Transcript #00000030 (NM_007294.2, BRCA1 gene)

Transcript name breast cancer 1, early onset (expired, new version available)
Gene name BRCA1 (BRCA1, DNA repair associated)
Chromosome 17
Transcript - NCBI ID NM_007294.2
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

229 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 02 c.-19-55_-19-56insG - -
./. 02 c.-19-55_-19-56insTG - -
./. 02 c.-2A>T - -
./. 21 c.5278-68insA - -
./. 24 c.5592*31G>A - -
./. 02 c.? - -
./. 02 c.43A>G - p.Ile15Val
./. 02 c.66dupA - p.Glu23ArgfsX18
./. 02 c.80+1G>T - -
./. 02 c.80+2delT - -
./. 02 c.80+2T>G - -
./. 03 c.114G>A - p.Lys38Lys
./. 03 c.114G>A - p.Lys38Lys
./. 03 c.114G>A - p.Leu38Lys
./. 03 c.114G>A - p.Lys38Lys
./. 03 c.114G>A - p.Lys38Lys
./. 05 c.154C>T - p.Leu52Val
./. 05 c.168A>T - p.Lys56Asn
./. 05 c.212G>A - p.Arg71Lys
./. 05 c.212+1G>T - -
./. 06 c.213-12A>G - -
./. 07 c.441+38T>C - -
./. 08 c.442-34T>C - -
./. 08 c.442-1G>T - -
./. 08 c.442-1G>T - -
./. 08 c.463C>T - p.Gln155X
./. 08 c.463C>T - p.Gln155X
./. 08 c.470_471delCT - p.Ser157X
./. 08 c.470_471delCT - p.Ser157X
./. 08 c.470_471delCT - p.Ser157X
./. 08 c.470_477del8 - p.Ser157TrpfsX22
./. 08 c.514C>T - p.Gln172X
./. 09 c.548-64delT - -
./. 09 c.548-58delT - -
./. 09 c.548-3delT - -
./. 09 c.548delG - p.Gly183AspfsX51
./. 09 c.571G>A - p.Val191Ile
./. 09 c.571G>A - p.Val191Ile
./. 09 c.571G>A - p.Val191Ile
./. 10 c.616C>T - p.Gln206X
./. 10 c.634C>T - p.Glu206X
./. 11 c.693G>A - p.Tyr231Tyr
./. 11 c.795T>C - p.Ser265Ser
./. 11 c.961delT - p.Trp321GlyfsX20
./. 11 c.962delG - p.Trp321TrpfsX20
./. 11 c.981_982delAT - p.Thr327ThrfsX2
./. 11 c.981_982delAT - p.Thr327ThrfsX2
./. 11 c.981_982delAT - p.Thr327ThrfsX2
./. 11 c.981_982delAT - p.Thr327ThrfsX2
./. 11 c.981_982delAT - p.Thr327ThrfsX2
./. 11 c.981_982delAT - p.Thr327ThrfsX2
./. 11 c.1016delA - p.Lys339ArgfsX2
./. 11 c.1016delA - p.Lys339ArgfsX2
./. 11 c.1036C>T - p.Pro346Ser
./. 11 c.1036C>T - p.Pro346Ser
./. 11 c.1066C>T - p.Gln356X
./. 11 c.1077C>T - p.Pro359Leu
./. 11 c.1116G>A - p.Trp372X
./. 11 c.1116G>A - p.Trp372X
./. 11 c.1279C>T - p.E427X
./. 11 c.1391delC - p.Thr464ThrfsX11
./. 11 c.1392C>T - p.Thr464Thr
./. 11 c.1404delG - p.Lys468LysfsX7
./. 11 c.1465G>T - p.Glu498X
./. 11 c.1548A>G - p.Lys1183Arg
./. 11 c.1548A>G - p.Lys1183Arg
./. 11 c.1846_1847insT - p.Ser616PhefsX9
./. 11 c.1945G>T - p.Glu649X
./. 11 c.2010_2011insTG - p.Gly671ValfsX31
./. 11 c.2082C>T - p.Ser694Ser
./. 11 c.2082C>T - p.Ser694Ser
./. 11 c.2082C>T - p.Ser694Ser
./. 11 c.2082C>T - p.Ser694Ser
./. 11 c.2082C>T - p.Ser694Ser
./. 11 c.2082C>T - p.Ser694Ser
./. 11 c.2082C>T - p.Ser694Ser
./. 11 c.2084A>G - p.ser695Ser
./. 11 c.2110_2111delAA - p.Asn704CysfsX7
./. 11 c.2252_2253delTG - p.Met751PhefsX10
./. 11 c.2252_2253delTG - P.Met751PhefsX10
./. 11 c.2311T>C - p.Leu771Leu
./. 11 c.2311T>C - p.Leu771Leu
./. 11 c.2311T>C - p.Leu771Leu
./. 11 c.2311T>C - p.Leu771Leu
./. 11 c.2311T>C - p.Leu771Leu
./. 11 c.2311T>C - P.Leu771Leu
./. 11 c.2311T>C - p.Leu771Leu
./. 11 c.2311T>C - p.Ler771Leu
./. 11 c.2311_2312insC - p.Leu771SerfsX6
./. 11 c.2312T>C - p.Leu771Leu
./. 11 c.2413T>C - p.Cys805Arg
./. 11 c.2511T>G - p.Val1837Val
./. 11 c.2566T>C - p.Tyr856His
./. 11 c.2566T>C - p.Tyr856His
./. 11 c.2566T>C - p.Tyr856His
./. 11 c.2566T>C - p.Tyr856His
./. 11 c.2566T>C - p.Tyr856His
./. 11 c.2572C>T - p.Gln858X
./. 11 c.2572C>T - p.Gln858X
./. 11 c.2603C>A - p.Ser868X
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