List of variants in gene LRAT reported as likely pathogenic for perceptual disorders

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_004744.5(LRAT):c.224C>T (p.Pro75Leu)	rs766279892	0.00003
NM_004744.5(LRAT):c.149T>G (p.Val50Gly)	rs1384466058	0.00001
NM_004744.5(LRAT):c.163C>G (p.Arg55Gly)	rs527236079	0.00001
NM_004744.5(LRAT):c.299G>A (p.Gly100Asp)	rs1396648864	0.00001
NM_004744.5(LRAT):c.40G>T (p.Glu14Ter)	rs768255532	0.00001
NM_004744.5(LRAT):c.163C>T (p.Arg55Trp)	rs527236079
NM_004744.5(LRAT):c.264_265dup (p.Gln89fs)	rs1578860254
NM_004744.5(LRAT):c.346T>C (p.Phe116Leu)	rs1578860322
NM_004744.5(LRAT):c.40_41delinsTT (p.Glu14Leu)
NM_004744.5(LRAT):c.470T>C (p.Leu157Pro)
NM_004744.5(LRAT):c.473G>A (p.Trp158Ter)	rs878853351
NM_004744.5(LRAT):c.481T>C (p.Cys161Arg)	rs1732848653
NM_004744.5(LRAT):c.487C>G (p.His163Asp)	rs1010347467
NM_004744.5(LRAT):c.487C>T (p.His163Tyr)	rs1010347467
NM_004744.5(LRAT):c.571G>T (p.Asp191Tyr)

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