List of variants in gene BRAT1 reported as pathogenic for not provided

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_152743.4(BRAT1):c.294dup (p.Leu99fs)	rs776913277	0.00022
NM_152743.4(BRAT1):c.1313_1314del (p.Gln438fs)	rs749240175	0.00004
NM_152743.4(BRAT1):c.1684C>T (p.Arg562Ter)	rs759216914	0.00003
NM_152743.4(BRAT1):c.1395G>A (p.Thr465=)	rs201855243	0.00002
NM_152743.4(BRAT1):c.1771-1G>A	rs1064796877	0.00001
NM_152743.4(BRAT1):c.1203_1204del (p.Cys401_Asp402delinsTer)	rs773772842
NM_152743.4(BRAT1):c.1710del (p.Gln571fs)	rs756489141
NM_152743.4(BRAT1):c.2125_2128del (p.Phe709fs)	rs763527391
NM_152743.4(BRAT1):c.2291dup (p.Gly765fs)	rs1463777746
NM_152743.4(BRAT1):c.638dup (p.Val214fs)	rs730880324
NM_152743.4(BRAT1):c.646C>T (p.Gln216Ter)	rs1779368057

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