Incidental Mutations

44 incidental mutations are currently displayed, and affect 44 genes.
8 are Possibly Damaging.
13 are Probably Damaging.
20 are Probably Benign.
3 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 44 of 44] 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 73990 APN Abhd18 0.074 IGL01319 G1 3 40933642 V307E T A missense Het probably benign 0.001 10/07/2013
2 73974 APN Bub1b 1.000 IGL01319 G1 2 118614994 I265T T C missense Het possibly damaging 0.485 phenotype 10/07/2013
3 73973 APN Cntnap3 0.059 IGL01319 G1 13 64787837 T404I G A missense Het probably damaging 1.000 phenotype 10/07/2013
4 73993 APN Disc1 0.425 IGL01319 G1 8 125087891 S165P T C missense Het probably damaging 0.991 phenotype 10/07/2013
5 73991 APN Dock1 1.000 IGL01319 G1 7 134789278 F756L T C missense Het probably benign 0.000 phenotype 10/07/2013
6 73962 APN Dock2 0.000 IGL01319 G1 11 34698790 V480A A G missense Het possibly damaging 0.608 phenotype 10/07/2013
7 73988 APN Drc3 0.154 IGL01319 G1 11 60364962 D125G A G missense Het probably null 0.697 10/07/2013
8 73971 APN Emid1 0.108 IGL01319 G1 11 5143859 C96Y C T missense Het probably damaging 1.000 10/07/2013
9 73977 APN F13b 0.000 IGL01319 G1 1 139506793 N99S A G missense Het probably damaging 0.980 phenotype 10/07/2013
10 74002 APN Fam20a 0.000 IGL01319 G1 11 109678458 A G splice site Het probably benign phenotype 10/07/2013
11 73967 APN Fancd2 1.000 IGL01319 G1 6 113584899 T1243K C A missense Het probably damaging 0.979 phenotype 10/07/2013
12 73992 APN Fbxw14 0.159 IGL01319 G1 9 109278791 K172E T C missense Het probably damaging 1.000 10/07/2013
13 73995 APN Gm13941 0.079 IGL01319 G1 2 111094805 T C critical splice acceptor site Het probably null 10/07/2013
14 73961 APN Gtpbp4 0.969 IGL01319 G1 13 8985260 N354K A T missense Het probably benign 0.050 phenotype 10/07/2013
15 73964 APN Igkv2-116 0.215 IGL01319 G1 6 68152404 L50P T C missense Het probably benign 0.102 10/07/2013
16 73969 APN Klrb1-ps1 0.068 IGL01319 G1 6 129116585 P23L C T missense Het possibly damaging 0.913 10/07/2013
17 73989 APN Kng2 0.000 IGL01319 G1 16 23028834 I26F T A missense Het probably damaging 0.988 10/07/2013
18 278271 APN Krt81 0.088 IGL01319 G1 15 101463388 H104Y G A missense Het probably benign 0.001 phenotype 04/16/2015
19 73998 APN Lrpprc 1.000 IGL01319 G1 17 84705412 T C utr 3 prime Het probably benign phenotype 10/07/2013
20 73972 APN Man2a2 0.184 IGL01319 G1 7 80361132 V704M C T missense Het possibly damaging 0.941 phenotype 10/07/2013
21 73981 APN Mbip 0.927 IGL01319 G1 12 56330242 V303A A G missense Het probably benign 0.349 10/07/2013
22 73975 APN Mipep 0.963 IGL01319 G1 14 60843271 M571L A T missense Het probably benign 0.001 phenotype 10/07/2013
23 73983 APN Ncan 0.000 IGL01319 G1 8 70097562 V1188D A T missense Het probably damaging 0.989 phenotype 10/07/2013
24 73963 APN Pcdhb4 0.058 IGL01319 G1 18 37308513 V292A T C missense Het probably benign 0.000 10/07/2013
25 73996 APN Pkd1 1.000 IGL01319 G1 17 24587919 T C unclassified Het probably benign phenotype 10/07/2013
26 73976 APN Ppp2r2c 0.412 IGL01319 G1 5 36947121 S282T T A missense Het possibly damaging 0.818 phenotype 10/07/2013
27 73965 APN Rad54l2 1.000 IGL01319 G1 9 106719046 G231D C T missense Het probably benign 0.183 phenotype 10/07/2013
28 73980 APN Rnf20 1.000 IGL01319 G1 4 49649326 D443E T G missense Het probably damaging 0.993 phenotype 10/07/2013
29 73982 APN Rptor 1.000 IGL01319 G1 11 119891170 M1108V A G missense Het probably benign 0.015 phenotype 10/07/2013
30 73970 APN Serpine2 0.000 IGL01319 G1 1 79810694 V182A A G missense Het probably damaging 0.980 0.805 phenotype 10/07/2013
31 73999 APN Sesn2 0.216 IGL01319 G1 4 132499967 C T splice site Het probably benign phenotype 10/07/2013
32 73986 APN Shank1 0.336 IGL01319 G1 7 44353123 A1422E C A missense Het possibly damaging 0.930 phenotype 10/07/2013
33 74001 APN Slc13a4 0.832 IGL01319 G1 6 35307353 C T splice site 5 bp Het probably null phenotype 10/07/2013
34 73994 APN Snrnp200 1.000 IGL01319 G1 2 127230127 T C splice site Het probably benign phenotype 10/07/2013
35 278270 APN Src 0.899 IGL01319 G1 2 157469503 G461R G A missense Het probably damaging 1.000 phenotype 04/16/2015
36 73978 APN Tbxas1 0.061 IGL01319 G1 6 39017973 I178V A G missense Het probably benign 0.092 phenotype 10/07/2013
37 73987 APN Tmem2 0.803 IGL01319 G1 19 21844757 P1172L C T missense Het possibly damaging 0.774 10/07/2013
38 73997 APN Triml1 0.135 IGL01319 G1 8 43141397 A G utr 5 prime Het probably benign phenotype 10/07/2013
39 73985 APN Tsen2 0.951 IGL01319 G1 6 115576984 Q441L A T missense Het probably damaging 0.999 phenotype 10/07/2013
40 74000 APN Ttc23l 0.083 IGL01319 G1 15 10509406 A G splice site Het probably benign 10/07/2013
41 73979 APN Ttc37 0.415 IGL01319 G1 13 76129379 H491R A G missense Het probably benign 0.293 phenotype 10/07/2013
42 73968 APN Ttn 1.000 IGL01319 G1 2 76881304 T C intron Het probably benign phenotype 10/07/2013
43 73966 APN Vsig10l 0.268 IGL01319 G1 7 43465254 S293L C T missense Het probably damaging 0.999 10/07/2013
44 73984 APN Zcchc13 IGL01319 G1 X 103631000 Q110K C A missense Het possibly damaging 0.901 10/07/2013
[records 1 to 44 of 44]