"Ambry Genetics"[submitter] AND "AFF1"[gene] - ClinVar

Search results

Items: 86

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2511477	NM_001166693.3(AFF1):c.44A>G (p.Tyr15Cys)	AFF1 (Y8C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385863	NM_001166693.3(AFF1):c.47A>G (p.Asn16Ser)	AFF1 (N16S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304850	NM_001166693.3(AFF1):c.80A>G (p.Lys27Arg)	AFF1 (K27R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330817	NM_001166693.3(AFF1):c.161C>T (p.Thr54Ile)	AFF1 (T47I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3092194	NM_001166693.3(AFF1):c.185G>A (p.Ser62Asn)	AFF1 (S62N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545285	NM_001166693.3(AFF1):c.215A>G (p.Glu72Gly)	AFF1 (E65G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232497	NM_001166693.3(AFF1):c.239C>T (p.Thr80Ile)	AFF1 (T73I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367877	NM_001166693.3(AFF1):c.256C>T (p.Arg86Cys)	AFF1 (R79C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3092263	NM_001166693.3(AFF1):c.257G>A (p.Arg86His)	AFF1 (R86H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535044	NM_001166693.3(AFF1):c.290C>T (p.Pro97Leu)	AFF1 (P90L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522475	NM_001166693.3(AFF1):c.380C>T (p.Ala127Val)	AFF1 (A120V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598066	NM_001166693.3(AFF1):c.533C>G (p.Ser178Cys)	AFF1 (S178C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3092323	NM_001166693.3(AFF1):c.617C>T (p.Ser206Phe)	AFF1 (S199F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2593240	NM_001166693.3(AFF1):c.715G>A (p.Gly239Ser)	AFF1 (G239S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2511832	NM_001166693.3(AFF1):c.722G>A (p.Ser241Asn)	AFF1 (S234N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2361761	NM_001166693.3(AFF1):c.740A>G (p.Tyr247Cys)	AFF1 (Y247C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2312762	NM_001166693.3(AFF1):c.805A>G (p.Ser269Gly)	AFF1 (S262G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401911	NM_001166693.3(AFF1):c.875C>T (p.Ala292Val)	AFF1 (A292V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364292	NM_001166693.3(AFF1):c.881A>T (p.Gln294Leu)	AFF1 (Q287L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295961	NM_001166693.3(AFF1):c.983C>T (p.Thr328Ile)	AFF1 (T328I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483908	NM_001166693.3(AFF1):c.993A>C (p.Lys331Asn)	AFF1 (K331N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3092125	NM_001166693.3(AFF1):c.1009C>T (p.Pro337Ser)	AFF1 (P330S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254120	NM_001166693.3(AFF1):c.1041G>T (p.Met347Ile)	AFF1 (M347I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3092130	NM_001166693.3(AFF1):c.1042C>T (p.Pro348Ser)	AFF1 (P341S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335666	NM_001166693.3(AFF1):c.1051T>A (p.Ser351Thr)	AFF1 (S344T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540227	NM_001166693.3(AFF1):c.1109T>C (p.Met370Thr)	AFF1 (M363T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372502	NM_001166693.3(AFF1):c.1141A>G (p.Ile381Val)	AFF1 (I381V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521753	NM_001166693.3(AFF1):c.1145A>G (p.His382Arg)	AFF1 (H382R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092142	NM_001166693.3(AFF1):c.1208G>A (p.Ser403Asn)	AFF1 (S403N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318912	NM_001166693.3(AFF1):c.1354C>G (p.Pro452Ala)	AFF1 (P452A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491303	NM_001166693.3(AFF1):c.1379C>A (p.Ala460Asp)	AFF1 (A460D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314316	NM_001166693.3(AFF1):c.1415A>T (p.His472Leu)	AFF1 (H465L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259832	NM_001166693.3(AFF1):c.1442C>G (p.Thr481Ser)	AFF1 (T112S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343614	NM_001166693.3(AFF1):c.1519A>T (p.Thr507Ser)	AFF1 (T138S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092167	NM_001166693.3(AFF1):c.1616C>G (p.Pro539Arg)	AFF1 (P539R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464061	NM_001166693.3(AFF1):c.1639C>T (p.Arg547Trp)	AFF1 (R178W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092172	NM_001166693.3(AFF1):c.1640G>A (p.Arg547Gln)	AFF1 (R547Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460803	NM_001166693.3(AFF1):c.1679G>A (p.Ser560Asn)	AFF1 (S553N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303388	NM_001166693.3(AFF1):c.1721C>G (p.Ser574Cys)	AFF1 (S574C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512420	NM_001166693.3(AFF1):c.1735C>T (p.Arg579Trp)	AFF1 (R572W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228179	NM_001166693.3(AFF1):c.1747G>A (p.Glu583Lys)	AFF1 (E214K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092183	NM_001166693.3(AFF1):c.1781A>G (p.Lys594Arg)	AFF1 (K225R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597975	NM_001166693.3(AFF1):c.1819G>A (p.Val607Ile)	AFF1 (V600I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482590	NM_001166693.3(AFF1):c.1819G>C (p.Val607Leu)	AFF1 (V607L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534933	NM_001166693.3(AFF1):c.1855T>C (p.Ser619Pro)	AFF1 (S619P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528141	NM_001166693.3(AFF1):c.1865C>T (p.Ala622Val)	AFF1 (A622V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570017	NM_001166693.3(AFF1):c.1903G>C (p.Gly635Arg)	AFF1 (G628R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092203	NM_001166693.3(AFF1):c.1916A>G (p.Tyr639Cys)	AFF1 (Y632C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468070	NM_001166693.3(AFF1):c.1949C>T (p.Pro650Leu)	AFF1 (P281L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216568	NM_001166693.3(AFF1):c.1969C>T (p.Arg657Trp)	AFF1 (R288W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366339	NM_001166693.3(AFF1):c.1975C>T (p.Arg659Trp)	AFF1 (R290W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092219	NM_001166693.3(AFF1):c.2002C>G (p.Pro668Ala)	AFF1 (P661A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092228	NM_001166693.3(AFF1):c.2015C>T (p.Pro672Leu)	AFF1 (P665L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589867	NM_001166693.3(AFF1):c.2015C>G (p.Pro672Arg)	AFF1 (P303R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302473	NM_001166693.3(AFF1):c.2032A>C (p.Lys678Gln)	AFF1 (K678Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092233	NM_001166693.3(AFF1):c.2056C>G (p.Pro686Ala)	AFF1 (P317A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553521	NM_001166693.3(AFF1):c.2066C>T (p.Ala689Val)	AFF1 (A682V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533890	NM_001166693.3(AFF1):c.2147G>A (p.Ser716Asn)	AFF1 (S716N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540743	NM_001166693.3(AFF1):c.2158C>T (p.Pro720Ser)	AFF1 (P713S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2588284	NM_001166693.3(AFF1):c.2225G>A (p.Arg742His)	AFF1 (R735H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549923	NM_001166693.3(AFF1):c.2290C>G (p.Pro764Ala)	AFF1 (P764A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381639	NM_001166693.3(AFF1):c.2294C>A (p.Pro765Gln)	AFF1 (P396Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374496	NM_001166693.3(AFF1):c.2335C>T (p.Arg779Trp)	AFF1 (R772W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230087	NM_001166693.3(AFF1):c.2410C>T (p.His804Tyr)	AFF1 (H804Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092254	NM_001166693.3(AFF1):c.2414G>T (p.Ser805Ile)	AFF1 (S798I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092255	NM_001166693.3(AFF1):c.2417C>G (p.Ser806Cys)	AFF1 (S437C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290212	NM_001166693.3(AFF1):c.2452G>T (p.Ala818Ser)	AFF1 (A811S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604475	NM_001166693.3(AFF1):c.2566A>G (p.Lys856Glu)	AFF1 (K487E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092260	NM_001166693.3(AFF1):c.2570C>G (p.Thr857Arg)	AFF1 (T850R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092268	NM_001166693.3(AFF1):c.2614C>T (p.Leu872Phe)	AFF1 (L865F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394968	NM_001166693.3(AFF1):c.2629G>A (p.Val877Met)	AFF1 (V508M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404707	NM_001166693.3(AFF1):c.2680C>T (p.Arg894Trp)	AFF1 (R525W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287813	NM_001166693.3(AFF1):c.2738A>G (p.Asn913Ser)	AFF1 (N913S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3092280	NM_001166693.3(AFF1):c.2789C>G (p.Ser930Cys)	AFF1 (S561C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092284	NM_001166693.3(AFF1):c.2821G>A (p.Gly941Arg)	AFF1 (G934R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610622	NM_001166693.3(AFF1):c.2827A>G (p.Thr943Ala)	AFF1 (T574A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369229	NM_001166693.3(AFF1):c.2852C>T (p.Ser951Phe)	AFF1 (S582F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298536	NM_001166693.3(AFF1):c.2941A>G (p.Met981Val)	AFF1 (M981V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314134	NM_001166693.3(AFF1):c.3046A>G (p.Ser1016Gly)	AFF1 (S1009G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621108	NM_001166693.3(AFF1):c.3071C>A (p.Ser1024Tyr)	AFF1 (S1017Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570191	NM_001166693.3(AFF1):c.3071C>G (p.Ser1024Cys)	AFF1 (S1017C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325776	NM_001166693.3(AFF1):c.3326C>T (p.Pro1109Leu)	AFF1 (P1101L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312492	NM_001166693.3(AFF1):c.3328T>C (p.Ser1110Pro)	AFF1 (S1102P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476112	NM_001166693.3(AFF1):c.3340C>T (p.Pro1114Ser)	AFF1 (P1106S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464527	NM_001166693.3(AFF1):c.3344T>A (p.Met1115Lys)	AFF1 (M1115K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508278	NM_001166693.3(AFF1):c.3400A>G (p.Ser1134Gly)	AFF1 (S1134G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

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Items: 86