Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
7 are Possibly Damaging.
7 are Probably Damaging.
11 are Probably Benign.
1 are Probably Null.
0 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 180410 APN 1810011H11Rik 0.062 IGL01930 G1 14 32816857 E92K G A missense Het probably benign 0.119 05/07/2014
2 180422 APN 4930433N12Rik 0.088 IGL01930 G1 9 3134875 C T unclassified Het noncoding transcript 05/07/2014
3 180417 APN Acsf3 0.330 IGL01930 G1 8 122780346 Y126C A G missense Het probably benign 0.032 phenotype 05/07/2014
4 180418 APN Akr1c20 0.000 IGL01930 G1 13 4507648 T A intron Het probably benign 05/07/2014
5 180420 APN Cdan1 1.000 IGL01930 G1 2 120726582 T C intron Het probably benign phenotype 05/07/2014
6 180400 APN Cdc42bpg 0.287 IGL01930 G1 19 6311368 A308V C T missense Het probably damaging 0.998 05/07/2014
7 180408 APN Dek 0.684 IGL01930 G1 13 47088135 I318V T C missense Het probably benign 0.373 phenotype 05/07/2014
8 180415 APN Dvl1 0.000 IGL01930 G1 4 155856188 M422V A G missense Het possibly damaging 0.718 phenotype 05/07/2014
9 180407 APN Erbin 0.000 IGL01930 G1 13 103841172 L626F G A missense Het probably damaging 1.000 phenotype 05/07/2014
10 180409 APN Fa2h 0.373 IGL01930 G1 8 111349304 V229E A T missense Het possibly damaging 0.545 phenotype 05/07/2014
11 180398 APN Gfpt1 1.000 IGL01930 G1 6 87059415 H193Q T A missense Het possibly damaging 0.883 phenotype 05/07/2014
12 279145 APN Gm10717 0.793 IGL01930 G1 9 3025616 S67L C T missense Het probably benign 0.002 04/16/2015
13 180413 APN Gpr162 0.116 IGL01930 G1 6 124861612 L25P A G missense Het possibly damaging 0.820 phenotype 05/07/2014
14 180402 APN Hsd3b5 0.068 IGL01930 G1 3 98622159 T52A T C missense Het probably benign 0.012 05/07/2014
15 180404 APN Megf8 0.920 IGL01930 G1 7 25334861 V668D T A missense Het probably damaging 0.999 phenotype 05/07/2014
16 180405 APN Olfr418 0.103 IGL01930 G1 1 173270610 V145A T C missense Het probably benign 0.000 phenotype 05/07/2014
17 180406 APN Prkdc 0.954 IGL01930 G1 16 15698887 T1042A A G missense Het probably damaging 1.000 phenotype 05/07/2014
18 180414 APN Rasgrf2 0.245 IGL01930 G1 13 91982738 S735P A G missense Het probably damaging 0.975 phenotype 05/07/2014
19 180403 APN Serpina3n 0.000 IGL01930 G1 12 104408972 L101H T A missense Het probably damaging 1.000 05/07/2014
20 180412 APN Sipa1l2 0.346 IGL01930 G1 8 125419239 D1674G T C missense Het probably damaging 0.989 phenotype 05/07/2014
21 180399 APN Sval3 0.102 IGL01930 G1 6 41972521 N98D A G missense Het probably benign 0.000 05/07/2014
22 180397 APN Tbc1d16 0.000 IGL01930 G1 11 119156075 R449C G A missense Het possibly damaging 0.695 05/07/2014
23 180416 APN Tm7sf3 0.149 IGL01930 G1 6 146610933 I321S A C missense Het possibly damaging 0.711 05/07/2014
24 180419 APN Trappc13 0.819 IGL01930 G1 13 104148078 A G splice site Het probably benign 05/07/2014
25 279146 APN Vmn2r-ps159 0.776 IGL01930 G1 4 156338254 C T exon Het noncoding transcript 04/16/2015
26 180421 APN Wdr60 1.000 IGL01930 G1 12 116225963 A G critical splice donor site 2 bp Het probably null phenotype 05/07/2014
27 180411 APN Wdr76 0.194 IGL01930 G1 2 121510822 D116G A G missense Het possibly damaging 0.820 05/07/2014
28 180401 APN Zscan18 0.081 IGL01930 G1 7 12775348 T C unclassified Het probably benign 05/07/2014
[records 1 to 28 of 28]