SPOUT1[gene] - ClinVar

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Items: 69

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 160862	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC126860768, LOC126860769 +3785 more	Copy number gain	See cases	GPathogenic
Select item 150340	GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3	LOC124310660, LOC124310661 +3784 more	Copy number gain	See cases	GPathogenic
Select item 150050	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3	LOC111413024, LOC111413033 +3785 more	Copy number gain	See cases	GPathogenic
Select item 149828	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3	ABCA1, ABCA2 +3785 more	Copy number gain	See cases	GPathogenic
Select item 59875	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3	ABCA1, ABCA2 +3785 more	Copy number gain	See cases	GPathogenic
Select item 33205	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC116216098, LOC116216099 +3785 more	Copy number gain	See cases	GPathogenic
Select item 153518	GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3	ABCA1, ABCA2 +3785 more	Copy number gain	See cases	GPathogenic
Select item 155409	GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	LCN15, LCN2 +3785 more	Copy number gain	See cases	GPathogenic
Select item 144309	GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445)	LOC126860765, LOC126860766 +3785 more	Copy number gain	See cases	GPathogenic
Select item 145579	GRCh38/hg38 9q33.2-34.3(chr9:121073102-138179445)x3	ABCA2, ABL1 +1272 more	Copy number gain	See cases	GPathogenic
Select item 57324	GRCh38/hg38 9q33.2-34.3(chr9:121112395-138075224)x3	LOC130003073, LOC130003074 +1268 more	Copy number gain	See cases	GPathogenic
Select item 57353	GRCh38/hg38 9q33.2-34.3(chr9:122792658-138124532)x3	LOC130002603, LOC130002604 +1210 more	Copy number gain	See cases	GPathogenic
Select item 59125	GRCh38/hg38 9q33.3-34.11(chr9:125993583-129682375)x1	AK1, ANGPTL2 +309 more	Copy number loss	See cases	GPathogenic
Select item 59134	GRCh38/hg38 9q34.11(chr9:127874581-130421811)x1	AK1, ASB6 +264 more	Copy number loss	See cases	GPathogenic
Select item 59906	GRCh38/hg38 9q34.11(chr9:127919476-130079974)x3	ASB6, BBLN +239 more	Copy number gain	See cases	GPathogenic
Select item 150008	GRCh38/hg38 9q34.11(chr9:128236347-128912067)x1	CERCAM, COQ4 +70 more	Copy number loss	See cases	GPathogenic
Select item 149067	GRCh38/hg38 9q34.11(chr9:128610170-129368351)x1	CRAT, DOLK +72 more	Copy number loss	See cases	GUncertain significance
Select item 58499	GRCh38/hg38 9q34.11(chr9:128808545-129002107)x3	DOLK, ENDOG +16 more	Copy number gain	See cases	GUncertain significance
Select item 2471708	NM_004435.2(ENDOG):c.536T>C (p.Leu179Pro)	ENDOG, KYAT1-SPOUT1 +1 more (L179P)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2462773	NM_004435.2(ENDOG):c.550C>T (p.Arg184Cys)	ENDOG, KYAT1-SPOUT1 +1 more (R184C)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2479810	NM_004435.2(ENDOG):c.577G>A (p.Val193Ile)	ENDOG, KYAT1-SPOUT1 +1 more (V193I)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 774205	NM_004435.2(ENDOG):c.654C>T (p.Ile218=)	ENDOG, KYAT1-SPOUT1 +1 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2395978	NM_004435.2(ENDOG):c.728A>G (p.Glu243Gly)	ENDOG, KYAT1-SPOUT1 +1 more (E243G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 789304	NM_004435.2(ENDOG):c.734G>T (p.Arg245Leu)	ENDOG, KYAT1-SPOUT1 +1 more (R245L)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 789305	NM_004435.2(ENDOG):c.737C>T (p.Thr246Ile)	ENDOG, KYAT1-SPOUT1 +1 more (T246I)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2345090	NM_004435.2(ENDOG):c.784C>T (p.Arg262Cys)	ENDOG, KYAT1-SPOUT1 +1 more (R262C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2351459	NM_004435.2(ENDOG):c.821C>T (p.Ser274Leu)	ENDOG, KYAT1-SPOUT1 +1 more (S274L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2391177	NM_004435.2(ENDOG):c.854G>A (p.Arg285Gln)	ENDOG, KYAT1-SPOUT1 +1 more (R285Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 218639	NM_004435.2(ENDOG):c.889_892del (p.Lys297fs)	ENDOG, KYAT1-SPOUT1 +1 more (K297fs)	Deletion (frameshift variant +1 more)	not specified	GBenign
Select item 3059891	NM_016390.4(SPOUT1):c.1106T>C (p.Ile369Thr)	KYAT1-SPOUT1, SPOUT1 (I369T +1 more)	Single nucleotide variant (missense variant +1 more)	SPOUT1-related condition	GBenign
Select item 3041881	NM_016390.4(SPOUT1):c.1089C>G (p.Ala363=)	KYAT1-SPOUT1, SPOUT1	Single nucleotide variant (synonymous variant +1 more)	SPOUT1-related condition	GBenign
Select item 2259029	NM_016390.4(SPOUT1):c.1070T>C (p.Ile357Thr)	KYAT1-SPOUT1, SPOUT1 (I357T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3034153	NM_016390.4(SPOUT1):c.1062+8C>T	KYAT1-SPOUT1, SPOUT1	Single nucleotide variant (intron variant)	SPOUT1-related condition	GLikely benign
Select item 2243683	NM_016390.4(SPOUT1):c.1028G>C (p.Cys343Ser)	KYAT1-SPOUT1, SPOUT1 (C343S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3059826	NM_016390.4(SPOUT1):c.891C>T (p.Ala297=)	KYAT1-SPOUT1, SPOUT1	Single nucleotide variant (synonymous variant +1 more)	SPOUT1-related condition	GBenign
Select item 2274948	NM_016390.4(SPOUT1):c.598C>T (p.Arg200Trp)	KYAT1-SPOUT1, SPOUT1 (R200W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3039768	NM_016390.4(SPOUT1):c.534C>T (p.Pro178=)	KYAT1-SPOUT1, SPOUT1	Single nucleotide variant (synonymous variant +1 more)	SPOUT1-related condition	GLikely benign
Select item 3043525	NM_016390.4(SPOUT1):c.508+5C>T	KYAT1-SPOUT1, SPOUT1	Single nucleotide variant (intron variant)	SPOUT1-related condition	GLikely benign
Select item 3059446	NM_016390.4(SPOUT1):c.458+6G>C	KYAT1-SPOUT1, SPOUT1	Single nucleotide variant (intron variant)	SPOUT1-related condition	GBenign
Select item 3053485	NM_016390.4(SPOUT1):c.418G>A (p.Val140Ile)	KYAT1-SPOUT1, SPOUT1 (V140I +1 more)	Single nucleotide variant (missense variant +1 more)	SPOUT1-related condition	GBenign
Select item 3059239	NM_016390.4(SPOUT1):c.389C>G (p.Thr130Arg)	KYAT1-SPOUT1, SPOUT1 (T130R +1 more)	Single nucleotide variant (missense variant +1 more)	SPOUT1-related condition	GBenign
Select item 3038672	NM_016390.4(SPOUT1):c.369-15TC[5]	KYAT1-SPOUT1, SPOUT1	Microsatellite (intron variant)	SPOUT1-related condition	GLikely benign
Select item 1050764	NM_016390.4(SPOUT1):c.366C>G (p.Ala122=)	KYAT1-SPOUT1, SPOUT1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 3041960	NM_016390.4(SPOUT1):c.270G>A (p.Pro90=)	KYAT1-SPOUT1, SPOUT1	Single nucleotide variant (synonymous variant +1 more)	SPOUT1-related condition	GBenign
Select item 2246665	NM_016390.4(SPOUT1):c.263A>T (p.Gln88Leu)	SPOUT1, KYAT1-SPOUT1 (Q537L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 547051	NM_016390.4(SPOUT1):c.256A>G (p.Asn86Asp)	KYAT1-SPOUT1, SPOUT1 (N86D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 771736	NM_016390.4(SPOUT1):c.189G>A (p.Ala63=)	KYAT1-SPOUT1, SPOUT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 547052	NM_016390.3(SPOUT1):c.102dup (p.Trp35Metfs)	SPOUT1, KYAT1-SPOUT1 (W35fs)	Duplication (frameshift variant)	SPOUT1-related condition +1 more	GConflicting classifications of pathogenicity
Select item 2659549	NM_016390.4(SPOUT1):c.91G>A (p.Glu31Lys)	KYAT1-SPOUT1, SPOUT1 (E31K +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2355368	NM_016390.4(SPOUT1):c.35C>G (p.Pro12Arg)	KYAT1-SPOUT1, SPOUT1 (P12R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3063071	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	ABCA1, ABCA2 +769 more	Copy number gain	not specified	GPathogenic
Select item 2426262	NC_000009.11:g.(?_131087402)_(141016451_?)dup	ABCA2, ABL1 +187 more	Duplication	Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome	GUncertain significance
Select item 1711101	GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3	ANKS6, ANP32B +596 more	Copy number gain	See cases	GPathogenic
Select item 1527562	GRCh37/hg19 9q34.11(chr9:130390139-132760275)	AK1, ASB6 +62 more	Copy number loss	not specified	GPathogenic
Select item 1527545	GRCh37/hg19 9q32-34.11(chr9:116422275-131713233)	ADGRD2, AK1 +141 more	Copy number gain	not specified	GPathogenic
Select item 1527491	GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389)	OR1L4, PTRH1 +768 more	Copy number gain	not specified	GPathogenic
Select item 1340206	GRCh37/hg19 9q33.3-34.11(chr9:128523763-132604808)x3	AK1, ANGPTL2 +75 more	Copy number gain	not provided	GPathogenic
Select item 988939	GRCh37/hg19 9q34.11(chr9:131282528-131720659)x3	DOLK, DYNC2I2 +13 more	Copy number gain	not provided	GUncertain significance
Select item 815298	GRCh37/hg19 9q34.11(chr9:131094304-131863858)x3	GLE1, SH3GLB2 +22 more	Copy number gain	not provided	GUncertain significance
Select item 815297	GRCh37/hg19 9q34.11(chr9:130957344-132310210)x1	ENDOG, SET +31 more	Copy number loss	not provided	GPathogenic
Select item 687100	GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3	ABCA1, ABCA2 +552 more	Copy number gain	not provided	GPathogenic
Select item 685192	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3	ABCA1, ABCA2 +769 more	Copy number gain	not provided	GPathogenic
Select item 523294	GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928)	SEC16A, SEC61B +553 more	Copy number gain	Hypotonia +2 more	GLikely pathogenic
Select item 443986	GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389)	SUSD3, SVEP1 +769 more	Copy number gain	See cases	GPathogenic
Select item 395707	GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407)	PPP1R26, PPP3R2 +771 more	Copy number gain	See cases	GPathogenic
Select item 395356	GRCh37/hg19 9q33.3-34.3(chr9:128652785-141044751)x3	ABCA2, ABL1 +228 more	Copy number gain	See cases	GPathogenic
Select item 394948	GRCh37/hg19 9q33.2-34.3(chr9:124642754-141146461)x3	ABCA2, ABL1 +279 more	Copy number gain	See cases	GPathogenic
Select item 253999	GRCh37/hg19 9q34.11(chr9:131550680-131775355)x3	LRRC8A, SPOUT1 +7 more	Copy number gain	See cases	GUncertain significance
Select item 253402	GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3	ANGPTL2, ANKRD18A +771 more	Copy number gain	See cases	GPathogenic

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Items: 69