Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
4 are Possibly Damaging.
12 are Probably Damaging.
10 are Probably Benign.
3 are Probably Null.
0 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 29 of 29] 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 92317 APN Adgrf5 0.000 IGL01614 G1 17 43424471 S143T T A missense Het possibly damaging 0.530 phenotype 12/09/2013
2 92333 APN Arhgap32 0.000 IGL01614 G1 9 32260505 S1527I G T missense Het probably damaging 0.996 phenotype 12/09/2013
3 278601 APN Atp8a2 0.262 IGL01614 G1 14 60044988 V128A A G missense Het probably damaging 0.994 phenotype 04/16/2015
4 92335 APN Bpi 0.000 IGL01614 G1 2 158271946 F255L T C missense Het probably damaging 0.996 phenotype 12/09/2013
5 92318 APN Clptm1 0.930 IGL01614 G1 7 19637700 D269E A T missense Het probably benign 0.136 12/09/2013
6 92322 APN E2f7 0.185 IGL01614 G1 10 110759978 V63A T C missense Het probably damaging 1.000 phenotype 12/09/2013
7 92329 APN Eif4e1b 0.000 IGL01614 G1 13 54786916 I184N T A missense Het probably damaging 0.999 12/09/2013
8 92338 APN Fam49a 0.458 IGL01614 G1 12 12361573 T C critical splice donor site 2 bp Het probably null 12/09/2013
9 92324 APN Gal3st1 0.000 IGL01614 G1 11 3998996 L401Q T A missense Het probably damaging 0.998 phenotype 12/09/2013
10 92315 APN Gm7808 IGL01614 G1 9 19928146 G A unclassified Het probably benign 12/09/2013
11 92325 APN Hdac5 0.000 IGL01614 G1 11 102200028 T741I G A missense Het probably benign 0.376 phenotype 12/09/2013
12 92316 APN Ipo5 0.921 IGL01614 G1 14 120935095 T522A A G missense Het probably benign 0.011 phenotype 12/09/2013
13 92330 APN Lama5 1.000 IGL01614 G1 2 180180864 F2832V A C missense Het probably damaging 0.997 phenotype 12/09/2013
14 92328 APN Ltk 0.000 IGL01614 G1 2 119753487 L230R A C missense Het probably damaging 1.000 phenotype 12/09/2013
15 92336 APN Mettl14 1.000 IGL01614 G1 3 123373960 A T splice site Het probably benign 12/09/2013
16 92319 APN Myom1 0.000 IGL01614 G1 17 71126178 F1507L T C missense Het possibly damaging 0.456 phenotype 12/09/2013
17 92326 APN Nsd3 0.206 IGL01614 G1 8 25666079 I554K T A missense Het possibly damaging 0.651 phenotype 12/09/2013
18 92320 APN Olfr1044 0.113 IGL01614 G1 2 86171397 I140N A T missense Het possibly damaging 0.900 phenotype 12/09/2013
19 92312 APN Olfr107 0.058 IGL01614 G1 17 37405638 C30Y G A missense Het probably benign 0.005 phenotype 12/09/2013
20 92313 APN Olfr340 0.104 IGL01614 G1 2 36452624 I13S T G missense Het probably benign 0.317 phenotype 12/09/2013
21 92321 APN Olfr644 0.268 IGL01614 G1 7 104068369 V221I C T missense Het probably benign 0.003 phenotype 12/09/2013
22 92311 APN Prr14 0.129 IGL01614 G1 7 127475133 L279H T A missense Het probably damaging 1.000 phenotype 12/09/2013
23 92323 APN Rbm25 1.000 IGL01614 G1 12 83659567 D229Y G T missense Het probably damaging 0.999 12/09/2013
24 92327 APN Sdk2 0.095 IGL01614 G1 11 113793858 K1926E T C missense Het probably damaging 1.000 phenotype 12/09/2013
25 92332 APN Slc25a23 0.000 IGL01614 G1 17 57045579 R435Q C T missense Het probably null 0.978 phenotype 12/09/2013
26 92331 APN Srebf2 1.000 IGL01614 G1 15 82178853 N457S A G missense Het probably benign 0.000 phenotype 12/09/2013
27 92314 APN Stac2 0.149 IGL01614 G1 11 98052948 D12G T C missense Het probably benign 0.103 12/09/2013
28 92337 APN Tal1 1.000 IGL01614 G1 4 115063128 A C critical splice acceptor site Het probably null phenotype 12/09/2013
29 92334 APN Usp25 0.000 IGL01614 G1 16 77077117 R527Q G A missense Het probably damaging 1.000 phenotype 12/09/2013
[records 1 to 29 of 29]