Incidental Mutations

46 incidental mutations are currently displayed, and affect 46 genes.
4 are Possibly Damaging.
20 are Probably Damaging.
14 are Probably Benign.
8 are Probably Null.
4 create premature stop codons.
4 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 46 of 46] 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 244647 UTSW 1110008L16Rik 0.425 R2307 G1 225 N 12 55304316 F137L T C missense Het probably damaging 0.999 10/30/2014
2 244648 UTSW Acot5 0.000 R2307 G1 225 N 12 84075601 F320L T C missense Het possibly damaging 0.898 10/30/2014
3 244643 UTSW Alox12e 0.000 R2307 G1 225 N 11 70321261 K170R T C missense Het probably damaging 1.000 10/30/2014
4 244634 UTSW Ano2 0.091 R2307 G1 225 N 6 125992886 S722P T C missense Het probably benign 0.004 phenotype 10/30/2014
5 244662 UTSW Cep192 0.000 R2307 G1 225 N 18 67813899 Y215C A G missense Het probably benign 0.068 10/30/2014
6 244639 UTSW Ces2g 0.050 R2307 G1 225 N 8 104968412 N555S A G missense Het probably benign 0.007 10/30/2014
7 244663 UTSW Cfap58 0.156 R2307 G1 225 N 19 47962486 Q429* C T nonsense Het probably null 10/30/2014
8 244623 UTSW Clcnkb 0.000 R2307 G1 225 N 4 141412329 S121P A G missense Het probably damaging 0.998 phenotype 10/30/2014
9 244649 UTSW Cltb 0.178 R2307 G1 215 N 13 54598751 E67D T A missense Het probably damaging 0.987 phenotype 10/30/2014
10 244651 UTSW Ddhd1 0.000 R2307 G1 178 N 14 45608990 L581Q A T missense Het probably damaging 0.999 phenotype 10/30/2014
11 244654 UTSW Dnajc3 0.286 R2307 G1 225 N 14 118953221 T C critical splice donor site 2 bp Het probably null phenotype 10/30/2014
12 244655 UTSW Fgf14 0.177 R2307 G1 225 N 14 123983822 N190I T A missense Het probably damaging 1.000 phenotype 10/30/2014
13 244627 UTSW Galnt17 0.000 R2307 G1 225 N 5 130900622 Y449S T G missense Het probably damaging 1.000 phenotype 10/30/2014
14 244622 UTSW Grin3a 0.000 R2307 G1 225 N 4 49793033 C T critical splice acceptor site Het probably null phenotype 10/30/2014
15 244632 UTSW Gxylt2 0.000 R2307 G1 225 N 6 100787212 N286S A G missense Het probably damaging 0.998 phenotype 10/30/2014
16 244657 UTSW H2-K1 0.104 R2307 G1 225 N 17 33997139 V120A A G missense Het probably benign 0.263 phenotype 10/30/2014
17 244637 UTSW Inpp5f 0.319 R2307 G1 225 N 7 128694310 V168A T C missense Het probably damaging 1.000 phenotype 10/30/2014
18 244613 UTSW Kif1a 0.763 R2307 G1 225 N 1 93078769 H59N G T missense Het probably damaging 1.000 phenotype 10/30/2014
19 244644 UTSW Krt24 0.121 R2307 G1 225 N 11 99284630 Q193R T C missense Het possibly damaging 0.480 phenotype 10/30/2014
20 244638 UTSW Krtap5-4 0.090 R2307 G1 225 N 7 142303614 S7* C A nonsense Het probably null 10/30/2014
21 244656 UTSW Ltn1 1.000 R2307 G1 157 N 16 87432424 A G critical splice donor site 2 bp Het probably null phenotype 10/30/2014
22 244631 UTSW Mcm2 1.000 R2307 G1 225 N 6 88893008 R60C G A missense Het probably damaging 0.993 0.264 phenotype 10/30/2014
23 244661 UTSW Mep1b 0.108 R2307 G1 225 N 18 21088575 D194V A T missense Het probably damaging 0.999 phenotype 10/30/2014
24 244620 UTSW Orc3 1.000 R2307 G1 225 N 4 34586503 V382M C T missense Het probably damaging 1.000 phenotype 10/30/2014
25 244624 UTSW Pclo 0.000 R2307 G1 225 N 5 14678651 T A unclassified Het probably benign phenotype 10/30/2014
26 244628 UTSW Pcolce 0.230 R2307 G1 225 N 5 137609094 H45R T C missense Het probably damaging 0.987 phenotype 10/30/2014
27 244642 UTSW Prf1 0.000 R2307 G1 225 N 10 61303163 V300A T C missense Het possibly damaging 0.800 phenotype 10/30/2014
28 244636 UTSW Prss53 0.489 R2307 G1 171 N 7 127890865 I18V T C missense Het probably benign 0.000 10/30/2014
29 244652 UTSW Rnase2b 0.050 R2307 G1 225 N 14 51162731 T90A A G missense Het probably benign 0.001 10/30/2014
30 244618 UTSW Rpap1 0.961 R2307 G1 157 N 2 119783766 P50L G A missense Het probably benign 0.001 phenotype 10/30/2014
31 244619 UTSW Rrnad1 0.085 R2307 G1 174 N 3 87926855 M171K A T missense Het possibly damaging 0.883 10/30/2014
32 244635 UTSW Rsf1 1.000 R2307 G1 215 N 7 97579908 CG CGACGGCGGGG unclassified Het probably benign phenotype 10/30/2014
33 244611 UTSW Rufy4 0.260 R2307 G1 194 N 1 74147663 C537R T C missense Het probably damaging 0.988 0.294 10/30/2014
34 244614 UTSW Sec16b 0.000 R2307 G1 225 N 1 157535492 V298I G A missense Het probably damaging 0.998 phenotype 10/30/2014
35 244625 UTSW Smarcd3 1.000 R2307 G1 225 N 5 24595748 R156Q C T missense Het probably damaging 0.999 phenotype 10/30/2014
36 244646 UTSW St6galnac2 0.139 R2307 G1 225 N 11 116681905 A242T C T missense Het probably damaging 0.999 phenotype 10/30/2014
37 244640 UTSW Syce1l 0.000 R2307 G1 225 N 8 113643305 T C critical splice donor site 2 bp Het probably null 10/30/2014
38 244645 UTSW Tcam1 0.000 R2307 G1 190 N 11 106284114 C132R T C missense Het probably damaging 0.999 phenotype 10/30/2014
39 244609 UTSW Trpa1 0.113 R2307 G1 225 N 1 14912381 I84V T C missense Het probably benign 0.003 phenotype 10/30/2014
40 244616 UTSW Ttn 1.000 R2307 G1 225 N 2 76886998 R455* G A nonsense Het probably null phenotype 10/30/2014
41 244641 UTSW Ubl5 0.935 R2307 G1 225 N 9 20646580 T A intron Het probably benign phenotype 10/30/2014
42 244659 UTSW Ubr2 0.882 R2307 G1 225 N 17 46966215 K779* T A nonsense Het probably null phenotype 10/30/2014
43 244612 UTSW Ugt1a10 0.098 R2307 G1 225 N 1 88055947 I156V A G missense Het probably benign 0.007 10/30/2014
44 244621 UTSW Unc13b 0.586 R2307 G1 225 N 4 43239854 T3513A A G missense Het probably damaging 0.981 phenotype 10/30/2014
45 244630 UTSW Vmn1r20 0.525 R2307 G1 225 N 6 57432136 T149I C T missense Het probably benign 0.027 10/30/2014
46 244617 UTSW Zfp804a 0.197 R2307 G1 225 N 2 82256857 D343E T A missense Het probably benign 0.044 phenotype 10/30/2014
[records 1 to 46 of 46]