Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
3 are Possibly Damaging.
6 are Probably Damaging.
15 are Probably Benign.
3 are Probably Null.
0 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 29 of 29] 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 84635 APN 1700003H04Rik 0.020 IGL01451 G1 3 124579878 S23P A G missense Het possibly damaging 0.827 11/11/2013
2 84646 APN Adam1a 0.069 IGL01451 G1 5 121519376 Y618C T C missense Het probably benign 0.095 phenotype 11/11/2013
3 84633 APN Amigo2 0.166 IGL01451 G1 15 97245226 S438R A C missense Het probably benign 0.221 11/11/2013
4 84632 APN Atp5k 0.147 IGL01451 G1 5 108434056 I21V T C missense Het probably benign 0.001 11/11/2013
5 84650 APN Dnah2 0.474 IGL01451 G1 11 69474191 T C splice site Het probably benign phenotype 11/11/2013
6 84641 APN Dock2 0.000 IGL01451 G1 11 34310390 Y984H A G missense Het probably damaging 0.999 phenotype 11/11/2013
7 84644 APN Dpysl2 0.498 IGL01451 G1 14 66807918 I469F T A missense Het possibly damaging 0.639 phenotype 11/11/2013
8 84636 APN Edem3 0.326 IGL01451 G1 1 151818628 T886I C T missense Het probably benign 0.209 phenotype 11/11/2013
9 84639 APN Gart 0.983 IGL01451 G1 16 91625512 T706A T C missense Het probably benign 0.000 phenotype 11/11/2013
10 84648 APN Gfpt2 0.703 IGL01451 G1 11 49807690 A T splice site Het probably benign 11/11/2013
11 84629 APN Gm11541 0.182 IGL01451 G1 11 94695669 D84A T G missense Het unknown 11/11/2013
12 84637 APN Gne 1.000 IGL01451 G1 4 44041860 T C intron 303 bp Het probably null phenotype 11/11/2013
13 84638 APN Gria4 0.366 IGL01451 G1 9 4503652 D321E A T missense Het probably benign 0.044 phenotype 11/11/2013
14 84655 APN Ift122 1.000 IGL01451 G1 6 115912604 T G critical splice donor site 2 bp Het probably null phenotype 11/11/2013
15 84647 APN Lcp2 0.115 IGL01451 G1 11 34047345 A T start gained Het probably benign phenotype 11/11/2013
16 84654 APN Mcm2 1.000 IGL01451 G1 6 88891966 C T splice site Het probably benign phenotype 11/11/2013
17 84628 APN Olfr921 0.018 IGL01451 G1 9 38775929 I225V A G missense Het probably benign 0.040 phenotype 11/11/2013
18 84653 APN Ptpru 0.658 IGL01451 G1 4 131769492 C A utr 3 prime Het probably benign phenotype 11/11/2013
19 84649 APN Rpap2 0.921 IGL01451 G1 5 107603626 T C critical splice donor site 2 bp Het probably null 11/11/2013
20 84645 APN Slc25a39 0.674 IGL01451 G1 11 102404900 T138A T C missense Het probably damaging 1.000 phenotype 11/11/2013
21 84627 APN St6galnac1 0.058 IGL01451 G1 11 116769339 S49R A C missense Het probably benign 0.001 phenotype 11/11/2013
22 84640 APN Stat1 0.000 IGL01451 G1 1 52139343 L312P T C missense Het probably damaging 1.000 phenotype 11/11/2013
23 84652 APN Tmem198 0.341 IGL01451 G1 1 75484370 T C unclassified Het probably benign 11/11/2013
24 84631 APN Top2a 0.984 IGL01451 G1 11 99011030 L458Q A T missense Het probably damaging 1.000 phenotype 11/11/2013
25 84651 APN Treml4 0.049 IGL01451 G1 17 48264995 T C splice site Het probably benign phenotype 11/11/2013
26 84643 APN Trpm6 1.000 IGL01451 G1 19 18809569 D503G A G missense Het probably damaging 1.000 phenotype 11/11/2013
27 84634 APN Ttn 1.000 IGL01451 G1 2 76945273 E1854D C A missense Het unknown phenotype 11/11/2013
28 84642 APN Ubqln3 0.075 IGL01451 G1 7 104142196 M229K A T missense Het possibly damaging 0.712 phenotype 11/11/2013
29 84630 APN Zfyve9 0.390 IGL01451 G1 4 108682260 T939A T C missense Het probably damaging 0.983 phenotype 11/11/2013
[records 1 to 29 of 29]