Incidental Mutations

28 incidental mutations are currently displayed, and affect 27 genes.
4 are Possibly Damaging.
9 are Probably Damaging.
11 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 28 of 28] 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 398020 UTSW 2700049A03Rik 1.000 R5188 G1 225 N 12 71164546 E685* G T nonsense Het probably null 0.976 phenotype 07/06/2016
2 398021 UTSW 2700049A03Rik 1.000 R5188 G1 225 N 12 71164547 E685V A T missense Het possibly damaging 0.931 0.181 phenotype 07/06/2016
3 398000 UTSW Abca12 1.000 R5188 G1 225 N 1 71291492 I1335F T A missense Het probably benign 0.229 phenotype 07/06/2016
4 398016 UTSW Amigo3 0.000 R5188 G1 225 N 9 108054683 A435E C A missense Het probably damaging 0.989 07/06/2016
5 398015 UTSW Atr 1.000 R5188 G1 225 N 9 95921725 N1871K T A missense Het probably benign 0.001 phenotype 07/06/2016
6 398028 UTSW Ctsw 0.000 R5188 G1 225 N 19 5467092 A71T C T missense Het probably damaging 1.000 phenotype 07/06/2016
7 398009 UTSW Decr1 0.776 R5188 G1 225 N 4 15924270 V217M C T missense Het probably damaging 1.000 phenotype 07/06/2016
8 398024 UTSW Golgb1 0.842 R5188 G1 225 N 16 36918465 T2389A A G missense Het probably benign 0.128 phenotype 07/06/2016
9 398026 UTSW Gpr151 0.000 R5188 G1 225 N 18 42578755 M286T A G missense Het probably benign 0.000 phenotype 07/06/2016
10 398005 UTSW Katnbl1 0.785 R5188 G1 225 N 2 112410154 I262N T A missense Het probably damaging 0.998 07/06/2016
11 398018 UTSW Lrp1 1.000 R5188 G1 225 N 10 127607952 C149R A G missense Het probably damaging 1.000 phenotype 07/06/2016
12 398025 UTSW Mpc1 0.111 R5188 G1 225 N 17 8296383 A T intron Het probably benign phenotype 07/06/2016
13 398027 UTSW Ndufv1 1.000 R5188 G1 225 N 19 4009988 N37K A T missense Het probably damaging 1.000 phenotype 07/06/2016
14 398004 UTSW Olfr1046 0.092 R5188 G1 225 N 2 86217177 S178R T G missense Het probably benign 0.001 phenotype 07/06/2016
15 398014 UTSW Olfr150 0.126 R5188 G1 225 N 9 39737235 V140A T C missense Het probably benign 0.005 phenotype 07/06/2016
16 398019 UTSW Olfr313 0.056 R5188 G1 225 N 11 58817320 T104K C A missense Het probably damaging 0.960 phenotype 07/06/2016
17 398003 UTSW Olfr353 0.142 R5188 G1 225 N 2 36890393 I152L T A missense Het probably benign 0.000 phenotype 07/06/2016
18 398002 UTSW Pnpla7 0.199 R5188 G1 225 N 2 24997300 P52Q C A missense Het probably benign 0.063 phenotype 07/06/2016
19 398013 UTSW Prh1 R5188 G1 225 N 6 132571707 Q59R A G missense Het unknown phenotype 07/06/2016
20 398001 UTSW Ren1 1.000 R5188 G1 225 N 1 133350613 A G unclassified Het probably benign phenotype 07/06/2016
21 398012 UTSW Rnf148 0.085 R5188 G1 225 N 6 23654140 T286A T C missense Het probably damaging 0.998 07/06/2016
22 398011 UTSW Sdk1 0.065 R5188 G1 225 N 5 141956260 T C critical splice donor site 2 bp Het probably null phenotype 07/06/2016
23 398010 UTSW Srp72 0.951 R5188 G1 208 N 5 76974751 S10T T A missense Het possibly damaging 0.543 phenotype 07/06/2016
24 398017 UTSW Stk11 1.000 R5188 G1 225 N 10 80126279 G215V G T missense Het probably damaging 1.000 phenotype 07/06/2016
25 398006 UTSW Stk4 0.000 R5188 G1 225 N 2 164088908 M143T T C missense Het possibly damaging 0.850 phenotype 07/06/2016
26 398007 UTSW Supt20 0.933 R5188 G1 225 N 3 54710428 S318T T A missense Het possibly damaging 0.872 phenotype 07/06/2016
27 398008 UTSW Tchh 0.058 R5188 G1 225 N 3 93446679 R1142P G C missense Het unknown 07/06/2016
28 398022 UTSW Vipas39 0.380 R5188 G1 225 N 12 87254247 R161S G T missense Het probably benign 0.210 phenotype 07/06/2016
[records 1 to 28 of 28]