Transcript #00017370

Transcript name transcript variant 1
Gene name RAD51C (RAD51 homolog C (S. cerevisiae))
Chromosome 17
Transcript - NCBI ID NM_058216.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_478123.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Haplotype     
-?/. 1 c.-26C>T - r.(?) p.(=) -
-?/. 1 c.-26C>T - r.(?) p.(=) -
-?/. 1 c.-26C>T - r.(?) p.(=) -
-?/. 1 c.-26C>T - r.(?) p.(=) -
?/. 1 c.-2C>G - r.(?) p.(=) -
?/. 1 c.4C>G - r.(?) p.(Arg2Gly) -
-?/. 1 c.7G>A - r.(?) p.(Gly3Arg) -
?/. 1 c.9G>C - r.(?) p.(=) -
+/. 1 c.68_72dup - r.(?) p.(Val25Cysfs*3) -
-?/. 1 c.87T>C - r.(?) p.(=) -
+/. 1 c.93delG - r.(?) p.fs -
+/. 1i c.145+1G>T - r.-11_145del p.0? -
?/. 1i c.145+12T>G - r.(=) p.(=) -
-?/. 1i c.146-8A>G - r.(=) p.(=) -
-?/. 1i c.146-8A>G - - p.= -
-?/. 2 c.154A>C - r.(?) p.(Ile52Leu) -
-?/. 2 c.195A>G - r.(?) p.(=) -
-?/. 2 c.195A>G - r.(?) p.(=) -
-/. - c.195A>G benign r.(=) p.(=) -
+/. 2 c.224dupA - r.(?) p.(Tyr75*) -
+/. 2 c.224dupA - r.(?) p.(Tyr75*) -
+/. 2 c.230delG - r.(?) p.(Gly77Valfs*24) -
-?/. 2 c.237T>G - r.(?) p.(=) -
-?/. 2 c.237T>G - - p.= -
-?/. 2 c.237T>G - r.(?) p.(=) -
-?/. 2 c.237T>G - r.(?) p.(=) -
?/. 2 c.308_310del - r.(?) p.(Phe103del) -
?/. 2 c.341G>T - r.(?) p.(Gly114Val) -
+/. 2 c.374G>T - r.(?) p.(Gly125Val) -
-?/. - c.376G>A likely benign r.(?) p.(Ala126Thr) -
-?/. 2 c.376G>A - r.(?) p.(Ala126Thr) -
-?/. - c.376G>A likely benign r.(?) p.(Ala126Thr) -
-?/. 2 c.376G>A - r.(?) p.(Ala126Thr) -
-?/. 2 c.376G>A - r.(?) p.(Ala126Thr) -
-?/. 2 c.376G>A - r.(?) p.(Ala126Thr) -
-?/. 2 c.376G>A - r.(?) p.(Ala126Thr) -
-?/. 2 c.376G>A - r.(?) p.(Ala126Thr) -
?/. 2 c.376G>A - r.(?) p.(Ala126Thr) -
?/. 2 c.376G>A - r.(?) p.(Ala126Thr) -
?/. 2 c.376G>A - r.(?) p.(Ala126Thr) -
-/. - c.376G>A benign r.(?) p.(Ala126Thr) -
?/. - c.397C>A VUS r.(?) p.(Gln133Lys) -
+/. 2 c.397C>T - r.(?) p.(Gln133*) -
+/. 3 c.414G>C - r.(?) p.(Leu138Phe) -
+?/. 3 c.428A>G - - p.(Gln143Arg) -
+?/. 3 c.428A>G - r.(?) p.(Gln143Arg) -
?/. 3 c.431T>C - r.(?) p.(Ile144Thr) -
+/. 3 c.458G>A - r.(?) p.(Gly153Asp) -
-?/. 3 c.475G>A - r.(?) p.(Asp159Asn) -
?/. 3 c.485G>A - r.(?) p.(Gly162Glu) -
?/. 3 c.485G>A - r.(?) p.(Gly162Glu) -
-?/. 3 c.506T>C - r.(?) p.(Val169Ala) -
-?/. 3 c.506T>C - r.(?) p.(Val169Ala) -
?/. 3 c.506T>C - r.(?) p.(Val169Ala) -
?/. 3 c.506T>C - r.(?) p.(Val169Ala) -
-?/. - c.514C>T likely benign r.(?) p.(Leu172Phe) -
?/. 3 c.523G>A - r.(?) p.(Ala175Thr) -
+/. 3 c.525dupC - r.(?) p.(Cys176Leufs*26) -
?/. 3 c.533A>C - r.(?) p.(Gln178Pro) -
?/. 3i c.571+64C>A - r.(spl?) p.(?) -
-?/. 3i c.572-17G>T - r.(=) p.(=) -
-?/. 3i c.572-17G>T - r.(=) p.(=) -
-?/. 3i c.572-17G>T - r.(=) p.(=) -
-?/. 3i c.572-17G>T - r.(=) p.(=) -
?/. 3i c.572-17G>T - r.(spl?) p.(?) -
?/. 3i c.572-17G>T - r.(spl?) p.(?) -
-/. - c.572-17G>T benign r.(=) p.(=) -
?/. 4i c.644A>G - r.(?) p.(Asp215Gly) -
?/. - c.666A>G - r.(=) p.(=) -
+?/. 4i c.706-2A>G - r.spl p.? -
?/. 5 c.745C>T - r.(?) p.(Arg249Cys) -
+/. 5 c.773G>A - r.(?) p.(Agr258His) FA
+/. 5 c.773G>A - r.(?) p.(Agr258His) FA
+/. 5 c.773G>A - r.(?) p.(Agr258His) FA
+/. 5 c.773G>A - r.(?) p.(Agr258His) FA
+/. 5 c.773G>A - r.(?) p.(Agr258His) FA
+/. 5 c.773G>A - r.(?) p.(Agr258His) FA
+/. 5 c.774delT - r.(?) p.fs -
-?/. 5 c.783A>G - r.(?) p.(=) -
?/. 5 c.784T>G - r.(?) p.(Leu262Val) -
?/. 5 c.784T>G - r.(?) p.(Leu262Val) -
-?/. - c.790G>A likely benign r.(?) p.(Gly264Ser) -
?/. 5 c.790G>A - r.(?) p.(Gly264Ser) -
?/. 5 c.790G>A - r.(?) p.(Gly264Ser) -
?/. 5 c.790G>A - - p.(Gly264Ser) -
-?/. 5 c.790G>A - r.(?) p.(Gly264Ser) -
-?/. 5 c.790G>A - r.(?) p.(Gly264Ser) -
-?/. 5 c.790G>A - r.(?) p.(Gly264Ser) -
?/. 5 c.790G>A - r.(?) p.(Gly264Ser) -
?/. 5 c.790G>A - r.(?) p.(Gly264Ser) -
?/. 5 c.790G>A - r.(?) p.(Gly264Ser) -
?/. 5 c.790G>A - r.(?) p.(Gly264Ser) -
?/. 5 c.790G>A - r.(?) p.(Gly264Ser) -
-?/. - c.790G>A likely benign r.(?) p.(Gly264Ser) -
-?/. 5 c.791G>T - r.(?) p.(Gly264Val) -
+/. - c.837+1del pathogenic r.spl? p.? -
+/. 5i c.837+1G>A - r.spl p.? -
-?/. 6 c.859A>G - r.(?) p.(Thr287Ala) -
-/. - c.859A>G benign r.(?) p.(Thr287Ala) -
-?/. 6 c.859A>G - r.(?) p.(Thr287Ala) -
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