Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
2 are Possibly Damaging.
7 are Probably Damaging.
13 are Probably Benign.
5 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 28 of 28] 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 184322 APN Adam26a 0.000 IGL02030 G1 8 43568857 D532G T C missense Het probably benign 0.003 phenotype 05/07/2014
2 184328 APN Adam29 0.087 IGL02030 G1 8 55872122 M432I C T missense Het probably benign 0.351 phenotype 05/07/2014
3 184347 APN Cbs 0.732 IGL02030 G1 17 31625489 A G critical splice donor site 2 bp Het probably null phenotype 05/07/2014
4 184338 APN Ccer1 0.068 IGL02030 G1 10 97693610 Y45C A G missense Het unknown 05/07/2014
5 184323 APN Clu 0.132 IGL02030 G1 14 65975791 G209S G A missense Het probably benign 0.077 phenotype 05/07/2014
6 184334 APN Ddx17 1.000 IGL02030 G1 15 79530376 D530G T C missense Het probably benign 0.000 0.058 phenotype 05/07/2014
7 184349 APN Ddx4 0.567 IGL02030 G1 13 112624777 T C splice site Het probably benign phenotype 05/07/2014
8 184348 APN Fry 0.744 IGL02030 G1 5 150471618 C T splice site Het probably benign 05/07/2014
9 184330 APN Fut10 0.126 IGL02030 G1 8 31235978 Q254* C T nonsense Het probably null 05/07/2014
10 184341 APN Gucy2e 0.295 IGL02030 G1 11 69223816 F1002S A G missense Het probably damaging 0.999 phenotype 05/07/2014
11 184333 APN Hsd3b6 0.087 IGL02030 G1 3 98806173 Y270C T C missense Het probably benign 0.071 05/07/2014
12 184339 APN Jup 1.000 IGL02030 G1 11 100376991 I502T A G missense Het probably damaging 0.965 phenotype 05/07/2014
13 184335 APN Lrrc71 0.000 IGL02030 G1 3 87745224 T A splice site Het probably null 05/07/2014
14 184340 APN Mei1 0.263 IGL02030 G1 15 82115743 V1127A T C missense Het probably benign 0.000 phenotype 05/07/2014
15 184346 APN Ncstn 1.000 IGL02030 G1 1 172072457 A T splice site Het probably benign phenotype 05/07/2014
16 184331 APN Nin 0.000 IGL02030 G1 12 70045268 R756G T C missense Het probably damaging 0.998 phenotype 05/07/2014
17 184345 APN Notch2 1.000 IGL02030 G1 3 98099421 C A splice site Het probably null phenotype 05/07/2014
18 184337 APN Oacyl 0.057 IGL02030 G1 18 65737910 V394A T C missense Het probably damaging 0.994 05/07/2014
19 184332 APN Olfr1444 0.184 IGL02030 G1 19 12862435 F220S T C missense Het probably benign 0.002 phenotype 05/07/2014
20 184326 APN Olfr348 0.054 IGL02030 G1 2 36787398 Y291C A G missense Het probably damaging 1.000 phenotype 05/07/2014
21 184342 APN Olfr524 0.061 IGL02030 G1 7 140202632 I46T A G missense Het probably damaging 0.970 phenotype 05/07/2014
22 184344 APN Parn 0.962 IGL02030 G1 16 13664650 A G splice site 6 bp Het probably null phenotype 05/07/2014
23 184329 APN Rspo3 1.000 IGL02030 G1 10 29500048 E173A T G missense Het probably damaging 0.998 phenotype 05/07/2014
24 184325 APN Rusc2 0.123 IGL02030 G1 4 43416095 V467E T A missense Het possibly damaging 0.862 phenotype 05/07/2014
25 184343 APN Sema7a 0.239 IGL02030 G1 9 57955140 E209K G A missense Het possibly damaging 0.907 phenotype 05/07/2014
26 184324 APN Uchl4 1.000 IGL02030 G1 9 64235629 S131P T C missense Het probably benign 0.000 05/07/2014
27 184327 APN Usp54 0.000 IGL02030 G1 14 20565946 I769V T C missense Het probably benign 0.439 05/07/2014
28 184336 APN Xirp2 0.223 IGL02030 G1 2 67508981 M522T T C missense Het probably benign 0.057 phenotype 05/07/2014
[records 1 to 28 of 28]