List of variants in gene ALOX12B reported by OMIM

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_001139.3(ALOX12B):c.1562A>G (p.Tyr521Cys)	rs199766569	0.00014
NM_001139.3(ALOX12B):c.1642C>T (p.Arg548Trp)	rs397514532	0.00003
NM_001139.3(ALOX12B):c.1180G>A (p.Glu394Lys)	rs397514529	0.00001
NM_001139.3(ALOX12B):c.1207C>T (p.His403Tyr)	rs397514531	0.00001
NM_001139.3(ALOX12B):c.1294C>T (p.Arg432Ter)	rs397514527	0.00001
NM_001139.3(ALOX12B):c.199A>T (p.Ile67Phe)	rs397514533	0.00001
NM_001139.3(ALOX12B):c.340C>T (p.Arg114Trp)	rs397514526	0.00001
NM_001139.3(ALOX12B):c.1277T>C (p.Leu426Pro)	rs137853023
NM_001139.3(ALOX12B):c.1389del (p.Phe463fs)	rs387906349
NM_001139.3(ALOX12B):c.1734C>A (p.His578Gln)	rs137853024
NM_001139.3(ALOX12B):c.2036G>T (p.Arg679Leu)	rs397514528
NM_001139.3(ALOX12B):c.353-1G>A	rs1598181810
NM_001139.3(ALOX12B):c.410T>A (p.Ile137Asn)	rs397514530

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