List of variants in gene BRCA2 reported by King Laboratory, University of Washington

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.750G>A (p.Val250=)	rs143214959	0.00005
NM_000059.4(BRCA2):c.9648+127G>A	rs182622896	0.00003
NM_000059.4(BRCA2):c.426-252A>G	rs948639481	0.00002
NM_000059.4(BRCA2):c.8331+3A>C	rs876659382	0.00002
NM_000059.4(BRCA2):c.7466A>G (p.Asp2489Gly)	rs80358970	0.00001
NM_000059.4(BRCA2):c.7992T>A (p.Ile2664=)	rs80359800	0.00001
NM_000059.4(BRCA2):c.8009C>T (p.Ser2670Leu)	rs80359035	0.00001
NM_000059.4(BRCA2):c.8350C>T (p.Arg2784Trp)	rs80359075	0.00001
NM_000059.4(BRCA2):c.8359C>T (p.Arg2787Cys)	rs41293517	0.00001
NM_000059.4(BRCA2):c.9076C>G (p.Gln3026Glu)	rs80359159	0.00001
NM_000059.4(BRCA2):c.9117G>A (p.Pro3039=)	rs28897756	0.00001
NM_000059.4(BRCA2):c.128A>G (p.Asn43Ser)	rs2072285447
NM_000059.4(BRCA2):c.28A>G (p.Thr10Ala)	rs786203080
NM_000059.4(BRCA2):c.517-2A>G	rs81002858
NM_000059.4(BRCA2):c.7007+1G>C	rs397507891
NM_000059.4(BRCA2):c.7007+5G>A	rs81002816
NM_000059.4(BRCA2):c.7007G>C (p.Arg2336Pro)	rs28897743
NM_000059.4(BRCA2):c.7559G>C (p.Arg2520Pro)	rs80358982
NM_000059.4(BRCA2):c.7618-1G>A	rs397507389
NM_000059.4(BRCA2):c.7802A>G (p.Tyr2601Cys)	rs786202344
NM_000059.4(BRCA2):c.7820C>T (p.Thr2607Ile)	rs1555286821
NM_000059.4(BRCA2):c.7879A>T (p.Ile2627Phe)	rs80359014
NM_000059.4(BRCA2):c.7902G>A (p.Met2634Ile)	rs1483170360
NM_000059.4(BRCA2):c.7976+2C>G	rs886040943
NM_000059.4(BRCA2):c.7976G>A (p.Arg2659Lys)	rs80359027
NM_000059.4(BRCA2):c.8206C>T (p.Leu2736Phe)	rs1555287042
NM_000059.4(BRCA2):c.8285C>G (p.Pro2762Arg)	rs398122600
NM_000059.4(BRCA2):c.8510G>T (p.Gly2837Val)	rs587780663
NM_000059.4(BRCA2):c.9344A>G (p.Lys3115Arg)	rs276174923

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