Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
4 are Possibly Damaging.
14 are Probably Damaging.
7 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 28 of 28] 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 8511 APN Aadat 0.000 IGL00822 G1 8 60535758 S332P T C missense Het probably benign 0.112 phenotype 12/06/2012
2 8532 APN Abcb4 0.000 IGL00822 G1 5 8950046 F1005L T C missense Het probably benign 0.000 phenotype 12/06/2012
3 8561 APN Actr2 0.950 IGL00822 G1 11 20094367 R80W G A missense Het probably damaging 1.000 phenotype 12/06/2012
4 8584 APN Adck1 0.000 IGL00822 G1 12 88455516 I299T T C missense Het probably damaging 0.992 12/06/2012
5 9060 APN Armc4 0.153 IGL00822 G1 18 7181817 L836M A T missense Het probably damaging 0.998 phenotype 12/06/2012
6 277995 APN Camk2g 0.000 IGL00822 G1 14 20737330 G500S C T missense Het probably damaging 0.992 phenotype 04/16/2015
7 9378 APN Car15 0.059 IGL00822 G1 16 17836634 M146K A T missense Het probably damaging 0.997 12/06/2012
8 10014 APN Cyp4f39 0.309 IGL00822 G1 17 32470832 N84S A G missense Het probably benign 0.025 phenotype 12/06/2012
9 10280 APN Dock8 0.098 IGL00822 G1 19 25188409 E1886* G T nonsense Het probably null phenotype 12/06/2012
10 11536 APN Kansl2 0.941 IGL00822 G1 15 98528853 T C splice site Het probably benign 12/06/2012
11 11646 APN Klc2 0.000 IGL00822 G1 19 5111513 V323E A T missense Het probably damaging 1.000 phenotype 12/06/2012
12 11832 APN Lrrc7 0.771 IGL00822 G1 3 158185474 V352A A G missense Het probably damaging 0.985 phenotype 12/06/2012
13 11842 APN Lrrc8c 0.000 IGL00822 G1 5 105608308 A650S G T missense Het probably benign 0.043 phenotype 12/06/2012
14 11866 APN Ltbp1 1.000 IGL00822 G1 17 75151321 Y299C A G missense Het probably damaging 0.998 phenotype 12/06/2012
15 12156 APN Myh13 0.119 IGL00822 G1 11 67361328 T1421A A G missense Het probably damaging 0.978 12/06/2012
16 12162 APN Myl3 0.258 IGL00822 G1 9 110766489 T56K C A missense Het possibly damaging 0.951 phenotype 12/06/2012
17 12400 APN Nod1 0.000 IGL00822 G1 6 54944946 Y129C T C missense Het probably damaging 1.000 phenotype 12/06/2012
18 12886 APN Otog 0.679 IGL00822 G1 7 46295880 S2187N G A missense Het probably benign 0.237 phenotype 12/06/2012
19 12902 APN Pank4 0.136 IGL00822 G1 4 154980602 R786H G A missense Het possibly damaging 0.501 phenotype 12/06/2012
20 26575 APN Sag 0.000 IGL00822 G1 1 87845026 A G unclassified 3 bp Het probably null phenotype 04/17/2013
21 13933 APN Scn2b 0.000 IGL00822 G1 9 45125544 V117M G A missense Het probably damaging 1.000 phenotype 12/06/2012
22 13947 APN Sec16b 0.000 IGL00822 G1 1 157564555 A886S G T missense Het probably benign 0.048 phenotype 12/06/2012
23 277994 APN Slit2 1.000 IGL00822 G1 5 47989151 E95K G A missense Het possibly damaging 0.877 phenotype 04/16/2015
24 14224 APN Spns3 0.000 IGL00822 G1 11 72499353 A T critical splice donor site 2 bp Het probably null 12/06/2012
25 14295 APN Styk1 0.325 IGL00822 G1 6 131301662 K350E T C missense Het possibly damaging 0.754 phenotype 12/06/2012
26 14540 APN Tns3 0.284 IGL00822 G1 11 8443976 T1291I G A missense Het probably damaging 0.987 phenotype 12/06/2012
27 14597 APN Xntrpc 0.449 IGL00822 G1 7 102084368 I175V A G missense Het probably damaging 0.998 phenotype 12/06/2012
28 14937 APN Zfp106 0.000 IGL00822 G1 2 120514160 R1745C G A missense Het probably damaging 1.000 phenotype 12/06/2012
[records 1 to 28 of 28]