Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
4 are Possibly Damaging.
13 are Probably Damaging.
11 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
0 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 154468 APN 0610010F05Rik 0.155 IGL01819 G1 11 23584561 S105P A G missense Het probably benign 0.288 02/04/2014
2 154481 APN Adora2b 0.000 IGL01819 G1 11 62265184 N153S A G missense Het possibly damaging 0.884 phenotype 02/04/2014
3 154476 APN Afm 0.053 IGL01819 G1 5 90524906 T200I C T missense Het probably benign 0.013 phenotype 02/04/2014
4 154473 APN Cyp2c67 0.078 IGL01819 G1 19 39615721 D397G T C missense Het probably damaging 0.977 02/04/2014
5 154484 APN Dnah9 0.251 IGL01819 G1 11 66108126 V1032A A G missense Het probably benign 0.326 phenotype 02/04/2014
6 154471 APN Elovl7 0.177 IGL01819 G1 13 108274320 V143G T G missense Het probably damaging 0.993 02/04/2014
7 154465 APN Fhl4 0.146 IGL01819 G1 10 85098870 K16E T C missense Het probably damaging 0.999 02/04/2014
8 154477 APN Golga1 0.177 IGL01819 G1 2 39034149 C383Y C T missense Het probably benign 0.002 phenotype 02/04/2014
9 154460 APN Gucy1a2 0.341 IGL01819 G1 9 3865409 R628* C T nonsense Het probably null phenotype 02/04/2014
10 154478 APN Hectd4 0.933 IGL01819 G1 5 121328418 D2432G A G missense Het possibly damaging 0.845 02/04/2014
11 154483 APN Iqcf5 0.071 IGL01819 G1 9 106515990 *149R T A makesense Het probably null 02/04/2014
12 154467 APN Kcnab1 0.085 IGL01819 G1 3 65319454 Y185N T A missense Het probably damaging 1.000 phenotype 02/04/2014
13 154472 APN Lars 1.000 IGL01819 G1 18 42202550 T1167K G T missense Het probably benign 0.001 phenotype 02/04/2014
14 154475 APN Mib2 0.000 IGL01819 G1 4 155655258 A T splice site 1685 bp Het probably null phenotype 02/04/2014
15 154466 APN Mrps2 0.918 IGL01819 G1 2 28468336 V46A T C missense Het probably benign 0.001 phenotype 02/04/2014
16 154485 APN Myo18b 1.000 IGL01819 G1 5 112878050 T45A T C missense Het unknown phenotype 02/04/2014
17 154486 APN Myo1e 0.000 IGL01819 G1 9 70343040 C T splice site Het probably benign phenotype 02/04/2014
18 154457 APN Olfr1129 0.072 IGL01819 G1 2 87575479 I132V A G missense Het probably damaging 1.000 phenotype 02/04/2014
19 154456 APN Olfr1285 0.103 IGL01819 G1 2 111408733 V106E T A missense Het probably damaging 0.990 phenotype 02/04/2014
20 154461 APN Osbp2 0.102 IGL01819 G1 11 3717127 I8N A T missense Het probably damaging 1.000 phenotype 02/04/2014
21 154455 APN Pcdhb22 0.000 IGL01819 G1 18 37519921 N481Y A T missense Het probably damaging 1.000 phenotype 02/04/2014
22 154482 APN Pde3a 0.379 IGL01819 G1 6 141487537 W765R T C missense Het probably damaging 0.998 phenotype 02/04/2014
23 154463 APN Phf11c 0.000 IGL01819 G1 14 59393137 T40A T C missense Het probably benign 0.003 02/04/2014
24 154474 APN Pih1d2 0.056 IGL01819 G1 9 50621877 S268R T A missense Het probably benign 0.090 02/04/2014
25 154479 APN Pkd1l2 0.000 IGL01819 G1 8 116998174 N2333D T C missense Het probably damaging 0.998 phenotype 02/04/2014
26 154462 APN Prex1 0.344 IGL01819 G1 2 166621245 I62T A G missense Het probably damaging 1.000 phenotype 02/04/2014
27 154469 APN Ptcd2 0.236 IGL01819 G1 13 99326711 N245S T C missense Het possibly damaging 0.783 phenotype 02/04/2014
28 154459 APN Ripor3 0.098 IGL01819 G1 2 167980843 V933F C A missense Het probably damaging 0.989 02/04/2014
29 154458 APN Sphk2 0.000 IGL01819 G1 7 45711056 A G splice site 942 bp Het probably null phenotype 02/04/2014
30 154464 APN Tfcp2 0.000 IGL01819 G1 15 100504439 E492D T G missense Het probably benign 0.024 phenotype 02/04/2014
31 154470 APN Ttn 1.000 IGL01819 G1 2 76798762 V14411I C T missense Het possibly damaging 0.955 phenotype 02/04/2014
32 154480 APN Utp20 0.950 IGL01819 G1 10 88792687 Q915R T C missense Het probably damaging 0.995 phenotype 02/04/2014
33 154454 APN Vmn2r45 0.078 IGL01819 G1 7 8485557 S158I C A missense Het probably benign 0.001 02/04/2014
[records 1 to 33 of 33]