Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933436I01Rik |
T |
A |
X: 66,964,308 (GRCm39) |
I184L |
probably benign |
Het |
9530002B09Rik |
T |
A |
4: 122,583,115 (GRCm39) |
|
probably benign |
Het |
Actr1b |
A |
G |
1: 36,741,168 (GRCm39) |
F138L |
possibly damaging |
Het |
Adamts14 |
G |
T |
10: 61,041,301 (GRCm39) |
P803Q |
probably benign |
Het |
Afap1l1 |
A |
T |
18: 61,872,193 (GRCm39) |
|
probably null |
Het |
Akt3 |
A |
G |
1: 176,930,551 (GRCm39) |
S136P |
possibly damaging |
Het |
Aldh16a1 |
C |
T |
7: 44,796,585 (GRCm39) |
|
probably null |
Het |
Alg12 |
A |
G |
15: 88,696,318 (GRCm39) |
W238R |
probably damaging |
Het |
Amy2a1 |
T |
C |
3: 113,324,217 (GRCm39) |
I108V |
probably benign |
Het |
Arhgap23 |
T |
A |
11: 97,383,888 (GRCm39) |
C1144S |
probably benign |
Het |
Arhgef40 |
G |
A |
14: 52,233,640 (GRCm39) |
V829M |
probably damaging |
Het |
Atg7 |
C |
A |
6: 114,680,324 (GRCm39) |
N344K |
probably damaging |
Het |
Aunip |
T |
A |
4: 134,250,618 (GRCm39) |
S188T |
probably benign |
Het |
Bmpr1b |
A |
T |
3: 141,576,568 (GRCm39) |
H88Q |
probably benign |
Het |
Brpf3 |
G |
A |
17: 29,040,338 (GRCm39) |
G920S |
probably benign |
Het |
Cdc123 |
C |
T |
2: 5,800,354 (GRCm39) |
|
probably benign |
Het |
Cdhr1 |
T |
C |
14: 36,817,062 (GRCm39) |
R100G |
probably benign |
Het |
Cdkn2d |
A |
G |
9: 21,202,175 (GRCm39) |
V24A |
probably damaging |
Het |
Cirbp |
T |
C |
10: 80,006,166 (GRCm39) |
|
probably benign |
Het |
Clptm1l |
C |
T |
13: 73,755,842 (GRCm39) |
Q153* |
probably null |
Het |
Col12a1 |
A |
G |
9: 79,569,736 (GRCm39) |
|
probably benign |
Het |
Cplane1 |
T |
A |
15: 8,215,649 (GRCm39) |
S402T |
probably damaging |
Het |
Cpox |
T |
A |
16: 58,494,772 (GRCm39) |
C270S |
probably benign |
Het |
Cspg4 |
A |
G |
9: 56,803,940 (GRCm39) |
D1677G |
probably damaging |
Het |
Cyp4a10 |
T |
A |
4: 115,381,917 (GRCm39) |
|
probably benign |
Het |
Dctn4 |
T |
C |
18: 60,671,349 (GRCm39) |
F74L |
possibly damaging |
Het |
Dennd5a |
G |
A |
7: 109,497,900 (GRCm39) |
|
probably benign |
Het |
Dnaaf3 |
T |
C |
7: 4,526,798 (GRCm39) |
I426M |
possibly damaging |
Het |
Dnah9 |
C |
T |
11: 66,036,261 (GRCm39) |
S185N |
probably benign |
Het |
Dqx1 |
T |
G |
6: 83,035,524 (GRCm39) |
|
probably benign |
Het |
Dtx2 |
C |
T |
5: 136,059,431 (GRCm39) |
S493F |
probably damaging |
Het |
Ehd1 |
T |
C |
19: 6,348,108 (GRCm39) |
L362P |
probably benign |
Het |
Endov |
T |
C |
11: 119,390,408 (GRCm39) |
F12S |
probably damaging |
Het |
Ep400 |
A |
C |
5: 110,883,270 (GRCm39) |
|
probably benign |
Het |
Epha1 |
G |
T |
6: 42,342,987 (GRCm39) |
H187Q |
probably benign |
Het |
Exoc2 |
T |
C |
13: 31,119,544 (GRCm39) |
D119G |
probably benign |
Het |
Fbn2 |
C |
T |
18: 58,181,921 (GRCm39) |
E1827K |
probably damaging |
Het |
Fbxo41 |
C |
T |
6: 85,455,453 (GRCm39) |
W577* |
probably null |
Het |
Fgd6 |
G |
A |
10: 93,880,903 (GRCm39) |
A586T |
probably damaging |
Het |
Gm12695 |
T |
C |
4: 96,657,963 (GRCm39) |
T69A |
probably benign |
Het |
Gm12888 |
A |
T |
4: 121,182,069 (GRCm39) |
W8R |
unknown |
Het |
Gm2959 |
A |
G |
14: 42,235,658 (GRCm39) |
|
noncoding transcript |
Het |
Gm6214 |
A |
G |
3: 140,544,978 (GRCm39) |
|
noncoding transcript |
Het |
Gm9912 |
T |
C |
3: 148,890,795 (GRCm39) |
T113A |
unknown |
Het |
Gmeb2 |
A |
G |
2: 180,895,763 (GRCm39) |
L469P |
probably benign |
Het |
Gosr1 |
T |
C |
11: 76,628,224 (GRCm39) |
I177V |
probably benign |
Het |
Gria1 |
T |
C |
11: 57,208,534 (GRCm39) |
F810L |
probably damaging |
Het |
Gtf2ird2 |
C |
T |
5: 134,245,340 (GRCm39) |
Q533* |
probably null |
Het |
Hadhb |
T |
A |
5: 30,378,796 (GRCm39) |
|
probably null |
Het |
Hat1 |
A |
T |
2: 71,240,504 (GRCm39) |
Y66F |
possibly damaging |
Het |
Hk1 |
T |
C |
10: 62,122,315 (GRCm39) |
Y488C |
probably benign |
Het |
Htt |
C |
T |
5: 34,983,326 (GRCm39) |
T975I |
probably benign |
Het |
Ifnb1 |
T |
A |
4: 88,440,996 (GRCm39) |
I6F |
possibly damaging |
Het |
Il19 |
T |
C |
1: 130,866,854 (GRCm39) |
H42R |
probably benign |
Het |
Il2rg |
A |
G |
X: 100,311,416 (GRCm39) |
L57P |
possibly damaging |
Het |
Impg2 |
G |
A |
16: 56,063,993 (GRCm39) |
|
probably null |
Het |
Invs |
T |
A |
4: 48,396,287 (GRCm39) |
L320Q |
probably damaging |
Het |
Itga9 |
T |
C |
9: 118,636,361 (GRCm39) |
F683S |
probably damaging |
Het |
Itih2 |
A |
G |
2: 10,135,385 (GRCm39) |
S2P |
possibly damaging |
Het |
Itpr3 |
G |
A |
17: 27,317,050 (GRCm39) |
M768I |
probably benign |
Het |
Kcnab1 |
A |
G |
3: 65,272,060 (GRCm39) |
E315G |
probably benign |
Het |
Kcnmb2 |
A |
C |
3: 32,252,437 (GRCm39) |
I213L |
probably damaging |
Het |
Khdc1a |
T |
A |
1: 21,421,196 (GRCm39) |
M127K |
probably benign |
Het |
Klhl28 |
T |
C |
12: 64,990,246 (GRCm39) |
N565S |
probably benign |
Het |
Lcp1 |
A |
G |
14: 75,435,515 (GRCm39) |
|
probably null |
Het |
Mcm4 |
T |
C |
16: 15,452,333 (GRCm39) |
T267A |
possibly damaging |
Het |
Mlxipl |
A |
T |
5: 135,161,631 (GRCm39) |
T517S |
possibly damaging |
Het |
Mpp3 |
T |
A |
11: 101,891,516 (GRCm39) |
I541L |
probably benign |
Het |
Mpp4 |
G |
A |
1: 59,182,941 (GRCm39) |
P322L |
possibly damaging |
Het |
Myh15 |
G |
A |
16: 48,975,984 (GRCm39) |
A1351T |
possibly damaging |
Het |
Nacc1 |
A |
T |
8: 85,399,747 (GRCm39) |
M490K |
probably benign |
Het |
Nbeal1 |
C |
A |
1: 60,309,515 (GRCm39) |
Q496K |
possibly damaging |
Het |
Oas1g |
T |
C |
5: 121,023,946 (GRCm39) |
E121G |
probably damaging |
Het |
Or14j1 |
T |
A |
17: 38,145,893 (GRCm39) |
M1K |
probably null |
Het |
Pard3 |
T |
C |
8: 128,337,092 (GRCm39) |
L1236P |
probably damaging |
Het |
Phc2 |
T |
C |
4: 128,640,929 (GRCm39) |
F672S |
probably damaging |
Het |
Phf21a |
C |
A |
2: 92,157,422 (GRCm39) |
N183K |
possibly damaging |
Het |
Plxnb3 |
T |
A |
X: 72,815,357 (GRCm39) |
Y1845* |
probably null |
Het |
Prl3c1 |
G |
A |
13: 27,380,720 (GRCm39) |
|
probably null |
Het |
Prl7a2 |
T |
A |
13: 27,844,870 (GRCm39) |
Y172F |
probably damaging |
Het |
Psg16 |
T |
G |
7: 16,827,673 (GRCm39) |
S210A |
possibly damaging |
Het |
Psg25 |
T |
A |
7: 18,255,178 (GRCm39) |
K446M |
probably damaging |
Het |
Rgs7 |
A |
T |
1: 174,949,508 (GRCm39) |
F160L |
probably damaging |
Het |
Rpl22l1 |
A |
T |
3: 28,860,957 (GRCm39) |
E57D |
possibly damaging |
Het |
Rpl35 |
A |
G |
2: 38,894,753 (GRCm39) |
L44P |
possibly damaging |
Het |
Rtn4r |
T |
C |
16: 17,969,121 (GRCm39) |
L183P |
probably damaging |
Het |
Skint1 |
T |
A |
4: 111,882,730 (GRCm39) |
V258D |
probably benign |
Het |
Slc4a7 |
G |
A |
14: 14,733,773 (GRCm38) |
R67H |
probably damaging |
Het |
Smg1 |
C |
T |
7: 117,756,090 (GRCm39) |
|
probably benign |
Het |
Smurf2 |
T |
C |
11: 106,762,374 (GRCm39) |
T39A |
probably damaging |
Het |
Sspo |
A |
T |
6: 48,450,596 (GRCm39) |
D2595V |
probably damaging |
Het |
Tatdn2 |
A |
G |
6: 113,681,103 (GRCm39) |
K379E |
probably benign |
Het |
Tbc1d14 |
G |
A |
5: 36,680,274 (GRCm39) |
R68* |
probably null |
Het |
Tgm1 |
A |
G |
14: 55,946,928 (GRCm39) |
I360T |
probably damaging |
Het |
Thrap3 |
T |
C |
4: 126,069,189 (GRCm39) |
Y654C |
possibly damaging |
Het |
Traf1 |
A |
T |
2: 34,838,202 (GRCm39) |
I212N |
probably benign |
Het |
Ttc17 |
C |
A |
2: 94,196,892 (GRCm39) |
W485L |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,768,675 (GRCm39) |
V2920F |
probably damaging |
Het |
Tyr |
T |
C |
7: 87,142,051 (GRCm39) |
I93V |
probably benign |
Het |
Ubap2 |
C |
T |
4: 41,199,872 (GRCm39) |
A752T |
probably benign |
Het |
Vmn1r212 |
A |
G |
13: 23,068,285 (GRCm39) |
V16A |
probably benign |
Het |
Vmn1r55 |
A |
G |
7: 5,150,048 (GRCm39) |
V125A |
possibly damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,831,553 (GRCm39) |
H412L |
possibly damaging |
Het |
Xirp1 |
T |
C |
9: 119,845,962 (GRCm39) |
I974V |
probably benign |
Het |
Zap70 |
A |
G |
1: 36,818,215 (GRCm39) |
T301A |
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,463,987 (GRCm39) |
K1382E |
probably damaging |
Het |
Zfp280b |
T |
A |
10: 75,875,017 (GRCm39) |
C299S |
probably damaging |
Het |
Zfp352 |
C |
T |
4: 90,113,357 (GRCm39) |
S499L |
probably benign |
Het |
Zfp423 |
G |
A |
8: 88,507,986 (GRCm39) |
A661V |
probably benign |
Het |
Zfp57 |
T |
A |
17: 37,320,568 (GRCm39) |
F141I |
possibly damaging |
Het |
Zfp946 |
A |
T |
17: 22,674,446 (GRCm39) |
H400L |
probably damaging |
Het |
Zgrf1 |
T |
C |
3: 127,406,999 (GRCm39) |
C1589R |
probably damaging |
Het |
|
Other mutations in Ptprz1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00486:Ptprz1
|
APN |
6 |
22,973,053 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00773:Ptprz1
|
APN |
6 |
23,002,628 (GRCm39) |
missense |
probably benign |
0.41 |
IGL01458:Ptprz1
|
APN |
6 |
22,972,843 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01481:Ptprz1
|
APN |
6 |
22,999,979 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01501:Ptprz1
|
APN |
6 |
22,973,081 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01601:Ptprz1
|
APN |
6 |
23,000,437 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01882:Ptprz1
|
APN |
6 |
23,000,463 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02058:Ptprz1
|
APN |
6 |
23,002,502 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02089:Ptprz1
|
APN |
6 |
23,033,447 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02136:Ptprz1
|
APN |
6 |
22,972,821 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02215:Ptprz1
|
APN |
6 |
22,965,181 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02220:Ptprz1
|
APN |
6 |
23,042,742 (GRCm39) |
splice site |
probably benign |
|
IGL02556:Ptprz1
|
APN |
6 |
22,972,844 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02601:Ptprz1
|
APN |
6 |
23,000,686 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02620:Ptprz1
|
APN |
6 |
22,959,739 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02666:Ptprz1
|
APN |
6 |
23,001,209 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02718:Ptprz1
|
APN |
6 |
23,001,348 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02792:Ptprz1
|
APN |
6 |
22,959,722 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02894:Ptprz1
|
APN |
6 |
23,035,148 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02952:Ptprz1
|
APN |
6 |
23,036,925 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03003:Ptprz1
|
APN |
6 |
23,002,582 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03060:Ptprz1
|
APN |
6 |
22,972,834 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03170:Ptprz1
|
APN |
6 |
22,959,766 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03246:Ptprz1
|
APN |
6 |
22,986,159 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03349:Ptprz1
|
APN |
6 |
23,000,331 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03365:Ptprz1
|
APN |
6 |
23,030,581 (GRCm39) |
splice site |
probably benign |
|
Elevator
|
UTSW |
6 |
23,030,661 (GRCm39) |
missense |
probably benign |
0.03 |
escalator
|
UTSW |
6 |
22,986,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R0044:Ptprz1
|
UTSW |
6 |
23,007,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R0054:Ptprz1
|
UTSW |
6 |
22,986,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R0054:Ptprz1
|
UTSW |
6 |
22,986,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R0107:Ptprz1
|
UTSW |
6 |
23,000,569 (GRCm39) |
missense |
probably damaging |
0.98 |
R0278:Ptprz1
|
UTSW |
6 |
23,000,816 (GRCm39) |
missense |
probably benign |
0.31 |
R0345:Ptprz1
|
UTSW |
6 |
23,016,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R0359:Ptprz1
|
UTSW |
6 |
22,973,175 (GRCm39) |
splice site |
probably benign |
|
R0743:Ptprz1
|
UTSW |
6 |
23,044,366 (GRCm39) |
nonsense |
probably null |
|
R1014:Ptprz1
|
UTSW |
6 |
23,000,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R1016:Ptprz1
|
UTSW |
6 |
23,000,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R1106:Ptprz1
|
UTSW |
6 |
22,965,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R1391:Ptprz1
|
UTSW |
6 |
23,001,728 (GRCm39) |
missense |
probably benign |
0.33 |
R1424:Ptprz1
|
UTSW |
6 |
23,000,382 (GRCm39) |
missense |
probably benign |
0.00 |
R1445:Ptprz1
|
UTSW |
6 |
23,050,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Ptprz1
|
UTSW |
6 |
23,049,523 (GRCm39) |
splice site |
probably benign |
|
R1544:Ptprz1
|
UTSW |
6 |
23,000,747 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1626:Ptprz1
|
UTSW |
6 |
23,001,573 (GRCm39) |
missense |
probably benign |
|
R1641:Ptprz1
|
UTSW |
6 |
23,049,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R1757:Ptprz1
|
UTSW |
6 |
23,044,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R1812:Ptprz1
|
UTSW |
6 |
22,959,711 (GRCm39) |
missense |
probably benign |
0.07 |
R1917:Ptprz1
|
UTSW |
6 |
23,035,039 (GRCm39) |
splice site |
probably benign |
|
R1930:Ptprz1
|
UTSW |
6 |
23,007,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R1931:Ptprz1
|
UTSW |
6 |
23,007,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R1974:Ptprz1
|
UTSW |
6 |
22,986,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R1992:Ptprz1
|
UTSW |
6 |
22,959,747 (GRCm39) |
missense |
probably benign |
0.24 |
R1997:Ptprz1
|
UTSW |
6 |
23,050,496 (GRCm39) |
missense |
probably damaging |
0.99 |
R2002:Ptprz1
|
UTSW |
6 |
23,027,833 (GRCm39) |
nonsense |
probably null |
|
R2012:Ptprz1
|
UTSW |
6 |
23,001,026 (GRCm39) |
missense |
probably benign |
0.03 |
R2059:Ptprz1
|
UTSW |
6 |
22,986,322 (GRCm39) |
splice site |
probably benign |
|
R2061:Ptprz1
|
UTSW |
6 |
23,049,674 (GRCm39) |
critical splice donor site |
probably null |
|
R2067:Ptprz1
|
UTSW |
6 |
23,050,388 (GRCm39) |
splice site |
probably benign |
|
R2108:Ptprz1
|
UTSW |
6 |
23,033,476 (GRCm39) |
missense |
probably damaging |
0.99 |
R2152:Ptprz1
|
UTSW |
6 |
23,030,670 (GRCm39) |
missense |
probably damaging |
0.99 |
R2166:Ptprz1
|
UTSW |
6 |
23,045,632 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2183:Ptprz1
|
UTSW |
6 |
23,002,284 (GRCm39) |
missense |
probably benign |
|
R2202:Ptprz1
|
UTSW |
6 |
23,000,649 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2238:Ptprz1
|
UTSW |
6 |
22,987,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Ptprz1
|
UTSW |
6 |
23,000,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R3027:Ptprz1
|
UTSW |
6 |
23,016,196 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3861:Ptprz1
|
UTSW |
6 |
23,036,894 (GRCm39) |
missense |
probably damaging |
0.98 |
R4012:Ptprz1
|
UTSW |
6 |
23,002,584 (GRCm39) |
missense |
probably damaging |
0.99 |
R4020:Ptprz1
|
UTSW |
6 |
22,959,623 (GRCm39) |
splice site |
probably benign |
|
R4158:Ptprz1
|
UTSW |
6 |
23,022,204 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4158:Ptprz1
|
UTSW |
6 |
23,001,683 (GRCm39) |
nonsense |
probably null |
|
R4159:Ptprz1
|
UTSW |
6 |
23,001,683 (GRCm39) |
nonsense |
probably null |
|
R4160:Ptprz1
|
UTSW |
6 |
23,022,204 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4606:Ptprz1
|
UTSW |
6 |
23,001,486 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4621:Ptprz1
|
UTSW |
6 |
23,001,453 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4640:Ptprz1
|
UTSW |
6 |
22,972,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Ptprz1
|
UTSW |
6 |
23,002,609 (GRCm39) |
missense |
probably benign |
0.06 |
R4732:Ptprz1
|
UTSW |
6 |
23,002,609 (GRCm39) |
missense |
probably benign |
0.06 |
R4733:Ptprz1
|
UTSW |
6 |
23,002,609 (GRCm39) |
missense |
probably benign |
0.06 |
R4803:Ptprz1
|
UTSW |
6 |
23,001,545 (GRCm39) |
missense |
probably benign |
0.00 |
R4890:Ptprz1
|
UTSW |
6 |
23,024,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R5035:Ptprz1
|
UTSW |
6 |
23,016,214 (GRCm39) |
missense |
probably benign |
0.06 |
R5052:Ptprz1
|
UTSW |
6 |
23,045,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R5106:Ptprz1
|
UTSW |
6 |
23,000,027 (GRCm39) |
missense |
probably benign |
0.04 |
R5248:Ptprz1
|
UTSW |
6 |
23,001,900 (GRCm39) |
missense |
probably benign |
0.11 |
R5292:Ptprz1
|
UTSW |
6 |
23,002,581 (GRCm39) |
missense |
probably benign |
0.31 |
R5373:Ptprz1
|
UTSW |
6 |
23,007,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5374:Ptprz1
|
UTSW |
6 |
23,007,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5378:Ptprz1
|
UTSW |
6 |
23,007,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R5408:Ptprz1
|
UTSW |
6 |
23,002,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R5479:Ptprz1
|
UTSW |
6 |
23,001,665 (GRCm39) |
missense |
probably benign |
|
R5524:Ptprz1
|
UTSW |
6 |
22,986,317 (GRCm39) |
splice site |
probably null |
|
R5527:Ptprz1
|
UTSW |
6 |
23,000,052 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5557:Ptprz1
|
UTSW |
6 |
23,001,000 (GRCm39) |
missense |
probably benign |
0.04 |
R5654:Ptprz1
|
UTSW |
6 |
22,986,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Ptprz1
|
UTSW |
6 |
22,999,772 (GRCm39) |
missense |
probably benign |
0.00 |
R5658:Ptprz1
|
UTSW |
6 |
23,016,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R5663:Ptprz1
|
UTSW |
6 |
23,035,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R5765:Ptprz1
|
UTSW |
6 |
23,000,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R5822:Ptprz1
|
UTSW |
6 |
23,001,444 (GRCm39) |
missense |
probably benign |
0.01 |
R5837:Ptprz1
|
UTSW |
6 |
23,001,417 (GRCm39) |
missense |
probably benign |
0.00 |
R6108:Ptprz1
|
UTSW |
6 |
23,045,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R6199:Ptprz1
|
UTSW |
6 |
23,002,470 (GRCm39) |
missense |
probably benign |
0.01 |
R6245:Ptprz1
|
UTSW |
6 |
23,051,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Ptprz1
|
UTSW |
6 |
22,959,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R6488:Ptprz1
|
UTSW |
6 |
23,001,516 (GRCm39) |
nonsense |
probably null |
|
R6606:Ptprz1
|
UTSW |
6 |
23,002,500 (GRCm39) |
missense |
probably benign |
0.27 |
R6612:Ptprz1
|
UTSW |
6 |
23,052,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R6824:Ptprz1
|
UTSW |
6 |
23,002,130 (GRCm39) |
missense |
probably benign |
0.05 |
R6834:Ptprz1
|
UTSW |
6 |
22,999,632 (GRCm39) |
missense |
probably benign |
0.38 |
R6836:Ptprz1
|
UTSW |
6 |
23,030,664 (GRCm39) |
nonsense |
probably null |
|
R6991:Ptprz1
|
UTSW |
6 |
23,002,686 (GRCm39) |
missense |
probably benign |
0.00 |
R7044:Ptprz1
|
UTSW |
6 |
23,044,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R7048:Ptprz1
|
UTSW |
6 |
22,961,622 (GRCm39) |
missense |
probably benign |
0.18 |
R7225:Ptprz1
|
UTSW |
6 |
23,000,928 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7284:Ptprz1
|
UTSW |
6 |
23,000,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R7360:Ptprz1
|
UTSW |
6 |
23,000,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R7501:Ptprz1
|
UTSW |
6 |
23,001,746 (GRCm39) |
nonsense |
probably null |
|
R7515:Ptprz1
|
UTSW |
6 |
23,022,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R7538:Ptprz1
|
UTSW |
6 |
22,999,895 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7567:Ptprz1
|
UTSW |
6 |
22,959,779 (GRCm39) |
missense |
probably damaging |
0.97 |
R7599:Ptprz1
|
UTSW |
6 |
23,002,518 (GRCm39) |
missense |
not run |
|
R7611:Ptprz1
|
UTSW |
6 |
23,001,219 (GRCm39) |
missense |
probably benign |
|
R7685:Ptprz1
|
UTSW |
6 |
23,024,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R7707:Ptprz1
|
UTSW |
6 |
23,002,295 (GRCm39) |
missense |
probably benign |
0.00 |
R7733:Ptprz1
|
UTSW |
6 |
23,000,383 (GRCm39) |
missense |
probably benign |
0.31 |
R7786:Ptprz1
|
UTSW |
6 |
23,036,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R7868:Ptprz1
|
UTSW |
6 |
23,000,963 (GRCm39) |
missense |
not run |
|
R7882:Ptprz1
|
UTSW |
6 |
23,002,256 (GRCm39) |
missense |
probably benign |
0.13 |
R7968:Ptprz1
|
UTSW |
6 |
22,959,675 (GRCm39) |
missense |
probably damaging |
0.98 |
R8024:Ptprz1
|
UTSW |
6 |
23,042,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R8157:Ptprz1
|
UTSW |
6 |
23,002,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R8159:Ptprz1
|
UTSW |
6 |
23,001,662 (GRCm39) |
missense |
probably benign |
|
R8354:Ptprz1
|
UTSW |
6 |
22,999,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R8496:Ptprz1
|
UTSW |
6 |
22,972,797 (GRCm39) |
missense |
probably damaging |
0.96 |
R8757:Ptprz1
|
UTSW |
6 |
22,972,716 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8767:Ptprz1
|
UTSW |
6 |
22,986,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R8783:Ptprz1
|
UTSW |
6 |
23,002,026 (GRCm39) |
missense |
probably benign |
0.00 |
R8811:Ptprz1
|
UTSW |
6 |
23,030,661 (GRCm39) |
missense |
probably benign |
0.03 |
R8817:Ptprz1
|
UTSW |
6 |
23,007,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R8822:Ptprz1
|
UTSW |
6 |
23,002,588 (GRCm39) |
missense |
probably damaging |
0.98 |
R8874:Ptprz1
|
UTSW |
6 |
23,042,747 (GRCm39) |
missense |
|
|
R9009:Ptprz1
|
UTSW |
6 |
23,001,653 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9126:Ptprz1
|
UTSW |
6 |
23,002,334 (GRCm39) |
nonsense |
probably null |
|
R9201:Ptprz1
|
UTSW |
6 |
22,972,869 (GRCm39) |
critical splice donor site |
probably null |
|
R9210:Ptprz1
|
UTSW |
6 |
23,050,493 (GRCm39) |
missense |
probably damaging |
0.99 |
R9212:Ptprz1
|
UTSW |
6 |
23,050,493 (GRCm39) |
missense |
probably damaging |
0.99 |
R9229:Ptprz1
|
UTSW |
6 |
22,986,283 (GRCm39) |
missense |
probably null |
0.03 |
R9279:Ptprz1
|
UTSW |
6 |
23,002,444 (GRCm39) |
missense |
probably benign |
|
R9336:Ptprz1
|
UTSW |
6 |
23,000,855 (GRCm39) |
missense |
probably benign |
0.01 |
R9372:Ptprz1
|
UTSW |
6 |
23,045,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R9577:Ptprz1
|
UTSW |
6 |
23,002,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R9594:Ptprz1
|
UTSW |
6 |
23,025,026 (GRCm39) |
missense |
probably damaging |
0.98 |
R9632:Ptprz1
|
UTSW |
6 |
23,007,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R9636:Ptprz1
|
UTSW |
6 |
22,999,994 (GRCm39) |
missense |
probably benign |
|
R9657:Ptprz1
|
UTSW |
6 |
23,042,377 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9694:Ptprz1
|
UTSW |
6 |
22,959,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R9716:Ptprz1
|
UTSW |
6 |
22,959,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R9794:Ptprz1
|
UTSW |
6 |
23,000,204 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Ptprz1
|
UTSW |
6 |
23,051,994 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Ptprz1
|
UTSW |
6 |
23,052,023 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ptprz1
|
UTSW |
6 |
22,999,839 (GRCm39) |
missense |
possibly damaging |
0.51 |
|