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 -


Variants

268 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     
?/. 2 c.-32142499G>A - r.(=) p.(=) - -
+/. - c.-39-1_-39del c.-39-1_-39delGA r.spl? p.? - Likely pathogenic
-/. - c.68-7T>A - r.(=) p.(=) - ClinVar
-/. - c.68-7T>A - r.(=) p.(=) - ClinVar
?/. 3 c.215A>G - r.(?) p.(Asn72Ser) - ClinVar
./. - c.215A>G - r.(?) p.(Asn72Ser) - ClinVar
+/. - c.262_263del - r.(?) p.(Leu88Alafs*12) - ClinVar
+/. - c.262_263del - r.(?) p.(Leu88Alafs*12) - Pathogenic
+/. 13 c.262_263delCT - r.(?) p.(Leu88Alafs*12) - ClinVar
+/. - c.262_263delCT - r.(?) p.(Leu88Alafs*12) - pathogenic
+/. - c.262_263delCT - r.(?) p.(Leu88Alafs*12) frameshift Pathogenic
+/. 3 c.262_263delCT - r.(?) p.(Leu88Alafs*12) - Pathogenic
-/. 10 c.317-1875G>A - r.(=) p.(=) - ClinVar
-/. 5 c.440A>G - r.(?) p.(Gln147Arg) - ClinVar
-/. - c.440A>G - r.(?) p.(Gln147Arg) - ClinVar
-/. - c.516+18T>C - r.(=) p.(=) - ClinVar
+/. - c.582G>A - r.(?) p.(Trp194*) - ClinVar
+/. - c.631+1G>A - r.spl? p.? - Pathogenic
-/. - c.631+541T>C - r.(=) p.(=) - ClinVar
+/. - c.755_758del - r.(?) p.(Asp252Valfs*24) - ClinVar
+/. - c.774_775del - r.(?) p.(Glu260Serfs*15) - Pathogenic
+/. - c.774_775delAA - r.(?) p.(Glu260Serfs*15) - Pathogenic
+/. 9 c.774_775delAA - r.(?) p.(Glu260Serfs*15) - Pathogenic
+/. - c.809C>G - r.(?) p.(Ser270*) - Pathogenic
+/. - c.809C>G - r.(?) p.(Ser270*) - Pathogenic
+/. 10 c.809C>G - r.(?) p.(Ser270*) - Pathogenic
-/. 10 c.865A>C - r.(?) p.(Asn289His) - ClinVar
+/. 10 c.865A>C c.856A>C r.(?) p.(Asn289His) - Benign
?/. 10 c.943T>A - r.(?) p.(Cys315Ser) - ClinVar
./. - c.943T>A - r.(?) p.(Cys315Ser) - ClinVar
+/. 10 c.943T>A - r.(?) p.(Cys315Ser) - Benign/Likely benign
+/. 10 c.956dupA - r.(?) p.(Asn319Lysfs*8) - ClinVar
+/. - c.956dupA - r.(?) p.(Asn319Lysfs*8) - Pathogenic
+/. 10 c.956dupA - r.(?) p.(Asn319Lysfs*8) - pathogenic
+/. 10 c.956_957insA - r.(?) p.(Asn319Lysfs*8) - -
+/. 10 c.1114A>C - r.(?) p.(Asn372His) - Benign
-/. 10 c.1275A>G - r.(=) p.(=) - ClinVar
?/. 10 c.1342C>T - r.(?) p.(Arg448Cys) - ClinVar
-/. 10 c.1362A>G - r.(=) p.(=) - ClinVar
-/. 10 c.1365A>G - r.(=) p.(=) - ClinVar
-/. 10 c.1644G>A - r.(=) p.(=) - ClinVar
+/. - c.1763_1766del - r.(?) p.(Asn588Serfs*25) - ClinVar
+/. - c.1773_1776del c.1773_1776delTTAT r.(?) p.(Ile591Metfs*22) - Pathogenic
+/. - c.1773_1776del - r.(?) p.(Ile591Metfs*22) - Pathogenic
+/. 10 c.1773_1776delTTAT - r.(?) p.(Ile591Metfs*22) - ClinVar
+/. 10 c.1773_1776delTTAT - r.(?) p.(Ile591Metfs*22) - Pathogenic
+/. 10 c.1813dupA - r.(?) p.(Ile605Asnfs*11) - Pathogenic
?/. - c.1825C>G - r.(?) p.(Gln609Glu) - ClinVar
+/. - c.1855C>T - r.(?) p.(Gln619*) - Pathogenic
+/. - c.1888dup - r.(?) p.(Thr630Asnfs*6) - ClinVar
./. - c.2186T>C - r.(?) p.(Ile729Thr) - ClinVar
-/. 11 c.2229T>C - r.(=) p.(=) - ClinVar
+/. 11 c.2229T>C - r.(=) p.(=) - Benign
+/. - c.2442del - r.(?) p.(Met815Trpfs*10) - ClinVar
+/. - c.2471_2476del 2471_2476delTAAATG r.(?) p.(Leu824*) - Pathogenic
+/. - c.2471_2476del - r.(?) p.(Leu824*) - Pathogenic
+/. 11 c.2471_2476delTAAATG - r.(?) p.(Leu824*) - ClinVar
+/. 11 c.2471_2476delTAAATG - r.(?) p.(Leu824*) - Pathogenic
+/. - c.2595del 2595delA r.(?) p.(Glu866Lysfs*8) - Pathogenic
+/. - c.2595del - r.(?) p.(Glu866Lysfs*8) - Pathogenic
+/. - c.2612C>A - r.(?) p.(Ser871*) - Pathogenic
+/. - c.2636_2637del - r.(?) p.(Ser879*) - Pathogenic
+/. 11 c.2636_2637delCT - r.(?) p.(Ser879*) - ClinVar
+/. 11 c.2636_2637delCT - r.(?) p.(Ser879*) - Pathogenic
+/. - c.2808_2811del - r.(?) p.(Ala938Profs*21) - ClinVar
+/. 11 c.2808_2811del - r.(?) p.(Ala938Profs*21) - ClinVar
+/. - c.2808_2811del 2808_2811delACAA r.(?) p.(Ala938Profs*21) - Pathogenic
+/. - c.2808_2811del - r.(?) p.(Ala938Profs*21) - Pathogenic
+/. 11 c.2808_2811delACAA - r.(?) p.(Ala938Profs*21) - Pathogenic
+/. 11 c.2808_2811delACAA - r.(?) p.(Ala938Profs*21) - Pathogenic
+/. - c.2830A>T - r.(?) p.(Lys944*) - Pathogenic
+/. - c.2830A>T - r.(?) p.(Lys944*) - Pathogenic
+/. 11 c.2830A>T - r.(?) p.(Lys944*) - Pathogenic
?/. 11 c.2860_2862delGAG - r.(?) p.(Glu954del) - ClinVar
-/. 11 c.2971A>G - r.(?) p.(Asn991Asp) - ClinVar
+/. 11 c.2971A>G - r.(?) p.(Asn991Asp) - Benign
+/. 11 c.3109C>T - r.(?) p.(Gln1037*) - ClinVar
+/. - c.3109C>T - r.(?) p.(Gln1037*) - ClinVar
+/. 11 c.3109C>T - r.(?) p.(Gln1037*) - ClinVar
+/. - c.3109C>T - r.(?) p.(Gln1037*) - Pathogenic
+/. - c.3109C>T - r.(?) p.(Gln1037*) - Pathogenic
+/. 11 c.3109C>T - r.(?) p.(Gln1037*) - Pathogenic
+/. - c.3391A>G - r.(?) p.(Arg1131Gly) missense Uncertain significance​
-/. 11 c.3396A>G - r.(=) p.(=) - ClinVar
+/. 11 c.3396A>G - r.(=) p.(=) - Benign
-/. 11 c.3420T>C - r.(=) p.(=) - ClinVar
?/. 11 c.3445A>G - r.(?) p.(Met1149Val) - ClinVar
./. - c.3445A>G - r.(?) p.(Met1149Val) - ClinVar
+/. 11 c.3445A>G - r.(?) p.(Met1149Val) - Uncertain significance
+/. - c.3569G>T - r.(?) p.(Arg1190Leu) missense Uncertain significance​
+/. - c.3599_3600del - r.(?) p.(Cys1200*) - Pathogenic
+/. 11 c.3599_3600delGT - r.(?) p.(Cys1200*) - Pathogenic
-?/. 11 c.3675A>G - r.(=) p.(=) - ClinVar
+/. - c.3680_3681del 3680_3681delTG r.(?) p.(Leu1227Glnfs*5) frameshift Pathogenic
?/. 11 c.3782C>G - r.(?) p.(Ser1261Cys) - ClinVar
-/. 11 c.3807T>C - r.(=) p.(=) - ClinVar
+/. 11 c.3807T>C - r.(=) p.(=) - Benign
+/. 11 c.3821delA - r.(?) p.(Lys1274Argfs*2) - -
+/. - c.3847_3848del 3847_3848delGT r.(?) p.(Val1283Lysfs*2) - Pathogenic
+/. - c.3865_3868del 3865_3868delAAAT r.(?) p.(Lys1289Alafs*3) frameshift Pathogenic
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