Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730061H03Rik |
C |
T |
14: 55,797,574 (GRCm39) |
|
probably benign |
Het |
Acsf2 |
A |
C |
11: 94,460,155 (GRCm39) |
M399R |
possibly damaging |
Het |
Adra2c |
C |
A |
5: 35,438,268 (GRCm39) |
R347S |
probably benign |
Het |
Akap9 |
A |
G |
5: 4,011,466 (GRCm39) |
K723R |
possibly damaging |
Het |
Anxa9 |
A |
C |
3: 95,215,324 (GRCm39) |
|
probably benign |
Het |
Aqr |
T |
C |
2: 113,943,832 (GRCm39) |
H1102R |
probably damaging |
Het |
Armh3 |
A |
T |
19: 45,808,726 (GRCm39) |
F655Y |
probably damaging |
Het |
Arrdc2 |
A |
G |
8: 71,290,162 (GRCm39) |
V173A |
probably benign |
Het |
Aspm |
T |
C |
1: 139,405,748 (GRCm39) |
V1545A |
probably benign |
Het |
Bbs5 |
C |
T |
2: 69,477,578 (GRCm39) |
|
probably benign |
Het |
Bnip2 |
A |
G |
9: 69,910,716 (GRCm39) |
T255A |
possibly damaging |
Het |
Cacna1b |
T |
C |
2: 24,538,535 (GRCm39) |
T1531A |
probably damaging |
Het |
Cast |
T |
C |
13: 74,955,942 (GRCm39) |
K9R |
probably benign |
Het |
Cfap46 |
A |
T |
7: 139,187,104 (GRCm39) |
|
probably null |
Het |
Cfap57 |
G |
T |
4: 118,450,251 (GRCm39) |
L624M |
probably damaging |
Het |
Cyp2c39 |
A |
T |
19: 39,552,323 (GRCm39) |
M339L |
probably benign |
Het |
Dcst1 |
T |
A |
3: 89,265,110 (GRCm39) |
T247S |
probably benign |
Het |
Dnajc18 |
T |
A |
18: 35,816,372 (GRCm39) |
I189F |
possibly damaging |
Het |
Eef2kmt |
T |
C |
16: 5,066,876 (GRCm39) |
T126A |
probably benign |
Het |
Epha2 |
A |
G |
4: 141,049,016 (GRCm39) |
E624G |
probably damaging |
Het |
Erbb3 |
G |
A |
10: 128,408,317 (GRCm39) |
H866Y |
probably benign |
Het |
F13a1 |
C |
T |
13: 37,100,837 (GRCm39) |
|
probably null |
Het |
Fgd3 |
T |
A |
13: 49,432,078 (GRCm39) |
N392I |
probably damaging |
Het |
Fgf7 |
A |
T |
2: 125,930,160 (GRCm39) |
M98L |
probably benign |
Het |
G2e3 |
T |
A |
12: 51,415,922 (GRCm39) |
S553T |
probably benign |
Het |
Glipr1 |
C |
A |
10: 111,829,411 (GRCm39) |
E117* |
probably null |
Het |
Gm11060 |
A |
T |
2: 104,924,128 (GRCm39) |
|
probably benign |
Het |
Gm4787 |
A |
G |
12: 81,424,403 (GRCm39) |
I585T |
probably damaging |
Het |
Gm6055 |
A |
T |
14: 48,316,915 (GRCm39) |
|
noncoding transcript |
Het |
Gpbar1 |
TACCAC |
TAC |
1: 74,318,704 (GRCm39) |
|
probably benign |
Het |
Gpt2 |
T |
A |
8: 86,246,068 (GRCm39) |
|
probably benign |
Het |
Gtf2ird1 |
A |
T |
5: 134,386,685 (GRCm39) |
Y345* |
probably null |
Het |
Hmcn1 |
T |
A |
1: 150,695,200 (GRCm39) |
T235S |
probably benign |
Het |
Igkv5-48 |
A |
G |
6: 69,703,738 (GRCm39) |
Y56H |
possibly damaging |
Het |
Il17re |
C |
T |
6: 113,446,530 (GRCm39) |
T427I |
probably benign |
Het |
Itpr3 |
A |
T |
17: 27,302,582 (GRCm39) |
D80V |
probably damaging |
Het |
Kif21a |
G |
T |
15: 90,833,213 (GRCm39) |
H1317N |
probably benign |
Het |
Kif28 |
T |
C |
1: 179,526,209 (GRCm39) |
K144E |
probably damaging |
Het |
Kif4-ps |
A |
C |
12: 101,113,330 (GRCm39) |
|
noncoding transcript |
Het |
Klk1b11 |
C |
T |
7: 43,427,160 (GRCm39) |
T148I |
probably damaging |
Het |
Klkb1 |
T |
A |
8: 45,739,995 (GRCm39) |
H99L |
probably damaging |
Het |
Kpna6 |
A |
C |
4: 129,550,198 (GRCm39) |
|
probably null |
Het |
Lama3 |
G |
T |
18: 12,685,883 (GRCm39) |
K1132N |
probably damaging |
Het |
Lcp1 |
T |
A |
14: 75,445,911 (GRCm39) |
L264* |
probably null |
Het |
Map2 |
T |
C |
1: 66,452,664 (GRCm39) |
V360A |
probably benign |
Het |
Med13 |
A |
T |
11: 86,189,673 (GRCm39) |
S1079T |
probably damaging |
Het |
Mettl13 |
A |
G |
1: 162,364,789 (GRCm39) |
M162T |
probably damaging |
Het |
Mppe1 |
T |
G |
18: 67,361,133 (GRCm39) |
E208A |
probably benign |
Het |
Msantd2 |
A |
C |
9: 37,400,675 (GRCm39) |
K19T |
possibly damaging |
Het |
Mylk3 |
A |
G |
8: 86,091,412 (GRCm39) |
V131A |
probably damaging |
Het |
Myocd |
A |
T |
11: 65,074,299 (GRCm39) |
S609T |
possibly damaging |
Het |
Ncbp3 |
G |
A |
11: 72,944,355 (GRCm39) |
|
probably null |
Het |
Neb |
T |
A |
2: 52,136,871 (GRCm39) |
L3203F |
probably damaging |
Het |
Notch2 |
C |
A |
3: 98,046,949 (GRCm39) |
T1756K |
probably benign |
Het |
Nphp4 |
A |
T |
4: 152,622,250 (GRCm39) |
R544W |
probably damaging |
Het |
Or3a1c |
A |
T |
11: 74,046,745 (GRCm39) |
Y255F |
probably benign |
Het |
Or4p18 |
T |
G |
2: 88,232,756 (GRCm39) |
H174P |
probably damaging |
Het |
Or5c1 |
A |
T |
2: 37,222,578 (GRCm39) |
D273V |
probably damaging |
Het |
Parp4 |
T |
A |
14: 56,827,355 (GRCm39) |
V163E |
possibly damaging |
Het |
Pcdhgb1 |
C |
A |
18: 37,815,425 (GRCm39) |
Q639K |
probably benign |
Het |
Pcnx2 |
A |
G |
8: 126,577,869 (GRCm39) |
V936A |
probably benign |
Het |
Pcsk7 |
T |
A |
9: 45,830,160 (GRCm39) |
M418K |
probably damaging |
Het |
Pglyrp4 |
T |
C |
3: 90,640,314 (GRCm39) |
I188T |
probably benign |
Het |
Pgs1 |
A |
G |
11: 117,896,345 (GRCm39) |
R339G |
probably benign |
Het |
Pik3r3 |
A |
G |
4: 116,143,388 (GRCm39) |
I294V |
probably benign |
Het |
Pik3r6 |
A |
G |
11: 68,430,771 (GRCm39) |
D520G |
probably damaging |
Het |
Pkdrej |
A |
G |
15: 85,704,610 (GRCm39) |
V442A |
probably benign |
Het |
Ppfibp1 |
T |
A |
6: 146,931,917 (GRCm39) |
|
probably benign |
Het |
Ppp3ca |
C |
A |
3: 136,640,810 (GRCm39) |
Q454K |
possibly damaging |
Het |
Ppp5c |
A |
T |
7: 16,743,861 (GRCm39) |
M191K |
probably damaging |
Het |
Prl4a1 |
A |
T |
13: 28,207,308 (GRCm39) |
Y194F |
possibly damaging |
Het |
Ptpn21 |
G |
T |
12: 98,646,362 (GRCm39) |
T1032K |
probably damaging |
Het |
Ptprh |
A |
T |
7: 4,554,006 (GRCm39) |
|
probably null |
Het |
Ptprm |
T |
A |
17: 66,985,062 (GRCm39) |
R1447S |
probably benign |
Het |
Pxk |
T |
A |
14: 8,140,734 (GRCm38) |
D236E |
probably damaging |
Het |
Qars1 |
T |
C |
9: 108,386,130 (GRCm39) |
F107S |
probably damaging |
Het |
Rbbp6 |
A |
G |
7: 122,599,031 (GRCm39) |
|
probably benign |
Het |
Rptor |
A |
T |
11: 119,712,466 (GRCm39) |
|
probably benign |
Het |
Rtn4 |
T |
A |
11: 29,690,994 (GRCm39) |
M1095K |
probably damaging |
Het |
Serpinb3b |
T |
A |
1: 107,082,445 (GRCm39) |
H273L |
probably benign |
Het |
Sgce |
G |
A |
6: 4,689,630 (GRCm39) |
T401M |
probably benign |
Het |
Slc12a6 |
C |
T |
2: 112,188,870 (GRCm39) |
R1083W |
probably damaging |
Het |
Slc45a4 |
A |
T |
15: 73,456,299 (GRCm39) |
M635K |
probably damaging |
Het |
Slc6a1 |
T |
A |
6: 114,284,662 (GRCm39) |
V240D |
probably damaging |
Het |
Snx9 |
G |
A |
17: 5,952,794 (GRCm39) |
|
probably null |
Het |
Spred3 |
A |
G |
7: 28,867,249 (GRCm39) |
V49A |
probably damaging |
Het |
Tars1 |
A |
G |
15: 11,390,477 (GRCm39) |
F334S |
probably damaging |
Het |
Tdpoz1 |
A |
G |
3: 93,578,454 (GRCm39) |
V110A |
probably benign |
Het |
Tfrc |
T |
G |
16: 32,437,097 (GRCm39) |
V252G |
probably damaging |
Het |
Tm6sf2 |
T |
C |
8: 70,528,128 (GRCm39) |
|
probably benign |
Het |
Txlnb |
T |
C |
10: 17,714,717 (GRCm39) |
V383A |
probably damaging |
Het |
Vmn2r12 |
A |
T |
5: 109,239,372 (GRCm39) |
V397E |
probably damaging |
Het |
Zdhhc12 |
G |
A |
2: 29,981,538 (GRCm39) |
R175W |
probably damaging |
Het |
Zfyve9 |
A |
G |
4: 108,538,097 (GRCm39) |
|
probably null |
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 |
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 |
|