470725	NM_001102416.3(KNG1):c.1430T>G (p.Phe477Cys)	KNG1 (F477C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2431559	NM_001102416.3(KNG1):c.166T>G (p.Leu56Val)	KNG1 (L56V)	Single nucleotide variant (missense variant)	Angioedema, hereditary, 6	GUncertain significance
Select item 2426290	NC_000003.11:g.(?_186256485)_(187009420_?)dup	ADIPOQ, AHSG +14 more	Duplication	3MC syndrome 1	GUncertain significance
Select item 2409725	NM_001102416.3(KNG1):c.323C>T (p.Thr108Met)	KNG1 (T108M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400167	NM_001102416.3(KNG1):c.1409G>T (p.Gly470Val)	KNG1 (G470V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390023	NM_001102416.3(KNG1):c.1404G>C (p.Gln468His)	KNG1 (Q468H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389557	NM_001102416.3(KNG1):c.986C>G (p.Ser329Cys)	KNG1 (S329C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377713	NM_001102416.3(KNG1):c.374C>A (p.Thr125Asn)	KNG1 (T125N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334368	NM_001102416.3(KNG1):c.1166G>T (p.Arg389Leu)	KNG1 (R353L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324476	NM_001102416.3(KNG1):c.1846G>A (p.Gly616Arg)	KNG1 (G616R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307889	NM_001102416.3(KNG1):c.*1428C>T	KNG1 (P384S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294572	NM_001102416.3(KNG1):c.711T>G (p.Ile237Met)	KNG1 (I201M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271525	NM_001102416.3(KNG1):c.1345C>T (p.Arg449Cys)	KNG1 (R449C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2230552	NM_001102416.3(KNG1):c.1202C>T (p.Thr401Ile)	KNG1 (T365I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227771	NM_001102416.3(KNG1):c.1012G>A (p.Glu338Lys)	KNG1 (E302K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212582	NM_001102416.3(KNG1):c.908A>G (p.Asn303Ser)	KNG1 (N303S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809046	GRCh37/hg19 3q27.1-28(chr3:184170962-188047867)x1	ADIPOQ, AHSG +32 more	Copy number loss	not provided	GLikely pathogenic
Select item 1803726	NM_001102416.3(KNG1):c.1165C>T (p.Arg389Ter)	KNG1 (R353* +1 more)	Single nucleotide variant (nonsense)	High molecular weight kininogen deficiency	GPathogenic
Select item 1707630	GRCh37/hg19 3q26.31-29(chr3:171558472-197871052)x3	CCDC50, MELTF +155 more	Copy number gain	Isolated anorectal malformation	GLikely pathogenic
Select item 1707428	GRCh37/hg19 3q27.1-29(chr3:183498520-197851986)x3	ABCC5, ABCF3 +118 more	Copy number gain	See cases	GPathogenic
Select item 1703771	NM_001102416.3(KNG1):c.162T>G (p.Phe54Leu)	KNG1 (F54L)	Single nucleotide variant (missense variant)	Thrombus +1 more	GUncertain significance
Select item 1703654	GRCh37/hg19 3q27.1-28(chr3:183556940-188083060)	ABCC5, ABCF3 +53 more	Copy number loss	Short stature	GPathogenic
Select item 1527065	GRCh37/hg19 3q27.3(chr3:186149060-186599706)	ADIPOQ, AHSG +10 more	Copy number loss	not specified	GUncertain significance
Select item 1527063	GRCh37/hg19 3q27.1-27.3(chr3:183178932-186838042)	ABCC5, ABCF3 +49 more	Copy number loss	not specified	GPathogenic
Select item 1527061	GRCh37/hg19 3q26.33-27.3(chr3:182189525-187212935)	ABCC5, ABCF3 +59 more	Copy number loss	not specified	GPathogenic
Select item 1328104	GRCh37/hg19 3q26.31-27.3(chr3:175119199-187592480)x3	ABCC5, ABCF3 +82 more	Copy number gain	not provided	GPathogenic
Select item 1162307	NM_001102416.3(KNG1):c.1720C>G (p.Pro574Ala)	KNG1 (P574A)	Single nucleotide variant (missense variant +1 more)	Angioedema, hereditary, 6	GPathogenic
Select item 1162306	NM_001102416.3(KNG1):c.1136T>A (p.Met379Lys)	KNG1 (M379K +1 more)	Single nucleotide variant (missense variant)	Angioedema, hereditary, 6	GPathogenic
Select item 1049825	NM_001102416.3(KNG1):c.1234G>A (p.Ala412Thr)	KNG1 (A412T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 980554	GRCh37/hg19 3q27.1-27.3(chr3:182877291-186830759)x1	CLCN2, YEATS2 +52 more	Copy number loss	not provided	GPathogenic
Select item 832891	NC_000003.11:g.(?_186256465)_(187009440_?)del	ADIPOQ, AHSG +14 more	Deletion	3MC syndrome 1	GPathogenic
Select item 827590	NM_001102416.3(KNG1):c.421G>A (p.Asp141Asn)	KNG1 (D141N)	Single nucleotide variant (missense variant)	Hereditary angioedema with normal C1Inh	Gnot provided
Select item 827589	NM_001102416.3(KNG1):c.-85T>A	KNG1	Single nucleotide variant (5 prime UTR variant)	Hereditary angioedema with normal C1Inh	Gnot provided
Select item 814507	GRCh37/hg19 3q27.2-27.3(chr3:185879162-187446035)x1	ST6GAL1, DNAJB11 +19 more	Copy number loss	not provided	GPathogenic
Select item 814497	GRCh37/hg19 3q26.2-28(chr3:169617690-190593854)x3	FXR1, HTR3D +113 more	Copy number gain	not provided	GPathogenic
Select item 730929	NM_001102416.3(KNG1):c.747C>T (p.Asp249=)	KNG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 721323	NM_001102416.3(KNG1):c.757+3A>G	KNG1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 562852	GRCh37/hg19 3q27.3-29(chr3:186374365-197851986)x3	PCYT1A, TNK2-AS1 +77 more	Copy number gain	not provided	GPathogenic
Select item 562850	GRCh37/hg19 3q27.1-29(chr3:184003967-197851986)x3	FYTTD1, FAM43A +103 more	Copy number gain	not provided	GPathogenic
Select item 562848	GRCh37/hg19 3q26.33-28(chr3:182650681-191275809)x1	KNG1, FETUB +75 more	Copy number loss	not provided	GPathogenic
Select item 562847	GRCh37/hg19 3q26.33-29(chr3:182539234-197851986)x3	PPP1R2, TBCCD1 +126 more	Copy number gain	not provided	GPathogenic
Select item 531899	NC_000003.11:g.(?_186256465)_(186980528_?)del	ADIPOQ, AHSG +14 more	Deletion	3MC syndrome 1	GPathogenic
Select item 523279	GRCh37/hg19 3q27.1-28(chr3:184300169-188285627)	FETUB, HRG +32 more	Copy number loss	Cognitive impairment +1 more	GPathogenic
Select item 442401	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	HHLA2, HIGD1A +1054 more	Copy number gain	See cases	GPathogenic
Select item 442400	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	A4GNT, AADAC +1054 more	Copy number gain	See cases	GPathogenic
Select item 403021	NM_001102416.3(KNG1):c.*1404C>T	KNG1 (R412* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided +1 more	GBenign
Select item 394816	GRCh37/hg19 3q27.2-27.3(chr3:185419048-186575415)x1	ADIPOQ, AHSG +14 more	Copy number loss	See cases	GPathogenic
Select item 393885	GRCh37/hg19 3q25.32-29(chr3:158980631-197766890)x3	ABCC5, ABCF3 +198 more	Copy number gain	See cases	GPathogenic
Select item 253655	GRCh37/hg19 3q27.3-28(chr3:186291045-191037240)x1	GMNC, UTS2B +28 more	Copy number loss	See cases	GPathogenic
Select item 253377	GRCh37/hg19 3q24-29(chr3:142995020-192997215)x4	AADAC, AADACL2 +220 more	Copy number gain	See cases	GPathogenic
Select item 225401	NM_001102416.3(KNG1):c.1866_1869del (p.Ser623fs)	KNG1 (S623fs)	Deletion (frameshift variant +1 more)	High molecular weight kininogen deficiency	GUncertain significance
Select item 156903	CM000665.1:g.186411076_186494422dup	KNG1	Duplication	Normal pregnancy	Gnot provided
Select item 155627	GRCh38/hg38 3q26.1-29(chr3:166137209-198125115)x3	LOC129938260, LOC129938261 +1064 more	Copy number gain	See cases	GPathogenic
Select item 154213	GRCh38/hg38 3q25.31-29(chr3:156118441-198125115)x3	LOC108281160, LOC108281177 +1247 more	Copy number gain	See cases	GPathogenic
Select item 153893	GRCh38/hg38 3q26.1-28(chr3:167717962-188365272)x3	ABCC5, ABCC5-AS1 +627 more	Copy number gain	See cases	GLikely pathogenic
Select item 153734	GRCh38/hg38 3q26.33-28(chr3:181138664-192512023)x1	ABCC5, ABCC5-AS1 +399 more	Copy number loss	See cases	GPathogenic

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