Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actrt3 |
T |
A |
3: 30,652,781 (GRCm39) |
E104D |
probably damaging |
Het |
Arih2 |
A |
T |
9: 108,493,890 (GRCm39) |
D174E |
probably damaging |
Het |
Asprv1 |
T |
C |
6: 86,606,077 (GRCm39) |
F308L |
probably damaging |
Het |
Baiap2l2 |
A |
G |
15: 79,168,205 (GRCm39) |
|
probably null |
Het |
Btla |
T |
C |
16: 45,064,656 (GRCm39) |
F203L |
possibly damaging |
Het |
C1rb |
A |
T |
6: 124,551,947 (GRCm39) |
D283V |
probably damaging |
Het |
C87436 |
C |
G |
6: 86,442,813 (GRCm39) |
Q462E |
probably benign |
Het |
Ccdc149 |
T |
C |
5: 52,563,352 (GRCm39) |
D147G |
possibly damaging |
Het |
Chd6 |
A |
T |
2: 160,871,793 (GRCm39) |
L214* |
probably null |
Het |
Chrna4 |
C |
A |
2: 180,670,643 (GRCm39) |
R371L |
possibly damaging |
Het |
Cit |
C |
A |
5: 115,984,161 (GRCm39) |
|
probably benign |
Het |
Cpne5 |
A |
G |
17: 29,444,163 (GRCm39) |
|
probably null |
Het |
Cr1l |
T |
C |
1: 194,789,204 (GRCm39) |
E400G |
possibly damaging |
Het |
Creb3l2 |
T |
C |
6: 37,332,583 (GRCm39) |
N304D |
probably damaging |
Het |
Cyp17a1 |
T |
C |
19: 46,656,030 (GRCm39) |
T420A |
probably benign |
Het |
Cyp24a1 |
A |
G |
2: 170,327,853 (GRCm39) |
I463T |
probably damaging |
Het |
Cyp3a41b |
A |
T |
5: 145,514,973 (GRCm39) |
I84N |
probably damaging |
Het |
Dnajc6 |
G |
A |
4: 101,496,559 (GRCm39) |
V909M |
possibly damaging |
Het |
Dtl |
A |
G |
1: 191,288,923 (GRCm39) |
Y264H |
probably damaging |
Het |
Dysf |
C |
T |
6: 84,077,216 (GRCm39) |
R660* |
probably null |
Het |
Egf |
A |
G |
3: 129,529,449 (GRCm39) |
|
probably null |
Het |
Eva1c |
T |
C |
16: 90,701,231 (GRCm39) |
S402P |
probably benign |
Het |
Fcho2 |
A |
T |
13: 98,925,869 (GRCm39) |
|
probably null |
Het |
Fhdc1 |
G |
A |
3: 84,352,290 (GRCm39) |
R197C |
unknown |
Het |
Foxa2 |
T |
A |
2: 147,886,426 (GRCm39) |
M136L |
probably benign |
Het |
Gm10226 |
T |
C |
17: 21,910,866 (GRCm39) |
C34R |
possibly damaging |
Het |
Gm29735 |
ACAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAACAGCAGGATTCGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAAGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCA |
ACAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAACAGCAGGATTCGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAAGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCA |
7: 141,710,266 (GRCm39) |
|
probably benign |
Het |
Gm8947 |
T |
C |
1: 151,068,853 (GRCm39) |
S229P |
probably benign |
Het |
Ighv9-2 |
A |
T |
12: 114,072,896 (GRCm39) |
S26T |
probably damaging |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kat6a |
T |
G |
8: 23,420,190 (GRCm39) |
I745M |
probably damaging |
Het |
Klhdc1 |
T |
C |
12: 69,309,968 (GRCm39) |
L290P |
probably damaging |
Het |
Lcp2 |
C |
T |
11: 34,039,688 (GRCm39) |
T496I |
|
Het |
Map4k4 |
T |
C |
1: 40,042,923 (GRCm39) |
W593R |
probably benign |
Het |
Mefv |
T |
G |
16: 3,535,841 (GRCm39) |
Q29P |
probably damaging |
Het |
Mgat5b |
T |
C |
11: 116,859,269 (GRCm39) |
Y34H |
|
Het |
Mlip |
C |
T |
9: 77,137,080 (GRCm39) |
R609Q |
probably benign |
Het |
Muc2 |
A |
G |
7: 141,290,816 (GRCm39) |
D34G |
|
Het |
Nbeal1 |
C |
T |
1: 60,307,548 (GRCm39) |
P1687S |
possibly damaging |
Het |
Notch1 |
T |
A |
2: 26,369,895 (GRCm39) |
I477L |
probably damaging |
Het |
Odad2 |
T |
A |
18: 7,217,846 (GRCm39) |
K623* |
probably null |
Het |
Or1l4b |
G |
A |
2: 37,037,047 (GRCm39) |
M274I |
probably benign |
Het |
Or1s2 |
T |
C |
19: 13,758,333 (GRCm39) |
V117A |
probably benign |
Het |
Or4a2 |
A |
T |
2: 89,248,712 (GRCm39) |
L15Q |
probably damaging |
Het |
Or51v8 |
T |
A |
7: 103,320,124 (GRCm39) |
N38I |
probably damaging |
Het |
Or6c214 |
A |
G |
10: 129,591,148 (GRCm39) |
M57T |
probably damaging |
Het |
Pak5 |
A |
T |
2: 135,958,688 (GRCm39) |
S133R |
probably damaging |
Het |
Pcyt1a |
C |
A |
16: 32,285,332 (GRCm39) |
D187E |
probably benign |
Het |
Pdlim7 |
G |
T |
13: 55,655,354 (GRCm39) |
T161K |
probably damaging |
Het |
Phf8-ps |
A |
C |
17: 33,286,701 (GRCm39) |
C34G |
probably damaging |
Het |
Pik3r4 |
A |
G |
9: 105,547,108 (GRCm39) |
K962R |
probably benign |
Het |
Pkd1l2 |
T |
C |
8: 117,759,433 (GRCm39) |
K1516E |
probably damaging |
Het |
Plk5 |
C |
G |
10: 80,193,830 (GRCm39) |
R40G |
probably damaging |
Het |
Ptchd3 |
A |
T |
11: 121,733,180 (GRCm39) |
Y690F |
probably benign |
Het |
Rbm27 |
C |
T |
18: 42,438,829 (GRCm39) |
A410V |
probably benign |
Het |
Rnase4 |
A |
G |
14: 51,342,662 (GRCm39) |
T129A |
probably benign |
Het |
Serpinb11 |
C |
T |
1: 107,304,533 (GRCm39) |
T166I |
probably benign |
Het |
Shank2 |
A |
G |
7: 143,963,705 (GRCm39) |
T438A |
possibly damaging |
Het |
Slc13a2 |
T |
C |
11: 78,295,258 (GRCm39) |
N172D |
probably damaging |
Het |
Slc2a8 |
A |
G |
2: 32,864,864 (GRCm39) |
F428L |
probably damaging |
Het |
Slc38a6 |
T |
C |
12: 73,398,544 (GRCm39) |
M358T |
probably benign |
Het |
Snx29 |
A |
G |
16: 11,213,155 (GRCm39) |
H107R |
probably benign |
Het |
Sorbs2 |
T |
G |
8: 46,248,774 (GRCm39) |
V675G |
probably benign |
Het |
Spint3 |
G |
A |
2: 164,415,154 (GRCm39) |
A21V |
probably benign |
Het |
Susd1 |
A |
T |
4: 59,412,226 (GRCm39) |
V162E |
probably benign |
Het |
Syne2 |
T |
G |
12: 75,977,834 (GRCm39) |
N1426K |
probably damaging |
Het |
Synj2 |
T |
C |
17: 6,067,875 (GRCm39) |
V638A |
possibly damaging |
Het |
Thada |
A |
T |
17: 84,538,589 (GRCm39) |
L1473Q |
probably damaging |
Het |
Trim36 |
G |
A |
18: 46,300,580 (GRCm39) |
S697L |
possibly damaging |
Het |
Ttbk1 |
A |
T |
17: 46,781,517 (GRCm39) |
I412N |
possibly damaging |
Het |
Tubb2a |
T |
C |
13: 34,258,578 (GRCm39) |
D404G |
probably damaging |
Het |
Tyk2 |
T |
A |
9: 21,035,841 (GRCm39) |
N114Y |
probably damaging |
Het |
Umodl1 |
A |
G |
17: 31,185,678 (GRCm39) |
D139G |
probably damaging |
Het |
Vmn2r101 |
T |
A |
17: 19,810,244 (GRCm39) |
N343K |
probably benign |
Het |
Vnn1 |
A |
G |
10: 23,780,464 (GRCm39) |
D484G |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,770,919 (GRCm39) |
T2121A |
probably benign |
Het |
Wdr81 |
T |
C |
11: 75,345,216 (GRCm39) |
E17G |
probably benign |
Het |
Wnk2 |
T |
G |
13: 49,224,505 (GRCm39) |
K1117Q |
probably benign |
Het |
Zbtb46 |
C |
T |
2: 181,066,138 (GRCm39) |
R4Q |
probably benign |
Het |
Zfp608 |
T |
A |
18: 55,032,190 (GRCm39) |
K583N |
probably damaging |
Het |
Zfp729b |
A |
T |
13: 67,740,480 (GRCm39) |
L595H |
probably damaging |
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 |
R0230:Ptpn13
|
UTSW |
5 |
103,674,997 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|