IL19[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58112	GRCh38/hg38 1q31.1-42.11(chr1:187143981-224299417)x3	PIK3C2B, PKP1 +1147 more	Copy number gain	See cases	GPathogenic
Select item 545154	NC_000001.11:g.(?_204033173)_(208209798_?)del	LOC129932391, PIK3C2B +278 more	Deletion	Autism	GLikely pathogenic
Select item 153790	GRCh38/hg38 1q32.1-42.12(chr1:204764914-225408698)x3	LOC129388734, LOC129388735 +723 more	Copy number gain	See cases	GPathogenic
Select item 1568337	NM_153758.5(IL19):c.-340_-339delinsGG	IL10, IL19	Indel (5 prime UTR variant +1 more)	Inflammatory bowel disease	GLikely benign
Select item 1166834	NM_153758.5(IL19):c.-339A>G	IL10, IL19	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +1 more	GBenign
Select item 2808342	NM_153758.5(IL19):c.-336C>G	IL10, IL19	Single nucleotide variant (5 prime UTR variant +1 more)	Inflammatory bowel disease	GLikely benign
Select item 2787055	NM_153758.5(IL19):c.-335T>G	IL10, IL19	Single nucleotide variant (5 prime UTR variant +1 more)	Inflammatory bowel disease	GLikely benign
Select item 2078691	NM_153758.5(IL19):c.-326A>G	IL10, IL19	Single nucleotide variant (5 prime UTR variant +1 more)	Inflammatory bowel disease	GUncertain significance
Select item 1144455	NM_000572.3(IL10):c.375C>A (p.Arg125=)	IL10, IL19	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 1482256	NM_000572.3(IL10):c.374G>T (p.Arg125Leu)	IL10, IL19 (R125L +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 1420500	NM_000572.3(IL10):c.374G>A (p.Arg125His)	IL10, IL19 (R125H +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 2044601	NM_000572.3(IL10):c.372G>A (p.Arg124=)	IL10, IL19	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 1432945	NM_000572.3(IL10):c.371G>A (p.Arg124Gln)	IL10, IL19 (R124Q +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 1011995	NM_000572.3(IL10):c.370C>T (p.Arg124Trp)	IL10, IL19 (R124W +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease +1 more	GUncertain significance
Select item 1025334	NM_000572.3(IL10):c.365G>A (p.Arg122Lys)	IL10, IL19 (R122K +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 2103299	NM_000572.3(IL10):c.361C>T (p.Leu121=)	IL10, IL19	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 745482	NM_000572.3(IL10):c.345C>T (p.Asn115=)	IL10, IL19 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 1005651	NM_000572.3(IL10):c.343A>T (p.Asn115Tyr)	IL10, IL19 +1 more (N115Y +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 757750	NM_000572.3(IL10):c.336G>C (p.Leu112=)	IL19, LOC129932369 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 1298449	NM_000572.3(IL10):c.334C>T (p.Leu112=)	IL10, IL19 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	not provided +1 more	GLikely benign
Select item 1004415	NM_000572.3(IL10):c.332C>T (p.Ser111Phe)	IL10, IL19 +1 more (S111F +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 1907986	NM_000572.3(IL10):c.327G>A (p.Val109=)	IL10, IL19 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 1525940	NM_000572.3(IL10):c.323A>G (p.His108Arg)	IL10, IL19 +1 more (H108R +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 1107004	NM_000572.3(IL10):c.321G>A (p.Ala107=)	IL10, IL19 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 1716474	NM_000572.3(IL10):c.320C>A (p.Ala107Glu)	IL10, IL19 +1 more (A107E +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 1399178	NM_000572.3(IL10):c.320C>T (p.Ala107Val)	IL10, IL19 +1 more (A107V +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 1056748	NM_000572.3(IL10):c.314T>G (p.Ile105Ser)	IL10, IL19 +1 more (I105S +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 1086791	NM_000572.3(IL10):c.309A>G (p.Pro103=)	IL10, IL19 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 1441711	NM_000572.3(IL10):c.301C>A (p.Gln101Lys)	IL10, IL19 +1 more (Q101K +1 more)	Single nucleotide variant (missense variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 1086136	NM_000572.3(IL10):c.297G>A (p.Glu99=)	LOC129932369, IL10 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 1095429	NM_000572.3(IL10):c.276G>A (p.Glu92=)	IL10, IL19 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 956183	NM_000572.3(IL10):c.274G>A (p.Glu92Lys)	IL10, IL19 +1 more (E7K +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 1641485	NM_000572.3(IL10):c.273G>A (p.Leu91=)	IL10, IL19 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 1926667	NM_000572.3(IL10):c.261C>T (p.Ile87=)	IL10, IL19 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 2112161	NM_000572.3(IL10):c.257T>A (p.Met86Lys)	IL10, IL19 +1 more (M1K +1 more)	Single nucleotide variant (missense variant +4 more)	Inflammatory bowel disease	GUncertain significance
Select item 1150550	NM_000572.3(IL10):c.255G>A (p.Glu85=)	IL10, IL19 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 1899952	NM_000572.3(IL10):c.252T>G (p.Ser84=)	IL10, IL19 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 1495514	NM_000572.3(IL10):c.241C>A (p.Gln81Lys)	IL19, IL10 +1 more (Q81K)	Single nucleotide variant (intron variant +3 more)	Inflammatory bowel disease	GUncertain significance
Select item 756187	NM_000572.3(IL10):c.228T>C (p.Gly76=)	IL10, IL19 +1 more	Single nucleotide variant (5 prime UTR variant +3 more)	Inflammatory bowel disease	GLikely benign
Select item 1166835	NM_153758.5(IL19):c.-149+222T>C	IL10, IL19	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 2748293	NM_153758.5(IL19):c.-149+258C>T	IL10, IL19	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GLikely benign
Select item 1574665	NM_153758.5(IL19):c.-149+260C>T	IL19, IL10	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GLikely benign
Select item 1612200	NM_153758.5(IL19):c.-149+261C>T	IL10, IL19	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GLikely benign
Select item 1576436	NM_153758.5(IL19):c.-149+263C>T	IL10, IL19	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GLikely benign
Select item 1480748	NM_153758.5(IL19):c.-149+272T>C	IL10, IL19	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GUncertain significance
Select item 2297180	NM_000572.3(IL10):c.215A>G (p.Glu72Gly)	IL10, IL19 (E72G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2779997	NM_000572.3(IL10):c.213G>T (p.Leu71=)	IL10, IL19	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease	GLikely benign
Select item 1367861	NM_000572.3(IL10):c.209T>A (p.Leu70Ter)	IL10, IL19 (L70*)	Single nucleotide variant (nonsense +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 1108648	NM_000572.3(IL10):c.201G>A (p.Lys67=)	IL10, IL19	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease	GLikely benign
Select item 2708725	NM_153758.5(IL19):c.-149+344G>A	IL19, IL10	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GLikely benign
Select item 1673878	NM_153758.5(IL19):c.-149+352A>G	IL10, IL19	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GBenign
Select item 2032719	NM_153758.5(IL19):c.-149+356G>A	IL10, IL19	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GLikely benign
Select item 2628131	NM_153758.5(IL19):c.-149+438A>C	IL10, IL19	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 1149147	NM_153758.5(IL19):c.-149+1173C>T	IL10, IL19 +1 more	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GLikely benign
Select item 1598090	NM_153758.5(IL19):c.-149+1178A>G	IL10, IL19 +1 more	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GLikely benign
Select item 2718333	NM_153758.5(IL19):c.-149+1179G>A	IL10, IL19 +1 more	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GLikely benign
Select item 729486	NM_153758.5(IL19):c.-149+1185A>G	IL10, IL19 +1 more	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GBenign
Select item 2100551	NM_000572.3(IL10):c.137A>G (p.Asp46Gly)	IL10, IL19 +1 more (D46G)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 2034096	NM_000572.3(IL10):c.135A>C (p.Arg45=)	IL10, IL19 +1 more	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease	GLikely benign
Select item 840379	NM_000572.3(IL10):c.134G>A (p.Arg45Gln)	LOC128462409, IL10 +1 more (R45Q)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 1493990	NM_000572.3(IL10):c.121C>T (p.Leu41Phe)	IL10, IL19 +1 more (L41F)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 2168240	NM_000572.3(IL10):c.118A>G (p.Met40Val)	IL10, IL19 +1 more (M40V)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 1963390	NM_000572.3(IL10):c.112C>G (p.Pro38Ala)	IL10, IL19 +1 more (P38A)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 1051340	NM_000572.3(IL10):c.100C>A (p.Pro34Thr)	IL10, IL19 +1 more (P34T)	Single nucleotide variant (intron variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 526787	NM_000572.3(IL10):c.94C>A (p.His32Asn)	IL10, IL19 +1 more (H32N)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 2120422	NM_000572.3(IL10):c.92C>T (p.Thr31Ile)	IL10, IL19 +1 more (T31I)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 1122395	NM_000572.3(IL10):c.84C>T (p.Asn28=)	IL10, IL19 +1 more	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease	GLikely benign
Select item 946285	NM_000572.3(IL10):c.71C>G (p.Thr24Ser)	IL10, IL19 +1 more (T24S)	Single nucleotide variant (intron variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 2177646	NM_000572.3(IL10):c.62G>A (p.Gly21Asp)	IL10, IL19 +1 more (G21D)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 526788	NM_000572.3(IL10):c.58C>T (p.Pro20Ser)	IL10, IL19 +1 more (P20S)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 729261	NM_000572.3(IL10):c.56G>A (p.Ser19Asn)	IL10, IL19 +1 more (S19N)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease	GLikely benign
Select item 726782	NM_000572.3(IL10):c.48G>A (p.Val16=)	LOC128462409, IL10 +1 more	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease	GLikely benign
Select item 1484774	NM_000572.3(IL10):c.46G>T (p.Val16Leu)	LOC128462409, IL10 +1 more (V16L)	Single nucleotide variant (intron variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 456662	NM_000572.3(IL10):c.43G>A (p.Gly15Arg)	IL10, IL19 +1 more (G15R)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease +4 more	GConflicting classifications of pathogenicity
Select item 1522939	NM_000572.3(IL10):c.37C>A (p.Leu13Met)	IL10, IL19 +1 more (L13M)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease	GUncertain significance
Select item 1656712	NM_000572.3(IL10):c.30G>C (p.Leu10=)	IL10, IL19 +1 more	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease	GLikely benign
Select item 1140946	NM_000572.3(IL10):c.18G>A (p.Leu6=)	IL10, IL19 +1 more	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease	GLikely benign
Select item 1131513	NM_000572.3(IL10):c.6C>T (p.His2=)	IL10, IL19 +1 more	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease +1 more	GLikely benign
Select item 16873	NM_153758.5(IL19):c.-149+1984T>G	IL10, IL19	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GBenign
Select item 1166836	NM_153758.5(IL19):c.-149+2211A>G	IL10, IL19	Single nucleotide variant (intron variant)	Inflammatory bowel disease	GBenign
Select item 1710531	NM_153758.5(IL19):c.-149+2474T>C	IL10, IL19	Single nucleotide variant (intron variant)	Leprosy, susceptibility to, 1	GUncertain risk allele
Select item 16874	NM_153758.5(IL19):c.-149+4208T>C	IL10, IL19	Single nucleotide variant (intron variant)	Rheumatoid arthritis, progression of	GPathogenic
Select item 3109216	NM_153758.5(IL19):c.-24C>T	IL19	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2360866	NM_153758.5(IL19):c.-6C>T	IL19	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 3109211	NM_153758.5(IL19):c.70G>A (p.Gly24Ser)	IL19 (G24S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2308177	NM_153758.5(IL19):c.133A>G (p.Lys45Glu)	IL19 (K45E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325793	NM_153758.5(IL19):c.229G>A (p.Val77Met)	IL19 (V77M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3109212	NM_153758.5(IL19):c.259G>C (p.Asp87His)	IL19 (D87H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456620	NM_153758.5(IL19):c.355C>T (p.Arg119Trp)	IL19 (R119W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109213	NM_153758.5(IL19):c.394G>A (p.Glu132Lys)	IL19 (E132K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248011	NM_153758.5(IL19):c.405T>G (p.Asn135Lys)	IL19 (N135K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292070	NM_153758.5(IL19):c.430T>G (p.Tyr144Asp)	IL19 (Y144D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109214	NM_153758.5(IL19):c.448C>T (p.His150Tyr)	IL19 (H150Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233592	NM_153758.5(IL19):c.458C>G (p.Ala153Gly)	IL19 (A153G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109215	NM_153758.5(IL19):c.481G>A (p.Asp161Asn)	IL19 (D161N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226551	NM_153758.5(IL19):c.522G>A (p.Met174Ile)	IL19 (M174I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3248093	NC_000001.10:g.(?_190829412)_(216061974_?)del	CFHR5, CHI3L1 +185 more	Deletion	not provided	GPathogenic
Select item 2422293	NC_000001.10:g.(?_200522516)_(208391267_?)dup	C4BPA, FMOD +110 more	Duplication	not provided	GUncertain significance
Select item 1809264	GRCh37/hg19 1q25.3-32.3(chr1:181453460-213107248)x3	IGFN1, IKBKE +211 more	Copy number gain	not provided	GPathogenic
Select item 1708464	GRCh37/hg19 1q31.3-44(chr1:197867914-249224684)x3	ABCB10, ACBD3 +381 more	Copy number gain	See cases	GPathogenic

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