Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
T |
A |
9: 44,190,691 (GRCm39) |
Q278H |
probably benign |
Het |
Ace3 |
T |
C |
11: 105,895,436 (GRCm39) |
|
probably null |
Het |
Aco1 |
T |
C |
4: 40,176,499 (GRCm39) |
V221A |
probably damaging |
Het |
Adamts20 |
T |
A |
15: 94,301,891 (GRCm39) |
H27L |
probably benign |
Het |
Adamts8 |
A |
G |
9: 30,867,808 (GRCm39) |
D544G |
probably benign |
Het |
Angptl4 |
C |
A |
17: 34,000,249 (GRCm39) |
E40* |
probably null |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Atf7ip2 |
T |
A |
16: 10,059,567 (GRCm39) |
I369N |
possibly damaging |
Het |
Atp6ap1l |
T |
A |
13: 91,031,806 (GRCm39) |
Y292F |
probably damaging |
Het |
Atp6v1b2 |
A |
T |
8: 69,555,459 (GRCm39) |
K217* |
probably null |
Het |
Bid |
C |
T |
6: 120,874,216 (GRCm39) |
A110T |
possibly damaging |
Het |
Blvra |
T |
A |
2: 126,937,068 (GRCm39) |
W174R |
probably damaging |
Het |
Catsperg1 |
C |
T |
7: 28,897,568 (GRCm39) |
G239R |
probably damaging |
Het |
Ccdc157 |
G |
T |
11: 4,096,549 (GRCm39) |
A400D |
probably damaging |
Het |
Chd2 |
G |
T |
7: 73,104,193 (GRCm39) |
P1298T |
probably damaging |
Het |
CK137956 |
G |
A |
4: 127,840,651 (GRCm39) |
L352F |
possibly damaging |
Het |
Col22a1 |
G |
A |
15: 71,741,989 (GRCm39) |
P503S |
unknown |
Het |
Cox15 |
C |
T |
19: 43,735,224 (GRCm39) |
R181H |
probably benign |
Het |
Crem |
C |
T |
18: 3,299,284 (GRCm39) |
G47R |
probably benign |
Het |
Crygs |
T |
A |
16: 22,625,304 (GRCm39) |
T46S |
probably benign |
Het |
Cts8 |
T |
A |
13: 61,401,429 (GRCm39) |
H62L |
probably damaging |
Het |
Cyp4a32 |
T |
A |
4: 115,468,474 (GRCm39) |
F319I |
possibly damaging |
Het |
Dchs1 |
T |
C |
7: 105,415,109 (GRCm39) |
S692G |
probably damaging |
Het |
Ddx23 |
G |
A |
15: 98,548,599 (GRCm39) |
R370W |
possibly damaging |
Het |
Defa29 |
A |
T |
8: 21,816,865 (GRCm39) |
S43T |
probably damaging |
Het |
Dnajc14 |
A |
G |
10: 128,652,661 (GRCm39) |
D573G |
probably damaging |
Het |
Drd5 |
A |
G |
5: 38,477,319 (GRCm39) |
Y104C |
probably benign |
Het |
Efcab7 |
C |
T |
4: 99,768,215 (GRCm39) |
P102L |
probably damaging |
Het |
Efhc1 |
A |
G |
1: 21,037,624 (GRCm39) |
Y267C |
probably damaging |
Het |
Eif2ak4 |
T |
C |
2: 118,278,967 (GRCm39) |
Y243H |
probably damaging |
Het |
Gfm2 |
T |
A |
13: 97,278,475 (GRCm39) |
I7N |
probably damaging |
Het |
Gmds |
A |
G |
13: 32,311,980 (GRCm39) |
F150L |
possibly damaging |
Het |
Gp2 |
T |
C |
7: 119,053,455 (GRCm39) |
T169A |
possibly damaging |
Het |
Grb14 |
A |
G |
2: 64,743,146 (GRCm39) |
F508L |
probably damaging |
Het |
Hdac5 |
T |
A |
11: 102,086,698 (GRCm39) |
|
probably benign |
Het |
Heatr1 |
T |
A |
13: 12,450,066 (GRCm39) |
M620K |
probably damaging |
Het |
Herc3 |
A |
G |
6: 58,853,778 (GRCm39) |
E608G |
probably damaging |
Het |
Hoxb4 |
T |
C |
11: 96,210,867 (GRCm39) |
Y156H |
probably damaging |
Het |
Ifi205 |
T |
A |
1: 173,855,980 (GRCm39) |
I17F |
possibly damaging |
Het |
Il2rb |
A |
T |
15: 78,375,977 (GRCm39) |
S25T |
possibly damaging |
Het |
Kansl1 |
T |
C |
11: 104,225,923 (GRCm39) |
T998A |
probably damaging |
Het |
Kcna6 |
G |
T |
6: 126,715,451 (GRCm39) |
H479Q |
probably benign |
Het |
Kif2a |
T |
C |
13: 107,114,599 (GRCm39) |
K350R |
probably benign |
Het |
Lct |
G |
T |
1: 128,221,898 (GRCm39) |
A1547E |
probably damaging |
Het |
Lhx9 |
T |
A |
1: 138,769,747 (GRCm39) |
|
probably benign |
Het |
Lingo1 |
T |
A |
9: 56,526,934 (GRCm39) |
I552F |
possibly damaging |
Het |
Lrp4 |
G |
A |
2: 91,327,700 (GRCm39) |
W1516* |
probably null |
Het |
Lrp5 |
C |
T |
19: 3,660,131 (GRCm39) |
V978I |
probably benign |
Het |
Ltbp1 |
T |
A |
17: 75,620,029 (GRCm39) |
D719E |
probably benign |
Het |
Ltbp4 |
A |
G |
7: 27,007,191 (GRCm39) |
|
probably null |
Het |
Macf1 |
A |
G |
4: 123,345,830 (GRCm39) |
I1326T |
probably damaging |
Het |
Manba |
T |
C |
3: 135,250,501 (GRCm39) |
F376S |
probably benign |
Het |
Mink1 |
T |
C |
11: 70,499,254 (GRCm39) |
|
probably null |
Het |
Nfatc2ip |
C |
T |
7: 125,984,164 (GRCm39) |
V410I |
probably damaging |
Het |
Nlrp1b |
A |
T |
11: 71,072,964 (GRCm39) |
I293N |
probably damaging |
Het |
Or10aa3 |
T |
C |
1: 173,878,244 (GRCm39) |
Y102H |
probably damaging |
Het |
Otol1 |
A |
C |
3: 69,935,437 (GRCm39) |
E476D |
probably benign |
Het |
Pcdhb4 |
C |
T |
18: 37,442,594 (GRCm39) |
P635S |
probably benign |
Het |
Pfkfb4 |
T |
A |
9: 108,828,237 (GRCm39) |
F91I |
probably damaging |
Het |
Polq |
G |
A |
16: 36,882,666 (GRCm39) |
R1610Q |
possibly damaging |
Het |
Polr3c |
A |
T |
3: 96,626,614 (GRCm39) |
L270H |
probably damaging |
Het |
Ppp1r15b |
C |
T |
1: 133,059,363 (GRCm39) |
|
probably benign |
Het |
Prkca |
T |
G |
11: 108,082,975 (GRCm39) |
D90A |
probably benign |
Het |
Sall3 |
T |
C |
18: 81,012,968 (GRCm39) |
D1156G |
probably benign |
Het |
Scn7a |
A |
T |
2: 66,506,446 (GRCm39) |
L1481H |
probably damaging |
Het |
Selenon |
A |
T |
4: 134,271,929 (GRCm39) |
I292N |
probably damaging |
Het |
Sema6d |
T |
A |
2: 124,501,806 (GRCm39) |
|
probably null |
Het |
Sgpp1 |
G |
T |
12: 75,762,953 (GRCm39) |
Y409* |
probably null |
Het |
Sh3pxd2a |
A |
G |
19: 47,255,947 (GRCm39) |
S924P |
probably benign |
Het |
Slc25a13 |
A |
G |
6: 6,042,264 (GRCm39) |
V638A |
probably benign |
Het |
Snhg11 |
T |
C |
2: 158,218,746 (GRCm39) |
|
probably benign |
Het |
Sorbs2 |
A |
G |
8: 46,249,389 (GRCm39) |
Q800R |
probably benign |
Het |
Srf |
C |
A |
17: 46,860,912 (GRCm39) |
G401C |
probably damaging |
Het |
Stradb |
A |
C |
1: 59,030,264 (GRCm39) |
N173H |
probably benign |
Het |
Swap70 |
C |
T |
7: 109,878,470 (GRCm39) |
A480V |
possibly damaging |
Het |
Sycp2 |
A |
G |
2: 178,023,750 (GRCm39) |
V422A |
probably damaging |
Het |
Taf4 |
G |
A |
2: 179,573,822 (GRCm39) |
T682M |
probably damaging |
Het |
Tet3 |
T |
C |
6: 83,381,361 (GRCm39) |
N269S |
possibly damaging |
Het |
Thap12 |
A |
T |
7: 98,366,045 (GRCm39) |
I738F |
possibly damaging |
Het |
Tiam2 |
C |
T |
17: 3,565,000 (GRCm39) |
R1413C |
possibly damaging |
Het |
Tmem229a |
A |
T |
6: 24,955,010 (GRCm39) |
F248Y |
probably damaging |
Het |
Tmprss7 |
G |
A |
16: 45,504,956 (GRCm39) |
Q145* |
probably null |
Het |
Tnc |
A |
T |
4: 63,911,262 (GRCm39) |
|
probably null |
Het |
Tonsl |
A |
T |
15: 76,508,797 (GRCm39) |
Y21N |
probably damaging |
Het |
Trpm2 |
G |
A |
10: 77,776,992 (GRCm39) |
A435V |
probably damaging |
Het |
Ubr3 |
T |
A |
2: 69,783,820 (GRCm39) |
|
probably null |
Het |
Vcan |
T |
C |
13: 89,853,653 (GRCm39) |
N436D |
possibly damaging |
Het |
Vmn2r104 |
T |
A |
17: 20,261,031 (GRCm39) |
Y464F |
probably damaging |
Het |
Vmn2r44 |
T |
A |
7: 8,370,981 (GRCm39) |
R688S |
probably benign |
Het |
Wdr74 |
G |
T |
19: 8,715,311 (GRCm39) |
V157L |
probably benign |
Het |
Wnt7a |
T |
A |
6: 91,371,530 (GRCm39) |
D144V |
probably benign |
Het |
Zfp106 |
C |
T |
2: 120,362,162 (GRCm39) |
A986T |
possibly damaging |
Het |
|
Other mutations in Tpr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00327:Tpr
|
APN |
1 |
150,299,447 (GRCm39) |
splice site |
probably benign |
|
IGL00424:Tpr
|
APN |
1 |
150,274,346 (GRCm39) |
splice site |
probably benign |
|
IGL01095:Tpr
|
APN |
1 |
150,285,891 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01347:Tpr
|
APN |
1 |
150,302,738 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01519:Tpr
|
APN |
1 |
150,306,919 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01768:Tpr
|
APN |
1 |
150,320,199 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01939:Tpr
|
APN |
1 |
150,289,496 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01988:Tpr
|
APN |
1 |
150,302,750 (GRCm39) |
splice site |
probably null |
|
IGL02065:Tpr
|
APN |
1 |
150,289,525 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02110:Tpr
|
APN |
1 |
150,311,493 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02311:Tpr
|
APN |
1 |
150,274,404 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02454:Tpr
|
APN |
1 |
150,306,943 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02569:Tpr
|
APN |
1 |
150,301,382 (GRCm39) |
unclassified |
probably benign |
|
IGL03168:Tpr
|
APN |
1 |
150,284,508 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03193:Tpr
|
APN |
1 |
150,315,831 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03333:Tpr
|
APN |
1 |
150,302,718 (GRCm39) |
missense |
probably benign |
0.04 |
gridiron
|
UTSW |
1 |
150,299,267 (GRCm39) |
missense |
probably damaging |
1.00 |
Pouch
|
UTSW |
1 |
150,309,523 (GRCm39) |
missense |
probably damaging |
1.00 |
punt
|
UTSW |
1 |
150,293,790 (GRCm39) |
missense |
probably benign |
0.02 |
Turf
|
UTSW |
1 |
150,317,996 (GRCm39) |
critical splice donor site |
probably null |
|
F6893:Tpr
|
UTSW |
1 |
150,269,313 (GRCm39) |
missense |
possibly damaging |
0.84 |
PIT4305001:Tpr
|
UTSW |
1 |
150,315,888 (GRCm39) |
missense |
possibly damaging |
0.85 |
PIT4469001:Tpr
|
UTSW |
1 |
150,279,707 (GRCm39) |
missense |
probably benign |
0.41 |
R0085:Tpr
|
UTSW |
1 |
150,293,164 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0101:Tpr
|
UTSW |
1 |
150,285,053 (GRCm39) |
splice site |
probably benign |
|
R0116:Tpr
|
UTSW |
1 |
150,285,898 (GRCm39) |
missense |
probably damaging |
0.98 |
R0136:Tpr
|
UTSW |
1 |
150,306,346 (GRCm39) |
missense |
probably benign |
0.01 |
R0207:Tpr
|
UTSW |
1 |
150,293,178 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0219:Tpr
|
UTSW |
1 |
150,319,009 (GRCm39) |
splice site |
probably null |
|
R0380:Tpr
|
UTSW |
1 |
150,288,698 (GRCm39) |
missense |
probably benign |
0.27 |
R0403:Tpr
|
UTSW |
1 |
150,283,165 (GRCm39) |
splice site |
probably benign |
|
R0469:Tpr
|
UTSW |
1 |
150,299,418 (GRCm39) |
frame shift |
probably null |
|
R0480:Tpr
|
UTSW |
1 |
150,303,992 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0514:Tpr
|
UTSW |
1 |
150,278,024 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0563:Tpr
|
UTSW |
1 |
150,284,609 (GRCm39) |
missense |
probably benign |
0.13 |
R0631:Tpr
|
UTSW |
1 |
150,298,282 (GRCm39) |
missense |
probably damaging |
0.98 |
R0685:Tpr
|
UTSW |
1 |
150,309,476 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0730:Tpr
|
UTSW |
1 |
150,269,158 (GRCm39) |
utr 5 prime |
probably benign |
|
R0739:Tpr
|
UTSW |
1 |
150,283,248 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0780:Tpr
|
UTSW |
1 |
150,307,092 (GRCm39) |
missense |
probably benign |
0.00 |
R1018:Tpr
|
UTSW |
1 |
150,317,934 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1084:Tpr
|
UTSW |
1 |
150,317,912 (GRCm39) |
missense |
probably benign |
0.18 |
R1532:Tpr
|
UTSW |
1 |
150,293,751 (GRCm39) |
missense |
probably damaging |
0.99 |
R1551:Tpr
|
UTSW |
1 |
150,312,552 (GRCm39) |
missense |
probably benign |
0.00 |
R1608:Tpr
|
UTSW |
1 |
150,302,644 (GRCm39) |
missense |
probably damaging |
0.96 |
R1759:Tpr
|
UTSW |
1 |
150,305,275 (GRCm39) |
missense |
probably benign |
0.19 |
R1817:Tpr
|
UTSW |
1 |
150,295,654 (GRCm39) |
missense |
probably damaging |
0.98 |
R1978:Tpr
|
UTSW |
1 |
150,295,658 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2031:Tpr
|
UTSW |
1 |
150,317,870 (GRCm39) |
missense |
probably benign |
|
R2176:Tpr
|
UTSW |
1 |
150,295,691 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2235:Tpr
|
UTSW |
1 |
150,317,843 (GRCm39) |
missense |
probably benign |
0.33 |
R2339:Tpr
|
UTSW |
1 |
150,289,525 (GRCm39) |
missense |
probably benign |
0.01 |
R2367:Tpr
|
UTSW |
1 |
150,309,479 (GRCm39) |
missense |
probably damaging |
0.99 |
R2507:Tpr
|
UTSW |
1 |
150,268,695 (GRCm39) |
start codon destroyed |
probably null |
|
R3931:Tpr
|
UTSW |
1 |
150,311,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R4320:Tpr
|
UTSW |
1 |
150,299,325 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4439:Tpr
|
UTSW |
1 |
150,279,712 (GRCm39) |
missense |
probably benign |
0.01 |
R4568:Tpr
|
UTSW |
1 |
150,268,710 (GRCm39) |
unclassified |
probably benign |
|
R4644:Tpr
|
UTSW |
1 |
150,299,250 (GRCm39) |
missense |
probably benign |
0.01 |
R4665:Tpr
|
UTSW |
1 |
150,320,150 (GRCm39) |
missense |
probably damaging |
0.97 |
R4672:Tpr
|
UTSW |
1 |
150,299,318 (GRCm39) |
missense |
probably benign |
0.45 |
R4673:Tpr
|
UTSW |
1 |
150,299,318 (GRCm39) |
missense |
probably benign |
0.45 |
R4735:Tpr
|
UTSW |
1 |
150,317,947 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4767:Tpr
|
UTSW |
1 |
150,306,280 (GRCm39) |
intron |
probably benign |
|
R4772:Tpr
|
UTSW |
1 |
150,288,864 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4815:Tpr
|
UTSW |
1 |
150,274,359 (GRCm39) |
missense |
probably benign |
0.01 |
R4839:Tpr
|
UTSW |
1 |
150,324,948 (GRCm39) |
nonsense |
probably null |
|
R4844:Tpr
|
UTSW |
1 |
150,321,630 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4925:Tpr
|
UTSW |
1 |
150,308,316 (GRCm39) |
missense |
probably benign |
0.00 |
R4967:Tpr
|
UTSW |
1 |
150,285,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R5017:Tpr
|
UTSW |
1 |
150,274,388 (GRCm39) |
missense |
probably benign |
0.00 |
R5096:Tpr
|
UTSW |
1 |
150,321,953 (GRCm39) |
missense |
probably damaging |
0.99 |
R5353:Tpr
|
UTSW |
1 |
150,321,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Tpr
|
UTSW |
1 |
150,321,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R5484:Tpr
|
UTSW |
1 |
150,302,639 (GRCm39) |
missense |
probably benign |
0.33 |
R5601:Tpr
|
UTSW |
1 |
150,311,604 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5642:Tpr
|
UTSW |
1 |
150,299,569 (GRCm39) |
missense |
probably damaging |
0.99 |
R5779:Tpr
|
UTSW |
1 |
150,299,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R5787:Tpr
|
UTSW |
1 |
150,271,037 (GRCm39) |
missense |
probably benign |
0.01 |
R5892:Tpr
|
UTSW |
1 |
150,283,151 (GRCm39) |
missense |
probably benign |
0.44 |
R5915:Tpr
|
UTSW |
1 |
150,301,400 (GRCm39) |
missense |
probably benign |
0.15 |
R5928:Tpr
|
UTSW |
1 |
150,303,878 (GRCm39) |
missense |
probably benign |
0.30 |
R6146:Tpr
|
UTSW |
1 |
150,298,913 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6154:Tpr
|
UTSW |
1 |
150,299,567 (GRCm39) |
missense |
probably benign |
0.00 |
R6234:Tpr
|
UTSW |
1 |
150,293,790 (GRCm39) |
missense |
probably benign |
0.02 |
R6263:Tpr
|
UTSW |
1 |
150,317,996 (GRCm39) |
critical splice donor site |
probably null |
|
R6318:Tpr
|
UTSW |
1 |
150,321,639 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6550:Tpr
|
UTSW |
1 |
150,299,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R6592:Tpr
|
UTSW |
1 |
150,287,656 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6704:Tpr
|
UTSW |
1 |
150,282,259 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6716:Tpr
|
UTSW |
1 |
150,290,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6836:Tpr
|
UTSW |
1 |
150,312,424 (GRCm39) |
splice site |
probably null |
|
R6886:Tpr
|
UTSW |
1 |
150,299,716 (GRCm39) |
missense |
probably benign |
0.00 |
R6894:Tpr
|
UTSW |
1 |
150,312,598 (GRCm39) |
missense |
probably benign |
0.28 |
R6928:Tpr
|
UTSW |
1 |
150,284,536 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7011:Tpr
|
UTSW |
1 |
150,309,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R7034:Tpr
|
UTSW |
1 |
150,299,358 (GRCm39) |
missense |
probably benign |
0.02 |
R7036:Tpr
|
UTSW |
1 |
150,299,358 (GRCm39) |
missense |
probably benign |
0.02 |
R7183:Tpr
|
UTSW |
1 |
150,282,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7221:Tpr
|
UTSW |
1 |
150,321,929 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7223:Tpr
|
UTSW |
1 |
150,315,007 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7294:Tpr
|
UTSW |
1 |
150,279,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Tpr
|
UTSW |
1 |
150,269,245 (GRCm39) |
missense |
unknown |
|
R7361:Tpr
|
UTSW |
1 |
150,323,372 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7405:Tpr
|
UTSW |
1 |
150,317,878 (GRCm39) |
missense |
probably benign |
0.02 |
R7637:Tpr
|
UTSW |
1 |
150,299,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R7720:Tpr
|
UTSW |
1 |
150,305,283 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7721:Tpr
|
UTSW |
1 |
150,320,180 (GRCm39) |
missense |
probably benign |
|
R7751:Tpr
|
UTSW |
1 |
150,295,646 (GRCm39) |
missense |
probably benign |
0.17 |
R7804:Tpr
|
UTSW |
1 |
150,308,310 (GRCm39) |
missense |
probably damaging |
0.99 |
R7878:Tpr
|
UTSW |
1 |
150,299,411 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7973:Tpr
|
UTSW |
1 |
150,279,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R8013:Tpr
|
UTSW |
1 |
150,274,359 (GRCm39) |
missense |
probably benign |
|
R8220:Tpr
|
UTSW |
1 |
150,308,164 (GRCm39) |
missense |
probably benign |
0.05 |
R8274:Tpr
|
UTSW |
1 |
150,299,230 (GRCm39) |
splice site |
probably benign |
|
R8428:Tpr
|
UTSW |
1 |
150,290,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R8482:Tpr
|
UTSW |
1 |
150,309,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R8699:Tpr
|
UTSW |
1 |
150,293,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R8859:Tpr
|
UTSW |
1 |
150,284,597 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9119:Tpr
|
UTSW |
1 |
150,279,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R9326:Tpr
|
UTSW |
1 |
150,301,407 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9618:Tpr
|
UTSW |
1 |
150,321,979 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9680:Tpr
|
UTSW |
1 |
150,314,887 (GRCm39) |
missense |
probably benign |
0.32 |
R9776:Tpr
|
UTSW |
1 |
150,324,939 (GRCm39) |
missense |
probably benign |
0.00 |
X0021:Tpr
|
UTSW |
1 |
150,270,958 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tpr
|
UTSW |
1 |
150,303,986 (GRCm39) |
missense |
probably damaging |
0.99 |
|