Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
2 are Possibly Damaging.
13 are Probably Damaging.
14 are Probably Benign.
4 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 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 27588 APN Aak1 0.515 IGL00904 G1 6 86946153 G236C G T missense Het probably damaging 1.000 phenotype 04/17/2013
2 26838 APN Abi1 0.725 IGL00904 G1 2 22941930 R404Q C T missense Het possibly damaging 0.711 phenotype 04/17/2013
3 28308 APN Atp8b3 0.142 IGL00904 G1 10 80528764 G532R C T missense Het probably damaging 1.000 phenotype 04/17/2013
4 29248 APN Bysl 1.000 IGL00904 G1 17 47601871 M331I C T missense Het probably benign 0.250 phenotype 04/17/2013
5 29398 APN Cndp1 0.103 IGL00904 G1 18 84611665 S468P A G missense Het probably benign 0.051 phenotype 04/17/2013
6 28929 APN Esd 0.288 IGL00904 G1 14 74749688 *266W A G makesense Het probably null 04/17/2013
7 26606 APN F5 1.000 IGL00904 G1 1 164194009 V1351A T C missense Het probably benign 0.000 phenotype 04/17/2013
8 27776 APN Fchsd2 0.165 IGL00904 G1 7 101271622 D454G A G missense Het probably benign 0.263 04/17/2013
9 29250 APN Fndc1 0.067 IGL00904 G1 17 7756363 M1415L T A missense Het probably benign 0.355 04/17/2013
10 29036 APN Ghr 0.000 IGL00904 G1 15 3328120 Y222F T A missense Het probably benign 0.003 phenotype 04/17/2013
11 27385 APN Gm6583 0.067 IGL00904 G1 5 112355128 R237* G A nonsense Het probably null 04/17/2013
12 27384 APN Gtf3c2 0.578 IGL00904 G1 5 31172858 S299N C T missense Het probably damaging 0.996 04/17/2013
13 28831 APN Ice1 0.930 IGL00904 G1 13 70602289 D93N C T missense Het probably damaging 1.000 04/17/2013
14 26607 APN Ints7 0.947 IGL00904 G1 1 191596164 T A splice site Het probably null phenotype 04/17/2013
15 26836 APN Kif18a 0.000 IGL00904 G1 2 109292126 D182G A G missense Het probably damaging 1.000 phenotype 04/17/2013
16 28307 APN Mcm9 0.000 IGL00904 G1 10 53622921 H308Q A T missense Het possibly damaging 0.887 phenotype 04/17/2013
17 27777 APN Mesp2 1.000 IGL00904 G1 7 79812653 D319G A G missense Het probably benign 0.000 phenotype 04/17/2013
18 28493 APN Mrpl55 IGL00904 G1 11 59205673 S84T T A missense Het probably benign 0.431 phenotype 04/17/2013
19 26837 APN Mybpc3 0.580 IGL00904 G1 2 91120029 V123A T C missense Het probably benign 0.000 phenotype 04/17/2013
20 29251 APN Myom1 0.000 IGL00904 G1 17 71099949 T C splice site Het probably benign phenotype 04/17/2013
21 27209 APN Nfia 1.000 IGL00904 G1 4 98065386 P325S C T missense Het probably damaging 0.966 phenotype 04/17/2013
22 29252 APN Notch4 0.000 IGL00904 G1 17 34575561 T C critical splice donor site 2 bp Het probably null phenotype 04/17/2013
23 28492 APN Npepps 0.888 IGL00904 G1 11 97258306 V130G A C missense Het probably damaging 0.988 phenotype 04/17/2013
24 28309 APN Olfr1356 0.185 IGL00904 G1 10 78847763 S51T A T missense Het probably damaging 0.997 phenotype 04/17/2013
25 29249 APN Pja2 0.000 IGL00904 G1 17 64283531 T669K G T missense Het probably damaging 1.000 04/17/2013
26 28491 APN Rnf112 0.000 IGL00904 G1 11 61452784 D98E G T missense Het probably damaging 0.998 phenotype 04/17/2013
27 29133 APN Rsl1d1 0.936 IGL00904 G1 16 11199694 T136I G A missense Het probably damaging 0.999 04/17/2013
28 29134 APN Samsn1 0.000 IGL00904 G1 16 75909120 A T splice site Het probably benign phenotype 04/17/2013
29 27208 APN Slc6a9 1.000 IGL00904 G1 4 117864617 L280P T C missense Het probably damaging 1.000 phenotype 04/17/2013
30 27207 APN Svep1 1.000 IGL00904 G1 4 58097398 N1382D T C missense Het probably benign 0.004 phenotype 04/17/2013
31 29247 APN Vmn2r100 0.065 IGL00904 G1 17 19526000 C474G T G missense Het probably damaging 1.000 04/17/2013
32 27775 APN Vmn2r74 0.083 IGL00904 G1 7 85957580 R186H C T missense Het probably benign 0.052 04/17/2013
33 29399 APN Wdr7 0.891 IGL00904 G1 18 63796231 I1046T T C missense Het probably benign 0.428 phenotype 04/17/2013
[records 1 to 33 of 33]