Incidental Mutations

38 incidental mutations are currently displayed, and affect 37 genes.
4 are Possibly Damaging.
14 are Probably Damaging.
15 are Probably Benign.
4 are Probably Null.
0 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 38 of 38] 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 51571 APN Ano1 1.000 IGL01112 G1 7 144637145 I401V T C missense Het possibly damaging 0.520 phenotype 06/21/2013
2 51573 APN Ap2a2 0.332 IGL01112 G1 7 141605019 A T splice site Het probably benign phenotype 06/21/2013
3 52816 APN Apol7c 0.068 IGL01112 G1 15 77526437 D103V T A missense Het probably damaging 0.999 06/21/2013
4 52463 APN Arid4a 0.000 IGL01112 G1 12 71072733 T C critical splice donor site 2 bp Het probably null phenotype 06/21/2013
5 51572 APN Atp2a1 1.000 IGL01112 G1 7 126450307 V521A A G missense Het probably benign 0.127 phenotype 06/21/2013
6 52462 APN Ccdc88c 0.000 IGL01112 G1 12 100916803 D1603E G T missense Het probably benign 0.044 phenotype 06/21/2013
7 51332 APN Clec4f 0.057 IGL01112 G1 6 83653200 I125M T C missense Het probably benign 0.010 phenotype 06/21/2013
8 53184 APN Dsc1 0.104 IGL01112 G1 18 20094622 I520V T C missense Het probably benign 0.023 phenotype 06/21/2013
9 51945 APN Eomes 1.000 IGL01112 G1 9 118482266 A386T G A missense Het probably damaging 1.000 phenotype 06/21/2013
10 53266 APN Gldc 1.000 IGL01112 G1 19 30158513 C T critical splice donor site 1 bp Het probably null phenotype 06/21/2013
11 51125 APN Hectd4 0.845 IGL01112 G1 5 121306950 M1420I G T missense Het probably benign 0.009 06/21/2013
12 50289 APN Hmcn1 0.000 IGL01112 G1 1 150632552 A T splice site Het probably benign phenotype 06/21/2013
13 52461 APN Ighv6-3 0.094 IGL01112 G1 12 114391715 T118I G A missense Het possibly damaging 0.910 06/21/2013
14 52815 APN Krt82 0.056 IGL01112 G1 15 101545523 F250S A G missense Het probably damaging 1.000 phenotype 06/21/2013
15 53071 APN Ltb 0.137 IGL01112 G1 17 35194600 T27A A G missense Het probably benign 0.039 phenotype 06/21/2013
16 51574 APN Mex3b 0.317 IGL01112 G1 7 82869703 S409T T A missense Het probably benign 0.413 phenotype 06/21/2013
17 51570 APN Mki67 0.873 IGL01112 G1 7 135714016 I39N A T missense Het probably damaging 0.998 phenotype 06/21/2013
18 51569 APN Olfr576 0.142 IGL01112 G1 7 102966028 A G splice site Het probably benign phenotype 06/21/2013
19 50753 APN Palmd 0.108 IGL01112 G1 3 116924273 S192P A G missense Het probably damaging 1.000 06/21/2013
20 52692 APN Pcdh20 0.000 IGL01112 G1 14 88467200 M888K A T missense Het probably benign 0.009 phenotype 06/21/2013
21 51126 APN Pclo 0.000 IGL01112 G1 5 14681069 H3195L A T missense Het unknown phenotype 06/21/2013
22 51124 APN Pgm1 0.000 IGL01112 G1 5 64102882 I137F A T missense Het possibly damaging 0.864 phenotype 06/21/2013
23 52938 APN Polq 0.444 IGL01112 G1 16 37017309 N194K T A missense Het probably damaging 1.000 phenotype 06/21/2013
24 52113 APN Rmnd1 0.775 IGL01112 G1 10 4410793 T C unclassified Het probably null phenotype 06/21/2013
25 50547 APN Rnf114 0.000 IGL01112 G1 2 167512539 M180T T C missense Het probably damaging 1.000 06/21/2013
26 51783 APN Sap30 0.631 IGL01112 G1 8 57485089 F165L A G missense Het possibly damaging 0.953 phenotype 06/21/2013
27 53186 APN Scgb3a2 0.072 IGL01112 G1 18 43766994 T A intron Het probably benign phenotype 06/21/2013
28 52691 APN Sftpa1 0.122 IGL01112 G1 14 41132570 N38I A T missense Het probably benign 0.102 phenotype 06/21/2013
29 51331 APN Sumf1 0.204 IGL01112 G1 6 108176016 F137S A G missense Het probably damaging 1.000 phenotype 06/21/2013
30 51946 APN Tln2 0.235 IGL01112 G1 9 67311811 R284L C A missense Het probably damaging 1.000 phenotype 06/21/2013
31 50548 APN Ttn 1.000 IGL01112 G1 2 76710464 R25732S T A missense Het probably damaging 0.985 phenotype 06/21/2013
32 50545 APN Ttn 1.000 IGL01112 G1 2 76740359 R26730Q C T missense Het probably damaging 1.000 phenotype 06/21/2013
33 50546 APN Tubgcp4 1.000 IGL01112 G1 2 121173601 V41A T C missense Het probably benign 0.105 phenotype 06/21/2013
34 50752 APN Usp53 0.171 IGL01112 G1 3 122957718 Q230L T A missense Het probably damaging 0.985 phenotype 06/21/2013
35 51568 APN Vmn2r57 0.134 IGL01112 G1 7 41425043 E532G T C missense Het probably damaging 0.995 06/21/2013
36 51784 APN Vps9d1 0.000 IGL01112 G1 8 123246030 N454K G T missense Het probably damaging 0.998 06/21/2013
37 53185 APN Wdr55 1.000 IGL01112 G1 18 36762079 T C critical splice donor site 2 bp Het probably null phenotype 06/21/2013
38 52937 APN Zfp263 0.163 IGL01112 G1 16 3748912 C76S T A missense Het probably benign 0.090 06/21/2013
[records 1 to 38 of 38]