Table 3 Overview of variants of high and moderate impact, their impact and the gene affected.

Strain	Chr	Position	ALT	Gene name	Ensembl ID	Modification
WMI	3	148895880	TA	Asxl1	ENSRNOG00000001603	Splice donor variant & splice region variant & intron variant
WMI	5	50287827	A	Zfp292	ENSRNOG00000031031	Missense variant
WMI	5	171455130	C	Wrap73	ENSRNOG00000014805	Splice donor variant & splice region variant & intron variant
WMI	8	21788512	A	Col5a3	ENSRNOG00000020525	Missense variant & splice region variant
WMI	11	84399496	C	Abcc5	ENSRNOG00000029178	Frameshift variant
WMI	12	13660098	C	Fscn1	ENSRNOG00000056585	Frameshift variant
WMI	14	9266419	GA	Wdfy3	ENSRNOG00000061121	Frameshift variant
WMI	17	49440318	G	Pou6f2	ENSRNOG00000013237	Splice donor variant & intron variant
WMI	17	55289842	T	Svil	ENSRNOG00000018110	Missense variant
WLI	2	60302395	CCT	Prlr	ENSRNOG00000057557	Frameshift variant & splice region variant
WLI	2	210884044	A	Gnat2	ENSRNOG00000019296	Missense variant
WLI	2	218889177	C	Slc30a7	ENSRNOG00000013912	Stop lost
WLI	4	152938803	T	Kdm5a	ENSRNOG00000010591	Missense variant
WLI	4	176505968	T	Slco1a2	ENSRNOG00000031249	Splice donor variant & intron variant
WLI	10	57738003	A	Nlrp1a	ENSRNOG00000023143	Missense variant
WLI	10	67392591	CA	Crlf3	ENSRNOG00000050657	Frameshift variant & splice region variant
WLI	12	41544356	C	Tpcn1	ENSRNOG00000059344	Missense variant
WLI	13	47589399	G	Pigr	ENSRNOG00000004405	Missense variant
WLI	17	49440316	AG	Pou6f2	ENSRNOG00000013237	Frameshift variant
WLI	20	22913769	A	Reep3	ENSRNOG00000000645	Missense variant

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