Incidental Mutations

42 incidental mutations are currently displayed, and affect 42 genes.
5 are Possibly Damaging.
14 are Probably Damaging.
15 are Probably Benign.
8 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 42 of 42] 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 89979 APN Atp5a1 1.000 IGL01536 G1 18 77780312 T C intron Het probably benign phenotype 12/03/2013
2 89958 APN Ccnc 1.000 IGL01536 G1 4 21732505 I81V A G missense Het probably benign 0.014 phenotype 12/03/2013
3 89974 APN Cep112 0.438 IGL01536 G1 11 108531411 D560G A G missense Het probably null 0.082 phenotype 12/03/2013
4 89959 APN Dis3 1.000 IGL01536 G1 14 99079423 Y826H A G missense Het probably damaging 1.000 12/03/2013
5 89980 APN Dtx2 0.000 IGL01536 G1 5 136010086 A G utr 5 prime Het probably benign phenotype 12/03/2013
6 89966 APN Enpp4 0.187 IGL01536 G1 17 44099603 K361E T C missense Het possibly damaging 0.555 12/03/2013
7 89953 APN Erap1 0.195 IGL01536 G1 13 74662423 K294* A T nonsense Het probably null phenotype 12/03/2013
8 89949 APN Erbb4 1.000 IGL01536 G1 1 68290282 Y636F T A missense Het probably benign 0.001 phenotype 12/03/2013
9 89960 APN Fads1 0.000 IGL01536 G1 19 10194030 Q342K C A missense Het probably benign 0.356 phenotype 12/03/2013
10 89945 APN Fntb 1.000 IGL01536 G1 12 76920130 T447S A T missense Het probably benign 0.000 phenotype 12/03/2013
11 89961 APN Hdac4 1.000 IGL01536 G1 1 91930146 A G utr 3 prime Het probably benign phenotype 12/03/2013
12 89969 APN Kcnh2 0.567 IGL01536 G1 5 24326524 I463T A G missense Het probably damaging 1.000 phenotype 12/03/2013
13 89950 APN Kif13a 0.337 IGL01536 G1 13 46752289 T726K G T missense Het probably damaging 0.962 phenotype 12/03/2013
14 89970 APN Lcmt1 1.000 IGL01536 G1 7 123422743 S275P T C missense Het possibly damaging 0.460 phenotype 12/03/2013
15 89971 APN Lmnb1 1.000 IGL01536 G1 18 56740796 S425P T C missense Het probably benign 0.370 phenotype 12/03/2013
16 89964 APN Lrp1b 0.000 IGL01536 G1 2 41110883 I2224V T C missense Het probably benign 0.012 phenotype 12/03/2013
17 89973 APN Lrrc45 0.183 IGL01536 G1 11 120715584 T173S A T missense Het probably benign 0.009 12/03/2013
18 89968 APN Muc4 0.106 IGL01536 G1 16 32763966 Y2590H T C missense Het possibly damaging 0.931 phenotype 12/03/2013
19 89972 APN Myo18a 1.000 IGL01536 G1 11 77820851 P676L C T missense Het probably damaging 1.000 phenotype 12/03/2013
20 89943 APN Olfr1023 0.068 IGL01536 G1 2 85887600 S267P T C missense Het probably damaging 0.997 phenotype 12/03/2013
21 89941 APN Pcdhb15 0.077 IGL01536 G1 18 37474993 M426T T C missense Het probably benign 0.010 phenotype 12/03/2013
22 89967 APN Pik3cd 0.963 IGL01536 G1 4 149652666 V891A A G missense Het probably damaging 1.000 phenotype 12/03/2013
23 89952 APN Polr1b 1.000 IGL01536 G1 2 129125555 N956S A G missense Het probably benign 0.001 phenotype 12/03/2013
24 89965 APN Ppil3 0.262 IGL01536 G1 1 58444591 M1V T C start codon destroyed Het probably null 0.015 phenotype 12/03/2013
25 89942 APN Rad1 0.938 IGL01536 G1 15 10493200 S238T T A missense Het possibly damaging 0.944 phenotype 12/03/2013
26 89962 APN Shc3 0.121 IGL01536 G1 13 51516559 S51A A C missense Het probably damaging 1.000 phenotype 12/03/2013
27 89976 APN Slc9c1 0.452 IGL01536 G1 16 45589629 T C critical splice donor site 2 bp Het probably null phenotype 12/03/2013
28 89963 APN Smg5 1.000 IGL01536 G1 3 88349245 K273E A G missense Het possibly damaging 0.580 phenotype 12/03/2013
29 89978 APN Sntg1 0.086 IGL01536 G1 1 8583200 C T splice site 5 bp Het probably null phenotype 12/03/2013
30 89948 APN Sstr4 0.145 IGL01536 G1 2 148395880 L137P T C missense Het probably damaging 1.000 phenotype 12/03/2013
31 89946 APN Taar8b 0.121 IGL01536 G1 10 24091595 V234I C T missense Het probably benign 0.000 12/03/2013
32 89957 APN Tbc1d9 0.350 IGL01536 G1 8 83260992 Y860C A G missense Het probably damaging 1.000 12/03/2013
33 89954 APN Tll1 1.000 IGL01536 G1 8 64074289 S399R A T missense Het probably damaging 0.998 phenotype 12/03/2013
34 89977 APN Tns1 0.406 IGL01536 G1 1 73919648 T C splice site Het probably benign phenotype 12/03/2013
35 89955 APN Trim10 0.115 IGL01536 G1 17 36877288 T A unclassified 4557 bp Het probably null phenotype 12/03/2013
36 89975 APN Ttn 1.000 IGL01536 G1 2 76732351 C T critical splice donor site 1 bp Het probably null phenotype 12/03/2013
37 89956 APN Usp43 0.000 IGL01536 G1 11 67855938 D981G T C missense Het probably benign 0.010 12/03/2013
38 89951 APN Vmn2r108 0.074 IGL01536 G1 17 20463281 C554S A T missense Het probably damaging 1.000 12/03/2013
39 89947 APN Vmn2r112 0.113 IGL01536 G1 17 22605155 Y464N T A missense Het probably damaging 1.000 12/03/2013
40 89940 APN Vmn2r31 0.247 IGL01536 G1 7 7384848 K575E T C missense Het probably damaging 0.996 12/03/2013
41 89944 APN Vmn2r50 0.129 IGL01536 G1 7 10037683 C697Y C T missense Het probably damaging 1.000 12/03/2013
42 89981 APN Zcchc8 0.419 IGL01536 G1 5 123720719 A C critical splice donor site 2 bp Het probably null 12/03/2013
[records 1 to 42 of 42]