List of variants in gene ALDH3A2 reported by Mayo Clinic Laboratories, Mayo Clinic

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000382.3(ALDH3A2):c.1446A>T (p.Ala482=)	rs7216	0.56713
NM_000382.3(ALDH3A2):c.563C>T (p.Ala188Val)	rs115977487	0.01228
NM_000382.3(ALDH3A2):c.1270C>T (p.Pro424Ser)	rs61737992	0.00419
NM_000382.3(ALDH3A2):c.465A>G (p.Leu155=)	rs149865400	0.00030
NM_000382.3(ALDH3A2):c.1208-30A>C	rs376485655	0.00011
NM_000382.3(ALDH3A2):c.1412T>C (p.Phe471Ser)	rs141112437	0.00009
NM_000382.3(ALDH3A2):c.941_942insTAAAAGTA (p.Pro315fs)	rs1555534430	0.00001
NM_000382.3(ALDH3A2):c.1064G>A (p.Arg355His)
NM_000382.3(ALDH3A2):c.1297_1298del (p.Glu433fs)	rs387906256
NM_000382.3(ALDH3A2):c.1307_1311dup (p.Leu438fs)	rs387906257
NM_000382.3(ALDH3A2):c.386-6A>G	rs117330764
NM_000382.3(ALDH3A2):c.941-1_941insGGG	rs1208451634
NM_000382.3(ALDH3A2):c.943delinsTGTTGGGG (p.Pro315fs)	rs1555534434

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