List of variants reported as likely pathogenic for ATTRV122I amyloidosis by Invitae

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Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.280G>C (p.Asp94His)	rs730881164	0.00007
NM_000371.4(TTR):c.119T>C (p.Val40Ala)
NM_000371.4(TTR):c.131C>T (p.Pro44Leu)	rs1415606768
NM_000371.4(TTR):c.155T>C (p.Val52Ala)	rs2073493951
NM_000371.4(TTR):c.163A>G (p.Lys55Glu)
NM_000371.4(TTR):c.193G>A (p.Ala65Thr)	rs121918078
NM_000371.4(TTR):c.194C>A (p.Ala65Asp)	rs730881169
NM_000371.4(TTR):c.200G>T (p.Gly67Val)	rs121918090
NM_000371.4(TTR):c.206C>G (p.Thr69Ser)	rs1555631387
NM_000371.4(TTR):c.208A>G (p.Ser70Gly)
NM_000371.4(TTR):c.217G>A (p.Gly73Arg)	rs2144409459
NM_000371.4(TTR):c.220_221inv (p.Glu74Ser)
NM_000371.4(TTR):c.221A>C (p.Glu74Ala)	rs1598845097
NM_000371.4(TTR):c.235A>G (p.Thr79Ala)
NM_000371.4(TTR):c.251T>A (p.Phe84Tyr)
NM_000371.4(TTR):c.251T>C (p.Phe84Ser)	rs121918099
NM_000371.4(TTR):c.258A>T (p.Glu86Asp)	rs2073510816
NM_000371.4(TTR):c.259G>C (p.Gly87Arg)	rs11541799
NM_000371.4(TTR):c.268A>C (p.Lys90Gln)
NM_000371.4(TTR):c.268A>G (p.Lys90Glu)
NM_000371.4(TTR):c.326A>G (p.Glu109Gly)
NM_000371.4(TTR):c.326A>T (p.Glu109Val)	rs2073511444
NM_000371.4(TTR):c.328C>G (p.His110Asp)	rs121918074
NM_000371.4(TTR):c.350C>A (p.Ala117Asp)
NM_000371.4(TTR):c.377C>A (p.Thr126Asn)
NM_000371.4(TTR):c.407A>C (p.Tyr136Ser)	rs730881167
NM_000371.4(TTR):c.89G>A (p.Cys30Tyr)	rs2144406508

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