Incidental Mutations

41 incidental mutations are currently displayed, and affect 41 genes.
6 are Possibly Damaging.
13 are Probably Damaging.
16 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 41 of 41] 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 411591 APN Adgrb3 0.338 IGL03165 1 25094394 I334V T C missense Het probably benign 0.049 phenotype 08/02/2016
2 411589 APN Axdnd1 0.176 IGL03165 1 156378389 Y519F T A missense Het probably benign 0.001 08/02/2016
3 411578 APN C4b 0.000 IGL03165 17 34739955 F500S A G missense Het probably benign 0.129 phenotype 08/02/2016
4 411603 APN Cacng2 0.000 IGL03165 15 77995663 I153N A T missense Het possibly damaging 0.936 phenotype 08/02/2016
5 411587 APN Ces1d 0.000 IGL03165 8 93189519 H160L T A missense Het probably benign 0.021 phenotype 08/02/2016
6 411616 APN Cnnm3 0.151 IGL03165 1 36525232 T G unclassified Het probably benign 08/02/2016
7 411599 APN Ctnna3 0.340 IGL03165 10 64945941 T728A A G missense Het probably damaging 0.984 phenotype 08/02/2016
8 411601 APN Cyp2g1 0.000 IGL03165 7 26809776 V92M G A missense Het possibly damaging 0.940 phenotype 08/02/2016
9 411602 APN Dock2 0.000 IGL03165 11 34687533 V35F C A missense Het probably damaging 0.989 phenotype 08/02/2016
10 411604 APN Eif2a 0.000 IGL03165 3 58548628 Y349* C A nonsense Het probably null phenotype 08/02/2016
11 411614 APN Erp44 0.941 IGL03165 4 48236872 C T critical splice donor site 1 bp Het probably null phenotype 08/02/2016
12 411583 APN Flg2 0.131 IGL03165 3 93214611 H1363Y C T missense Het unknown 08/02/2016
13 411608 APN Flnc 1.000 IGL03165 6 29449378 G1425W G T missense Het probably damaging 1.000 phenotype 08/02/2016
14 411607 APN Frem3 0.109 IGL03165 8 80612529 N484D A G missense Het probably benign 0.260 phenotype 08/02/2016
15 411592 APN Fstl3 0.000 IGL03165 10 79779965 D95G A G missense Het probably benign 0.022 phenotype 08/02/2016
16 411609 APN Gldc 1.000 IGL03165 19 30098993 S1018P A G missense Het possibly damaging 0.605 phenotype 08/02/2016
17 411596 APN Gstk1 0.139 IGL03165 6 42249434 I159S T G missense Het probably benign 0.016 phenotype 08/02/2016
18 411606 APN Herc2 0.907 IGL03165 7 56191912 E3513G A G missense Het probably damaging 0.997 phenotype 08/02/2016
19 411579 APN Hpca 0.158 IGL03165 4 129118590 I51N A T missense Het probably damaging 0.996 phenotype 08/02/2016
20 411588 APN Hsd17b7 1.000 IGL03165 1 169953080 E320K C T missense Het probably damaging 0.975 0.796 phenotype 08/02/2016
21 411610 APN Igkv4-74 IGL03165 6 69185305 T C splice site Het probably benign 08/02/2016
22 411611 APN Kdm7a 0.000 IGL03165 6 39170914 C A splice site Het probably benign phenotype 08/02/2016
23 411580 APN Olfr1040 0.146 IGL03165 2 86146068 L222R A C missense Het possibly damaging 0.907 phenotype 08/02/2016
24 411577 APN Olfr382 0.177 IGL03165 11 73516884 L105* A T nonsense Het probably null phenotype 08/02/2016
25 411576 APN Olfr619 0.062 IGL03165 7 103604011 I119T T C missense Het probably damaging 0.984 phenotype 08/02/2016
26 411612 APN Pa2g4 0.616 IGL03165 10 128559060 A T critical splice donor site 2 bp Het probably null phenotype 08/02/2016
27 411586 APN Pdlim3 0.537 IGL03165 8 45918998 L360Q T A missense Het possibly damaging 0.819 phenotype 08/02/2016
28 411582 APN Pkd1l2 0.000 IGL03165 8 117065745 T436I G A missense Het probably benign 0.070 0.072 phenotype 08/02/2016
29 411584 APN Polk 0.163 IGL03165 13 96516688 Q68L T A missense Het probably benign 0.226 phenotype 08/02/2016
30 411600 APN Ppfia2 0.000 IGL03165 10 106767487 L195R T G missense Het probably damaging 1.000 phenotype 08/02/2016
31 411613 APN Ranbp1 0.000 IGL03165 16 18247281 A T unclassified Het probably benign phenotype 08/02/2016
32 411595 APN Rbm12b1 0.163 IGL03165 4 12145845 R606G A G missense Het possibly damaging 0.936 08/02/2016
33 411590 APN Ryr1 1.000 IGL03165 7 29105040 V488A A G missense Het probably benign 0.223 phenotype 08/02/2016
34 411598 APN Sall2 0.000 IGL03165 14 52314168 D521E A T missense Het probably damaging 0.999 phenotype 08/02/2016
35 411585 APN Sntg1 0.118 IGL03165 1 8445104 C402S A T missense Het probably damaging 0.996 phenotype 08/02/2016
36 411615 APN Spg7 0.135 IGL03165 8 123080812 T C critical splice donor site 2 bp Het probably null phenotype 08/02/2016
37 411605 APN Stk31 0.000 IGL03165 6 49445264 E750K G A missense Het probably damaging 0.977 phenotype 08/02/2016
38 411594 APN Tlr2 0.000 IGL03165 3 83837948 I276T A G missense Het probably benign 0.001 phenotype 08/02/2016
39 411581 APN Trav12-2 0.149 IGL03165 14 53616749 H60L A T missense Het probably benign 0.006 08/02/2016
40 411593 APN Urb1 1.000 IGL03165 16 90780304 L775S A G missense Het probably damaging 0.999 08/02/2016
41 411597 APN Utp14b 0.000 IGL03165 1 78664520 D45G A G missense Het probably damaging 0.967 phenotype 08/02/2016
[records 1 to 41 of 41]