Incidental Mutations

32 incidental mutations are currently displayed, and affect 32 genes.
4 are Possibly Damaging.
6 are Probably Damaging.
18 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 32 of 32] 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 178426 APN Afg1l 0.107 IGL01863 G1 10 42339911 I326F T A missense Het possibly damaging 0.864 phenotype 05/07/2014
2 178428 APN Aimp1 0.812 IGL01863 G1 3 132672092 T171A T C missense Het probably benign 0.033 phenotype 05/07/2014
3 178429 APN Armc4 0.221 IGL01863 G1 18 7222617 T551A T C missense Het probably damaging 0.998 phenotype 05/07/2014
4 178418 APN Ash1l 1.000 IGL01863 G1 3 88985506 L1564* T A nonsense Het probably null phenotype 05/07/2014
5 178408 APN Atp1a1 1.000 IGL01863 G1 3 101591889 Y131* G T nonsense Het probably null phenotype 05/07/2014
6 178424 APN Celsr2 0.000 IGL01863 G1 3 108394022 E2686G T C missense Het probably benign 0.004 phenotype 05/07/2014
7 178416 APN Cyp4f18 0.000 IGL01863 G1 8 71989926 V395A A G missense Het possibly damaging 0.489 phenotype 05/07/2014
8 178413 APN Ephb2 0.731 IGL01863 G1 4 136659777 Q713R T C missense Het probably benign 0.032 phenotype 05/07/2014
9 178411 APN Esf1 0.937 IGL01863 G1 2 140120679 M824K A T missense Het probably benign 0.001 05/07/2014
10 178431 APN Fam46c 1.000 IGL01863 G1 3 100472664 D259N C T missense Het probably benign 0.047 phenotype 05/07/2014
11 178436 APN Fat4 1.000 IGL01863 G1 3 38970619 T C splice site Het probably benign phenotype 05/07/2014
12 178430 APN Gem 0.214 IGL01863 G1 4 11705980 I23V A G missense Het probably benign 0.000 phenotype 05/07/2014
13 278936 APN Gm10718 0.600 IGL01863 G1 9 3025118 Y194F A T missense Het probably benign 0.001 04/16/2015
14 278937 APN Gm5862 0.199 IGL01863 G1 5 26022771 W41G A C missense Het probably benign 0.000 04/16/2015
15 178414 APN Il6st 1.000 IGL01863 G1 13 112504210 E779G A G missense Het possibly damaging 0.880 phenotype 05/07/2014
16 178435 APN Lama3 1.000 IGL01863 G1 18 12419936 T A splice site Het probably benign phenotype 05/07/2014
17 178427 APN Lipi 0.072 IGL01863 G1 16 75550226 I435R A C missense Het probably damaging 0.999 phenotype 05/07/2014
18 178432 APN Lrrc6 0.230 IGL01863 G1 15 66396974 A T splice site Het probably benign phenotype 05/07/2014
19 178422 APN Olfr291 0.054 IGL01863 G1 7 84856411 L14P T C missense Het probably damaging 1.000 phenotype 05/07/2014
20 178423 APN Omg 1.000 IGL01863 G1 11 79502224 M269I C T missense Het probably benign 0.000 phenotype 05/07/2014
21 178434 APN Optn 0.256 IGL01863 G1 2 5021487 A T splice site Het probably benign phenotype 05/07/2014
22 178419 APN Pex1 0.564 IGL01863 G1 5 3606066 T298A A G missense Het probably benign 0.010 phenotype 05/07/2014
23 178412 APN Rab27b 0.000 IGL01863 G1 18 69989554 R111S T A missense Het probably damaging 1.000 phenotype 05/07/2014
24 178417 APN Rhbdf1 0.137 IGL01863 G1 11 32213484 E329D T G missense Het probably benign 0.000 phenotype 05/07/2014
25 178421 APN Slc2a13 0.000 IGL01863 G1 15 91516492 I176V T C missense Het probably benign 0.003 05/07/2014
26 178410 APN Slc30a1 1.000 IGL01863 G1 1 191909084 C281S T A missense Het probably damaging 1.000 phenotype 05/07/2014
27 178420 APN Slc4a7 0.883 IGL01863 G1 14 14762430 C509S T A missense Het probably damaging 0.974 phenotype 05/07/2014
28 178415 APN Slfn9 0.064 IGL01863 G1 11 82981325 R862G T C missense Het probably benign 0.273 05/07/2014
29 178425 APN Tbc1d2 0.138 IGL01863 G1 4 46607064 I782T A G missense Het possibly damaging 0.659 05/07/2014
30 278938 APN Vmn2r-ps159 0.716 IGL01863 G1 4 156338254 C T exon Het noncoding transcript 04/16/2015
31 178433 APN Vps33b 1.000 IGL01863 G1 7 80274311 T C critical splice donor site 2 bp Het probably null phenotype 05/07/2014
32 178409 APN Wrap73 0.707 IGL01863 G1 4 154145333 I54V A G missense Het probably benign 0.018 phenotype 05/07/2014
[records 1 to 32 of 32]