Transcript #00000178

Transcript name transcript variant 1
Gene name RAD51C (RAD51 paralog C)
Chromosome 17
Transcript - NCBI ID NM_058216.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_478123.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-39C>A r.(=) p.(=)
./. - c.-19G>A r.(=) p.(=)
./. - c.4C>G r.(?) p.(Arg2Gly)
./. - c.80T>C r.(?) p.(Leu27Pro)
./. - c.80T>C r.(?) p.(Leu27Pro)
./. - c.80T>C r.(?) p.(Leu27Pro)
./. - c.80T>C r.(?) p.(Leu27Pro)
./. - c.80T>C r.(?) p.(Leu27Pro)
./. - c.80T>C r.(?) p.(Leu27Pro)
./. - c.80T>C r.(?) p.(Leu27Pro)
./. - c.80T>C r.(?) p.(Leu27Pro)
./. - c.80T>C r.(?) p.(Leu27Pro)
./. - c.80T>C r.(?) p.(Leu27Pro)
./. - c.141C>T r.(=) p.(=)
./. - c.145+49C>T r.(=) p.(=)
./. - c.158C>G r.(?) p.(Ser53Cys)
./. - c.158C>G r.(?) p.(Ser53Cys)
./. - c.198A>G r.(=) p.(=)
./. - c.335G>C r.(?) p.(Gly112Ala)
./. - c.335G>C r.(?) p.(Gly112Ala)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.376G>A r.(?) p.(Ala126Thr)
./. - c.404+42_404+43del r.(=) p.(=)
./. - c.404+42_404+43del r.(=) p.(=)
./. - c.404+42_404+43del r.(=) p.(=)
./. - c.404+42_404+43del r.(=) p.(=)
./. - c.431T>C r.(?) p.(Ile144Thr)
./. - c.431T>C r.(?) p.(Ile144Thr)
./. - c.431T>C r.(?) p.(Ile144Thr)
./. - c.523G>A r.(?) p.(Ala175Thr)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-17G>T r.(=) p.(=)
./. - c.572-10G>T r.(=) p.(=)
./. - c.577C>T r.(?) p.(Arg193*)
./. - c.577C>T r.(?) p.(Arg193*)
./. - c.577C>T r.(?) p.(Arg193*)
./. - c.622A>G r.(?) p.(Ile208Val)
./. - c.622A>G r.(?) p.(Ile208Val)
./. - c.622A>G r.(?) p.(Ile208Val)
./. - c.696A>G r.(=) p.(=)
./. - c.696A>G r.(=) p.(=)
./. - c.705+3A>G r.spl? p.?
./. - c.705+3A>G r.spl? p.?
./. - c.705+3A>G r.spl? p.?
./. - c.705+3A>G r.spl? p.?
./. - c.705+4T>G r.spl? p.?
./. - c.705+14T>C r.(=) p.(=)
./. - c.705+14T>C r.(=) p.(=)
./. - c.705+14T>C r.(=) p.(=)
./. - c.706-2A>G r.spl? p.?
./. - c.706-2A>G r.spl? p.?
./. - c.706-2A>G r.spl? p.?
./. - c.706-2A>G r.spl? p.?
./. - c.706-2A>G r.spl? p.?
./. - c.706-2A>G r.spl? p.?
./. - c.706-2A>G r.spl? p.?
./. - c.709C>T r.(?) p.(Arg237*)
./. - c.709C>T r.(?) p.(Arg237*)
./. - c.709C>T r.(?) p.(Arg237*)
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