List of variants in gene MIP reported as pathogenic for cataract

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_012064.4(MIP):c.401A>G (p.Glu134Gly)	rs121917869
NM_012064.4(MIP):c.413C>G (p.Thr138Arg)	rs121917867
NM_012064.4(MIP):c.508dup (p.Leu170fs)	rs1057519616
NM_012064.4(MIP):c.606+1G>C	rs1220143491
NM_012064.4(MIP):c.606+1G>T
NM_012064.4(MIP):c.616_632del (p.Val206fs)
NM_012064.4(MIP):c.623del (p.Pro208fs)	rs1555179713
NM_012064.4(MIP):c.638del (p.Gly213fs)	rs398122378
NM_012064.4(MIP):c.97C>T (p.Arg33Cys)	rs864309693

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