Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432M17Rik |
A |
C |
3: 121,679,446 (GRCm38) |
K83N |
unknown |
Het |
Abca13 |
A |
T |
11: 9,294,649 (GRCm38) |
N2171Y |
probably damaging |
Het |
Abcc8 |
G |
A |
7: 46,105,498 (GRCm38) |
T1532I |
possibly damaging |
Het |
Abtb2 |
A |
T |
2: 103,702,424 (GRCm38) |
|
probably null |
Het |
Agk |
A |
T |
6: 40,329,517 (GRCm38) |
T7S |
possibly damaging |
Het |
Akap9 |
C |
A |
5: 4,032,696 (GRCm38) |
T1940K |
probably damaging |
Het |
Armc4 |
T |
C |
18: 7,222,635 (GRCm38) |
K545E |
probably damaging |
Het |
BC024978 |
G |
A |
7: 27,201,123 (GRCm38) |
A176T |
probably damaging |
Het |
Ccdc8 |
A |
G |
7: 16,996,031 (GRCm38) |
T482A |
unknown |
Het |
Cd2ap |
G |
A |
17: 42,830,013 (GRCm38) |
R212* |
probably null |
Het |
Cenpt |
G |
A |
8: 105,849,904 (GRCm38) |
Q45* |
probably null |
Het |
Cnga1 |
T |
C |
5: 72,605,432 (GRCm38) |
I246M |
probably benign |
Het |
Cnot7 |
A |
G |
8: 40,507,545 (GRCm38) |
I74T |
probably damaging |
Het |
Cog6 |
T |
C |
3: 53,002,507 (GRCm38) |
S275G |
probably benign |
Het |
Csmd2 |
C |
A |
4: 128,528,262 (GRCm38) |
D2797E |
|
Het |
Ddx24 |
A |
G |
12: 103,419,450 (GRCm38) |
M298T |
possibly damaging |
Het |
Eif2b3 |
T |
A |
4: 117,052,822 (GRCm38) |
S185T |
probably benign |
Het |
Ergic2 |
T |
A |
6: 148,188,112 (GRCm38) |
Y249F |
probably damaging |
Het |
Exoc1 |
T |
A |
5: 76,542,159 (GRCm38) |
M182K |
probably damaging |
Het |
Fhdc1 |
T |
C |
3: 84,444,540 (GRCm38) |
E1126G |
probably damaging |
Het |
Gabrr2 |
T |
A |
4: 33,095,284 (GRCm38) |
M391K |
probably benign |
Het |
Gap43 |
T |
C |
16: 42,292,252 (GRCm38) |
K49E |
probably damaging |
Het |
Gata4 |
T |
A |
14: 63,203,742 (GRCm38) |
T276S |
probably damaging |
Het |
Gca |
C |
T |
2: 62,689,976 (GRCm38) |
P160L |
probably benign |
Het |
Ghdc |
C |
T |
11: 100,768,116 (GRCm38) |
V397I |
possibly damaging |
Het |
Gm3409 |
T |
A |
5: 146,539,547 (GRCm38) |
D169E |
probably benign |
Het |
Gtf3c3 |
G |
A |
1: 54,417,708 (GRCm38) |
P511L |
probably benign |
Het |
Hal |
T |
C |
10: 93,492,561 (GRCm38) |
V233A |
probably benign |
Het |
Ighv1-4 |
T |
C |
12: 114,487,288 (GRCm38) |
I67V |
probably benign |
Het |
Itgb8 |
T |
C |
12: 119,202,461 (GRCm38) |
N112D |
probably benign |
Het |
Klhl38 |
G |
A |
15: 58,322,980 (GRCm38) |
R118W |
probably damaging |
Het |
Krtap26-1 |
T |
C |
16: 88,647,244 (GRCm38) |
Y163C |
possibly damaging |
Het |
Kyat1 |
T |
C |
2: 30,191,995 (GRCm38) |
D44G |
probably benign |
Het |
Mob1a |
G |
A |
6: 83,338,449 (GRCm38) |
|
probably null |
Het |
Mst1r |
G |
T |
9: 107,914,790 (GRCm38) |
A842S |
possibly damaging |
Het |
Nhsl1 |
A |
G |
10: 18,527,671 (GRCm38) |
|
probably null |
Het |
Nos1 |
A |
T |
5: 117,867,905 (GRCm38) |
D230V |
possibly damaging |
Het |
Nppb |
T |
C |
4: 147,986,323 (GRCm38) |
S52P |
probably benign |
Het |
Olfml3 |
T |
C |
3: 103,735,860 (GRCm38) |
K402E |
probably damaging |
Het |
Olfr1496 |
G |
A |
19: 13,781,324 (GRCm38) |
W235* |
probably null |
Het |
Pcdha3 |
G |
A |
18: 36,946,924 (GRCm38) |
E240K |
possibly damaging |
Het |
Podxl |
G |
T |
6: 31,524,436 (GRCm38) |
P395T |
probably damaging |
Het |
Prr5l |
T |
A |
2: 101,717,286 (GRCm38) |
D298V |
probably damaging |
Het |
Rad9b |
A |
G |
5: 122,352,614 (GRCm38) |
V13A |
possibly damaging |
Het |
Ralgps1 |
T |
C |
2: 33,157,873 (GRCm38) |
K365R |
probably benign |
Het |
Reep1 |
A |
T |
6: 71,761,389 (GRCm38) |
I44L |
probably benign |
Het |
Ripor2 |
T |
C |
13: 24,725,001 (GRCm38) |
I1034T |
possibly damaging |
Het |
Rtn4ip1 |
T |
C |
10: 43,936,020 (GRCm38) |
Y338H |
probably damaging |
Het |
Shisa5 |
G |
T |
9: 109,054,884 (GRCm38) |
|
probably benign |
Het |
Snx24 |
G |
T |
18: 53,340,172 (GRCm38) |
V63F |
probably damaging |
Het |
Svep1 |
G |
A |
4: 58,046,587 (GRCm38) |
Q3515* |
probably null |
Het |
Tfap2a |
T |
C |
13: 40,721,308 (GRCm38) |
K276E |
probably damaging |
Het |
Tmem158 |
C |
A |
9: 123,260,301 (GRCm38) |
S82I |
probably damaging |
Het |
Tmem263 |
T |
A |
10: 85,114,397 (GRCm38) |
|
probably null |
Het |
Tmtc3 |
G |
T |
10: 100,447,474 (GRCm38) |
H740N |
not run |
Het |
Tnrc6a |
A |
C |
7: 123,170,913 (GRCm38) |
N642T |
probably benign |
Het |
Top3a |
A |
T |
11: 60,748,148 (GRCm38) |
F559I |
probably damaging |
Het |
Trak1 |
A |
G |
9: 121,451,863 (GRCm38) |
|
probably null |
Het |
Trpc4 |
T |
C |
3: 54,317,627 (GRCm38) |
I799T |
possibly damaging |
Het |
Ttc7 |
T |
C |
17: 87,346,542 (GRCm38) |
I549T |
possibly damaging |
Het |
Tysnd1 |
C |
A |
10: 61,696,549 (GRCm38) |
P327T |
possibly damaging |
Het |
Ulk4 |
T |
A |
9: 121,145,059 (GRCm38) |
D969V |
probably benign |
Het |
Vcan |
T |
A |
13: 89,705,266 (GRCm38) |
Y525F |
probably benign |
Het |
Vmn1r204 |
G |
A |
13: 22,556,805 (GRCm38) |
S202N |
probably damaging |
Het |
Vmn2r107 |
A |
G |
17: 20,345,616 (GRCm38) |
I64M |
probably benign |
Het |
Wrn |
A |
G |
8: 33,292,718 (GRCm38) |
F728S |
probably damaging |
Het |
Zfp280b |
C |
G |
10: 76,038,703 (GRCm38) |
Q139E |
probably damaging |
Het |
Zfp322a |
C |
T |
13: 23,357,144 (GRCm38) |
G143S |
probably benign |
Het |
Zfp322a |
C |
A |
13: 23,357,143 (GRCm38) |
G143V |
probably damaging |
Het |
Zfp418 |
T |
A |
7: 7,182,828 (GRCm38) |
C597S |
possibly damaging |
Het |
Zfp568 |
A |
G |
7: 30,017,244 (GRCm38) |
T190A |
probably benign |
Het |
Zfyve26 |
A |
T |
12: 79,282,984 (GRCm38) |
V476D |
probably benign |
Het |
|
Other mutations in Ptpro |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Ptpro
|
APN |
6 |
137,394,909 (GRCm38) |
critical splice donor site |
probably null |
|
IGL00844:Ptpro
|
APN |
6 |
137,414,239 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00983:Ptpro
|
APN |
6 |
137,418,248 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01073:Ptpro
|
APN |
6 |
137,377,088 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01832:Ptpro
|
APN |
6 |
137,393,668 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL02308:Ptpro
|
APN |
6 |
137,454,700 (GRCm38) |
missense |
probably benign |
0.37 |
IGL02387:Ptpro
|
APN |
6 |
137,410,980 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL02605:Ptpro
|
APN |
6 |
137,380,318 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02666:Ptpro
|
APN |
6 |
137,378,059 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL03275:Ptpro
|
APN |
6 |
137,450,006 (GRCm38) |
missense |
probably damaging |
1.00 |
Brau
|
UTSW |
6 |
137,454,598 (GRCm38) |
missense |
probably damaging |
1.00 |
court
|
UTSW |
6 |
137,393,675 (GRCm38) |
nonsense |
probably null |
|
Hoff
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
Jester
|
UTSW |
6 |
137,449,917 (GRCm38) |
missense |
probably damaging |
1.00 |
mann
|
UTSW |
6 |
137,411,116 (GRCm38) |
splice site |
probably null |
|
R0017:Ptpro
|
UTSW |
6 |
137,416,827 (GRCm38) |
missense |
probably benign |
0.03 |
R0017:Ptpro
|
UTSW |
6 |
137,416,827 (GRCm38) |
missense |
probably benign |
0.03 |
R0020:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0022:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0023:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0024:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0094:Ptpro
|
UTSW |
6 |
137,386,352 (GRCm38) |
missense |
probably benign |
0.08 |
R0094:Ptpro
|
UTSW |
6 |
137,386,352 (GRCm38) |
missense |
probably benign |
0.08 |
R0103:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0106:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0316:Ptpro
|
UTSW |
6 |
137,376,989 (GRCm38) |
missense |
possibly damaging |
0.81 |
R0427:Ptpro
|
UTSW |
6 |
137,368,296 (GRCm38) |
missense |
possibly damaging |
0.81 |
R0456:Ptpro
|
UTSW |
6 |
137,414,230 (GRCm38) |
missense |
probably benign |
0.04 |
R0536:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0537:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0552:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0555:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0664:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0708:Ptpro
|
UTSW |
6 |
137,386,253 (GRCm38) |
missense |
probably benign |
0.26 |
R0730:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0735:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0738:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0786:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0811:Ptpro
|
UTSW |
6 |
137,368,079 (GRCm38) |
missense |
probably benign |
0.00 |
R0812:Ptpro
|
UTSW |
6 |
137,368,079 (GRCm38) |
missense |
probably benign |
0.00 |
R0881:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0973:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1145:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1145:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1146:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1146:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1147:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1147:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1259:Ptpro
|
UTSW |
6 |
137,392,741 (GRCm38) |
missense |
probably damaging |
0.98 |
R1340:Ptpro
|
UTSW |
6 |
137,441,081 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1381:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1382:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1385:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1396:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1401:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1416:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1422:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1448:Ptpro
|
UTSW |
6 |
137,441,116 (GRCm38) |
missense |
probably damaging |
1.00 |
R1513:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1518:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1526:Ptpro
|
UTSW |
6 |
137,461,726 (GRCm38) |
missense |
probably damaging |
1.00 |
R1540:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1571:Ptpro
|
UTSW |
6 |
137,378,130 (GRCm38) |
missense |
probably benign |
|
R1573:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1587:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1588:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1649:Ptpro
|
UTSW |
6 |
137,444,017 (GRCm38) |
nonsense |
probably null |
|
R1700:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1701:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1745:Ptpro
|
UTSW |
6 |
137,400,645 (GRCm38) |
missense |
probably benign |
0.03 |
R1772:Ptpro
|
UTSW |
6 |
137,430,743 (GRCm38) |
missense |
probably damaging |
1.00 |
R1911:Ptpro
|
UTSW |
6 |
137,400,619 (GRCm38) |
splice site |
probably benign |
|
R1958:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1967:Ptpro
|
UTSW |
6 |
137,416,865 (GRCm38) |
missense |
probably benign |
0.38 |
R2025:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R2026:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R2040:Ptpro
|
UTSW |
6 |
137,386,164 (GRCm38) |
splice site |
probably benign |
|
R2115:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R2117:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R2130:Ptpro
|
UTSW |
6 |
137,411,116 (GRCm38) |
splice site |
probably null |
|
R2161:Ptpro
|
UTSW |
6 |
137,449,887 (GRCm38) |
missense |
probably benign |
0.01 |
R2431:Ptpro
|
UTSW |
6 |
137,443,585 (GRCm38) |
nonsense |
probably null |
|
R2915:Ptpro
|
UTSW |
6 |
137,414,241 (GRCm38) |
start gained |
probably benign |
|
R2988:Ptpro
|
UTSW |
6 |
137,443,599 (GRCm38) |
nonsense |
probably null |
|
R3772:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R3773:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R3795:Ptpro
|
UTSW |
6 |
137,380,309 (GRCm38) |
missense |
probably benign |
|
R3885:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R3886:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R3887:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R3888:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R3893:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R4032:Ptpro
|
UTSW |
6 |
137,461,742 (GRCm38) |
missense |
probably damaging |
1.00 |
R4133:Ptpro
|
UTSW |
6 |
137,420,372 (GRCm38) |
missense |
probably damaging |
1.00 |
R4377:Ptpro
|
UTSW |
6 |
137,380,266 (GRCm38) |
missense |
probably benign |
0.26 |
R4455:Ptpro
|
UTSW |
6 |
137,393,659 (GRCm38) |
missense |
probably damaging |
1.00 |
R4613:Ptpro
|
UTSW |
6 |
137,416,836 (GRCm38) |
nonsense |
probably null |
|
R4827:Ptpro
|
UTSW |
6 |
137,442,710 (GRCm38) |
missense |
probably damaging |
1.00 |
R4863:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R4870:Ptpro
|
UTSW |
6 |
137,377,132 (GRCm38) |
missense |
probably damaging |
0.96 |
R4910:Ptpro
|
UTSW |
6 |
137,368,338 (GRCm38) |
missense |
probably damaging |
0.99 |
R4932:Ptpro
|
UTSW |
6 |
137,411,105 (GRCm38) |
nonsense |
probably null |
|
R4941:Ptpro
|
UTSW |
6 |
137,392,765 (GRCm38) |
missense |
probably damaging |
1.00 |
R4989:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R5009:Ptpro
|
UTSW |
6 |
137,377,132 (GRCm38) |
missense |
probably damaging |
0.96 |
R5032:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R5033:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R5162:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R5393:Ptpro
|
UTSW |
6 |
137,380,224 (GRCm38) |
missense |
probably benign |
0.04 |
R5423:Ptpro
|
UTSW |
6 |
137,442,707 (GRCm38) |
missense |
probably damaging |
1.00 |
R5782:Ptpro
|
UTSW |
6 |
137,399,498 (GRCm38) |
missense |
possibly damaging |
0.80 |
R6103:Ptpro
|
UTSW |
6 |
137,400,706 (GRCm38) |
missense |
possibly damaging |
0.76 |
R6239:Ptpro
|
UTSW |
6 |
137,380,608 (GRCm38) |
missense |
probably benign |
0.28 |
R6488:Ptpro
|
UTSW |
6 |
137,393,675 (GRCm38) |
nonsense |
probably null |
|
R6494:Ptpro
|
UTSW |
6 |
137,382,642 (GRCm38) |
missense |
probably benign |
0.20 |
R6746:Ptpro
|
UTSW |
6 |
137,394,823 (GRCm38) |
missense |
probably damaging |
1.00 |
R6763:Ptpro
|
UTSW |
6 |
137,418,281 (GRCm38) |
splice site |
probably null |
|
R6888:Ptpro
|
UTSW |
6 |
137,380,200 (GRCm38) |
missense |
probably benign |
0.30 |
R6983:Ptpro
|
UTSW |
6 |
137,449,917 (GRCm38) |
missense |
probably damaging |
1.00 |
R7019:Ptpro
|
UTSW |
6 |
137,380,478 (GRCm38) |
missense |
probably benign |
|
R7218:Ptpro
|
UTSW |
6 |
137,454,598 (GRCm38) |
missense |
probably damaging |
1.00 |
R7236:Ptpro
|
UTSW |
6 |
137,368,337 (GRCm38) |
missense |
probably damaging |
1.00 |
R7381:Ptpro
|
UTSW |
6 |
137,399,561 (GRCm38) |
missense |
possibly damaging |
0.93 |
R7493:Ptpro
|
UTSW |
6 |
137,382,649 (GRCm38) |
missense |
probably benign |
0.01 |
R7733:Ptpro
|
UTSW |
6 |
137,414,286 (GRCm38) |
nonsense |
probably null |
|
R7793:Ptpro
|
UTSW |
6 |
137,416,820 (GRCm38) |
missense |
probably damaging |
0.99 |
R7804:Ptpro
|
UTSW |
6 |
137,399,601 (GRCm38) |
splice site |
probably null |
|
R7833:Ptpro
|
UTSW |
6 |
137,416,863 (GRCm38) |
nonsense |
probably null |
|
R7859:Ptpro
|
UTSW |
6 |
137,392,807 (GRCm38) |
critical splice donor site |
probably null |
|
R7873:Ptpro
|
UTSW |
6 |
137,430,739 (GRCm38) |
missense |
probably benign |
0.44 |
R8042:Ptpro
|
UTSW |
6 |
137,416,883 (GRCm38) |
missense |
possibly damaging |
0.71 |
R8859:Ptpro
|
UTSW |
6 |
137,426,784 (GRCm38) |
nonsense |
probably null |
|
R8979:Ptpro
|
UTSW |
6 |
137,368,142 (GRCm38) |
missense |
probably benign |
|
R9138:Ptpro
|
UTSW |
6 |
137,411,115 (GRCm38) |
critical splice donor site |
probably null |
|
R9309:Ptpro
|
UTSW |
6 |
137,454,658 (GRCm38) |
missense |
probably damaging |
1.00 |
R9420:Ptpro
|
UTSW |
6 |
137,443,935 (GRCm38) |
missense |
probably benign |
0.08 |
R9612:Ptpro
|
UTSW |
6 |
137,414,320 (GRCm38) |
missense |
probably benign |
0.31 |
R9625:Ptpro
|
UTSW |
6 |
137,394,875 (GRCm38) |
missense |
probably damaging |
1.00 |
R9697:Ptpro
|
UTSW |
6 |
137,386,290 (GRCm38) |
missense |
probably damaging |
1.00 |
R9715:Ptpro
|
UTSW |
6 |
137,368,110 (GRCm38) |
missense |
probably damaging |
0.96 |
Z1177:Ptpro
|
UTSW |
6 |
137,378,140 (GRCm38) |
missense |
probably damaging |
1.00 |
|