Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
3 are Possibly Damaging.
4 are Probably Damaging.
16 are Probably Benign.
4 are Probably Null.
3 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 27 of 27] 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 8603 APN Adcyap1r1 0.336 IGL00837 G1 6 55461620 T C splice site Het probably benign phenotype 12/06/2012
2 8619 APN Adig IGL00837 G1 2 158502789 F16Y T A missense Het possibly damaging 0.518 12/06/2012
3 8806 APN Alox12e 0.000 IGL00837 G1 11 70321054 T210A T C missense Het probably benign 0.000 12/06/2012
4 8874 APN Ankfy1 1.000 IGL00837 G1 11 72755898 T A splice site Het probably benign phenotype 12/06/2012
5 8546 APN Aoc1 0.000 IGL00837 G1 6 48908664 I701N T A missense Het possibly damaging 0.921 phenotype 12/06/2012
6 9052 APN Armc1 0.192 IGL00837 G1 3 19144420 N125K A C missense Het probably benign 0.210 12/06/2012
7 9252 APN Bcl2a1c 0.213 IGL00837 G1 9 114330492 T113S A T missense Het probably benign 0.005 12/06/2012
8 9534 APN Cdh10 0.102 IGL00837 G1 15 19013404 I697L A T missense Het probably benign 0.000 phenotype 12/06/2012
9 9626 APN Cep350 0.957 IGL00837 G1 1 155953391 S256T A T missense Het probably damaging 0.999 phenotype 12/06/2012
10 9672 APN Chd6 0.796 IGL00837 G1 2 161042079 N82S T C missense Het probably benign 0.006 phenotype 12/06/2012
11 10920 APN Gart 1.000 IGL00837 G1 16 91638720 T C unclassified Het probably benign phenotype 12/06/2012
12 11182 APN Gtf3c6 0.846 IGL00837 G1 10 40254474 A G splice site Het probably benign phenotype 12/06/2012
13 11418 APN Igf1r 1.000 IGL00837 G1 7 68201352 T C splice site Het probably benign phenotype 12/06/2012
14 12120 APN Mtmr6 0.000 IGL00837 G1 14 60280217 Y92* T A nonsense Het probably null 12/06/2012
15 12134 APN Muc13 0.062 IGL00837 G1 16 33807959 K360* A T nonsense Het probably null phenotype 12/06/2012
16 12344 APN Nfyc 0.967 IGL00837 G1 4 120781547 A G intron Het probably benign phenotype 12/06/2012
17 13085 APN Pole 1.000 IGL00837 G1 5 110302009 V774E T A missense Het possibly damaging 0.911 phenotype 12/06/2012
18 13843 APN Rnf217 0.126 IGL00837 G1 10 31503774 L484P A G missense Het probably damaging 0.992 phenotype 12/06/2012
19 14049 APN Slc18a2 1.000 IGL00837 G1 19 59284384 I373F A T missense Het probably benign 0.017 phenotype 12/06/2012
20 14115 APN Slc5a9 0.074 IGL00837 G1 4 111893690 A G intron Het probably benign 12/06/2012
21 14385 APN Tbc1d30 0.000 IGL00837 G1 10 121296845 I205V T C missense Het probably damaging 0.999 12/06/2012
22 14405 APN Tfap2d 0.000 IGL00837 G1 1 19119206 D270V A T missense Het probably damaging 0.999 phenotype 12/06/2012
23 14501 APN Tmem63c 0.099 IGL00837 G1 12 87077197 S483N G A missense Het probably benign 0.000 12/06/2012
24 26576 APN Tor1aip1 1.000 IGL00837 G1 1 156006916 T A utr 3 prime Het probably benign phenotype 04/17/2013
25 14615 APN Tsga10 0.181 IGL00837 G1 1 37801911 A C splice site Het probably benign 12/06/2012
26 14629 APN Ttc21b 1.000 IGL00837 G1 2 66235571 A T critical splice donor site 2 bp Het probably null phenotype 12/06/2012
27 14859 APN Wdr89 0.000 IGL00837 G1 12 75633051 L143* A T nonsense Het probably null phenotype 12/06/2012
[records 1 to 27 of 27]