ClinVar Miner

List of variants in gene CHAT reported as benign for not specified

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Gene type:
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Total variants: 26
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HGVS dbSNP
NM_020549.4(CHAT):c.-10T>G rs7923716
NM_020549.4(CHAT):c.-17G>A rs77152496
NM_020549.4(CHAT):c.-44G>C rs7903315
NM_020549.4(CHAT):c.1111+45G>A rs58788269
NM_020549.4(CHAT):c.1122C>T (p.Asn374=) rs61115650
NM_020549.4(CHAT):c.1131G>A (p.Ser377=) rs115126024
NM_020549.4(CHAT):c.1135G>C (p.Asp379His) rs115212829
NM_020549.4(CHAT):c.1198G>A (p.Asp400Asn) rs8178991
NM_020549.4(CHAT):c.1281+16G>A rs61132699
NM_020549.4(CHAT):c.1281+47G>A rs11101192
NM_020549.4(CHAT):c.1372C>T (p.Leu458Phe) rs76014951
NM_020549.4(CHAT):c.1381= (p.Met461=) rs4838544
NM_020549.4(CHAT):c.1381A>G (p.Met461Val) rs4838544
NM_020549.4(CHAT):c.141C>G (p.Asp47Glu) rs3810948
NM_020549.4(CHAT):c.1641T>C (p.His547=) rs8178992
NM_020549.4(CHAT):c.1674C>T (p.Ser558=) rs7073028
NM_020549.4(CHAT):c.1682G>A (p.Arg561Gln) rs80097077
NM_020549.4(CHAT):c.2067C>T (p.Ile689=) rs3793801
NM_020549.4(CHAT):c.287-431G>A rs1880676
NM_020549.4(CHAT):c.358G>A (p.Ala120Thr) rs3810950
NM_020549.4(CHAT):c.388-50C>T rs4838537
NM_020549.4(CHAT):c.438C>T (p.Tyr146=) rs61731734
NM_020549.4(CHAT):c.711C>G (p.Ser237Arg) rs78925077
NM_020549.4(CHAT):c.727C>T (p.Leu243Phe) rs8178990
NM_020549.4(CHAT):c.753-26C>T rs12257601
NM_020549.4(CHAT):c.903T>C (p.Pro301=) rs113897064

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