ClinVar Miner

List of variants in gene NTRK1 reported as likely benign for not specified

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Total variants: 31
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HGVS dbSNP
NM_001007792.1(NTRK1):c.*7G>T rs145060242
NM_001007792.1(NTRK1):c.1128C>T (p.Asp376=) rs147438950
NM_001007792.1(NTRK1):c.1144-15C>G rs186649954
NM_001007792.1(NTRK1):c.1149G>A (p.Ser383=) rs750968694
NM_001007792.1(NTRK1):c.123-3404C>T rs201472270
NM_001007792.1(NTRK1):c.123-3447C>A rs753655855
NM_001007792.1(NTRK1):c.123-3458A>G rs570123832
NM_001007792.1(NTRK1):c.123-3463C>T rs1057522593
NM_001007792.1(NTRK1):c.1246+18A>T rs73004759
NM_001007792.1(NTRK1):c.1246+8G>A rs763576316
NM_001007792.1(NTRK1):c.1414C>A (p.Arg472=) rs200575096
NM_001007792.1(NTRK1):c.1449C>T (p.Gly483=) rs564775946
NM_001007792.1(NTRK1):c.164G>A (p.Arg55His) rs79678945
NM_001007792.1(NTRK1):c.1800G>A (p.Ala600=) rs17838192
NM_001007792.1(NTRK1):c.189G>A (p.Leu63=) rs147983523
NM_001007792.1(NTRK1):c.1939-6T>C rs762866535
NM_001007792.1(NTRK1):c.1959G>A (p.Leu653=) rs1057521447
NM_001007792.1(NTRK1):c.201C>T (p.Thr67=) rs1057522997
NM_001007792.1(NTRK1):c.2061C>T (p.Tyr687=) rs140852621
NM_001007792.1(NTRK1):c.2164G>A (p.Ala722Thr) rs62640939
NM_001007792.1(NTRK1):c.231G>T (p.Ala77=) rs774351278
NM_001007792.1(NTRK1):c.338+12C>T rs41267425
NM_001007792.1(NTRK1):c.441T>C (p.Cys147=) rs1057523619
NM_001007792.1(NTRK1):c.484+10G>A rs201336491
NM_001007792.1(NTRK1):c.485-16C>T rs143312136
NM_001007792.1(NTRK1):c.522G>A (p.Ser174=) rs114320051
NM_001007792.1(NTRK1):c.540C>T (p.Asp180=) rs147882947
NM_001007792.1(NTRK1):c.621G>A (p.Thr207=) rs537430475
NM_001007792.1(NTRK1):c.628-15T>C rs778745696
NM_001007792.1(NTRK1):c.978C>T (p.Asn326=) rs145823996
NM_001007792.1(NTRK1):c.987C>T (p.Tyr329=) rs1057521034

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