Incidental Mutations

40 incidental mutations are currently displayed, and affect 40 genes.
12 are Possibly Damaging.
16 are Probably Damaging.
6 are Probably Benign.
6 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 40 of 40] 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 522531 UTSW 2410131K14Rik 0.184 R6563 G1 212.01 Y 5 118258982 V92A T C missense Het possibly damaging 0.945 0.513 06/06/2018
2 522523 UTSW Arhgap11a 0.000 R6563 G1 225.01 Y 2 113833902 C679S A T missense Het probably benign 0.001 phenotype 06/06/2018
3 522551 UTSW Atg4d 0.000 R6563 G1 225.01 Y 9 21268460 L235F C T missense Het possibly damaging 0.803 phenotype 06/06/2018
4 522577 UTSW Cyp2d22 0.064 R6563 G1 225.01 Y 15 82371912 W174R A T missense Het probably damaging 1.000 0.968 06/06/2018
5 522527 UTSW Cyp4a14 0.072 R6563 G1 225.01 Y 4 115492086 H259L T A missense Het probably benign 0.232 phenotype 06/06/2018
6 522575 UTSW Dennd3 0.145 R6563 G1 225.01 Y 15 73544380 H493L A T missense Het probably damaging 0.984 0.414 06/06/2018
7 522517 UTSW Diexf 0.969 R6563 G1 225.01 Y 1 193118390 R374L C A missense Het probably damaging 1.000 06/06/2018
8 522519 UTSW Dnm1 1.000 R6563 G1 196.01 N 2 32312726 D759V T A missense Het probably damaging 1.000 phenotype 06/06/2018
9 522529 UTSW Dvl1 0.000 R6563 G1 225.01 Y 4 155856253 N443K T A missense Het probably damaging 0.995 phenotype 06/06/2018
10 522549 UTSW Dync2h1 1.000 R6563 G1 225.01 Y 9 7120819 V2156A A G missense Het probably benign 0.267 phenotype 06/06/2018
11 522583 UTSW Enpp5 0.000 R6563 G1 225.01 Y 17 44085264 G356S G A missense Het probably damaging 1.000 0.917 phenotype 06/06/2018
12 522587 UTSW Ermp1 0.000 R6563 G1 225.01 Y 19 29623778 D523G T C missense Het probably damaging 0.999 0.736 phenotype 06/06/2018
13 522525 UTSW Fam83c 0.069 R6563 G1 225.01 Y 2 155830952 V295A A G missense Het probably damaging 0.983 06/06/2018
14 522571 UTSW Gphn 1.000 R6563 G1 225.01 Y 12 78680396 T C critical splice donor site 2 bp Het probably null phenotype 06/06/2018
15 522513 UTSW Irs1 0.592 R6563 G1 225.01 Y 1 82288407 N696I T A missense Het probably damaging 0.984 0.299 phenotype 06/06/2018
16 522535 UTSW Kmt5c 0.000 R6563 G1 225.01 Y 7 4742629 Y96C A G missense Het probably damaging 1.000 phenotype 06/06/2018
17 522579 UTSW Krt77 0.000 R6563 G1 225.01 Y 15 101862923 T315N G T missense Het probably damaging 1.000 0.280 phenotype 06/06/2018
18 522553 UTSW L3mbtl3 1.000 R6563 G1 225.01 Y 10 26302863 A C splice site Het probably null phenotype 06/06/2018
19 522585 UTSW Lama3 1.000 R6563 G1 225.01 Y 18 12537766 Y2409F A T missense Het probably damaging 0.999 0.135 phenotype 06/06/2018
20 522569 UTSW Lrrc9 0.167 R6563 G1 225.01 Y 12 72486395 A G splice site 4 bp Het probably null 06/06/2018
21 522539 UTSW Ltbp4 1.000 R6563 G1 195.01 Y 7 27309063 N1273K A T missense Het probably damaging 0.999 phenotype 06/06/2018
22 522545 UTSW Mfsd13b 0.179 R6563 G1 225.01 Y 7 120995467 A321T G A missense Het probably damaging 0.990 0.647 06/06/2018
23 522521 UTSW Mvb12b 0.848 R6563 G1 225.01 Y 2 33825116 H167Q A T missense Het probably benign 0.037 phenotype 06/06/2018
24 522559 UTSW Myo1g 0.000 R6563 G1 225.01 Y 11 6517146 N230Y T A missense Het possibly damaging 0.907 0.182 phenotype 06/06/2018
25 522557 UTSW Olfr57 0.090 R6563 G1 225.01 Y 10 79035217 R140S A T missense Het possibly damaging 0.667 phenotype 06/06/2018
26 522567 UTSW Prkar2b 0.457 R6563 G1 225.01 Y 12 31993786 G T splice site Het probably null phenotype 06/06/2018
27 522561 UTSW Pwwp2a 0.159 R6563 G1 225.01 Y 11 43705765 A586S G T missense Het possibly damaging 0.880 06/06/2018
28 522541 UTSW Ryr1 1.000 R6563 G1 225.01 Y 7 29095492 V1150A A G missense Het possibly damaging 0.922 phenotype 06/06/2018
29 543445 UTSW Sh3bgr 0.106 R6563 G1 225.01 Y 16 96205943 A G splice site 4 bp Het probably null 12/21/2018
30 522589 UTSW Slk 1.000 R6563 G1 225.01 Y 19 47636469 T C critical splice donor site 2 bp Het probably null phenotype 06/06/2018
31 522555 UTSW Snx3 1.000 R6563 G1 225.01 Y 10 42526036 E82G A G missense Het possibly damaging 0.540 phenotype 06/06/2018
32 522565 UTSW Srcin1 0.000 R6563 G1 112.01 Y 11 97534774 Y486N A T missense Het possibly damaging 0.737 phenotype 06/06/2018
33 522573 UTSW Tecpr2 0.000 R6563 G1 225.01 Y 12 110929087 E336G A G missense Het probably benign 0.002 phenotype 06/06/2018
34 522547 UTSW Terf2ip 1.000 R6563 G1 225.01 Y 8 112018202 V384F G T missense Het probably damaging 0.999 phenotype 06/06/2018
35 522515 UTSW Tnn 0.520 R6563 G1 189.01 Y 1 160088398 S1250C T A missense Het probably damaging 1.000 0.855 06/06/2018
36 522563 UTSW Tspoap1 0.000 R6563 G1 225.01 Y 11 87777159 E1263G A G missense Het possibly damaging 0.865 0.074 Rimbp2tm1.2Geno does not exacerbate the phenotype of the latter single KO. [provided by MGI curators] (source: MGI)">phenotype 06/06/2018
37 522543 UTSW Tubgcp5 0.965 R6563 G1 225.01 Y 7 55825661 R932G A G missense Het possibly damaging 0.903 06/06/2018
38 522537 UTSW Vmn1r175 0.076 R6563 G1 225.01 Y 7 23808605 I199T A G missense Het possibly damaging 0.611 06/06/2018
39 522581 UTSW Vmn1r225 0.062 R6563 G1 225.01 Y 17 20502501 A68V C T missense Het probably benign 0.034 0.183 06/06/2018
40 522533 UTSW Vmn2r24 0.071 R6563 G1 225.01 Y 6 123804178 N448Y A T missense Het possibly damaging 0.858 06/06/2018
[records 1 to 40 of 40]