List of variants in gene MFSD8 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001371596.2(MFSD8):c.1006G>C (p.Glu336Gln)	rs150418024	0.00299
NM_001371596.2(MFSD8):c.1444C>T (p.Arg482Ter)	rs724159971	0.00003
NM_001371596.2(MFSD8):c.1141G>T (p.Glu381Ter)	rs724159970	0.00001
NM_001371596.2(MFSD8):c.1235C>T (p.Pro412Leu)	rs267607235	0.00001
NM_001371596.2(MFSD8):c.1102G>C (p.Asp368His)	rs727502800
NM_001371596.2(MFSD8):c.1286G>A (p.Gly429Asp)	rs118203976
NM_001371596.2(MFSD8):c.362A>G (p.Tyr121Cys)	rs118203978
NM_001371596.2(MFSD8):c.468_469delinsCC (p.Ala157Pro)	rs1740291234
NM_001371596.2(MFSD8):c.863+3_863+4insT	rs727502801
NM_001371596.2(MFSD8):c.881C>A (p.Thr294Lys)	rs140948465
NM_001371596.2(MFSD8):c.894T>G (p.Tyr298Ter)	rs118203977
NM_001371596.2(MFSD8):c.929G>A (p.Gly310Asp)	rs118203975

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