List of variants in gene MYO1E reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_004998.4(MYO1E):c.643-4C>T	rs73422973	0.00956
NM_004998.4(MYO1E):c.1617-12C>G	rs192317472	0.00636
NM_004998.4(MYO1E):c.2304C>T (p.Asp768=)	rs145459485	0.00334
NM_004998.4(MYO1E):c.978G>A (p.Arg326=)	rs141570155	0.00199
NM_004998.4(MYO1E):c.147+14G>T	rs183374173	0.00123
NM_004998.4(MYO1E):c.1616+17A>G	rs138790400	0.00120
NM_004998.4(MYO1E):c.554A>G (p.Asp185Gly)	rs141565214	0.00101
NM_004998.4(MYO1E):c.511-17C>T	rs118012522	0.00071
NM_004998.4(MYO1E):c.669G>A (p.Gln223=)	rs142105673	0.00049
NM_004998.4(MYO1E):c.1530+14C>T	rs116371817	0.00043
NM_004998.4(MYO1E):c.2878+19G>A	rs200710336	0.00043
NM_004998.4(MYO1E):c.2335-13C>T	rs775751894	0.00034
NM_004998.4(MYO1E):c.1065C>T (p.Leu355=)	rs146652440	0.00030
NM_004998.4(MYO1E):c.1805+7G>A	rs561678142	0.00021
NM_004998.4(MYO1E):c.2628-8T>C	rs373053697	0.00021
NM_004998.4(MYO1E):c.2640G>A (p.Lys880=)	rs144794852	0.00021
NM_004998.4(MYO1E):c.2164+12A>G	rs187897054	0.00020
NM_004998.4(MYO1E):c.1734A>G (p.Lys578=)	rs200987052	0.00015
NM_004998.4(MYO1E):c.2298C>T (p.Phe766=)	rs370612369	0.00007
NM_004998.4(MYO1E):c.1275+12C>G	rs373603961	0.00004
NM_004998.4(MYO1E):c.3060C>T (p.Val1020=)	rs140388346	0.00004
NM_004998.4(MYO1E):c.1770C>T (p.Asn590=)	rs149553440	0.00003
NM_004998.4(MYO1E):c.2179T>C (p.Leu727=)	rs774695459	0.00001
NM_004998.4(MYO1E):c.2334+10_2334+11delinsGC	rs2140317179
NM_004998.4(MYO1E):c.2878+18C>T	rs759274124

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