List of variants in gene DCC reported as pathogenic for mirror movements 1 and/or agenesis of the corpus callosum

Minimum submission review status:		Collection method:
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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_005215.3(DCC):c.698-?_985+?del (p.Asp233_Leu328del)
NM_005215.4(DCC):c.1140+1G>A	rs797044553
NM_005215.4(DCC):c.1154T>A (p.Leu385Ter)
NM_005215.4(DCC):c.1573+2T>G
NM_005215.4(DCC):c.2266C>T (p.Arg756Ter)	rs764481922
NM_005215.4(DCC):c.2280_2286del (p.Ile760fs)
NM_005215.4(DCC):c.2377_2381del (p.Val793fs)
NM_005215.4(DCC):c.2378T>G (p.Val793Gly)	rs1057519054
NM_005215.4(DCC):c.2414G>A (p.Gly805Glu)	rs1057519055
NM_005215.4(DCC):c.2774dup (p.Asn925fs)	rs2145024323
NM_005215.4(DCC):c.3073C>T (p.Arg1025Ter)	rs1909920586
NM_005215.4(DCC):c.3577C>T (p.Gln1193Ter)
NM_005215.4(DCC):c.3836_3837del (p.Leu1279fs)	rs797044556
NM_005215.4(DCC):c.571dup (p.Val191fs)	rs797044552
NM_005215.4(DCC):c.823C>T (p.Arg275Ter)	rs754914260
NM_005215.4(DCC):c.925del (p.Thr309fs)	rs1057519053

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