List of variants in gene GRM6 studied for perceptual disorders

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000843.4(GRM6):c.176A>C (p.Gln59Pro)	rs2645329	0.57334
NM_000843.4(GRM6):c.643T>C (p.Tyr215His)	rs144362143	0.00025
NM_000843.4(GRM6):c.137C>T (p.Pro46Leu)	rs62638197	0.00009
NM_000843.4(GRM6):c.448G>A (p.Gly150Ser)	rs62638202	0.00003
NM_000843.3(GRM6):c.(1354+1_1355-1)_(2436+1_2437-1)del
NM_000843.4(GRM6):c.118_132del (p.Thr40_Leu44del)	rs1237461749
NM_000843.4(GRM6):c.2497G>C (p.Gly833Arg)
NM_000843.4(GRM6):c.292A>C (p.Thr98Pro)
NM_000843.4(GRM6):c.340C>T (p.Gln114Ter)
NM_000843.4(GRM6):c.527C>T (p.Ser176Phe)	rs1581898677
NM_000843.4(GRM6):c.541C>A (p.Leu181Ile)
NM_000843.4(GRM6):c.577del (p.Val193fs)	rs781463257
NM_000843.4(GRM6):c.722-1G>T	rs766594761
NM_000843.4(GRM6):c.727G>T (p.Val243Phe)	rs17078894
NM_000843.4(GRM6):c.727dup	rs281865186
NM_000843.4(GRM6):c.824G>A (p.Gly275Asp)
NM_000843.4(GRM6):c.953G>T (p.Ser318Ile)	rs755939082

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