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BRCA2 c.4631del 37913

Variant:BRCA2 c.4631del 37913 Gene:BRCA2Coding Change (c.):c.4631delProtein Change (p.):p.Asn1544fsVariant Forum:Other Names:4859delAGene:BRCA2

CHEK2 c.593-11_593-7del 215865

Variant:CHEK2 c.593-11_593-7del 215865Gene:CHEK2Coding Change (c.):c.593-11_593-7delProtein Change (p.):p.?Variant Forum:Gene:CHEK2

ATM c.3402+3A>G 187380

Variant:ATM c.3402+3A>G 187380Gene:ATMCoding Change (c.):c.3402+3A>GVariant Forum:https://community.breastcancer.org/forum/112/topics/862062?page=1#post_5154931Notes:The variant is mentioned once by a one forum user here Gene:ATM

BRCA1 c.2869C>T 54703

Variant:BRCA1 c.2869C>T 54703Gene:BRCA1Coding Change (c.):c.2869C>TProtein Change (p.):p.Gln957TerVariant Forum:https://messageboard.facingourrisk.org/t/brca1-c-2869c-t-p-q957/1568Gene:BRCA1

BRCA1 c.5096G>A 37636

Variant:BRCA1 c.5096G>A 37636Gene:BRCA1Coding Change (c.):c.5096G>AProtein Change (p.):p.Arg1699GlnVariant Forum:https://messageboard.facingourrisk.org/t/r1699q-intermediate-risk/925Notes:Additional Links: https://messageboard.facingourrisk.org/t/brca1 c 5096g a p arg1699gln/6014 This variant has been estimated t have intermediate risk compared to other BRCA1 variants. Cumulative risk of breast cancer age 70 years was 20% and cumulative risk of ovarian by age 70 was 6%. See https://pubmed.ncbi.nlm.nih.gov/28490613/ Other Names:p.R1699Q:CGG>CAG 5215G>AGene:BRCA1

BRCA1 c.53T>A 55559

Variant:BRCA1 c.53T>A 55559Gene:BRCA1Coding Change (c.):c.53T>AProtein Change (p.):p.Met18LysVariant Forum:https://messageboard.facingourrisk.org/t/brca1-c-53t-a/1387Notes:FORCE "Share your Mutation" Gene:BRCA1

BRCA1 c.68_69del 17662

Variant:BRCA1 c.68_69del 17662Gene:BRCA1Coding Change (c.):c.68_69delProtein Change (p.):p.Glu23fsVariant Forum:https://messageboard.facingourrisk.org/t/brca1-c-68-69del-p-glu23valfs-17/1429Notes:Additional links: https://messageboard.facingourrisk.org/t/brca1 c 68 69del/5811/11 Other Names:c.66_67AG[1] 185_186delAG 187delAG 185delAGGene:BRCA1

BRCA1 exon 21 del

Variant:BRCA1 exon 21 delGene:BRCA1Coding Change (c.):exon 21 delProtein Change (p.):?Variant Forum:https://messageboard.facingourrisk.org/t/brca1-del-exon-21/147Gene:BRCA1

BRCA2 c.4449del 37904

Variant:BRCA2 c.4449del 37904Gene:BRCA2Coding Change (c.):c.4449delAProtein Change (p.):p.Asp1484fsVariant Forum:https://messageboard.facingourrisk.org/t/brca2-c-4449dela/2159Other Names:4677delA c.4449delGene:BRCA2

BRCA2 c.5303_5304delTT 37957

Variant:BRCA2 c.5303_5304delTT 37957Gene:BRCA2Coding Change (c.):c.5303_5304delTTProtein Change (p.):p.Leu1768ArgfsVariant Forum:https://messageboard.facingourrisk.org/t/brca2-5303-5304deltt/1318Notes:FORCE "Share your Mutation" forum Other Names:5531delTTGene:BRCA2

BRCA2 c.538_539dup 51851

Variant:BRCA2 c.538_539dup 51851Gene:BRCA2Coding Change (c.):c.538_539dupProtein Change (p.):p.Ser181fsVariant Forum:https://messageboard.facingourrisk.org/t/brca2c-538-539dupat-anyone-else/1494Notes:This is a FORCE "Share your mutation" forum Other Names:767_768insAT 767insATGene:BRCA2

BRCA1 c.4951T>C 246002

Variant:BRCA1 c.4951T>C 246002Gene:BRCA1Coding Change (c.):c.4951T>CProtein Change (p.):p.Ser1651PrVariant Forum:https://messageboard.facingourrisk.org/t/c-4951t-c-p-ser1651pro/2168Gene:BRCA1

BRCA2 c.8165C>G 9340

Variant:BRCA2 c.8165C>G 9340Gene:BRCA2Coding Change (c.):c.8165C>GProtein Change (p.):p.Thr2722ArgVariant Forum:https://messageboard.facingourrisk.org/t/c-8165c-g/2181Other Names:8393C>GGene:BRCA2

BRCA2 c.316+5G>A 51409

Variant:BRCA2 c.316+5G>A 51409Gene:BRCA2Coding Change (c.):c.316+5G>AVariant Forum:https://messageboard.facingourrisk.org/t/brca2-c-316-5g-a/1836Other Names:IVS3+5G>AGene:BRCA2

BRCA2 c.36dupT 51509

Variant:BRCA2 c.36dupT 51509Gene:BRCA2Coding Change (c.):c.36dupProtein Change (p.):p.Glu13TerVariant Forum:https://messageboard.facingourrisk.org/t/brca-2-c-36dupt-p-glu13-aka-264inst/1402Notes:FORCE "Share your mutation" Other Names:264insTGene:BRCA2

PALB2 c.3549C>G 1245

Variant:PALB2 c.3549C>G 1245Gene:PALB2Coding Change (c.):c.3549C>GProtein Change (p.):p.Y1183*Variant Forum:https://csn.cancer.org/node/311776Notes:PALB2 c.3549C> A is a different variant that also creates the same protein change (same p. identifier) Gene:PALB2

BRCA2 c.2957dup 51378

Variant:BRCA2 c.2957dup 51378Gene:BRCA2Coding Change (c.):c. 2957dupProtein Change (p.):p.Asn986fsVariant Forum:https://messageboard.facingourrisk.org/t/brca2-3185insa/2128Other Names:3185insA c.2957dupAGene:BRCA2

BRCA2 c.9097del 38209

Variant:BRCA2 c.9097del 38209Gene:BRCA2Coding Change (c.):c.9097delProtein Change (p.):p.Thr3033fsVariant Forum:https://messageboard.facingourrisk.org/t/brca-2-c-9097dela/533Notes:Also known as 9325delA Other Names:9325delAGene:BRCA2

BRCA2 c.9182T>A 52769

Variant:BRCA2 c.9182T>A 52769Gene:BRCA2Coding Change (c.):c.9182T>AProtein Change (p.):p.Leu3061TerVariant Forum:https://messageboard.facingourrisk.org/t/looking-for-origin-of-this-mutation/1140/8Gene:BRCA2

BRIP1 c.341C>A 407838

Variant:BRIP1 c.341C>A 407838Gene:BRIP1Coding Change (c.):c:341C>AProtein Change (p.):p.Pro114GInVariant Forum:https://messageboard.facingourrisk.org/t/brip1-variant-of-uncertain-significance/983Gene:BRIP1