List of variants in gene MYO6 studied for obsolete rare genetic deafness

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_004999.4(MYO6):c.826C>T (p.Arg276Ter)	rs727503326	0.00002
NM_004999.4(MYO6):c.238C>T (p.Arg80Ter)	rs727504567	0.00001
NM_004999.4(MYO6):c.2545C>T (p.Arg849Ter)	rs121912561	0.00001
NM_004999.4(MYO6):c.1383G>C (p.Glu461Asp)	rs727504548
NM_004999.4(MYO6):c.2111dup (p.Tyr705fs)	rs397517045
NM_004999.4(MYO6):c.258_259delinsCTTTACTAAA (p.Tyr87fs)	rs1583208411
NM_004999.4(MYO6):c.2814_2815del (p.Arg939fs)	rs876657709
NM_004999.4(MYO6):c.2839C>T (p.Arg947Ter)	rs876657653
NM_004999.4(MYO6):c.3207_3212delinsATCCTACATACTTAAAATTTCTT (p.Ala1070fs)	rs727505015
NM_004999.4(MYO6):c.458C>G (p.Ser153Ter)	rs876657710
NM_004999.4(MYO6):c.535G>T (p.Asp179Tyr)	rs1554205683
NM_004999.4(MYO6):c.737A>G (p.His246Arg)	rs121912560

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