Incidental Mutations

35 incidental mutations are currently displayed, and affect 34 genes.
7 are Possibly Damaging.
12 are Probably Damaging.
13 are Probably Benign.
1 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 35 of 35] 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 103325 APN Akap13 1.000 IGL01667 G1 7 75570019 T57A A G missense Het probably damaging 1.000 phenotype 01/21/2014
2 103338 APN Akna 0.134 IGL01667 G1 4 63379159 T886N G T missense Het probably benign 0.345 phenotype 01/21/2014
3 103339 APN Aqp9 0.116 IGL01667 G1 9 71138213 V38A A G missense Het probably benign 0.129 phenotype 01/21/2014
4 103352 APN Awat2 IGL01667 G1 X 100404254 G124D C T missense Het probably damaging 1.000 phenotype 01/21/2014
5 103357 APN Camsap1 0.283 IGL01667 G1 2 25945281 A G splice site Het probably benign 01/21/2014
6 103345 APN Catsperg2 0.130 IGL01667 G1 7 29710133 Y545C T C missense Het probably damaging 0.979 01/21/2014
7 103331 APN Cldn23 0.108 IGL01667 G1 8 35825920 F138S A G missense Het possibly damaging 0.808 phenotype 01/21/2014
8 103353 APN Clec4a3 0.000 IGL01667 G1 6 122952860 A C utr 5 prime Het probably benign 01/21/2014
9 103349 APN Dlgap3 0.107 IGL01667 G1 4 127233897 T786K C A missense Het probably benign 0.013 phenotype 01/21/2014
10 103328 APN Dnah2 0.000 IGL01667 G1 11 69544395 S50A A C missense Het probably benign 0.000 phenotype 01/21/2014
11 103334 APN Dnah2 0.000 IGL01667 G1 11 69520941 I285N A T missense Het probably damaging 0.978 phenotype 01/21/2014
12 103333 APN Dnah7a 0.126 IGL01667 G1 1 53547292 Y1467H A G missense Het probably damaging 1.000 01/21/2014
13 103356 APN Fgf22 0.000 IGL01667 G1 10 79756754 P115L C T missense Het probably damaging 0.958 phenotype 01/21/2014
14 103329 APN Fzd2 0.533 IGL01667 G1 11 102605782 V351L G T missense Het possibly damaging 0.938 phenotype 01/21/2014
15 103335 APN Gapdhs 0.160 IGL01667 G1 7 30736637 E174V T A missense Het possibly damaging 0.905 phenotype 01/21/2014
16 103330 APN Gjc2 0.000 IGL01667 G1 11 59177518 I46S A C missense Het probably damaging 1.000 phenotype 01/21/2014
17 103344 APN Gm5581 0.080 IGL01667 G1 6 131167772 T C unclassified Het noncoding transcript 01/21/2014
18 103324 APN Krt2 0.141 IGL01667 G1 15 101816330 V282L C A missense Het possibly damaging 0.847 phenotype 01/21/2014
19 103348 APN Myh15 0.173 IGL01667 G1 16 49195579 V1873M G A missense Het probably benign 0.205 01/21/2014
20 103347 APN Myo1b 0.215 IGL01667 G1 1 51760377 T931A T C missense Het probably damaging 0.999 01/21/2014
21 103336 APN Myo6 0.000 IGL01667 G1 9 80289893 K965N A T missense Het unknown phenotype 01/21/2014
22 103326 APN Olfr1441 0.084 IGL01667 G1 19 12422756 V149A T C missense Het probably benign 0.000 phenotype 01/21/2014
23 103332 APN Pcnx3 0.000 IGL01667 G1 19 5686630 R160G T C missense Het probably benign 0.026 01/21/2014
24 103323 APN Slc22a16 0.108 IGL01667 G1 10 40585018 I272T T C missense Het probably damaging 0.997 phenotype 01/21/2014
25 103351 APN Slc35b4 1.000 IGL01667 G1 6 34167675 Y82H A G missense Het possibly damaging 0.808 phenotype 01/21/2014
26 103341 APN Spdya 0.478 IGL01667 G1 17 71556259 M1T T C start codon destroyed Het probably null 0.999 phenotype 01/21/2014
27 103343 APN St6gal1 0.079 IGL01667 G1 16 23321424 N115S A G missense Het probably benign 0.001 phenotype 01/21/2014
28 103355 APN Tbc1d12 0.530 IGL01667 G1 19 38914300 A T splice site Het probably benign 01/21/2014
29 103354 APN Tfrc 1.000 IGL01667 G1 16 32624443 A G unclassified Het probably benign phenotype 01/21/2014
30 103337 APN Trip11 1.000 IGL01667 G1 12 101878862 F1539C A C missense Het probably damaging 1.000 phenotype 01/21/2014
31 103342 APN Ttn 1.000 IGL01667 G1 2 76781078 I15624N A T missense Het possibly damaging 0.916 phenotype 01/21/2014
32 103350 APN Vmn1r169 0.064 IGL01667 G1 7 23577800 M206L A T missense Het probably benign 0.172 01/21/2014
33 103346 APN Zfp362 0.250 IGL01667 G1 4 128787109 L141P A G missense Het probably damaging 1.000 01/21/2014
34 103327 APN Zfp692 0.000 IGL01667 G1 11 58311553 H378R A G missense Het probably damaging 1.000 01/21/2014
35 103340 APN Zfp799 0.204 IGL01667 G1 17 32821820 Q52R T C missense Het possibly damaging 0.734 01/21/2014
[records 1 to 35 of 35]