"PreventionGenetics, part of Exact Sciences"[submitter] AND "AFF2"[gen - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1336054	NM_002025.4(AFF2):c.303T>C (p.Ser101=)	AFF2	Single nucleotide variant (synonymous variant)	AFF2-related disorder +1 more	GBenign
Select item 3047582	NM_002025.4(AFF2):c.891G>A (p.Gln297=)	AFF2	Single nucleotide variant (synonymous variant)	AFF2-related disorder	GLikely benign
Select item 2632526	NM_002025.4(AFF2):c.1041+56452_1041+56454del	AFF2 (F14del)	Microsatellite (inframe_deletion +1 more)	AFF2-related disorder	GUncertain significance
Select item 283357	NM_002025.4(AFF2):c.1097A>G (p.His366Arg)	AFF2 (H366R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity
Select item 197738	NM_002025.4(AFF2):c.1121C>A (p.Ser374Tyr)	AFF2 (S374Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GBenign
Select item 3033268	NM_002025.4(AFF2):c.1287G>T (p.Leu429=)	AFF2	Single nucleotide variant (synonymous variant)	AFF2-related disorder	GLikely benign
Select item 2537940	NM_002025.4(AFF2):c.1330A>G (p.Thr444Ala)	AFF2 (T405A +5 more)	Single nucleotide variant (missense variant)	not provided +2 more	GLikely benign
Select item 128282	NM_002025.4(AFF2):c.1653A>G (p.Thr551=)	AFF2	Single nucleotide variant (synonymous variant)	AFF2-related disorder +1 more	GBenign
Select item 283886	NM_002025.4(AFF2):c.1858A>G (p.Thr620Ala)	AFF2 (T620A +5 more)	Single nucleotide variant (missense variant)	not specified +1 more	GLikely benign
Select item 2661609	NM_002025.4(AFF2):c.2351T>G (p.Met784Arg)	AFF2 (M425R +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2636273	NM_002025.4(AFF2):c.2459A>G (p.His820Arg)	AFF2 (H461R +5 more)	Single nucleotide variant (missense variant)	AFF2-related disorder	GUncertain significance
Select item 166659	NM_002025.4(AFF2):c.2656C>G (p.Pro886Ala)	AFF2 (P886A +5 more)	Single nucleotide variant (missense variant)	AFF2-related disorder +3 more	GBenign/Likely benign
Select item 194202	NM_002025.4(AFF2):c.2780G>A (p.Arg927His)	AFF2 (R927H +5 more)	Single nucleotide variant (missense variant)	not specified +3 more	GLikely benign
Select item 774549	NM_002025.4(AFF2):c.3002_3031del (p.Ile1001_Ala1010del)	AFF2	Deletion (inframe_deletion)	AFF2-related disorder +1 more	GLikely benign
Select item 3034121	NM_002025.4(AFF2):c.3033C>T (p.Thr1011=)	AFF2	Single nucleotide variant (synonymous variant)	AFF2-related disorder	GLikely benign
Select item 94027	NM_002025.4(AFF2):c.3088A>C (p.Ile1030Leu)	AFF2 (I1030L +4 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 3043521	NM_002025.4(AFF2):c.3543C>T (p.Tyr1181=)	AFF2	Single nucleotide variant (synonymous variant)	AFF2-related disorder	GLikely benign
Select item 128284	NM_002025.4(AFF2):c.3837G>A (p.Thr1279=)	AFF2	Single nucleotide variant (synonymous variant)	AFF2-related disorder	GBenign