Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
6 are Possibly Damaging.
9 are Probably Damaging.
16 are Probably Benign.
2 are Probably Null.
0 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 33 of 33] 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 178672 APN Agtr1a 0.000 IGL01870 G1 13 30381327 (GRCm38) D125G A G missense Het probably damaging 1.000 phenotype 2014-05-07
2 178690 APN Arhgap31 0.202 IGL01870 G1 16 38618242 (GRCm38) K300E T C missense Het probably damaging 1.000 phenotype 2014-05-07
3 278959 APN Cma2 0.066 IGL01870 G1 14 55973737 (GRCm38) S162Y C A missense Het probably benign 0.001 2015-04-16
4 178679 APN Cntn4 0.347 IGL01870 G1 6 106489715 (GRCm38) T193A A G missense Het possibly damaging 0.953 phenotype 2014-05-07
5 178685 APN Col22a1 0.000 IGL01870 G1 15 71952528 (GRCm38) M556L T A missense Het probably benign 0.073 phenotype 2014-05-07
6 178680 APN Dld 0.971 IGL01870 G1 12 31335467 (GRCm38) S292P A G missense Het possibly damaging 0.894 phenotype 2014-05-07
7 178695 APN Dnah6 0.123 IGL01870 G1 6 73032569 (GRCm38) D3746E A T missense Het probably benign 0.035 phenotype 2014-05-07
8 178683 APN Eea1 0.261 IGL01870 G1 10 95973986 (GRCm38) T9A A G missense Het probably damaging 0.998 2014-05-07
9 178681 APN Fam102a 0.236 IGL01870 G1 2 32566282 (GRCm38) S319P T C missense Het probably benign 0.010 2014-05-07
10 178677 APN Gbf1 1.000 IGL01870 G1 19 46285669 (GRCm38) K1714R A G missense Het probably benign 0.001 phenotype 2014-05-07
11 278958 APN Gm10718 0.539 IGL01870 G1 9 3025118 (GRCm38) Y194F A T missense Het probably benign 0.001 2015-04-16
12 178682 APN Gm12794 0.048 IGL01870 G1 4 101940690 (GRCm38) L95H T A missense Het probably benign 0.032 2014-05-07
13 178669 APN H2-M1 0.054 IGL01870 G1 17 36670063 (GRCm38) M327K A T missense Het probably benign 0.375 2014-05-07
14 178694 APN Ifnz IGL01870 G1 4 88783311 (GRCm38) S176T T A missense Het possibly damaging 0.780 2014-05-07
15 178678 APN Irak4 0.482 IGL01870 G1 15 94547870 (GRCm38) Y10H T C missense Het probably benign 0.276 phenotype 2014-05-07
16 178673 APN Irx5 0.000 IGL01870 G1 8 92359777 (GRCm38) F163L T C missense Het probably damaging 1.000 phenotype 2014-05-07
17 178670 APN Jak3 0.689 IGL01870 G1 8 71680790 (GRCm38) P376S C T missense Het probably damaging 1.000 phenotype 2014-05-07
18 178684 APN Lrrc25 0.080 IGL01870 G1 8 70617787 (GRCm38) S73P T C missense Het possibly damaging 0.827 2014-05-07
19 178676 APN Macf1 1.000 IGL01870 G1 4 123474113 (GRCm38) G2285D C T missense Het probably damaging 0.991 phenotype 2014-05-07
20 178668 APN Muc4 0.099 IGL01870 G1 16 32753196 (GRCm38) T1025S A T missense Het probably benign 0.015 phenotype 2014-05-07
21 178693 APN Mylk2 0.259 IGL01870 G1 2 152915214 (GRCm38) N303S A G missense Het probably benign 0.205 phenotype 2014-05-07
22 178667 APN Olfr111 0.505 IGL01870 G1 17 37530664 (GRCm38) R229H G A missense Het probably benign 0.004 0.085 phenotype 2014-05-07
23 178675 APN Pcnx 0.000 IGL01870 G1 12 81975893 (GRCm38) V1512A T C missense Het probably benign 0.007 phenotype 2014-05-07
24 178689 APN Phlda3 0.073 IGL01870 G1 1 135766638 (GRCm38) S64G A G missense Het probably benign 0.036 phenotype 2014-05-07
25 178691 APN Pptc7 0.185 IGL01870 G1 5 122313602 (GRCm38) S40R C A missense Het probably damaging 1.000 2014-05-07
26 178696 APN Ptpn4 0.236 IGL01870 G1 1 119675547 (GRCm38) A C critical splice donor site 2 bp Het probably null phenotype 2014-05-07
27 178674 APN Slc10a1 0.000 IGL01870 G1 12 80960528 (GRCm38) M160V T C missense Het probably benign 0.001 phenotype 2014-05-07
28 178692 APN Stac 0.212 IGL01870 G1 9 111572332 (GRCm38) I349V T C missense Het probably benign 0.223 2014-05-07
29 178671 APN Synm 0.000 IGL01870 G1 7 67736118 (GRCm38) S157P A G missense Het possibly damaging 0.862 phenotype 2014-05-07
30 178687 APN Tbc1d9b 0.203 IGL01870 G1 11 50162088 (GRCm38) L924P T C missense Het probably damaging 0.997 2014-05-07
31 178686 APN Tcaf2 0.102 IGL01870 G1 6 42624477 (GRCm38) V883I C T missense Het possibly damaging 0.469 2014-05-07
32 178697 APN Upp1 0.234 IGL01870 G1 11 9125700 (GRCm38) T C critical splice donor site 2 bp Het probably null 0.946 phenotype 2014-05-07
33 178688 APN Whamm 0.000 IGL01870 G1 7 81595974 (GRCm38) T726I C T missense Het probably damaging 0.960 phenotype 2014-05-07
[records 1 to 33 of 33]