Incidental Mutations

39 incidental mutations are currently displayed, and affect 38 genes.
7 are Possibly Damaging.
14 are Probably Damaging.
16 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 39 of 39] 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 104495 APN 1110008L16Rik 0.653 IGL01701 G1 12 55308875 T G splice site Het probably benign 01/21/2014
2 104493 APN 2410089E03Rik 1.000 IGL01701 G1 15 8203257 T C splice site Het probably benign phenotype 01/21/2014
3 104459 APN 4930568D16Rik 0.214 IGL01701 G1 2 35364764 Y36H A G missense Het possibly damaging 0.951 01/21/2014
4 104463 APN Adgrv1 0.000 IGL01701 G1 13 81419631 D5141G T C missense Het possibly damaging 0.553 phenotype 01/21/2014
5 104469 APN Adk 1.000 IGL01701 G1 14 21103854 E42K G A missense Het probably damaging 0.995 phenotype 01/21/2014
6 104474 APN Akap1 0.000 IGL01701 G1 11 88845132 V268L C A missense Het probably benign 0.028 phenotype 01/21/2014
7 104492 APN Arl6ip5 0.109 IGL01701 G1 6 97210813 A G utr 5 prime Het probably benign phenotype 01/21/2014
8 104473 APN Atrx 0.937 IGL01701 G1 X 105830920 S1945P A G missense Het probably damaging 0.999 phenotype 01/21/2014
9 104490 APN Clec5a 0.021 IGL01701 G1 6 40582226 G A splice site Het probably benign phenotype 01/21/2014
10 104464 APN Cul3 1.000 IGL01701 G1 1 80277423 H6Q G T missense Het probably damaging 0.971 phenotype 01/21/2014
11 104471 APN D11Wsu47e 0.079 IGL01701 G1 11 113689101 F441L T C missense Het probably benign 0.271 01/21/2014
12 104460 APN E330021D16Rik 0.255 IGL01701 G1 6 136400806 Y342F T A missense Het probably damaging 0.988 01/21/2014
13 104494 APN Fn1 1.000 IGL01701 G1 1 71629853 T C splice site Het probably benign phenotype 01/21/2014
14 104472 APN Furin 1.000 IGL01701 G1 7 80392492 V452F C A missense Het probably benign 0.112 phenotype 01/21/2014
15 104486 APN Furin 1.000 IGL01701 G1 7 80390759 D777V T A missense Het probably benign 0.001 phenotype 01/21/2014
16 104467 APN Hmgb4 0.274 IGL01701 G1 4 128260373 T134I G A missense Het probably benign 0.012 01/21/2014
17 104487 APN Ift74 0.496 IGL01701 G1 4 94662658 E349V A T missense Het possibly damaging 0.938 phenotype 01/21/2014
18 104457 APN Igkv6-23 0.178 IGL01701 G1 6 70260896 L13Q A T missense Het probably damaging 1.000 01/21/2014
19 104488 APN Lekr1 0.297 IGL01701 G1 3 65684004 Y54F A T missense Het probably damaging 1.000 01/21/2014
20 104476 APN Lman1 0.610 IGL01701 G1 18 65994850 V241E A T missense Het possibly damaging 0.912 phenotype 01/21/2014
21 104465 APN Mat1a 0.120 IGL01701 G1 14 41114815 D167E T A missense Het probably benign 0.000 phenotype 01/21/2014
22 104458 APN Myl6 0.399 IGL01701 G1 10 128492097 A130V G A missense Het probably damaging 0.999 phenotype 01/21/2014
23 104491 APN Myo9a 0.374 IGL01701 G1 9 59884594 T C critical splice donor site 2 bp Het probably null phenotype 01/21/2014
24 104480 APN Nlrp4f 0.249 IGL01701 G1 13 65199409 W12R A T missense Het probably damaging 1.000 01/21/2014
25 104462 APN Nr1h4 0.420 IGL01701 G1 10 89478807 R276G T C missense Het probably benign 0.419 phenotype 01/21/2014
26 104466 APN Olfr1026 0.043 IGL01701 G1 2 85924077 Q270K C A missense Het possibly damaging 0.814 phenotype 01/21/2014
27 104461 APN Olfr1314 0.055 IGL01701 G1 2 112092506 N65S T C missense Het possibly damaging 0.693 phenotype 01/21/2014
28 104484 APN Pag1 0.000 IGL01701 G1 3 9693826 E411K C T missense Het probably damaging 0.966 phenotype 01/21/2014
29 104478 APN Rttn 1.000 IGL01701 G1 18 89064215 N1422D A G missense Het probably damaging 0.999 phenotype 01/21/2014
30 104475 APN Ryr1 1.000 IGL01701 G1 7 29059810 R3345Q C T missense Het probably damaging 0.976 phenotype 01/21/2014
31 104477 APN Slc12a8 0.000 IGL01701 G1 16 33540910 L85P T C missense Het probably damaging 1.000 phenotype 01/21/2014
32 104482 APN Slc22a17 0.174 IGL01701 G1 14 54907261 H565R T C missense Het probably damaging 0.999 01/21/2014
33 104479 APN Slc46a3 0.303 IGL01701 G1 5 147886298 T245A T C missense Het probably benign 0.005 phenotype 01/21/2014
34 104489 APN Thsd7b 0.267 IGL01701 G1 1 129430928 H33R A G missense Het probably benign 0.068 01/21/2014
35 104470 APN Tmem131 0.578 IGL01701 G1 1 36808237 V1260A A G missense Het probably benign 0.017 01/21/2014
36 104483 APN Tmem30a 0.783 IGL01701 G1 9 79774179 F236Y A T missense Het probably damaging 1.000 phenotype 01/21/2014
37 104468 APN Trim30b 0.000 IGL01701 G1 7 104366051 Y43* A C nonsense Het probably null 01/21/2014
38 104481 APN Trpc3 1.000 IGL01701 G1 3 36671594 K78E T C missense Het possibly damaging 0.920 phenotype 01/21/2014
39 104485 APN Twist2 IGL01701 G1 1 91802014 M130L A T missense Het probably benign 0.000 phenotype 01/21/2014
[records 1 to 39 of 39]