Incidental Mutations

46 incidental mutations are currently displayed, and affect 46 genes.
6 are Possibly Damaging.
13 are Probably Damaging.
19 are Probably Benign.
7 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 46 of 46] 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 326829 UTSW 1110017D15Rik 0.000 R4416 G1 225 N 4 41505574 T183A T C missense Het possibly damaging 0.707 0.179 phenotype 07/07/2015
2 326853 UTSW 4933412E24Rik 0.063 R4416 G1 225 N 15 60016423 E56V T A missense Het possibly damaging 0.881 07/07/2015
3 326852 UTSW Adam28 0.120 R4416 G1 225 N 14 68622082 A G critical splice donor site 2 bp Het probably null phenotype 07/07/2015
4 326840 UTSW Bnc1 0.000 R4416 G1 225 N 7 81968960 H786N G T missense Het probably benign 0.000 phenotype 07/07/2015
5 326836 UTSW Cav1 0.653 R4416 G1 225 N 6 17339249 M100K T A missense Het probably benign 0.360 phenotype 07/07/2015
6 326820 UTSW Cdk9 1.000 R4416 G1 225 N 2 32708072 L273P A G missense Het probably damaging 1.000 phenotype 07/07/2015
7 500615 UTSW Celsr1 0.787 R4416 G1 225 N 15 85927999 V2065A A G missense Het probably damaging 1.000 0.267 phenotype 12/01/2017
8 326857 UTSW Cyp2c54 0.127 R4416 G1 225 N 19 40038259 Q484R T C missense Het probably benign 0.041 07/07/2015
9 326834 UTSW Elfn1 0.131 R4416 G1 225 N 5 139972194 S318P T C missense Het possibly damaging 0.519 phenotype 07/07/2015
10 326860 UTSW Fam160b1 0.146 R4416 G1 225 N 19 57385397 G T splice site 3 bp Het probably null 07/07/2015
11 500614 UTSW Fbxl6 0.127 R4416 G1 225 N 15 76537724 E205G T C missense Het possibly damaging 0.759 0.179 phenotype 12/01/2017
12 326850 UTSW Frmd6 0.000 R4416 G1 225 N 12 70877249 Y94N T A missense Het probably benign 0.037 07/07/2015
13 326849 UTSW Gdpd1 0.108 R4416 G1 225 N 11 87035288 V277D A T missense Het probably benign 0.443 phenotype 07/07/2015
14 326861 UTSW Gm1141 0.123 R4416 G1 222 N X 71939619 C399Y G A missense Het possibly damaging 0.827 0.179 07/07/2015
15 326855 UTSW Grik1 0.000 R4416 G1 225 N 16 88051461 V140L C A missense Het probably benign 0.001 phenotype 07/07/2015
16 326832 UTSW Grpel1 0.949 R4416 G1 225 N 5 36471272 H175R A G missense Het probably damaging 1.000 07/07/2015
17 326822 UTSW Gtdc1 0.081 R4416 G1 225 N 2 44575590 G T splice site Het probably null 07/07/2015
18 326845 UTSW Hivep2 0.895 R4416 G1 225 N 10 14129170 Q504L A T missense Het probably benign 0.000 phenotype 07/07/2015
19 326816 UTSW Icos 0.152 R4416 G1 225 N 1 60994690 I160L A T missense Het probably benign 0.004 phenotype 07/07/2015
20 326843 UTSW Igsf9b 0.908 R4416 G1 225 N 9 27322917 C442F G T missense Het probably damaging 1.000 07/07/2015
21 326828 UTSW Itga10 0.212 R4416 G1 225 N 3 96658246 V1062A T C missense Het possibly damaging 0.577 phenotype 07/07/2015
22 326821 UTSW Lrp1b 0.000 R4416 G1 225 N 2 40663667 V386I C T missense Het unknown phenotype 07/07/2015
23 326823 UTSW Lrp2 1.000 R4416 G1 225 N 2 69527231 F409L G T missense Het probably benign 0.177 phenotype 07/07/2015
24 326831 UTSW Nadk 0.953 R4416 G1 225 N 4 155587726 Y291* T G nonsense Het probably null phenotype 07/07/2015
25 326825 UTSW Nudt6 0.270 R4416 G1 225 N 3 37405229 A T unclassified 127 bp Het probably null phenotype 07/07/2015
26 326846 UTSW Oit3 0.271 R4416 G1 225 N 10 59428103 Y403C T C missense Het probably damaging 1.000 0.515 phenotype 07/07/2015
27 326841 UTSW Olfr694 0.102 R4416 G1 225 N 7 106689011 T240I G A missense Het probably benign 0.072 phenotype 07/07/2015
28 326848 UTSW Olfr814 0.061 R4416 G1 225 N 10 129873957 T267A T C missense Het probably benign 0.003 phenotype 07/07/2015
29 326844 UTSW Olfr974 0.084 R4416 G1 225 N 9 39942428 H56R A G missense Het probably damaging 0.995 phenotype 07/07/2015
30 326835 UTSW Pds5b 1.000 R4416 G1 225 N 5 150736396 P275S C T missense Het probably damaging 1.000 phenotype 07/07/2015
31 326858 UTSW Pdzd7 0.277 R4416 G1 225 N 19 45040580 E117V T A missense Het probably damaging 0.999 phenotype 07/07/2015
32 326824 UTSW Pik3ca 1.000 R4416 G1 225 N 3 32461530 V784A T C missense Het probably damaging 0.987 phenotype 07/07/2015
33 326842 UTSW Polr3e 0.964 R4416 G1 225 N 7 120939057 T C critical splice donor site 2 bp Het probably null 07/07/2015
34 326818 UTSW Rab3gap2 0.000 R4416 G1 225 N 1 185282347 D1231V A T missense Het probably benign 0.001 phenotype 07/07/2015
35 326827 UTSW Rapgef2 1.000 R4416 G1 225 N 3 79069057 G1481* C A nonsense Het probably null phenotype 07/07/2015
36 326838 UTSW Rho 0.133 R4416 G1 225 N 6 115935230 V76I G A missense Het probably benign 0.000 0.090 phenotype 07/07/2015
37 500613 UTSW Rrm1 0.969 R4416 G1 225 N 7 102447801 D96G A G missense Het probably benign 0.059 phenotype 12/01/2017
38 326856 UTSW Slc35b2 0.147 R4416 G1 201 N 17 45566429 V161M G A missense Het probably benign 0.337 0.108 phenotype 07/07/2015
39 326817 UTSW Srp9 R4416 G1 225 N 1 182131411 M50L A T missense Het probably benign 0.049 07/07/2015
40 326847 UTSW Stox1 0.307 R4416 G1 225 N 10 62659569 N975S T C missense Het probably benign 0.001 0.090 phenotype 07/07/2015
41 326833 UTSW Sult1d1 0.059 R4416 G1 225 N 5 87558576 F169S A G missense Het probably damaging 1.000 phenotype 07/07/2015
42 326851 UTSW Tmem63c 0.092 R4416 G1 225 N 12 87081902 T567R C G missense Het probably benign 0.144 07/07/2015
43 326837 UTSW Tmf1 0.150 R4416 G1 135 N 6 97178988 F12L G T missense Het probably damaging 0.999 phenotype 07/07/2015
44 326819 UTSW Ush2a 0.485 R4416 G1 225 N 1 188356874 I342T T C missense Het probably damaging 0.972 phenotype 07/07/2015
45 326826 UTSW Veph1 0.000 R4416 G1 225 N 3 66061185 N712K A T missense Het probably damaging 0.987 phenotype 07/07/2015
46 326859 UTSW Vti1a 0.000 R4416 G1 225 N 19 55380948 S91A T G missense Het probably benign 0.317 phenotype 07/07/2015
[records 1 to 46 of 46]