List of variants in gene combination ASTN2, TRIM32 reported by Athena Diagnostics Inc

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_012210.4(TRIM32):c.1222C>T (p.Arg408Cys)	rs3747835	0.00113
NM_012210.4(TRIM32):c.*1G>A	rs142781513	0.00053
NM_012210.4(TRIM32):c.863C>A (p.Pro288His)	rs367574371	0.00012
NM_012210.4(TRIM32):c.979A>G (p.Met327Val)	rs373287765	0.00009
NM_012210.4(TRIM32):c.1012G>A (p.Ala338Thr)	rs141806013	0.00008
NM_012210.4(TRIM32):c.1688G>A (p.Arg563His)	rs138056275	0.00006
NM_012210.4(TRIM32):c.693A>C (p.Ala231=)	rs368455215	0.00005
NM_012210.4(TRIM32):c.127A>G (p.Ile43Val)	rs764366522	0.00004
NM_012210.4(TRIM32):c.907G>A (p.Val303Met)	rs144532174	0.00002
NM_012210.4(TRIM32):c.938C>T (p.Ala313Val)	rs794727284	0.00001
NM_012210.4(TRIM32):c.164G>T (p.Ser55Ile)	rs1564215128
NM_012210.4(TRIM32):c.1710G>A (p.Ser570=)	rs555217187

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