List of variants in gene NTRK1 reported as not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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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.470G>A (p.Arg157His)	rs141021604	0.00006
NM_002529.4(NTRK1):c.2242C>T (p.Arg748Trp)	rs778520978	0.00003
NM_002529.4(NTRK1):c.851-33T>A	rs80356674	0.00003
NM_002529.4(NTRK1):c.287+2dup	rs768373757	0.00002
NM_002529.4(NTRK1):c.1633-1G>T	rs1571699664
NM_002529.4(NTRK1):c.1660del (p.Arg554fs)	rs80356675
NM_002529.4(NTRK1):c.1860_1861insT (p.Pro621fs)	rs80356676
NM_002529.4(NTRK1):c.2020G>T (p.Asp674Tyr)	rs80356677

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