RIT2[gene] - ClinVar

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Items: 61

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58718	GRCh38/hg38 18p11.32-q23(chr18:53345-80209986)x3	ABHD3, ACAA2 +1646 more	Copy number gain	See cases	GPathogenic
Select item 149674	GRCh38/hg38 18p11.32-q23(chr18:118760-80254946)x3	LOC126862711, LOC126862712 +1643 more	Copy number gain	See cases	GPathogenic
Select item 155151	GRCh38/hg38 18p11.32-q23(chr18:136226-80256240)x3	LOC130062667, LOC130062668 +1643 more	Copy number gain	See cases	GPathogenic
Select item 154106	GRCh38/hg38 18p11.32-q23(chr18:136227-80256240)x3	LOC130062278, LOC130062279 +1643 more	Copy number gain	See cases	GPathogenic
Select item 160810	GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3	LOC126862732, LOC126862733 +1643 more	Copy number gain	See cases	GPathogenic
Select item 58729	GRCh38/hg38 18p11.32-q23(chr18:148963-80244381)x3	ANKRD12, ANKRD29 +1642 more	Copy number gain	See cases	GPathogenic
Select item 33085	GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3	SERPINB12, SERPINB13 +1643 more	Copy number gain	See cases	GPathogenic
Select item 150559	GRCh38/hg38 18p11.32-q23(chr18:149089-80254936)x3	LOC125368553, LOC125368554 +1643 more	Copy number gain	See cases	GPathogenic
Select item 144654	GRCh38/hg38 18p11.32-q23(chr18:149089-80234391)x3	LOC130062355, LOC130062356 +1642 more	Copy number gain	See cases	GPathogenic
Select item 58756	GRCh38/hg38 18q11.1-23(chr18:20960320-80234429)x3	LOC126862717, LOC126862718 +1266 more	Copy number gain	See cases	GPathogenic
Select item 154990	GRCh38/hg38 18q11.1-22.3(chr18:20962119-74691446)x3	LOC132090510, LOC132090511 +1089 more	Copy number gain	See cases	GPathogenic
Select item 58762	GRCh38/hg38 18q11.1-23(chr18:20989762-80209986)x3	LOC132211113, LOC132211114 +1266 more	Copy number gain	See cases	GPathogenic
Select item 59958	GRCh38/hg38 18q12.1-12.3(chr18:32111530-44070219)x1	ASXL3, C18orf21 +129 more	Copy number loss	See cases	GPathogenic
Select item 147738	GRCh38/hg38 18q12.1-23(chr18:32123105-80252149)x3	LOC130062787, LOC130062788 +1005 more	Copy number gain	See cases	GPathogenic
Select item 59960	GRCh38/hg38 18q12.2-21.1(chr18:36859191-47164436)x1	ARK2C, ARK2N +119 more	Copy number loss	See cases	GPathogenic
Select item 147762	GRCh38/hg38 18q12.2-22.1(chr18:38794728-65632804)x3	ACAA2, ALPK2 +596 more	Copy number gain	See cases	GPathogenic
Select item 154074	GRCh38/hg38 18q12.3-23(chr18:40367455-80256240)x3	LOC130062694, LOC130062695 +887 more	Copy number gain	See cases	GPathogenic
Select item 154629	GRCh38/hg38 18q12.3-21.1(chr18:41722823-49043887)x1	ARK2C, ARK2N +147 more	Copy number loss	See cases	GPathogenic
Select item 147605	GRCh38/hg38 18q12.3-21.1(chr18:42335174-46726460)x1	ARK2C, ARK2N +74 more	Copy number loss	See cases	GPathogenic
Select item 148972	GRCh38/hg38 18q12.3-23(chr18:42651392-80254946)x3	LINC01929, LINC02565 +879 more	Copy number gain	See cases	GPathogenic
Select item 2468710	NM_002930.4(RIT2):c.578A>C (p.Lys193Thr)	RIT2 (K193T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3154716	NM_002930.4(RIT2):c.509T>C (p.Ile170Thr)	RIT2 (I170T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2529401	NM_002930.4(RIT2):c.413A>G (p.Glu138Gly)	RIT2 (E138G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314561	NM_002930.4(RIT2):c.371A>G (p.Tyr124Cys)	RIT2 (Y124C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328221	NM_002930.4(RIT2):c.345G>C (p.Glu115Asp)	RIT2 (E115D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 769441	NM_002930.4(RIT2):c.235-8del	RIT2	Deletion (intron variant)	not provided	GBenign
Select item 3154714	NM_002930.4(RIT2):c.188T>C (p.Ile63Thr)	RIT2 (I63T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247838	NM_002930.4(RIT2):c.74T>C (p.Met25Thr)	RIT2 (M25T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154715	NM_002930.4(RIT2):c.49G>A (p.Gly17Arg)	RIT2 (G17R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393597	NM_002930.4(RIT2):c.29C>A (p.Ser10Tyr)	RIT2 (S10Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517126	NM_002930.4(RIT2):c.20C>G (p.Ala7Gly)	RIT2 (A7G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3242272	GRCh37/hg19 18q12.3(chr18:38682015-40447305)x1	PIK3C3, RIT2	Copy number loss	not provided	GUncertain significance
Select item 3063562	GRCh37/hg19 18q12.2-21.1(chr18:36823620-44030870)x1	ARK2C, ARK2N +11 more	Copy number loss	not specified	GLikely pathogenic
Select item 3063545	GRCh37/hg19 18q12.2-21.1(chr18:33793283-46823898)x1	ARK2C, ARK2N +29 more	Copy number loss	not specified	GPathogenic
Select item 1808951	GRCh37/hg19 18q12.3(chr18:39703214-40584221)x3	RIT2	Copy number gain	not provided	GUncertain significance
Select item 1703574	GRCh37/hg19 18p11.32-q23(chr18:1-78077248)	CABYR, CBLN2 +267 more	Copy number gain	Trisomy 18	GPathogenic
Select item 1526597	GRCh37/hg19 18p11.32-q23(chr18:136226-78014123)	ABHD3, ACAA2 +267 more	Copy number gain	not specified	GPathogenic
Select item 1340795	GRCh37/hg19 18q12.3(chr18:38661177-41507765)x1	PIK3C3, RIT2 +1 more	Copy number loss	not provided	GUncertain significance
Select item 1340187	GRCh37/hg19 18q12.3(chr18:39565952-42338070)x3	PIK3C3, RIT2 +2 more	Copy number gain	not provided	GUncertain significance
Select item 1326872	Single allele	AKAIN1, LIPG +174 more	Deletion	Intellectual disability	GPathogenic
Select item 1180529	GRCh37/hg19 18q11.2-23(chr18:23626739-78014976)x3	MAPRE2, TSHZ1 +176 more	Copy number gain	not provided	GPathogenic
Select item 979697	GRCh37/hg19 18q12.3(chr18:40100890-40503349)x3	RIT2	Copy number gain	not provided	GUncertain significance
Select item 816014	GRCh37/hg19 18q11.2-21.2(chr18:20689919-49455212)x3	ACAA2, ANKRD29 +97 more	Copy number gain	not provided	GPathogenic
Select item 816010	GRCh37/hg19 18q12.3-21.1(chr18:39800804-44365152)x1	ST8SIA5, RNF165 +12 more	Copy number loss	not provided	GPathogenic
Select item 816008	GRCh37/hg19 18q12.2-12.3(chr18:35075741-42526183)x1	RIT2, SYT4 +3 more	Copy number loss	not provided	GPathogenic
Select item 816006	GRCh37/hg19 18q12.3(chr18:38040162-41956192)x1	RIT2, SYT4 +1 more	Copy number loss	not provided	GUncertain significance
Select item 816005	GRCh37/hg19 18q12.3(chr18:40548003-40825757)x3	RIT2	Copy number gain	not provided	GUncertain significance
Select item 816004	GRCh37/hg19 18q12.2-12.3(chr18:37132106-40414893)x3	PIK3C3, RIT2	Copy number gain	not provided	GUncertain significance
Select item 564568	GRCh37/hg19 18q12.2-21.31(chr18:35866313-55082983)x3	ACAA2, ATP5F1A +55 more	Copy number gain	not provided	GPathogenic
Select item 564537	GRCh37/hg19 18q12.3(chr18:40602410-42148160)x3	SYT4, RIT2	Copy number gain	not provided	GLikely benign
Select item 564493	GRCh37/hg19 18q12.3(chr18:40586824-40806895)x1	RIT2	Copy number loss	not provided	GUncertain significance
Select item 443993	GRCh37/hg19 18p11.32-q23(chr18:136227-78014123)	ABHD3, ACAA2 +267 more	Copy number gain	See cases	GPathogenic
Select item 443662	GRCh37/hg19 18p11.21-q23(chr18:14869204-78014123)x3	ABHD3, ACAA2 +200 more	Copy number gain	See cases	GPathogenic
Select item 443196	GRCh37/hg19 18q12.1-23(chr18:31879854-78014123)x3	ACAA2, ADNP2 +150 more	Copy number gain	See cases	GPathogenic
Select item 443054	GRCh37/hg19 18q11.2-21.1(chr18:24835114-46917217)x3	ARK2C, ARK2N +62 more	Copy number gain	See cases	GLikely benign
Select item 442451	GRCh37/hg19 18p11.32-q21.1(chr18:136227-46171053)x3	ABHD3, ADCYAP1 +157 more	Copy number gain	See cases	GPathogenic
Select item 442013	GRCh37/hg19 18q11.1-22.1(chr18:18521285-64495798)x3	ABHD3, ACAA2 +163 more	Copy number gain	See cases	GPathogenic
Select item 441853	GRCh37/hg19 18q12.2-23(chr18:33417216-78014123)x3	ACAA2, ADNP2 +142 more	Copy number gain	See cases	GPathogenic
Select item 395441	GRCh37/hg19 18p11.32-q23(chr18:163323-78005185)x3	ABHD3, ACAA2 +267 more	Copy number gain	See cases	GPathogenic
Select item 253620	GRCh37/hg19 18q11.1-23(chr18:18548019-77954165)x3	ABHD3, ACAA2 +200 more	Copy number gain	See cases	GPathogenic
Select item 253424	GRCh37/hg19 18p11.32-q23(chr18:163323-78005236)x3	TNFRSF11A, TXNL1 +267 more	Copy number gain	See cases	GPathogenic

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Items: 61