Transcript #00000115 (NM_007294.4, BRCA1 gene)

Transcript name transcript variant 1
Gene name BRCA1 (BRCA1, DNA repair associated)
Chromosome 17
Transcript - NCBI ID NM_007294.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_009225.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

51 entries on 1 page. Showing entries 1 - 51.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Zygosity     

Co_ocurrence     

Review status     
+/+ 1-2 Deletion r.? p.? Hetero N/A -
+/+ 1-2 deletion r.? p.? Hetero N/A -
+/+ 10-14 deletion (Exons 10-14) r.? p.? Hetero N/A -
?/+? 12 duplication exon 12 r.? p.? Hetero BLM -
+/+ 2 c.53T>C r.(53u>c) (p.Met18Thr) Hetero N/A -
+/+ 2 c.68_69delAG r.(68_69del) p.(Glu23Valfs*17) Hetero N/A -
+/+ 2 c.68_69delAG r.(68_69del) p.(Glu23Valfs*17) Hetero N/A -
+/+ 2 c.68_69delAG r.(68_69del) p.(Glu23Valfs*17) Hetero N/A -
+/+ 2 c.68_69delAG r.(68_69del) p.(Glu23Valfs*17) Hetero N/A -
+/+ 2 c.68_69delAG r.(68_69del) p.(Glu23Valfs*17) Hetero N/A -
+/+ 2 c.68_69delAG r.(68_69del) p.(Glu23Valfs*17) Hetero no -
?/? 3 c.107C>A r.(107c>a) p.(Ser36Tyr) Hetero no -
+?/+? 3 c.121C>T r.? p.(His41Tyr) Hetero no -
+/+ 3 c.131G>T r.? p.(Cys44Phe) Hetero N/A -
+/+ 4 c.190T>C r.(190u>c) p.Cys64Arg Hetero N/A -
+/+ 4 c.190T>C r.(190u>c) p.(Cys64Arg) Hetero N/A -
?/? 4 c.206C>T r.? p.(Thr69Ile) Hetero no -
+/+ 4 c.211A>G r.? p.(Arg71Gly) Hetero N/A -
+/+ 4 c.211A>G r.? p.(Arg71Gly) Hetero N/A -
+/+ 4 c.211A>G r.(211a>g) p.(Arg71Gly) Hetero N/A -
+/+ 4 c.211A>G r.(211a>g) p.(Arg71Gly) Hetero N/A -
+/+ 6 c.411dup r.(411dup) p.(Leu138Serfs*4) Hetero N/A -
+/+ 10 c.689_692del r.(689_692del) p.(Glu230Glyfs*3) Hetero N/A -
+/+ 10 c.798_799del r.? p.(Ser267Lysfs*19) Hetero N/A -
+/+ 11 c.1175_1214del r.(?) p.(Leu392Glnfs*5) Hetero N/A -
?/? 10 c.1367T>C r.(1367u>c) p.(Ile456Thr) Hetero no -
?/? 15 c.2296A>C r.(2296a>c) p.(Ser766Arg) Hetero no -
?/? 10 c.2750T>C r.(2750u>c) p.Ile917Thr Hetero no -
?/? 10 c.3119G>A r.(3119g>a) p.(Ser1040Asn) Hetero no -
+/+ 10 c.3228_3229del r.(?) p.(Gly1077Alafs*8) Hetero N/A -
+/+ 10 c.3257T>G r.(3257u>g) p.(Leu1086*) Hetero N/A -
+/+ 10 c.3292_3293del r.(3292_3293del) p.Leu1098fs Hetero N/A -
?/? 10 c.3433G>T r.? p.(Val1145Phe) Hetero no -
?/? 10 c.3878C>T r.(3878c>u) p.(Ala1293Val) Hetero no -
?/? 13 c.(4146_4242)_(4357+159_4417)dup r.? p.? Hetero N/A -
+/+ 13 c.4327C>T r.(?) p.(R1443*) Hetero no -
?/? 13 c.4408G>A r.(4408g>a) p.(Glu1470Lys) Homo no -
+/+ 15-16 c.4484_4987del r.(4484_4987del) p.(Arg1495_Phe1662del) Hetero N/A -
+/+ 15 c.4964_4982del r.(4964_4982del) p.(Ser1655Tyrfs*16) Hetero N/A -
+/+ 15 c.4964_4982del r.(4964_4982del) p.(Ser1655Tyrfs*16) Hetero N/A -
+/+ 16 c.5030_5033del r.? p.(Thr1677Ilefs*2) Hetero N/A -
+/+ 16 c.5030_5033del r.? p.(Thr1677Ilefs*2) Hetero N/A -
+/+ 16 c.5035_5039del r.? p.(Leu1679fs) Hetero N/A -
+?/+? 17 c.5108A>G r.? p.(Tyr1703Cys) Hetero no -
+/+ 17 c.5117G>A r.(5117g>a) p.(Gly1706Glu) Hetero N/A -
+/+ 17 c.5123C>A r.(5123c>a) p.(Ala1708Glu) Hetero N/A -
+/+ 17 c.5123C>A r.(5123c>a) p.(Ala1708Glu) Hetero N/A -
+/+ 17 c.5123C>A r.(5123c>a) p.(Ala1708Glu) Hetero N/A -
+/+ 20 c.5266dup r.(5266dup) p.Gln1756fs Hetero N/A Other names: 5382insC
+/+ 23 c.5476C>T r.(5476c>u) p.Gln1826Ter Hetero N/A -
+/+ 23 c.5476C>T r.(5476c>u) p.Gln1826Ter Hetero N/A -
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