Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700066M21Rik |
T |
A |
1: 57,422,302 (GRCm39) |
M226K |
probably benign |
Het |
4921524L21Rik |
T |
G |
18: 6,626,385 (GRCm39) |
S132R |
probably damaging |
Het |
A4gnt |
T |
G |
9: 99,502,335 (GRCm39) |
I165S |
probably damaging |
Het |
Abca14 |
G |
A |
7: 119,877,534 (GRCm39) |
D1061N |
probably benign |
Het |
Abcc9 |
G |
A |
6: 142,617,319 (GRCm39) |
P582S |
probably damaging |
Het |
Abhd5 |
G |
A |
9: 122,208,638 (GRCm39) |
V343I |
probably benign |
Het |
Adam6a |
C |
T |
12: 113,509,192 (GRCm39) |
R522C |
probably damaging |
Het |
Ankle2 |
G |
A |
5: 110,385,590 (GRCm39) |
R313H |
probably damaging |
Het |
Aplf |
G |
A |
6: 87,623,197 (GRCm39) |
T315I |
probably damaging |
Het |
Asic5 |
C |
T |
3: 81,928,383 (GRCm39) |
P491S |
probably benign |
Het |
Atp5f1b |
T |
C |
10: 127,921,391 (GRCm39) |
Y230H |
probably benign |
Het |
B4galt6 |
A |
T |
18: 20,861,099 (GRCm39) |
I51N |
probably damaging |
Het |
Bmal2 |
G |
A |
6: 146,723,632 (GRCm39) |
V321I |
not run |
Het |
C4b |
A |
G |
17: 34,962,633 (GRCm39) |
L23S |
probably damaging |
Het |
Cables2 |
A |
G |
2: 179,902,129 (GRCm39) |
V410A |
|
Het |
Ccdc168 |
T |
A |
1: 44,100,076 (GRCm39) |
K341* |
probably null |
Het |
Cdyl |
A |
G |
13: 36,047,378 (GRCm39) |
M489V |
probably damaging |
Het |
Clip4 |
T |
C |
17: 72,096,996 (GRCm39) |
M40T |
probably damaging |
Het |
Col12a1 |
T |
C |
9: 79,589,348 (GRCm39) |
Y1069C |
probably damaging |
Het |
Col6a3 |
T |
C |
1: 90,755,708 (GRCm39) |
M194V |
probably benign |
Het |
Colec11 |
T |
A |
12: 28,644,714 (GRCm39) |
D260V |
probably damaging |
Het |
Cracdl |
T |
C |
1: 37,653,699 (GRCm39) |
T1036A |
possibly damaging |
Het |
Cux2 |
T |
C |
5: 121,999,319 (GRCm39) |
D1207G |
probably benign |
Het |
Cyp2d34 |
G |
T |
15: 82,501,436 (GRCm39) |
N297K |
possibly damaging |
Het |
Dmbt1 |
A |
G |
7: 130,713,861 (GRCm39) |
Y1643C |
unknown |
Het |
Dnmt3c |
A |
G |
2: 153,556,946 (GRCm39) |
T288A |
probably benign |
Het |
Dock8 |
T |
A |
19: 25,162,245 (GRCm39) |
F1842I |
probably benign |
Het |
Dysf |
A |
G |
6: 84,083,880 (GRCm39) |
I740V |
probably benign |
Het |
Epha6 |
T |
A |
16: 59,736,201 (GRCm39) |
M778L |
probably benign |
Het |
Eri2 |
A |
T |
7: 119,385,739 (GRCm39) |
L254* |
probably null |
Het |
Fam43b |
A |
G |
4: 138,123,152 (GRCm39) |
F56S |
probably damaging |
Het |
Fat4 |
C |
A |
3: 38,943,294 (GRCm39) |
S729* |
probably null |
Het |
Fbxw22 |
C |
A |
9: 109,211,143 (GRCm39) |
W386L |
probably benign |
Het |
Fgd6 |
T |
A |
10: 93,879,909 (GRCm39) |
C254* |
probably null |
Het |
Fgd6 |
C |
A |
10: 93,975,743 (GRCm39) |
T1386K |
probably benign |
Het |
Fkbp7 |
G |
T |
2: 76,502,108 (GRCm39) |
D98E |
possibly damaging |
Het |
Hectd1 |
C |
T |
12: 51,832,635 (GRCm39) |
C913Y |
possibly damaging |
Het |
Hgf |
T |
A |
5: 16,769,841 (GRCm39) |
M105K |
probably benign |
Het |
Icam1 |
A |
C |
9: 20,930,311 (GRCm39) |
D55A |
probably benign |
Het |
Itga2 |
A |
C |
13: 114,993,930 (GRCm39) |
|
probably null |
Het |
Kcnj5 |
A |
C |
9: 32,234,045 (GRCm39) |
L90R |
probably damaging |
Het |
Klra17 |
T |
A |
6: 129,808,555 (GRCm39) |
N226I |
possibly damaging |
Het |
Krt1 |
T |
A |
15: 101,759,064 (GRCm39) |
R33S |
unknown |
Het |
L3mbtl3 |
T |
A |
10: 26,158,728 (GRCm39) |
D615V |
unknown |
Het |
Lrp2 |
T |
A |
2: 69,312,725 (GRCm39) |
Y2521F |
probably benign |
Het |
Megf10 |
A |
T |
18: 57,408,825 (GRCm39) |
N589I |
probably damaging |
Het |
Metap1d |
G |
C |
2: 71,337,129 (GRCm39) |
G14A |
probably benign |
Het |
Mfap5 |
T |
A |
6: 122,505,381 (GRCm39) |
D162E |
probably benign |
Het |
Mixl1 |
T |
C |
1: 180,524,523 (GRCm39) |
I19V |
probably benign |
Het |
Mtrr |
G |
T |
13: 68,716,979 (GRCm39) |
Y411* |
probably null |
Het |
Myh7 |
T |
C |
14: 55,227,482 (GRCm39) |
T318A |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,349,383 (GRCm39) |
Y2348* |
probably null |
Het |
Nhsl3 |
A |
G |
4: 129,119,211 (GRCm39) |
Y170H |
probably damaging |
Het |
Niban2 |
T |
C |
2: 32,812,654 (GRCm39) |
S468P |
possibly damaging |
Het |
Nlrc3 |
T |
C |
16: 3,781,454 (GRCm39) |
S668G |
probably damaging |
Het |
Nutm1 |
G |
A |
2: 112,080,401 (GRCm39) |
R505C |
probably damaging |
Het |
Or10ag59 |
T |
A |
2: 87,406,052 (GRCm39) |
V208E |
probably damaging |
Het |
Or12j2 |
A |
T |
7: 139,916,654 (GRCm39) |
D293V |
possibly damaging |
Het |
Or4c117 |
C |
A |
2: 88,955,180 (GRCm39) |
R298S |
probably benign |
Het |
Pcna |
A |
G |
2: 132,094,797 (GRCm39) |
S54P |
probably benign |
Het |
Pde6a |
A |
G |
18: 61,391,364 (GRCm39) |
T570A |
probably damaging |
Het |
Phf21b |
A |
T |
15: 84,739,918 (GRCm39) |
M1K |
probably null |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Prob1 |
A |
G |
18: 35,786,352 (GRCm39) |
F634S |
possibly damaging |
Het |
Prss50 |
A |
G |
9: 110,690,357 (GRCm39) |
T167A |
probably damaging |
Het |
Ptpn1 |
T |
C |
2: 167,816,692 (GRCm39) |
V249A |
probably damaging |
Het |
Rai1 |
G |
A |
11: 60,079,499 (GRCm39) |
V1188I |
probably benign |
Het |
Ric1 |
G |
A |
19: 29,561,978 (GRCm39) |
|
probably null |
Het |
Robo1 |
C |
T |
16: 72,786,519 (GRCm39) |
Q844* |
probably null |
Het |
Rpn1 |
A |
G |
6: 88,061,619 (GRCm39) |
D36G |
possibly damaging |
Het |
Serpinb1b |
A |
T |
13: 33,277,810 (GRCm39) |
M348L |
probably benign |
Het |
Setd4 |
T |
C |
16: 93,380,830 (GRCm39) |
|
probably null |
Het |
Setd5 |
T |
G |
6: 113,124,518 (GRCm39) |
S1124A |
probably benign |
Het |
Slc35c1 |
C |
A |
2: 92,289,084 (GRCm39) |
V154F |
probably damaging |
Het |
Slc7a6os |
G |
T |
8: 106,937,121 (GRCm39) |
S113* |
probably null |
Het |
Syne2 |
T |
A |
12: 76,149,810 (GRCm39) |
D1787E |
probably benign |
Het |
Tas2r144 |
A |
C |
6: 42,192,373 (GRCm39) |
I38L |
probably damaging |
Het |
Tepsin |
G |
T |
11: 119,982,534 (GRCm39) |
T512K |
possibly damaging |
Het |
Utp20 |
A |
G |
10: 88,606,586 (GRCm39) |
V1662A |
probably benign |
Het |
Vmn1r201 |
C |
T |
13: 22,659,509 (GRCm39) |
A241V |
possibly damaging |
Het |
Vmn2r60 |
T |
A |
7: 41,785,826 (GRCm39) |
S210T |
probably benign |
Het |
Wdr6 |
G |
T |
9: 108,451,784 (GRCm39) |
H700N |
probably damaging |
Het |
Zdhhc8 |
T |
C |
16: 18,052,790 (GRCm39) |
T29A |
probably benign |
Het |
Zfp335 |
A |
G |
2: 164,742,052 (GRCm39) |
I614T |
probably damaging |
Het |
Zfp54 |
T |
A |
17: 21,653,844 (GRCm39) |
S113T |
probably benign |
Het |
Zfp873 |
T |
A |
10: 81,897,071 (GRCm39) |
C601S |
probably damaging |
Het |
Zmynd8 |
T |
C |
2: 165,681,929 (GRCm39) |
T201A |
probably damaging |
Het |
|
Other mutations in Zfyve26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Zfyve26
|
APN |
12 |
79,296,234 (GRCm39) |
unclassified |
probably benign |
|
IGL00940:Zfyve26
|
APN |
12 |
79,327,674 (GRCm39) |
missense |
probably benign |
|
IGL01148:Zfyve26
|
APN |
12 |
79,307,644 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01347:Zfyve26
|
APN |
12 |
79,298,957 (GRCm39) |
splice site |
probably null |
|
IGL01472:Zfyve26
|
APN |
12 |
79,323,117 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01490:Zfyve26
|
APN |
12 |
79,291,147 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01516:Zfyve26
|
APN |
12 |
79,334,625 (GRCm39) |
missense |
probably benign |
0.37 |
IGL01642:Zfyve26
|
APN |
12 |
79,308,348 (GRCm39) |
splice site |
probably null |
|
IGL01689:Zfyve26
|
APN |
12 |
79,330,827 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01877:Zfyve26
|
APN |
12 |
79,334,218 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01997:Zfyve26
|
APN |
12 |
79,291,174 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02077:Zfyve26
|
APN |
12 |
79,323,169 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02437:Zfyve26
|
APN |
12 |
79,315,621 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02933:Zfyve26
|
APN |
12 |
79,326,854 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02937:Zfyve26
|
APN |
12 |
79,285,794 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02982:Zfyve26
|
APN |
12 |
79,310,644 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03064:Zfyve26
|
APN |
12 |
79,308,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03086:Zfyve26
|
APN |
12 |
79,342,338 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03146:Zfyve26
|
APN |
12 |
79,330,846 (GRCm39) |
nonsense |
probably null |
|
challenge
|
UTSW |
12 |
79,317,610 (GRCm39) |
critical splice donor site |
probably null |
|
fourteener
|
UTSW |
12 |
79,302,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02799:Zfyve26
|
UTSW |
12 |
79,320,084 (GRCm39) |
missense |
probably benign |
0.28 |
R0318:Zfyve26
|
UTSW |
12 |
79,323,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R0513:Zfyve26
|
UTSW |
12 |
79,291,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R0582:Zfyve26
|
UTSW |
12 |
79,292,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R0586:Zfyve26
|
UTSW |
12 |
79,315,502 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0718:Zfyve26
|
UTSW |
12 |
79,312,576 (GRCm39) |
splice site |
probably benign |
|
R0738:Zfyve26
|
UTSW |
12 |
79,342,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Zfyve26
|
UTSW |
12 |
79,326,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R0894:Zfyve26
|
UTSW |
12 |
79,320,372 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1109:Zfyve26
|
UTSW |
12 |
79,318,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Zfyve26
|
UTSW |
12 |
79,326,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R1186:Zfyve26
|
UTSW |
12 |
79,310,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Zfyve26
|
UTSW |
12 |
79,321,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1430:Zfyve26
|
UTSW |
12 |
79,329,591 (GRCm39) |
missense |
probably benign |
0.07 |
R1439:Zfyve26
|
UTSW |
12 |
79,298,937 (GRCm39) |
missense |
probably benign |
0.03 |
R1517:Zfyve26
|
UTSW |
12 |
79,298,925 (GRCm39) |
missense |
probably damaging |
0.98 |
R1553:Zfyve26
|
UTSW |
12 |
79,334,535 (GRCm39) |
missense |
probably benign |
0.00 |
R1721:Zfyve26
|
UTSW |
12 |
79,308,573 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1758:Zfyve26
|
UTSW |
12 |
79,285,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Zfyve26
|
UTSW |
12 |
79,325,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1786:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1826:Zfyve26
|
UTSW |
12 |
79,315,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R1833:Zfyve26
|
UTSW |
12 |
79,333,032 (GRCm39) |
missense |
probably benign |
0.36 |
R1868:Zfyve26
|
UTSW |
12 |
79,308,573 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1900:Zfyve26
|
UTSW |
12 |
79,311,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R1928:Zfyve26
|
UTSW |
12 |
79,286,744 (GRCm39) |
nonsense |
probably null |
|
R1982:Zfyve26
|
UTSW |
12 |
79,302,017 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2062:Zfyve26
|
UTSW |
12 |
79,330,806 (GRCm39) |
splice site |
probably null |
|
R2071:Zfyve26
|
UTSW |
12 |
79,334,220 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2130:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2132:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2133:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2135:Zfyve26
|
UTSW |
12 |
79,292,826 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2207:Zfyve26
|
UTSW |
12 |
79,292,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R2280:Zfyve26
|
UTSW |
12 |
79,321,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R2352:Zfyve26
|
UTSW |
12 |
79,330,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R2398:Zfyve26
|
UTSW |
12 |
79,329,573 (GRCm39) |
splice site |
probably null |
|
R3084:Zfyve26
|
UTSW |
12 |
79,312,457 (GRCm39) |
splice site |
probably benign |
|
R3086:Zfyve26
|
UTSW |
12 |
79,312,457 (GRCm39) |
splice site |
probably benign |
|
R4626:Zfyve26
|
UTSW |
12 |
79,315,844 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4727:Zfyve26
|
UTSW |
12 |
79,291,170 (GRCm39) |
missense |
probably benign |
0.16 |
R4908:Zfyve26
|
UTSW |
12 |
79,296,469 (GRCm39) |
splice site |
probably null |
|
R4926:Zfyve26
|
UTSW |
12 |
79,321,785 (GRCm39) |
missense |
probably benign |
|
R4990:Zfyve26
|
UTSW |
12 |
79,334,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R4999:Zfyve26
|
UTSW |
12 |
79,327,159 (GRCm39) |
nonsense |
probably null |
|
R5029:Zfyve26
|
UTSW |
12 |
79,333,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R5070:Zfyve26
|
UTSW |
12 |
79,302,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R5100:Zfyve26
|
UTSW |
12 |
79,326,832 (GRCm39) |
nonsense |
probably null |
|
R5252:Zfyve26
|
UTSW |
12 |
79,315,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R5318:Zfyve26
|
UTSW |
12 |
79,317,624 (GRCm39) |
missense |
probably benign |
0.35 |
R5509:Zfyve26
|
UTSW |
12 |
79,293,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R5574:Zfyve26
|
UTSW |
12 |
79,286,698 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5735:Zfyve26
|
UTSW |
12 |
79,320,147 (GRCm39) |
missense |
probably damaging |
0.96 |
R5756:Zfyve26
|
UTSW |
12 |
79,311,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R5773:Zfyve26
|
UTSW |
12 |
79,334,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R5834:Zfyve26
|
UTSW |
12 |
79,313,311 (GRCm39) |
missense |
probably benign |
0.30 |
R6075:Zfyve26
|
UTSW |
12 |
79,340,628 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6184:Zfyve26
|
UTSW |
12 |
79,315,501 (GRCm39) |
missense |
probably damaging |
0.98 |
R6235:Zfyve26
|
UTSW |
12 |
79,296,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Zfyve26
|
UTSW |
12 |
79,329,758 (GRCm39) |
missense |
probably benign |
0.04 |
R6320:Zfyve26
|
UTSW |
12 |
79,286,776 (GRCm39) |
missense |
probably damaging |
0.97 |
R6548:Zfyve26
|
UTSW |
12 |
79,285,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R6887:Zfyve26
|
UTSW |
12 |
79,313,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Zfyve26
|
UTSW |
12 |
79,330,926 (GRCm39) |
missense |
probably benign |
0.06 |
R7152:Zfyve26
|
UTSW |
12 |
79,325,888 (GRCm39) |
missense |
probably benign |
0.42 |
R7165:Zfyve26
|
UTSW |
12 |
79,327,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R7181:Zfyve26
|
UTSW |
12 |
79,315,182 (GRCm39) |
missense |
probably benign |
0.00 |
R7223:Zfyve26
|
UTSW |
12 |
79,292,945 (GRCm39) |
missense |
probably damaging |
0.99 |
R7299:Zfyve26
|
UTSW |
12 |
79,329,758 (GRCm39) |
missense |
probably benign |
0.01 |
R7301:Zfyve26
|
UTSW |
12 |
79,329,758 (GRCm39) |
missense |
probably benign |
0.01 |
R7302:Zfyve26
|
UTSW |
12 |
79,297,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R7355:Zfyve26
|
UTSW |
12 |
79,286,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:Zfyve26
|
UTSW |
12 |
79,334,581 (GRCm39) |
missense |
probably benign |
0.00 |
R7540:Zfyve26
|
UTSW |
12 |
79,315,450 (GRCm39) |
missense |
probably damaging |
0.99 |
R7552:Zfyve26
|
UTSW |
12 |
79,337,731 (GRCm39) |
missense |
probably damaging |
0.97 |
R7762:Zfyve26
|
UTSW |
12 |
79,315,409 (GRCm39) |
missense |
probably benign |
0.02 |
R7806:Zfyve26
|
UTSW |
12 |
79,327,129 (GRCm39) |
critical splice donor site |
probably null |
|
R7821:Zfyve26
|
UTSW |
12 |
79,302,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R8141:Zfyve26
|
UTSW |
12 |
79,315,331 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8190:Zfyve26
|
UTSW |
12 |
79,327,610 (GRCm39) |
missense |
probably benign |
0.00 |
R8207:Zfyve26
|
UTSW |
12 |
79,307,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R8210:Zfyve26
|
UTSW |
12 |
79,302,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R8500:Zfyve26
|
UTSW |
12 |
79,334,454 (GRCm39) |
missense |
probably damaging |
0.99 |
R8686:Zfyve26
|
UTSW |
12 |
79,334,227 (GRCm39) |
missense |
probably benign |
|
R8758:Zfyve26
|
UTSW |
12 |
79,311,083 (GRCm39) |
critical splice donor site |
probably benign |
|
R8826:Zfyve26
|
UTSW |
12 |
79,285,742 (GRCm39) |
missense |
probably benign |
0.05 |
R8877:Zfyve26
|
UTSW |
12 |
79,334,152 (GRCm39) |
missense |
probably benign |
0.05 |
R9067:Zfyve26
|
UTSW |
12 |
79,318,915 (GRCm39) |
missense |
probably damaging |
0.99 |
R9195:Zfyve26
|
UTSW |
12 |
79,311,168 (GRCm39) |
missense |
probably benign |
0.12 |
R9269:Zfyve26
|
UTSW |
12 |
79,323,076 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9273:Zfyve26
|
UTSW |
12 |
79,317,610 (GRCm39) |
critical splice donor site |
probably null |
|
R9340:Zfyve26
|
UTSW |
12 |
79,321,680 (GRCm39) |
nonsense |
probably null |
|
R9348:Zfyve26
|
UTSW |
12 |
79,315,231 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9482:Zfyve26
|
UTSW |
12 |
79,291,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R9536:Zfyve26
|
UTSW |
12 |
79,298,046 (GRCm39) |
missense |
probably benign |
0.32 |
R9653:Zfyve26
|
UTSW |
12 |
79,334,418 (GRCm39) |
missense |
probably benign |
|
R9676:Zfyve26
|
UTSW |
12 |
79,330,959 (GRCm39) |
missense |
probably benign |
0.01 |
R9797:Zfyve26
|
UTSW |
12 |
79,293,006 (GRCm39) |
missense |
probably damaging |
0.98 |
RF010:Zfyve26
|
UTSW |
12 |
79,302,112 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Zfyve26
|
UTSW |
12 |
79,285,779 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Zfyve26
|
UTSW |
12 |
79,315,307 (GRCm39) |
missense |
probably benign |
0.07 |
Z1177:Zfyve26
|
UTSW |
12 |
79,334,149 (GRCm39) |
missense |
probably null |
1.00 |
|