Incidental Mutations

24 incidental mutations are currently displayed, and affect 24 genes.
3 are Possibly Damaging.
13 are Probably Damaging.
5 are Probably Benign.
3 are Probably Null.
0 create premature stop codons.
1 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 330182 UTSW Adcyap1r1 0.342 R4462 G1 225 N 6 55480099 I272F A T missense Het possibly damaging 0.902 phenotype 07/21/2015
2 500631 UTSW Adgrl3 0.000 R4462 G1 225 N 5 81688510 A705V C T missense Het probably damaging 1.000 phenotype 12/01/2017
3 330189 UTSW Arhgef12 0.922 R4462 G1 225 N 9 42981982 V975E A T missense Het probably damaging 1.000 phenotype 07/21/2015
4 330176 UTSW Bahd1 0.000 R4462 G1 171 N 2 118916406 P169S C T missense Het probably damaging 0.999 0.066 phenotype 07/21/2015
5 330201 UTSW Btnl6 0.059 R4462 G1 225 N 17 34508057 S500P A G missense Het probably damaging 1.000 07/21/2015
6 330178 UTSW Ccdc39 0.448 R4462 G1 225 N 3 33814668 R798Q C T missense Het probably damaging 1.000 0.647 phenotype 07/21/2015
7 330186 UTSW Cdkn2d 0.275 R4462 G1 215 N 9 21290889 V21L C G missense Het probably benign 0.000 0.059 phenotype 07/21/2015
8 330187 UTSW Cdon 0.457 R4462 G1 225 N 9 35457580 V34A T C missense Het probably damaging 0.969 phenotype 07/21/2015
9 330184 UTSW Defa17 R4462 G1 84 N 8 21656537 R60G A G missense Het probably benign 0.006 07/21/2015
10 330191 UTSW Egr2 1.000 R4462 G1 217 N 10 67539903 GAA GA frame shift Het probably null 0.976 phenotype 07/21/2015
11 330190 UTSW Fuca2 0.182 R4462 G1 225 N 10 13503235 V41A T C missense Het probably damaging 0.998 phenotype 07/21/2015
12 330196 UTSW Ggt6 0.000 R4462 G1 225 N 11 72437828 H385N C A missense Het possibly damaging 0.518 phenotype 07/21/2015
13 330185 UTSW Hgsnat 0.000 R4462 G1 225 N 8 25954636 T428I G A missense Het probably damaging 0.996 phenotype 07/21/2015
14 330192 UTSW Nefh 0.000 R4462 G1 225 N 11 4941015 S535P A G missense Het probably damaging 0.978 phenotype 07/21/2015
15 330194 UTSW Olfr1371 0.056 R4462 G1 225 N 11 52213974 N5I T A missense Het probably damaging 1.000 phenotype 07/21/2015
16 330188 UTSW Olfr905 0.064 R4462 G1 225 N 9 38473064 F106I T A missense Het probably benign 0.325 phenotype 07/21/2015
17 330200 UTSW Pkhd1l1 0.000 R4462 G1 225 N 15 44581804 F3691L T C missense Het probably damaging 0.999 07/21/2015
18 330195 UTSW Polr2a 0.965 R4462 G1 225 N 11 69746403 D282G T C missense Het probably damaging 0.998 phenotype 07/21/2015
19 330193 UTSW Ranbp17 0.000 R4462 G1 225 N 11 33217421 T C critical splice acceptor site Het probably null phenotype 07/21/2015
20 330197 UTSW Slc13a2 0.000 R4462 G1 225 N 11 78404387 T187A T C missense Het probably benign 0.440 phenotype 07/21/2015
21 330183 UTSW Slco3a1 0.224 R4462 G1 97 N 7 74554563 S10A A C missense Het probably benign 0.177 07/21/2015
22 330177 UTSW Snph 0.000 R4462 G1 219 N 2 151594115 S229T A T missense Het probably damaging 0.999 0.064 phenotype 07/21/2015
23 330199 UTSW Trim38 0.055 R4462 G1 225 N 13 23791452 Y458C A G missense Het probably null 1.000 phenotype 07/21/2015
24 330180 UTSW Ubr4 1.000 R4462 G1 192 N 4 139418502 M1537V A G missense Het possibly damaging 0.466 phenotype 07/21/2015
[records 1 to 24 of 24]