Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arfgef3 |
A |
T |
10: 18,522,007 (GRCm39) |
I673K |
probably benign |
Het |
Arhgap32 |
C |
A |
9: 32,093,235 (GRCm39) |
T196K |
probably benign |
Het |
Azi2 |
T |
A |
9: 117,879,960 (GRCm39) |
|
probably null |
Het |
B3gnt2 |
A |
T |
11: 22,786,482 (GRCm39) |
C235* |
probably null |
Het |
Capn5 |
C |
T |
7: 97,780,426 (GRCm39) |
V315M |
probably benign |
Het |
Ccl24 |
T |
A |
5: 135,599,676 (GRCm39) |
R111S |
possibly damaging |
Het |
Cdk9 |
A |
G |
2: 32,602,083 (GRCm39) |
V45A |
probably damaging |
Het |
Cep162 |
G |
T |
9: 87,130,547 (GRCm39) |
S21* |
probably null |
Het |
Chil3 |
T |
A |
3: 106,071,496 (GRCm39) |
Y56F |
probably damaging |
Het |
Ctr9 |
T |
A |
7: 110,642,378 (GRCm39) |
L368* |
probably null |
Het |
Ctss |
A |
G |
3: 95,436,852 (GRCm39) |
E45G |
probably benign |
Het |
Cyp2c29 |
A |
T |
19: 39,296,211 (GRCm39) |
Q214L |
probably null |
Het |
Cyp2d34 |
T |
A |
15: 82,502,587 (GRCm39) |
N183I |
probably benign |
Het |
Dhx29 |
T |
A |
13: 113,099,393 (GRCm39) |
N1139K |
probably benign |
Het |
Elp1 |
C |
A |
4: 56,781,211 (GRCm39) |
Q487H |
possibly damaging |
Het |
Elp1 |
T |
G |
4: 56,781,212 (GRCm39) |
Q487P |
probably benign |
Het |
Ermp1 |
C |
A |
19: 29,604,468 (GRCm39) |
|
probably null |
Het |
Ermp1 |
T |
A |
19: 29,604,469 (GRCm39) |
|
probably null |
Het |
Evi2 |
A |
G |
11: 79,406,493 (GRCm39) |
S361P |
probably benign |
Het |
Ext2 |
T |
A |
2: 93,560,612 (GRCm39) |
K518M |
probably damaging |
Het |
Fgl1 |
A |
C |
8: 41,663,483 (GRCm39) |
M15R |
probably benign |
Het |
Fsip2 |
T |
G |
2: 82,820,663 (GRCm39) |
D5465E |
possibly damaging |
Het |
Hdlbp |
A |
T |
1: 93,358,783 (GRCm39) |
I256N |
possibly damaging |
Het |
Hmmr |
G |
T |
11: 40,598,613 (GRCm39) |
|
probably null |
Het |
Hnrnpu |
T |
C |
1: 178,164,643 (GRCm39) |
Q165R |
unknown |
Het |
Homer3 |
G |
A |
8: 70,742,134 (GRCm39) |
A132T |
probably benign |
Het |
Ift70a1 |
T |
C |
2: 75,810,359 (GRCm39) |
K575E |
probably benign |
Het |
Kcnb1 |
T |
C |
2: 166,947,370 (GRCm39) |
R493G |
probably damaging |
Het |
Kcnn3 |
A |
T |
3: 89,516,778 (GRCm39) |
T396S |
probably benign |
Het |
Krt15 |
A |
T |
11: 100,026,386 (GRCm39) |
V100E |
possibly damaging |
Het |
Krtap4-1 |
A |
G |
11: 99,518,810 (GRCm39) |
S67P |
unknown |
Het |
Lama4 |
G |
T |
10: 38,963,383 (GRCm39) |
|
probably null |
Het |
Lrrtm2 |
T |
A |
18: 35,345,818 (GRCm39) |
I495F |
possibly damaging |
Het |
Mical2 |
A |
T |
7: 111,919,816 (GRCm39) |
E442V |
probably damaging |
Het |
Muc16 |
C |
T |
9: 18,550,832 (GRCm39) |
V5154I |
probably benign |
Het |
Nav3 |
A |
T |
10: 109,539,317 (GRCm39) |
M2028K |
probably benign |
Het |
Ncr1 |
T |
A |
7: 4,347,470 (GRCm39) |
W249R |
possibly damaging |
Het |
Neurod6 |
T |
C |
6: 55,656,616 (GRCm39) |
D7G |
probably damaging |
Het |
Nwd1 |
A |
G |
8: 73,389,046 (GRCm39) |
E158G |
probably damaging |
Het |
Or10ak7 |
A |
T |
4: 118,791,198 (GRCm39) |
N282K |
possibly damaging |
Het |
Or2h15 |
A |
T |
17: 38,441,941 (GRCm39) |
F47L |
probably benign |
Het |
Or2t26 |
A |
G |
11: 49,039,806 (GRCm39) |
T241A |
probably damaging |
Het |
Or2y11 |
T |
C |
11: 49,443,371 (GRCm39) |
S266P |
probably damaging |
Het |
Or51a39 |
T |
C |
7: 102,363,189 (GRCm39) |
N144D |
probably benign |
Het |
Padi2 |
A |
G |
4: 140,665,266 (GRCm39) |
D457G |
probably benign |
Het |
Parn |
C |
A |
16: 13,485,870 (GRCm39) |
|
probably null |
Het |
Pcdh1 |
C |
T |
18: 38,335,838 (GRCm39) |
E266K |
possibly damaging |
Het |
Pigr |
A |
G |
1: 130,777,303 (GRCm39) |
D703G |
probably damaging |
Het |
Ppm1f |
T |
A |
16: 16,732,098 (GRCm39) |
S183T |
probably benign |
Het |
Ppp2r5b |
T |
A |
19: 6,278,544 (GRCm39) |
Q455L |
probably benign |
Het |
Pramel20 |
T |
A |
4: 143,298,876 (GRCm39) |
L273H |
probably damaging |
Het |
R3hdm4 |
T |
C |
10: 79,746,943 (GRCm39) |
K240R |
probably benign |
Het |
Rin1 |
T |
C |
19: 5,100,888 (GRCm39) |
M1T |
probably null |
Het |
Rundc3b |
T |
A |
5: 8,609,455 (GRCm39) |
M170L |
probably benign |
Het |
Ryr3 |
A |
T |
2: 112,611,322 (GRCm39) |
|
probably null |
Het |
Scn11a |
T |
C |
9: 119,624,783 (GRCm39) |
D513G |
probably damaging |
Het |
Slc27a2 |
C |
A |
2: 126,395,082 (GRCm39) |
P3Q |
unknown |
Het |
Slc4a8 |
A |
G |
15: 100,682,743 (GRCm39) |
I187M |
probably damaging |
Het |
Slc6a11 |
A |
T |
6: 114,215,422 (GRCm39) |
I441F |
probably benign |
Het |
Stx2 |
C |
T |
5: 129,065,867 (GRCm39) |
R263Q |
probably damaging |
Het |
Svep1 |
A |
T |
4: 58,145,185 (GRCm39) |
W427R |
probably damaging |
Het |
Tes |
T |
A |
6: 17,096,166 (GRCm39) |
H51Q |
probably damaging |
Het |
Thnsl2 |
T |
C |
6: 71,108,914 (GRCm39) |
D299G |
probably damaging |
Het |
Tmem30b |
T |
C |
12: 73,592,702 (GRCm39) |
S138G |
probably benign |
Het |
Tmprss11c |
T |
A |
5: 86,385,650 (GRCm39) |
H274L |
probably damaging |
Het |
Trim10 |
G |
A |
17: 37,180,773 (GRCm39) |
M1I |
probably null |
Het |
Unc13b |
A |
G |
4: 43,216,459 (GRCm39) |
I253V |
probably benign |
Het |
Unc80 |
A |
G |
1: 66,734,687 (GRCm39) |
S3305G |
probably benign |
Het |
Ush2a |
TCACC |
TC |
1: 188,694,205 (GRCm39) |
|
probably benign |
Het |
Virma |
A |
G |
4: 11,508,099 (GRCm39) |
D267G |
probably damaging |
Het |
Vmn1r46 |
C |
T |
6: 89,953,607 (GRCm39) |
S152L |
probably benign |
Het |
Wdr90 |
T |
C |
17: 26,065,502 (GRCm39) |
N1621S |
probably benign |
Het |
Zfhx3 |
G |
A |
8: 109,674,475 (GRCm39) |
A1842T |
probably damaging |
Het |
Zfp583 |
A |
G |
7: 6,319,498 (GRCm39) |
S505P |
probably damaging |
Het |
Zfp608 |
T |
C |
18: 55,030,619 (GRCm39) |
Y1107C |
possibly damaging |
Het |
Zfp616 |
A |
G |
11: 73,976,155 (GRCm39) |
H808R |
probably benign |
Het |
Zfp677 |
T |
C |
17: 21,618,653 (GRCm39) |
F570S |
possibly damaging |
Het |
Zfp85 |
A |
T |
13: 67,897,410 (GRCm39) |
Y221N |
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 |
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 |
|