Incidental Mutations

22 incidental mutations are currently displayed, and affect 21 genes.
6 are Possibly Damaging.
7 are Probably Damaging.
4 are Probably Benign.
4 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 22 of 22] 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 531109 UTSW 0610010F05Rik 0.174 R6758 G1 97.01 N 11 23588475 T C intron 160 bp Het probably null 08/01/2018
2 531106 UTSW Ankrd17 1.000 R6758 G1 225.01 N 5 90263313 D1374E A T missense Het probably damaging 0.997 phenotype 08/01/2018
3 531118 UTSW Cd96 0.000 R6758 G1 225.01 N 16 46118004 V33L C A missense Het possibly damaging 0.505 phenotype 08/01/2018
4 531113 UTSW Drd1 0.122 R6758 G1 225.01 N 13 54053289 E295G T C missense Het probably benign 0.000 phenotype 08/01/2018
5 531123 UTSW Fzd8 0.000 R6758 G1 225.01 N 18 9213238 C107S T A missense Het possibly damaging 0.783 phenotype 08/01/2018
6 531103 UTSW Gm10801 0.244 R6758 G1 142.47 N 2 98663807 C CGTG nonsense Het probably null 08/01/2018
7 531110 UTSW Gm11595 0.198 R6758 G1 185.01 N 11 99772540 V105L C A missense Het unknown 08/01/2018
8 531111 UTSW Gm11595 0.198 R6758 G1 192.01 N 11 99772541 C104* A T nonsense Het probably null 08/01/2018
9 531105 UTSW Igsf3 0.289 R6758 G1 202.01 N 3 101425498 Y31H T C missense Het probably damaging 0.976 phenotype 08/01/2018
10 531102 UTSW Ikzf2 0.869 R6758 G1 225.01 N 1 69538900 H483Q A T missense Het probably damaging 0.966 phenotype 08/01/2018
11 531117 UTSW Itgbl1 0.100 R6758 G1 225.01 N 14 123857489 K309E A G missense Het probably benign 0.230 phenotype 08/01/2018
12 531112 UTSW Myt1l 0.873 R6758 G1 225.01 N 12 29842600 Y79D T G missense Het possibly damaging 0.935 phenotype 08/01/2018
13 531116 UTSW Nid2 0.200 R6758 G1 225.01 N 14 19802483 S1086R T A missense Het probably damaging 1.000 phenotype 08/01/2018
14 531122 UTSW Olfr107 0.037 R6758 G1 225.01 N 17 37405695 D49G A G missense Het probably damaging 0.973 phenotype 08/01/2018
15 531119 UTSW Olfr192 0.115 R6758 G1 225.01 N 16 59098965 E9G T C missense Het probably damaging 0.962 08/01/2018
16 531108 UTSW Olfr808 0.084 R6758 G1 225.01 N 10 129768051 I185T T C missense Het probably damaging 0.972 phenotype 08/01/2018
17 531104 UTSW Rorc 0.657 R6758 G1 225.01 N 3 94387518 N51S A G missense Het possibly damaging 0.904 phenotype 08/01/2018
18 531114 UTSW Simc1 0.089 R6758 G1 225.01 N 13 54525548 P570S C T missense Het possibly damaging 0.574 08/01/2018
19 531115 UTSW Smn1 1.000 R6758 G1 225.01 N 13 100132438 M264K T A missense Het possibly damaging 0.879 phenotype 08/01/2018
20 531120 UTSW Tiam2 0.000 R6758 G1 225.01 N 17 3518403 D1608G A G missense Het probably benign 0.006 phenotype 08/01/2018
21 531107 UTSW Tll1 1.000 R6758 G1 225.01 N 8 64041405 C A critical splice donor site 1 bp Het probably null phenotype 08/01/2018
22 531121 UTSW Trim15 0.196 R6758 G1 225.01 N 17 36862341 L284P A G missense Het probably benign 0.159 phenotype 08/01/2018
[records 1 to 22 of 22]