TNFSF15[gene] - ClinVar

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Items: 52

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 160862	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC124210612, LOC124210613 +3786 more	Copy number gain	See cases	GPathogenic
Select item 150340	GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3	LOC121331326, LOC121331327 +3785 more	Copy number gain	See cases	GPathogenic
Select item 150050	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3	LOC126860737, LOC126860738 +3786 more	Copy number gain	See cases	GPathogenic
Select item 149828	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 59875	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3	LOC110121197, LOC110121234 +3786 more	Copy number gain	See cases	GPathogenic
Select item 33205	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC121331342, LOC121331343 +3786 more	Copy number gain	See cases	GPathogenic
Select item 153518	GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3	LOC113839542, LOC113839543 +3786 more	Copy number gain	See cases	GPathogenic
Select item 155409	GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 144309	GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445)	LOC130002189, LOC130002190 +3786 more	Copy number gain	See cases	GPathogenic
Select item 161058	GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1	LOC126860732, LOC126860733 +514 more	Copy number loss	See cases	GPathogenic
Select item 32222	GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1	ABCA1, ABITRAM +514 more	Copy number loss	See cases	GPathogenic
Select item 59123	GRCh38/hg38 9q22.33-33.1(chr9:99349916-115767475)x1	CT70, CTNNAL1 +509 more	Copy number loss	See cases	GPathogenic
Select item 152171	GRCh38/hg38 9q31.2-33.1(chr9:107530314-117965944)x1	PALM2AKAP2, PAPPA +377 more	Copy number loss	See cases	GPathogenic
Select item 1710538	NC_000009.12:g.114776054C>T	TNFSF15	Single nucleotide variant	Leprosy, susceptibility to, 1	GUncertain risk allele
Select item 1710526	NM_005118.4(TNFSF15):c.*4960A>G	TNFSF15	Single nucleotide variant (3 prime UTR variant)	Leprosy, susceptibility to, 1	GUncertain risk allele
Select item 3327546	NM_005118.4(TNFSF15):c.688G>A (p.Val230Ile)	TNFSF15 (V171I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180328	NM_005118.4(TNFSF15):c.563A>G (p.Tyr188Cys)	TNFSF15 (Y188C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180327	NM_005118.4(TNFSF15):c.545C>T (p.Thr182Ile)	TNFSF15 (T123I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213536	NM_005118.4(TNFSF15):c.431C>T (p.Ser144Leu)	TNFSF15 (S85L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272923	NM_005118.4(TNFSF15):c.394A>G (p.Met132Val)	TNFSF15 (M132V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322783	NM_005118.4(TNFSF15):c.341T>A (p.Phe114Tyr)	TNFSF15 (F55Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 768323	NM_005118.4(TNFSF15):c.330T>A (p.Phe110Leu)	TNFSF15 (F51L +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3327547	NM_005118.4(TNFSF15):c.319A>C (p.Thr107Pro)	TNFSF15 (T107P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 737466	NM_005118.4(TNFSF15):c.276A>C (p.Gly92=)	TNFSF15	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 745318	NM_005118.4(TNFSF15):c.273C>T (p.Asp91=)	TNFSF15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2550148	NM_005118.4(TNFSF15):c.217A>G (p.Lys73Glu)	TNFSF15 (K73E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1710525	NM_005118.4(TNFSF15):c.211-2855G>C	TNFSF15	Single nucleotide variant (intron variant)	Leprosy, susceptibility to, 1	Gconfers sensitivity
Select item 2520163	NM_005118.4(TNFSF15):c.178C>T (p.Arg60Trp)	TNFSF15 (R60W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535765	NM_005118.4(TNFSF15):c.149T>A (p.Leu50His)	TNFSF15 (L50H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 750521	NM_005118.4(TNFSF15):c.120C>T (p.Cys40=)	TNFSF15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2368830	NM_005118.4(TNFSF15):c.101G>A (p.Arg34His)	TNFSF15 (R34H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180330	NM_005118.4(TNFSF15):c.82G>T (p.Ala28Ser)	TNFSF15 (A28S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 730004	NM_005118.4(TNFSF15):c.74G>A (p.Arg25Lys)	TNFSF15 (R25K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3180329	NM_005118.4(TNFSF15):c.63C>A (p.His21Gln)	TNFSF15 (H21Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063071	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	DMAC1, DMRT1 +769 more	Copy number gain	not specified	GPathogenic
Select item 1711101	GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3	ADAMTSL1, CEP78 +596 more	Copy number gain	See cases	GPathogenic
Select item 1703688	GRCh37/hg19 9p22.1-q33.1(chr9:19356861-119513311)	ATOSB, ATP6V1G1 +417 more	Copy number loss	Distal tetrasomy 15q	GUncertain significance
Select item 1527546	GRCh37/hg19 9q32-33.1(chr9:116506015-119942279)	AKNA, AMBP +16 more	Copy number loss	not specified	GUncertain significance
Select item 1527545	GRCh37/hg19 9q32-34.11(chr9:116422275-131713233)	ADGRD2, AK1 +141 more	Copy number gain	not specified	GPathogenic
Select item 1527542	GRCh37/hg19 9q31.2-32(chr9:109265628-117650999)	ABITRAM, ACTL7A +61 more	Copy number loss	not specified	GLikely pathogenic
Select item 1527539	GRCh37/hg19 9q31.1-33.3(chr9:104604851-126253089)	ABCA1, ABITRAM +130 more	Copy number loss	not specified	GPathogenic
Select item 1527521	GRCh37/hg19 9q21.11-33.2(chr9:71349994-122603410)	ABCA1, ABHD17B +261 more	Copy number gain	not specified	GLikely pathogenic
Select item 1527491	GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389)	ANKRD18A, ANKRD18B +768 more	Copy number gain	not specified	GPathogenic
Select item 815278	GRCh37/hg19 9q32(chr9:116642144-117613527)x1	ORM1, TNFSF15 +9 more	Copy number loss	not provided	GUncertain significance
Select item 687100	GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3	AMBP, ANAPC2 +552 more	Copy number gain	not provided	GPathogenic
Select item 685192	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3	MSMP, OR13D1 +769 more	Copy number gain	not provided	GPathogenic
Select item 523294	GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928)	ANGPTL2, ANKS6 +555 more	Copy number gain	Seizure +2 more	GLikely pathogenic
Select item 443986	GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389)	ODF2, OGN +769 more	Copy number gain	See cases	GPathogenic
Select item 442115	GRCh37/hg19 9q31.3-33.2(chr9:114299780-123267736)x1	AKNA, ALAD +48 more	Copy number loss	See cases	GPathogenic
Select item 395707	GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407)	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic
Select item 394605	GRCh37/hg19 9q31.3-33.1(chr9:111348809-118687200)x1	ABITRAM, ACTL7A +61 more	Copy number loss	See cases	GPathogenic
Select item 253402	GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic

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Items: 52