Incidental Mutations

35 incidental mutations are currently displayed, and affect 35 genes.
8 are Possibly Damaging.
15 are Probably Damaging.
10 are Probably Benign.
2 are Probably Null.
2 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 35 of 35] 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 361092 APN 2210408I21Rik 0.000 IGL02823 13 77261955 S194P T C missense Het probably damaging 0.958 12/18/2015
2 361106 APN 3110043O21Rik 0.000 IGL02823 4 35213031 C215S A T missense Het probably damaging 0.981 phenotype 12/18/2015
3 361077 APN Abca7 0.000 IGL02823 10 80008822 D1488E T A missense Het probably damaging 1.000 phenotype 12/18/2015
4 361110 APN Abhd18 0.099 IGL02823 3 40933518 A G splice site Het probably benign 12/18/2015
5 361085 APN Atp6ap1l 0.069 IGL02823 13 90899525 V56A A G missense Het probably benign 0.002 12/18/2015
6 361086 APN Atrip 1.000 IGL02823 9 109061178 Y631H A G missense Het probably damaging 1.000 phenotype 12/18/2015
7 361090 APN Dst 0.417 IGL02823 1 34192083 H3097L A T missense Het possibly damaging 0.834 phenotype 12/18/2015
8 361100 APN Ear1 0.069 IGL02823 14 43819045 S122* G T nonsense Het probably null 12/18/2015
9 361099 APN Eif2a 0.000 IGL02823 3 58548671 A364S G T missense Het probably benign 0.006 phenotype 12/18/2015
10 361079 APN Eps8l2 0.000 IGL02823 7 141342075 D22V A T missense Het probably damaging 0.998 phenotype 12/18/2015
11 361107 APN Fam84b 0.076 IGL02823 15 60823123 D258G T C missense Het probably damaging 0.972 12/18/2015
12 361088 APN Fndc7 0.000 IGL02823 3 108869171 F432S A G missense Het probably damaging 1.000 12/18/2015
13 361109 APN Gemin5 1.000 IGL02823 11 58167705 T C splice site Het probably benign phenotype 12/18/2015
14 361095 APN Grxcr2 0.000 IGL02823 18 41991981 K121E T C missense Het probably damaging 0.999 phenotype 12/18/2015
15 361081 APN Gucy1a2 0.402 IGL02823 9 3894656 I713T T C missense Het possibly damaging 0.787 phenotype 12/18/2015
16 361097 APN Hs3st1 0.140 IGL02823 5 39614757 L181P A G missense Het probably damaging 0.998 phenotype 12/18/2015
17 361078 APN Ksr1 0.162 IGL02823 11 79021403 V627L C A missense Het probably benign 0.347 phenotype 12/18/2015
18 361104 APN Lama2 0.453 IGL02823 10 27001145 N2682D T C missense Het probably damaging 1.000 phenotype 12/18/2015
19 361087 APN Map3k19 0.111 IGL02823 1 127822264 H1117N G T missense Het probably benign 0.010 12/18/2015
20 361082 APN Mdc1 0.944 IGL02823 17 35852923 A1121V C T missense Het probably damaging 0.987 phenotype 12/18/2015
21 361098 APN Nlrp1a 0.161 IGL02823 11 71092423 S1239N C T missense Het probably damaging 0.958 phenotype 12/18/2015
22 361103 APN Olfr322 0.072 IGL02823 11 58665967 M136T T C missense Het possibly damaging 0.952 phenotype 12/18/2015
23 361105 APN Prkra 0.651 IGL02823 2 76630424 A310E G T missense Het probably damaging 1.000 phenotype 12/18/2015
24 361108 APN Prl2c1 0.066 IGL02823 13 27856433 T C splice site Het probably benign 12/18/2015
25 361091 APN Prl7a2 0.063 IGL02823 13 27662751 Y93C T C missense Het possibly damaging 0.947 12/18/2015
26 361096 APN Prob1 0.174 IGL02823 18 35652747 V818E A T missense Het possibly damaging 0.861 12/18/2015
27 361089 APN Rbbp8 1.000 IGL02823 18 11732213 S720G A G missense Het possibly damaging 0.892 phenotype 12/18/2015
28 361080 APN Rexo4 0.000 IGL02823 2 26962477 T149A T C missense Het probably benign 0.062 12/18/2015
29 361094 APN Slc39a2 0.060 IGL02823 14 51895412 Y271N T A missense Het probably damaging 0.999 phenotype 12/18/2015
30 361076 APN Sprr2d IGL02823 3 92340427 C58* T A nonsense Het probably null 12/18/2015
31 361101 APN Srebf2 1.000 IGL02823 15 82199774 G965D G A missense Het possibly damaging 0.870 phenotype 12/18/2015
32 361083 APN Tcof1 1.000 IGL02823 18 60816048 E1265G T C missense Het probably benign 0.002 phenotype 12/18/2015
33 361102 APN Terf2 1.000 IGL02823 8 107072625 N389S T C missense Het possibly damaging 0.893 phenotype 12/18/2015
34 361093 APN Vsig10l 0.138 IGL02823 7 43466464 S410P T C missense Het probably damaging 0.997 12/18/2015
35 361084 APN Vwa3b 0.062 IGL02823 1 37186904 A T utr 3 prime Het probably benign 12/18/2015
[records 1 to 35 of 35]