Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
5 are Possibly Damaging.
13 are Probably Damaging.
10 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 33 of 33] per page Full List
 
ID question?
Source question?
Gene question?
E-score question?
 
Stock # question?
Gen question?
Quality
-
Vld question?
Strain question?
Chr question?
Position question?
 
Mutation question?
Ref
Var
Type question?
Exon Dist question?
 
Zygosity question?
Predicted Effect question?
PPH Score question?
-
Meta Score question?
 
MGI Phenotype question?
Posted question?
 
1 8752 APN Akr1c20 0.051 IGL00834 G1 13 4512665 A G critical splice donor site 2 bp Het probably null 12/06/2012
2 8783 APN Alg5 0.230 IGL00834 G1 3 54744719 T C splice site Het probably benign phenotype 12/06/2012
3 9002 APN App 0.520 IGL00834 G1 16 84965711 F675I A T missense Het probably damaging 0.989 phenotype 12/06/2012
4 9100 APN Atad1 0.274 IGL00834 G1 19 32698568 C152F C A missense Het probably benign 0.016 phenotype 12/06/2012
5 9136 APN Atp2a3 0.356 IGL00834 G1 11 72982787 I829L A C missense Het probably damaging 0.982 phenotype 12/06/2012
6 9178 APN B3galt1 0.150 IGL00834 G1 2 68118706 S255L C T missense Het probably damaging 1.000 phenotype 12/06/2012
7 9292 APN Bptf 1.000 IGL00834 G1 11 107073928 V1417A A G missense Het possibly damaging 0.587 phenotype 12/06/2012
8 9406 APN Cast 0.000 IGL00834 G1 13 74736974 T219S T A missense Het probably damaging 1.000 phenotype 12/06/2012
9 9442 APN Cep95 0.357 IGL00834 G1 11 106818217 I705F A T missense Het probably damaging 0.976 12/06/2012
10 9758 APN Cnot3 1.000 IGL00834 G1 7 3650855 A2V C T missense Het probably damaging 0.999 phenotype 12/06/2012
11 9810 APN Col1a1 1.000 IGL00834 G1 11 94949378 D1084G A G missense Het unknown phenotype 12/06/2012
12 9826 APN Col5a3 0.248 IGL00834 G1 9 20786389 Q873* G A nonsense Het probably null phenotype 12/06/2012
13 9948 APN Cubn 1.000 IGL00834 G1 2 13381927 G1509D C T missense Het probably damaging 1.000 phenotype 12/06/2012
14 10106 APN Defb10 0.123 IGL00834 G1 8 21861936 C66S T A missense Het possibly damaging 0.931 12/06/2012
15 10116 APN Dennd4b 0.576 IGL00834 G1 3 90279686 T C critical splice donor site 2 bp Het probably null 12/06/2012
16 10170 APN Dido1 0.878 IGL00834 G1 2 180689526 T43M G A missense Het possibly damaging 0.797 phenotype 12/06/2012
17 11290 APN Hmcn1 0.314 IGL00834 G1 1 150630340 V3812I C T missense Het probably benign 0.001 phenotype 12/06/2012
18 11492 APN Islr2 1.000 IGL00834 G1 9 58199786 T64A T C missense Het probably benign 0.028 phenotype 12/06/2012
19 11624 APN Kif2b 0.571 IGL00834 G1 11 91576380 I359N A T missense Het probably damaging 1.000 12/06/2012
20 11638 APN Kit 0.852 IGL00834 G1 5 75645959 N704T A C missense Het probably damaging 1.000 phenotype 12/06/2012
21 11706 APN Ksr1 0.240 IGL00834 G1 11 79027517 F604L A G missense Het probably damaging 1.000 phenotype 12/06/2012
22 11820 APN Lrp5 0.768 IGL00834 G1 19 3649404 F294I A T missense Het probably benign 0.000 phenotype 12/06/2012
23 11856 APN Lrrn1 0.306 IGL00834 G1 6 107568308 T356A A G missense Het probably benign 0.060 phenotype 12/06/2012
24 12092 APN Mrps17 IGL00834 G1 5 129716765 V8I G A missense Het probably benign 0.014 phenotype 12/06/2012
25 12764 APN Nop56 0.975 IGL00834 G1 2 130275995 H130Q T A missense Het possibly damaging 0.769 phenotype 12/06/2012
26 13053 APN Plg 0.238 IGL00834 G1 17 12411493 L639Q T A missense Het probably damaging 0.997 phenotype 12/06/2012
27 13108 APN Ppcdc 0.869 IGL00834 G1 9 57415140 F159L A G missense Het probably benign 0.005 phenotype 12/06/2012
28 13122 APN Ppp1ca 0.950 IGL00834 G1 19 4194520 T193A A G missense Het probably benign 0.197 phenotype 12/06/2012
29 13181 APN Prpf39 0.947 IGL00834 G1 12 65043263 D117G A G missense Het probably damaging 0.989 12/06/2012
30 13745 APN Ranbp2 1.000 IGL00834 G1 10 58453323 T51K C A missense Het possibly damaging 0.935 phenotype 12/06/2012
31 14335 APN Sytl2 0.242 IGL00834 G1 7 90382636 A G intron Het probably benign phenotype 12/06/2012
32 12830 APN Tenm2 0.000 IGL00834 G1 11 36024258 I2150F T A missense Het probably damaging 0.998 phenotype 12/06/2012
33 14833 APN Wdr11 0.524 IGL00834 G1 7 129593093 T G splice site 6 bp Het probably null phenotype 12/06/2012
[records 1 to 33 of 33]