List of variants reported as likely benign for channelopathy-associated congenital insensitivity to pain, autosomal recessive

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Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.*3038C>T	rs115766730	0.01421
NM_001365536.1(SCN9A):c.2827A>C (p.Met943Leu)	rs12478318	0.01339
NM_001365536.1(SCN9A):c.-294T>C	rs141521157	0.00704
NM_001365536.1(SCN9A):c.554G>A (p.Arg185His)	rs73969684	0.00574
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser)	rs141268327	0.00496
NM_001365536.1(SCN9A):c.2517+6C>T	rs145316463	0.00460
NM_001365536.1(SCN9A):c.1398C>T (p.Ser466=)	rs201531206	0.00386
NM_001365536.1(SCN9A):c.2190G>C (p.Trp730Cys)	rs202055175	0.00341
NM_001365536.1(SCN9A):c.5779C>T (p.Leu1927Phe)	rs111558968	0.00315
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val)	rs182650126	0.00278
NM_001365536.1(SCN9A):c.*2312A>T	rs185580193	0.00248
NM_001365536.1(SCN9A):c.*2212T>C	rs200750861	0.00201
NM_001365536.1(SCN9A):c.1997A>G (p.Lys666Arg)	rs121908919	0.00180
NM_001365536.1(SCN9A):c.3832C>G (p.Leu1278Val)	rs180922748	0.00174
NM_001365536.1(SCN9A):c.4645T>C (p.Trp1549Arg)	rs202084411	0.00173
NM_001365536.1(SCN9A):c.*362C>T	rs185832567	0.00092
NM_001365536.1(SCN9A):c.4315G>A (p.Val1439Ile)	rs149346064	0.00061
NM_001365536.1(SCN9A):c.1555G>A (p.Glu519Lys)	rs187453572	0.00059
NM_001365536.1(SCN9A):c.*3317A>G	rs191667986	0.00039
NM_001365536.1(SCN9A):c.2192T>A (p.Ile731Lys)	rs200945460	0.00019
NM_001365536.1(SCN9A):c.4495C>A (p.Arg1499=)	rs187558439	0.00019
NM_001365536.1(SCN9A):c.3472+14T>C	rs201979079	0.00017
NM_001365536.1(SCN9A):c.2875-6A>G	rs760470229	0.00011
NM_001365536.1(SCN9A):c.2165T>C (p.Leu722Ser)	rs187526567	0.00009
NM_001365536.1(SCN9A):c.5711G>A (p.Arg1904His)	rs79805025	0.00009
NM_001365536.1(SCN9A):c.29A>G (p.Gln10Arg)	rs267607030	0.00006
NM_001365536.1(SCN9A):c.561G>A (p.Pro187=)	rs200182914	0.00006
NM_001365536.1(SCN9A):c.1838C>T (p.Pro613Leu)	rs200671761	0.00005
NM_001365536.1(SCN9A):c.*2721C>G	rs199595958	0.00001
NM_001365536.1(SCN9A):c.5245C>T (p.Leu1749=)	rs200636760	0.00001
NM_001365536.1(SCN9A):c.*920T>A	rs201424899
NM_001365536.1(SCN9A):c.2874+11_2874+13del

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