FAS[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1966792	NM_000043.6(FAS):c.31-13T>A	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 301522	NM_000043.6(FAS):c.31-9A>G	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 661911	NM_000043.6(FAS):c.31-8T>G	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 3013405	NM_000043.6(FAS):c.32T>C (p.Val11Ala)	FAS (V11A +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 2025749	NM_000043.6(FAS):c.33T>C (p.Val11=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 301523	NM_000043.6(FAS):c.33T>A (p.Val11=)	FAS	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 2097629	NM_000043.6(FAS):c.38C>A (p.Thr13Lys)	FAS (T13K +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1397597	NM_000043.6(FAS):c.38C>T (p.Thr13Met)	FAS (T13M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 851315	NM_000043.6(FAS):c.38del (p.Thr13fs)	FAS (T13fs)	Deletion (frameshift variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GPathogenic
Select item 1563845	NM_000043.6(FAS):c.39G>A (p.Thr13=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 872242	NM_000043.6(FAS):c.46_47del (p.Val15_Ala16insTer)	FAS	Deletion (nonsense +1 more)	Autoimmune lymphoproliferative syndrome type 1 +1 more	GPathogenic
Select item 134371	NM_000043.6(FAS):c.46G>A (p.Ala16Thr)	FAS (A16T)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1 +1 more	GBenign/Likely benign
Select item 2083953	NM_000043.6(FAS):c.55T>C (p.Ser19Pro)	FAS (S19P +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 2787069	NM_000043.6(FAS):c.56C>T (p.Ser19Leu)	FAS (S19L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1150743	NM_000043.6(FAS):c.57G>A (p.Ser19=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +1 more	GLikely benign
Select item 3257941	NM_000043.6(FAS):c.61A>T (p.Lys21Ter)	FAS (K21* +1 more)	Single nucleotide variant (nonsense +1 more)	Neoplasm	OLikely oncogenic
Select item 2983914	NM_000043.6(FAS):c.66T>C (p.Ser22=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 2723129	NM_000043.6(FAS):c.67G>A (p.Val23Ile)	FAS (V23I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 16508	NM_000043.6(FAS):c.73G>A (p.Ala25Thr)	FAS (A25T)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome, type 1a	GPathogenic
Select item 1409348	NM_000043.6(FAS):c.77A>G (p.Gln26Arg)	FAS (Q26R)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 878041	NM_000043.6(FAS):c.78A>G (p.Gln26=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GBenign/Likely benign
Select item 1520853	NM_000043.6(FAS):c.79G>A (p.Val27Met)	FAS (V27M)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 879503	NM_000043.6(FAS):c.84T>C (p.Thr28=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1136089	NM_000043.6(FAS):c.87C>T (p.Asp29=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 1044705	NM_000043.6(FAS):c.95C>A (p.Ser32Tyr)	FAS (S32Y)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1449112	NM_000043.6(FAS):c.97A>C (p.Lys33Gln)	FAS (K33Q)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1040507	NM_000043.6(FAS):c.97A>G (p.Lys33Glu)	FAS (K33E)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 2498466	NM_000043.6(FAS):c.98A>C (p.Lys33Thr)	FAS (K33T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 532232	NM_000043.6(FAS):c.102A>G (p.Gly34=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 2155954	NM_000043.6(FAS):c.103T>A (p.Leu35Met)	FAS (L35M +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 301524	NM_000043.6(FAS):c.103T>C (p.Leu35=)	FAS	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 1509252	NM_000043.6(FAS):c.104T>G (p.Leu35Trp)	FAS (L35W)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 580709	NM_000043.6(FAS):c.110T>A (p.Leu37Ter)	FAS (L37*)	Single nucleotide variant (nonsense +1 more)	Autoimmune lymphoproliferative syndrome type 1	GPathogenic
Select item 2698574	NM_000043.6(FAS):c.115A>T (p.Lys39Ter)	FAS (K54* +1 more)	Single nucleotide variant (nonsense +1 more)	Autoimmune lymphoproliferative syndrome type 1	GPathogenic
Select item 2836853	NM_000043.6(FAS):c.136A>C (p.Thr46Pro)	FAS (T46P +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 2081225	NM_000043.6(FAS):c.140A>G (p.Gln47Arg)	FAS (Q47R +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1 +1 more	GConflicting classifications of pathogenicity
Select item 301525	NM_000043.6(FAS):c.141G>A (p.Gln47=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1 +2 more	GBenign
Select item 2012302	NM_000043.6(FAS):c.144C>T (p.Asn48=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 2414133	NM_000043.6(FAS):c.145T>C (p.Leu49=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 3017042	NM_000043.6(FAS):c.155_169dup (p.Gly56_Gln57insLeuHisHisAspGly)	FAS	Duplication (inframe_insertion +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 2640668	NM_000043.6(FAS):c.153C>T (p.Gly51=)	FAS	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 857680	NM_000043.6(FAS):c.161A>G (p.His54Arg)	FAS (H54R)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 2169310	NM_000043.6(FAS):c.162T>C (p.His54=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 1429679	NM_000043.6(FAS):c.163G>C (p.Asp55His)	FAS (D55H)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1 +1 more	GUncertain significance
Select item 2002840	NM_000043.6(FAS):c.174C>T (p.Phe58=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 2762517	NM_000043.6(FAS):c.175T>A (p.Cys59Ser)	FAS (C74S +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 301526	NM_000043.6(FAS):c.176G>T (p.Cys59Phe)	FAS (C59F)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 802617	NM_000043.6(FAS):c.178del (p.His60fs)	FAS (H60fs)	Deletion (frameshift variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GPathogenic
Select item 1439236	NM_000043.6(FAS):c.179A>G (p.His60Arg)	FAS (H60R)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1413808	NM_000043.6(FAS):c.182_183insTTAT (p.Lys61fs)	FAS (K61fs)	Insertion (frameshift variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GPathogenic
Select item 155871	NM_000043.6(FAS):c.183G>A (p.Lys61=)	FAS	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign
Select item 806000	NM_000043.6(FAS):c.185C>G (p.Pro62Arg)	FAS (P62R)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 2811621	NM_000043.6(FAS):c.187T>C (p.Cys63Arg)	FAS (C78R +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 636739	NM_000043.6(FAS):c.191del (p.Pro64fs)	FAS (P64fs)	Deletion (frameshift variant +1 more)	not provided	GLikely pathogenic
Select item 2047175	NM_000043.6(FAS):c.195A>G (p.Pro65=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 2105287	NM_000043.6(FAS):c.196+2dup	FAS	Duplication (splice donor variant)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1003135	NM_000043.6(FAS):c.196+3A>C	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 2851870	NM_000043.6(FAS):c.196+5G>T	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 2159363	NM_000043.6(FAS):c.196+17A>G	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 1291169	NM_000043.6(FAS):c.196+176C>T	FAS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238747	NM_000043.6(FAS):c.197-110C>T	FAS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277444	NM_000043.6(FAS):c.197-62G>C	FAS	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1588642	NM_000043.6(FAS):c.197-18C>G	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 1632415	NM_000043.6(FAS):c.197-11T>C	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 1529362	NM_000043.6(FAS):c.197-11T>A	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 1566764	NM_000043.6(FAS):c.197-8T>C	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 598753	NM_000043.6(FAS):c.197-2A>G	FAS	Single nucleotide variant (splice acceptor variant)	Autoimmune lymphoproliferative syndrome type 1	GLikely pathogenic
Select item 1473254	NM_000043.6(FAS):c.197-1G>A	FAS	Single nucleotide variant (splice acceptor variant)	Autoimmune lymphoproliferative syndrome type 1	GLikely pathogenic
Select item 2959237	NM_000043.6(FAS):c.204G>T (p.Arg68Ser)	FAS (R83S +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 749195	NM_000043.6(FAS):c.216C>T (p.Asp72=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 1023229	NM_000043.6(FAS):c.217T>G (p.Cys73Gly)	FAS (C73G)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1415216	NM_000043.6(FAS):c.218G>C (p.Cys73Ser)	FAS (C73S)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 301527	NM_000043.6(FAS):c.222A>G (p.Thr74=)	FAS	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign
Select item 2879692	NM_000043.6(FAS):c.226A>C (p.Asn76His)	FAS (N76H +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 16497	NM_000043.6(FAS):c.232del (p.Asp78fs)	FAS (D78fs)	Deletion (frameshift variant +1 more)	Autoimmune lymphoproliferative syndrome, type 1a	GPathogenic
Select item 2991381	NM_000043.6(FAS):c.230G>A (p.Gly77Glu)	FAS (G77E +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 2441356	NM_000043.6(FAS):c.245G>A (p.Cys82Tyr)	FAS (C82Y +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1155659	NM_000043.6(FAS):c.246C>T (p.Cys82=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1 +1 more	GLikely benign
Select item 1001817	NM_000043.6(FAS):c.247G>A (p.Val83Met)	FAS (V83M)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 2172165	NM_000043.6(FAS):c.249G>A (p.Val83=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 879504	NM_000043.6(FAS):c.251C>T (p.Pro84Leu)	FAS (P84L)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1451181	NM_000043.6(FAS):c.259G>T (p.Glu87Ter)	FAS (E87*)	Single nucleotide variant (nonsense +1 more)	Autoimmune lymphoproliferative syndrome type 1	GPathogenic
Select item 1392172	NM_000043.6(FAS):c.259G>A (p.Glu87Lys)	FAS (E87K)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1143163	NM_000043.6(FAS):c.264G>A (p.Gly88=)	FAS	Single nucleotide variant (non-coding transcript variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 3381062	NM_000043.6(FAS):c.265A>T (p.Lys89Ter)	FAS (K104* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided	GLikely pathogenic
Select item 1129893	NM_000043.6(FAS):c.270G>A (p.Glu90=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 2977588	NM_000043.6(FAS):c.279C>A (p.Asp93Glu)	FAS (D93E +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 653447	NM_000043.6(FAS):c.287A>G (p.His96Arg)	FAS (H96R)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1879140	NM_000043.6(FAS):c.301T>A (p.Cys101Ser)	FAS (C101S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2708956	NM_000043.6(FAS):c.310T>C (p.Cys104Arg)	FAS (C104R +1 more)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 1443489	NM_000043.6(FAS):c.312dup (p.Arg105Ter)	FAS (R105*)	Duplication (nonsense +1 more)	Autoimmune lymphoproliferative syndrome type 1	GPathogenic
Select item 1336616	NM_000043.6(FAS):c.318G>C (p.Leu106Phe)	FAS (L106F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 864610	NM_000043.6(FAS):c.323A>G (p.Asp108Gly)	FAS (D108G)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely pathogenic
Select item 1673935	NM_000043.6(FAS):c.324T>C (p.Asp108=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign
Select item 1395111	NM_000043.6(FAS):c.332A>G (p.His111Arg)	FAS (H111R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 2040054	NM_000043.6(FAS):c.333T>C (p.His111=)	FAS	Single nucleotide variant (synonymous variant +1 more)	Autoimmune lymphoproliferative syndrome type 1	GUncertain significance
Select item 16498	NM_000043.6(FAS):c.334+2dup	FAS	Duplication (splice donor variant)	Autoimmune lymphoproliferative syndrome type 1	GPathogenic
Select item 1802177	NM_000043.6(FAS):c.334+2T>C	FAS	Single nucleotide variant (splice donor variant)	Autoimmune lymphoproliferative syndrome type 1	GPathogenic
Select item 1406327	NM_000043.6(FAS):c.334+3A>C	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1 +1 more	GUncertain significance
Select item 2919915	NM_000043.6(FAS):c.334+11T>C	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1	GLikely benign

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