Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503B20Rik |
A |
G |
3: 146,356,363 (GRCm39) |
F182L |
probably damaging |
Het |
4930503B20Rik |
T |
C |
3: 146,356,713 (GRCm39) |
Y65C |
probably damaging |
Het |
4930590J08Rik |
A |
G |
6: 91,896,174 (GRCm39) |
T341A |
probably benign |
Het |
Adamts13 |
G |
A |
2: 26,876,570 (GRCm39) |
V495I |
probably benign |
Het |
Alms1 |
C |
A |
6: 85,600,070 (GRCm39) |
T2101K |
probably benign |
Het |
Als2 |
T |
C |
1: 59,214,105 (GRCm39) |
D1361G |
probably benign |
Het |
Ankdd1a |
A |
T |
9: 65,412,496 (GRCm39) |
M275K |
probably benign |
Het |
Arfip2 |
A |
T |
7: 105,286,183 (GRCm39) |
Y161* |
probably null |
Het |
Asap3 |
A |
T |
4: 135,968,570 (GRCm39) |
E707D |
probably benign |
Het |
Atm |
C |
T |
9: 53,419,077 (GRCm39) |
|
probably null |
Het |
Atp9b |
A |
T |
18: 80,820,052 (GRCm39) |
S577R |
probably benign |
Het |
Bltp1 |
G |
T |
3: 36,971,817 (GRCm39) |
V517F |
probably damaging |
Het |
Camk1d |
G |
C |
2: 5,308,177 (GRCm39) |
D274E |
probably benign |
Het |
Cebpz |
C |
T |
17: 79,229,634 (GRCm39) |
D907N |
probably benign |
Het |
Cmtm1 |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
8: 105,036,102 (GRCm39) |
|
probably benign |
Het |
Cnst |
T |
A |
1: 179,429,301 (GRCm39) |
|
probably benign |
Het |
Cog2 |
G |
T |
8: 125,259,268 (GRCm39) |
V196L |
probably benign |
Het |
Col11a1 |
A |
G |
3: 113,987,833 (GRCm39) |
|
probably null |
Het |
Cops6 |
T |
A |
5: 138,161,762 (GRCm39) |
|
probably null |
Het |
Cspg4 |
A |
G |
9: 56,797,484 (GRCm39) |
E1316G |
probably damaging |
Het |
Cwc22 |
G |
C |
2: 77,759,683 (GRCm39) |
D122E |
possibly damaging |
Het |
Dapk2 |
G |
A |
9: 66,176,000 (GRCm39) |
V300M |
probably benign |
Het |
Dcp1b |
C |
A |
6: 119,152,328 (GRCm39) |
D25E |
probably damaging |
Het |
Ddx10 |
A |
T |
9: 53,145,157 (GRCm39) |
Y273* |
probably null |
Het |
Dhx58 |
T |
C |
11: 100,589,034 (GRCm39) |
E504G |
probably benign |
Het |
Dync2h1 |
C |
T |
9: 7,120,899 (GRCm39) |
W2129* |
probably null |
Het |
Egr4 |
A |
T |
6: 85,489,442 (GRCm39) |
L206Q |
probably damaging |
Het |
Eif4g3 |
A |
G |
4: 137,830,709 (GRCm39) |
|
probably null |
Het |
Fbxo46 |
A |
G |
7: 18,870,541 (GRCm39) |
N387D |
possibly damaging |
Het |
Fpr-rs3 |
T |
G |
17: 20,844,470 (GRCm39) |
M224L |
probably benign |
Het |
Gm14325 |
G |
A |
2: 177,474,777 (GRCm39) |
H102Y |
possibly damaging |
Het |
Gxylt2 |
A |
G |
6: 100,682,075 (GRCm39) |
K91E |
probably benign |
Het |
Hecw1 |
A |
T |
13: 14,497,174 (GRCm39) |
V278E |
probably damaging |
Het |
Hydin |
A |
G |
8: 111,266,474 (GRCm39) |
|
probably null |
Het |
Iars1 |
T |
C |
13: 49,875,641 (GRCm39) |
L776P |
probably damaging |
Het |
Kcnh2 |
T |
A |
5: 24,537,039 (GRCm39) |
T182S |
probably benign |
Het |
Kplce |
T |
C |
3: 92,776,005 (GRCm39) |
E226G |
probably damaging |
Het |
Lats2 |
T |
G |
14: 57,928,810 (GRCm39) |
S1022R |
probably benign |
Het |
Lef1 |
C |
T |
3: 130,988,308 (GRCm39) |
P264S |
probably damaging |
Het |
Lyrm1 |
A |
C |
7: 119,513,471 (GRCm39) |
I79L |
possibly damaging |
Het |
Macroh2a2 |
G |
A |
10: 61,587,466 (GRCm39) |
T156M |
possibly damaging |
Het |
Man2b2 |
T |
G |
5: 36,971,862 (GRCm39) |
Q618P |
probably benign |
Het |
Mei1 |
T |
C |
15: 81,976,957 (GRCm39) |
V180A |
possibly damaging |
Het |
Mmp15 |
A |
T |
8: 96,093,032 (GRCm39) |
N137I |
probably damaging |
Het |
Mms22l |
A |
G |
4: 24,517,115 (GRCm39) |
D222G |
possibly damaging |
Het |
Mmut |
T |
A |
17: 41,258,075 (GRCm39) |
S414T |
probably benign |
Het |
Myo18a |
T |
C |
11: 77,744,176 (GRCm39) |
M1846T |
probably benign |
Het |
Neo1 |
A |
T |
9: 58,897,517 (GRCm39) |
N146K |
probably benign |
Het |
Nos3 |
A |
G |
5: 24,588,888 (GRCm39) |
T1174A |
probably benign |
Het |
Or10d4b |
A |
T |
9: 39,534,430 (GRCm39) |
T4S |
probably benign |
Het |
Or10x1 |
T |
C |
1: 174,196,836 (GRCm39) |
Y118H |
probably damaging |
Het |
Or4c125 |
A |
T |
2: 89,169,806 (GRCm39) |
I280N |
probably damaging |
Het |
Or51f1 |
A |
T |
7: 102,505,686 (GRCm39) |
S268T |
probably damaging |
Het |
Pax8 |
A |
T |
2: 24,332,922 (GRCm39) |
|
probably benign |
Het |
Pde5a |
G |
A |
3: 122,611,658 (GRCm39) |
C532Y |
probably damaging |
Het |
Pigq |
T |
C |
17: 26,150,446 (GRCm39) |
D442G |
possibly damaging |
Het |
Pik3c2g |
T |
C |
6: 139,665,808 (GRCm39) |
V43A |
probably benign |
Het |
Pik3cb |
T |
C |
9: 98,970,716 (GRCm39) |
N325S |
probably benign |
Het |
Pot1b |
T |
C |
17: 56,007,063 (GRCm39) |
K18R |
probably benign |
Het |
Ppp1r42 |
A |
T |
1: 10,069,630 (GRCm39) |
L144Q |
probably damaging |
Het |
Prdm13 |
T |
A |
4: 21,679,455 (GRCm39) |
Q345L |
unknown |
Het |
Pyroxd2 |
T |
A |
19: 42,728,898 (GRCm39) |
K167N |
probably benign |
Het |
Rnf123 |
T |
C |
9: 107,947,930 (GRCm39) |
Y131C |
probably damaging |
Het |
Rnf25 |
T |
C |
1: 74,634,411 (GRCm39) |
D204G |
probably damaging |
Het |
Rpf2 |
G |
A |
10: 40,109,181 (GRCm39) |
T60I |
possibly damaging |
Het |
Scaf11 |
T |
C |
15: 96,317,339 (GRCm39) |
N742D |
probably benign |
Het |
Shank1 |
G |
A |
7: 44,002,075 (GRCm39) |
D1257N |
possibly damaging |
Het |
Shc2 |
A |
G |
10: 79,465,933 (GRCm39) |
V168A |
probably damaging |
Het |
Slc16a4 |
G |
A |
3: 107,199,758 (GRCm39) |
V2M |
probably benign |
Het |
Slc24a3 |
T |
C |
2: 145,455,494 (GRCm39) |
V461A |
probably benign |
Het |
Slc45a2 |
C |
T |
15: 11,027,871 (GRCm39) |
T480I |
probably damaging |
Het |
Slc4a4 |
T |
A |
5: 89,345,623 (GRCm39) |
|
probably null |
Het |
Snx30 |
T |
A |
4: 59,879,329 (GRCm39) |
D189E |
probably benign |
Het |
Sspo |
A |
G |
6: 48,472,194 (GRCm39) |
Q4653R |
possibly damaging |
Het |
Tpte |
G |
T |
8: 22,817,806 (GRCm39) |
R264I |
probably damaging |
Het |
Tsc22d4 |
T |
A |
5: 137,757,036 (GRCm39) |
|
probably benign |
Het |
Ubn1 |
T |
C |
16: 4,892,233 (GRCm39) |
L585P |
possibly damaging |
Het |
Usp24 |
A |
T |
4: 106,265,210 (GRCm39) |
D1781V |
probably damaging |
Het |
Vmn1r55 |
A |
T |
7: 5,149,995 (GRCm39) |
Y143N |
probably damaging |
Het |
Vmn2r65 |
A |
G |
7: 84,595,862 (GRCm39) |
V274A |
probably benign |
Het |
Wdr17 |
A |
G |
8: 55,092,524 (GRCm39) |
S1087P |
possibly damaging |
Het |
Wnt5b |
C |
A |
6: 119,417,283 (GRCm39) |
R156L |
probably damaging |
Het |
Zan |
T |
C |
5: 137,433,896 (GRCm39) |
D2279G |
unknown |
Het |
Zan |
T |
C |
5: 137,462,336 (GRCm39) |
T948A |
unknown |
Het |
Zfp758 |
T |
C |
17: 22,591,049 (GRCm39) |
S4P |
probably damaging |
Het |
Zfp839 |
A |
G |
12: 110,822,020 (GRCm39) |
E278G |
probably benign |
Het |
Zfp994 |
T |
A |
17: 22,419,506 (GRCm39) |
H481L |
probably damaging |
Het |
Zswim9 |
G |
A |
7: 12,994,909 (GRCm39) |
R416C |
probably damaging |
Het |
|
Other mutations in Utp20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00530:Utp20
|
APN |
10 |
88,661,306 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL00858:Utp20
|
APN |
10 |
88,644,987 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL00858:Utp20
|
APN |
10 |
88,645,000 (GRCm39) |
missense |
probably benign |
|
IGL00946:Utp20
|
APN |
10 |
88,584,177 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01061:Utp20
|
APN |
10 |
88,606,566 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01399:Utp20
|
APN |
10 |
88,594,164 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01548:Utp20
|
APN |
10 |
88,600,643 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01587:Utp20
|
APN |
10 |
88,623,397 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01789:Utp20
|
APN |
10 |
88,634,141 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01819:Utp20
|
APN |
10 |
88,628,549 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02070:Utp20
|
APN |
10 |
88,657,739 (GRCm39) |
splice site |
probably benign |
|
IGL02231:Utp20
|
APN |
10 |
88,627,030 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02244:Utp20
|
APN |
10 |
88,651,818 (GRCm39) |
splice site |
probably benign |
|
IGL02367:Utp20
|
APN |
10 |
88,607,715 (GRCm39) |
unclassified |
probably benign |
|
IGL02553:Utp20
|
APN |
10 |
88,600,657 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02748:Utp20
|
APN |
10 |
88,653,157 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02831:Utp20
|
APN |
10 |
88,651,770 (GRCm39) |
missense |
probably benign |
|
IGL02986:Utp20
|
APN |
10 |
88,611,147 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02997:Utp20
|
APN |
10 |
88,649,896 (GRCm39) |
missense |
probably benign |
|
IGL03105:Utp20
|
APN |
10 |
88,626,958 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03251:Utp20
|
APN |
10 |
88,653,188 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03337:Utp20
|
APN |
10 |
88,590,428 (GRCm39) |
missense |
probably benign |
|
IGL03348:Utp20
|
APN |
10 |
88,594,179 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03381:Utp20
|
APN |
10 |
88,657,867 (GRCm39) |
missense |
probably damaging |
0.99 |
Bell
|
UTSW |
10 |
88,628,487 (GRCm39) |
missense |
probably benign |
0.29 |
elite
|
UTSW |
10 |
88,606,670 (GRCm39) |
missense |
probably benign |
|
Margin
|
UTSW |
10 |
88,604,541 (GRCm39) |
missense |
probably benign |
0.04 |
Percentile
|
UTSW |
10 |
88,611,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R0037:Utp20
|
UTSW |
10 |
88,634,266 (GRCm39) |
missense |
probably benign |
0.05 |
R0107:Utp20
|
UTSW |
10 |
88,614,253 (GRCm39) |
missense |
probably benign |
0.03 |
R0197:Utp20
|
UTSW |
10 |
88,613,378 (GRCm39) |
missense |
probably benign |
0.22 |
R0219:Utp20
|
UTSW |
10 |
88,600,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R0315:Utp20
|
UTSW |
10 |
88,643,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R0328:Utp20
|
UTSW |
10 |
88,602,969 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0329:Utp20
|
UTSW |
10 |
88,653,841 (GRCm39) |
missense |
probably benign |
0.00 |
R0330:Utp20
|
UTSW |
10 |
88,653,841 (GRCm39) |
missense |
probably benign |
0.00 |
R0395:Utp20
|
UTSW |
10 |
88,654,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R0399:Utp20
|
UTSW |
10 |
88,656,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Utp20
|
UTSW |
10 |
88,657,931 (GRCm39) |
missense |
probably benign |
0.00 |
R0456:Utp20
|
UTSW |
10 |
88,590,435 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0491:Utp20
|
UTSW |
10 |
88,596,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R0557:Utp20
|
UTSW |
10 |
88,584,173 (GRCm39) |
missense |
probably damaging |
0.99 |
R0600:Utp20
|
UTSW |
10 |
88,603,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Utp20
|
UTSW |
10 |
88,606,613 (GRCm39) |
missense |
probably benign |
0.14 |
R1076:Utp20
|
UTSW |
10 |
88,608,405 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1076:Utp20
|
UTSW |
10 |
88,608,321 (GRCm39) |
missense |
probably benign |
0.36 |
R1330:Utp20
|
UTSW |
10 |
88,637,051 (GRCm39) |
missense |
probably damaging |
0.96 |
R1440:Utp20
|
UTSW |
10 |
88,655,201 (GRCm39) |
missense |
probably benign |
0.19 |
R1529:Utp20
|
UTSW |
10 |
88,588,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R1554:Utp20
|
UTSW |
10 |
88,600,599 (GRCm39) |
nonsense |
probably null |
|
R1621:Utp20
|
UTSW |
10 |
88,598,733 (GRCm39) |
missense |
probably benign |
|
R1641:Utp20
|
UTSW |
10 |
88,593,834 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1709:Utp20
|
UTSW |
10 |
88,585,159 (GRCm39) |
missense |
probably benign |
0.29 |
R1734:Utp20
|
UTSW |
10 |
88,603,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R1755:Utp20
|
UTSW |
10 |
88,645,631 (GRCm39) |
missense |
probably benign |
0.01 |
R1775:Utp20
|
UTSW |
10 |
88,606,670 (GRCm39) |
missense |
probably benign |
|
R1866:Utp20
|
UTSW |
10 |
88,598,632 (GRCm39) |
nonsense |
probably null |
|
R1867:Utp20
|
UTSW |
10 |
88,585,305 (GRCm39) |
missense |
probably benign |
|
R1901:Utp20
|
UTSW |
10 |
88,588,888 (GRCm39) |
missense |
probably benign |
0.02 |
R1902:Utp20
|
UTSW |
10 |
88,588,888 (GRCm39) |
missense |
probably benign |
0.02 |
R1967:Utp20
|
UTSW |
10 |
88,652,841 (GRCm39) |
missense |
probably benign |
0.03 |
R2060:Utp20
|
UTSW |
10 |
88,610,657 (GRCm39) |
missense |
probably damaging |
0.98 |
R2102:Utp20
|
UTSW |
10 |
88,608,779 (GRCm39) |
missense |
probably damaging |
0.99 |
R2110:Utp20
|
UTSW |
10 |
88,603,313 (GRCm39) |
critical splice donor site |
probably null |
|
R2115:Utp20
|
UTSW |
10 |
88,621,865 (GRCm39) |
missense |
probably benign |
0.02 |
R2128:Utp20
|
UTSW |
10 |
88,649,917 (GRCm39) |
missense |
probably damaging |
0.99 |
R2129:Utp20
|
UTSW |
10 |
88,649,917 (GRCm39) |
missense |
probably damaging |
0.99 |
R2180:Utp20
|
UTSW |
10 |
88,656,801 (GRCm39) |
missense |
probably damaging |
0.98 |
R2280:Utp20
|
UTSW |
10 |
88,661,365 (GRCm39) |
splice site |
probably null |
|
R2435:Utp20
|
UTSW |
10 |
88,656,753 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2914:Utp20
|
UTSW |
10 |
88,590,337 (GRCm39) |
critical splice donor site |
probably null |
|
R3005:Utp20
|
UTSW |
10 |
88,613,317 (GRCm39) |
missense |
probably damaging |
0.97 |
R3546:Utp20
|
UTSW |
10 |
88,618,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R3547:Utp20
|
UTSW |
10 |
88,618,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R3622:Utp20
|
UTSW |
10 |
88,593,855 (GRCm39) |
unclassified |
probably benign |
|
R3737:Utp20
|
UTSW |
10 |
88,598,668 (GRCm39) |
missense |
probably benign |
0.00 |
R3738:Utp20
|
UTSW |
10 |
88,598,668 (GRCm39) |
missense |
probably benign |
0.00 |
R3841:Utp20
|
UTSW |
10 |
88,611,065 (GRCm39) |
unclassified |
probably benign |
|
R4034:Utp20
|
UTSW |
10 |
88,598,668 (GRCm39) |
missense |
probably benign |
0.00 |
R4035:Utp20
|
UTSW |
10 |
88,598,668 (GRCm39) |
missense |
probably benign |
0.00 |
R4157:Utp20
|
UTSW |
10 |
88,597,729 (GRCm39) |
missense |
probably benign |
|
R4243:Utp20
|
UTSW |
10 |
88,643,187 (GRCm39) |
critical splice donor site |
probably null |
|
R4295:Utp20
|
UTSW |
10 |
88,590,381 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4632:Utp20
|
UTSW |
10 |
88,614,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R4633:Utp20
|
UTSW |
10 |
88,588,814 (GRCm39) |
missense |
probably benign |
|
R4684:Utp20
|
UTSW |
10 |
88,643,307 (GRCm39) |
nonsense |
probably null |
|
R4731:Utp20
|
UTSW |
10 |
88,590,382 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4735:Utp20
|
UTSW |
10 |
88,652,780 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4772:Utp20
|
UTSW |
10 |
88,645,797 (GRCm39) |
missense |
probably benign |
0.09 |
R4912:Utp20
|
UTSW |
10 |
88,607,822 (GRCm39) |
missense |
probably benign |
0.01 |
R4974:Utp20
|
UTSW |
10 |
88,652,811 (GRCm39) |
missense |
probably benign |
0.08 |
R4991:Utp20
|
UTSW |
10 |
88,582,796 (GRCm39) |
missense |
probably benign |
0.09 |
R5004:Utp20
|
UTSW |
10 |
88,584,135 (GRCm39) |
missense |
probably damaging |
0.98 |
R5037:Utp20
|
UTSW |
10 |
88,611,192 (GRCm39) |
missense |
probably benign |
0.00 |
R5043:Utp20
|
UTSW |
10 |
88,634,608 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5108:Utp20
|
UTSW |
10 |
88,604,735 (GRCm39) |
missense |
probably benign |
0.00 |
R5138:Utp20
|
UTSW |
10 |
88,583,239 (GRCm39) |
missense |
probably damaging |
0.96 |
R5252:Utp20
|
UTSW |
10 |
88,586,532 (GRCm39) |
missense |
probably benign |
0.01 |
R5470:Utp20
|
UTSW |
10 |
88,653,758 (GRCm39) |
missense |
probably benign |
0.14 |
R5558:Utp20
|
UTSW |
10 |
88,587,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R5678:Utp20
|
UTSW |
10 |
88,644,979 (GRCm39) |
missense |
probably benign |
0.00 |
R5822:Utp20
|
UTSW |
10 |
88,653,147 (GRCm39) |
missense |
probably benign |
0.00 |
R5866:Utp20
|
UTSW |
10 |
88,608,421 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5924:Utp20
|
UTSW |
10 |
88,651,784 (GRCm39) |
missense |
probably benign |
0.00 |
R6026:Utp20
|
UTSW |
10 |
88,604,541 (GRCm39) |
missense |
probably benign |
0.04 |
R6363:Utp20
|
UTSW |
10 |
88,592,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R6434:Utp20
|
UTSW |
10 |
88,608,395 (GRCm39) |
nonsense |
probably null |
|
R6477:Utp20
|
UTSW |
10 |
88,604,780 (GRCm39) |
missense |
probably benign |
0.05 |
R6480:Utp20
|
UTSW |
10 |
88,591,048 (GRCm39) |
critical splice donor site |
probably null |
|
R6989:Utp20
|
UTSW |
10 |
88,614,102 (GRCm39) |
missense |
probably benign |
0.00 |
R7033:Utp20
|
UTSW |
10 |
88,590,337 (GRCm39) |
critical splice donor site |
probably null |
|
R7192:Utp20
|
UTSW |
10 |
88,608,321 (GRCm39) |
missense |
probably benign |
0.09 |
R7236:Utp20
|
UTSW |
10 |
88,585,204 (GRCm39) |
missense |
probably benign |
0.28 |
R7260:Utp20
|
UTSW |
10 |
88,587,334 (GRCm39) |
missense |
probably benign |
0.39 |
R7296:Utp20
|
UTSW |
10 |
88,606,586 (GRCm39) |
missense |
probably benign |
0.21 |
R7317:Utp20
|
UTSW |
10 |
88,598,797 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7318:Utp20
|
UTSW |
10 |
88,649,811 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7330:Utp20
|
UTSW |
10 |
88,623,424 (GRCm39) |
frame shift |
probably null |
|
R7367:Utp20
|
UTSW |
10 |
88,631,305 (GRCm39) |
missense |
probably benign |
0.21 |
R7432:Utp20
|
UTSW |
10 |
88,634,260 (GRCm39) |
missense |
probably benign |
0.00 |
R7447:Utp20
|
UTSW |
10 |
88,608,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7473:Utp20
|
UTSW |
10 |
88,656,572 (GRCm39) |
splice site |
probably null |
|
R7520:Utp20
|
UTSW |
10 |
88,654,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R7530:Utp20
|
UTSW |
10 |
88,588,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R7539:Utp20
|
UTSW |
10 |
88,627,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R7651:Utp20
|
UTSW |
10 |
88,590,457 (GRCm39) |
missense |
probably benign |
0.41 |
R7728:Utp20
|
UTSW |
10 |
88,634,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R7831:Utp20
|
UTSW |
10 |
88,598,632 (GRCm39) |
nonsense |
probably null |
|
R7833:Utp20
|
UTSW |
10 |
88,636,998 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7909:Utp20
|
UTSW |
10 |
88,611,192 (GRCm39) |
missense |
probably benign |
|
R7956:Utp20
|
UTSW |
10 |
88,618,476 (GRCm39) |
missense |
probably benign |
0.23 |
R7999:Utp20
|
UTSW |
10 |
88,606,250 (GRCm39) |
missense |
probably benign |
|
R8080:Utp20
|
UTSW |
10 |
88,618,577 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8098:Utp20
|
UTSW |
10 |
88,588,810 (GRCm39) |
missense |
probably benign |
0.13 |
R8104:Utp20
|
UTSW |
10 |
88,593,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R8129:Utp20
|
UTSW |
10 |
88,628,487 (GRCm39) |
missense |
probably benign |
0.29 |
R8147:Utp20
|
UTSW |
10 |
88,594,306 (GRCm39) |
missense |
probably benign |
0.02 |
R8199:Utp20
|
UTSW |
10 |
88,634,337 (GRCm39) |
missense |
probably benign |
|
R8222:Utp20
|
UTSW |
10 |
88,614,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R8415:Utp20
|
UTSW |
10 |
88,662,466 (GRCm39) |
critical splice donor site |
probably null |
|
R8466:Utp20
|
UTSW |
10 |
88,654,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R8505:Utp20
|
UTSW |
10 |
88,653,870 (GRCm39) |
missense |
probably benign |
0.03 |
R8774:Utp20
|
UTSW |
10 |
88,588,763 (GRCm39) |
splice site |
probably benign |
|
R8802:Utp20
|
UTSW |
10 |
88,583,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R8923:Utp20
|
UTSW |
10 |
88,627,604 (GRCm39) |
nonsense |
probably null |
|
R8945:Utp20
|
UTSW |
10 |
88,628,532 (GRCm39) |
nonsense |
probably null |
|
R9065:Utp20
|
UTSW |
10 |
88,592,972 (GRCm39) |
missense |
probably benign |
0.32 |
R9092:Utp20
|
UTSW |
10 |
88,611,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R9092:Utp20
|
UTSW |
10 |
88,604,679 (GRCm39) |
missense |
probably benign |
|
R9094:Utp20
|
UTSW |
10 |
88,611,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R9095:Utp20
|
UTSW |
10 |
88,611,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R9096:Utp20
|
UTSW |
10 |
88,611,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R9229:Utp20
|
UTSW |
10 |
88,594,239 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9323:Utp20
|
UTSW |
10 |
88,583,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R9336:Utp20
|
UTSW |
10 |
88,649,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R9467:Utp20
|
UTSW |
10 |
88,640,390 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9545:Utp20
|
UTSW |
10 |
88,618,511 (GRCm39) |
missense |
probably benign |
0.38 |
R9659:Utp20
|
UTSW |
10 |
88,653,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R9788:Utp20
|
UTSW |
10 |
88,653,171 (GRCm39) |
missense |
probably damaging |
1.00 |
RF005:Utp20
|
UTSW |
10 |
88,661,319 (GRCm39) |
missense |
probably damaging |
1.00 |
RF024:Utp20
|
UTSW |
10 |
88,661,319 (GRCm39) |
missense |
probably damaging |
1.00 |
|