List of variants in gene TRPM1 studied for Congenital stationary night blindness

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001252024.2(TRPM1):c.3070A>T (p.Ile1024Phe)	rs369484186	0.00003
NM_001252024.2(TRPM1):c.1263G>A (p.Pro421=)	rs768701595	0.00001
NM_001252024.2(TRPM1):c.2633G>A (p.Trp878Ter)	rs765645888	0.00001
NM_001252024.2(TRPM1):c.2695C>T (p.Arg899Ter)	rs1485132228	0.00001
NM_001252024.2(TRPM1):c.3214dup (p.Trp1072fs)	rs770380556	0.00001
NM_001252024.2(TRPM1):c.3155G>A (p.Cys1052Tyr)	rs1555418784
NM_001252024.2(TRPM1):c.3174T>A (p.Asp1058Glu)	rs748046539
NM_001252024.2(TRPM1):c.380G>A (p.Gly127Glu)	rs1555424849
NM_001252024.2(TRPM1):c.618+3_618+6del	rs781610444
NM_001252024.2(TRPM1):c.832G>A (p.Gly278Arg)	rs1555424166
NM_001252024.2(TRPM1):c.946A>T (p.Lys316Ter)	rs1596029830

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