Transcript #00000006 (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 -


Variants

112 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 02 c.-39-26G>A - -
./. 02 c.-39-26G>A - -
./. 02 c.-39-26G>A - -
./. 17 C.7806-9T>G - -
./. 17 C.7806-9T>G - -
./. 03 c.78A>G - p.Pro26Pro
./. 05 c.425-79T>C - -
./. 05 c.425-79T>C - -
./. 05 c.425-79T>C - -
./. 04 c.425+67A>C - -
./. 04 c.425+67A>C - -
./. 04 c.425+67A>C - -
./. 05 c.440A>G - p.Glu147Arg
./. 05 c.464_468del5 - p.Arg155LysfsX26
./. 05 c.470_474del5 - p.Lys157SerfsX24
./. 08 c.681+56C>T - -
./. 10 c.865A>C - p.Asn289His
./. 10 c.865A>C - p.Asn991Asp
./. 10 c.1080delA - p.Pro360ProfsX7
./. 10 c.1114A>C - p.Asn372His
./. 10 c.1114A>C - p.Asn372His
./. 10 c.1114A>C - p.Asn372His
./. 10 c.1114A>C - p.Asn372His
./. 10 c.1114A>C - p.Asn372His
./. 10 c.1261C>T - p.Gln421X
./. 10 c.1303dupA - p.Arg435LysfsX17
./. 10 c.1365A>G - p.Ser455Ser
./. 10 c.1365A>G - p.Ser455Ser
./. 10 c.1365A>G - p.Ser455Ser
./. 10 c.1365A>G - p.Ser455Ser
./. 10 c.1365A>G - p.Ser455Ser
./. 10 c.1773_1776delTTAT - p.Ile591MetfsX22
./. 10 c.1813delA - p.Ile605TyrfsX9
./. 10 c.1881delA - p.Ala672AlafsX16
./. 10 c.1901delC - p.Ala634ValfsX10
./. 11 c.1910-51G>T - -
./. 11 c.1910-51G>T - -
./. 11 c.1910-51G>T - -
./. 11 c.2229T>C - p.His743His
./. 11 c.2229T>C - p.His743His
./. 11 c.2229T>C - p.His743His
./. 11 c.2229T>C - p.His743His
./. 11 c.2229T>C - p.His743His
./. 11 c.2442delC - p.Pro814ProfsX10
./. 11 c.2442delC - p.Pro814ProfsX10
./. 11 c.2588_2589insA - p.Asn863LysfsX18
./. 11 c.2731A>G - p.Asn991Asp
./. 11 c.2731A>G - p.Asn991Asp
./. 11 c.2731A>G - p.Asn991Asp
./. 11 c.2731A>G - p.Asn991Asp
./. 11 c.2731A>G - p.Asn991Asp
./. 11 c.2806_2809delAAAC - p.Lys936LysfsX23
./. 11 c.2845delT - p.Tyr949MetfsX11
./. 11 c.3109C>T - p.Gln1037X
./. 11 c.3109C>T - p.Gln1037X
./. 11 c.3109C>T - p.Gln1037X
./. 11 c.3195_3198delTAAT - p.Ile1065IlefsX11
./. 11 c.3396A>G - p.Lys1132Lys
./. 11 c.3396A>G - p.Lys1132Lys
./. 11 c.3396A>G - p.Lys1132Lys
./. 11 c.3396A>G - p.Lys1132Lys
./. 11 c.3406A>G - p.Lys1132Lys
./. 11 c.3744_3747delTGAG - p.Ser1248ArgfsX10
./. 11 c.3807T>C - p.Val1269Val
./. 11 c.3807T>C - p.Val1269Val
./. 11 c.3807T>C r.(=) p.(=)
./. 11 c.3807T>C - p.Val1269Val
./. 11 c.3807T>C - p.Val1269Val
./. 11 c.3871C>T - p.Gln1291X
./. 11 c.4563_4564delGT - p.Leu1522GlyfsX6
./. 11 c.5164_5165delAG - p.Ser1722TyrfsX4
./. 11 c.5574_5577delAATT - p.Thr1858ThrfsX4
./. 11 c.5574_5577delAATT - p.Thr1858ThrfsX4
./. 11 c.5574_5577delAATT - p.Thr1858ThrfsX4
./. 11 c.5574_5577delAATT - p.Thr1858ThrfsX4
./. 11 c.5645C>A - p.Ser1882X
./. 11 c.5681dupA - p.Tyr1894X
./. 11 c.5683G>C - p.Glu1895Gln
./. 11 c.5683G>C - p.Glu1895Gln
./. 11 c.5722_5723delCT - p.Leu1908ArgfsX2
./. 11 c.5722_5723delCT - p.Leu1908ArgfsX2
./. 11 c.5722_5723delCT - p.Leu1908ArgfsX2
./. 11 c.5851_5854delAGTT - p.Ser1951TrpfsX11
./. 11 c.5946delT - p.Ser1982ArgfsX22
./. 11 c.6033_6034delTT - p.Phe2011PhefsX6
./. 11 c.6468_6469delTC - p.Ser2156SerfsX19
./. 14 c.7242A>G - p.Ser2414Ser
./. 14 c.7435+53C>T - -
./. 14 c.7435+53C>T - -
./. 14 c.7435+53C>T - -
./. 15 c.7467_7468insT - p.Ile2490TyrfsX7
./. 15 c.7471C>T - p.Gln2491X
./. 16 c.7655_7658delTTAA - p.Ile2552ThrfsX95
./. 17 c.7806-15C>T - -
./. 17 c.7806-14T>C - -
./. 17 c.7806-14T>C - -
./. 17 c.7806-14T>C - -
./. 17 c.7806-14T>C - -
./. 17 c.7976+1G>A - -
./. 18 c.8047_8054dupGCAAAAAC - p.Leu2686GlufsX10
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