Incidental Mutations

31 incidental mutations are currently displayed, and affect 31 genes.
6 are Possibly Damaging.
8 are Probably Damaging.
14 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 31 of 31] 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 97432 UTSW Aldh1l2 0.000 R1117 G1 225 N 10 83508623 (GRCm38) T353I G A missense Het probably benign 0.012 phenotype 2014-01-05
2 97408 UTSW Arpc1b 0.000 R1117 G1 225 N 5 145125754 (GRCm38) V226A T C missense Het possibly damaging 0.950 phenotype 2014-01-05
3 97400 UTSW Casz1 1.000 R1117 G1 225 N 4 148934595 (GRCm38) T451K C A missense Het probably damaging 0.996 phenotype 2014-01-05
4 97430 UTSW Ccr4 0.000 R1117 G1 225 N 9 114492017 (GRCm38) V327M C T missense Het probably benign 0.004 phenotype 2014-01-05
5 97386 UTSW Cntrl 0.864 R1117 G1 225 N 2 35127973 (GRCm38) E465G A G missense Het probably damaging 1.000 phenotype 2014-01-05
6 97410 UTSW Cpa1 0.000 R1117 G1 225 N 6 30645261 (GRCm38) D412G A G missense Het probably benign 0.164 phenotype 2014-01-05
7 97368 UTSW Crispld1 0.079 R1117 G1 225 N 1 17749622 (GRCm38) N281K T A missense Het probably benign 0.028 2014-01-05
8 97376 UTSW Cul3 1.000 R1117 G1 225 N 1 80280924 (GRCm38) Q465R T C missense Het probably damaging 0.999 phenotype 2014-01-05
9 97468 UTSW Cyp2c68 0.000 R1117 G1 225 N 19 39712459 (GRCm38) T305M G A missense Het probably damaging 1.000 2014-01-05
10 97390 UTSW Elp4 0.965 R1117 G1 225 N 2 105842311 (GRCm38) D143G T C missense Het probably benign 0.003 phenotype 2014-01-05
11 97394 UTSW Etnppl 0.088 R1117 G1 225 N 3 130634563 (GRCm38) I462M A G missense Het probably benign 0.005 2014-01-05
12 97380 UTSW Fmo4 0.101 R1117 G1 225 N 1 162803663 (GRCm38) V245A A G missense Het probably benign 0.033 phenotype 2014-01-05
13 97443 UTSW Gm4076 0.286 R1117 G1 225 N 13 85127318 (GRCm38) A G exon Het noncoding transcript 2014-01-05
14 97460 UTSW Gm9573 0.076 R1117 G1 221 N 17 35620028 (GRCm38) T C intron Het probably benign 2014-01-05
15 97374 UTSW Gtf3c3 0.965 R1117 G1 225 N 1 54417778 (GRCm38) A488T C T missense Het probably damaging 0.998 0.654 phenotype 2014-01-05
16 97456 UTSW Kcnj15 0.000 R1117 G1 225 N 16 95295625 (GRCm38) M8I G A missense Het probably benign 0.282 phenotype 2014-01-05
17 97414 UTSW Klk1b22 0.052 R1117 G1 225 N 7 44116859 (GRCm38) M255L A T missense Het probably benign 0.004 phenotype 2014-01-05
18 97412 UTSW Mmrn1 0.000 R1117 G1 225 N 6 60976325 (GRCm38) I530K T A missense Het possibly damaging 0.513 phenotype 2014-01-05
19 97444 UTSW Nid2 0.188 R1117 G1 225 N 14 19763664 (GRCm38) A C critical splice acceptor site Het probably null phenotype 2014-01-05
20 97438 UTSW Olfr311 0.088 R1117 G1 225 N 11 58841815 (GRCm38) K234E A G missense Het possibly damaging 0.643 phenotype 2014-01-05
21 97458 UTSW Olfr63 0.085 R1117 G1 225 N 17 33268966 (GRCm38) R81* C T nonsense Het probably null 0.976 phenotype 2014-01-05
22 97420 UTSW Olfr981 0.132 R1117 G1 225 N 9 40022762 (GRCm38) F123S T C missense Het probably damaging 0.994 phenotype 2014-01-05
23 97422 UTSW Peak1 0.336 R1117 G1 225 N 9 56258418 (GRCm38) T742M G A missense Het probably benign 0.045 phenotype 2014-01-05
24 97402 UTSW Sel1l3 0.000 R1117 G1 225 N 5 53172607 (GRCm38) T469S T A missense Het probably benign 0.004 2014-01-05
25 97440 UTSW Sez6 0.000 R1117 G1 225 N 11 77974514 (GRCm38) Y659C A G missense Het probably damaging 1.000 phenotype 2014-01-05
26 97382 UTSW Slc19a2 0.160 R1117 G1 219 N 1 164263456 (GRCm38) I278F A T missense Het possibly damaging 0.858 phenotype 2014-01-05
27 97436 UTSW Slc36a3 0.096 R1117 G1 221 N 11 55146180 (GRCm38) I100V T C missense Het possibly damaging 0.778 2014-01-05
28 97464 UTSW Tcerg1 1.000 R1117 G1 225 N 18 42574652 (GRCm38) D1079G A G missense Het probably damaging 0.991 phenotype 2014-01-05
29 97426 UTSW Trim43c 0.081 R1117 G1 225 N 9 88844977 (GRCm38) S286P T C missense Het probably benign 0.204 0.090 2014-01-05
30 97416 UTSW Umod 0.117 R1117 G1 191 N 7 119477306 (GRCm38) N79S T C missense Het possibly damaging 0.707 phenotype 2014-01-05
31 97462 UTSW Wdr43 0.964 R1117 G1 148 N 17 71616387 (GRCm38) T43A A G missense Het probably benign 0.353 2014-01-05
[records 1 to 31 of 31]