Incidental Mutations

33 incidental mutations are currently displayed, and affect 32 genes.
3 are Possibly Damaging.
12 are Probably Damaging.
11 are Probably Benign.
5 are Probably Null.
3 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 33 of 33] 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 297437 APN Aggf1 0.516 IGL02534 13 95369522 E186K C T missense Het possibly damaging 0.759 phenotype 04/16/2015
2 297424 APN Anks1b 0.000 IGL02534 10 90895117 I932V A G missense Het probably benign 0.448 phenotype 04/16/2015
3 297427 APN Atg2b 0.191 IGL02534 12 105643267 Y1361H A G missense Het probably damaging 1.000 phenotype 04/16/2015
4 297423 APN Bcl9 0.895 IGL02534 3 97215229 L85M G T missense Het probably damaging 0.999 phenotype 04/16/2015
5 297442 APN Bcl9l 0.000 IGL02534 9 44505739 S291R T G missense Het probably benign 0.005 phenotype 04/16/2015
6 297418 APN Cpa2 0.000 IGL02534 6 30550768 D201E T A missense Het probably benign 0.199 phenotype 04/16/2015
7 297429 APN Efna5 0.000 IGL02534 17 62613389 C164* A T nonsense Het probably null phenotype 04/16/2015
8 297425 APN Fam160b2 0.102 IGL02534 14 70585688 H642Q A T missense Het probably damaging 0.980 04/16/2015
9 297436 APN Fam160b2 0.102 IGL02534 14 70586190 H580L T A missense Het probably benign 0.000 04/16/2015
10 297415 APN Gm6316 IGL02534 12 69920989 A G intron Het probably benign 04/16/2015
11 297431 APN Gm996 0.100 IGL02534 2 25577031 S956* G T nonsense Het probably null 0.976 04/16/2015
12 297438 APN Gucy2g 0.000 IGL02534 19 55241068 S57P A G missense Het probably damaging 1.000 phenotype 04/16/2015
13 297434 APN Inf2 0.000 IGL02534 12 112610496 A968E C A missense Het unknown phenotype 04/16/2015
14 297419 APN Man2a2 0.237 IGL02534 7 80359640 A822V G A missense Het probably damaging 0.992 phenotype 04/16/2015
15 297439 APN Mcm5 1.000 IGL02534 8 75114233 V222E T A missense Het probably damaging 0.997 phenotype 04/16/2015
16 297435 APN Muc5b 0.145 IGL02534 7 141844719 Y287C A G missense Het unknown phenotype 04/16/2015
17 297432 APN Olfr1037 0.070 IGL02534 2 86085369 M136T A G missense Het probably damaging 0.999 phenotype 04/16/2015
18 297421 APN Olfr1121 0.061 IGL02534 2 87372254 S241A T G missense Het probably benign 0.000 phenotype 04/16/2015
19 297416 APN Olfr292 0.074 IGL02534 7 86694731 V92M G A missense Het probably benign 0.173 phenotype 04/16/2015
20 297414 APN Olfr538 0.070 IGL02534 7 140574641 M163L A T missense Het probably benign 0.005 phenotype 04/16/2015
21 297422 APN Pabpc1l 0.000 IGL02534 2 164027490 D70G A G missense Het probably damaging 0.999 phenotype 04/16/2015
22 297433 APN Pkhd1 0.125 IGL02534 1 20117720 I3455F T A missense Het probably damaging 0.992 phenotype 04/16/2015
23 297426 APN Ppp1r17 0.000 IGL02534 6 56026460 S86* C A nonsense Het probably null phenotype 04/16/2015
24 297443 APN Rasd1 0.000 IGL02534 11 59964789 M6T A G missense Het possibly damaging 0.862 phenotype 04/16/2015
25 297417 APN Rsph14 0.117 IGL02534 10 74957634 V345F C A missense Het probably damaging 0.966 phenotype 04/16/2015
26 297430 APN Slc11a2 0.416 IGL02534 15 100401326 Q121L T A missense Het probably benign 0.026 phenotype 04/16/2015
27 297444 APN Smc5 1.000 IGL02534 19 23228172 A T critical splice donor site 2 bp Het probably null phenotype 04/16/2015
28 297441 APN Tanc2 1.000 IGL02534 11 105835168 L386P T C missense Het probably damaging 0.996 phenotype 04/16/2015
29 297428 APN Tmem9b 0.207 IGL02534 7 109736957 L160Q A T missense Het probably damaging 1.000 04/16/2015
30 297440 APN Trim32 0.817 IGL02534 4 65614669 T488A A G missense Het possibly damaging 0.724 phenotype 04/16/2015
31 297420 APN Tubb1 0.169 IGL02534 2 174455669 I24V A G missense Het probably benign 0.037 phenotype 04/16/2015
32 297446 APN Upf1 0.966 IGL02534 8 70335652 A T critical splice donor site 2 bp Het probably null phenotype 04/16/2015
33 297445 APN Zfp263 0.130 IGL02534 16 3746415 T A unclassified Het probably benign 04/16/2015
[records 1 to 33 of 33]