Incidental Mutations

27 incidental mutations are currently displayed, and affect 26 genes.
4 are Possibly Damaging.
6 are Probably Damaging.
13 are Probably Benign.
4 are Probably Null.
3 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 27 of 27] 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 88581 APN Adck1 0.000 IGL01480 G1 12 88456865 C379* T A nonsense Het probably null 11/18/2013
2 88583 APN Ankrd10 0.087 IGL01480 G1 8 11635592 V9A A G missense Het probably benign 0.000 11/18/2013
3 88586 APN Ankrd13a 0.138 IGL01480 G1 5 114800818 A T splice site Het probably benign 11/18/2013
4 88574 APN Bbs1 0.723 IGL01480 G1 19 4894393 K403E T C missense Het probably damaging 0.998 phenotype 11/18/2013
5 88571 APN Cd200r2 0.069 IGL01480 G1 16 44909266 I95V A G missense Het probably null 0.996 11/18/2013
6 88565 APN Cyba 0.000 IGL01480 G1 8 122424945 E171G T C missense Het probably benign 0.001 phenotype 11/18/2013
7 88572 APN Dnah2 0.000 IGL01480 G1 11 69458371 M2480L T A missense Het possibly damaging 0.910 phenotype 11/18/2013
8 88566 APN Fxyd7 0.000 IGL01480 G1 7 31047374 Y20* A T nonsense Het probably null phenotype 11/18/2013
9 88568 APN Il22ra1 0.000 IGL01480 G1 4 135744801 V216A T C missense Het probably benign 0.033 phenotype 11/18/2013
10 88588 APN Mapk10 0.000 IGL01480 G1 5 102926152 G A splice site Het probably benign phenotype 11/18/2013
11 88584 APN Mgat5b 0.111 IGL01480 G1 11 116978452 T607K C A missense Het probably benign 0.001 phenotype 11/18/2013
12 88573 APN Nov 0.129 IGL01480 G1 15 54752291 Y284C A G missense Het probably damaging 1.000 phenotype 11/18/2013
13 278523 APN Olfr344 0.083 IGL01480 G1 2 36568742 L48H T A missense Het probably damaging 1.000 phenotype 04/16/2015
14 88578 APN Olfr406 0.055 IGL01480 G1 11 74269601 I71L A T missense Het possibly damaging 0.637 phenotype 11/18/2013
15 88587 APN Olfr8 0.210 IGL01480 G1 10 78956144 T C utr 3 prime Het probably benign phenotype 11/18/2013
16 88582 APN Olfr975 0.060 IGL01480 G1 9 39949988 A261V G A missense Het probably benign 0.014 phenotype 11/18/2013
17 88575 APN Optn 0.192 IGL01480 G1 2 5046018 S184L G A missense Het probably benign 0.008 phenotype 11/18/2013
18 88576 APN Plxna1 0.803 IGL01480 G1 6 89344096 L462P A G missense Het possibly damaging 0.699 phenotype 11/18/2013
19 88579 APN Prkca 0.282 IGL01480 G1 11 107986289 F339L A G missense Het possibly damaging 0.934 phenotype 11/18/2013
20 88570 APN Prkca 0.282 IGL01480 G1 11 108192201 V73M C T missense Het probably damaging 0.999 phenotype 11/18/2013
21 88577 APN Ptch2 0.000 IGL01480 G1 4 117114082 V1062A T C missense Het probably damaging 1.000 phenotype 11/18/2013
22 88564 APN Serpina11 0.060 IGL01480 G1 12 103982851 K354* T A nonsense Het probably null 11/18/2013
23 88589 APN Sf1 1.000 IGL01480 G1 19 6372022 T C unclassified Het probably benign phenotype 11/18/2013
24 88580 APN Stam2 0.000 IGL01480 G1 2 52716439 S112P A G missense Het probably benign 0.000 phenotype 11/18/2013
25 88567 APN Tlr5 0.240 IGL01480 G1 1 182973499 E123K G A missense Het probably benign 0.086 phenotype 11/18/2013
26 88585 APN Tpp1 1.000 IGL01480 G1 7 105749053 E301G T C missense Het probably damaging 1.000 phenotype 11/18/2013
27 88569 APN Vmn2r58 0.314 IGL01480 G1 7 41864692 I176F T A missense Het probably benign 0.013 11/18/2013
[records 1 to 27 of 27]