List of variants in gene BRCA2 reported as uncertain significance by GeneKor MSA

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.3032C>G (p.Thr1011Arg)	rs80358548	0.00004
NM_000059.4(BRCA2):c.10089A>G (p.Ile3363Met)	rs80358390	0.00002
NM_000059.4(BRCA2):c.2944A>C (p.Ile982Leu)	rs28897717	0.00002
NM_000059.4(BRCA2):c.5921C>T (p.Thr1974Ile)	rs55730620	0.00002
NM_000059.4(BRCA2):c.3562A>G (p.Ile1188Val)	rs202230438	0.00001
NM_000059.4(BRCA2):c.425+4T>G	rs757612558	0.00001
NM_000059.4(BRCA2):c.5081G>C (p.Arg1694Thr)	rs753721331	0.00001
NM_000059.4(BRCA2):c.6613G>A (p.Val2205Met)	rs80358889	0.00001
NM_000059.4(BRCA2):c.9472A>G (p.Thr3158Ala)	rs786204284	0.00001
NM_000059.4(BRCA2):c.9863C>T (p.Thr3288Ile)	rs754588394	0.00001
NM_000059.4(BRCA2):c.3437A>G (p.Glu1146Gly)	rs80358588
NM_000059.4(BRCA2):c.3547G>C (p.Glu1183Gln)	rs1566228768
NM_000059.4(BRCA2):c.3608G>A (p.Ser1203Asn)	rs745817393
NM_000059.4(BRCA2):c.3861TAA[1] (p.Asn1288del)	rs276174837
NM_000059.4(BRCA2):c.4412_4414del (p.Arg1471del)	rs886039317
NM_000059.4(BRCA2):c.6160G>A (p.Ala2054Thr)	rs80358855
NM_000059.4(BRCA2):c.6296G>C (p.Arg2099Thr)	rs80358868
NM_000059.4(BRCA2):c.6607G>T (p.Val2203Phe)	rs587782136
NM_000059.4(BRCA2):c.6983A>G (p.Glu2328Gly)	rs201500887
NM_000059.4(BRCA2):c.7985C>T (p.Thr2662Met)	rs431825362
NM_000059.4(BRCA2):c.8944A>C (p.Lys2982Gln)	rs80359145
NM_000059.4(BRCA2):c.8981C>T (p.Ser2994Leu)	rs1566253076

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