List of variants in gene combination PRPH, TROAP reported by Epithelial Biology; Institute of Medical Biology, Singapore

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_006262.4(PRPH):c.545+69G>C	rs7488343	0.39633
NM_006262.4(PRPH):c.702+27T>C	rs2070760	0.29573
NM_006262.4(PRPH):c.1267+58T>C	rs2236746	0.21972
NM_006262.4(PRPH):c.-24G>C	rs74089010	0.05436
NM_006262.4(PRPH):c.63C>T (p.Phe21=)	rs58403142	0.02123
NM_006262.4(PRPH):c.829G>A (p.Ala277Thr)	rs62636520	0.02098
NM_006262.4(PRPH):c.26G>A (p.Arg9Gln)	rs57451017	0.00997
NM_006262.4(PRPH):c.421G>T (p.Asp141Tyr)	rs58599399	0.00363
NM_006262.4(PRPH):c.*82C>A	rs7137584	0.00027
NM_006262.4(PRPH):c.398G>C (p.Arg133Pro)	rs267607528	0.00003
NM_006262.4(PRPH):c.-23G>C	rs267607670
NM_006262.4(PRPH):c.1348-36dup	rs267607672
NM_006262.4(PRPH):c.229del (p.Arg77fs)	rs56843567
NM_006262.4(PRPH):c.547T>C (p.Leu183=)	rs267607530
NM_006262.4(PRPH):c.606+52T>G	rs267607673
NM_006262.4(PRPH):c.607-77A>C	rs267607671
NM_006262.4(PRPH):c.703-13C>T	rs267607529

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