Transcript #00000031 (NM_032043.2, BRIP1 gene)

Transcript name BRCA1 interacting protein C-terminal helicase 1
Gene name BRIP1 (BRCA1 interacting protein C-terminal helicase 1)
Chromosome 17
Transcript - NCBI ID NM_032043.2
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 01 c.-64G>A - -
./. 01 c.-64G>A - -
./. 01 c.-31+12G>A - -
./. 01 c.-31+22G>C - -
./. 17 c.? - -
./. 02 c.10A>G - p.Met4Val
./. 02 c.93+72T>G - -
./. 03 c.139C>G - p.Pro47Ala
./. 03 c.139C>G - p.Pro47Ala
./. 03 c.141delC - p.Thr48GlnfsX7
./. 03 c.155A>G - p.Lys52Arg
./. 03 c.193C>T - p.Gln65X
./. 03 c.205+5G>T - -
./. 04 c.265delG - p.Ala89HisfsX12
./. 04 c.316C>T - p.Arg106Cys
./. 04 c.317G>A - p.Arg106His
./. 04 c.370A>G - p.Thr124Ala
./. 04 c.379+28G>A - p.=
./. 05 c.380-28G>A - -
./. 05 c.380-28G>A - p.=
./. 05 c.430G>A - p.Ala144Thr
./. 05 c.430G>A - p.Ala144Thr
./. 05 c.430G>A - p.Ala144Thr
./. 05 c.485G>A - p.Arg162Gln
./. 06 c.508-31C>G - -
./. 06 c.508-31C>G - p.=
./. 06 c.508-31C>G - -
./. 06 c.512G>T - p.Arg171Ile
./. 06 c.517C>T - p.Arg173Cys
./. 06 c.517C>T - p.Arg173Cys
./. 06 c.517C>T - p.Arg173Cys
./. 06 c.517C>T - p.Arg173Cys
./. 06 c.517C>T - p.Arg173Cys
./. 06 c.577G>A - p.Val193Ile
./. 06 c.577G>A - p.Val193Ile
./. 06 c.577G>A - p.Val193Ile
./. 06 c.577G>A - p.Val193Ile
./. 06 c.577G>A - p.Val193Ile
./. 06 c.577G>A - p.Val193Ile
./. 06 c.584T>C - p.Leu195Pro
./. 06 c.584T>C - p.Leu195Pro
./. 06 c.584T>C - p.Leu195Pro
./. 06 c.584T>C - p.Leu195Pro
./. 06 c.584T>C - p.Leu195Pro
./. 06 c.584T>C - p.Leu195Pro
./. 06 c.587A>G - p.Asn196Ser
./. 07 c.628C>T - p.Pro210Ser
./. 07 c.629C>T - p.Pro210Leu
./. 07 c.644C>A - p.Ser215Tyr
./. 07 c.679C>G - p.Gln227Glu
./. 07 c.765G>T - p.Gln255His
./. 07 c.778A>G - p.Thr260Ala
./. 07 c.790C>T - p.Arg264Trp
./. 07 c.790C>T - p.Arg264Trp
./. 07 c.790C>T - p.Arg264Trp
./. 07 c.820A>G - p.Thr274Ala
./. 07 c.845C>G - p.Thr282Ser
./. 07 c.854A>G - p.His285Arg
./. 07 c.868G>A - p.Gly290Ser
./. 07 c.869G>A - p.Gly290Asp
./. 07 c.890A>G - p.Lys297Arg
./. 07 c.890A>G - p.Lys297Arg
./. 07 c.918+15T>A - -
./. 08 c.941A>G - p.His314Arg
./. 08 c.1045G>C - p.Ala349Pro
./. 08 c.1045G>C - p.Ala349Pro
./. 08 c.1045G>C - p.Ala349Pro
./. 09 c.1238T>C - p.Val413Ala
./. 09 c.1254del - p.Arg419GlyfsX4
./. 09 c.1255C>T - p.Arg419Trp
./. 09 c.1255C>T - p.Arg419Trp
./. 09 c.1255C>T - p.Arg419Trp
./. 10 c.1433A>G - p.His478Arg
./. 10 c.1444A>G - p.Ile482Val
./. 11 c.1586G>A - p.Gly529Glu
./. 11 c.1591T>G - p.Phe531Val
./. 11 c.1591T>G - p.Phe531Val
./. 11 c.1605C>G - p.Asp535Glu
./. 11 c.1619A>T - p.Gln540Leu
./. 11 c.1619A>T - p.Gln540Leu
./. 12 c.1629-498A>T - -
./. 12 c.1629-498A>T - -
./. 12 c.1629-439_1629-436del - p.=
./. 12 c.1684A>G - p.Ile562Val
./. 12 c.1704T>G - p.Asn568Lys
./. 12 c.1735C>T - p.Arg579Cys
./. 13 c.1795-47G>C - p.=
./. 13 c.1795-47G>C - -
./. 13 c.1823A>G - p.Gln608Arg
./. 13 c.1831G>A - p.Val611Ile
./. 13 c.1899C>G - p.Ile633Met
./. 14 c.1941G>C - p.Trp647Cys
./. 14 c.1993dup - p.Gln665ProfsX4
./. 14 c.2010dupT - p.Glu671X
./. 14 c.2056A>G - p.Thr686Ala
./. 14 c.2076G>A - p.Leu692Leu
./. 14 c.2087C>T - p.Pro696Leu
./. 14 c.2097+7G>A - -
./. 14 c.2097+7G>A - -
./. 14 c.2097+26delT - -
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