Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Amy1 |
T |
C |
3: 113,352,079 (GRCm39) |
D371G |
probably benign |
Het |
Asrgl1 |
T |
A |
19: 9,095,883 (GRCm39) |
|
probably benign |
Het |
Asxl3 |
T |
A |
18: 22,585,383 (GRCm39) |
|
probably benign |
Het |
B3galnt1 |
T |
C |
3: 69,482,673 (GRCm39) |
N196S |
possibly damaging |
Het |
Bbof1 |
A |
G |
12: 84,471,978 (GRCm39) |
H74R |
probably damaging |
Het |
Bpifb9b |
C |
T |
2: 154,158,995 (GRCm39) |
T504M |
probably damaging |
Het |
Cdk12 |
T |
G |
11: 98,094,817 (GRCm39) |
S208R |
probably damaging |
Het |
Cdk5r1 |
T |
C |
11: 80,368,576 (GRCm39) |
L81P |
probably damaging |
Het |
Chrd |
T |
C |
16: 20,552,025 (GRCm39) |
L43P |
probably benign |
Het |
Col6a4 |
A |
C |
9: 105,949,565 (GRCm39) |
M690R |
probably benign |
Het |
Cyp39a1 |
A |
T |
17: 44,042,903 (GRCm39) |
R418W |
probably damaging |
Het |
Dars2 |
C |
T |
1: 160,890,357 (GRCm39) |
V162M |
probably benign |
Het |
Dixdc1 |
C |
T |
9: 50,606,807 (GRCm39) |
V270M |
possibly damaging |
Het |
Dnah11 |
C |
A |
12: 117,946,791 (GRCm39) |
E1194* |
probably null |
Het |
Dnah7b |
T |
C |
1: 46,258,508 (GRCm39) |
S1900P |
probably damaging |
Het |
Dnah9 |
C |
T |
11: 65,746,141 (GRCm39) |
E3991K |
probably damaging |
Het |
Dsp |
A |
T |
13: 38,381,681 (GRCm39) |
I2210F |
probably benign |
Het |
Ebf1 |
A |
G |
11: 44,886,949 (GRCm39) |
S556G |
probably damaging |
Het |
Enam |
G |
A |
5: 88,637,514 (GRCm39) |
|
probably benign |
Het |
Eno1b |
T |
C |
18: 48,180,806 (GRCm39) |
I328T |
probably benign |
Het |
Epc1 |
T |
C |
18: 6,440,168 (GRCm39) |
D579G |
probably damaging |
Het |
Ephb3 |
A |
T |
16: 21,039,525 (GRCm39) |
I426F |
probably damaging |
Het |
Fam135b |
T |
G |
15: 71,317,886 (GRCm39) |
I1359L |
probably benign |
Het |
Fcgbpl1 |
T |
A |
7: 27,856,250 (GRCm39) |
H2012Q |
probably damaging |
Het |
Gm16519 |
T |
C |
17: 71,236,128 (GRCm39) |
S26P |
probably benign |
Het |
Gm17622 |
T |
A |
13: 96,627,594 (GRCm39) |
|
probably null |
Het |
Gpat2 |
G |
A |
2: 127,277,765 (GRCm39) |
V764I |
possibly damaging |
Het |
Gpx4 |
G |
A |
10: 79,890,838 (GRCm39) |
A81T |
probably benign |
Het |
Gss |
C |
A |
2: 155,420,326 (GRCm39) |
R83L |
probably damaging |
Het |
Hcls1 |
C |
A |
16: 36,758,216 (GRCm39) |
Q36K |
probably damaging |
Het |
Hepacam2 |
A |
G |
6: 3,463,336 (GRCm39) |
V438A |
probably benign |
Het |
Hnf4a |
T |
C |
2: 163,401,005 (GRCm39) |
F184S |
probably damaging |
Het |
Katnal1 |
T |
A |
5: 148,855,460 (GRCm39) |
D90V |
possibly damaging |
Het |
Kcnt2 |
A |
G |
1: 140,174,083 (GRCm39) |
D30G |
probably benign |
Het |
Kyat1 |
T |
C |
2: 30,084,087 (GRCm39) |
E11G |
probably benign |
Het |
Lefty1 |
T |
A |
1: 180,764,579 (GRCm39) |
V168E |
probably damaging |
Het |
Map2k6 |
C |
T |
11: 110,387,281 (GRCm39) |
P218S |
probably damaging |
Het |
Mlkl |
C |
G |
8: 112,041,694 (GRCm39) |
K415N |
probably benign |
Het |
Myh7 |
A |
T |
14: 55,211,390 (GRCm39) |
M1593K |
probably benign |
Het |
Myo19 |
T |
A |
11: 84,784,159 (GRCm39) |
C186S |
possibly damaging |
Het |
Ngp |
T |
C |
9: 110,249,069 (GRCm39) |
L47P |
probably damaging |
Het |
Nkiras1 |
A |
G |
14: 18,280,185 (GRCm38) |
N192S |
probably benign |
Het |
Or1j17 |
G |
A |
2: 36,578,628 (GRCm39) |
V205M |
probably benign |
Het |
Or2n1 |
A |
G |
17: 38,486,841 (GRCm39) |
I289V |
probably damaging |
Het |
Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
Or8u9 |
T |
C |
2: 86,001,886 (GRCm39) |
I92V |
probably benign |
Het |
Pdcd6ip |
A |
G |
9: 113,514,361 (GRCm39) |
|
probably benign |
Het |
Pde4b |
T |
C |
4: 102,454,707 (GRCm39) |
Y186H |
probably benign |
Het |
Pex7 |
A |
G |
10: 19,780,331 (GRCm39) |
V101A |
possibly damaging |
Het |
Phldb3 |
G |
A |
7: 24,312,004 (GRCm39) |
R106Q |
probably benign |
Het |
Plxnc1 |
A |
G |
10: 94,635,209 (GRCm39) |
V1339A |
probably benign |
Het |
Proser1 |
A |
G |
3: 53,386,383 (GRCm39) |
N755S |
probably damaging |
Het |
Rassf8 |
A |
C |
6: 145,765,700 (GRCm39) |
|
probably benign |
Het |
Rfc4 |
G |
A |
16: 22,932,849 (GRCm39) |
Q363* |
probably null |
Het |
Rxfp1 |
T |
C |
3: 79,552,282 (GRCm39) |
N673S |
probably damaging |
Het |
Scn7a |
T |
C |
2: 66,556,628 (GRCm39) |
E319G |
probably damaging |
Het |
Scnn1g |
A |
G |
7: 121,345,984 (GRCm39) |
|
probably benign |
Het |
Scube2 |
C |
T |
7: 109,423,971 (GRCm39) |
|
probably null |
Het |
Slc4a4 |
A |
C |
5: 89,304,195 (GRCm39) |
H502P |
possibly damaging |
Het |
Slc6a13 |
A |
G |
6: 121,301,262 (GRCm39) |
N184D |
probably benign |
Het |
Slco1a5 |
T |
A |
6: 142,182,054 (GRCm39) |
|
probably benign |
Het |
Slf1 |
T |
A |
13: 77,260,867 (GRCm39) |
|
probably benign |
Het |
Smarca4 |
G |
A |
9: 21,612,168 (GRCm39) |
V1518I |
probably damaging |
Het |
Smyd3 |
A |
G |
1: 179,250,993 (GRCm39) |
|
probably benign |
Het |
Sox5 |
A |
G |
6: 144,155,064 (GRCm39) |
F11L |
probably benign |
Het |
Spag17 |
T |
C |
3: 100,014,143 (GRCm39) |
S2139P |
probably benign |
Het |
Spice1 |
A |
T |
16: 44,185,939 (GRCm39) |
|
probably benign |
Het |
Sptan1 |
T |
A |
2: 29,900,704 (GRCm39) |
|
probably benign |
Het |
Srebf2 |
T |
A |
15: 82,066,286 (GRCm39) |
N571K |
probably damaging |
Het |
Tbl3 |
A |
G |
17: 24,920,307 (GRCm39) |
L670P |
probably damaging |
Het |
Tmem45a2 |
A |
G |
16: 56,867,359 (GRCm39) |
V114A |
possibly damaging |
Het |
Tmigd3 |
A |
G |
3: 105,826,053 (GRCm39) |
N132D |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,567,778 (GRCm39) |
D19378G |
probably damaging |
Het |
Ugcg |
C |
A |
4: 59,189,739 (GRCm39) |
Y32* |
probably null |
Het |
Ush2a |
C |
T |
1: 188,582,301 (GRCm39) |
P3788L |
probably damaging |
Het |
Usp22 |
T |
A |
11: 61,050,023 (GRCm39) |
|
probably benign |
Het |
Xaf1 |
T |
C |
11: 72,197,381 (GRCm39) |
|
probably benign |
Het |
Zbtb41 |
C |
T |
1: 139,374,673 (GRCm39) |
T711I |
probably damaging |
Het |
Zfp457 |
T |
C |
13: 67,442,180 (GRCm39) |
T132A |
possibly damaging |
Het |
Zfp64 |
T |
G |
2: 168,754,150 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ptpn13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Ptpn13
|
APN |
5 |
103,698,924 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00569:Ptpn13
|
APN |
5 |
103,738,872 (GRCm39) |
splice site |
probably benign |
|
IGL00764:Ptpn13
|
APN |
5 |
103,745,584 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00805:Ptpn13
|
APN |
5 |
103,702,595 (GRCm39) |
missense |
probably benign |
0.33 |
IGL00922:Ptpn13
|
APN |
5 |
103,735,954 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00959:Ptpn13
|
APN |
5 |
103,665,437 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01090:Ptpn13
|
APN |
5 |
103,689,180 (GRCm39) |
missense |
probably null |
0.80 |
IGL01352:Ptpn13
|
APN |
5 |
103,634,641 (GRCm39) |
splice site |
probably null |
|
IGL01510:Ptpn13
|
APN |
5 |
103,710,166 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01515:Ptpn13
|
APN |
5 |
103,703,979 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01896:Ptpn13
|
APN |
5 |
103,649,389 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02094:Ptpn13
|
APN |
5 |
103,742,483 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02561:Ptpn13
|
APN |
5 |
103,710,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02562:Ptpn13
|
APN |
5 |
103,710,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02567:Ptpn13
|
APN |
5 |
103,710,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02604:Ptpn13
|
APN |
5 |
103,649,769 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02679:Ptpn13
|
APN |
5 |
103,717,320 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02981:Ptpn13
|
APN |
5 |
103,676,670 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03131:Ptpn13
|
APN |
5 |
103,665,425 (GRCm39) |
missense |
probably benign |
|
IGL03136:Ptpn13
|
APN |
5 |
103,691,329 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03163:Ptpn13
|
APN |
5 |
103,739,212 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03271:Ptpn13
|
APN |
5 |
103,610,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03297:Ptpn13
|
APN |
5 |
103,688,943 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03328:Ptpn13
|
APN |
5 |
103,664,214 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03343:Ptpn13
|
APN |
5 |
103,702,816 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02835:Ptpn13
|
UTSW |
5 |
103,707,891 (GRCm39) |
missense |
probably damaging |
0.98 |
P0021:Ptpn13
|
UTSW |
5 |
103,676,686 (GRCm39) |
missense |
probably benign |
0.39 |
R0017:Ptpn13
|
UTSW |
5 |
103,634,638 (GRCm39) |
critical splice donor site |
probably null |
|
R0090:Ptpn13
|
UTSW |
5 |
103,717,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0111:Ptpn13
|
UTSW |
5 |
103,728,629 (GRCm39) |
splice site |
probably benign |
|
R0183:Ptpn13
|
UTSW |
5 |
103,664,274 (GRCm39) |
missense |
probably benign |
0.00 |
R0302:Ptpn13
|
UTSW |
5 |
103,713,091 (GRCm39) |
missense |
probably benign |
|
R0360:Ptpn13
|
UTSW |
5 |
103,681,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R0364:Ptpn13
|
UTSW |
5 |
103,681,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R0388:Ptpn13
|
UTSW |
5 |
103,702,928 (GRCm39) |
missense |
probably benign |
0.31 |
R0504:Ptpn13
|
UTSW |
5 |
103,649,362 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0558:Ptpn13
|
UTSW |
5 |
103,677,583 (GRCm39) |
missense |
probably damaging |
0.99 |
R0562:Ptpn13
|
UTSW |
5 |
103,664,291 (GRCm39) |
critical splice donor site |
probably null |
|
R0568:Ptpn13
|
UTSW |
5 |
103,637,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Ptpn13
|
UTSW |
5 |
103,704,011 (GRCm39) |
missense |
probably benign |
|
R0669:Ptpn13
|
UTSW |
5 |
103,703,975 (GRCm39) |
missense |
probably benign |
|
R0739:Ptpn13
|
UTSW |
5 |
103,722,998 (GRCm39) |
missense |
probably benign |
|
R1006:Ptpn13
|
UTSW |
5 |
103,734,655 (GRCm39) |
missense |
probably benign |
0.04 |
R1164:Ptpn13
|
UTSW |
5 |
103,637,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R1274:Ptpn13
|
UTSW |
5 |
103,698,126 (GRCm39) |
missense |
probably damaging |
0.98 |
R1501:Ptpn13
|
UTSW |
5 |
103,664,230 (GRCm39) |
missense |
probably benign |
0.01 |
R1529:Ptpn13
|
UTSW |
5 |
103,711,998 (GRCm39) |
missense |
probably benign |
0.00 |
R1533:Ptpn13
|
UTSW |
5 |
103,704,044 (GRCm39) |
nonsense |
probably null |
|
R1613:Ptpn13
|
UTSW |
5 |
103,684,737 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1616:Ptpn13
|
UTSW |
5 |
103,713,103 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1830:Ptpn13
|
UTSW |
5 |
103,691,325 (GRCm39) |
missense |
probably benign |
0.00 |
R1892:Ptpn13
|
UTSW |
5 |
103,649,545 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1907:Ptpn13
|
UTSW |
5 |
103,728,575 (GRCm39) |
missense |
probably null |
0.45 |
R2143:Ptpn13
|
UTSW |
5 |
103,703,999 (GRCm39) |
missense |
probably benign |
|
R2145:Ptpn13
|
UTSW |
5 |
103,703,999 (GRCm39) |
missense |
probably benign |
|
R2151:Ptpn13
|
UTSW |
5 |
103,673,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R2180:Ptpn13
|
UTSW |
5 |
103,717,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R2264:Ptpn13
|
UTSW |
5 |
103,637,527 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2313:Ptpn13
|
UTSW |
5 |
103,712,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R3522:Ptpn13
|
UTSW |
5 |
103,737,720 (GRCm39) |
splice site |
probably benign |
|
R3773:Ptpn13
|
UTSW |
5 |
103,624,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R3924:Ptpn13
|
UTSW |
5 |
103,698,607 (GRCm39) |
splice site |
probably benign |
|
R4289:Ptpn13
|
UTSW |
5 |
103,681,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R4348:Ptpn13
|
UTSW |
5 |
103,717,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R4385:Ptpn13
|
UTSW |
5 |
103,681,273 (GRCm39) |
splice site |
probably null |
|
R4526:Ptpn13
|
UTSW |
5 |
103,649,335 (GRCm39) |
missense |
probably benign |
0.32 |
R4557:Ptpn13
|
UTSW |
5 |
103,688,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R4596:Ptpn13
|
UTSW |
5 |
103,671,558 (GRCm39) |
missense |
probably benign |
0.06 |
R4632:Ptpn13
|
UTSW |
5 |
103,717,726 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4727:Ptpn13
|
UTSW |
5 |
103,717,721 (GRCm39) |
missense |
probably benign |
|
R4780:Ptpn13
|
UTSW |
5 |
103,734,639 (GRCm39) |
missense |
probably benign |
0.04 |
R4793:Ptpn13
|
UTSW |
5 |
103,730,644 (GRCm39) |
critical splice donor site |
probably null |
|
R4812:Ptpn13
|
UTSW |
5 |
103,671,481 (GRCm39) |
missense |
probably benign |
0.00 |
R4939:Ptpn13
|
UTSW |
5 |
103,665,335 (GRCm39) |
splice site |
probably null |
|
R4951:Ptpn13
|
UTSW |
5 |
103,735,912 (GRCm39) |
missense |
probably benign |
0.00 |
R5052:Ptpn13
|
UTSW |
5 |
103,709,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R5148:Ptpn13
|
UTSW |
5 |
103,640,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R5309:Ptpn13
|
UTSW |
5 |
103,688,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R5521:Ptpn13
|
UTSW |
5 |
103,649,294 (GRCm39) |
missense |
probably benign |
0.03 |
R5545:Ptpn13
|
UTSW |
5 |
103,709,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Ptpn13
|
UTSW |
5 |
103,702,625 (GRCm39) |
missense |
probably benign |
0.20 |
R5735:Ptpn13
|
UTSW |
5 |
103,702,686 (GRCm39) |
missense |
probably benign |
0.03 |
R5815:Ptpn13
|
UTSW |
5 |
103,745,556 (GRCm39) |
splice site |
probably null |
|
R5876:Ptpn13
|
UTSW |
5 |
103,624,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R5878:Ptpn13
|
UTSW |
5 |
103,624,984 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6366:Ptpn13
|
UTSW |
5 |
103,698,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R6455:Ptpn13
|
UTSW |
5 |
103,689,150 (GRCm39) |
missense |
probably benign |
0.00 |
R6492:Ptpn13
|
UTSW |
5 |
103,649,478 (GRCm39) |
missense |
probably benign |
0.02 |
R6709:Ptpn13
|
UTSW |
5 |
103,734,622 (GRCm39) |
missense |
probably benign |
0.18 |
R6759:Ptpn13
|
UTSW |
5 |
103,713,121 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6944:Ptpn13
|
UTSW |
5 |
103,624,857 (GRCm39) |
missense |
probably null |
1.00 |
R7079:Ptpn13
|
UTSW |
5 |
103,649,752 (GRCm39) |
missense |
probably benign |
0.00 |
R7253:Ptpn13
|
UTSW |
5 |
103,713,150 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7254:Ptpn13
|
UTSW |
5 |
103,742,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R7391:Ptpn13
|
UTSW |
5 |
103,688,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R7451:Ptpn13
|
UTSW |
5 |
103,674,961 (GRCm39) |
missense |
probably benign |
0.16 |
R7614:Ptpn13
|
UTSW |
5 |
103,649,331 (GRCm39) |
missense |
probably benign |
0.13 |
R7652:Ptpn13
|
UTSW |
5 |
103,677,578 (GRCm39) |
missense |
probably benign |
0.12 |
R7655:Ptpn13
|
UTSW |
5 |
103,688,849 (GRCm39) |
missense |
probably benign |
0.00 |
R7656:Ptpn13
|
UTSW |
5 |
103,688,849 (GRCm39) |
missense |
probably benign |
0.00 |
R7683:Ptpn13
|
UTSW |
5 |
103,713,018 (GRCm39) |
missense |
probably benign |
0.01 |
R7734:Ptpn13
|
UTSW |
5 |
103,709,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Ptpn13
|
UTSW |
5 |
103,640,090 (GRCm39) |
missense |
probably benign |
0.06 |
R7834:Ptpn13
|
UTSW |
5 |
103,610,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R7911:Ptpn13
|
UTSW |
5 |
103,688,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:Ptpn13
|
UTSW |
5 |
103,707,803 (GRCm39) |
nonsense |
probably null |
|
R8308:Ptpn13
|
UTSW |
5 |
103,688,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R8493:Ptpn13
|
UTSW |
5 |
103,717,671 (GRCm39) |
missense |
probably benign |
0.01 |
R8493:Ptpn13
|
UTSW |
5 |
103,712,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Ptpn13
|
UTSW |
5 |
103,705,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R8556:Ptpn13
|
UTSW |
5 |
103,707,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Ptpn13
|
UTSW |
5 |
103,739,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R8933:Ptpn13
|
UTSW |
5 |
103,727,671 (GRCm39) |
missense |
probably benign |
0.00 |
R8958:Ptpn13
|
UTSW |
5 |
103,698,973 (GRCm39) |
missense |
probably benign |
0.15 |
R8975:Ptpn13
|
UTSW |
5 |
103,649,266 (GRCm39) |
missense |
probably benign |
0.32 |
R9080:Ptpn13
|
UTSW |
5 |
103,637,494 (GRCm39) |
missense |
probably damaging |
0.99 |
R9091:Ptpn13
|
UTSW |
5 |
103,649,735 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9219:Ptpn13
|
UTSW |
5 |
103,745,632 (GRCm39) |
missense |
probably benign |
0.16 |
R9270:Ptpn13
|
UTSW |
5 |
103,649,735 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9577:Ptpn13
|
UTSW |
5 |
103,676,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R9593:Ptpn13
|
UTSW |
5 |
103,674,998 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9705:Ptpn13
|
UTSW |
5 |
103,681,221 (GRCm39) |
missense |
possibly damaging |
0.89 |
RF017:Ptpn13
|
UTSW |
5 |
103,741,446 (GRCm39) |
missense |
probably benign |
0.45 |
Z1177:Ptpn13
|
UTSW |
5 |
103,717,422 (GRCm39) |
missense |
probably damaging |
1.00 |
|