Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
3 are Possibly Damaging.
10 are Probably Damaging.
16 are Probably Benign.
3 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 33 of 33] 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 46592 UTSW 2700099C18Rik 0.288 R0574 G1 225 Y 17 94761491 T C splice site Het noncoding transcript 0.087 06/11/2013
2 46574 UTSW Abca14 0.000 R0574 G1 225 Y 7 120224497 I416V A G missense Het probably damaging 0.957 0.119 06/11/2013
3 46565 UTSW Actrt3 0.000 R0574 G1 199 Y 3 30599680 E57G T C missense Het probably benign 0.209 0.090 06/11/2013
4 46589 UTSW Adamts5 0.219 R0574 G1 216 Y 16 85899484 S262P A G missense Het probably damaging 0.994 0.164 phenotype 06/11/2013
5 46577 UTSW Aldh1a2 1.000 R0574 G1 225 Y 9 71281708 T C critical splice donor site 2 bp Het probably null 0.948 phenotype 06/11/2013
6 46568 UTSW Arhgap29 1.000 R0574 G1 225 Y 3 122007625 I670V A G missense Het probably benign 0.015 0.090 phenotype 06/11/2013
7 46582 UTSW Bptf 1.000 R0574 G1 178 Y 11 107076527 D1009G T C missense Het probably damaging 0.998 0.067 phenotype 06/11/2013
8 46562 UTSW Ddr2 0.000 R0574 G1 218 Y 1 169981963 G T splice site Het probably benign 0.090 phenotype 06/11/2013
9 46590 UTSW Ift140 1.000 R0574 G1 225 Y 17 25051760 T A splice site Het probably null 0.976 phenotype 06/11/2013
10 46587 UTSW Itga1 0.296 R0574 G1 225 Y 13 114966561 S1111R A C missense Het probably damaging 0.997 0.101 phenotype 06/11/2013
11 46571 UTSW Klk1b27 0.061 R0574 G1 225 Y 7 44056101 L199Q T A missense Het probably damaging 1.000 0.858 phenotype 06/11/2013
12 46564 UTSW Lhx3 1.000 R0574 G1 225 Y 2 26201311 S329G T C missense Het probably benign 0.004 0.060 phenotype 06/11/2013
13 46575 UTSW Man2b1 0.000 R0574 G1 221 Y 8 85096776 M913R T G missense Het probably benign 0.000 0.070 phenotype 06/11/2013
14 46576 UTSW Mmp15 0.000 R0574 G1 196 Y 8 95365401 A80T G A missense Het possibly damaging 0.727 0.181 phenotype 06/11/2013
15 46581 UTSW Mpo 0.000 R0574 G1 225 Y 11 87796076 Y177F A T missense Het probably damaging 0.991 0.413 phenotype 06/11/2013
16 46566 UTSW Mynn 0.455 R0574 G1 225 Y 3 30616739 S587P T C missense Het probably benign 0.013 0.073 phenotype 06/11/2013
17 46570 UTSW Nfkbib 0.209 R0574 G1 225 Y 7 28761788 V145I C T missense Het probably benign 0.276 0.090 phenotype 06/11/2013
18 46563 UTSW Olfr421-ps1 R0574 G1 225 Y 1 174151566 F17L T C missense Het probably benign 0.126 0.293 06/11/2013
19 46588 UTSW Olfr727 0.098 R0574 G1 201 Y 14 50126682 Y35F A T missense Het probably damaging 1.000 0.091 phenotype 06/11/2013
20 46591 UTSW Olfr98 0.062 R0574 G1 225 Y 17 37262881 S261Y G T missense Het probably damaging 1.000 0.316 phenotype 06/11/2013
21 46583 UTSW Pole2 1.000 R0574 G1 225 Y 12 69211457 G A splice site Het probably benign 0.090 phenotype 06/11/2013
22 46593 UTSW Ppargc1b 0.444 R0574 G1 152 Y 18 61302739 G906D C T missense Het probably benign 0.337 0.090 phenotype 06/11/2013
23 46586 UTSW Prl8a2 0.058 R0574 G1 216 Y 13 27348900 C32S T A missense Het probably damaging 1.000 0.647 phenotype 06/11/2013
24 46569 UTSW Rhno1 0.061 R0574 G1 225 Y 6 128358150 A T splice site Het probably null 0.976 06/11/2013
25 46567 UTSW Rprd2 0.680 R0574 G1 225 Y 3 95774357 E408G T C missense Het possibly damaging 0.577 0.074 06/11/2013
26 46584 UTSW Ryr2 1.000 R0574 G1 225 Y 13 11731669 H1999L T A missense Het probably benign 0.021 0.397 phenotype 06/11/2013
27 46578 UTSW Shprh 0.000 R0574 G1 225 Y 10 11163077 T C unclassified Het probably benign 0.090 Pcna. Neither homozygous truncation nor KO affect B cell somatic hypermutation or class switching. [provided by MGI curators] (source: MGI)">phenotype 06/11/2013
28 46579 UTSW Snx3 1.000 R0574 G1 139 Y 10 42502387 N19K T A missense Het probably benign 0.002 0.098 phenotype 06/11/2013
29 46580 UTSW Stx8 0.000 R0574 G1 225 Y 11 67973252 T46M C T missense Het probably damaging 0.987 0.647 phenotype 06/11/2013
30 46572 UTSW Tbc1d17 0.155 R0574 G1 225 Y 7 44843123 A G unclassified Het probably benign 0.090 06/11/2013
31 46573 UTSW Ush1c 0.000 R0574 G1 225 Y 7 46196804 S855P A G missense Het possibly damaging 0.676 0.076 phenotype 06/11/2013
32 192607 UTSW Usp54 0.000 R0574 G1 43 Y 14 20556254 V1338A A G missense Het probably benign 0.005 0.090 05/14/2014
33 46585 UTSW Vmn1r214 0.060 R0574 G1 225 Y 13 23034493 I52M A G missense Het probably benign 0.195 0.090 06/11/2013
[records 1 to 33 of 33]