Transcript #00000002 (NM_000059.3, BRCA2 gene)

Transcript name breast cancer 2, early onset
Gene name BRCA2 (BRCA2, DNA repair associated)
Chromosome 13
Transcript - NCBI ID NM_000059.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000050.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2016-06-24 09:35:13 +00:00 (UTC)
Date last edited N/A


Variants

42 entries on 1 page. Showing entries 1 - 42.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Class     
-?/+? 2i c.68-7T>A r.(=) p.(=) benign
?/+ 5 c.462_463del r.(?) p.(Asp156*) likely pathogenic
+/+ 9 c.731del r.(?) p.(Asp244Valfs*7) pathogenic
?/-? 10 c.1775A>T r.(?) p.(Tyr592Phe) likely benign
+/+ 10 c.1813dupA r.(?) p.(Ile605Asnfs*11) pathogenic
+/+ 11 c.1945C>T r.(?) p.(Gln649*) pathogenic
+/+ 11 c.2099T>G r.(?) p.(Leu700*) pathogenic
-/-? 11 c.2245A>G r.(?) p.(Ser749Gly) -
-/-? 11 c.2320A>G r.(?) p.(Thr774Ala) likely benign
+/+ 11 c.2808_2811del r.(?) p.(Ala938Profs*21) pathogenic
?/? 11 c.3839A>T r.(?) p.(Asp1280Val) -
+/+ 11 c.3847_3848del r.(?) p.(Val1283Lysfs*2) pathogenic
+/+ 11 c.4284dup r.(?) p.(Gln1429Serfs*9) pathogenic
-?/-? 11 c.4307T>C r.(?) p.(Ile1436Thr) likely benign
?/-? 11 c.4662T>G r.(?) p.(Ser1554Arg) likely benign
?/-? 11 c.4960T>G r.(?) p.(Cys1654Gly) -
?/? 11 c.5070A>C r.(?) p.(Lys1690Asn) likely benign
+/+ 11 c.5238dup r.(?) p.(Asn1747*) pathogenic
?/-? 11 c.5552T>G r.(?) p.(Ile1851Ser) benign
+/+ 11 c.5614A>T r.(?) p.(Lys1872*) pathogenic
-?/-? 11 c.5634C>T r.(=) p.(=) benign
+/+ 2 c.5641_5644del r.(?) p.(Lys1881Glnfs*27) pathogenic
+?/+? 11 c.5645C>A r.(?) p.(Ser1882*) pathogenic
+/+ 11 c.5851_5854del r.(?) p.(Ser1951Trpfs*11) pathogenic
+/+ 11 c.5946del r.(?) p.(Ser1982Argfs*22) pathogenic
+/+ 11 c.6275_6276del r.(?) p.(Leu2092Profs*7) pathogenic
?/-? 11 c.6443C>A r.(?) p.(Ser2148Tyr) likely benign
?/-? 11 c.6523G>A r.(?) p.(Glu2175Lys) -
+/+ 11 c.6553del r.(?) p.(Ala2185Leufs*6) pathogenic
+/+ 11 c.6644_6647del r.(?) p.(Tyr2215Serfs*13) pathogenic
+?/+? E14-E17 c.7008-20_7976+20del r.(?) p.(Thr2337_Arg2659del) pathogenic
+/+ 14 c.7301del r.(?) p.(Lys2434Serfs*33) pathogenic
?/-? 15 c.7448G>A r.(?) p.(Ser2483Asn) likely benign
+/+ 15 c.7516C>T r.(?) p.(Gln2506*) pathogenic
?/? 12 c.7630G>A r.(?) p.(Gly2544Ser) VUS
?/? 18 c.8035G>T r.(?) p.(Asp2679Tyr) VUS
?/? 18 c.8111C>T r.(?) p.(Ser2704Phe) VUS
?/? 18 c.8327T>C r.(?) p.(Leu2776Ser) -
+/? 22 c.8941G>A r.(?) p.(Glu2981Lys) VUS
+/+ 24 c.9196C>T r.(?) p.(Gln3066*) pathogenic
?/+? 25 c.9501+1G>C r.spl? p.? likely pathogenic
?/? 27 c.9976A>T r.(?) p.(Lys3326*) VUS
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