List of variants in gene NTRK1 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_002529.4(NTRK1):c.1838G>T (p.Gly613Val)	rs6339	0.03698
NM_002529.4(NTRK1):c.1810C>T (p.His604Tyr)	rs6336	0.03696
NM_002529.4(NTRK1):c.851-33T>A	rs80356674	0.00003
NM_002529.4(NTRK1):c.1550G>A (p.Gly517Glu)	rs606231467	0.00001
NM_002529.4(NTRK1):c.207_208del (p.Glu70fs)	rs398122810	0.00001
NM_002529.4(NTRK1):c.1076A>G (p.Tyr359Cys)	rs121964869
NM_002529.4(NTRK1):c.1660del (p.Arg554fs)	rs80356675
NM_002529.4(NTRK1):c.1729G>C (p.Gly577Arg)	rs121964866
NM_002529.4(NTRK1):c.1759A>G (p.Met587Val)	rs121964870
NM_002529.4(NTRK1):c.1860_1861insT (p.Pro621fs)	rs80356676
NM_002529.4(NTRK1):c.2046+3A>C	rs914061514
NM_002529.4(NTRK1):c.2084C>T (p.Pro695Leu)	rs121964868
NM_002529.4(NTRK1):c.2339G>C (p.Arg780Pro)	rs35669708
NM_002529.4(NTRK1):c.717+4A>T	rs606231466
NM_002529.4(NTRK1):c.[253C>A;429-1G>C]

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