Table 1.

Nineteen SNPs in twelve candidate genes.

Δ (SNP Index)	Accession	Location (bp)	Reference Base (WT)	Altered Base in wb1	Type of Mutation	Gene Annotation
0.758	ORF1	21550665	T	G	Missense (T to P)	Helicase conserved C-terminal domain containing protein
0.754		21550664	G	T	Missense (T to K)
0.663		21550888	C	T	Intron mutation
0.655		21550286	T	A	Missense (T to S)
0.649		21551279	G	A	Intron mutation
0.754	ORF2	21539737	A	G	3′-UTR mutation	Protein of unknown function DUF668 family protein
0.612		21539457	G	T	Splice region mutation
0.743	ORF3	21331260	G	A	Missense (D to N)	40S ribosomal protein S10
0.734	ORF4	21514382	C	T	Intron mutation	Similar to H0315E07.10 protein
0.708		21513793	A	G	Intron mutation
0.734	ORF5	21612944	C	A	Missense (K to N)	CENP-E-like kinetochore protein
0.663		21610862	C	A	Missense (S to I)
0.733	ORF6	20423829	G	A	Missense (A to T)	Glycosyl hydrolases
0.733	ORF7	21795109	G	A	Missense (L to F)	Expressed protein
0.672	ORF8	21493980	G	A	Intron mutation	Similar to H0315E07.7 protein
0.639	ORF9	21897538	C	T	3′-UTR mutation	Nonsense-mediated decay UPF3
0.634	ORF10	21970357	C	T	5′-UTR mutation	Peptide transporter PTR2
0.631	ORF11	21710470	C	G	Intron mutation	Conserved hypothetical protein
0.61	ORF12	21734385	C	T	Nonsense (R to *)	No apical meristem protein

The asterisk indicates the stop codon.