List of variants in gene combination CORO7-PAM16, PAM16 studied for not specified

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_016069.11(PAM16):c.374C>T (p.Thr125Met)	rs148571756	0.00020
NM_016069.11(PAM16):c.118C>T (p.Arg40Cys)	rs146773339	0.00013
NM_016069.11(PAM16):c.47T>C (p.Val16Ala)	rs757446733	0.00005
NM_001201479.2(CORO7-PAM16):c.2843G>A (p.Arg948Gln)	rs770759571	0.00003
NM_001201479.2(CORO7-PAM16):c.2833C>T (p.Arg945Trp)	rs200006600	0.00002
NM_001201479.2(CORO7-PAM16):c.2999A>G (p.Tyr1000Cys)	rs530133377	0.00001
NM_016069.11(PAM16):c.130C>T (p.Arg44Trp)	rs781160994	0.00001
NM_001201479.2(CORO7-PAM16):c.2890G>A (p.Ala964Thr)	rs143616972
NM_001201479.2(CORO7-PAM16):c.3001G>A (p.Glu1001Lys)	rs2505630936
NM_001201479.2(CORO7-PAM16):c.3022G>C (p.Asp1008His)	rs1260237933

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