Incidental Mutations

46 incidental mutations are currently displayed, and affect 45 genes.
7 are Possibly Damaging.
17 are Probably Damaging.
17 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 46 of 46] 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 594985 UTSW 0610010F05Rik 0.191 R7717 G1 225.01 N 11 23606757 (GRCm38) C408G A C missense Het probably benign 0.048 2019-11-12
2 595001 UTSW Adgrf5 0.000 R7717 G1 225.01 N 17 43450753 (GRCm38) L1113P T C missense Het probably damaging 1.000 phenotype 2019-11-12
3 595004 UTSW Aldh3b3 0.150 R7717 G1 225.01 N 19 3963970 (GRCm38) L57P T C missense Het probably damaging 1.000 2019-11-12
4 594970 UTSW Asb15 0.000 R7717 G1 225.01 N 6 24559252 (GRCm38) D132G A G missense Het probably benign 0.000 phenotype 2019-11-12
5 594984 UTSW Cep290 0.902 R7717 G1 225.01 N 10 100492681 (GRCm38) R111W C T missense Het probably benign 0.031 phenotype 2019-11-12
6 594999 UTSW Cfap44 0.000 R7717 G1 225.01 N 16 44429935 (GRCm38) D792G A G missense Het probably damaging 0.974 phenotype 2019-11-12
7 594961 UTSW Col20a1 0.000 R7717 G1 225.01 N 2 181007615 (GRCm38) R1029W C T missense Het probably damaging 0.999 2019-11-12
8 594967 UTSW Csf3r 0.317 R7717 G1 225.01 N 4 126037610 (GRCm38) Y462C A G missense Het probably damaging 1.000 phenotype 2019-11-12
9 594996 UTSW Cthrc1 0.000 R7717 G1 156.01 N 15 39077116 (GRCm38) V38A T C missense Het probably benign 0.000 phenotype 2019-11-12
10 594960 UTSW Cxcr2 0.000 R7717 G1 225.01 N 1 74158839 (GRCm38) V164A T C missense Het probably benign 0.052 phenotype 2019-11-12
11 594981 UTSW D230025D16Rik 0.260 R7717 G1 225.01 N 8 105251604 (GRCm38) Q397K C A missense Het probably benign 0.117 2019-11-12
12 594990 UTSW Efr3b 0.000 R7717 G1 225.01 N 12 3984574 (GRCm38) S199P A G missense Het probably damaging 0.997 2019-11-12
13 594965 UTSW Elavl4 0.429 R7717 G1 225.01 N 4 110206466 (GRCm38) C342R A G missense Het probably damaging 1.000 phenotype 2019-11-12
14 594987 UTSW Gemin5 1.000 R7717 G1 225.01 N 11 58151530 (GRCm38) A T critical splice donor site 2 bp Het probably null phenotype 2019-11-12
15 594988 UTSW Gm14190 R7717 G1 225.01 N 11 99690650 (GRCm38) C31S A T missense Het unknown 2019-11-12
16 594972 UTSW Golt1b 0.000 R7717 G1 225.01 N 6 142394043 (GRCm38) V78D T A missense Het probably damaging 1.000 2019-11-12
17 594997 UTSW Gsdmc3 0.058 R7717 G1 225.01 N 15 63869212 (GRCm38) D29V T A missense Het probably damaging 1.000 2019-11-12
18 594992 UTSW Itih1 0.090 R7717 G1 225.01 N 14 30931185 (GRCm38) D766V T A missense Het probably damaging 1.000 phenotype 2019-11-12
19 594962 UTSW Larp1b 0.000 R7717 G1 225.01 N 3 40972444 (GRCm38) S251F C T missense Het probably damaging 0.968 2019-11-12
20 594964 UTSW Lrp8 0.534 R7717 G1 225.01 N 4 107834743 (GRCm38) T115A A G missense Het probably benign 0.003 phenotype 2019-11-12
21 594989 UTSW Lrrc37a 0.098 R7717 G1 225.01 N 11 103504300 (GRCm38) S100P A G missense Het probably benign 0.015 2019-11-12
22 594983 UTSW Lss 1.000 R7717 G1 225.01 N 10 76545452 (GRCm38) V424A T C missense Het possibly damaging 0.883 phenotype 2019-11-12
23 595002 UTSW Ltbp1 1.000 R7717 G1 225.01 N 17 75290078 (GRCm38) V568A T C missense Het possibly damaging 0.898 phenotype 2019-11-12
24 594995 UTSW Myo10 0.000 R7717 G1 225.01 N 15 25731970 (GRCm38) T311S A T missense Het probably benign 0.009 phenotype 2019-11-12
25 594979 UTSW Nsd3 0.247 R7717 G1 225.01 N 8 25682562 (GRCm38) V779A T C missense Het probably benign 0.000 phenotype 2019-11-12
26 594966 UTSW Olfr1335 0.076 R7717 G1 225.01 N 4 118808933 (GRCm38) S310R A T missense Het probably damaging 0.991 phenotype 2019-11-12
27 595000 UTSW Olfr138 0.053 R7717 G1 225.01 N 17 38275580 (GRCm38) Q270K C A missense Het probably damaging 0.999 phenotype 2019-11-12
28 595005 UTSW Olfr1444 0.302 R7717 G1 225.01 N 19 12861795 (GRCm38) I7F A T missense Het probably benign 0.072 phenotype 2019-11-12
29 594976 UTSW Olfr624 0.273 R7717 G1 225.01 N 7 103670945 (GRCm38) T29A T C missense Het probably benign 0.000 phenotype 2019-11-12
30 594977 UTSW Olfr698 0.070 R7717 G1 225.01 N 7 106752636 (GRCm38) W251R A G missense Het possibly damaging 0.577 phenotype 2019-11-12
31 594993 UTSW Olfr748 0.061 R7717 G1 225.01 N 14 50710762 (GRCm38) L144Q T A missense Het probably damaging 1.000 phenotype 2019-11-12
32 594975 UTSW Pak1 0.000 R7717 G1 225.01 N 7 97886348 (GRCm38) D215E T A missense Het probably benign 0.001 phenotype 2019-11-12
33 594982 UTSW Pde7b 0.000 R7717 G1 225.01 N 10 20407191 (GRCm38) F355L A G missense Het probably benign 0.051 phenotype 2019-11-12
34 594998 UTSW Pi4ka 1.000 R7717 G1 225.01 N 16 17376923 (GRCm38) S204P A G missense Het phenotype 2019-11-12
35 594973 UTSW Pirb 0.000 R7717 G1 176.01 N 7 3717783 (GRCm38) K239E T C missense Het not run phenotype 2019-11-12
36 594974 UTSW Pirb 0.000 R7717 G1 116.01 N 7 3717801 (GRCm38) G233R C T missense Het not run phenotype 2019-11-12
37 594994 UTSW Pnp 0.138 R7717 G1 225.01 N 14 50951003 (GRCm38) M211I G A missense Het probably benign 0.001 phenotype 2019-11-12
38 594971 UTSW Pot1a 1.000 R7717 G1 225.01 N 6 25758823 (GRCm38) L319Q A T missense Het probably benign 0.451 phenotype 2019-11-12
39 594980 UTSW Rspry1 0.363 R7717 G1 225.01 N 8 94623122 (GRCm38) C46F G T missense Het probably damaging 0.998 phenotype 2019-11-12
40 595003 UTSW Sec11c 0.000 R7717 G1 225.01 N 18 65812712 (GRCm38) T82M C T missense Het possibly damaging 0.672 2019-11-12
41 594991 UTSW Secisbp2 0.099 R7717 G1 225.01 N 13 51673098 (GRCm38) V414A T C missense Het probably benign 0.002 phenotype 2019-11-12
42 594986 UTSW Tenm2 0.480 R7717 G1 225.01 N 11 36864935 (GRCm38) F79L A G missense Het probably damaging 0.972 phenotype 2019-11-12
43 594963 UTSW Vmn2r2 0.082 R7717 G1 225.01 N 3 64134598 (GRCm38) V232A A G missense Het possibly damaging 0.947 2019-11-12
44 594968 UTSW Zbtb17 1.000 R7717 G1 225.01 N 4 141466083 (GRCm38) S593P T C missense Het probably damaging 0.998 phenotype 2019-11-12
45 594978 UTSW Zfp143 0.946 R7717 G1 225.01 N 7 110086220 (GRCm38) C419G T G missense Het possibly damaging 0.930 phenotype 2019-11-12
46 594969 UTSW Zfp804b 0.140 R7717 G1 225.01 N 5 6771293 (GRCm38) N590S T C missense Het possibly damaging 0.505 2019-11-12
[records 1 to 46 of 46]