Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J04Rik |
A |
G |
12: 11,272,143 (GRCm39) |
S20P |
unknown |
Het |
4921528I07Rik |
G |
A |
9: 114,108,386 (GRCm39) |
|
noncoding transcript |
Het |
4930562C15Rik |
G |
A |
16: 4,669,422 (GRCm39) |
|
probably null |
Het |
4933427I04Rik |
A |
G |
4: 123,754,286 (GRCm39) |
T67A |
possibly damaging |
Het |
Abcc2 |
A |
T |
19: 43,786,858 (GRCm39) |
N160Y |
possibly damaging |
Het |
Acaca |
A |
G |
11: 84,191,248 (GRCm39) |
D155G |
possibly damaging |
Het |
Afg3l1 |
G |
A |
8: 124,219,639 (GRCm39) |
R389Q |
possibly damaging |
Het |
Ank2 |
G |
A |
3: 126,728,196 (GRCm39) |
T799M |
probably benign |
Het |
Anxa2 |
T |
C |
9: 69,395,363 (GRCm39) |
Y202H |
possibly damaging |
Het |
Arhgef33 |
A |
G |
17: 80,681,172 (GRCm39) |
T771A |
probably benign |
Het |
Atp12a |
T |
C |
14: 56,610,046 (GRCm39) |
V182A |
probably benign |
Het |
Birc6 |
T |
C |
17: 74,919,281 (GRCm39) |
L210S |
probably damaging |
Het |
Car3 |
A |
G |
3: 14,929,492 (GRCm39) |
T73A |
probably benign |
Het |
Cd5l |
T |
C |
3: 87,275,966 (GRCm39) |
L312P |
probably damaging |
Het |
Celf5 |
A |
G |
10: 81,303,138 (GRCm39) |
|
probably benign |
Het |
Cep290 |
T |
A |
10: 100,332,672 (GRCm39) |
V257E |
probably damaging |
Het |
Cntrob |
T |
C |
11: 69,211,693 (GRCm39) |
D177G |
possibly damaging |
Het |
Copg2 |
A |
T |
6: 30,787,271 (GRCm39) |
F658I |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,763,135 (GRCm39) |
T1234A |
probably damaging |
Het |
Dhx35 |
A |
G |
2: 158,648,357 (GRCm39) |
T72A |
probably damaging |
Het |
Dmrtc2 |
A |
T |
7: 24,573,792 (GRCm39) |
H209L |
possibly damaging |
Het |
Eml5 |
G |
T |
12: 98,818,963 (GRCm39) |
|
probably null |
Het |
Evpl |
T |
C |
11: 116,114,486 (GRCm39) |
E1068G |
possibly damaging |
Het |
Ezh2 |
A |
G |
6: 47,553,594 (GRCm39) |
M41T |
probably damaging |
Het |
Fmo3 |
A |
G |
1: 162,796,294 (GRCm39) |
S93P |
possibly damaging |
Het |
Gdi2 |
A |
G |
13: 3,610,018 (GRCm39) |
Y213C |
possibly damaging |
Het |
Gpr15 |
A |
T |
16: 58,538,921 (GRCm39) |
I56K |
probably benign |
Het |
Gria2 |
G |
T |
3: 80,598,645 (GRCm39) |
S796R |
probably benign |
Het |
Hectd4 |
T |
A |
5: 121,429,254 (GRCm39) |
|
probably benign |
Het |
Hgfac |
T |
C |
5: 35,200,194 (GRCm39) |
|
probably benign |
Het |
Hspg2 |
C |
T |
4: 137,247,467 (GRCm39) |
R1200W |
probably damaging |
Het |
Ift52 |
G |
A |
2: 162,867,275 (GRCm39) |
D78N |
possibly damaging |
Het |
Iqca1 |
C |
A |
1: 90,009,138 (GRCm39) |
W415L |
probably damaging |
Het |
Ism1 |
A |
T |
2: 139,587,963 (GRCm39) |
K236N |
probably damaging |
Het |
Itgb6 |
C |
T |
2: 60,502,988 (GRCm39) |
W43* |
probably null |
Het |
Kcnk18 |
T |
A |
19: 59,223,773 (GRCm39) |
I306N |
probably damaging |
Het |
Kctd8 |
T |
C |
5: 69,497,903 (GRCm39) |
K248E |
probably damaging |
Het |
Layn |
T |
A |
9: 50,970,833 (GRCm39) |
I237F |
probably benign |
Het |
Lce3f |
C |
T |
3: 92,900,248 (GRCm39) |
P23L |
unknown |
Het |
Lct |
A |
G |
1: 128,228,038 (GRCm39) |
F1152L |
probably damaging |
Het |
Mettl25b |
A |
G |
3: 87,831,124 (GRCm39) |
S404P |
probably damaging |
Het |
Mxra8 |
T |
C |
4: 155,927,531 (GRCm39) |
I413T |
probably damaging |
Het |
Nedd9 |
A |
G |
13: 41,471,438 (GRCm39) |
V187A |
probably benign |
Het |
Net1 |
A |
G |
13: 3,937,642 (GRCm39) |
L207P |
probably damaging |
Het |
Neurod1 |
G |
T |
2: 79,284,781 (GRCm39) |
P201T |
probably benign |
Het |
Nlrp1b |
A |
G |
11: 71,052,647 (GRCm39) |
F927S |
probably damaging |
Het |
Ntrk3 |
T |
A |
7: 78,005,789 (GRCm39) |
H524L |
possibly damaging |
Het |
Nup98 |
A |
C |
7: 101,784,144 (GRCm39) |
S1063A |
probably benign |
Het |
Or10ak11 |
T |
A |
4: 118,687,065 (GRCm39) |
M191L |
probably benign |
Het |
Or11h4b |
G |
T |
14: 50,918,623 (GRCm39) |
P156Q |
possibly damaging |
Het |
Or56b1 |
G |
A |
7: 104,285,366 (GRCm39) |
V162I |
probably benign |
Het |
Or5b97 |
C |
A |
19: 12,878,599 (GRCm39) |
V182F |
probably benign |
Het |
Or5m9b |
G |
A |
2: 85,905,104 (GRCm39) |
V7I |
possibly damaging |
Het |
Or6d15 |
T |
C |
6: 116,559,925 (GRCm39) |
|
probably benign |
Het |
Pdzd2 |
G |
A |
15: 12,592,546 (GRCm39) |
R33W |
probably damaging |
Het |
Phf21a |
G |
A |
2: 92,160,860 (GRCm39) |
V243I |
probably damaging |
Het |
Ppp1r12b |
A |
G |
1: 134,821,086 (GRCm39) |
|
probably null |
Het |
Rexo5 |
T |
C |
7: 119,444,634 (GRCm39) |
V703A |
probably benign |
Het |
Rgs4 |
A |
G |
1: 169,572,847 (GRCm39) |
S30P |
probably benign |
Het |
Rxra |
C |
A |
2: 27,646,256 (GRCm39) |
D340E |
probably damaging |
Het |
Samhd1 |
A |
G |
2: 156,949,467 (GRCm39) |
V473A |
probably benign |
Het |
Scn3a |
T |
A |
2: 65,302,686 (GRCm39) |
K1253N |
probably damaging |
Het |
Scn7a |
T |
C |
2: 66,511,299 (GRCm39) |
N1207S |
probably benign |
Het |
Sec24d |
T |
A |
3: 123,130,166 (GRCm39) |
I443N |
probably damaging |
Het |
Sema4g |
T |
A |
19: 44,987,681 (GRCm39) |
|
probably null |
Het |
Sema5b |
A |
G |
16: 35,480,694 (GRCm39) |
K787R |
probably benign |
Het |
Serpinc1 |
A |
G |
1: 160,817,217 (GRCm39) |
N104D |
probably benign |
Het |
Sfn |
T |
C |
4: 133,328,542 (GRCm39) |
H180R |
probably damaging |
Het |
Slc22a6 |
G |
T |
19: 8,596,471 (GRCm39) |
|
probably null |
Het |
Slc9a8 |
T |
C |
2: 167,299,278 (GRCm39) |
S217P |
probably benign |
Het |
Smc6 |
A |
G |
12: 11,359,270 (GRCm39) |
N965D |
probably benign |
Het |
Sod2 |
T |
A |
17: 13,233,919 (GRCm39) |
I177N |
probably damaging |
Het |
Sp4 |
A |
T |
12: 118,263,335 (GRCm39) |
I237K |
probably damaging |
Het |
Sulf2 |
T |
C |
2: 165,921,532 (GRCm39) |
K697R |
probably benign |
Het |
Svs4 |
A |
T |
2: 164,119,005 (GRCm39) |
D110E |
unknown |
Het |
Tas1r1 |
T |
A |
4: 152,122,675 (GRCm39) |
R57* |
probably null |
Het |
Tlr5 |
T |
C |
1: 182,801,287 (GRCm39) |
I197T |
probably damaging |
Het |
Tmc3 |
T |
C |
7: 83,261,740 (GRCm39) |
V606A |
probably benign |
Het |
Tmem241 |
T |
A |
18: 12,251,469 (GRCm39) |
L37F |
probably damaging |
Het |
Tmem59l |
A |
T |
8: 70,938,903 (GRCm39) |
N90K |
probably damaging |
Het |
Tram1 |
A |
C |
1: 13,646,680 (GRCm39) |
|
probably benign |
Het |
Trim15 |
T |
A |
17: 37,176,061 (GRCm39) |
H162L |
probably benign |
Het |
Ttc28 |
T |
A |
5: 111,424,677 (GRCm39) |
Y1501N |
probably benign |
Het |
Ttc34 |
T |
C |
4: 154,946,671 (GRCm39) |
V857A |
probably benign |
Het |
Tulp4 |
A |
G |
17: 6,189,321 (GRCm39) |
T48A |
probably damaging |
Het |
Usp9y |
T |
C |
Y: 1,368,089 (GRCm39) |
E939G |
probably damaging |
Het |
Vmn2r72 |
T |
C |
7: 85,387,378 (GRCm39) |
M729V |
probably benign |
Het |
Vps13c |
C |
T |
9: 67,788,729 (GRCm39) |
T334M |
probably damaging |
Het |
Wnk4 |
C |
G |
11: 101,167,166 (GRCm39) |
|
probably benign |
Het |
Xpo1 |
A |
G |
11: 23,221,193 (GRCm39) |
N97D |
probably benign |
Het |
Xpo4 |
A |
T |
14: 57,841,129 (GRCm39) |
F518Y |
probably benign |
Het |
Zfp668 |
C |
T |
7: 127,465,778 (GRCm39) |
V469I |
possibly damaging |
Het |
Zfp85 |
C |
A |
13: 67,897,823 (GRCm39) |
C83F |
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 |
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 |
R5394:Utp20
|
UTSW |
10 |
88,608,777 (GRCm39) |
nonsense |
probably null |
|
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 |
|