Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
5 are Possibly Damaging.
11 are Probably Damaging.
11 are Probably Benign.
5 are Probably Null.
1 create premature stop codons.
3 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 306550 APN Acp4 0.087 IGL00157 G1 7 44253451 (GRCm38) V331A A G missense Het possibly damaging 0.558 phenotype 2015-04-16
2 852 APN Casr 1.000 IGL00157 G1 16 36495810 (GRCm38) V633F C A missense Het probably damaging 0.999 phenotype 2011-07-12
3 844 APN Cblb 0.276 IGL00157 G1 16 52183307 (GRCm38) V716G T G missense Het probably benign 0.279 phenotype 2011-07-12
4 725 APN Cbln2 0.083 IGL00157 G1 18 86716384 (GRCm38) Q156* C T nonsense Het probably null phenotype 2011-07-12
5 306555 APN Cnn1 0.000 IGL00157 G1 9 22099397 (GRCm38) L14F G T missense Het possibly damaging 0.950 phenotype 2015-04-16
6 306553 APN D830013O20Rik 0.210 IGL00157 G1 12 73364247 (GRCm38) T C unclassified Het noncoding transcript 2015-04-16
7 1021 APN Drd1 0.407 IGL00157 G1 13 54053878 (GRCm38) S99P A G missense Het probably damaging 1.000 phenotype 2011-07-12
8 974 APN Fam35a 0.082 IGL00157 G1 14 34268625 (GRCm38) V108A A G missense Het probably benign 0.019 2011-07-12
9 306551 APN Fat1 1.000 IGL00157 G1 8 44951670 (GRCm38) V486A T C missense Het possibly damaging 0.956 phenotype 2015-04-16
10 1400 APN Galnt7 0.732 IGL00157 G1 8 57540039 (GRCm38) N416S T C missense Het probably damaging 0.996 phenotype 2011-07-12
11 306554 APN Gm10735 0.059 IGL00157 G1 13 113041484 (GRCm38) T C unclassified Het probably benign 2015-04-16
12 791 APN Gm8909 0.058 IGL00157 G1 17 36165354 (GRCm38) A T critical splice donor site 2 bp Het probably null 2011-07-12
13 1048 APN Jag2 1.000 IGL00157 G1 12 112912718 (GRCm38) T790A T C missense Het probably benign 0.198 phenotype 2011-07-12
14 1080 APN Klhdc1 0.000 IGL00157 G1 12 69242008 (GRCm38) Y31N T A missense Het possibly damaging 0.920 2011-07-12
15 769 APN Lama1 1.000 IGL00157 G1 17 67815928 (GRCm38) M2769L A T missense Het probably benign 0.000 phenotype 2011-07-12
16 698 APN Mms19 0.968 IGL00157 G1 19 41945457 (GRCm38) A G critical splice donor site 2 bp Het probably null 2011-07-12
17 1921 APN Msrb2 0.086 IGL00157 G1 2 19394341 (GRCm38) P172T C A missense Het probably damaging 0.977 2011-07-12
18 1877 APN Olfr228 0.137 IGL00157 G1 2 86483218 (GRCm38) S175G T C missense Het probably benign 0.048 phenotype 2011-07-12
19 1323 APN Olfr955 0.072 IGL00157 G1 9 39470243 (GRCm38) V161A A G missense Het probably benign 0.003 phenotype 2011-07-12
20 744 APN Pcdhb9 0.085 IGL00157 G1 18 37403279 (GRCm38) D775E T A missense Het possibly damaging 0.594 2011-07-12
21 2011 APN Pkhd1 0.104 IGL00157 G1 1 20566874 (GRCm38) T C critical splice acceptor site Het probably null phenotype 2011-07-12
22 1664 APN Preb 0.951 IGL00157 G1 5 30955964 (GRCm38) D375E A T missense Het probably damaging 1.000 phenotype 2011-07-12
23 867 APN Prkdc 0.959 IGL00157 G1 16 15697226 (GRCm38) I1010T T C missense Het probably damaging 0.998 phenotype 2011-07-12
24 1287 APN Rbp2 0.123 IGL00157 G1 9 98498897 (GRCm38) A G splice site 3 bp Het probably null phenotype 2011-07-12
25 2017 APN Sept9 1.000 IGL00157 G1 11 117352184 (GRCm38) T66A A G missense Het probably damaging 1.000 phenotype 2011-07-12
26 1035 APN Serpinb9b 0.000 IGL00157 G1 13 33035625 (GRCm38) E178D A T missense Het probably benign 0.001 2011-07-12
27 918 APN Tg 0.114 IGL00157 G1 15 66847166 (GRCm38) Y258C A G missense Het probably damaging 1.000 phenotype 2011-07-12
28 847 APN Tmprss7 0.084 IGL00157 G1 16 45663368 (GRCm38) R548G T C missense Het probably benign 0.000 2011-07-12
29 1278 APN Uba7 0.148 IGL00157 G1 9 107979111 (GRCm38) A536T G A missense Het probably benign 0.311 phenotype 2011-07-12
30 306549 APN Vmn2r114 0.108 IGL00157 G1 17 23291665 (GRCm38) P614S G A missense Het probably damaging 1.000 2015-04-16
31 1566 APN Xpc 0.434 IGL00157 G1 6 91492264 (GRCm38) A G unclassified Het probably benign phenotype 2011-07-12
32 1703 APN Yrdc 0.959 IGL00157 G1 4 124853961 (GRCm38) S86P T C missense Het probably damaging 1.000 2011-07-12
33 306552 APN Zbed6 IGL00157 G1 1 133657376 (GRCm38) A741D G T missense Het probably damaging 0.999 phenotype 2015-04-16
[records 1 to 33 of 33]