Incidental Mutations

24 incidental mutations are currently displayed, and affect 24 genes.
3 are Possibly Damaging.
7 are Probably Damaging.
14 are Probably Benign.
0 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 24 of 24] 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 175063 UTSW 2610507B11Rik 0.960 R1313 G1 225 N 11 78265672 T226A A G missense Het probably benign 0.017 04/24/2014
2 175057 UTSW Ankle1 0.490 R1313 G1 225 N 8 71407213 E145G A G missense Het possibly damaging 0.606 phenotype 04/24/2014
3 175052 UTSW C1qtnf12 0.221 R1313 G1 225 N 4 155965874 E223K G A missense Het probably damaging 0.962 04/24/2014
4 175048 UTSW Cep250 0.711 R1313 G1 225 N 2 155972079 A589V C T missense Het probably damaging 0.980 phenotype 04/24/2014
5 175062 UTSW Clhc1 0.073 R1313 G1 225 N 11 29571678 I404V A G missense Het probably benign 0.000 04/24/2014
6 175059 UTSW Ddi1 0.090 R1313 G1 225 N 9 6265769 E200G T C missense Het probably damaging 0.993 04/24/2014
7 175068 UTSW Dmxl1 0.863 R1313 G1 225 N 18 49878483 S1236P T C missense Het probably damaging 0.996 phenotype 04/24/2014
8 175051 UTSW Dpyd 0.265 R1313 G1 225 N 3 118899161 G T splice site Het probably benign phenotype 04/24/2014
9 175065 UTSW Ercc6 0.509 R1313 G1 225 N 14 32552720 C T splice site Het probably benign phenotype 04/24/2014
10 500213 UTSW Gtf3c3 0.934 R1313 G1 225 N 1 54417778 A488T C T missense Het probably damaging 0.998 0.348 phenotype 12/01/2017
11 175055 UTSW Hnrnpul1 0.492 R1313 G1 225 N 7 25722916 G T unclassified Het probably benign phenotype 04/24/2014
12 262749 UTSW Ints1 1.000 R1313 G1 93 N 5 139762906 T1049A T C missense Het probably benign 0.000 phenotype 02/04/2015
13 175060 UTSW Lilrb4 0.000 R1313 G1 150 N 10 51480736 T6I C T missense Het probably benign 0.254 phenotype 04/24/2014
14 500215 UTSW Mocs1 1.000 R1313 G1 225 N 17 49454269 T464S A T missense Het probably benign 0.002 phenotype 12/01/2017
15 175064 UTSW Myo15b 0.048 R1313 G1 225 N 11 115885129 S816P T C missense Het probably damaging 1.000 04/24/2014
16 175049 UTSW Ogfr 0.433 R1313 G1 225 N 2 180594630 L336P T C missense Het probably benign 0.000 phenotype 04/24/2014
17 175056 UTSW Olfr473 0.143 R1313 G1 225 N 7 107933768 M83L A T missense Het probably benign 0.010 phenotype 04/24/2014
18 175050 UTSW Pet112l R1313 G1 225 N 3 85653826 I550V A G missense Het probably benign 0.008 04/24/2014
19 175053 UTSW Psapl1 0.071 R1313 G1 225 N 5 36205266 Q401K C A missense Het probably benign 0.010 phenotype 04/24/2014
20 175058 UTSW Rps26-ps1 R1313 G1 119 N 8 107439457 T A intron Het probably benign 04/24/2014
21 175061 UTSW Sh3rf3 0.195 R1313 G1 212 N 10 59071999 Q450K C A missense Het possibly damaging 0.919 04/24/2014
22 500214 UTSW Sned1 0.070 R1313 G1 225 N 1 93281654 V830M G A missense Het possibly damaging 0.895 0.144 12/01/2017
23 175045 UTSW Stat1 0.000 R1313 G1 225 N 1 52156006 T720I C T missense Het probably damaging 0.984 phenotype 04/24/2014
24 175067 UTSW Vav1 0.253 R1313 G1 225 N 17 57309498 G A splice site Het probably benign phenotype 04/24/2014
[records 1 to 24 of 24]