Incidental Mutations

37 incidental mutations are currently displayed, and affect 37 genes.
5 are Possibly Damaging.
17 are Probably Damaging.
11 are Probably Benign.
1 are Probably Null.
1 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 37 of 37] 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 538983 UTSW 0610010F05Rik 0.191 R6910 G1 225.01 Y 11 23620447 (GRCm38) V151A A G missense Het probably damaging 0.986 2018-11-06
2 538982 UTSW Cfap54 0.072 R6910 G1 225.01 Y 10 92836512 (GRCm38) S2899P A G missense Het probably benign 0.290 phenotype 2018-11-06
3 543656 UTSW Chil5 0.066 R6910 G1 225.01 Y 3 106019661 (GRCm38) W82R A G missense Het probably damaging 1.000 2019-04-30
4 538990 UTSW Dennd3 0.214 R6910 G1 225.01 Y 15 73555116 (GRCm38) T781A A G missense Het probably benign 0.011 0.086 2018-11-06
5 538971 UTSW Epha2 0.760 R6910 G1 225.01 Y 4 141321513 (GRCm38) D597G A G missense Het probably damaging 1.000 0.845 phenotype 2018-11-06
6 538973 UTSW Gcn1l1 0.925 R6910 G1 225.01 Y 5 115606538 (GRCm38) T1598A A G missense Het probably benign 0.424 0.075 2018-11-06
7 538984 UTSW Glp2r 0.000 R6910 G1 225.01 Y 11 67730671 (GRCm38) F162S A G missense Het probably benign 0.283 phenotype 2018-11-06
8 538965 UTSW Gm10130 0.098 R6910 G1 225.01 Y 2 150324067 (GRCm38) Q56L A T missense Het probably benign 0.031 2018-11-06
9 538972 UTSW Gm17655 0.086 R6910 G1 211.01 Y 5 110047173 (GRCm38) R248* T A nonsense Het probably null 0.976 2018-11-06
10 538976 UTSW Gm9268 0.103 R6910 G1 225.01 Y 7 43024051 (GRCm38) F178L T C missense Het probably benign 0.008 2018-11-06
11 538981 UTSW Gnptab 0.950 R6910 G1 225.01 Y 10 88431396 (GRCm38) G450S G A missense Het probably damaging 1.000 0.521 phenotype 2018-11-06
12 538987 UTSW Gpatch2l 0.000 R6910 G1 225.01 Y 12 86244184 (GRCm38) R47H G A missense Het probably damaging 0.999 0.143 2018-11-06
13 538968 UTSW Hapln2 0.117 R6910 G1 225.01 Y 3 88023828 (GRCm38) Y127H A G missense Het probably damaging 1.000 phenotype 2018-11-06
14 538962 UTSW Hdac4 1.000 R6910 G1 207.01 Y 1 91982153 (GRCm38) T463K G T missense Het probably damaging 0.999 0.647 phenotype 2018-11-06
15 538967 UTSW Ift80 0.191 R6910 G1 225.01 Y 3 68927735 (GRCm38) S458A A C missense Het probably benign 0.009 0.063 phenotype 2018-11-06
16 538993 UTSW Lama1 1.000 R6910 G1 225.01 Y 17 67791464 (GRCm38) D1846G A G missense Het possibly damaging 0.603 phenotype 2018-11-06
17 538994 UTSW Map3k8 0.000 R6910 G1 225.01 Y 18 4340801 (GRCm38) I171T A G missense Het probably benign 0.025 0.090 phenotype 2018-11-06
18 538980 UTSW Micu1 0.746 R6910 G1 225.01 Y 10 59740667 (GRCm38) E115G A G missense Het probably damaging 0.999 phenotype 2018-11-06
19 538992 UTSW Mrpl39 0.946 R6910 G1 225.01 Y 16 84735192 (GRCm38) V9A A G missense Het unknown 0.087 phenotype 2018-11-06
20 538979 UTSW Ncoa7 0.000 R6910 G1 225.01 Y 10 30694121 (GRCm38) I281L T G missense Het possibly damaging 0.891 2018-11-06
21 538961 UTSW Nms 0.050 R6910 G1 225.01 Y 1 38941895 (GRCm38) E54G A G missense Het probably benign 0.038 0.090 phenotype 2018-11-06
22 538991 UTSW Nrip1 0.000 R6910 G1 225.01 Y 16 76294417 (GRCm38) A84V G A missense Het probably damaging 1.000 0.486 phenotype 2018-11-06
23 538970 UTSW Olfr1331 0.050 R6910 G1 225.01 Y 4 118869138 (GRCm38) M119K T A missense Het probably damaging 1.000 0.197 phenotype 2018-11-06
24 538988 UTSW Olfr743 0.076 R6910 G1 225.01 Y 14 50533873 (GRCm38) V154M G A missense Het probably benign 0.312 phenotype 2018-11-06
25 538995 UTSW Pcdhga10 0.118 R6910 G1 225.01 Y 18 37748232 (GRCm38) S349T T A missense Het probably damaging 0.991 0.249 phenotype 2018-11-06
26 538989 UTSW R3hcc1 0.107 R6910 G1 225.01 Y 14 69697575 (GRCm38) P454L G A missense Het probably damaging 1.000 0.756 2018-11-06
27 538966 UTSW Rsrc1 0.134 R6910 G1 225.01 Y 3 66994649 (GRCm38) P44L C T missense Het unknown 0.087 phenotype 2018-11-06
28 538964 UTSW Ryr3 0.414 R6910 G1 225.01 Y 2 112958175 (GRCm38) D170G T C missense Het probably damaging 0.997 phenotype 2018-11-06
29 538969 UTSW Scp2 0.101 R6910 G1 225.01 Y 4 108105086 (GRCm38) G81C C A missense Het probably damaging 1.000 0.975 phenotype 2018-11-06
30 538986 UTSW Sez6 0.000 R6910 G1 225.01 Y 11 77953869 (GRCm38) T173A A G missense Het possibly damaging 0.853 phenotype 2018-11-06
31 538978 UTSW Syne1 1.000 R6910 G1 225.01 Y 10 5048887 (GRCm38) H8142R T C missense Het probably benign 0.006 phenotype 2018-11-06
32 538996 UTSW Tcof1 1.000 R6910 G1 225.01 Y 18 60829051 (GRCm38) A702G G C missense Het possibly damaging 0.837 0.242 phenotype 2018-11-06
33 538963 UTSW Tnfrsf11a 0.124 R6910 G1 225.01 Y 1 105844546 (GRCm38) T520A A G missense Het probably damaging 1.000 0.168 phenotype 2018-11-06
34 538977 UTSW Tpm1 1.000 R6910 G1 225.01 Y 9 67031974 (GRCm38) S170P A G missense Het probably damaging 1.000 0.948 phenotype 2018-11-06
35 538975 UTSW Try5 0.070 R6910 G1 225.01 Y 6 41311799 (GRCm38) D54G T C missense Het possibly damaging 0.623 2018-11-06
36 538974 UTSW Zan 0.068 R6910 G1 225.01 Y 5 137419080 (GRCm38) E3041G T C missense Het unknown phenotype 2018-11-06
37 538985 UTSW Zfp616 0.000 R6910 G1 225.01 Y 11 74085002 (GRCm38) H699L A T missense Het probably damaging 1.000 2018-11-06
[records 1 to 37 of 37]