List of variants in gene TGM5 reported as benign for Acral peeling skin syndrome

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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_201631.4(TGM5):c.660C>T (p.Tyr220=)	rs555001	0.42220
NM_201631.4(TGM5):c.1055C>G (p.Ala352Gly)	rs28756768	0.20951
NM_201631.4(TGM5):c.*252C>T	rs7176183	0.04835
NM_201631.4(TGM5):c.1510G>A (p.Val504Met)	rs7171797	0.03875
NM_201631.4(TGM5):c.960C>T (p.Asn320=)	rs34222269	0.03866
NM_201631.4(TGM5):c.44C>G (p.Ser15Cys)	rs61744878	0.02998
NM_201631.4(TGM5):c.10+11C>T	rs113296343	0.02990
NM_201631.4(TGM5):c.654C>T (p.Pro218=)	rs77256087	0.02739
NM_201631.4(TGM5):c.1106-7C>T	rs113249183	0.01507
NM_201631.4(TGM5):c.1562A>G (p.Gln521Arg)	rs35985214	0.01269
NM_201631.4(TGM5):c.1822A>G (p.Lys608Glu)	rs76456763	0.01253
NM_201631.4(TGM5):c.1970T>C (p.Val657Ala)	rs80058195	0.00967
NM_201631.4(TGM5):c.326C>T (p.Thr109Met)	rs113463533	0.00516
NM_201631.4(TGM5):c.314G>A (p.Cys105Tyr)	rs116753155	0.00185
NM_201631.4(TGM5):c.1309C>T (p.Arg437Trp)	rs375323388	0.00001

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