List of variants in gene BRCA2 reported as likely benign for digestive system cancer

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.3264T>C (p.Pro1088=)	rs36060526	0.00793
NM_000059.4(BRCA2):c.5199C>T (p.Ser1733=)	rs28897734	0.00488
NM_000059.4(BRCA2):c.8182G>A (p.Val2728Ile)	rs28897749	0.00239
NM_000059.4(BRCA2):c.8503T>C (p.Ser2835Pro)	rs11571746	0.00202
NM_000059.4(BRCA2):c.1938C>T (p.Ser646=)	rs28897711	0.00096
NM_000059.4(BRCA2):c.1151C>T (p.Ser384Phe)	rs41293475	0.00074
NM_000059.4(BRCA2):c.5198C>T (p.Ser1733Phe)	rs55639415	0.00069
NM_000059.4(BRCA2):c.1964C>G (p.Pro655Arg)	rs28897712	0.00054
NM_000059.4(BRCA2):c.2803G>A (p.Asp935Asn)	rs28897716	0.00054
NM_000059.4(BRCA2):c.5785A>G (p.Ile1929Val)	rs79538375	0.00031
NM_000059.4(BRCA2):c.1395A>C (p.Val465=)	rs11571641	0.00026
NM_000059.4(BRCA2):c.1786G>C (p.Asp596His)	rs56328701	0.00025
NM_000059.4(BRCA2):c.9876G>A (p.Pro3292=)	rs369047997	0.00025
NM_000059.4(BRCA2):c.3445A>G (p.Met1149Val)	rs80358589	0.00013
NM_000059.4(BRCA2):c.4656T>C (p.Gly1552=)	rs41293491	0.00009
NM_000059.4(BRCA2):c.6935A>T (p.Asp2312Val)	rs80358916	0.00003
NM_000059.4(BRCA2):c.1538A>G (p.Lys513Arg)	rs28897709	0.00002
NM_000059.4(BRCA2):c.7986G>A (p.Thr2662=)	rs1057522378	0.00002
NM_000059.4(BRCA2):c.10111A>G (p.Thr3371Ala)	rs80358393	0.00001
NM_000059.4(BRCA2):c.10113T>C (p.Thr3371=)	rs779075029	0.00001
NM_000059.4(BRCA2):c.1179T>C (p.Cys393=)	rs786201237	0.00001
NM_000059.4(BRCA2):c.441A>G (p.Gln147=)	rs80358676	0.00001
NM_000059.4(BRCA2):c.5028T>C (p.Ser1676=)	rs762458631	0.00001
NM_000059.4(BRCA2):c.6264T>C (p.Thr2088=)	rs750651726	0.00001
NM_000059.4(BRCA2):c.5025T>C (p.Cys1675=)	rs370591460
NM_000059.4(BRCA2):c.5661G>A (p.Thr1887=)	rs80359793
NM_000059.4(BRCA2):c.6030C>A (p.Val2010=)	rs786201328
NM_000059.4(BRCA2):c.68-7dup	rs276174878

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