Transcript #00000001 (NM_007294.3, BRCA1 gene)

Transcript name breast cancer 1, early onset, transcript variant 1
Gene name BRCA1 (BRCA1, DNA repair associated)
Chromosome 17
Transcript - NCBI ID NM_007294.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_009225.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
+/. - c.-232_4484del c.-232-?_4484+?del r.spl? p.? - Pathogenic
?/? - c.-19-10T>C - r.(=) p.(=) - ClinVar
+/. - c.61del - r.(?) p.(Ile21Serfs*2) - ClinVar
+/. - c.61del - r.(?) p.(Ile21Serfs*2) - Pathogenic
+/? 2 c.61delA - r.(?) p.(Ile21Serfs*2) - ClinVar
+/. 2 c.61delA - r.(?) p.(Ile21Serfs*2) - Pathogenic
+/. - c.66dup - r.(?) p.(Glu23Argfs*18) - Pathogenic
+/? 2 c.66dupA - r.(?) p.(Glu23Argfs*18) - ClinVar
+/. - c.66dupA - r.(?) p.(Glu23Argfs*18) - ClinVar
+/. - c.66dupA - r.(?) p.(Glu23Argfs*18) - ClinVar
+/. 2 c.66dupA - r.(?) p.(Glu23Argfs*18) - Pathogenic
+/. - c.68_69del - r.(?) p.(Glu23Valfs*17) - ClinVar
+/. - c.68_69del - r.(?) p.(Glu23Valfs*17) - -
+/. - c.68_69del - r.(?) p.(Glu23Valfs*17) - Pathogenic
+/? 2 c.68_69delAG - r.(?) p.(Glu23Valfs*17) - ClinVar
+/. - c.68_69delAG - r.(?) p.(Glu23Valfs*17) - -
+/. 2 c.68_69delAG - r.(?) p.(Glu23Valfs*17) - Pathogenic
-/? - c.81-14C>T - r.(?) p.(Glu1148Argfs*7) - ClinVar
+/. - c.81_134del c.81-?_134+?del r.(?) p.(Cys27*) - ClinVar
+/. - c.110C>A - r.(?) p.(Thr37Lys) - ClinVar
-/? 3 c.114G>A - r.(=) p.(=) - ClinVar
-/. 3 c.114G>A - r.(=) p.(=) - ClinVar
+/. 3 c.114G>A - r.(=) p.(=) - Benign
+/. 3 c.115T>C - r.(?) p.(Cys39Arg) - ClinVar
+/. - c.115T>C C39R r.(?) p.(Cys39Arg) frameshift ClinVar
+/. - c.134+1G>T - r.spl? p.? - ClinVar
+/. - c.134+1G>T - r.spl? p.? - Pathogenic/Likely pathogenic
+/. IVS3 c.134+1G>T - r.spl? p.? - Pathogenic/Likely pathogenic
+/. 3 c.134+2del - r.spl? p.? - ClinVar
+/. - c.134+2del - r.spl? p.? - Pathogenic
+/. - c.134+2del - r.spl? p.? - Pathogenic
+/. - c.134+2delT - r.spl? p.? - -
+/. IVS3 c.134+2delT - r.spl? p.? - Pathogenic
+/. 4i c.135-1G>C - r.spl? p.? - ClinVar
+/. - c.135-1G>C - r.spl? p.? - ClinVar
+/. - c.135-1G>C - r.spl? p.? - Pathogenic
+/. IVS4 c.135-1G>C - r.spl? p.? - Pathogenic
+/. - c.150del - r.(?) p.(Lys50Asnfs*19) - Pathogenic
+/. - c.150delA - r.(?) p.(Lys50Asnfs*19) - ClinVar
+/. 5 c.150delA - r.(?) p.(Lys50Asnfs*19) - Pathogenic
./. 5 c.181T>C - r.(?) p.(Cys61Arg) - ClinVar
+/. - c.182G>A - r.(?) p.(Cys61Tyr) - ClinVar
+/. - c.190T>C - r.(?) p.(Cys64Arg) missense Pathogenic​
+/. - c.211A>G - r.(?) p.(Arg71Gly) - ClinVar
+/? - c.212+1G>T - r.spl? p.? - ClinVar
+/? - c.213-12A>G - r.(=) p.(=) - ClinVar
+/. - c.213-12A>G - r.(=) p.(=) - ClinVar
+/. - c.213-12A>G - r.(=) p.(=) - Pathogenic
+/. IVS5 c.213-12A>G - r.(=) p.(=) - Pathogenic
+/. - c.216C>G - r.(?) p.(Ser72Arg) missense Uncertain significance
-?/? 7 c.372C>A - r.(=) p.(=) - ClinVar
+/. - c.470_471del - r.(?) p.(Ser157*) - ClinVar
+/. - c.470_471del - r.(?) p.(Ser157*) - Pathogenic
+/? 8 c.470_471delCT - r.(?) p.(Ser157*) - ClinVar
+/. - c.470_471delCT - r.(?) p.(Ser157*) - ClinVar
+/. 8 c.470_471delCT - r.(?) p.(Ser157*) - Pathogenic
+/. - c.505C>T - r.(?) p.(Gln169*) - ClinVar
+/. - c.505C>T - r.(?) p.(Gln169*) - Pathogenic
+/. 8 c.505C>T - r.(?) p.(Gln169*) - Pathogenic
+/. - c.533T>A - r.(?) p.(Val178Asp) missense Uncertain significance
-/. - c.548-58del IVS8-57delT r.(=) p.(=) - ClinVar
-/. - c.548-58del IVS8-57delT r.(=) p.(=) - ClinVar
+/. - c.548-57del - r.(=) p.(=) - ClinVar
-/? 9 c.571G>A - r.(?) p.(Val191Ile) - ClinVar
-/. - c.571G>A - r.(?) p.(Val191Ile) - ClinVar
?/. 10 c.594-2A>G - r.spl? p.? - ClinVar
+/. - c.594-2A>G - r.spl? p.? - ClinVar
+/. 11 c.686_687delCT - r.(?) p.(Ser229*) - ClinVar
+/. - c.686_687delCT - r.(?) p.(Ser229*) - -
+/. 11 c.726delT - r.(?) p.(Ser242Argfs*5) - -
+/. - c.726delT - r.(?) p.(Ser242Argfs*5) - -
+/. - c.726delT - r.(?) p.(Ser242Argfs*5) - -
?/? 11 c.754C>T - r.(?) p.(Arg252Cys) - ClinVar
-/? 11 c.795T>C - r.(=) p.(=) - ClinVar
-/. - c.823G>A - r.(?) p.(Gly275Ser) - ClinVar
+/. 11 c.829_830del - r.(?) p.(Asn277Tyrfs*9) - ClinVar
+/. - c.829_830del - r.(?) p.(Asn277Tyrfs*9) - Pathogenic
+/. 11 c.829_830delAA - r.(?) p.(Asn277Tyrfs*9) - Pathogenic
+/. - c.850C>T - r.(?) p.(Gln284*) - ClinVar
+/. - c.850C>T - r.(?) p.(Gln284*) - Pathogenic
+/. 11 c.850C>T - r.(?) p.(Gln284*) - Pathogenic
+/. - c.964del - r.(?) p.(Ala322Leufs*19) - Pathogenic
+/. 11 c.964delG - r.(?) p.(Ala322Leufs*19) - Pathogenic
+/. - c.981_982del - r.(?) p.(Cys328*) - ClinVar
+/. - c.981_982del - r.(?) p.(Cys328*) - Pathogenic
+/? 11 c.981_982delAT - r.(?) p.(Cys328*) - ClinVar
+/. - c.981_982delAT - r.(?) p.(Cys328*) - ClinVar
+/. 11 c.981_982delAT - r.(?) p.(Cys328*) - Pathogenic
-/. - c.1036C>T - r.(?) p.(Pro346Ser) - ClinVar
+/. - c.1054G>T - r.(?) p.(Glu352*) - ClinVar
+/. - c.1054G>T - r.(?) p.(Glu352*) - Pathogenic
+/. 11 c.1054G>T - r.(?) p.(Glu352*) - Pathogenic
+/. - c.1104del - r.(?) p.(Asp369Metfs*5) - Pathogenic
+/. - c.1104delA - r.(?) p.(Asp369Metfs*5) - -
+/. 11 c.1104delA - r.(?) p.(Asp369Metfs*5) - Pathogenic
+/. - c.1140dup - r.(?) p.(Lys381Glufs*3) - ClinVar
+/. - c.1204G>T - r.(?) p.(Glu402*) - ClinVar
+/. - c.1204G>T - r.(?) p.(Glu402*) - ClinVar
+/. - c.1204G>T - r.(?) p.(Glu402*) - Pathogenic
+/. 11 c.1204G>T - r.(?) p.(Glu402*) - Pathogenic
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