List of variants in gene combination ASTN2, TRIM32 reported by Breakthrough Genomics, Breakthrough Genomics

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_012210.4(TRIM32):c.*129C>T	rs3019	0.93884
NM_012210.4(TRIM32):c.*1206T>C	rs2281627	0.28861
NM_012210.4(TRIM32):c.-133G>C	rs12342207	0.27173
NM_012210.4(TRIM32):c.1254G>A (p.Val418=)	rs1661300	0.10569
NM_012210.4(TRIM32):c.-81-98G>A	rs73515229	0.04415
NM_012210.4(TRIM32):c.1411_1414dup	rs758130716	0.00031
NM_012210.4(TRIM32):c.521C>T (p.Ser174Phe)	rs138699534	0.00019
NM_012210.4(TRIM32):c.1275T>C (p.Asp425=)	rs150813870	0.00005
NM_012210.4(TRIM32):c.277G>A (p.Glu93Lys)	rs754449534	0.00003
NM_012210.4(TRIM32):c.1046C>G (p.Ala349Gly)	rs774316527	0.00002

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