Incidental Mutations

65 incidental mutations are currently displayed, and affect 63 genes.
8 are Possibly Damaging.
24 are Probably Damaging.
22 are Probably Benign.
7 are Probably Null.
1 create premature stop codons.
4 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 65 of 65] 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 93537 APN 1700034H15Rik IGL01634 G1 1 191900904 A T unclassified Het noncoding transcript 12/09/2013
2 93523 APN 4933421I07Rik 0.063 IGL01634 G1 7 42447699 D63N C T missense Het probably benign 0.000 12/09/2013
3 93580 APN Alg9 1.000 IGL01634 G1 9 50775377 C A splice site Het probably null phenotype 12/09/2013
4 93530 APN Anln 0.967 IGL01634 G1 9 22360475 T695A T C missense Het probably benign 0.002 phenotype 12/09/2013
5 93557 APN Aox4 0.000 IGL01634 G1 1 58221930 D141Y G T missense Het possibly damaging 0.812 phenotype 12/09/2013
6 93541 APN Arhgap21 0.269 IGL01634 G1 2 20914644 Q84H C A missense Het probably benign 0.003 phenotype 12/09/2013
7 93579 APN Arnt 1.000 IGL01634 G1 3 95470398 G A splice site Het probably benign phenotype 12/09/2013
8 93556 APN Atp8a2 0.302 IGL01634 G1 14 59998062 Y677F T A missense Het probably benign 0.014 phenotype 12/09/2013
9 93540 APN Car6 0.000 IGL01634 G1 4 150198153 V12M C T missense Het probably benign 0.383 phenotype 12/09/2013
10 93577 APN Cd209d 0.000 IGL01634 G1 8 3877974 A T splice site Het probably null phenotype 12/09/2013
11 93525 APN Ctnna1 1.000 IGL01634 G1 18 35223448 V390E T A missense Het probably damaging 0.968 phenotype 12/09/2013
12 93555 APN Cypt4 0.067 IGL01634 G1 9 24625656 N147K T A missense Het possibly damaging 0.816 12/09/2013
13 93535 APN Dnah10 0.000 IGL01634 G1 5 124821341 A3729E C A missense Het probably damaging 0.981 phenotype 12/09/2013
14 93565 APN Dusp8 0.109 IGL01634 G1 7 142084423 V156A A G missense Het probably benign 0.050 phenotype 12/09/2013
15 93518 APN Ecm1 0.154 IGL01634 G1 3 95734899 P458L G A missense Het probably damaging 0.998 phenotype 12/09/2013
16 93543 APN Fat3 0.540 IGL01634 G1 9 15998358 Y2116S T G missense Het probably damaging 1.000 phenotype 12/09/2013
17 93526 APN Fscn3 0.156 IGL01634 G1 6 28430538 Y236N T A missense Het probably damaging 0.999 12/09/2013
18 93548 APN Gaa 0.715 IGL01634 G1 11 119274076 S265N G A missense Het possibly damaging 0.792 phenotype 12/09/2013
19 93578 APN Gas7 0.000 IGL01634 G1 11 67674231 T C splice site Het probably benign phenotype 12/09/2013
20 93521 APN Gbp8 0.075 IGL01634 G1 5 105018572 K297R T C missense Het probably damaging 0.961 12/09/2013
21 93519 APN Gm1818 0.906 IGL01634 G1 12 48556209 G A exon Het noncoding transcript 12/09/2013
22 93564 APN Gm5114 0.063 IGL01634 G1 7 39408647 T516K G T missense Het probably benign 0.000 12/09/2013
23 93547 APN Hectd1 1.000 IGL01634 G1 12 51803779 S165P A G missense Het probably damaging 0.975 phenotype 12/09/2013
24 93568 APN Hoxb4 0.900 IGL01634 G1 11 96318900 R44L G T missense Het probably damaging 0.996 phenotype 12/09/2013
25 93531 APN Ivd 1.000 IGL01634 G1 2 118876382 R285H G A missense Het probably damaging 1.000 phenotype 12/09/2013
26 93539 APN Krtap20-2 0.195 IGL01634 G1 16 89206089 F59S T C missense Het unknown 12/09/2013
27 93575 APN Megf8 0.930 IGL01634 G1 7 25358781 G A splice site Het probably benign phenotype 12/09/2013
28 93566 APN Mgat4d 0.000 IGL01634 G1 8 83368116 M261L A T missense Het possibly damaging 0.712 12/09/2013
29 93573 APN Mlc1 0.000 IGL01634 G1 15 88974718 A T splice site Het probably benign phenotype 12/09/2013
30 93554 APN Mmp20 0.067 IGL01634 G1 9 7635148 Y43* T A nonsense Het probably null phenotype 12/09/2013
31 93561 APN Morc3 1.000 IGL01634 G1 16 93873237 V767I G A missense Het probably benign 0.024 phenotype 12/09/2013
32 93558 APN Myo15 0.000 IGL01634 G1 11 60495472 T1808A A G missense Het probably damaging 0.998 phenotype 12/09/2013
33 93534 APN Notch4 0.000 IGL01634 G1 17 34572588 F574L T C missense Het probably damaging 1.000 phenotype 12/09/2013
34 93569 APN Npas3 0.916 IGL01634 G1 12 53947163 V164M G A missense Het probably damaging 1.000 phenotype 12/09/2013
35 93563 APN Nptx1 0.000 IGL01634 G1 11 119544672 Y273H A G missense Het probably damaging 1.000 phenotype 12/09/2013
36 93562 APN Oaf 0.000 IGL01634 G1 9 43224004 N159S T C missense Het probably damaging 1.000 12/09/2013
37 93520 APN Olfr1216 0.056 IGL01634 G1 2 89013444 I207F T A missense Het probably damaging 0.985 phenotype 12/09/2013
38 93517 APN Olfr519 0.070 IGL01634 G1 7 108894085 F107L A T missense Het probably benign 0.220 phenotype 12/09/2013
39 93536 APN Olfr994 0.098 IGL01634 G1 2 85430439 L130H A T missense Het probably damaging 1.000 phenotype 12/09/2013
40 93528 APN Pgm1 0.000 IGL01634 G1 5 64100974 F101L T C missense Het probably benign 0.006 phenotype 12/09/2013
41 93572 APN Pkd1l3 0.000 IGL01634 G1 8 109667525 A C critical splice acceptor site Het probably null phenotype 12/09/2013
42 93567 APN Plcd1 0.396 IGL01634 G1 9 119073789 R527H C T missense Het probably damaging 0.988 phenotype 12/09/2013
43 93559 APN Rexo2 1.000 IGL01634 G1 9 48468915 E206K C T missense Het probably damaging 1.000 phenotype 12/09/2013
44 93570 APN Ropn1 0.116 IGL01634 G1 16 34666778 T28N C A missense Het possibly damaging 0.953 phenotype 12/09/2013
45 278781 APN Ropn1 0.116 IGL01634 G1 16 34666771 I26F A T missense Het probably damaging 1.000 phenotype 04/16/2015
46 93529 APN Rpgrip1l 1.000 IGL01634 G1 8 91252544 S998C T A missense Het probably benign 0.251 phenotype 12/09/2013
47 93527 APN Rpgrip1l 1.000 IGL01634 G1 8 91252543 S998I C A missense Het probably benign 0.000 phenotype 12/09/2013
48 93571 APN Scap 0.000 IGL01634 G1 9 110378789 T C critical splice donor site 2 bp Het probably null phenotype 12/09/2013
49 93549 APN Sec23b 1.000 IGL01634 G1 2 144559230 Y4H T C missense Het probably damaging 0.963 phenotype 12/09/2013
50 93524 APN Sfrp4 0.284 IGL01634 G1 13 19623630 D66E C A missense Het possibly damaging 0.833 phenotype 12/09/2013
51 93550 APN Slc25a36 0.167 IGL01634 G1 9 97080481 T13A T C missense Het probably benign 0.001 12/09/2013
52 93551 APN Synpr 0.077 IGL01634 G1 14 13608576 I119F A T missense Het possibly damaging 0.861 12/09/2013
53 93538 APN Tamm41 0.928 IGL01634 G1 6 115016098 H109Q A C missense Het probably benign 0.001 phenotype 12/09/2013
54 93532 APN Tet1 0.000 IGL01634 G1 10 62878588 I476K A T missense Het possibly damaging 0.939 phenotype 12/09/2013
55 93552 APN Tg 0.105 IGL01634 G1 15 66729566 I142F A T missense Het probably benign 0.337 phenotype 12/09/2013
56 93574 APN Thada 0.000 IGL01634 G1 17 84393358 A T critical splice donor site 2 bp Het probably null phenotype 12/09/2013
57 93542 APN Triobp 1.000 IGL01634 G1 15 78993368 L1654P T C missense Het probably damaging 1.000 phenotype 12/09/2013
58 93553 APN Trpm7 1.000 IGL01634 G1 2 126826818 V726A A G missense Het probably damaging 0.999 phenotype 12/09/2013
59 93522 APN Txndc15 0.093 IGL01634 G1 13 55721625 V197G T G missense Het probably damaging 0.988 12/09/2013
60 93560 APN Ubr3 1.000 IGL01634 G1 2 69973572 T1169S A T missense Het probably benign 0.000 phenotype 12/09/2013
61 93576 APN Uhmk1 0.823 IGL01634 G1 1 170207113 C T critical splice donor site 1 bp Het probably null phenotype 12/09/2013
62 93533 APN Vmn2r16 0.200 IGL01634 G1 5 109340311 M350K T A missense Het probably benign 0.002 12/09/2013
63 93544 APN Vmn2r77 0.100 IGL01634 G1 7 86811649 V728I G A missense Het probably benign 0.000 12/09/2013
64 93546 APN Wipf1 0.161 IGL01634 G1 2 73447881 P7S G A missense Het unknown phenotype 12/09/2013
65 93545 APN Zswim3 0.086 IGL01634 G1 2 164820002 D134G A G missense Het probably damaging 0.987 12/09/2013
[records 1 to 65 of 65]