Merged Table S5 and Table S6.

Excluded SSTR1:c.1170_1793del (large deletion.)

Used transvar to infer coordinates from cDNA mutation (or protein if cDNA failed.) Matching between transcript and variant prioritized VALIDATED refseq transcript and excluded (XM_*) transcripts. See "Inherited-variants_S11-S12-S13.ods" and "transvar_results.txt.csv" for raw data.

Merged overlapping EVC2 variants for sample A9 to chr4:g.5633570_5633573delATTC/c.1417_1420delGAAT/p.E473*fs*1. Transcript chosen was NM_001166136 as it agreed with the protein deletion call (Leucine reference amino acid).