Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310030G06Rik |
A |
G |
9: 50,651,866 (GRCm39) |
Y121H |
probably damaging |
Het |
Abca13 |
G |
T |
11: 9,349,303 (GRCm39) |
G3626W |
probably damaging |
Het |
Acvr1c |
A |
G |
2: 58,174,973 (GRCm39) |
Y192H |
probably damaging |
Het |
Afm |
A |
T |
5: 90,698,200 (GRCm39) |
D534V |
probably damaging |
Het |
Agl |
T |
C |
3: 116,565,021 (GRCm39) |
E1076G |
probably benign |
Het |
Ahcyl |
T |
C |
16: 45,974,211 (GRCm39) |
K389E |
probably benign |
Het |
Angptl3 |
A |
T |
4: 98,925,757 (GRCm39) |
H361L |
probably benign |
Het |
Apob |
T |
C |
12: 8,061,421 (GRCm39) |
F3301S |
possibly damaging |
Het |
Arhgef33 |
T |
A |
17: 80,674,730 (GRCm39) |
C376S |
possibly damaging |
Het |
Ass1 |
A |
G |
2: 31,410,428 (GRCm39) |
*413W |
probably null |
Het |
Atp6v1h |
T |
A |
1: 5,165,911 (GRCm39) |
L127Q |
probably damaging |
Het |
Bcl2l1 |
G |
A |
2: 152,671,870 (GRCm39) |
S14F |
probably damaging |
Het |
Bhmt1b |
T |
G |
18: 87,775,382 (GRCm39) |
F302V |
probably damaging |
Het |
Birc6 |
G |
A |
17: 74,930,853 (GRCm39) |
A2477T |
probably benign |
Het |
Bpifb9a |
G |
A |
2: 154,112,941 (GRCm39) |
A589T |
possibly damaging |
Het |
Casp9 |
C |
A |
4: 141,533,151 (GRCm39) |
T252K |
probably benign |
Het |
Cct4 |
G |
A |
11: 22,952,922 (GRCm39) |
D533N |
probably damaging |
Het |
Clcn6 |
A |
C |
4: 148,098,358 (GRCm39) |
I555S |
probably damaging |
Het |
Col4a4 |
A |
T |
1: 82,475,543 (GRCm39) |
|
probably null |
Het |
Cyp2d10 |
A |
T |
15: 82,288,129 (GRCm39) |
|
probably null |
Het |
D930048N14Rik |
A |
G |
11: 51,545,740 (GRCm39) |
|
probably benign |
Het |
Dhfr |
A |
G |
13: 92,504,815 (GRCm39) |
|
probably benign |
Het |
Dlg5 |
T |
C |
14: 24,204,764 (GRCm39) |
|
probably null |
Het |
Dnah11 |
T |
C |
12: 118,002,430 (GRCm39) |
E2240G |
probably damaging |
Het |
Dnmt3a |
A |
G |
12: 3,916,088 (GRCm39) |
E17G |
probably damaging |
Het |
Dock1 |
A |
G |
7: 134,384,138 (GRCm39) |
T670A |
probably benign |
Het |
Dpy19l2 |
A |
G |
9: 24,580,618 (GRCm39) |
M241T |
probably benign |
Het |
Dpy19l4 |
A |
G |
4: 11,296,034 (GRCm39) |
S212P |
probably damaging |
Het |
Ephb6 |
T |
C |
6: 41,593,040 (GRCm39) |
F426S |
probably damaging |
Het |
Faah |
A |
T |
4: 115,856,755 (GRCm39) |
V469E |
probably damaging |
Het |
Fas |
T |
C |
19: 34,294,013 (GRCm39) |
C123R |
probably damaging |
Het |
Fhod1 |
T |
C |
8: 106,065,546 (GRCm39) |
|
probably benign |
Het |
Filip1 |
A |
G |
9: 79,805,589 (GRCm39) |
V55A |
probably benign |
Het |
Frmpd1 |
G |
A |
4: 45,273,197 (GRCm39) |
R372Q |
probably damaging |
Het |
Glyctk |
C |
T |
9: 106,034,806 (GRCm39) |
G87S |
probably damaging |
Het |
Golga3 |
T |
C |
5: 110,357,744 (GRCm39) |
L1080P |
probably damaging |
Het |
Gpr137 |
T |
C |
19: 6,915,812 (GRCm39) |
T281A |
probably benign |
Het |
Grap2 |
T |
A |
15: 80,532,612 (GRCm39) |
|
probably null |
Het |
Hlcs |
T |
C |
16: 94,069,151 (GRCm39) |
D170G |
probably damaging |
Het |
Hook1 |
A |
G |
4: 95,901,493 (GRCm39) |
T484A |
probably benign |
Het |
Hoxa5 |
T |
A |
6: 52,180,771 (GRCm39) |
H187L |
probably benign |
Het |
Inpp1 |
G |
T |
1: 52,829,253 (GRCm39) |
S255R |
probably benign |
Het |
Inpp4b |
T |
A |
8: 82,494,786 (GRCm39) |
V67E |
probably damaging |
Het |
Iqgap3 |
A |
G |
3: 87,994,616 (GRCm39) |
N105S |
probably damaging |
Het |
Kcnq5 |
A |
G |
1: 21,539,692 (GRCm39) |
|
probably null |
Het |
Klhl1 |
T |
C |
14: 96,477,649 (GRCm39) |
N473S |
probably benign |
Het |
Klk1b24 |
C |
A |
7: 43,840,785 (GRCm39) |
T71N |
probably benign |
Het |
Loxhd1 |
A |
G |
18: 77,468,269 (GRCm39) |
|
probably null |
Het |
Lrp1b |
C |
T |
2: 41,001,071 (GRCm39) |
R2165Q |
probably benign |
Het |
Lrp2bp |
A |
T |
8: 46,478,272 (GRCm39) |
Q328L |
possibly damaging |
Het |
Lrrc63 |
T |
A |
14: 75,344,829 (GRCm39) |
K419N |
possibly damaging |
Het |
Lrrc9 |
A |
G |
12: 72,547,533 (GRCm39) |
N150S |
probably benign |
Het |
Lrrn4 |
C |
A |
2: 132,713,995 (GRCm39) |
C317F |
probably damaging |
Het |
Ltbp2 |
T |
C |
12: 84,860,074 (GRCm39) |
S627G |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,386,947 (GRCm39) |
S1224T |
probably damaging |
Het |
Meis2 |
A |
C |
2: 115,889,151 (GRCm39) |
H200Q |
probably benign |
Het |
Mesd |
C |
A |
7: 83,544,790 (GRCm39) |
A80E |
probably benign |
Het |
Mtor |
G |
T |
4: 148,610,450 (GRCm39) |
|
probably benign |
Het |
Myo3a |
T |
C |
2: 22,467,939 (GRCm39) |
F398L |
probably benign |
Het |
Nagpa |
G |
T |
16: 5,019,392 (GRCm39) |
|
probably benign |
Het |
Nanp |
A |
G |
2: 150,872,749 (GRCm39) |
C60R |
probably benign |
Het |
Nectin2 |
T |
G |
7: 19,464,041 (GRCm39) |
M313L |
probably benign |
Het |
Nek4 |
C |
T |
14: 30,678,844 (GRCm39) |
H123Y |
probably damaging |
Het |
Nploc4 |
A |
G |
11: 120,299,607 (GRCm39) |
V371A |
probably damaging |
Het |
Ntrk3 |
T |
C |
7: 78,005,762 (GRCm39) |
|
probably benign |
Het |
Or11g7 |
A |
G |
14: 50,690,634 (GRCm39) |
T42A |
possibly damaging |
Het |
Or13c7b |
A |
G |
4: 43,820,723 (GRCm39) |
F213L |
probably benign |
Het |
Or52n4 |
T |
C |
7: 104,294,153 (GRCm39) |
N140S |
probably benign |
Het |
Or5b109 |
T |
A |
19: 13,212,265 (GRCm39) |
V217E |
possibly damaging |
Het |
Pcdh20 |
T |
A |
14: 88,706,673 (GRCm39) |
Q209L |
probably benign |
Het |
Pcdhb20 |
G |
A |
18: 37,637,750 (GRCm39) |
R92H |
probably damaging |
Het |
Pgap1 |
T |
C |
1: 54,567,714 (GRCm39) |
H377R |
probably benign |
Het |
Phyhipl |
G |
T |
10: 70,406,798 (GRCm39) |
P52Q |
probably damaging |
Het |
Plekhg4 |
T |
C |
8: 106,107,672 (GRCm39) |
|
probably benign |
Het |
Pwwp2a |
T |
A |
11: 43,596,383 (GRCm39) |
V516E |
possibly damaging |
Het |
Rack1 |
T |
C |
11: 48,692,586 (GRCm39) |
V69A |
probably damaging |
Het |
Rexo5 |
T |
A |
7: 119,400,581 (GRCm39) |
|
probably null |
Het |
Rnf123 |
T |
C |
9: 107,948,665 (GRCm39) |
|
probably benign |
Het |
Rock1 |
G |
T |
18: 10,072,863 (GRCm39) |
Q1161K |
possibly damaging |
Het |
Rps6ka2 |
T |
C |
17: 7,560,266 (GRCm39) |
L568P |
probably damaging |
Het |
Seh1l |
T |
C |
18: 67,917,054 (GRCm39) |
S78P |
probably damaging |
Het |
Serpinb3b |
A |
T |
1: 107,083,573 (GRCm39) |
|
probably null |
Het |
Setd1a |
T |
C |
7: 127,387,512 (GRCm39) |
|
probably benign |
Het |
Setx |
G |
T |
2: 29,030,401 (GRCm39) |
|
probably null |
Het |
Sh3bp1 |
T |
C |
15: 78,791,545 (GRCm39) |
|
probably benign |
Het |
Shc2 |
G |
T |
10: 79,467,136 (GRCm39) |
R146S |
probably damaging |
Het |
Skap2 |
T |
C |
6: 51,886,348 (GRCm39) |
T5A |
probably benign |
Het |
Skor2 |
A |
T |
18: 76,964,340 (GRCm39) |
|
probably benign |
Het |
Slc35a3 |
T |
C |
3: 116,480,983 (GRCm39) |
I93M |
probably benign |
Het |
Sohlh1 |
C |
T |
2: 25,733,359 (GRCm39) |
G295D |
probably damaging |
Het |
Speg |
A |
G |
1: 75,405,128 (GRCm39) |
|
probably benign |
Het |
Sult2a8 |
A |
C |
7: 14,150,208 (GRCm39) |
C168G |
probably benign |
Het |
Tax1bp1 |
T |
C |
6: 52,704,179 (GRCm39) |
|
probably benign |
Het |
Tbc1d4 |
T |
C |
14: 101,685,124 (GRCm39) |
I1176V |
possibly damaging |
Het |
Tcof1 |
A |
G |
18: 60,952,026 (GRCm39) |
|
probably benign |
Het |
Thada |
A |
T |
17: 84,744,104 (GRCm39) |
F735I |
possibly damaging |
Het |
Tle1 |
A |
C |
4: 72,058,068 (GRCm39) |
H52Q |
probably damaging |
Het |
Tmem101 |
A |
T |
11: 102,044,155 (GRCm39) |
V244E |
probably damaging |
Het |
Tnfrsf26 |
C |
A |
7: 143,171,668 (GRCm39) |
C95F |
probably damaging |
Het |
Uspl1 |
T |
C |
5: 149,150,842 (GRCm39) |
S482P |
probably benign |
Het |
Vmn2r118 |
G |
T |
17: 55,917,935 (GRCm39) |
N192K |
probably benign |
Het |
Vmn2r14 |
C |
T |
5: 109,368,195 (GRCm39) |
V266I |
possibly damaging |
Het |
Vmn2r51 |
A |
G |
7: 9,834,249 (GRCm39) |
I263T |
probably damaging |
Het |
Zfp937 |
T |
A |
2: 150,080,967 (GRCm39) |
C332* |
probably null |
Het |
Zscan21 |
T |
A |
5: 138,123,470 (GRCm39) |
S50T |
probably benign |
Het |
|
Other mutations in F5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00840:F5
|
APN |
1 |
164,007,093 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00843:F5
|
APN |
1 |
164,039,360 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00904:F5
|
APN |
1 |
164,021,578 (GRCm39) |
missense |
probably benign |
|
IGL00913:F5
|
APN |
1 |
164,032,465 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01099:F5
|
APN |
1 |
164,021,903 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01134:F5
|
APN |
1 |
164,019,548 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01313:F5
|
APN |
1 |
164,021,181 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01635:F5
|
APN |
1 |
164,035,427 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01697:F5
|
APN |
1 |
164,021,621 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01768:F5
|
APN |
1 |
164,003,914 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01795:F5
|
APN |
1 |
164,021,959 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01835:F5
|
APN |
1 |
164,021,937 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01843:F5
|
APN |
1 |
164,039,395 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01989:F5
|
APN |
1 |
164,003,876 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02036:F5
|
APN |
1 |
164,010,571 (GRCm39) |
splice site |
probably benign |
|
IGL02065:F5
|
APN |
1 |
164,017,695 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02077:F5
|
APN |
1 |
164,026,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02139:F5
|
APN |
1 |
164,020,243 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02210:F5
|
APN |
1 |
164,017,710 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02415:F5
|
APN |
1 |
164,019,498 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02440:F5
|
APN |
1 |
164,034,635 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02471:F5
|
APN |
1 |
164,001,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02535:F5
|
APN |
1 |
164,026,302 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02537:F5
|
APN |
1 |
164,020,686 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02628:F5
|
APN |
1 |
164,021,644 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02638:F5
|
APN |
1 |
164,012,177 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02824:F5
|
APN |
1 |
164,021,916 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02977:F5
|
APN |
1 |
164,021,590 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03028:F5
|
APN |
1 |
164,020,569 (GRCm39) |
nonsense |
probably null |
|
IGL03064:F5
|
APN |
1 |
164,023,163 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03127:F5
|
APN |
1 |
164,021,107 (GRCm39) |
missense |
probably benign |
0.45 |
IGL03131:F5
|
APN |
1 |
163,989,388 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03348:F5
|
APN |
1 |
164,021,721 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03387:F5
|
APN |
1 |
164,020,801 (GRCm39) |
missense |
probably damaging |
1.00 |
James_dean
|
UTSW |
1 |
164,032,389 (GRCm39) |
missense |
probably benign |
0.43 |
BB002:F5
|
UTSW |
1 |
164,003,935 (GRCm39) |
critical splice donor site |
probably null |
|
BB012:F5
|
UTSW |
1 |
164,003,935 (GRCm39) |
critical splice donor site |
probably null |
|
R0002:F5
|
UTSW |
1 |
164,029,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0095:F5
|
UTSW |
1 |
164,019,537 (GRCm39) |
nonsense |
probably null |
|
R0116:F5
|
UTSW |
1 |
164,012,483 (GRCm39) |
missense |
probably benign |
0.01 |
R0359:F5
|
UTSW |
1 |
164,007,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R0426:F5
|
UTSW |
1 |
164,010,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R0452:F5
|
UTSW |
1 |
164,012,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R0457:F5
|
UTSW |
1 |
164,021,769 (GRCm39) |
missense |
probably benign |
0.00 |
R0520:F5
|
UTSW |
1 |
164,037,156 (GRCm39) |
missense |
probably benign |
0.15 |
R0522:F5
|
UTSW |
1 |
164,039,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R0554:F5
|
UTSW |
1 |
164,007,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R0575:F5
|
UTSW |
1 |
164,003,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R0734:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R0739:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1062:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1063:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1149:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1149:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1150:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1151:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1152:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1221:F5
|
UTSW |
1 |
163,989,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1284:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1286:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1358:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1360:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1362:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1383:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:F5
|
UTSW |
1 |
164,026,402 (GRCm39) |
missense |
probably benign |
0.02 |
R1545:F5
|
UTSW |
1 |
164,036,529 (GRCm39) |
nonsense |
probably null |
|
R1561:F5
|
UTSW |
1 |
164,014,472 (GRCm39) |
nonsense |
probably null |
|
R1623:F5
|
UTSW |
1 |
164,023,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:F5
|
UTSW |
1 |
164,035,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R1673:F5
|
UTSW |
1 |
164,007,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R1689:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1705:F5
|
UTSW |
1 |
164,045,059 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1732:F5
|
UTSW |
1 |
164,001,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R1763:F5
|
UTSW |
1 |
164,020,104 (GRCm39) |
missense |
probably benign |
0.04 |
R1774:F5
|
UTSW |
1 |
164,020,104 (GRCm39) |
missense |
probably benign |
0.04 |
R1799:F5
|
UTSW |
1 |
164,021,100 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1800:F5
|
UTSW |
1 |
164,010,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R1842:F5
|
UTSW |
1 |
164,012,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R1915:F5
|
UTSW |
1 |
164,010,486 (GRCm39) |
missense |
probably damaging |
0.97 |
R1926:F5
|
UTSW |
1 |
164,007,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2025:F5
|
UTSW |
1 |
164,037,044 (GRCm39) |
missense |
probably benign |
0.05 |
R2198:F5
|
UTSW |
1 |
164,034,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R2258:F5
|
UTSW |
1 |
164,019,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R2264:F5
|
UTSW |
1 |
164,021,971 (GRCm39) |
missense |
probably benign |
0.32 |
R2281:F5
|
UTSW |
1 |
164,023,289 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2407:F5
|
UTSW |
1 |
164,039,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R2445:F5
|
UTSW |
1 |
164,017,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R2860:F5
|
UTSW |
1 |
164,012,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2861:F5
|
UTSW |
1 |
164,012,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2862:F5
|
UTSW |
1 |
164,012,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2899:F5
|
UTSW |
1 |
164,014,469 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2910:F5
|
UTSW |
1 |
164,032,389 (GRCm39) |
missense |
probably benign |
0.43 |
R2912:F5
|
UTSW |
1 |
164,021,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R2996:F5
|
UTSW |
1 |
164,010,486 (GRCm39) |
missense |
probably damaging |
0.97 |
R3745:F5
|
UTSW |
1 |
164,014,348 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3901:F5
|
UTSW |
1 |
164,003,798 (GRCm39) |
missense |
probably benign |
0.08 |
R3902:F5
|
UTSW |
1 |
164,003,798 (GRCm39) |
missense |
probably benign |
0.08 |
R4365:F5
|
UTSW |
1 |
164,012,519 (GRCm39) |
missense |
probably damaging |
0.98 |
R4448:F5
|
UTSW |
1 |
164,026,468 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4490:F5
|
UTSW |
1 |
164,044,964 (GRCm39) |
missense |
probably benign |
0.40 |
R4514:F5
|
UTSW |
1 |
163,979,566 (GRCm39) |
unclassified |
probably benign |
|
R4598:F5
|
UTSW |
1 |
164,032,366 (GRCm39) |
missense |
probably benign |
0.05 |
R4608:F5
|
UTSW |
1 |
164,036,598 (GRCm39) |
missense |
probably benign |
0.12 |
R4661:F5
|
UTSW |
1 |
164,012,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:F5
|
UTSW |
1 |
164,001,755 (GRCm39) |
missense |
probably benign |
0.00 |
R4689:F5
|
UTSW |
1 |
163,979,542 (GRCm39) |
unclassified |
probably benign |
|
R4716:F5
|
UTSW |
1 |
164,021,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R4732:F5
|
UTSW |
1 |
164,009,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:F5
|
UTSW |
1 |
164,009,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R4854:F5
|
UTSW |
1 |
164,019,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:F5
|
UTSW |
1 |
164,039,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:F5
|
UTSW |
1 |
164,021,755 (GRCm39) |
missense |
probably benign |
|
R5001:F5
|
UTSW |
1 |
164,023,139 (GRCm39) |
missense |
probably benign |
0.00 |
R5042:F5
|
UTSW |
1 |
164,047,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R5056:F5
|
UTSW |
1 |
164,019,601 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5061:F5
|
UTSW |
1 |
164,021,749 (GRCm39) |
missense |
probably benign |
0.00 |
R5143:F5
|
UTSW |
1 |
164,039,397 (GRCm39) |
missense |
probably damaging |
0.98 |
R5622:F5
|
UTSW |
1 |
164,020,134 (GRCm39) |
missense |
probably benign |
0.09 |
R5626:F5
|
UTSW |
1 |
164,036,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R5658:F5
|
UTSW |
1 |
164,019,907 (GRCm39) |
missense |
probably damaging |
0.96 |
R5702:F5
|
UTSW |
1 |
164,022,116 (GRCm39) |
nonsense |
probably null |
|
R5795:F5
|
UTSW |
1 |
163,979,578 (GRCm39) |
missense |
probably benign |
0.09 |
R5884:F5
|
UTSW |
1 |
164,023,215 (GRCm39) |
missense |
probably benign |
0.01 |
R6036:F5
|
UTSW |
1 |
164,012,565 (GRCm39) |
missense |
probably damaging |
0.99 |
R6036:F5
|
UTSW |
1 |
164,012,565 (GRCm39) |
missense |
probably damaging |
0.99 |
R6151:F5
|
UTSW |
1 |
164,017,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:F5
|
UTSW |
1 |
164,009,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R6345:F5
|
UTSW |
1 |
164,019,520 (GRCm39) |
missense |
probably benign |
0.13 |
R6391:F5
|
UTSW |
1 |
164,021,062 (GRCm39) |
missense |
probably damaging |
0.99 |
R6542:F5
|
UTSW |
1 |
164,022,037 (GRCm39) |
missense |
probably benign |
0.32 |
R6620:F5
|
UTSW |
1 |
164,014,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:F5
|
UTSW |
1 |
164,021,076 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6754:F5
|
UTSW |
1 |
164,021,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R6774:F5
|
UTSW |
1 |
164,014,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R6802:F5
|
UTSW |
1 |
164,006,925 (GRCm39) |
missense |
probably damaging |
0.98 |
R6810:F5
|
UTSW |
1 |
164,014,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R6983:F5
|
UTSW |
1 |
164,021,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R7000:F5
|
UTSW |
1 |
164,007,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R7151:F5
|
UTSW |
1 |
164,029,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R7193:F5
|
UTSW |
1 |
164,046,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R7230:F5
|
UTSW |
1 |
164,012,522 (GRCm39) |
missense |
probably benign |
|
R7324:F5
|
UTSW |
1 |
164,021,150 (GRCm39) |
small deletion |
probably benign |
|
R7350:F5
|
UTSW |
1 |
164,020,277 (GRCm39) |
missense |
probably benign |
0.08 |
R7466:F5
|
UTSW |
1 |
164,020,897 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7503:F5
|
UTSW |
1 |
164,019,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R7626:F5
|
UTSW |
1 |
164,014,481 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7742:F5
|
UTSW |
1 |
164,035,453 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7837:F5
|
UTSW |
1 |
164,014,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R7848:F5
|
UTSW |
1 |
163,989,446 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7925:F5
|
UTSW |
1 |
164,003,935 (GRCm39) |
critical splice donor site |
probably null |
|
R8053:F5
|
UTSW |
1 |
164,020,338 (GRCm39) |
missense |
probably benign |
0.26 |
R8094:F5
|
UTSW |
1 |
164,036,509 (GRCm39) |
missense |
probably benign |
0.06 |
R8175:F5
|
UTSW |
1 |
164,019,834 (GRCm39) |
nonsense |
probably null |
|
R8209:F5
|
UTSW |
1 |
164,021,959 (GRCm39) |
missense |
probably benign |
0.00 |
R8226:F5
|
UTSW |
1 |
164,021,959 (GRCm39) |
missense |
probably benign |
0.00 |
R8266:F5
|
UTSW |
1 |
164,012,693 (GRCm39) |
critical splice donor site |
probably null |
|
R8517:F5
|
UTSW |
1 |
164,003,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R8684:F5
|
UTSW |
1 |
164,045,111 (GRCm39) |
missense |
probably benign |
0.01 |
R8941:F5
|
UTSW |
1 |
164,026,440 (GRCm39) |
missense |
probably benign |
0.19 |
R9130:F5
|
UTSW |
1 |
164,001,830 (GRCm39) |
missense |
probably benign |
0.37 |
R9181:F5
|
UTSW |
1 |
164,019,895 (GRCm39) |
missense |
probably benign |
0.00 |
R9186:F5
|
UTSW |
1 |
164,021,470 (GRCm39) |
missense |
probably benign |
|
R9233:F5
|
UTSW |
1 |
164,047,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R9314:F5
|
UTSW |
1 |
164,029,146 (GRCm39) |
missense |
probably benign |
0.01 |
R9631:F5
|
UTSW |
1 |
164,014,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:F5
|
UTSW |
1 |
164,021,730 (GRCm39) |
missense |
probably benign |
0.15 |
X0024:F5
|
UTSW |
1 |
164,020,557 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:F5
|
UTSW |
1 |
163,981,954 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:F5
|
UTSW |
1 |
164,012,085 (GRCm39) |
missense |
probably damaging |
0.97 |
|