Incidental Mutations

40 incidental mutations are currently displayed, and affect 40 genes.
6 are Possibly Damaging.
12 are Probably Damaging.
15 are Probably Benign.
5 are Probably Null.
1 create premature stop codons.
3 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 88394 APN Acot12 0.066 IGL01474 G1 13 91772783 K336I A T missense Het possibly damaging 0.529 11/18/2013
2 88383 APN Acsbg2 0.073 IGL01474 G1 17 56861621 I166T A G missense Het possibly damaging 0.898 phenotype 11/18/2013
3 88390 APN Bpifc 0.124 IGL01474 G1 10 86000639 M1L T A start codon destroyed Het probably damaging 0.982 11/18/2013
4 88370 APN Ccnb2 0.669 IGL01474 G1 9 70419023 N44I T A missense Het probably benign 0.000 phenotype 11/18/2013
5 88380 APN Cdc73 1.000 IGL01474 G1 1 143671332 V276M C T missense Het probably benign 0.105 phenotype 11/18/2013
6 88405 APN Cnot7 0.635 IGL01474 G1 8 40507449 A G splice site 6 bp Het probably null phenotype 11/18/2013
7 88384 APN Col11a1 0.867 IGL01474 G1 3 114217134 T A utr 3 prime Het probably benign phenotype 11/18/2013
8 88404 APN Coro1c 0.000 IGL01474 G1 5 113882155 T C splice site Het probably benign phenotype 11/18/2013
9 88403 APN Crocc 0.211 IGL01474 G1 4 141035392 A G splice site Het probably benign phenotype 11/18/2013
10 88391 APN Dync2h1 1.000 IGL01474 G1 9 7102493 Y396N A T missense Het probably benign 0.009 phenotype 11/18/2013
11 88368 APN Gm2888 IGL01474 G1 14 3032041 D116E T A missense Het probably damaging 0.997 11/18/2013
12 88376 APN Gm29326 IGL01474 G1 7 29562589 A T exon Het noncoding transcript 11/18/2013
13 88392 APN Gm9774 0.400 IGL01474 G1 3 92428343 Q351K G T missense Het probably damaging 0.989 11/18/2013
14 88377 APN Greb1 0.000 IGL01474 G1 12 16684501 V1496A A G missense Het probably benign 0.000 phenotype 11/18/2013
15 88402 APN Hdac7 1.000 IGL01474 G1 15 97797939 A G critical splice donor site 2 bp Het probably null phenotype 11/18/2013
16 88395 APN Hectd4 0.904 IGL01474 G1 5 121336649 T2778A A G missense Het possibly damaging 0.528 11/18/2013
17 88393 APN Hist2h2bb 0.395 IGL01474 G1 3 96269809 A G unclassified Het probably benign phenotype 11/18/2013
18 88371 APN Hivep2 0.876 IGL01474 G1 10 14143662 H2059L A T missense Het probably damaging 0.999 phenotype 11/18/2013
19 88387 APN Ift88 1.000 IGL01474 G1 14 57478074 I525F A T missense Het probably benign 0.235 phenotype 11/18/2013
20 88382 APN Itga5 1.000 IGL01474 G1 15 103354270 Q324* G A nonsense Het probably null phenotype 11/18/2013
21 88372 APN Klhl14 0.592 IGL01474 G1 18 21557854 H513P T G missense Het probably damaging 0.985 phenotype 11/18/2013
22 88386 APN Lama5 1.000 IGL01474 G1 2 180196570 D837E A T missense Het probably damaging 0.998 phenotype 11/18/2013
23 88374 APN Mrvi1 0.099 IGL01474 G1 7 110871433 S898T A T missense Het possibly damaging 0.653 phenotype 11/18/2013
24 88369 APN Muc6 0.126 IGL01474 G1 7 141651307 C215F C A missense Het probably damaging 1.000 phenotype 11/18/2013
25 88388 APN Myh15 0.203 IGL01474 G1 16 49132098 K844E A G missense Het probably damaging 0.999 11/18/2013
26 88396 APN Neb 0.762 IGL01474 G1 2 52328905 V31A A G missense Het unknown phenotype 11/18/2013
27 88399 APN Nipbl 0.966 IGL01474 G1 15 8311209 I2009T A G missense Het possibly damaging 0.628 phenotype 11/18/2013
28 88375 APN Olfr700 0.080 IGL01474 G1 7 106805940 I174T A G missense Het probably benign 0.233 phenotype 11/18/2013
29 88378 APN Piwil2 0.000 IGL01474 G1 14 70398218 R536G T C missense Het probably benign 0.347 phenotype 11/18/2013
30 88373 APN Pld3 0.000 IGL01474 G1 7 27532619 V412A A G missense Het probably damaging 0.999 phenotype 11/18/2013
31 88401 APN Prkaa2 0.000 IGL01474 G1 4 105049332 A C critical splice donor site 2 bp Het probably null phenotype 11/18/2013
32 88367 APN Rdh9 0.000 IGL01474 G1 10 127790945 L289P T C missense Het probably damaging 0.996 phenotype 11/18/2013
33 88379 APN Rusc2 0.202 IGL01474 G1 4 43416434 S580L C T missense Het probably damaging 0.975 phenotype 11/18/2013
34 88406 APN Sidt2 0.153 IGL01474 G1 9 45946982 A G critical splice donor site 2 bp Het probably null phenotype 11/18/2013
35 88398 APN Slc18b1 0.067 IGL01474 G1 10 23803850 K92N A T missense Het probably benign 0.350 phenotype 11/18/2013
36 88389 APN Slc20a2 0.082 IGL01474 G1 8 22535557 V92M G A missense Het possibly damaging 0.659 phenotype 11/18/2013
37 88385 APN Slc4a11 0.163 IGL01474 G1 2 130685544 F644I A T missense Het probably damaging 1.000 phenotype 11/18/2013
38 88400 APN Spata31d1d 0.000 IGL01474 G1 13 59730215 A T splice site Het probably benign 11/18/2013
39 88381 APN Spef2 0.120 IGL01474 G1 15 9663158 M846V T C missense Het probably benign 0.001 phenotype 11/18/2013
40 88397 APN Syncrip 0.762 IGL01474 G1 9 88480747 T3A T C missense Het probably benign 0.036 phenotype 11/18/2013
[records 1 to 40 of 40]