Incidental Mutations

45 incidental mutations are currently displayed, and affect 45 genes.
3 are Possibly Damaging.
18 are Probably Damaging.
17 are Probably Benign.
6 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 45 of 45] 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 73227 APN 1600012H06Rik 0.125 IGL01301 G1 17 14943919 (GRCm38) C T splice site 1090 bp Het probably null phenotype 2013-10-07
2 73243 APN Acacb 0.000 IGL01301 G1 5 114246498 (GRCm38) I2238L A T missense Het probably benign 0.000 phenotype 2013-10-07
3 73247 APN Aldh1l2 0.000 IGL01301 G1 10 83522846 (GRCm38) Y95C T C missense Het probably damaging 0.999 phenotype 2013-10-07
4 73244 APN Asxl2 0.920 IGL01301 G1 12 3501425 (GRCm38) T1056A A G missense Het probably damaging 1.000 phenotype 2013-10-07
5 73231 APN B4galnt1 0.000 IGL01301 G1 10 127169779 (GRCm38) T250A A G missense Het possibly damaging 0.555 phenotype 2013-10-07
6 73253 APN Cela3b 0.063 IGL01301 G1 4 137423843 (GRCm38) A T critical splice donor site 2 bp Het probably null phenotype 2013-10-07
7 73226 APN Chst3 0.197 IGL01301 G1 10 60185832 (GRCm38) T398A T C missense Het probably damaging 0.999 phenotype 2013-10-07
8 73225 APN Cngb3 0.083 IGL01301 G1 4 19425625 (GRCm38) T478A A G missense Het probably damaging 1.000 phenotype 2013-10-07
9 73223 APN Cyp4a10 0.060 IGL01301 G1 4 115518455 (GRCm38) L45P T C missense Het probably damaging 1.000 phenotype 2013-10-07
10 73238 APN Defb21 0.065 IGL01301 G1 2 152574751 (GRCm38) E49G A G missense Het possibly damaging 0.847 2013-10-07
11 73237 APN Dnajc1 0.130 IGL01301 G1 2 18308834 (GRCm38) T159A T C missense Het probably damaging 0.989 phenotype 2013-10-07
12 73234 APN Dnmbp 0.000 IGL01301 G1 19 43902354 (GRCm38) S325P A G missense Het probably benign 0.036 phenotype 2013-10-07
13 73233 APN Fam91a1 0.000 IGL01301 G1 15 58442871 (GRCm38) F534L T C missense Het probably damaging 0.993 phenotype 2013-10-07
14 73236 APN Fermt2 1.000 IGL01301 G1 14 45464863 (GRCm38) E488G T C missense Het probably damaging 0.997 phenotype 2013-10-07
15 73219 APN Filip1 0.522 IGL01301 G1 9 79819180 (GRCm38) D719G T C missense Het possibly damaging 0.928 phenotype 2013-10-07
16 73245 APN Gad1-ps 0.186 IGL01301 G1 10 99445151 (GRCm38) A G exon Het noncoding transcript 2013-10-07
17 73224 APN Glra3 0.000 IGL01301 G1 8 55940962 (GRCm38) A36E C A missense Het probably benign 0.001 phenotype 2013-10-07
18 73261 APN Gm9884 IGL01301 G1 1 25830648 (GRCm38) T A unclassified Het probably benign 2013-10-07
19 73255 APN Hectd2 0.000 IGL01301 G1 19 36569370 (GRCm38) T C splice site Het probably benign 2013-10-07
20 73257 APN Hnrnpm 1.000 IGL01301 G1 17 33669168 (GRCm38) C T critical splice donor site 1 bp Het probably null phenotype 2013-10-07
21 73218 APN Lrrk2 0.405 IGL01301 G1 15 91767339 (GRCm38) Y1733N T A missense Het probably damaging 1.000 phenotype 2013-10-07
22 73248 APN Mindy1 0.000 IGL01301 G1 3 95288390 (GRCm38) L148P T C missense Het probably damaging 1.000 2013-10-07
23 73242 APN Mkrn2 0.000 IGL01301 G1 6 115611789 (GRCm38) Y164* C A nonsense Het probably null phenotype 2013-10-07
24 73240 APN Msra 0.119 IGL01301 G1 14 64210435 (GRCm38) Y135C T C missense Het probably damaging 1.000 phenotype 2013-10-07
25 73241 APN Ndst3 0.248 IGL01301 G1 3 123548916 (GRCm38) A749T C T missense Het probably damaging 0.970 phenotype 2013-10-07
26 73235 APN Ngdn 1.000 IGL01301 G1 14 55017114 (GRCm38) A41S G T missense Het probably benign 0.148 phenotype 2013-10-07
27 73249 APN Nlrp12 0.145 IGL01301 G1 7 3240092 (GRCm38) S597T A T missense Het probably damaging 0.999 phenotype 2013-10-07
28 73220 APN Olfr1451 0.194 IGL01301 G1 19 12999417 (GRCm38) I144F A T missense Het probably damaging 0.988 phenotype 2013-10-07
29 73251 APN Pabpc6 0.098 IGL01301 G1 17 9667970 (GRCm38) S551P A G missense Het probably benign 0.000 2013-10-07
30 73232 APN Plekhg5 0.138 IGL01301 G1 4 152112553 (GRCm38) A752V C T missense Het probably benign 0.000 phenotype 2013-10-07
31 73246 APN Prpf4b 1.000 IGL01301 G1 13 34884291 (GRCm38) S368P T C missense Het probably benign 0.226 phenotype 2013-10-07
32 73254 APN Pus7 0.638 IGL01301 G1 5 23746424 (GRCm38) A G critical splice donor site 2 bp Het probably null 2013-10-07
33 73259 APN Rad23b 1.000 IGL01301 G1 4 55366774 (GRCm38) T C splice site Het probably benign phenotype 2013-10-07
34 73260 APN Rgs13 0.000 IGL01301 G1 1 144171414 (GRCm38) T C splice site Het probably benign phenotype 2013-10-07
35 73262 APN Sfpq 1.000 IGL01301 G1 4 127026760 (GRCm38) T C splice site Het probably benign phenotype 2013-10-07
36 73221 APN Slc9a9 0.000 IGL01301 G1 9 95055459 (GRCm38) S455T T A missense Het probably benign 0.025 phenotype 2013-10-07
37 73256 APN Slco1a1 0.210 IGL01301 G1 6 141932530 (GRCm38) A G splice site Het probably benign phenotype 2013-10-07
38 73229 APN Tmem26 0.068 IGL01301 G1 10 68778606 (GRCm38) N284Y A T missense Het probably damaging 1.000 phenotype 2013-10-07
39 73239 APN Tmem87a 0.133 IGL01301 G1 2 120380769 (GRCm38) I232V T C missense Het probably benign 0.011 2013-10-07
40 73250 APN Trpm2 0.141 IGL01301 G1 10 77923984 (GRCm38) L1106P A G missense Het probably damaging 0.997 phenotype 2013-10-07
41 73258 APN Vmn1r18 0.055 IGL01301 G1 6 57389667 (GRCm38) T C utr 3 prime Het probably benign 2013-10-07
42 73230 APN Zfp213 0.056 IGL01301 G1 17 23561417 (GRCm38) A43D G T missense Het probably benign 0.176 phenotype 2013-10-07
43 73228 APN Zfp365 0.000 IGL01301 G1 10 67909354 (GRCm38) V198A A G missense Het probably damaging 0.997 phenotype 2013-10-07
44 73252 APN Zfp395 0.000 IGL01301 G1 14 65394751 (GRCm38) T A splice site Het probably null 2013-10-07
45 73222 APN Zfp618 0.156 IGL01301 G1 4 63132826 (GRCm38) V615M G A missense Het probably damaging 0.998 2013-10-07
[records 1 to 45 of 45]