List of variants in gene BRCA2 studied for notochordal tumor

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.5070A>C (p.Lys1690Asn)	rs56087561	0.00023
NM_000059.4(BRCA2):c.7010C>T (p.Thr2337Ile)	rs80358927	0.00004
NM_000059.4(BRCA2):c.7565C>T (p.Ser2522Phe)	rs80358985	0.00003
NM_000059.4(BRCA2):c.4779A>C (p.Glu1593Asp)	rs80358703	0.00002
NM_000059.4(BRCA2):c.3517A>T (p.Ile1173Phe)	rs431825308	0.00001
NM_000059.4(BRCA2):c.8117A>G (p.Asn2706Ser)	rs80359055	0.00001
NM_000059.4(BRCA2):c.8350C>T (p.Arg2784Trp)	rs80359075	0.00001
NM_000059.4(BRCA2):c.2141A>C (p.Glu714Ala)	rs2137483648
NM_000059.4(BRCA2):c.2143G>T (p.Gly715Ter)	rs1007336407
NM_000059.4(BRCA2):c.3599_3600del (p.Asp1199_Cys1200insTer)	rs80359391
NM_000059.4(BRCA2):c.6902A>G (p.Glu2301Gly)	rs2137537213

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