Incidental Mutations

20 incidental mutations are currently displayed, and affect 20 genes.
2 are Possibly Damaging.
6 are Probably Damaging.
7 are Probably Benign.
5 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 20 of 20] 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 269208 UTSW Acsf2 0.000 R3610 G1 167 N 11 94561346 V457L C A missense Het probably benign 0.001 phenotype 02/19/2015
2 269206 UTSW Cacna1a 0.927 R3610 G1 129 N 8 84559065 R733S C A missense Het probably damaging 0.996 phenotype 02/19/2015
3 269200 UTSW Cc2d2a 0.805 R3610 G1 225 N 5 43712326 E856D A T missense Het probably damaging 0.988 phenotype 02/19/2015
4 269199 UTSW Cpeb2 0.273 R3610 G1 225 N 5 43285933 F989S T C missense Het probably damaging 0.975 phenotype 02/19/2015
5 269198 UTSW Dcaf10 0.000 R3610 G1 225 N 4 45372962 E409* G T nonsense Het probably null 02/19/2015
6 269216 UTSW Ddx3y 0.029 R3610 G1 222 N Y 1263928 N545S T C missense Het probably null 0.995 phenotype 02/19/2015
7 269205 UTSW Eef2k 0.162 R3610 G1 225 N 7 120889235 S448G A G missense Het probably benign 0.000 phenotype 02/19/2015
8 269209 UTSW Irf2bpl 0.447 R3610 G1 225 N 12 86881857 I681V T C missense Het probably benign 0.029 phenotype 02/19/2015
9 269207 UTSW Kremen1 0.136 R3610 G1 166 N 11 5201791 CGGG CGGGGGG unclassified Het probably benign phenotype 02/19/2015
10 269214 UTSW Morc2b 0.233 R3610 G1 225 N 17 33136278 V840A A G missense Het probably damaging 0.999 phenotype 02/19/2015
11 269215 UTSW Rcl1 0.926 R3610 G1 225 N 19 29118230 T72A A G missense Het probably benign 0.001 02/19/2015
12 269211 UTSW Robo1 1.000 R3610 G1 225 N 16 72983770 F796S T C missense Het probably benign 0.001 phenotype 02/19/2015
13 269203 UTSW Rsf1 1.000 R3610 G1 113 N 7 97579904 A AAGGCGACGG start codon destroyed Het probably null phenotype 02/19/2015
14 269197 UTSW Setx 0.000 R3610 G1 217 N 2 29154061 GTGGCT GT frame shift Het probably null 0.642 phenotype 02/19/2015
15 269210 UTSW Tars 0.952 R3610 G1 225 N 15 11392904 Y152C T C missense Het probably damaging 0.994 phenotype 02/19/2015
16 269202 UTSW Tmem184a 0.327 R3610 G1 225 N 5 139807955 A G critical splice donor site 2 bp Het probably null 02/19/2015
17 269213 UTSW Tmem8 0.091 R3610 G1 225 N 17 26118886 V415I G A missense Het probably benign 0.228 02/19/2015
18 269212 UTSW Tsc2 1.000 R3610 G1 171 N 17 24622550 I365S A C missense Het possibly damaging 0.740 phenotype 02/19/2015
19 269204 UTSW Usp17la 0.075 R3610 G1 225 N 7 104861072 V295I G A missense Het probably damaging 1.000 02/19/2015
20 269196 UTSW Vim 0.704 R3610 G1 225 N 2 13578626 H253L A T missense Het possibly damaging 0.671 phenotype 02/19/2015
[records 1 to 20 of 20]