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 0.110 IGL01301 G1 17 14943919 C T splice site 1090 bp Het probably null phenotype 10/07/2013
2 73243 APN Acacb 0.000 IGL01301 G1 5 114246498 I2238L A T missense Het probably benign 0.000 phenotype 10/07/2013
3 73247 APN Aldh1l2 0.000 IGL01301 G1 10 83522846 Y95C T C missense Het probably damaging 0.999 phenotype 10/07/2013
4 73244 APN Asxl2 0.938 IGL01301 G1 12 3501425 T1056A A G missense Het probably damaging 1.000 phenotype 10/07/2013
5 73231 APN B4galnt1 0.000 IGL01301 G1 10 127169779 T250A A G missense Het possibly damaging 0.555 phenotype 10/07/2013
6 73253 APN Cela3b 0.077 IGL01301 G1 4 137423843 A T critical splice donor site 2 bp Het probably null phenotype 10/07/2013
7 73226 APN Chst3 0.197 IGL01301 G1 10 60185832 T398A T C missense Het probably damaging 0.999 phenotype 10/07/2013
8 73225 APN Cngb3 0.102 IGL01301 G1 4 19425625 T478A A G missense Het probably damaging 1.000 phenotype 10/07/2013
9 73223 APN Cyp4a10 0.073 IGL01301 G1 4 115518455 L45P T C missense Het probably damaging 1.000 phenotype 10/07/2013
10 73238 APN Defb21 0.102 IGL01301 G1 2 152574751 E49G A G missense Het possibly damaging 0.847 10/07/2013
11 73237 APN Dnajc1 0.093 IGL01301 G1 2 18308834 T159A T C missense Het probably damaging 0.989 phenotype 10/07/2013
12 73234 APN Dnmbp 0.000 IGL01301 G1 19 43902354 S325P A G missense Het probably benign 0.036 phenotype 10/07/2013
13 73233 APN Fam91a1 0.000 IGL01301 G1 15 58442871 F534L T C missense Het probably damaging 0.993 phenotype 10/07/2013
14 73236 APN Fermt2 1.000 IGL01301 G1 14 45464863 E488G T C missense Het probably damaging 0.997 phenotype 10/07/2013
15 73219 APN Filip1 0.367 IGL01301 G1 9 79819180 D719G T C missense Het possibly damaging 0.928 phenotype 10/07/2013
16 73245 APN Gad1-ps 0.174 IGL01301 G1 10 99445151 A G exon Het noncoding transcript 10/07/2013
17 73224 APN Glra3 0.000 IGL01301 G1 8 55940962 A36E C A missense Het probably benign 0.001 phenotype 10/07/2013
18 73261 APN Gm9884 IGL01301 G1 1 25830648 T A unclassified Het probably benign 10/07/2013
19 73255 APN Hectd2 0.000 IGL01301 G1 19 36569370 T C splice site Het probably benign 10/07/2013
20 73257 APN Hnrnpm 1.000 IGL01301 G1 17 33669168 C T critical splice donor site 1 bp Het probably null phenotype 10/07/2013
21 73218 APN Lrrk2 0.417 IGL01301 G1 15 91767339 Y1733N T A missense Het probably damaging 1.000 phenotype 10/07/2013
22 73248 APN Mindy1 0.000 IGL01301 G1 3 95288390 L148P T C missense Het probably damaging 1.000 10/07/2013
23 73242 APN Mkrn2 0.000 IGL01301 G1 6 115611789 Y164* C A nonsense Het probably null phenotype 10/07/2013
24 73240 APN Msra 0.125 IGL01301 G1 14 64210435 Y135C T C missense Het probably damaging 1.000 phenotype 10/07/2013
25 73241 APN Ndst3 0.271 IGL01301 G1 3 123548916 A749T C T missense Het probably damaging 0.970 phenotype 10/07/2013
26 73235 APN Ngdn 1.000 IGL01301 G1 14 55017114 A41S G T missense Het probably benign 0.148 phenotype 10/07/2013
27 73249 APN Nlrp12 0.125 IGL01301 G1 7 3240092 S597T A T missense Het probably damaging 0.999 phenotype 10/07/2013
28 73220 APN Olfr1451 0.154 IGL01301 G1 19 12999417 I144F A T missense Het probably damaging 0.988 phenotype 10/07/2013
29 73251 APN Pabpc6 0.094 IGL01301 G1 17 9667970 S551P A G missense Het probably benign 0.000 10/07/2013
30 73232 APN Plekhg5 0.135 IGL01301 G1 4 152112553 A752V C T missense Het probably benign 0.000 phenotype 10/07/2013
31 73246 APN Prpf4b 1.000 IGL01301 G1 13 34884291 S368P T C missense Het probably benign 0.226 phenotype 10/07/2013
32 73254 APN Pus7 0.246 IGL01301 G1 5 23746424 A G critical splice donor site 2 bp Het probably null 10/07/2013
33 73259 APN Rad23b 1.000 IGL01301 G1 4 55366774 T C splice site Het probably benign phenotype 10/07/2013
34 73260 APN Rgs13 0.000 IGL01301 G1 1 144171414 T C splice site Het probably benign phenotype 10/07/2013
35 73262 APN Sfpq 1.000 IGL01301 G1 4 127026760 T C splice site Het probably benign phenotype 10/07/2013
36 73221 APN Slc9a9 0.000 IGL01301 G1 9 95055459 S455T T A missense Het probably benign 0.025 phenotype 10/07/2013
37 73256 APN Slco1a1 0.289 IGL01301 G1 6 141932530 A G splice site Het probably benign phenotype 10/07/2013
38 73229 APN Tmem26 0.094 IGL01301 G1 10 68778606 N284Y A T missense Het probably damaging 1.000 phenotype 10/07/2013
39 73239 APN Tmem87a 0.158 IGL01301 G1 2 120380769 I232V T C missense Het probably benign 0.011 10/07/2013
40 73250 APN Trpm2 0.150 IGL01301 G1 10 77923984 L1106P A G missense Het probably damaging 0.997 phenotype 10/07/2013
41 73258 APN Vmn1r18 0.075 IGL01301 G1 6 57389667 T C utr 3 prime Het probably benign 10/07/2013
42 73230 APN Zfp213 0.058 IGL01301 G1 17 23561417 A43D G T missense Het probably benign 0.176 phenotype 10/07/2013
43 73228 APN Zfp365 0.000 IGL01301 G1 10 67909354 V198A A G missense Het probably damaging 0.997 phenotype 10/07/2013
44 73252 APN Zfp395 0.000 IGL01301 G1 14 65394751 T A splice site Het probably null 10/07/2013
45 73222 APN Zfp618 0.167 IGL01301 G1 4 63132826 V615M G A missense Het probably damaging 0.998 10/07/2013
[records 1 to 45 of 45]