Table 1 Frequency of apparently disabling mutations in B. nigra COb

Pop	n	St1	D1	St2	d2	d3	Sp1	Sp2	D4	St3	I1	I2	None
		4 ^a	33	264	630	643	723	724	863	977	987	1056
			197						1032		988	1057
Eth	22	0.05	0.05	0	0.05	0.09	0.41	0	0.09	0.41	0	0.18	0.27
Fra	8	0	0.38	0.38	0	0	0	0	0	0	0.38	0.38	0
Ger	10	0	0	0	0	0	1	0	0	1	0	0	0
Gre	20	0	0.15	0	0.10	0.30	0.65	0	0.20	0.40	0	0	0.30
Ind	10	0	0.50	0	0	0	0.70	0	0	0.80	0	0.20	0
Ita	26	0	0	0.04	0.35	0.15	0.27	0.04	0.15	0.42	0.04	0.08	0.19
Tur	10	0	0.60	0	0	0	0	0	0	0.10	0	0.50	0.30
Tot	106	0.01	0.17	0.04	0.11	0.11	0.43	0.01	0.09	0.44	0.04	0.15	0.19

Abbreviations: n, number of alleles sequenced.
Mutations denoted St result in premature stop codons, D denotes large deletions, d denotes one bp deletions resulting in frame shifts, Sp a mutation in a splice signal, and I denotes 2 bp insertions resulting in frame shifts.
^aNumbers below the names of mutations represent its position in nucleotides from the start codon. The positions of different mutations are also shown in Figure 1.

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