Incidental Mutations

39 incidental mutations are currently displayed, and affect 38 genes.
4 are Possibly Damaging.
14 are Probably Damaging.
19 are Probably Benign.
2 are Probably Null.
0 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 527330 UTSW Adgrb3 0.493 R6678 G1 225.01 Y 1 25460810 N644S T C missense Het possibly damaging 0.842 phenotype 07/23/2018
2 527339 UTSW Agl 0.230 R6678 G1 225.01 Y 3 116753320 V1294F C A missense Het probably damaging 0.985 phenotype 07/23/2018
3 527349 UTSW Ash2l 1.000 R6678 G1 225.01 Y 8 25833777 W125G A C missense Het probably damaging 1.000 phenotype 07/23/2018
4 527358 UTSW Dap 0.000 R6678 G1 225.01 Y 15 31273250 T51M C T missense Het probably benign 0.001 phenotype 07/23/2018
5 527357 UTSW Dnah12 0.232 R6678 G1 225.01 Y 14 26735692 R871H G A missense Het probably damaging 1.000 07/23/2018
6 527363 UTSW Filip1l 0.000 R6678 G1 225.01 Y 16 57569970 I307T T C missense Het probably benign 0.003 07/23/2018
7 527338 UTSW Gdap1l1 0.205 R6678 G1 214.01 Y 2 163438654 S37T T A missense Het probably benign 0.000 0.164 phenotype 07/23/2018
8 527343 UTSW Gm43302 0.052 R6678 G1 225.01 Y 5 105290954 Q23K G T missense Het probably benign 0.141 07/23/2018
9 527356 UTSW Gm8765 0.086 R6678 G1 225.01 N 13 50701910 K528R A G missense Het probably benign 0.137 07/23/2018
10 527334 UTSW Golga2 0.851 R6678 G1 225.01 Y 2 32299060 V227A T C missense Het probably damaging 0.992 phenotype 07/23/2018
11 527360 UTSW Gramd4 0.000 R6678 G1 225.01 Y 15 86091503 S74C A T missense Het probably damaging 0.993 0.016 phenotype 07/23/2018
12 527361 UTSW Gramd4 0.000 R6678 G1 225.01 Y 15 86091504 S74T G C missense Het possibly damaging 0.519 0.174 phenotype 07/23/2018
13 527344 UTSW Hsph1 0.498 R6678 G1 225.01 Y 5 149618497 S755A A C missense Het probably benign 0.001 phenotype 07/23/2018
14 527348 UTSW Inppl1 0.722 R6678 G1 225.01 Y 7 101832270 V235A A G missense Het probably damaging 0.986 0.224 phenotype 07/23/2018
15 527347 UTSW Kcnc1 0.135 R6678 G1 119.01 Y 7 46397805 H43R A G missense Het probably benign 0.300 phenotype 07/23/2018
16 527336 UTSW Klhl41 0.071 R6678 G1 225.01 Y 2 69670844 S216R T G missense Het probably benign 0.035 phenotype 07/23/2018
17 527342 UTSW Kmt2e 1.000 R6678 G1 191.01 Y 5 23499295 E1162G A G missense Het possibly damaging 0.539 phenotype 07/23/2018
18 527351 UTSW Lrp1 1.000 R6678 G1 221.01 Y 10 127560136 H2422Y G A missense Het probably damaging 0.997 phenotype 07/23/2018
19 527367 UTSW Ms4a13 0.049 R6678 G1 225.01 Y 19 11183858 I106V T C missense Het probably benign 0.336 07/23/2018
20 527364 UTSW Myo1f 0.166 R6678 G1 225.01 Y 17 33575845 D20N G A missense Het probably damaging 0.999 phenotype 07/23/2018
21 527353 UTSW Ndel1 1.000 R6678 G1 225.01 Y 11 68833413 T245A T C missense Het possibly damaging 0.867 phenotype 07/23/2018
22 527337 UTSW Olfr1042 0.056 R6678 G1 225.01 Y 2 86160185 F62I A T missense Het probably damaging 0.978 phenotype 07/23/2018
23 527362 UTSW P2rx6 0.000 R6678 G1 225.01 Y 16 17570956 N360K C A missense Het probably benign 0.002 phenotype 07/23/2018
24 527366 UTSW Pcdhgb5 0.137 R6678 G1 225.01 Y 18 37731202 L17F C T missense Het probably damaging 0.998 0.278 phenotype 07/23/2018
25 527331 UTSW Plcl1 0.849 R6678 G1 225.01 Y 1 55695776 K92R A G missense Het probably benign 0.133 phenotype 07/23/2018
26 527332 UTSW Prelp 0.000 R6678 G1 220.01 Y 1 133914775 D211N C T missense Het probably benign 0.002 0.100 phenotype 07/23/2018
27 527333 UTSW Rgl1 0.333 R6678 G1 225.01 Y 1 152524724 Y677C T C missense Het probably damaging 1.000 phenotype 07/23/2018
28 527354 UTSW Rnd2 0.000 R6678 G1 225.01 Y 11 101468999 L57F C T missense Het probably damaging 1.000 0.218 phenotype 07/23/2018
29 527355 UTSW Rreb1 0.944 R6678 G1 225.01 Y 13 37899699 D113Y G T missense Het probably damaging 1.000 0.370 phenotype 07/23/2018
30 543523 UTSW Sf1 1.000 R6678 G1 225.01 Y 19 6374513 T A splice site Het probably null 0.637 phenotype 02/15/2019
31 527359 UTSW Sh3bp1 0.192 R6678 G1 225.01 Y 15 78908514 T C critical splice donor site 2 bp Het probably null 07/23/2018
32 527350 UTSW Shprh 0.000 R6678 G1 225.01 Y 10 11166545 D757E T A missense Het probably benign 0.158 Pcna. Neither homozygous truncation nor KO affect B cell somatic hypermutation or class switching. [provided by MGI curators] (source: MGI)">phenotype 07/23/2018
33 527345 UTSW Slc6a1 0.123 R6678 G1 225.01 Y 6 114307776 K81R A G missense Het probably benign 0.001 phenotype 07/23/2018
34 527340 UTSW Ttc22 0.060 R6678 G1 172.01 Y 4 106623045 S165R T A missense Het probably benign 0.165 0.119 phenotype 07/23/2018
35 527346 UTSW Vmn1r113 0.059 R6678 G1 225.01 N 7 20787978 G232S G A missense Het probably benign 0.024 07/23/2018
36 527365 UTSW Vwa7 0.054 R6678 G1 225.01 Y 17 35019800 A288D C A missense Het probably damaging 1.000 07/23/2018
37 527352 UTSW Wdpcp 0.263 R6678 G1 225.01 Y 11 21721105 I449V A G missense Het probably benign 0.000 phenotype 07/23/2018
38 527335 UTSW Wdsub1 0.118 R6678 G1 225.01 Y 2 59862631 T313I G A missense Het probably benign 0.452 07/23/2018
39 527341 UTSW Zyg11a 0.182 R6678 G1 225.01 Y 4 108189681 V532A A G missense Het probably benign 0.013 0.006 07/23/2018
[records 1 to 39 of 39]