Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
4 are Possibly Damaging.
14 are Probably Damaging.
10 are Probably Benign.
4 are Probably Null.
1 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 332367 APN Abca16 0.000 IGL00417 G1 7 120423759 I39M A G missense Het probably benign 0.078 08/05/2015
2 7039 APN Acoxl 0.000 IGL00417 G1 2 127978804 C92Y G A missense Het probably damaging 1.000 04/20/2012
3 5518 APN Actl6b 0.752 IGL00417 G1 5 137554637 R76L G T missense Het probably damaging 0.994 phenotype 04/20/2012
4 4112 APN Ank 0.454 IGL00417 G1 15 27544351 M66T T C missense Het possibly damaging 0.528 phenotype 04/20/2012
5 29014 APN C6 0.098 IGL00417 G1 15 4759967 A298V C T missense Het possibly damaging 0.529 phenotype 04/17/2013
6 3426 APN Clip4 0.131 IGL00417 G1 17 71849942 N591Y A T missense Het probably damaging 0.999 04/20/2012
7 7400 APN Cntnap5b 0.145 IGL00417 G1 1 100050754 I165T T C missense Het probably damaging 0.999 04/20/2012
8 7363 APN Dennd1b 0.000 IGL00417 G1 1 139062940 R214H G A missense Het probably damaging 1.000 phenotype 04/20/2012
9 5139 APN Eri2 0.183 IGL00417 G1 7 119787741 T185I G A missense Het probably benign 0.444 04/20/2012
10 4412 APN Fbxo33 0.000 IGL00417 G1 12 59202670 V476A A G missense Het probably damaging 0.997 phenotype 04/20/2012
11 6992 APN Fer1l4 0.000 IGL00417 G1 2 156019920 R1826* G A nonsense Het probably null 04/20/2012
12 4130 APN Fyb 0.000 IGL00417 G1 15 6580777 K277I A T missense Het probably damaging 0.991 phenotype 04/20/2012
13 4338 APN Gli3 1.000 IGL00417 G1 13 15644299 H229N C A missense Het probably damaging 0.999 phenotype 04/20/2012
14 7351 APN Hmcn1 0.000 IGL00417 G1 1 150677278 I2554V T C missense Het probably benign 0.000 phenotype 04/20/2012
15 332368 APN Maml2 0.000 IGL00417 G1 9 13621604 A T unclassified Het probably benign 08/05/2015
16 7499 APN Map4k4 1.000 IGL00417 G1 1 40014532 F930L T C missense Het possibly damaging 0.915 phenotype 04/20/2012
17 7217 APN Mmadhc 0.512 IGL00417 G1 2 50289031 D125G T C missense Het probably benign 0.000 phenotype 04/20/2012
18 5848 APN Nipbl 0.963 IGL00417 G1 15 8366673 S139P A G missense Het probably damaging 0.978 phenotype 04/20/2012
19 332366 APN Obscn 0.687 IGL00417 G1 11 59006788 L6647P A G missense Het unknown phenotype 08/05/2015
20 4060 APN Ppara 0.000 IGL00417 G1 15 85801067 H406N C A missense Het probably benign 0.001 phenotype 04/20/2012
21 5318 APN Psg27 0.000 IGL00417 G1 7 18561917 H201L T A missense Het probably benign 0.216 04/20/2012
22 7102 APN Qser1 0.385 IGL00417 G1 2 104786903 I1188N A T missense Het probably damaging 1.000 04/20/2012
23 7341 APN Rc3h1 0.304 IGL00417 G1 1 160955981 T C critical splice donor site 2 bp Het probably null phenotype 04/20/2012
24 7409 APN Sept2 0.934 IGL00417 G1 1 93499142 H158Y C T missense Het probably damaging 1.000 04/20/2012
25 332365 APN Snx9 0.765 IGL00417 G1 17 5891897 Q100K C A missense Het probably benign 0.028 phenotype 08/05/2015
26 6903 APN Spata5 1.000 IGL00417 G1 3 37451802 I677V A G missense Het possibly damaging 0.600 phenotype 04/20/2012
27 5434 APN Thnsl2 0.126 IGL00417 G1 6 71131900 T309I G A missense Het probably damaging 0.999 phenotype 04/20/2012
28 7382 APN Thsd7b 0.239 IGL00417 G1 1 129595834 R125G A G missense Het probably damaging 1.000 04/20/2012
29 7066 APN Tmem62 0.298 IGL00417 G1 2 121006964 T G unclassified Het probably null 04/20/2012
30 5466 APN Tnpo3 1.000 IGL00417 G1 6 29578461 A T critical splice donor site 2 bp Het probably null phenotype 04/20/2012
31 4941 APN Trpc6 0.000 IGL00417 G1 9 8680438 D889V A T missense Het probably damaging 1.000 phenotype 04/20/2012
32 5815 APN Tubgcp6 0.964 IGL00417 G1 15 89104008 V913L C A missense Het probably benign 0.004 phenotype 04/20/2012
33 6736 APN Uox 0.491 IGL00417 G1 3 146627810 M255L A T missense Het probably benign 0.002 phenotype 04/20/2012
[records 1 to 33 of 33]