RASD2[gene] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144164	GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3	IL17RA, LINC01640 +2088 more	Copy number gain	See cases	GPathogenic
Select item 145336	GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3	LOC130067403, LOC130067404 +2088 more	Copy number gain	See cases	GPathogenic
Select item 148861	GRCh38/hg38 22q11.21-12.3(chr22:20907226-37187347)x3	ADORA2A, ADORA2A-AS1 +823 more	Copy number gain	See cases	GPathogenic
Select item 149114	GRCh38/hg38 22q11.23-12.3(chr22:23279231-36247369)x3	LOC130067187, LOC130067188 +556 more	Copy number gain	See cases	GPathogenic
Select item 57629	GRCh38/hg38 22q12.3-13.1(chr22:35333993-38900177)x1	ANKRD54, APOL1 +293 more	Copy number loss	See cases	GPathogenic
Select item 3312896	NM_014310.4(RASD2):c.32C>T (p.Thr11Met)	RASD2 (T11M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312893	NM_014310.4(RASD2):c.106G>A (p.Val36Met)	RASD2 (V36M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278328	NM_014310.4(RASD2):c.193G>A (p.Asp65Asn)	RASD2 (D65N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151774	NM_014310.4(RASD2):c.234C>A (p.His78Gln)	RASD2 (H78Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240123	NM_014310.4(RASD2):c.244G>A (p.Ala82Thr)	RASD2 (A82T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151775	NM_014310.4(RASD2):c.346A>T (p.Ile116Phe)	RASD2 (I116F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485730	NM_014310.4(RASD2):c.454C>T (p.Pro152Ser)	RASD2 (P152S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386357	NM_014310.4(RASD2):c.466G>C (p.Ala156Pro)	RASD2 (A156P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398612	NM_014310.4(RASD2):c.482C>T (p.Ser161Leu)	RASD2 (S161L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151777	NM_014310.4(RASD2):c.550T>C (p.Tyr184His)	RASD2 (Y184H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312894	NM_014310.4(RASD2):c.610A>G (p.Ile204Val)	RASD2 (I204V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151778	NM_014310.4(RASD2):c.661C>T (p.Arg221Cys)	RASD2 (R221C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151779	NM_014310.4(RASD2):c.758G>A (p.Arg253Gln)	RASD2 (R253Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2422150	NC_000022.10:g.(?_35776672)_(42486826_?)dup	ACO2, ADSL +132 more	Duplication	Adenylosuccinate lyase deficiency	GUncertain significance
Select item 983188	GRCh37/hg19 22q11.1-13.33(chr22:16197005-51224252)x3	A4GALT, ACO2 +438 more	Copy number gain	See cases	GPathogenic
Select item 816216	GRCh37/hg19 22q12.2-13.33(chr22:30654764-51197838)x3	CERK, CHADL +271 more	Copy number gain	not provided	GPathogenic
Select item 685636	GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3	TUBA8, TUBGCP6 +435 more	Copy number gain	not provided	GPathogenic
Select item 443342	GRCh37/hg19 22q12.3-13.1(chr22:35674826-39466442)x3	ANKRD54, APOBEC3A +76 more	Copy number gain	See cases	GLikely pathogenic
Select item 441826	GRCh37/hg19 22q11.23-12.3(chr22:23637907-36614412)x3	ADORA2A, AP1B1 +131 more	Copy number gain	See cases	GPathogenic
Select item 441654	GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)	ANKRD54, AP1B1 +435 more	Copy number gain	See cases	GPathogenic
Select item 441653	GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3	NEFH, NF2 +435 more	Copy number gain	See cases	GPathogenic
Select item 395140	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3	ZNF280A, ZNF280B +438 more	Copy number gain	See cases	GPathogenic
Select item 394709	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3	SMARCB1, SMC1B +438 more	Copy number gain	See cases	GPathogenic
Select item 253617	GRCh37/hg19 22q12.3-13.33(chr22:35728929-51220961)x3	A4GALT, ACO2 +223 more	Copy number gain	See cases	GPathogenic
Select item 253509	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3	A4GALT, ACO2 +438 more	Copy number gain	See cases	GPathogenic
Select item 221996	GRCh37/hg19 22q12.3-13.1(chr22:35680095-38098981)x1	APOL1, APOL2 +41 more	Copy number loss	See cases	GPathogenic

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Items: 31