Incidental Mutations

42 incidental mutations are currently displayed, and affect 41 genes.
4 are Possibly Damaging.
15 are Probably Damaging.
17 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 42 of 42] 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 89459 APN 0610010F05Rik 0.191 IGL01522 G1 11 23582865 (GRCm38) A G critical splice donor site 2 bp Het probably null 2013-12-03
2 89461 APN Adamts12 0.104 IGL01522 G1 15 11065159 (GRCm38) T C critical splice donor site 2 bp Het probably null phenotype 2013-12-03
3 89445 APN Adamts3 1.000 IGL01522 G1 5 89702943 (GRCm38) N579S T C missense Het probably benign 0.140 phenotype 2013-12-03
4 89457 APN Akr1c19 0.000 IGL01522 G1 13 4239099 (GRCm38) A G splice site Het probably benign 2013-12-03
5 89446 APN Ankrd39 0.075 IGL01522 G1 1 36542061 (GRCm38) H69L T A missense Het probably damaging 0.979 2013-12-03
6 89432 APN Apcdd1 0.154 IGL01522 G1 18 62952115 (GRCm38) M461K T A missense Het possibly damaging 0.495 phenotype 2013-12-03
7 89444 APN Bpifa3 0.051 IGL01522 G1 2 154137582 (GRCm38) C209Y G A missense Het probably damaging 1.000 2013-12-03
8 89439 APN Cep131 0.945 IGL01522 G1 11 120067163 (GRCm38) E779G T C missense Het probably benign 0.091 phenotype 2013-12-03
9 89441 APN Cep85 0.949 IGL01522 G1 4 134152255 (GRCm38) Q394R T C missense Het probably damaging 0.998 phenotype 2013-12-03
10 89442 APN Cep85 0.949 IGL01522 G1 4 134152256 (GRCm38) Q394K G T missense Het probably damaging 0.998 phenotype 2013-12-03
11 89424 APN Clcn6 0.104 IGL01522 G1 4 148017535 (GRCm38) Y364C T C missense Het probably benign 0.445 phenotype 2013-12-03
12 89425 APN Fetub 0.059 IGL01522 G1 16 22929641 (GRCm38) M1I G A start codon destroyed Het probably null 0.102 phenotype 2013-12-03
13 89455 APN Greb1 0.000 IGL01522 G1 12 16701201 (GRCm38) I1003V T C missense Het probably damaging 0.999 phenotype 2013-12-03
14 89456 APN Hsf3 IGL01522 G1 X 96320594 (GRCm38) A G splice site Het probably benign 2013-12-03
15 89449 APN Jcad 0.000 IGL01522 G1 18 4673312 (GRCm38) N358S A G missense Het probably damaging 0.974 2013-12-03
16 89458 APN Kndc1 0.000 IGL01522 G1 7 139913972 (GRCm38) T C splice site Het probably benign phenotype 2013-12-03
17 89460 APN Lama1 1.000 IGL01522 G1 17 67752774 (GRCm38) A T splice site Het probably benign phenotype 2013-12-03
18 89431 APN Mark2 0.900 IGL01522 G1 19 7281238 (GRCm38) V50A A G missense Het probably benign 0.056 phenotype 2013-12-03
19 89434 APN Mmp7 0.152 IGL01522 G1 9 7692228 (GRCm38) W35R T C missense Het probably damaging 1.000 phenotype 2013-12-03
20 89422 APN Ndc80 0.964 IGL01522 G1 17 71499325 (GRCm38) V578A A G missense Het probably benign 0.228 phenotype 2013-12-03
21 89423 APN Nfyc 0.968 IGL01522 G1 4 120781524 (GRCm38) E42G T C missense Het probably damaging 1.000 phenotype 2013-12-03
22 89447 APN Olfr1164 0.113 IGL01522 G1 2 88093016 (GRCm38) K307E T C missense Het possibly damaging 0.480 phenotype 2013-12-03
23 89437 APN Olfr1504 0.068 IGL01522 G1 19 13887358 (GRCm38) L284* A T nonsense Het probably null phenotype 2013-12-03
24 89421 APN Olfr344 0.091 IGL01522 G1 2 36569221 (GRCm38) T208A A G missense Het probably benign 0.004 phenotype 2013-12-03
25 89429 APN Olfr547 0.115 IGL01522 G1 7 102535184 (GRCm38) I146F A T missense Het probably damaging 0.972 phenotype 2013-12-03
26 89420 APN Olfr935 0.057 IGL01522 G1 9 38995100 (GRCm38) C112S A T missense Het probably benign 0.078 phenotype 2013-12-03
27 89453 APN Pcdha11 0.095 IGL01522 G1 18 37185008 (GRCm38) F925L T C missense Het probably damaging 0.999 phenotype 2013-12-03
28 89450 APN Pdcd1 0.055 IGL01522 G1 1 94040846 (GRCm38) R154S T G missense Het probably benign 0.002 phenotype 2013-12-03
29 89426 APN Pepd 0.000 IGL01522 G1 7 34924440 (GRCm38) D87E T A missense Het probably benign 0.000 phenotype 2013-12-03
30 89451 APN Pfn4 0.000 IGL01522 G1 12 4770240 (GRCm38) T30A A G missense Het probably benign 0.007 2013-12-03
31 89448 APN Pgpep1l 0.094 IGL01522 G1 7 68237708 (GRCm38) M48T A G missense Het possibly damaging 0.616 2013-12-03
32 89433 APN Pla2g15 0.253 IGL01522 G1 8 106163116 (GRCm38) N340S A G missense Het probably benign 0.001 phenotype 2013-12-03
33 89443 APN Plcb4 0.000 IGL01522 G1 2 136002627 (GRCm38) D155G A G missense Het probably damaging 1.000 phenotype 2013-12-03
34 89440 APN Plg 0.314 IGL01522 G1 17 12404069 (GRCm38) G499S G A missense Het probably damaging 1.000 phenotype 2013-12-03
35 89454 APN Plin3 0.089 IGL01522 G1 17 56280799 (GRCm38) W305* C T nonsense Het probably null phenotype 2013-12-03
36 89452 APN Polq 0.430 IGL01522 G1 16 37027903 (GRCm38) L291I C A missense Het probably damaging 1.000 phenotype 2013-12-03
37 89436 APN Sdf2l1 0.000 IGL01522 G1 16 17132150 (GRCm38) H54L T A missense Het probably damaging 1.000 2013-12-03
38 89430 APN Slc38a2 0.218 IGL01522 G1 15 96693055 (GRCm38) D276N C T missense Het possibly damaging 0.780 2013-12-03
39 89435 APN Syk 1.000 IGL01522 G1 13 52643061 (GRCm38) T576A A G missense Het probably benign 0.000 phenotype 2013-12-03
40 89428 APN Tas2r119 0.000 IGL01522 G1 15 32178193 (GRCm38) V302I G A missense Het probably benign 0.148 phenotype 2013-12-03
41 89438 APN Uso1 1.000 IGL01522 G1 5 92181419 (GRCm38) F389L T C missense Het probably damaging 0.960 phenotype 2013-12-03
42 89427 APN Wwc2 0.110 IGL01522 G1 8 47868633 (GRCm38) Y482F T A missense Het unknown phenotype 2013-12-03
[records 1 to 42 of 42]