Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
4 are Possibly Damaging.
9 are Probably Damaging.
11 are Probably Benign.
4 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 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 1762 APN Abca4 0.000 IGL00156 G1 3 122062704 G A splice site 5 bp Het probably null phenotype 07/12/2011
2 735 APN Adamts19 0.222 IGL00156 G1 18 59024465 V943E T A missense Het probably damaging 0.999 phenotype 07/12/2011
3 306544 APN C530025M09Rik 0.059 IGL00156 G1 2 149830726 C A unclassified Het probably benign 04/16/2015
4 732 APN Cep192 0.971 IGL00156 G1 18 67820336 W475G T G missense Het probably damaging 1.000 07/12/2011
5 1597 APN Col28a1 0.118 IGL00156 G1 6 8014795 Y870C T C missense Het probably damaging 1.000 phenotype 07/12/2011
6 1522 APN Cyp2a22 0.147 IGL00156 G1 7 26937738 M207K A T missense Het probably benign 0.092 07/12/2011
7 1816 APN Dpm1 0.326 IGL00156 G1 2 168210575 V247A A G missense Het probably benign 0.374 phenotype 07/12/2011
8 1619 APN Glt1d1 0.031 IGL00156 G1 5 127632285 M1T T C start codon destroyed Het probably null 0.996 07/12/2011
9 306548 APN Gm9507 IGL00156 G1 10 77811280 C188* A T nonsense Het probably null 04/16/2015
10 306547 APN Hectd4 0.426 IGL00156 G1 5 121363870 V4222A T C missense Het possibly damaging 0.511 04/16/2015
11 306541 APN Igkv3-3 0.219 IGL00156 G1 6 70687413 S80T T A missense Het possibly damaging 0.543 04/16/2015
12 306542 APN Lrrc49 0.229 IGL00156 G1 9 60601320 K520E T C missense Het probably damaging 0.999 04/16/2015
13 762 APN Ltbp1 1.000 IGL00156 G1 17 75385160 Y1273F A T missense Het probably damaging 0.967 phenotype 07/12/2011
14 1040 APN Lyst 0.411 IGL00156 G1 13 13648878 H1478Q T A missense Het probably benign 0.000 phenotype 07/12/2011
15 1345 APN Mre11a 0.000 IGL00156 G1 9 14825208 D518G A G missense Het probably benign 0.281 phenotype 07/12/2011
16 1870 APN Olfr1243 0.074 IGL00156 G1 2 89528207 D68N C T missense Het probably damaging 1.000 phenotype 07/12/2011
17 1159 APN Olfr381 0.086 IGL00156 G1 11 73486572 N84I T A missense Het probably benign 0.221 phenotype 07/12/2011
18 1342 APN Olfr859 0.084 IGL00156 G1 9 19808396 I26T T C missense Het probably benign 0.090 phenotype 07/12/2011
19 306543 APN Pkd1l1 1.000 IGL00156 G1 11 8950515 S9C T A missense Het probably damaging 1.000 phenotype 04/16/2015
20 1907 APN Prrc2b 0.212 IGL00156 G1 2 32208719 H681R A G missense Het probably damaging 1.000 07/12/2011
21 1909 APN Rapgef1 1.000 IGL00156 G1 2 29722269 S644G A G missense Het probably benign 0.000 phenotype 07/12/2011
22 1598 APN Sgce 0.219 IGL00156 G1 6 4689750 H361L T A missense Het probably damaging 1.000 phenotype 07/12/2011
23 306546 APN Specc1 0.360 IGL00156 G1 11 62118009 W117L G T missense Het probably benign 0.024 phenotype 04/16/2015
24 1634 APN Srrm4 0.480 IGL00156 G1 5 116446557 S485P A G missense Het possibly damaging 0.856 phenotype 07/12/2011
25 306545 APN Traf2 0.709 IGL00156 G1 2 25520451 Y395* G T nonsense Het probably null phenotype 04/16/2015
26 1284 APN Trf 1.000 IGL00156 G1 9 103220957 I34T A G missense Het probably benign 0.001 phenotype 07/12/2011
27 990 APN Vdac2 0.435 IGL00156 G1 14 21838524 Y165H T C missense Het possibly damaging 0.534 phenotype 07/12/2011
28 1742 APN Wwp1 0.000 IGL00156 G1 4 19650360 T269A T C missense Het probably benign 0.000 phenotype 07/12/2011
[records 1 to 28 of 28]