Incidental Mutations

57 incidental mutations are currently displayed, and affect 56 genes.
7 are Possibly Damaging.
21 are Probably Damaging.
16 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 57 of 57] 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 592189 UTSW 0610009O20Rik 0.231 R7671 G1 225.01 N 18 38259925 I394N T A missense Het probably damaging 0.993 11/12/2019
2 592184 UTSW 4930435E12Rik 0.054 R7671 G1 225.01 N 16 38828091 D219N C T missense Het possibly damaging 0.869 11/12/2019
3 592147 UTSW 4932438A13Rik 1.000 R7671 G1 225.01 N 3 36943231 F1146L T C missense Het probably damaging 0.987 phenotype 11/12/2019
4 592139 UTSW 4933406M09Rik 0.000 R7671 G1 225.01 N 1 134390062 C191R T C missense Het probably benign 0.272 11/12/2019
5 592160 UTSW Akap13 1.000 R7671 G1 225.01 N 7 75569900 T17K C A missense Het probably damaging 1.000 phenotype 11/12/2019
6 592188 UTSW Ankrd29 0.358 R7671 G1 225.01 N 18 12260986 K257I T A missense Het probably damaging 0.961 11/12/2019
7 592167 UTSW Bicc1 1.000 R7671 G1 225.01 N 10 70957167 L219P A G missense Het probably benign 0.012 phenotype 11/12/2019
8 592185 UTSW Boc 0.000 R7671 G1 225.01 N 16 44491849 V617M C T missense Het phenotype 11/12/2019
9 592173 UTSW Ccl8 0.000 R7671 G1 225.01 N 11 82115207 A G start gained Het probably benign Ccl12 also affect expression of this gene. [provided by MGI curators] (source: MGI)">phenotype 11/12/2019
10 592169 UTSW Col18a1 0.000 R7671 G1 225.01 N 10 77085383 L261P A G missense Het unknown phenotype 11/12/2019
11 592162 UTSW Col5a3 0.188 R7671 G1 225.01 N 9 20775086 T A critical splice acceptor site Het probably null phenotype 11/12/2019
12 592156 UTSW Cryba4 0.127 R7671 G1 225.01 N 5 112248173 A C critical splice donor site 2 bp Het probably null phenotype 11/12/2019
13 592182 UTSW Csf2rb 1.000 R7671 G1 225.01 N 15 78338930 Y114C A G missense Het probably damaging 0.999 phenotype 11/12/2019
14 592190 UTSW Ctif 0.113 R7671 G1 225.01 N 18 75472016 D484G T C missense Het probably damaging 0.990 phenotype 11/12/2019
15 592152 UTSW Ctnnal1 0.256 R7671 G1 225.01 N 4 56837848 F261L A G missense Het probably damaging 0.999 phenotype 11/12/2019
16 592146 UTSW Defb22 0.000 R7671 G1 225.01 N 2 152486030 N78K A T missense Het unknown 11/12/2019
17 592181 UTSW Efr3a 0.758 R7671 G1 225.01 N 15 65837434 G A critical splice acceptor site Het probably null phenotype 11/12/2019
18 592145 UTSW Elp4 0.966 R7671 G1 225.01 N 2 105904481 A3E G T missense Het probably damaging 0.989 phenotype 11/12/2019
19 592187 UTSW Emilin2 0.087 R7671 G1 225.01 N 17 71273910 V607A A G missense Het probably benign 0.004 phenotype 11/12/2019
20 592180 UTSW Epsti1 0.062 R7671 G1 225.01 N 14 77904490 Y2C A G missense Het probably damaging 0.997 phenotype 11/12/2019
21 592176 UTSW Fam81b 0.216 R7671 G1 225.01 N 13 76271293 L46R A C missense Het probably damaging 0.966 11/12/2019
22 592177 UTSW Fam81b 0.216 R7671 G1 225.01 N 13 76271294 L46I G T missense Het possibly damaging 0.942 11/12/2019
23 592191 UTSW Fbxo15 0.000 R7671 G1 225.01 N 18 84964153 H288Q T A missense Het probably damaging 0.999 phenotype 11/12/2019
24 592155 UTSW Gabrg1 0.074 R7671 G1 225.01 N 5 70815980 N77I T A missense Het probably damaging 0.995 phenotype 11/12/2019
25 592193 UTSW Ganab 0.889 R7671 G1 225.01 N 19 8912852 Y715C A G missense Het possibly damaging 0.944 phenotype 11/12/2019
26 592171 UTSW Hist3h2ba 0.185 R7671 G1 225.01 N 11 58949276 S113P T C missense Het possibly damaging 0.705 phenotype 11/12/2019
27 592178 UTSW Iqgap2 0.000 R7671 G1 225.01 N 13 95628119 D1539G T C missense Het probably damaging 0.977 phenotype 11/12/2019
28 592159 UTSW Kcp 0.217 R7671 G1 225.01 N 6 29496517 N633S T C missense Het probably benign 0.021 phenotype 11/12/2019
29 592183 UTSW Krt6a 0.286 R7671 G1 225.01 N 15 101690543 S529I C A missense Het unknown phenotype 11/12/2019
30 592165 UTSW Leo1 1.000 R7671 G1 225.01 N 9 75445562 H129R A G missense Het probably benign 0.002 phenotype 11/12/2019
31 592186 UTSW Lmf1 1.000 R7671 G1 225.01 N 17 25579349 V55M G A missense Het possibly damaging 0.752 phenotype 11/12/2019
32 592166 UTSW Mcm9 0.000 R7671 G1 225.01 N 10 53537569 S472P A G missense Het probably benign 0.006 phenotype 11/12/2019
33 592141 UTSW Med27 0.942 R7671 G1 225.01 N 2 29377938 V33D T A missense Het phenotype 11/12/2019
34 592153 UTSW Mup15 R7671 G1 225.01 N 4 61438289 E80K C T missense Het probably benign 0.019 11/12/2019
35 592172 UTSW Myo18a 1.000 R7671 G1 137.01 N 11 77859420 R199H G A missense Het phenotype 11/12/2019
36 592140 UTSW Nebl 0.000 R7671 G1 225.01 N 2 17390916 R558* T A nonsense Het probably null 11/12/2019
37 592143 UTSW Olfr1121 0.063 R7671 G1 225.01 N 2 87372269 T246A A G missense Het probably damaging 1.000 phenotype 11/12/2019
38 592144 UTSW Olfr1252 0.647 R7671 G1 225.01 N 2 89721259 I284K A T missense Het probably damaging 0.997 phenotype 11/12/2019
39 592154 UTSW Olfr1329 0.145 R7671 G1 225.01 N 4 118916986 H160Q A T missense Het probably benign 0.018 phenotype 11/12/2019
40 592161 UTSW Olfr506 0.114 R7671 G1 225.01 N 7 108612991 I228T T C missense Het probably damaging 0.999 phenotype 11/12/2019
41 592179 UTSW Olfr740 0.106 R7671 G1 225.01 N 14 50453885 V278L G T missense Het probably benign 0.038 phenotype 11/12/2019
42 592170 UTSW Olfr815 0.055 R7671 G1 225.01 N 10 129902353 D119G T C missense Het probably damaging 1.000 phenotype 11/12/2019
43 592163 UTSW Olfr890 0.070 R7671 G1 225.01 N 9 38143440 M97L A T missense Het probably benign 0.017 phenotype 11/12/2019
44 592142 UTSW Pde11a 0.198 R7671 G1 225.01 N 2 76215353 F376I A T missense Het possibly damaging 0.805 phenotype 11/12/2019
45 592175 UTSW Prima1 0.000 R7671 G1 147.01 N 12 103235661 C52S A T missense Het probably damaging 0.975 phenotype 11/12/2019
46 592157 UTSW Pxn 1.000 R7671 G1 225.01 N 5 115548547 R366H G A missense Het not run phenotype 11/12/2019
47 592158 UTSW Sgce 0.402 R7671 G1 225.01 N 6 4691564 Y337C T C missense Het probably damaging 1.000 phenotype 11/12/2019
48 592174 UTSW Slc25a10 0.000 R7671 G1 225.01 N 11 120495460 M130K T A missense Het probably benign 0.177 phenotype 11/12/2019
49 592192 UTSW Slc29a2 0.341 R7671 G1 225.01 N 19 5024262 N5I A T missense Het probably benign 0.154 phenotype 11/12/2019
50 592150 UTSW Slc35a1 1.000 R7671 G1 225.01 N 4 34673875 H150Q A T missense Het phenotype 11/12/2019
51 592168 UTSW Slc5a4a 0.075 R7671 G1 225.01 N 10 76147550 V7D T A missense Het unknown 11/12/2019
52 592138 UTSW Stk17b 0.097 R7671 G1 225.01 N 1 53766000 D134V T A missense Het probably damaging 0.992 phenotype 11/12/2019
53 592148 UTSW Thbs3 0.583 R7671 G1 225.01 N 3 89216707 S36T T A missense Het probably benign 0.006 phenotype 11/12/2019
54 592164 UTSW Thsd4 0.081 R7671 G1 225.01 N 9 60428174 S152P A G missense Het probably benign 0.000 11/12/2019
55 592149 UTSW Tmem67 1.000 R7671 G1 225.01 N 4 12063698 H422N G T missense Het probably benign 0.002 phenotype 11/12/2019
56 592137 UTSW Tram1 0.462 R7671 G1 225.01 N 1 13589644 V27F C A missense Het probably damaging 0.957 phenotype 11/12/2019
57 592151 UTSW Trim14 0.000 R7671 G1 225.01 N 4 46507238 V326A A G missense Het possibly damaging 0.895 phenotype 11/12/2019
[records 1 to 57 of 57]