RASSF2[gene] - ClinVar

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Items: 53

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150785	GRCh38/hg38 20p13-12.3(chr20:80093-6386012)x3	LOC130065401, LOC130065402 +348 more	Copy number gain	See cases	GPathogenic
Select item 149704	GRCh38/hg38 20p13-12.1(chr20:80106-13029401)x3	LOC130065344, LOC130065345 +455 more	Copy number gain	See cases	GPathogenic
Select item 144514	GRCh38/hg38 20p13-q11.1(chr20:80106-30227427)x3	LOC129456123, LOC130065248 +833 more	Copy number gain	See cases	GPathogenic
Select item 154176	GRCh38/hg38 20p13-12.3(chr20:80927-5447679)x3	LOC112694699, LOC112694712 +306 more	Copy number gain	See cases	GUncertain significance
Select item 153731	GRCh38/hg38 20p13-11.1(chr20:80927-26324843)x3	ABHD12, ACSS1 +828 more	Copy number gain	See cases	GPathogenic
Select item 155359	GRCh38/hg38 20p13-11.23(chr20:80928-18688031)x3	ADAM33, ADISSP +571 more	Copy number gain	See cases	GPathogenic
Select item 152841	GRCh38/hg38 20p13-12.3(chr20:84402-6159078)x3	LOC114004355, LOC116286198 +347 more	Copy number gain	See cases	GPathogenic
Select item 2579201	GRCh38/hg38 20p13-11.21(chr20:87153-23635465)x3	ADAM33, ADISSP +731 more	Copy number gain	Renal agenesis	GPathogenic
Select item 59191	GRCh38/hg38 20p13-11.23(chr20:89939-19071495)x3	ADAM33, ADISSP +579 more	Copy number gain	See cases	GPathogenic
Select item 57514	GRCh38/hg38 20p13-11.21(chr20:89939-25697564)x3	FASTKD5, FERMT1 +814 more	Copy number gain	See cases	GPathogenic
Select item 57354	GRCh38/hg38 20p13-11.23(chr20:89939-19146279)x3	LOC130065324, LOC130065325 +581 more	Copy number gain	See cases	GPathogenic
Select item 146596	GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3	JPH2, KAT14 +2522 more	Copy number gain	See cases	GPathogenic
Select item 154850	GRCh38/hg38 20p13-12.3(chr20:1269303-8626911)x3	LOC130065322, LOC130065323 +300 more	Copy number gain	See cases	GPathogenic
Select item 148627	GRCh38/hg38 20p13-12.3(chr20:4343033-6911730)x1	BMP2, CASC20 +101 more	Copy number loss	See cases	GPathogenic
Select item 146302	GRCh38/hg38 20p13(chr20:4594991-5050271)x3	LOC111240478, LOC111240479 +25 more	Copy number gain	See cases	GUncertain significance
Select item 3312973	NM_014737.3(RASSF2):c.955A>C (p.Ile319Leu)	RASSF2 (I319L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342244	NM_014737.3(RASSF2):c.919G>A (p.Val307Met)	RASSF2 (V307M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398117	NM_014737.3(RASSF2):c.908G>A (p.Arg303His)	RASSF2 (R303H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151926	NM_014737.3(RASSF2):c.842C>T (p.Pro281Leu)	RASSF2 (P281L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249760	NM_014737.3(RASSF2):c.839T>A (p.Met280Lys)	RASSF2 (M280K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312972	NM_014737.3(RASSF2):c.709G>T (p.Ala237Ser)	RASSF2 (A237S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312971	NM_014737.3(RASSF2):c.604C>T (p.Pro202Ser)	RASSF2 (P202S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246260	NM_014737.3(RASSF2):c.563G>T (p.Gly188Val)	RASSF2 (G188V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151925	NM_014737.3(RASSF2):c.455G>A (p.Arg152His)	RASSF2 (R152H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372386	NM_014737.3(RASSF2):c.451C>T (p.Arg151Cys)	RASSF2 (R151C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276196	NM_014737.3(RASSF2):c.317A>G (p.Lys106Arg)	RASSF2 (K106R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218605	NM_014737.3(RASSF2):c.307A>T (p.Thr103Ser)	RASSF2 (T103S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151924	NM_014737.3(RASSF2):c.227G>A (p.Arg76His)	RASSF2 (R76H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209869	NM_014737.3(RASSF2):c.200G>A (p.Arg67His)	RASSF2 (R67H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373071	NM_014737.3(RASSF2):c.191G>A (p.Arg64Gln)	RASSF2 (R64Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296015	NM_014737.3(RASSF2):c.130C>G (p.Arg44Gly)	RASSF2 (R44G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151923	NM_014737.3(RASSF2):c.124C>T (p.Arg42Trp)	RASSF2 (R42W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366403	NM_014737.3(RASSF2):c.89A>G (p.Tyr30Cys)	RASSF2 (Y30C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478746	NM_014737.3(RASSF2):c.10A>G (p.Ser4Gly)	RASSF2 (S4G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3248273	NC_000020.10:g.(?_3190198)_(6760201_?)del	DNAAF9, FERMT1 +35 more	Deletion	Inosine triphosphatase deficiency	GPathogenic
Select item 3024619	GRCh37/hg19 20p13-11.21(chr20:68351-23860313)x3	THBD, TMC2 +164 more	Copy number gain	not provided	GPathogenic
Select item 3024618	GRCh37/hg19 20p13-12.1(chr20:68351-16142323)x3	TMEM74B, TMX4 +114 more	Copy number gain	not provided	GPathogenic
Select item 2684899	GRCh37/hg19 20p13-12.2(chr20:61569-9542361)x3	ADAM33, ADISSP +100 more	Copy number gain	not provided	GPathogenic
Select item 2446383	GRCh37/hg19 20p13-12.3(chr20:3034557-5524417)x1	MAVS, OXT +36 more	Copy number loss	See cases	GLikely pathogenic
Select item 2422855	NC_000020.10:g.(?_1959939)_(6760201_?)dup	CDS2, CENPB +60 more	Duplication	Pigmentary pallidal degeneration +1 more	GUncertain significance
Select item 1703638	GRCh37/hg19 20p13-12.2(chr20:3178539-11848383)	ADAM33, ADRA1D +47 more	Copy number loss	20p12.3 microdeletion syndrome	GPathogenic
Select item 979727	GRCh37/hg19 20p13(chr20:3092739-4939933)x3	CDC25B, ADAM33 +25 more	Copy number gain	not provided	GUncertain significance
Select item 816102	GRCh37/hg19 20p13-11.1(chr20:61568-26305479)x3	ABHD12, ACSS1 +177 more	Copy number gain	not provided	GPathogenic
Select item 564645	GRCh37/hg19 20p13-12.1(chr20:3092739-17091453)x1	FERMT1, SPTLC3 +62 more	Copy number loss	not provided	GPathogenic
Select item 443885	GRCh37/hg19 20p13-12.3(chr20:2463101-8185680)x1	ADAM33, ADISSP +58 more	Copy number loss	See cases	GPathogenic
Select item 443774	GRCh37/hg19 20p13-12.2(chr20:61568-10486106)x3	ADAM33, ADISSP +104 more	Copy number gain	See cases	GLikely pathogenic
Select item 443340	GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3	AAR2, ABHD12 +540 more	Copy number gain	See cases	GPathogenic
Select item 443339	GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)	AAR2, ABHD12 +540 more	Copy number gain	See cases	GPathogenic
Select item 443248	GRCh37/hg19 20p13-12.3(chr20:213423-5483406)x3	ADAM33, ADISSP +80 more	Copy number gain	See cases	GUncertain significance
Select item 424642	GRCh37/hg19 20p13-q11.21(chr20:80198-26208081)x3	ESF1, FAM110A +178 more	Copy number gain	not provided	GPathogenic
Select item 394208	GRCh37/hg19 20p13-12.1(chr20:4392930-12667768)x1	ANKEF1, BMP2 +28 more	Copy number loss	See cases	GPathogenic
Select item 253647	GRCh37/hg19 20p13-11.1(chr20:80198-26075841)x3	ABHD12, ACSS1 +176 more	Copy number gain	See cases	GPathogenic
Select item 253566	GRCh37/hg19 20p13-12.3(chr20:121521-5564937)x3	ADAM33, ADISSP +85 more	Copy number gain	See cases	GPathogenic

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Items: 53