List of variants in gene LRRC51, LRTOMT studied for auditory system disorder

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_145309.6(LRRC51):c.352G>C (p.Gly118Arg)	rs149637884	0.00473
NM_145309.6(LRRC51):c.255C>T (p.Asp85=)	rs145851613	0.00232
NM_145309.6(LRRC51):c.150G>T (p.Leu50=)	rs144139038	0.00106
NM_145309.6(LRRC51):c.281T>C (p.Ile94Thr)	rs369105155	0.00032
NM_145309.6(LRRC51):c.-140+5G>A	rs767961368	0.00013
NM_145309.6(LRRC51):c.-162G>A	rs886048626	0.00006
NM_145309.6(LRRC51):c.347G>A (p.Arg116His)	rs145488053	0.00004
NM_145309.6(LRRC51):c.99G>A (p.Glu33=)	rs886048627	0.00002
NM_145309.6(LRTOMT):c.230A>G (p.His77Arg)	rs1382614042	0.00001
NM_145309.6(LRRC51):c.-140+1G>T	rs1565309133
NM_145309.6(LRRC51):c.330del (p.His110fs)	rs2136541413
NM_145309.6(LRRC51):c.340_346del (p.Ile114fs)	rs759544282

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