Other mutations in this stock |
Total: 139 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700031F05Rik |
G |
T |
X: 101,904,515 (GRCm39) |
N132K |
possibly damaging |
Het |
Aatf |
T |
C |
11: 84,362,023 (GRCm39) |
D313G |
possibly damaging |
Het |
Abcb11 |
T |
G |
2: 69,115,615 (GRCm39) |
D583A |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,676,914 (GRCm39) |
Y1252* |
probably null |
Het |
Aim2 |
T |
C |
1: 173,283,090 (GRCm39) |
|
silent |
Het |
Angpt1 |
T |
A |
15: 42,539,580 (GRCm39) |
Y93F |
probably benign |
Het |
Ankrd27 |
C |
T |
7: 35,337,659 (GRCm39) |
P991L |
probably benign |
Het |
Ap1s3 |
C |
T |
1: 79,591,920 (GRCm39) |
|
probably null |
Het |
Apbb1 |
A |
C |
7: 105,214,745 (GRCm39) |
S500A |
probably benign |
Het |
Arc |
G |
A |
15: 74,543,374 (GRCm39) |
A283V |
probably damaging |
Het |
Bbs10 |
A |
G |
10: 111,136,995 (GRCm39) |
K703E |
probably benign |
Het |
C1galt1c1 |
A |
T |
X: 37,720,349 (GRCm39) |
S216T |
probably benign |
Het |
C1qtnf4 |
T |
A |
2: 90,719,996 (GRCm39) |
S90T |
probably damaging |
Het |
Cachd1 |
A |
T |
4: 100,810,327 (GRCm39) |
K310* |
probably null |
Het |
Calhm1 |
A |
G |
19: 47,132,240 (GRCm39) |
L125P |
probably damaging |
Het |
Carmil1 |
G |
A |
13: 24,321,162 (GRCm39) |
L278F |
probably damaging |
Het |
Ccar1 |
A |
T |
10: 62,583,196 (GRCm39) |
Y972* |
probably null |
Het |
Cd163 |
C |
T |
6: 124,297,580 (GRCm39) |
P909S |
probably damaging |
Het |
Cd44 |
T |
A |
2: 102,668,274 (GRCm39) |
H268L |
possibly damaging |
Het |
Cdkl2 |
A |
T |
5: 92,165,072 (GRCm39) |
L517Q |
probably damaging |
Het |
Cep68 |
G |
T |
11: 20,189,349 (GRCm39) |
N554K |
probably benign |
Het |
Ces1d |
A |
G |
8: 93,893,038 (GRCm39) |
W515R |
probably damaging |
Het |
Clca4b |
A |
C |
3: 144,634,286 (GRCm39) |
H102Q |
probably benign |
Het |
Cldn15 |
T |
A |
5: 137,003,337 (GRCm39) |
I142N |
probably damaging |
Het |
Cmklr1 |
T |
A |
5: 113,752,701 (GRCm39) |
D100V |
probably damaging |
Het |
Crocc2 |
G |
A |
1: 93,096,516 (GRCm39) |
V24M |
possibly damaging |
Het |
D430041D05Rik |
G |
A |
2: 104,088,788 (GRCm39) |
P63S |
probably damaging |
Het |
Ddx39a |
A |
T |
8: 84,448,902 (GRCm39) |
H259L |
probably benign |
Het |
Dhx16 |
C |
G |
17: 36,196,527 (GRCm39) |
A565G |
probably benign |
Het |
Dimt1 |
A |
T |
13: 107,084,163 (GRCm39) |
D50V |
probably benign |
Het |
Dock9 |
A |
T |
14: 121,823,658 (GRCm39) |
L1428H |
probably damaging |
Het |
Dpp4 |
G |
T |
2: 62,164,949 (GRCm39) |
T700K |
probably damaging |
Het |
E030030I06Rik |
T |
A |
10: 22,024,744 (GRCm39) |
R56S |
unknown |
Het |
Eea1 |
A |
G |
10: 95,864,255 (GRCm39) |
T925A |
probably benign |
Het |
Ext1 |
A |
G |
15: 52,953,383 (GRCm39) |
S494P |
possibly damaging |
Het |
Fam171a1 |
G |
A |
2: 3,221,328 (GRCm39) |
E140K |
probably damaging |
Het |
Fgfr3 |
C |
T |
5: 33,892,330 (GRCm39) |
|
probably benign |
Het |
Gabra6 |
A |
G |
11: 42,198,199 (GRCm39) |
I407T |
probably damaging |
Het |
Gm16223 |
C |
A |
5: 42,371,954 (GRCm39) |
L115M |
unknown |
Het |
Gm4781 |
G |
T |
10: 100,232,862 (GRCm39) |
|
noncoding transcript |
Het |
Gm9772 |
T |
A |
17: 22,226,013 (GRCm39) |
I70F |
possibly damaging |
Het |
Gpr107 |
T |
A |
2: 31,100,513 (GRCm39) |
F497Y |
probably damaging |
Het |
Grm7 |
T |
A |
6: 110,891,344 (GRCm39) |
Y192* |
probably null |
Het |
Gtf2ird2 |
G |
A |
5: 134,245,034 (GRCm39) |
A431T |
probably damaging |
Het |
H2-K2 |
T |
A |
17: 34,194,989 (GRCm39) |
|
noncoding transcript |
Het |
H2-M11 |
T |
A |
17: 36,858,883 (GRCm39) |
V141D |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,551,262 (GRCm39) |
|
probably null |
Het |
Hmcn2 |
A |
T |
2: 31,289,031 (GRCm39) |
Q2280L |
possibly damaging |
Het |
Hmg20b |
T |
A |
10: 81,184,416 (GRCm39) |
Q129L |
probably damaging |
Het |
Igfbp7 |
T |
A |
5: 77,499,143 (GRCm39) |
Q285L |
possibly damaging |
Het |
Igkv13-85 |
T |
A |
6: 68,907,720 (GRCm39) |
|
probably benign |
Het |
Inpp5e |
A |
T |
2: 26,297,926 (GRCm39) |
L225H |
probably benign |
Het |
Inpp5f |
T |
A |
7: 128,260,833 (GRCm39) |
V91E |
possibly damaging |
Het |
Khdc3 |
A |
G |
9: 73,009,868 (GRCm39) |
E26G |
possibly damaging |
Het |
Klra5 |
T |
A |
6: 129,876,339 (GRCm39) |
D156V |
probably damaging |
Het |
Kmo |
C |
A |
1: 175,487,340 (GRCm39) |
Y430* |
probably null |
Het |
Lbx2 |
A |
G |
6: 83,065,027 (GRCm39) |
D188G |
probably damaging |
Het |
Lcorl |
A |
T |
5: 45,890,931 (GRCm39) |
L474* |
probably null |
Het |
Lnx1 |
C |
T |
5: 74,771,457 (GRCm39) |
V350I |
probably benign |
Het |
Lrrc45 |
T |
A |
11: 120,609,947 (GRCm39) |
S464T |
probably benign |
Het |
Ltc4s |
T |
A |
11: 50,128,052 (GRCm39) |
T61S |
probably benign |
Het |
Luc7l3 |
A |
C |
11: 94,200,467 (GRCm39) |
N50K |
probably damaging |
Het |
Ly75 |
G |
A |
2: 60,138,622 (GRCm39) |
T1415M |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,367,420 (GRCm39) |
E2447G |
probably benign |
Het |
Map3k21 |
A |
G |
8: 126,668,850 (GRCm39) |
D812G |
probably benign |
Het |
Mbtd1 |
C |
T |
11: 93,815,437 (GRCm39) |
H342Y |
probably damaging |
Het |
Mest |
C |
T |
6: 30,745,109 (GRCm39) |
R226* |
probably null |
Het |
Mindy1 |
A |
T |
3: 95,190,054 (GRCm39) |
|
probably benign |
Het |
Mmp13 |
A |
T |
9: 7,274,233 (GRCm39) |
D180V |
probably damaging |
Het |
Mn1 |
A |
G |
5: 111,567,949 (GRCm39) |
T640A |
probably benign |
Het |
Msi2 |
T |
C |
11: 88,608,864 (GRCm39) |
H18R |
possibly damaging |
Het |
Myo18a |
T |
A |
11: 77,708,776 (GRCm39) |
V61E |
probably damaging |
Het |
Myo19 |
T |
G |
11: 84,785,468 (GRCm39) |
I237S |
probably damaging |
Het |
Ncaph2 |
T |
A |
15: 89,254,635 (GRCm39) |
L416Q |
probably damaging |
Het |
Nlrp1a |
T |
A |
11: 70,987,952 (GRCm39) |
|
probably null |
Het |
Or1n1b |
A |
G |
2: 36,780,663 (GRCm39) |
F66L |
probably benign |
Het |
Or2d4 |
A |
T |
7: 106,543,547 (GRCm39) |
N220K |
probably benign |
Het |
Or51a25 |
A |
G |
7: 102,373,299 (GRCm39) |
S133P |
probably damaging |
Het |
Or5b98 |
A |
G |
19: 12,931,441 (GRCm39) |
I163V |
probably benign |
Het |
Or8s10 |
G |
T |
15: 98,335,457 (GRCm39) |
V36F |
probably benign |
Het |
Padi2 |
T |
C |
4: 140,671,757 (GRCm39) |
F495S |
probably damaging |
Het |
Pan3 |
G |
T |
5: 147,464,013 (GRCm39) |
D535Y |
probably damaging |
Het |
Paqr3 |
T |
A |
5: 97,256,069 (GRCm39) |
R102* |
probably null |
Het |
Patl1 |
T |
A |
19: 11,891,798 (GRCm39) |
D34E |
probably damaging |
Het |
Pcdha6 |
A |
T |
18: 37,102,189 (GRCm39) |
T461S |
probably damaging |
Het |
Pcnt |
T |
C |
10: 76,190,047 (GRCm39) |
S2830G |
probably benign |
Het |
Pdgfa |
G |
A |
5: 138,964,939 (GRCm39) |
T181I |
probably benign |
Het |
Pds5a |
C |
A |
5: 65,813,661 (GRCm39) |
D275Y |
probably damaging |
Het |
Plod2 |
T |
A |
9: 92,487,503 (GRCm39) |
Y607* |
probably null |
Het |
Pomt2 |
G |
T |
12: 87,164,857 (GRCm39) |
T517K |
possibly damaging |
Het |
Pramel23 |
T |
C |
4: 143,425,914 (GRCm39) |
M10V |
probably benign |
Het |
Prdm1 |
T |
C |
10: 44,315,686 (GRCm39) |
T817A |
probably damaging |
Het |
Prdm2 |
T |
C |
4: 142,859,525 (GRCm39) |
D1255G |
possibly damaging |
Het |
Prex2 |
T |
A |
1: 11,232,509 (GRCm39) |
C859S |
probably damaging |
Het |
Ralgapa2 |
A |
T |
2: 146,229,549 (GRCm39) |
M1077K |
possibly damaging |
Het |
Ralgds |
T |
C |
2: 28,435,532 (GRCm39) |
|
probably null |
Het |
Rasa3 |
T |
C |
8: 13,638,865 (GRCm39) |
E314G |
probably null |
Het |
Rasa4 |
T |
A |
5: 136,130,217 (GRCm39) |
D324E |
probably damaging |
Het |
Rbm46 |
A |
T |
3: 82,771,765 (GRCm39) |
D283E |
probably benign |
Het |
Rnf139 |
A |
T |
15: 58,771,836 (GRCm39) |
L620F |
probably benign |
Het |
Scaf11 |
A |
T |
15: 96,317,981 (GRCm39) |
|
probably null |
Het |
Sectm1b |
A |
T |
11: 120,946,760 (GRCm39) |
V45E |
probably damaging |
Het |
Selenon |
A |
G |
4: 134,272,968 (GRCm39) |
W157R |
probably damaging |
Het |
Sema3b |
C |
A |
9: 107,476,250 (GRCm39) |
R657L |
possibly damaging |
Het |
Setd1b |
C |
T |
5: 123,286,175 (GRCm39) |
A407V |
unknown |
Het |
Sh3tc1 |
C |
T |
5: 35,863,662 (GRCm39) |
A842T |
probably damaging |
Het |
Shank2 |
A |
G |
7: 143,965,566 (GRCm39) |
E1268G |
probably damaging |
Het |
Shmt1 |
G |
A |
11: 60,692,291 (GRCm39) |
S155F |
probably damaging |
Het |
Sim2 |
A |
G |
16: 93,924,385 (GRCm39) |
E510G |
possibly damaging |
Het |
Slc25a46 |
A |
T |
18: 31,733,245 (GRCm39) |
I168N |
probably damaging |
Het |
Slc26a4 |
T |
G |
12: 31,590,525 (GRCm39) |
D376A |
possibly damaging |
Het |
Slfn14 |
G |
T |
11: 83,167,484 (GRCm39) |
A677E |
probably benign |
Het |
Slk |
G |
T |
19: 47,608,713 (GRCm39) |
Q555H |
possibly damaging |
Het |
Synj1 |
A |
T |
16: 90,770,877 (GRCm39) |
D517E |
probably damaging |
Het |
Syvn1 |
G |
A |
19: 6,101,504 (GRCm39) |
R440Q |
probably benign |
Het |
Tafa5 |
T |
G |
15: 87,604,783 (GRCm39) |
S115A |
probably damaging |
Het |
Tas2r118 |
A |
T |
6: 23,969,467 (GRCm39) |
I198N |
probably damaging |
Het |
Tdh |
A |
G |
14: 63,731,205 (GRCm39) |
L323P |
possibly damaging |
Het |
Tet2 |
A |
T |
3: 133,193,843 (GRCm39) |
M197K |
probably benign |
Het |
Timeless |
A |
G |
10: 128,075,825 (GRCm39) |
Y19C |
possibly damaging |
Het |
Tnn |
T |
C |
1: 159,973,612 (GRCm39) |
M252V |
probably benign |
Het |
Trdn |
G |
T |
10: 33,071,977 (GRCm39) |
E215* |
probably null |
Het |
Trmt1l |
G |
T |
1: 151,333,632 (GRCm39) |
V712F |
possibly damaging |
Het |
Tti1 |
T |
C |
2: 157,848,940 (GRCm39) |
|
probably benign |
Het |
Ulk4 |
T |
C |
9: 120,970,918 (GRCm39) |
H1018R |
probably benign |
Het |
Vim |
A |
T |
2: 13,587,306 (GRCm39) |
H461L |
probably benign |
Het |
Vmn2r118 |
T |
A |
17: 55,917,665 (GRCm39) |
E282D |
probably damaging |
Het |
Vmn2r31 |
T |
A |
7: 7,387,367 (GRCm39) |
I735F |
probably damaging |
Het |
Vmn2r88 |
A |
G |
14: 51,656,250 (GRCm39) |
M829V |
probably benign |
Het |
Washc4 |
T |
A |
10: 83,410,407 (GRCm39) |
M665K |
possibly damaging |
Het |
Wbp2 |
T |
A |
11: 115,973,207 (GRCm39) |
M67L |
probably benign |
Het |
Wdr81 |
T |
A |
11: 75,336,814 (GRCm39) |
E1525V |
probably damaging |
Het |
Xbp1 |
A |
G |
11: 5,472,006 (GRCm39) |
D44G |
probably damaging |
Het |
Zfhx4 |
T |
G |
3: 5,464,341 (GRCm39) |
F1500V |
probably damaging |
Het |
Zfp286 |
A |
C |
11: 62,674,559 (GRCm39) |
Y95* |
probably null |
Het |
Zfp872 |
A |
G |
9: 22,111,057 (GRCm39) |
T178A |
possibly damaging |
Het |
Zkscan5 |
A |
G |
5: 145,155,640 (GRCm39) |
H364R |
possibly damaging |
Het |
Zp3r |
A |
T |
1: 130,505,697 (GRCm39) |
Y422N |
probably damaging |
Het |
Zscan10 |
C |
T |
17: 23,829,314 (GRCm39) |
R542C |
probably benign |
Het |
|
Other mutations in Rptor |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00537:Rptor
|
APN |
11 |
119,690,271 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01319:Rptor
|
APN |
11 |
119,781,996 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01375:Rptor
|
APN |
11 |
119,787,262 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01899:Rptor
|
APN |
11 |
119,748,279 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01927:Rptor
|
APN |
11 |
119,548,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02312:Rptor
|
APN |
11 |
119,737,741 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02620:Rptor
|
APN |
11 |
119,671,413 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02651:Rptor
|
APN |
11 |
119,783,438 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03182:Rptor
|
APN |
11 |
119,615,971 (GRCm39) |
missense |
probably damaging |
1.00 |
Velocipede
|
UTSW |
11 |
119,786,803 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0103:Rptor
|
UTSW |
11 |
119,775,793 (GRCm39) |
missense |
probably benign |
0.01 |
R0179:Rptor
|
UTSW |
11 |
119,763,193 (GRCm39) |
missense |
probably benign |
0.14 |
R0217:Rptor
|
UTSW |
11 |
119,785,738 (GRCm39) |
splice site |
probably benign |
|
R0219:Rptor
|
UTSW |
11 |
119,712,603 (GRCm39) |
intron |
probably benign |
|
R0324:Rptor
|
UTSW |
11 |
119,783,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R0432:Rptor
|
UTSW |
11 |
119,671,379 (GRCm39) |
nonsense |
probably null |
|
R0718:Rptor
|
UTSW |
11 |
119,763,202 (GRCm39) |
missense |
probably benign |
0.15 |
R0730:Rptor
|
UTSW |
11 |
119,775,780 (GRCm39) |
missense |
probably benign |
0.06 |
R1019:Rptor
|
UTSW |
11 |
119,734,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R1073:Rptor
|
UTSW |
11 |
119,634,717 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1424:Rptor
|
UTSW |
11 |
119,671,419 (GRCm39) |
nonsense |
probably null |
|
R1579:Rptor
|
UTSW |
11 |
119,786,827 (GRCm39) |
missense |
probably benign |
0.00 |
R1766:Rptor
|
UTSW |
11 |
119,615,887 (GRCm39) |
missense |
probably damaging |
0.99 |
R1844:Rptor
|
UTSW |
11 |
119,647,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R2180:Rptor
|
UTSW |
11 |
119,615,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R2274:Rptor
|
UTSW |
11 |
119,647,148 (GRCm39) |
nonsense |
probably null |
|
R2275:Rptor
|
UTSW |
11 |
119,647,148 (GRCm39) |
nonsense |
probably null |
|
R2408:Rptor
|
UTSW |
11 |
119,748,277 (GRCm39) |
missense |
probably damaging |
0.99 |
R2981:Rptor
|
UTSW |
11 |
119,756,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R2996:Rptor
|
UTSW |
11 |
119,747,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R3001:Rptor
|
UTSW |
11 |
119,763,197 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3002:Rptor
|
UTSW |
11 |
119,763,197 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3003:Rptor
|
UTSW |
11 |
119,763,197 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4358:Rptor
|
UTSW |
11 |
119,562,171 (GRCm39) |
missense |
probably damaging |
0.98 |
R4592:Rptor
|
UTSW |
11 |
119,689,666 (GRCm39) |
missense |
probably null |
1.00 |
R4666:Rptor
|
UTSW |
11 |
119,634,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R4958:Rptor
|
UTSW |
11 |
119,748,217 (GRCm39) |
missense |
probably benign |
0.29 |
R4974:Rptor
|
UTSW |
11 |
119,712,466 (GRCm39) |
intron |
probably benign |
|
R5073:Rptor
|
UTSW |
11 |
119,787,305 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5199:Rptor
|
UTSW |
11 |
119,494,642 (GRCm39) |
missense |
probably benign |
|
R5216:Rptor
|
UTSW |
11 |
119,734,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R5219:Rptor
|
UTSW |
11 |
119,734,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R5277:Rptor
|
UTSW |
11 |
119,713,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R5365:Rptor
|
UTSW |
11 |
119,734,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R5366:Rptor
|
UTSW |
11 |
119,734,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R5447:Rptor
|
UTSW |
11 |
119,734,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R5630:Rptor
|
UTSW |
11 |
119,647,075 (GRCm39) |
missense |
probably benign |
0.01 |
R6220:Rptor
|
UTSW |
11 |
119,788,268 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6567:Rptor
|
UTSW |
11 |
119,786,838 (GRCm39) |
missense |
probably benign |
0.00 |
R6741:Rptor
|
UTSW |
11 |
119,786,803 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6915:Rptor
|
UTSW |
11 |
119,647,171 (GRCm39) |
missense |
probably damaging |
0.99 |
R7032:Rptor
|
UTSW |
11 |
119,737,762 (GRCm39) |
missense |
probably benign |
0.00 |
R7051:Rptor
|
UTSW |
11 |
119,765,012 (GRCm39) |
utr 3 prime |
probably benign |
|
R7396:Rptor
|
UTSW |
11 |
119,763,181 (GRCm39) |
missense |
probably benign |
0.10 |
R7429:Rptor
|
UTSW |
11 |
119,737,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R7430:Rptor
|
UTSW |
11 |
119,737,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R7447:Rptor
|
UTSW |
11 |
119,775,805 (GRCm39) |
missense |
probably benign |
0.00 |
R7595:Rptor
|
UTSW |
11 |
119,634,779 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7776:Rptor
|
UTSW |
11 |
119,783,453 (GRCm39) |
missense |
probably benign |
0.01 |
R7854:Rptor
|
UTSW |
11 |
119,748,779 (GRCm39) |
missense |
probably benign |
0.02 |
R8288:Rptor
|
UTSW |
11 |
119,748,763 (GRCm39) |
missense |
probably benign |
0.02 |
R8305:Rptor
|
UTSW |
11 |
119,702,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R8328:Rptor
|
UTSW |
11 |
119,783,473 (GRCm39) |
missense |
probably benign |
0.00 |
R8351:Rptor
|
UTSW |
11 |
119,783,465 (GRCm39) |
missense |
probably benign |
0.22 |
R8772:Rptor
|
UTSW |
11 |
119,615,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Rptor
|
UTSW |
11 |
119,494,751 (GRCm39) |
missense |
probably benign |
0.01 |
R8925:Rptor
|
UTSW |
11 |
119,782,036 (GRCm39) |
missense |
probably benign |
0.11 |
R8927:Rptor
|
UTSW |
11 |
119,782,036 (GRCm39) |
missense |
probably benign |
0.11 |
R8981:Rptor
|
UTSW |
11 |
119,734,508 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9149:Rptor
|
UTSW |
11 |
119,777,896 (GRCm39) |
missense |
probably benign |
0.05 |
R9213:Rptor
|
UTSW |
11 |
119,494,765 (GRCm39) |
missense |
probably benign |
|
R9224:Rptor
|
UTSW |
11 |
119,785,113 (GRCm39) |
missense |
probably benign |
0.11 |
R9290:Rptor
|
UTSW |
11 |
119,702,823 (GRCm39) |
missense |
probably benign |
0.00 |
R9314:Rptor
|
UTSW |
11 |
119,786,772 (GRCm39) |
missense |
probably benign |
0.43 |
R9371:Rptor
|
UTSW |
11 |
119,562,152 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9719:Rptor
|
UTSW |
11 |
119,781,940 (GRCm39) |
missense |
probably benign |
0.13 |
R9751:Rptor
|
UTSW |
11 |
119,777,964 (GRCm39) |
missense |
probably benign |
0.02 |
X0050:Rptor
|
UTSW |
11 |
119,737,231 (GRCm39) |
missense |
probably benign |
0.14 |
X0066:Rptor
|
UTSW |
11 |
119,748,692 (GRCm39) |
missense |
probably benign |
0.31 |
Z0001:Rptor
|
UTSW |
11 |
119,762,318 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z0001:Rptor
|
UTSW |
11 |
119,748,279 (GRCm39) |
critical splice donor site |
probably benign |
|
Z0001:Rptor
|
UTSW |
11 |
119,742,294 (GRCm39) |
critical splice donor site |
probably benign |
|
Z0001:Rptor
|
UTSW |
11 |
119,737,578 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z0001:Rptor
|
UTSW |
11 |
119,690,145 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z0001:Rptor
|
UTSW |
11 |
119,647,241 (GRCm39) |
critical splice donor site |
probably benign |
|
Z0001:Rptor
|
UTSW |
11 |
119,647,062 (GRCm39) |
splice site |
probably null |
|
Z0001:Rptor
|
UTSW |
11 |
119,494,798 (GRCm39) |
critical splice donor site |
probably null |
|
Z0001:Rptor
|
UTSW |
11 |
119,787,375 (GRCm39) |
critical splice donor site |
probably benign |
|
Z0001:Rptor
|
UTSW |
11 |
119,764,977 (GRCm39) |
critical splice acceptor site |
probably benign |
|
|