Incidental Mutations

23 incidental mutations are currently displayed, and affect 23 genes.
2 are Possibly Damaging.
12 are Probably Damaging.
8 are Probably Benign.
1 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 23 of 23] 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 248360 UTSW AK157302 0.945 R2378 G1 225 N 13 21495562 I86T T C missense Het possibly damaging 0.688 11/11/2014
2 248337 UTSW Akr1cl 0.068 R2378 G1 184 N 1 65021988 M124K A T missense Het probably benign 0.143 11/11/2014
3 248358 UTSW Asap2 0.095 R2378 G1 225 N 12 21254318 L745P T C missense Het possibly damaging 0.955 phenotype 11/11/2014
4 248349 UTSW B3gnt9 0.102 R2378 G1 225 N 8 105254484 R91C G A missense Het probably damaging 1.000 11/11/2014
5 248346 UTSW Capg 0.169 R2378 G1 225 N 6 72555491 P13L C T missense Het probably benign 0.069 phenotype 11/11/2014
6 248348 UTSW Eif3c 0.000 R2378 G1 225 N 7 126552325 R609H C T missense Het probably damaging 0.989 phenotype 11/11/2014
7 248361 UTSW Ephb3 0.901 R2378 G1 225 N 16 21218243 H152R A G missense Het probably benign 0.000 phenotype 11/11/2014
8 248345 UTSW Gbp9 0.053 R2378 G1 225 N 5 105080176 D580G T C missense Het probably benign 0.023 11/11/2014
9 248356 UTSW Gm884 0.140 R2378 G1 225 N 11 103619711 A G unclassified Het probably benign 11/11/2014
10 248340 UTSW Iars2 1.000 R2378 G1 225 N 1 185327721 Y97H A G missense Het probably damaging 1.000 phenotype 11/11/2014
11 248352 UTSW Ip6k2 0.000 R2378 G1 225 N 9 108796301 A G splice site Het probably null phenotype 11/11/2014
12 248341 UTSW Itih2 0.122 R2378 G1 225 N 2 10094887 D907V T A missense Het probably damaging 0.997 phenotype 11/11/2014
13 248344 UTSW Msh4 0.383 R2378 G1 225 N 3 153863477 C732R A G missense Het probably damaging 0.994 phenotype 11/11/2014
14 248350 UTSW Mtss1l 0.000 R2378 G1 225 N 8 110738349 F474L T C missense Het probably damaging 0.999 11/11/2014
15 248354 UTSW Nbeal2 0.252 R2378 G1 168 N 9 110630808 E1175G T C missense Het probably damaging 0.989 phenotype 11/11/2014
16 248351 UTSW Pgm3 0.950 R2378 G1 225 N 9 86562667 C272S A T missense Het probably damaging 0.966 phenotype 11/11/2014
17 248364 UTSW R3hcc1l 0.000 R2378 G1 225 N 19 42563473 I303N T A missense Het probably damaging 0.991 11/11/2014
18 248343 UTSW Sla2 0.000 R2378 G1 225 N 2 156875942 R137C G A missense Het probably damaging 0.999 0.314 phenotype 11/11/2014
19 248363 UTSW Spsb3 0.111 R2378 G1 225 N 17 24886950 A G unclassified Het probably benign 11/11/2014
20 248355 UTSW Tgfbr2 1.000 R2378 G1 225 N 9 116129950 T132I G A missense Het probably benign 0.018 phenotype 11/11/2014
21 248336 UTSW Tpp2 0.630 R2378 G1 225 N 1 43999765 E223V A T missense Het probably damaging 0.992 phenotype 11/11/2014
22 248342 UTSW Ttn 1.000 R2378 G1 225 N 2 76889450 T A intron Het probably benign 0.111 phenotype 11/11/2014
23 248362 UTSW Vmn2r102 0.000 R2378 G1 225 N 17 19694668 L832V T G missense Het probably damaging 0.999 11/11/2014
[records 1 to 23 of 23]