List of variants in gene LPAR6, RB1 studied for cancer

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_001162498.3(LPAR6):c.921G>T (p.Trp307Cys)	rs17071686	0.00841
NM_001162498.3(LPAR6):c.819C>A (p.Tyr273Ter)	rs749894411	0.00001
NC_000013.10:g.(?_48877851)_(49054207_?)del
NC_000013.10:g.(?_48985727)_(49039514_?)dup
NC_000013.11:g.(?_48302747)_(48482890_?)del
NC_000013.11:g.(?_48303701)_(48412896_?)del
NC_000013.11:g.(?_48303701)_(48480071_?)del
NC_000013.11:g.(?_48379574)_(48480071_?)del
NM_001162498.3(LPAR6):c.341_344del (p.Arg114fs)	rs1198561901
NM_001162498.3(LPAR6):c.347del (p.Leu116fs)	rs1404056158
NM_001162498.3(LPAR6):c.350_352del (p.Ala117_Ile118delinsVal)	rs1200570253
NM_001162498.3(LPAR6):c.354T>G (p.Ile118Met)	rs1458608158
NM_001162498.3(LPAR6):c.358T>G (p.Tyr120Asp)	rs1344531248
NM_001162498.3(LPAR6):c.359del (p.Tyr120fs)	rs1275629547
NM_001162498.3(LPAR6):c.361_362insGTAT (p.Pro121fs)	rs1236830240
NM_001162498.3(LPAR6):c.366T>A (p.Phe122Leu)	rs977436301
NM_001162498.3(LPAR6):c.368_369insAAAAAAAA (p.Ser124fs)	rs1370123231
NM_001162498.3(LPAR6):c.369_370del (p.Lys123fs)	rs1177544722

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