List of variants studied for Autosomal recessive limb-girdle muscular dystrophy type 2G; Hypertrophic cardiomyopathy 25 by Fulgent Genetics, Fulgent Genetics

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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_003673.4(TCAP):c.*297C>T	rs772638575	0.00034
NM_003673.4(TCAP):c.458G>A (p.Arg153His)	rs149585781	0.00021
NM_003673.4(TCAP):c.337C>T (p.Leu113Phe)	rs372312912	0.00014
NM_003673.4(TCAP):c.209G>A (p.Arg70Gln)	rs552865793	0.00012
NM_003673.3(TCAP):c.-13A>G	rs368175926	0.00010
NM_003673.4(TCAP):c.*292G>A	rs185210946	0.00010
NM_003673.4(TCAP):c.223G>A (p.Gly75Ser)	rs753744791	0.00010
NM_003673.4(TCAP):c.388C>T (p.Arg130Cys)	rs374886575	0.00009
NM_003673.4(TCAP):c.448G>A (p.Gly150Ser)	rs762850913	0.00009
NM_003673.4(TCAP):c.97C>T (p.Arg33Trp)	rs145524909	0.00009
NM_003673.4(TCAP):c.54G>C (p.Arg18=)	rs754054712	0.00004
NM_003673.4(TCAP):c.208C>T (p.Arg70Trp)	rs775636212	0.00003
NM_003673.4(TCAP):c.267G>A (p.Leu89=)	rs1419129039	0.00002
NM_003673.4(TCAP):c.157C>T (p.Gln53Ter)	rs104894655	0.00001
NM_003673.4(TCAP):c.194C>T (p.Pro65Leu)	rs2057250642	0.00001
NM_003673.4(TCAP):c.37G>A (p.Glu13Lys)	rs1042724474	0.00001
NM_003673.4(TCAP):c.401C>A (p.Ala134Asp)	rs786205287	0.00001
NM_003673.4(TCAP):c.66G>A (p.Trp22Ter)	rs141019458	0.00001
NM_003673.4(TCAP):c.98G>A (p.Arg33Gln)	rs1085307822	0.00001
NM_003673.4(TCAP):c.110_110+1del	rs786205076
NM_003673.4(TCAP):c.294_295delinsAG (p.Met99Val)	rs2057251619
NM_003673.4(TCAP):c.313G>A (p.Glu105Lys)	rs146906267
NM_003673.4(TCAP):c.341A>G (p.Gln114Arg)	rs1355624192
NM_003673.4(TCAP):c.457C>A (p.Arg153Ser)	rs761498487
NM_003673.4(TCAP):c.478A>G (p.Met160Val)	rs1057106389
NM_003673.4(TCAP):c.50_51delinsCT (p.Arg17Pro)	rs1555606961

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