Incidental Mutations

31 incidental mutations are currently displayed, and affect 31 genes.
5 are Possibly Damaging.
13 are Probably Damaging.
9 are Probably Benign.
3 are Probably Null.
2 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 31 of 31] 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 76017 APN Acod1 0.000 IGL01368 G1 14 103051334 D93E T A missense Het probably damaging 0.998 phenotype 10/07/2013
2 76009 APN Adam22 1.000 IGL01368 G1 5 8127411 Y566C T C missense Het probably damaging 0.999 phenotype 10/07/2013
3 76031 APN Atp8b3 0.091 IGL01368 G1 10 80534229 G A splice site Het probably benign phenotype 10/07/2013
4 76022 APN Babam1 0.468 IGL01368 G1 8 71398406 D104E T A missense Het probably damaging 1.000 0.647 10/07/2013
5 76007 APN Bcl2a1a 0.135 IGL01368 G1 9 88957447 W133R T A missense Het probably damaging 1.000 phenotype 10/07/2013
6 76015 APN Ckm 0.280 IGL01368 G1 7 19416787 Q184* C T nonsense Het probably null phenotype 10/07/2013
7 76019 APN Clk4 0.654 IGL01368 G1 11 51281172 Y246* T A nonsense Het probably null phenotype 10/07/2013
8 76011 APN Cyp3a57 0.065 IGL01368 G1 5 145369068 S121P T C missense Het probably damaging 0.987 10/07/2013
9 76005 APN Gm5039 0.338 IGL01368 G1 12 88321088 D132N C T missense Het unknown 10/07/2013
10 76028 APN Gm5771 0.090 IGL01368 G1 6 41396686 D161G A G missense Het possibly damaging 0.938 10/07/2013
11 76032 APN Gm8011 IGL01368 G1 14 42465874 T C splice site Het probably benign 10/07/2013
12 76029 APN Gpr153 0.000 IGL01368 G1 4 152282994 F434S T C missense Het probably benign 0.403 phenotype 10/07/2013
13 76016 APN Gpr158 0.000 IGL01368 G1 2 21827098 W1003L G T missense Het probably damaging 1.000 10/07/2013
14 76006 APN Ighv5-9-1 0.154 IGL01368 G1 12 113736390 E34G T C missense Het probably damaging 1.000 10/07/2013
15 76025 APN Igkv16-104 0.084 IGL01368 G1 6 68425610 R2S G T missense Het possibly damaging 0.598 10/07/2013
16 76014 APN Map3k3 1.000 IGL01368 G1 11 106150389 F395L T C missense Het probably benign 0.015 phenotype 10/07/2013
17 76026 APN Myof 0.000 IGL01368 G1 19 37936457 T1161S T A missense Het probably damaging 0.972 phenotype 10/07/2013
18 76008 APN Nlrp9a 0.060 IGL01368 G1 7 26557874 S217P T C missense Het probably damaging 0.996 10/07/2013
19 76021 APN Nol9 0.960 IGL01368 G1 4 152058391 N687K T A missense Het probably benign 0.000 10/07/2013
20 76012 APN Olfr287 0.079 IGL01368 G1 15 98207500 I295V T C missense Het probably damaging 0.988 phenotype 10/07/2013
21 76010 APN Olfr697 0.092 IGL01368 G1 7 106741622 E104G T C missense Het probably benign 0.192 phenotype 10/07/2013
22 76003 APN Olfr748 0.061 IGL01368 G1 14 50710993 V221A T C missense Het possibly damaging 0.946 phenotype 10/07/2013
23 76004 APN Olfr952 0.060 IGL01368 G1 9 39426180 V297D A T missense Het probably damaging 1.000 phenotype 10/07/2013
24 76027 APN Rrh 0.113 IGL01368 G1 3 129808969 D229G T C missense Het probably benign 0.021 phenotype 10/07/2013
25 76018 APN Sclt1 0.246 IGL01368 G1 3 41711175 T153A T C missense Het probably damaging 0.962 phenotype 10/07/2013
26 76023 APN Slc41a1 0.000 IGL01368 G1 1 131839124 V127I G A missense Het probably damaging 0.988 10/07/2013
27 76024 APN Smarca2 0.000 IGL01368 G1 19 26774294 S214L C T missense Het possibly damaging 0.825 phenotype 10/07/2013
28 76013 APN Tmem63a 0.088 IGL01368 G1 1 180970232 V616A T C missense Het possibly damaging 0.690 10/07/2013
29 76033 APN Ubr1 0.746 IGL01368 G1 2 120941131 A G splice site Het probably benign phenotype 10/07/2013
30 76020 APN Vmn1r228 0.056 IGL01368 G1 17 20776512 L248P A G missense Het probably benign 0.071 10/07/2013
31 76030 APN Zdhhc16 0.637 IGL01368 G1 19 41941506 T A splice site Het probably null phenotype 10/07/2013
[records 1 to 31 of 31]