"PreventionGenetics, part of Exact Sciences"[submitter] AND "AFF3"[gen - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040901	NM_001386135.1(AFF3):c.3516C>T (p.Tyr1172=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GLikely benign
Select item 2651182	NM_001386135.1(AFF3):c.3474G>A (p.Ala1158=)	AFF3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3059808	NM_001386135.1(AFF3):c.2910C>T (p.Phe970=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GBenign
Select item 2631655	NM_001386135.1(AFF3):c.2805CAA[1] (p.Asn937del)	AFF3 (N937del +1 more)	Microsatellite (inframe_deletion)	AFF3-related condition	GUncertain significance
Select item 3048417	NM_001386135.1(AFF3):c.2766G>A (p.Gln922=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GBenign
Select item 2630555	NM_001386135.1(AFF3):c.2667C>G (p.His889Gln)	AFF3 (H889Q +1 more)	Single nucleotide variant (missense variant)	AFF3-related condition	GUncertain significance
Select item 3038615	NM_001386135.1(AFF3):c.2592-5T>C	AFF3	Single nucleotide variant (intron variant)	AFF3-related condition	GLikely benign
Select item 3035450	NM_001386135.1(AFF3):c.2591+5G>A	AFF3	Single nucleotide variant (intron variant)	AFF3-related condition	GBenign
Select item 3057773	NM_001386135.1(AFF3):c.2475C>T (p.Asn825=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GLikely benign
Select item 3054555	NM_001386135.1(AFF3):c.2307A>G (p.Lys769=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GLikely benign
Select item 3024997	NM_001386135.1(AFF3):c.2134G>A (p.Ala712Thr)	AFF3 (A712T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3041817	NM_001386135.1(AFF3):c.2061G>A (p.Glu687=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GLikely benign
Select item 3059122	NM_001386135.1(AFF3):c.1921C>G (p.Leu641Val)	AFF3 (L641V +1 more)	Single nucleotide variant (missense variant)	AFF3-related condition	GLikely benign
Select item 2630383	NM_001386135.1(AFF3):c.1815del (p.Glu606fs)	AFF3 (E606fs +1 more)	Deletion (frameshift variant)	AFF3-related condition	GUncertain significance
Select item 3059499	NM_001386135.1(AFF3):c.1788del (p.Asp598fs)	AFF3 (D598fs +1 more)	Deletion (frameshift variant)	KINSSHIP syndrome +1 more	GBenign
Select item 3059258	NM_001386135.1(AFF3):c.1781_1785del (p.Thr594fs)	AFF3 (T594fs +1 more)	Deletion (frameshift variant)	AFF3-related condition	GBenign
Select item 2651188	NM_001386135.1(AFF3):c.1722C>T (p.Asn574=)	AFF3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3052623	NM_001386135.1(AFF3):c.1689G>A (p.Pro563=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GBenign
Select item 3045882	NM_001386135.1(AFF3):c.1498G>T (p.Val500Leu)	AFF3 (V500L +1 more)	Single nucleotide variant (missense variant)	AFF3-related condition	GLikely benign
Select item 3060909	NM_001386135.1(AFF3):c.1395G>A (p.Lys465=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GLikely benign
Select item 3051733	NM_001386135.1(AFF3):c.1368C>T (p.Pro456=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GLikely benign
Select item 2651194	NM_001386135.1(AFF3):c.1308G>A (p.Ser436=)	AFF3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3048479	NM_001386135.1(AFF3):c.1197G>A (p.Gln399=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GLikely benign
Select item 3057346	NM_001386135.1(AFF3):c.1170C>T (p.Arg390=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GLikely benign
Select item 2630082	NM_001386135.1(AFF3):c.994C>A (p.Pro332Thr)	AFF3 (P332T +1 more)	Single nucleotide variant (missense variant)	AFF3-related condition	GUncertain significance
Select item 3050483	NM_001386135.1(AFF3):c.922-10C>T	AFF3	Single nucleotide variant (intron variant)	AFF3-related condition	GBenign
Select item 1270586	NM_001386135.1(AFF3):c.837C>T (p.Ala279=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition +1 more	GBenign
Select item 2633805	NM_001386135.1(AFF3):c.812A>C (p.Lys271Thr)	AFF3 (K271T +1 more)	Single nucleotide variant (missense variant)	AFF3-related condition	GUncertain significance
Select item 3031952	NM_001386135.1(AFF3):c.692C>G (p.Pro231Arg)	AFF3 (P231R +1 more)	Single nucleotide variant (missense variant)	AFF3-related condition	GUncertain significance
Select item 2636626	NM_001386135.1(AFF3):c.631C>A (p.His211Asn)	AFF3 (H211N +1 more)	Single nucleotide variant (missense variant)	AFF3-related condition	GUncertain significance
Select item 3037215	NM_001386135.1(AFF3):c.573G>A (p.Val191=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GBenign
Select item 2651204	NM_001386135.1(AFF3):c.354C>A (p.Ala118=)	AFF3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3035092	NM_001386135.1(AFF3):c.171C>T (p.Tyr57=)	AFF3	Single nucleotide variant (synonymous variant)	AFF3-related condition	GLikely benign

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Items: 33