List of variants in gene combination ASTN2, TRIM32 reported by Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_012210.4(TRIM32):c.480G>A (p.Met160Ile)	rs200196832	0.00006
NM_012210.4(TRIM32):c.1162G>A (p.Ala388Thr)	rs886042328	0.00001
NM_012210.4(TRIM32):c.1459G>A (p.Asp487Asn)	rs111033570	0.00001
NM_012210.4(TRIM32):c.236A>T (p.Asn79Ile)	rs775738712
NM_012210.4(TRIM32):c.946G>A (p.Ala316Thr)

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