Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
A |
T |
2: 69,115,068 (GRCm39) |
I626N |
probably damaging |
Het |
Abcc12 |
T |
A |
8: 87,258,179 (GRCm39) |
Y779F |
possibly damaging |
Het |
Abcc12 |
C |
T |
8: 87,284,859 (GRCm39) |
C252Y |
probably damaging |
Het |
Adam22 |
A |
T |
5: 8,180,535 (GRCm39) |
C521S |
probably damaging |
Het |
Adcy5 |
C |
A |
16: 34,977,570 (GRCm39) |
H368N |
probably benign |
Het |
Akap13 |
T |
A |
7: 75,392,390 (GRCm39) |
I2411N |
possibly damaging |
Het |
Ankrd12 |
A |
G |
17: 66,294,347 (GRCm39) |
F339S |
probably damaging |
Het |
Bmp1 |
T |
A |
14: 70,746,005 (GRCm39) |
R153W |
probably damaging |
Het |
Bmp6 |
T |
C |
13: 38,653,643 (GRCm39) |
F237L |
probably damaging |
Het |
Cacna1c |
A |
G |
6: 118,587,542 (GRCm39) |
S1628P |
|
Het |
Ccdc141 |
T |
C |
2: 76,889,889 (GRCm39) |
R468G |
possibly damaging |
Het |
Cdc40 |
A |
T |
10: 40,758,945 (GRCm39) |
S43T |
probably benign |
Het |
Celf4 |
A |
G |
18: 25,886,542 (GRCm39) |
M48T |
probably benign |
Het |
Clec4g |
A |
T |
8: 3,766,500 (GRCm39) |
M267K |
probably damaging |
Het |
Col6a1 |
G |
T |
10: 76,545,762 (GRCm39) |
S903R |
unknown |
Het |
Creg2 |
A |
G |
1: 39,689,802 (GRCm39) |
F103L |
probably damaging |
Het |
Cul9 |
T |
C |
17: 46,836,630 (GRCm39) |
|
probably null |
Het |
Dchs1 |
G |
A |
7: 105,414,774 (GRCm39) |
A756V |
probably benign |
Het |
Diaph1 |
G |
A |
18: 37,986,762 (GRCm39) |
|
probably benign |
Het |
Dmxl1 |
G |
A |
18: 50,054,044 (GRCm39) |
G2550D |
probably damaging |
Het |
Dst |
G |
T |
1: 34,233,186 (GRCm39) |
R3396I |
probably benign |
Het |
Dync2h1 |
T |
C |
9: 7,118,953 (GRCm39) |
T2171A |
probably benign |
Het |
Fgd2 |
C |
T |
17: 29,583,925 (GRCm39) |
T113M |
probably damaging |
Het |
Galnt6 |
G |
T |
15: 100,611,984 (GRCm39) |
S219R |
probably damaging |
Het |
Gbp6 |
T |
A |
5: 105,421,131 (GRCm39) |
E558V |
probably benign |
Het |
Gnas |
A |
T |
2: 174,140,783 (GRCm39) |
K377* |
probably null |
Het |
Hars2 |
T |
C |
18: 36,922,634 (GRCm39) |
I389T |
probably damaging |
Het |
Hsp90ab1 |
T |
C |
17: 45,882,091 (GRCm39) |
I123V |
possibly damaging |
Het |
Igkv6-14 |
A |
T |
6: 70,411,992 (GRCm39) |
N97K |
possibly damaging |
Het |
Isg20 |
T |
C |
7: 78,569,867 (GRCm39) |
L168P |
probably damaging |
Het |
Kcna1 |
C |
T |
6: 126,619,703 (GRCm39) |
D206N |
probably benign |
Het |
Kcnn3 |
A |
G |
3: 89,428,661 (GRCm39) |
I296V |
probably damaging |
Het |
Kif18a |
G |
A |
2: 109,127,119 (GRCm39) |
R351H |
probably damaging |
Het |
Klra5 |
A |
T |
6: 129,876,253 (GRCm39) |
|
probably null |
Het |
Krt9 |
T |
C |
11: 100,083,492 (GRCm39) |
T180A |
probably benign |
Het |
Lhx8 |
T |
C |
3: 154,017,174 (GRCm39) |
S323G |
probably null |
Het |
Lpcat2 |
T |
A |
8: 93,644,729 (GRCm39) |
L506H |
possibly damaging |
Het |
Map2 |
A |
G |
1: 66,455,647 (GRCm39) |
E1447G |
probably damaging |
Het |
Mapk8ip2 |
A |
T |
15: 89,345,576 (GRCm39) |
I779F |
probably damaging |
Het |
Mcmdc2 |
G |
A |
1: 9,982,399 (GRCm39) |
|
probably null |
Het |
Mrps15 |
G |
A |
4: 125,949,182 (GRCm39) |
E217K |
probably damaging |
Het |
Muc5b |
G |
A |
7: 141,412,807 (GRCm39) |
G1918R |
unknown |
Het |
Mug2 |
T |
C |
6: 122,013,241 (GRCm39) |
I336T |
probably benign |
Het |
Myh10 |
T |
C |
11: 68,676,652 (GRCm39) |
V878A |
probably damaging |
Het |
Nomo1 |
T |
C |
7: 45,706,162 (GRCm39) |
|
probably null |
Het |
Ogdhl |
T |
A |
14: 32,062,666 (GRCm39) |
I584N |
probably benign |
Het |
Pdzrn3 |
G |
A |
6: 101,128,156 (GRCm39) |
R837C |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,382,273 (GRCm39) |
M2626T |
probably benign |
Het |
Plat |
G |
T |
8: 23,262,248 (GRCm39) |
G91W |
probably damaging |
Het |
Pml |
C |
A |
9: 58,141,968 (GRCm39) |
R288L |
probably benign |
Het |
Pnliprp2 |
T |
C |
19: 58,762,591 (GRCm39) |
S399P |
probably benign |
Het |
Prelp |
T |
C |
1: 133,842,510 (GRCm39) |
T212A |
probably damaging |
Het |
Ptprb |
A |
C |
10: 116,175,329 (GRCm39) |
E821A |
probably benign |
Het |
Rabgap1 |
T |
C |
2: 37,359,419 (GRCm39) |
|
probably benign |
Het |
Reln |
C |
T |
5: 22,244,633 (GRCm39) |
V782M |
possibly damaging |
Het |
Rpl3l |
T |
C |
17: 24,952,437 (GRCm39) |
V52A |
possibly damaging |
Het |
Rrp1b |
T |
C |
17: 32,270,698 (GRCm39) |
V219A |
probably benign |
Het |
Rtn1 |
T |
A |
12: 72,350,806 (GRCm39) |
I468F |
probably damaging |
Het |
Safb |
T |
A |
17: 56,900,881 (GRCm39) |
M129K |
unknown |
Het |
Sall1 |
C |
A |
8: 89,760,002 (GRCm39) |
S34I |
probably benign |
Het |
Slc2a8 |
C |
T |
2: 32,866,919 (GRCm39) |
G227D |
probably damaging |
Het |
Slco4a1 |
G |
T |
2: 180,107,470 (GRCm39) |
V295L |
probably benign |
Het |
Slfn5 |
A |
T |
11: 82,851,278 (GRCm39) |
Q525L |
possibly damaging |
Het |
Speg |
C |
T |
1: 75,361,571 (GRCm39) |
T195M |
probably damaging |
Het |
Syne2 |
A |
T |
12: 76,014,021 (GRCm39) |
T3071S |
probably benign |
Het |
Syngr1 |
G |
T |
15: 79,995,818 (GRCm39) |
W119L |
probably damaging |
Het |
Tenm2 |
A |
G |
11: 35,915,681 (GRCm39) |
L1951P |
probably damaging |
Het |
Ulk4 |
C |
T |
9: 121,092,734 (GRCm39) |
E168K |
possibly damaging |
Het |
Ush2a |
G |
A |
1: 188,465,637 (GRCm39) |
W2735* |
probably null |
Het |
Usp17lb |
T |
A |
7: 104,490,718 (GRCm39) |
T70S |
probably damaging |
Het |
Vmn2r6 |
T |
G |
3: 64,445,443 (GRCm39) |
N761H |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,835,143 (GRCm39) |
I2741K |
|
Het |
Wdr38 |
A |
T |
2: 38,890,196 (GRCm39) |
Q110L |
possibly damaging |
Het |
Zfp872 |
A |
G |
9: 22,111,406 (GRCm39) |
K295R |
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 |
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 |
|