ClinVar Miner

List of variants in gene TRIO studied for not specified

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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_007118.4(TRIO):c.171C>T (p.Asn57=) rs55664610 0.00913
NM_007118.4(TRIO):c.2811C>G (p.Ala937=) rs143042118 0.00529
NM_007118.4(TRIO):c.1179C>T (p.Asn393=) rs56035446 0.00399
NM_007118.4(TRIO):c.8831A>G (p.Asn2944Ser) rs143213427 0.00279
NM_007118.4(TRIO):c.6914G>A (p.Gly2305Asp) rs552613615 0.00158
NM_007118.4(TRIO):c.6836-4dup rs758053482 0.00023
NM_007118.4(TRIO):c.3067-4A>T rs200412925 0.00005
NM_007118.4(TRIO):c.1143G>C (p.Gln381His) rs369621289 0.00004
NM_007118.4(TRIO):c.1467A>G (p.Gly489=) rs759501399 0.00003
NM_007118.4(TRIO):c.5221A>G (p.Ser1741Gly) rs1206287803 0.00001
GRCh37/hg19 5p15.2(chr5:14300651-14379344)x1
NM_007118.4(TRIO):c.1053+8C>T
NM_007118.4(TRIO):c.1368+19del
NM_007118.4(TRIO):c.2167G>T (p.Val723Leu)
NM_007118.4(TRIO):c.3562A>G (p.Thr1188Ala) rs1746074176
NM_007118.4(TRIO):c.3716G>A (p.Arg1239Lys) rs2152361600
NM_007118.4(TRIO):c.3825T>G (p.Leu1275=) rs2152361847
NM_007118.4(TRIO):c.3881+3A>T
NM_007118.4(TRIO):c.3948+26_3948+27dup rs57751910
NM_007118.4(TRIO):c.4519C>T (p.Arg1507Trp) rs2152373766
NM_007118.4(TRIO):c.5638C>T (p.Leu1880Phe)
NM_007118.4(TRIO):c.5926G>C (p.Glu1976Gln)
NM_007118.4(TRIO):c.6388-14C>T
NM_007118.4(TRIO):c.6611A>G (p.Lys2204Arg) rs141648983
NM_007118.4(TRIO):c.7059CTC[1] (p.Ser2355del)
NM_007118.4(TRIO):c.7416C>T (p.Pro2472=)
NM_007118.4(TRIO):c.7444G>C (p.Gly2482Arg)
NM_007118.4(TRIO):c.7574G>A (p.Arg2525His) rs1756164006
NM_007118.4(TRIO):c.761G>A (p.Arg254Gln)
NM_007118.4(TRIO):c.8915C>A (p.Thr2972Asn)
NM_007118.4(TRIO):c.905C>T (p.Ala302Val)

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