ClinVar Miner

List of variants in gene NTRK1 reported as benign for Hereditary insensitivity to pain with anhidrosis

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Total variants: 28
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HGVS dbSNP
NM_001007792.1(NTRK1):c.1128C>T (p.Asp376=) rs147438950
NM_001007792.1(NTRK1):c.1149G>A (p.Ser383=) rs750968694
NM_001007792.1(NTRK1):c.1223G>A (p.Arg408Gln) rs56320207
NM_001007792.1(NTRK1):c.123-3198C>T rs183517027
NM_001007792.1(NTRK1):c.123-3263G>C rs200815412
NM_001007792.1(NTRK1):c.123-3367G>A rs1007211
NM_001007792.1(NTRK1):c.1489C>T (p.Leu497=) rs760564817
NM_001007792.1(NTRK1):c.1566G>A (p.Gln522=) rs6334
NM_001007792.1(NTRK1):c.1620C>T (p.Phe540=) rs6335
NM_001007792.1(NTRK1):c.1695C>G (p.Leu565=) rs146129485
NM_001007792.1(NTRK1):c.1698-4del rs1799770
NM_001007792.1(NTRK1):c.1702C>T (p.His568Tyr) rs6336
NM_001007792.1(NTRK1):c.1730G>T (p.Gly577Val) rs6339
NM_001007792.1(NTRK1):c.1752C>T (p.Gly584=) rs6338
NM_001007792.1(NTRK1):c.1779C>T (p.Ala593=) rs6337
NM_001007792.1(NTRK1):c.1800G>A (p.Ala600=) rs17838192
NM_001007792.1(NTRK1):c.1887G>A (p.Lys629=) rs553270591
NM_001007792.1(NTRK1):c.1944A>G (p.Gly648=) rs34271945
NM_001007792.1(NTRK1):c.198-8C>T rs80026148
NM_001007792.1(NTRK1):c.2094G>A (p.Thr698=) rs55668752
NM_001007792.1(NTRK1):c.2164G>A (p.Ala722Thr) rs62640939
NM_001007792.1(NTRK1):c.2231G>A (p.Arg744Gln) rs35669708
NM_001007792.1(NTRK1):c.338+12C>A rs41267425
NM_001007792.1(NTRK1):c.522G>A (p.Ser174=) rs114320051
NM_001007792.1(NTRK1):c.620C>T (p.Thr207Met) rs55909005
NM_001007792.1(NTRK1):c.990G>A (p.Thr330=) rs2274498
NM_002529.3(NTRK1):c.2047-11G>A rs79173278
NM_002529.4(NTRK1):c.1149C>T (p.Phe383=)

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