Incidental Mutations

49 incidental mutations are currently displayed, and affect 49 genes.
10 are Possibly Damaging.
14 are Probably Damaging.
22 are Probably Benign.
3 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 49 of 49] 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 92255 APN Aacs 0.510 IGL01613 G1 5 125512652 M446R T G missense Het possibly damaging 0.478 12/09/2013
2 92256 APN Abca16 0.000 IGL01613 G1 7 120541277 N1599S A G missense Het probably benign 0.025 12/09/2013
3 92257 APN Ankib1 0.000 IGL01613 G1 5 3713146 Q528* G A nonsense Het probably null 12/09/2013
4 92253 APN Ano10 0.149 IGL01613 G1 9 122259540 L347M A T missense Het possibly damaging 0.751 phenotype 12/09/2013
5 92279 APN Bag6 1.000 IGL01613 G1 17 35143016 T C unclassified Het probably benign phenotype 12/09/2013
6 92250 APN Bpnt1 0.271 IGL01613 G1 1 185353994 V182A T C missense Het possibly damaging 0.951 phenotype 12/09/2013
7 92259 APN Capn13 0.052 IGL01613 G1 17 73331058 T450N G T missense Het probably benign 0.066 phenotype 12/09/2013
8 92270 APN Cbr3 0.234 IGL01613 G1 16 93683443 E40V A T missense Het probably benign 0.004 phenotype 12/09/2013
9 92241 APN Cdk10 0.190 IGL01613 G1 8 123228387 I159T T C missense Het probably damaging 0.991 phenotype 12/09/2013
10 92276 APN Cela3b 0.083 IGL01613 G1 4 137425071 D65G T C missense Het possibly damaging 0.657 phenotype 12/09/2013
11 92284 APN Csf2rb 1.000 IGL01613 G1 15 78335302 T G intron Het probably benign phenotype 12/09/2013
12 278597 APN Cyp2b19 0.064 IGL01613 G1 7 26763461 T256I C T missense Het possibly damaging 0.908 04/16/2015
13 92271 APN Dpp9 1.000 IGL01613 G1 17 56190713 H687R T C missense Het probably benign 0.000 phenotype 12/09/2013
14 92246 APN Elovl1 1.000 IGL01613 G1 4 118431270 V108A T C missense Het probably benign 0.062 phenotype 12/09/2013
15 92275 APN Emb 0.076 IGL01613 G1 13 117272078 N318K T A missense Het probably damaging 0.998 phenotype 12/09/2013
16 92263 APN Ermp1 0.000 IGL01613 G1 19 29639939 L36P A G missense Het probably damaging 1.000 phenotype 12/09/2013
17 92251 APN Esco2 1.000 IGL01613 G1 14 65826595 H380P T G missense Het possibly damaging 0.754 phenotype 12/09/2013
18 92267 APN Gm5724 0.078 IGL01613 G1 6 141713214 T552K G T missense Het possibly damaging 0.670 12/09/2013
19 92249 APN Gm9747 0.197 IGL01613 G1 1 82234088 G A utr 3 prime Het probably benign 12/09/2013
20 92264 APN Golga1 0.210 IGL01613 G1 2 39020126 M603T A G missense Het probably benign 0.144 phenotype 12/09/2013
21 92268 APN Hsph1 0.505 IGL01613 G1 5 149627278 V411A A G missense Het probably benign 0.343 phenotype 12/09/2013
22 278598 APN Igsf21 0.066 IGL01613 G1 4 140107364 G66S C T missense Het possibly damaging 0.754 phenotype 04/16/2015
23 92280 APN Ints11 1.000 IGL01613 G1 4 155885198 T C critical splice donor site 2 bp Het probably null phenotype 12/09/2013
24 92274 APN Jakmip1 0.647 IGL01613 G1 5 37100768 A253S G T missense Het probably damaging 0.997 phenotype 12/09/2013
25 92266 APN Met 1.000 IGL01613 G1 6 17540577 Y834C A G missense Het probably damaging 1.000 phenotype 12/09/2013
26 92269 APN Mgl2 0.000 IGL01613 G1 11 70134158 T2A A G missense Het probably benign 0.082 phenotype 12/09/2013
27 92273 APN Myh2 0.185 IGL01613 G1 11 67197344 V1929L G T missense Het probably benign 0.014 phenotype 12/09/2013
28 92262 APN Myh8 0.833 IGL01613 G1 11 67301710 S1472P T C missense Het probably benign 0.109 phenotype 12/09/2013
29 92281 APN Myo1e 0.000 IGL01613 G1 9 70341273 T C splice site Het probably benign phenotype 12/09/2013
30 92277 APN Ndufaf7 1.000 IGL01613 G1 17 78937502 I17V A G missense Het probably benign 0.015 phenotype 12/09/2013
31 92254 APN Olfr1046 0.112 IGL01613 G1 2 86217161 D183A T G missense Het probably damaging 1.000 phenotype 12/09/2013
32 92243 APN Olfr1256 0.063 IGL01613 G1 2 89835808 T46A T C missense Het probably damaging 0.980 phenotype 12/09/2013
33 92244 APN Olfr193 0.071 IGL01613 G1 16 59109921 S230T A T missense Het probably damaging 0.999 phenotype 12/09/2013
34 92238 APN Olfr804 0.097 IGL01613 G1 10 129705623 I248M A G missense Het probably benign 0.015 phenotype 12/09/2013
35 92283 APN Olfr830 0.145 IGL01613 G1 9 18875321 T A splice site Het probably benign phenotype 12/09/2013
36 92242 APN Olfr914 0.059 IGL01613 G1 9 38606554 I30V A G missense Het probably null 0.001 phenotype 12/09/2013
37 92261 APN Olfr992 0.062 IGL01613 G1 2 85400171 D121N C T missense Het probably damaging 0.999 phenotype 12/09/2013
38 92258 APN Ppef2 0.000 IGL01613 G1 5 92235820 E477G T C missense Het probably benign 0.013 phenotype 12/09/2013
39 92282 APN Scmh1 0.000 IGL01613 G1 4 120529900 T A utr 3 prime Het probably benign phenotype 12/09/2013
40 92272 APN Scn1a 1.000 IGL01613 G1 2 66285937 D1473Y C A missense Het probably damaging 1.000 phenotype 12/09/2013
41 92265 APN Sdr42e1 0.000 IGL01613 G1 8 117662937 V322I C T missense Het probably benign 0.137 12/09/2013
42 92260 APN Spta1 0.872 IGL01613 G1 1 174208394 A1089T G A missense Het probably damaging 1.000 phenotype 12/09/2013
43 92278 APN Sufu 1.000 IGL01613 G1 19 46475620 Y424H T C missense Het probably damaging 1.000 phenotype 12/09/2013
44 92248 APN Tgs1 1.000 IGL01613 G1 4 3585183 F108L T C missense Het possibly damaging 0.920 phenotype 12/09/2013
45 92245 APN Ttn 1.000 IGL01613 G1 2 76974964 N177S T C missense Het probably benign 0.256 phenotype 12/09/2013
46 92247 APN Tyk2 0.000 IGL01613 G1 9 21120576 D401G T C missense Het probably damaging 0.987 phenotype 12/09/2013
47 92239 APN Vav1 0.269 IGL01613 G1 17 57307067 F650L T C missense Het possibly damaging 0.930 phenotype 12/09/2013
48 92240 APN Wdr12 1.000 IGL01613 G1 1 60080559 H385R T C missense Het probably damaging 0.996 phenotype 12/09/2013
49 92252 APN Xab2 1.000 IGL01613 G1 8 3610880 M745V T C missense Het probably benign 0.010 phenotype 12/09/2013
[records 1 to 49 of 49]