List of variants in gene HSPB8 reported by CeGaT Center for Human Genetics Tuebingen

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_014365.3(HSPB8):c.233G>T (p.Arg78Met)	rs55826713	0.00058
NM_014365.3(HSPB8):c.503C>T (p.Ala168Val)	rs373049356	0.00011
NM_014365.3(HSPB8):c.14A>G (p.Gln5Arg)	rs146900850	0.00009
NM_014365.3(HSPB8):c.534A>G (p.Gly178=)	rs756610498	0.00003
NM_014365.3(HSPB8):c.163C>T (p.Arg55Cys)	rs1011669872	0.00001
NM_014365.3(HSPB8):c.135A>G (p.Thr45=)
NM_014365.3(HSPB8):c.266C>G (p.Pro89Arg)	rs35909818
NM_014365.3(HSPB8):c.421A>G (p.Lys141Glu)	rs104894351
NM_014365.3(HSPB8):c.85C>A (p.Arg29Ser)	rs748320300

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