List of variants in gene combination BRCA1, LOC126862571 reported as pathogenic by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_007294.4(BRCA1):c.3331_3334del (p.Gln1111fs)	rs80357701
NM_007294.4(BRCA1):c.3436_3439del (p.Cys1146fs)	rs397509067
NM_007294.4(BRCA1):c.3598C>T (p.Gln1200Ter)	rs62625307
NM_007294.4(BRCA1):c.3648dup (p.Ser1217fs)	rs80357902
NM_007294.4(BRCA1):c.3759_3760del (p.Lys1254fs)	rs80357520
NM_007294.4(BRCA1):c.3893C>A (p.Ser1298Ter)	rs80357440
NM_007294.4(BRCA1):c.4041_4042del (p.Gly1348fs)	rs80357727
NM_007294.4(BRCA1):c.4054G>T (p.Glu1352Ter)	rs80357202
NM_007294.4(BRCA1):c.4065_4068del (p.Asn1355fs)	rs80357508

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