Table 2. Genomic variants detected in eight exomes based on 2 454 GS FLX runs of aligned data.

Individual	10032	10033	10034	10035	10036	10037	10039	10082	Avg.	Range
KNOWN VARIANTS	7962	6342	6346	9480	9875	7924	9398	7165	8062	6342–9875
Non-Synonymous	3467	2687	2749	4059	4257	3363	3952	3108	3455	2687–4257
indel	49	38	34	69	73	41	65	56	53	34–73
SNP	3418	2649	2715	3990	4184	3322	3887	3052	3402	2649–4184
Synonymous	4495	3655	3597	5421	5618	4561	5446	4057	4606	3597–5618
indel	19	20	19	38	35	29	28	30	27	19–38
SNP	4476	3635	3578	5383	5583	4532	5418	4027	4579	3578–5583
NOVEL VARIANTS	607	456	444	844	1163	610	748	591	683	444–1163
Non-Synonymous	344	254	244	486	723	347	402	337	392	244–723
indel	49	44	31	118	296	48	58	115	95	31–296
SNP	295	210	213	368	427	299	344	222	297	210–427
Synonymous	263	202	200	358	440	263	346	254	291	200–440
indel	21	16	19	44	76	21	29	31	32	16–76
SNP	242	186	181	314	364	242	317	223	259	181–364
Total	8569	6798	6790	10324	11038	8534	10146	7756	8744	6790–11038