Incidental Mutations

36 incidental mutations are currently displayed, and affect 36 genes.
6 are Possibly Damaging.
13 are Probably Damaging.
13 are Probably Benign.
3 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 36 of 36] 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 363449 APN 1700093K21Rik 0.074 IGL02897 11 23517308 E108D T A missense Het probably benign 0.001 phenotype 12/18/2015
2 363443 APN Abca7 0.000 IGL02897 10 80001592 F437L T C missense Het probably damaging 0.998 phenotype 12/18/2015
3 363437 APN Abi2 0.000 IGL02897 1 60448194 V134A T C missense Het probably damaging 0.957 phenotype 12/18/2015
4 363455 APN Ablim2 0.201 IGL02897 5 35833126 I75T T C missense Het probably damaging 1.000 12/18/2015
5 363433 APN Aldh1a3 0.510 IGL02897 7 66427327 V29A A G missense Het probably benign 0.016 phenotype 12/18/2015
6 363456 APN Bptf 1.000 IGL02897 11 107047121 K2715E T C missense Het probably damaging 0.995 phenotype 12/18/2015
7 363452 APN Cd163 0.000 IGL02897 6 124325527 S1017C A T missense Het probably damaging 0.999 phenotype 12/18/2015
8 363438 APN Cdc14b 0.298 IGL02897 13 64247253 I76V T C missense Het probably benign 0.005 phenotype 12/18/2015
9 363428 APN Cers6 0.320 IGL02897 2 68934533 C63* T A nonsense Het probably null phenotype 12/18/2015
10 363459 APN Chd9 0.000 IGL02897 8 90933868 T C splice site Het probably benign 12/18/2015
11 363450 APN Col19a1 1.000 IGL02897 1 24534098 N198D T C missense Het unknown phenotype 12/18/2015
12 363445 APN Cse1l 1.000 IGL02897 2 166919708 C61R T C missense Het possibly damaging 0.465 phenotype 12/18/2015
13 363444 APN Cubn 1.000 IGL02897 2 13318312 T2815A T C missense Het possibly damaging 0.552 phenotype 12/18/2015
14 363440 APN Cyp19a1 0.000 IGL02897 9 54166911 T453K G T missense Het possibly damaging 0.948 phenotype 12/18/2015
15 363457 APN Dlg1 1.000 IGL02897 16 31771856 G T critical splice donor site 1 bp Het probably null phenotype 12/18/2015
16 363427 APN Dpp7 0.093 IGL02897 2 25353672 Y339C T C missense Het probably damaging 1.000 phenotype 12/18/2015
17 363461 APN Dtl 1.000 IGL02897 1 191541544 T C splice site Het probably benign phenotype 12/18/2015
18 363436 APN Gm5591 0.181 IGL02897 7 38520042 E469G T C missense Het probably damaging 0.998 12/18/2015
19 363434 APN Ing3 0.959 IGL02897 6 21969326 V202E T A missense Het probably benign 0.143 phenotype 12/18/2015
20 363429 APN Inpp5j 0.323 IGL02897 11 3500619 L578P A G missense Het probably damaging 1.000 phenotype 12/18/2015
21 363432 APN Irak4 0.823 IGL02897 15 94553991 N155S A G missense Het probably benign 0.001 phenotype 12/18/2015
22 363442 APN Kif2b 0.843 IGL02897 11 91576219 S413T A T missense Het probably damaging 0.999 12/18/2015
23 363439 APN L3mbtl1 0.000 IGL02897 2 162965772 Y490F A T missense Het probably damaging 0.999 phenotype 12/18/2015
24 363441 APN Med17 0.966 IGL02897 9 15267534 D447A T G missense Het probably damaging 0.997 phenotype 12/18/2015
25 363431 APN Med26 0.371 IGL02897 8 72496521 T245A T C missense Het probably benign 0.001 phenotype 12/18/2015
26 363451 APN Nlrc3 0.124 IGL02897 16 3964074 S490R A T missense Het possibly damaging 0.846 phenotype 12/18/2015
27 363460 APN Nme5 0.000 IGL02897 18 34569903 A G intron Het probably benign phenotype 12/18/2015
28 363446 APN Olfr611 0.090 IGL02897 7 103518130 R85G T C missense Het probably benign 0.009 phenotype 12/18/2015
29 363454 APN Rnf10 0.634 IGL02897 5 115248641 Q530K G T missense Het probably benign 0.000 phenotype 12/18/2015
30 363426 APN Robo3 1.000 IGL02897 9 37427502 Y281* A T nonsense Het probably null phenotype 12/18/2015
31 363447 APN Sclt1 0.217 IGL02897 3 41675387 I330V T C missense Het probably benign 0.015 phenotype 12/18/2015
32 363458 APN Smim14 0.112 IGL02897 5 65450396 A T intron Het probably benign 12/18/2015
33 363448 APN Trank1 0.000 IGL02897 9 111367517 H1536Q T G missense Het probably damaging 0.985 12/18/2015
34 363453 APN Tspan18 0.000 IGL02897 2 93220173 L35P A G missense Het possibly damaging 0.921 12/18/2015
35 363435 APN Ubr4 1.000 IGL02897 4 139472508 V4568M G A missense Het probably damaging 0.974 phenotype 12/18/2015
36 363430 APN Vmn1r63 0.052 IGL02897 7 5802745 V296A A G missense Het possibly damaging 0.511 12/18/2015
[records 1 to 36 of 36]