Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
A |
T |
2: 69,104,487 (GRCm39) |
V733E |
probably benign |
Het |
Adam34 |
A |
T |
8: 44,105,041 (GRCm39) |
N201K |
probably benign |
Het |
Aldh3b2 |
A |
C |
19: 4,029,592 (GRCm39) |
S322R |
probably damaging |
Het |
Anpep |
A |
T |
7: 79,475,058 (GRCm39) |
L914Q |
probably damaging |
Het |
Arhgap30 |
T |
C |
1: 171,235,139 (GRCm39) |
F535S |
probably damaging |
Het |
Baiap3 |
G |
A |
17: 25,462,814 (GRCm39) |
R1075C |
probably benign |
Het |
Baz2a |
G |
T |
10: 127,948,475 (GRCm39) |
G252V |
probably damaging |
Het |
Brinp3 |
T |
A |
1: 146,776,812 (GRCm39) |
S420T |
possibly damaging |
Het |
Carmil3 |
T |
C |
14: 55,733,695 (GRCm39) |
F359S |
possibly damaging |
Het |
Ccdc124 |
A |
T |
8: 71,321,170 (GRCm39) |
L190Q |
probably damaging |
Het |
Ccr6 |
T |
C |
17: 8,474,972 (GRCm39) |
V59A |
probably damaging |
Het |
Ccr8 |
T |
A |
9: 119,923,683 (GRCm39) |
I266N |
probably damaging |
Het |
Cdh23 |
T |
A |
10: 60,167,596 (GRCm39) |
E1798V |
probably damaging |
Het |
Cdk5rap2 |
T |
C |
4: 70,153,684 (GRCm39) |
N1713S |
probably benign |
Het |
Cep19 |
T |
A |
16: 31,922,833 (GRCm39) |
I33N |
probably damaging |
Het |
Cers3 |
A |
T |
7: 66,433,163 (GRCm39) |
Y196F |
probably damaging |
Het |
Cidea |
T |
C |
18: 67,499,491 (GRCm39) |
I126T |
probably damaging |
Het |
Copg2 |
A |
T |
6: 30,789,689 (GRCm39) |
Y546* |
probably null |
Het |
Cul3 |
A |
T |
1: 80,264,717 (GRCm39) |
V261E |
probably benign |
Het |
Cyp2g1 |
A |
T |
7: 26,514,057 (GRCm39) |
D221V |
probably damaging |
Het |
Cyp8b1 |
G |
A |
9: 121,744,163 (GRCm39) |
H390Y |
probably damaging |
Het |
Daam1 |
T |
C |
12: 72,035,717 (GRCm39) |
F971L |
probably damaging |
Het |
Dnajc24 |
G |
A |
2: 105,832,311 (GRCm39) |
S24L |
possibly damaging |
Het |
Dpysl3 |
T |
C |
18: 43,571,107 (GRCm39) |
S56G |
probably benign |
Het |
Esp1 |
A |
G |
17: 41,041,972 (GRCm39) |
D88G |
probably benign |
Het |
Fam171b |
A |
G |
2: 83,708,574 (GRCm39) |
T359A |
probably damaging |
Het |
Fam186b |
T |
C |
15: 99,177,718 (GRCm39) |
E536G |
possibly damaging |
Het |
Fbxo3 |
T |
C |
2: 103,873,357 (GRCm39) |
V156A |
possibly damaging |
Het |
Gls2 |
C |
A |
10: 128,035,063 (GRCm39) |
H65Q |
probably benign |
Het |
Gp2 |
A |
G |
7: 119,050,721 (GRCm39) |
|
probably null |
Het |
Gpcpd1 |
T |
A |
2: 132,375,976 (GRCm39) |
K435I |
probably benign |
Het |
Gpx6 |
T |
A |
13: 21,501,840 (GRCm39) |
|
probably null |
Het |
Hps3 |
A |
T |
3: 20,084,583 (GRCm39) |
S202T |
probably benign |
Het |
Htr1d |
T |
A |
4: 136,170,812 (GRCm39) |
L347H |
probably damaging |
Het |
Igfals |
T |
C |
17: 25,100,208 (GRCm39) |
L433P |
probably damaging |
Het |
Ilvbl |
C |
T |
10: 78,419,530 (GRCm39) |
H537Y |
probably benign |
Het |
Iqgap2 |
A |
T |
13: 95,765,480 (GRCm39) |
M1530K |
probably damaging |
Het |
Jarid2 |
A |
G |
13: 45,049,798 (GRCm39) |
T247A |
possibly damaging |
Het |
L3hypdh |
C |
T |
12: 72,120,783 (GRCm39) |
V323I |
possibly damaging |
Het |
Lama3 |
C |
T |
18: 12,715,665 (GRCm39) |
T1707I |
possibly damaging |
Het |
Map6 |
G |
T |
7: 98,917,232 (GRCm39) |
A2S |
probably damaging |
Het |
Mfap3 |
T |
A |
11: 57,421,066 (GRCm39) |
I349K |
probably benign |
Het |
Mybl2 |
A |
G |
2: 162,914,625 (GRCm39) |
T248A |
probably benign |
Het |
N6amt1 |
A |
G |
16: 87,159,548 (GRCm39) |
*151W |
probably null |
Het |
Nhlrc1 |
A |
G |
13: 47,167,684 (GRCm39) |
V191A |
probably benign |
Het |
Nkx2-5 |
T |
C |
17: 27,058,594 (GRCm39) |
E120G |
possibly damaging |
Het |
Or2y10 |
T |
A |
11: 49,454,925 (GRCm39) |
M59K |
probably damaging |
Het |
Or52r1b |
C |
A |
7: 102,690,839 (GRCm39) |
T46N |
possibly damaging |
Het |
Or8b41 |
T |
C |
9: 38,055,049 (GRCm39) |
V201A |
probably benign |
Het |
Or8k28 |
T |
A |
2: 86,286,211 (GRCm39) |
I135F |
possibly damaging |
Het |
Pcdha8 |
T |
G |
18: 37,126,201 (GRCm39) |
L228V |
probably benign |
Het |
Pcsk2 |
A |
G |
2: 143,532,253 (GRCm39) |
T134A |
possibly damaging |
Het |
Phldb3 |
G |
A |
7: 24,324,078 (GRCm39) |
R484Q |
probably benign |
Het |
Pipox |
A |
G |
11: 77,772,012 (GRCm39) |
S371P |
probably damaging |
Het |
Plekhg1 |
T |
C |
10: 3,823,343 (GRCm39) |
S159P |
|
Het |
Psme4 |
C |
T |
11: 30,824,226 (GRCm39) |
P1737S |
probably benign |
Het |
Pygm |
G |
A |
19: 6,438,893 (GRCm39) |
D328N |
probably benign |
Het |
Rabgef1 |
A |
T |
5: 130,219,801 (GRCm39) |
E88V |
probably benign |
Het |
Rims2 |
G |
T |
15: 39,300,428 (GRCm39) |
R245L |
probably benign |
Het |
Slc38a4 |
T |
C |
15: 96,908,226 (GRCm39) |
I172V |
probably damaging |
Het |
Slc4a10 |
T |
A |
2: 62,099,009 (GRCm39) |
Y586N |
probably damaging |
Het |
Snap91 |
C |
T |
9: 86,761,610 (GRCm39) |
|
probably benign |
Het |
Sorcs1 |
C |
T |
19: 50,178,480 (GRCm39) |
V881I |
probably benign |
Het |
Spef2 |
A |
T |
15: 9,601,726 (GRCm39) |
V1512E |
unknown |
Het |
Sufu |
T |
C |
19: 46,441,716 (GRCm39) |
I292T |
possibly damaging |
Het |
Tet1 |
T |
C |
10: 62,649,450 (GRCm39) |
N87D |
possibly damaging |
Het |
Tmem108 |
T |
C |
9: 103,376,733 (GRCm39) |
T239A |
not run |
Het |
Tmem121 |
A |
T |
12: 113,152,114 (GRCm39) |
K111* |
probably null |
Het |
Tpp2 |
T |
A |
1: 44,008,048 (GRCm39) |
D417E |
probably damaging |
Het |
Trappc3 |
C |
T |
4: 126,168,945 (GRCm39) |
A145V |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,721,325 (GRCm39) |
D6754G |
probably null |
Het |
Unc13c |
T |
A |
9: 73,536,473 (GRCm39) |
M1627L |
probably benign |
Het |
Ush2a |
A |
G |
1: 188,542,414 (GRCm39) |
I3327V |
probably benign |
Het |
Vmn1r74 |
C |
T |
7: 11,580,894 (GRCm39) |
Q65* |
probably null |
Het |
Wdr18 |
G |
A |
10: 79,796,202 (GRCm39) |
R69H |
probably damaging |
Het |
Zbed5 |
G |
T |
5: 129,929,279 (GRCm39) |
D132Y |
probably damaging |
Het |
Zfp644 |
A |
T |
5: 106,785,448 (GRCm39) |
Y366* |
probably null |
Het |
Zfyve26 |
T |
C |
12: 79,292,945 (GRCm39) |
N2068S |
probably damaging |
Het |
Zic2 |
T |
C |
14: 122,713,503 (GRCm39) |
F139S |
probably damaging |
Het |
Zmynd11 |
T |
C |
13: 9,760,198 (GRCm39) |
Q141R |
probably benign |
Het |
Zrsr2-ps1 |
A |
G |
11: 22,923,388 (GRCm39) |
E54G |
probably benign |
Het |
Zscan10 |
G |
A |
17: 23,828,456 (GRCm39) |
D333N |
probably benign |
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 |
R1932:Tpr
|
UTSW |
1 |
150,297,414 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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 |
|