Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022A10Rik |
T |
A |
7: 27,279,871 (GRCm39) |
V278D |
probably damaging |
Het |
Akap12 |
G |
T |
10: 4,307,122 (GRCm39) |
E1311* |
probably null |
Het |
Ankdd1a |
T |
A |
9: 65,415,957 (GRCm39) |
D186V |
probably benign |
Het |
Birc6 |
A |
G |
17: 74,869,090 (GRCm39) |
E346G |
probably damaging |
Het |
Brd10 |
A |
G |
19: 29,696,508 (GRCm39) |
L995S |
possibly damaging |
Het |
Ccr7 |
A |
C |
11: 99,036,130 (GRCm39) |
V264G |
probably damaging |
Het |
Col7a1 |
T |
C |
9: 108,812,987 (GRCm39) |
|
probably null |
Het |
Coq8a |
T |
C |
1: 180,006,633 (GRCm39) |
T132A |
probably benign |
Het |
Cplane1 |
A |
G |
15: 8,281,690 (GRCm39) |
E2843G |
unknown |
Het |
Cyp2b10 |
G |
A |
7: 25,616,780 (GRCm39) |
S407N |
probably benign |
Het |
Ddi2 |
A |
G |
4: 141,412,561 (GRCm39) |
V117A |
probably benign |
Het |
Ddx42 |
G |
A |
11: 106,129,970 (GRCm39) |
V421I |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,601,896 (GRCm39) |
L285* |
probably null |
Het |
Dip2c |
C |
T |
13: 9,684,868 (GRCm39) |
S1232F |
probably damaging |
Het |
Dner |
T |
A |
1: 84,454,123 (GRCm39) |
R402* |
probably null |
Het |
Dpysl3 |
A |
T |
18: 43,486,956 (GRCm39) |
I317N |
probably damaging |
Het |
Dusp23 |
T |
A |
1: 172,459,224 (GRCm39) |
Y146F |
probably benign |
Het |
Eef1a2 |
C |
A |
2: 180,790,421 (GRCm39) |
V412L |
possibly damaging |
Het |
Epha7 |
C |
T |
4: 28,821,489 (GRCm39) |
T218I |
probably damaging |
Het |
Gigyf2 |
T |
A |
1: 87,334,858 (GRCm39) |
C284S |
probably damaging |
Het |
Golm1 |
ACTTCTTCT |
ACTTCT |
13: 59,797,390 (GRCm39) |
|
probably benign |
Het |
Hao2 |
T |
A |
3: 98,784,068 (GRCm39) |
E327V |
probably damaging |
Het |
Hdhd5 |
A |
G |
6: 120,487,130 (GRCm39) |
V409A |
probably damaging |
Het |
Kif9 |
T |
C |
9: 110,323,690 (GRCm39) |
Y236H |
probably damaging |
Het |
Kri1 |
T |
C |
9: 21,199,050 (GRCm39) |
|
probably benign |
Het |
Lig4 |
A |
T |
8: 10,021,098 (GRCm39) |
V894E |
probably damaging |
Het |
Lrriq1 |
T |
C |
10: 103,023,319 (GRCm39) |
N982S |
probably damaging |
Het |
Mapk8 |
T |
C |
14: 33,132,841 (GRCm39) |
I32V |
possibly damaging |
Het |
Mstn |
T |
C |
1: 53,101,100 (GRCm39) |
I59T |
probably benign |
Het |
Mtrf1l |
T |
C |
10: 5,763,384 (GRCm39) |
E315G |
probably damaging |
Het |
Notch4 |
G |
T |
17: 34,803,774 (GRCm39) |
E1515* |
probably null |
Het |
Npw |
A |
C |
17: 24,877,029 (GRCm39) |
V124G |
probably benign |
Het |
Nxph3 |
A |
G |
11: 95,402,244 (GRCm39) |
S57P |
probably damaging |
Het |
Opn4 |
A |
T |
14: 34,315,864 (GRCm39) |
L390M |
probably benign |
Het |
Or12e10 |
G |
A |
2: 87,640,787 (GRCm39) |
D208N |
possibly damaging |
Het |
Or52e4 |
T |
C |
7: 104,705,771 (GRCm39) |
I106T |
probably damaging |
Het |
Or5b95 |
G |
T |
19: 12,658,112 (GRCm39) |
L213F |
probably benign |
Het |
Or5g23 |
T |
C |
2: 85,438,592 (GRCm39) |
I221V |
possibly damaging |
Het |
Or5p68 |
T |
A |
7: 107,945,295 (GRCm39) |
N298Y |
possibly damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Pla2g2e |
G |
A |
4: 138,607,986 (GRCm39) |
C62Y |
probably damaging |
Het |
Plcb4 |
G |
A |
2: 135,752,114 (GRCm39) |
V107M |
probably damaging |
Het |
Pramel33 |
T |
A |
5: 93,632,233 (GRCm39) |
N107I |
probably damaging |
Het |
Prorsd1 |
A |
C |
11: 29,464,486 (GRCm39) |
|
probably benign |
Het |
Prox2 |
A |
G |
12: 85,134,165 (GRCm39) |
L587P |
probably benign |
Het |
Prr22 |
A |
G |
17: 57,078,345 (GRCm39) |
D166G |
possibly damaging |
Het |
Ptprz1 |
G |
A |
6: 23,002,686 (GRCm39) |
R1592Q |
probably benign |
Het |
Rarg |
C |
G |
15: 102,150,350 (GRCm39) |
R74P |
probably damaging |
Het |
Rcan1 |
A |
G |
16: 92,194,251 (GRCm39) |
V54A |
probably benign |
Het |
Rmdn2 |
A |
G |
17: 79,928,739 (GRCm39) |
|
probably benign |
Het |
Sec16a |
G |
A |
2: 26,320,498 (GRCm39) |
R1361C |
probably damaging |
Het |
Serpina1a |
T |
C |
12: 103,820,092 (GRCm39) |
T385A |
probably benign |
Het |
Slc44a3 |
T |
C |
3: 121,325,814 (GRCm39) |
Y12C |
probably benign |
Het |
Smg1 |
C |
A |
7: 117,767,091 (GRCm39) |
|
probably benign |
Het |
Spock3 |
A |
G |
8: 63,808,415 (GRCm39) |
*437W |
probably null |
Het |
Sugct |
T |
A |
13: 17,728,965 (GRCm39) |
Q220H |
probably benign |
Het |
Tesk1 |
A |
G |
4: 43,447,006 (GRCm39) |
T465A |
probably benign |
Het |
Tnks |
C |
A |
8: 35,301,647 (GRCm39) |
R1274I |
probably damaging |
Het |
Trp53bp1 |
C |
T |
2: 121,038,521 (GRCm39) |
R1439H |
probably damaging |
Het |
Vmn1r16 |
G |
T |
6: 57,299,869 (GRCm39) |
S251* |
probably null |
Het |
Vmn2r15 |
T |
A |
5: 109,441,180 (GRCm39) |
Q226L |
probably damaging |
Het |
Vmn2r67 |
T |
G |
7: 84,804,953 (GRCm39) |
Y53S |
possibly damaging |
Het |
Vmn2r99 |
A |
G |
17: 19,598,372 (GRCm39) |
N132S |
probably benign |
Het |
Wdr73 |
T |
G |
7: 80,541,604 (GRCm39) |
T313P |
probably benign |
Het |
Zfp65 |
C |
T |
13: 67,856,640 (GRCm39) |
R213Q |
probably damaging |
Het |
|
Other mutations in Mast4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00703:Mast4
|
APN |
13 |
102,907,275 (GRCm39) |
nonsense |
probably null |
|
IGL00933:Mast4
|
APN |
13 |
102,871,874 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01113:Mast4
|
APN |
13 |
102,910,744 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01461:Mast4
|
APN |
13 |
102,890,576 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01569:Mast4
|
APN |
13 |
102,897,523 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01697:Mast4
|
APN |
13 |
102,904,401 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01725:Mast4
|
APN |
13 |
102,887,020 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01734:Mast4
|
APN |
13 |
102,874,123 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01738:Mast4
|
APN |
13 |
102,873,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01739:Mast4
|
APN |
13 |
102,910,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02299:Mast4
|
APN |
13 |
102,874,482 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02479:Mast4
|
APN |
13 |
102,878,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02485:Mast4
|
APN |
13 |
102,872,004 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02528:Mast4
|
APN |
13 |
102,990,331 (GRCm39) |
makesense |
probably null |
|
IGL02850:Mast4
|
APN |
13 |
102,890,740 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02900:Mast4
|
APN |
13 |
102,872,184 (GRCm39) |
missense |
probably benign |
|
IGL03064:Mast4
|
APN |
13 |
102,897,472 (GRCm39) |
nonsense |
probably null |
|
IGL03124:Mast4
|
APN |
13 |
102,874,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03146:Mast4
|
APN |
13 |
102,874,163 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03221:Mast4
|
APN |
13 |
102,890,764 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03284:Mast4
|
APN |
13 |
102,887,905 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03406:Mast4
|
APN |
13 |
102,873,615 (GRCm39) |
missense |
possibly damaging |
0.46 |
buck
|
UTSW |
13 |
102,897,801 (GRCm39) |
critical splice donor site |
probably null |
|
doe
|
UTSW |
13 |
103,042,185 (GRCm39) |
missense |
possibly damaging |
0.85 |
skinnybones
|
UTSW |
13 |
102,941,149 (GRCm39) |
critical splice donor site |
probably null |
|
BB010:Mast4
|
UTSW |
13 |
102,909,071 (GRCm39) |
missense |
probably damaging |
0.99 |
BB020:Mast4
|
UTSW |
13 |
102,909,071 (GRCm39) |
missense |
probably damaging |
0.99 |
FR4304:Mast4
|
UTSW |
13 |
102,871,370 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4340:Mast4
|
UTSW |
13 |
102,872,825 (GRCm39) |
small insertion |
probably benign |
|
FR4340:Mast4
|
UTSW |
13 |
102,871,365 (GRCm39) |
frame shift |
probably null |
|
FR4548:Mast4
|
UTSW |
13 |
102,872,826 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Mast4
|
UTSW |
13 |
102,875,755 (GRCm39) |
frame shift |
probably null |
|
FR4976:Mast4
|
UTSW |
13 |
102,872,820 (GRCm39) |
small insertion |
probably benign |
|
NA:Mast4
|
UTSW |
13 |
102,878,565 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4466001:Mast4
|
UTSW |
13 |
102,941,226 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4469001:Mast4
|
UTSW |
13 |
102,941,226 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4472001:Mast4
|
UTSW |
13 |
102,941,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R0009:Mast4
|
UTSW |
13 |
102,878,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Mast4
|
UTSW |
13 |
103,470,723 (GRCm39) |
start gained |
probably benign |
|
R0242:Mast4
|
UTSW |
13 |
102,990,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R0310:Mast4
|
UTSW |
13 |
102,890,669 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0395:Mast4
|
UTSW |
13 |
102,871,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Mast4
|
UTSW |
13 |
102,888,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Mast4
|
UTSW |
13 |
102,895,252 (GRCm39) |
splice site |
probably benign |
|
R0744:Mast4
|
UTSW |
13 |
102,873,895 (GRCm39) |
missense |
probably damaging |
0.98 |
R0883:Mast4
|
UTSW |
13 |
102,990,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R0905:Mast4
|
UTSW |
13 |
102,907,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R1023:Mast4
|
UTSW |
13 |
102,872,004 (GRCm39) |
missense |
probably benign |
0.02 |
R1281:Mast4
|
UTSW |
13 |
102,887,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R1376:Mast4
|
UTSW |
13 |
102,872,916 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1376:Mast4
|
UTSW |
13 |
102,872,916 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1473:Mast4
|
UTSW |
13 |
102,909,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Mast4
|
UTSW |
13 |
102,873,431 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1575:Mast4
|
UTSW |
13 |
102,875,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Mast4
|
UTSW |
13 |
102,930,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Mast4
|
UTSW |
13 |
102,887,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Mast4
|
UTSW |
13 |
102,875,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R2062:Mast4
|
UTSW |
13 |
102,895,601 (GRCm39) |
missense |
probably benign |
0.18 |
R2106:Mast4
|
UTSW |
13 |
102,887,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R2118:Mast4
|
UTSW |
13 |
102,890,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R2143:Mast4
|
UTSW |
13 |
102,871,983 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2256:Mast4
|
UTSW |
13 |
102,872,259 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2261:Mast4
|
UTSW |
13 |
102,934,715 (GRCm39) |
splice site |
probably benign |
|
R2370:Mast4
|
UTSW |
13 |
102,910,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Mast4
|
UTSW |
13 |
102,875,147 (GRCm39) |
missense |
probably damaging |
0.96 |
R2509:Mast4
|
UTSW |
13 |
102,990,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R2842:Mast4
|
UTSW |
13 |
102,872,939 (GRCm39) |
missense |
probably benign |
0.01 |
R3087:Mast4
|
UTSW |
13 |
102,990,434 (GRCm39) |
splice site |
probably benign |
|
R3434:Mast4
|
UTSW |
13 |
102,923,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R3435:Mast4
|
UTSW |
13 |
102,923,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R3763:Mast4
|
UTSW |
13 |
102,923,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Mast4
|
UTSW |
13 |
102,875,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R3829:Mast4
|
UTSW |
13 |
102,875,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R3830:Mast4
|
UTSW |
13 |
102,875,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R3913:Mast4
|
UTSW |
13 |
102,895,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R3914:Mast4
|
UTSW |
13 |
102,875,829 (GRCm39) |
nonsense |
probably null |
|
R4021:Mast4
|
UTSW |
13 |
102,875,829 (GRCm39) |
nonsense |
probably null |
|
R4022:Mast4
|
UTSW |
13 |
102,990,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R4022:Mast4
|
UTSW |
13 |
102,875,829 (GRCm39) |
nonsense |
probably null |
|
R4210:Mast4
|
UTSW |
13 |
102,875,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R4342:Mast4
|
UTSW |
13 |
102,910,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R4580:Mast4
|
UTSW |
13 |
102,873,766 (GRCm39) |
nonsense |
probably null |
|
R4627:Mast4
|
UTSW |
13 |
103,470,529 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4711:Mast4
|
UTSW |
13 |
103,470,627 (GRCm39) |
missense |
probably benign |
0.01 |
R4732:Mast4
|
UTSW |
13 |
102,909,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R4733:Mast4
|
UTSW |
13 |
102,909,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R4833:Mast4
|
UTSW |
13 |
102,910,692 (GRCm39) |
critical splice donor site |
probably null |
|
R4995:Mast4
|
UTSW |
13 |
103,042,262 (GRCm39) |
intron |
probably benign |
|
R5059:Mast4
|
UTSW |
13 |
102,887,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R5073:Mast4
|
UTSW |
13 |
102,875,391 (GRCm39) |
nonsense |
probably null |
|
R5101:Mast4
|
UTSW |
13 |
102,872,864 (GRCm39) |
missense |
probably benign |
0.01 |
R5526:Mast4
|
UTSW |
13 |
102,890,723 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5599:Mast4
|
UTSW |
13 |
102,873,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R5673:Mast4
|
UTSW |
13 |
102,930,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R5694:Mast4
|
UTSW |
13 |
102,910,701 (GRCm39) |
nonsense |
probably null |
|
R5906:Mast4
|
UTSW |
13 |
102,872,252 (GRCm39) |
missense |
probably benign |
0.31 |
R5908:Mast4
|
UTSW |
13 |
102,874,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R5947:Mast4
|
UTSW |
13 |
102,872,148 (GRCm39) |
missense |
probably benign |
|
R5987:Mast4
|
UTSW |
13 |
102,895,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R6143:Mast4
|
UTSW |
13 |
102,990,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R6154:Mast4
|
UTSW |
13 |
102,923,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R6169:Mast4
|
UTSW |
13 |
102,923,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R6239:Mast4
|
UTSW |
13 |
102,872,717 (GRCm39) |
missense |
probably benign |
0.01 |
R6327:Mast4
|
UTSW |
13 |
102,897,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R6356:Mast4
|
UTSW |
13 |
102,872,493 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6432:Mast4
|
UTSW |
13 |
103,042,185 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6522:Mast4
|
UTSW |
13 |
102,897,801 (GRCm39) |
critical splice donor site |
probably null |
|
R6667:Mast4
|
UTSW |
13 |
102,874,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R6941:Mast4
|
UTSW |
13 |
102,941,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Mast4
|
UTSW |
13 |
102,941,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Mast4
|
UTSW |
13 |
102,934,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R6970:Mast4
|
UTSW |
13 |
102,941,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6980:Mast4
|
UTSW |
13 |
102,941,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6992:Mast4
|
UTSW |
13 |
102,941,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6993:Mast4
|
UTSW |
13 |
102,872,482 (GRCm39) |
missense |
probably benign |
0.28 |
R6993:Mast4
|
UTSW |
13 |
102,941,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R7083:Mast4
|
UTSW |
13 |
102,874,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R7241:Mast4
|
UTSW |
13 |
103,470,508 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7242:Mast4
|
UTSW |
13 |
102,874,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R7246:Mast4
|
UTSW |
13 |
102,930,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R7332:Mast4
|
UTSW |
13 |
102,887,932 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7453:Mast4
|
UTSW |
13 |
102,941,149 (GRCm39) |
critical splice donor site |
probably null |
|
R7514:Mast4
|
UTSW |
13 |
102,923,934 (GRCm39) |
nonsense |
probably null |
|
R7697:Mast4
|
UTSW |
13 |
102,875,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R7820:Mast4
|
UTSW |
13 |
102,890,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R7874:Mast4
|
UTSW |
13 |
102,875,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R7933:Mast4
|
UTSW |
13 |
102,909,071 (GRCm39) |
missense |
probably damaging |
0.99 |
R8042:Mast4
|
UTSW |
13 |
102,917,753 (GRCm39) |
missense |
probably damaging |
0.96 |
R8060:Mast4
|
UTSW |
13 |
102,874,184 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8172:Mast4
|
UTSW |
13 |
103,089,633 (GRCm39) |
critical splice donor site |
probably null |
|
R8206:Mast4
|
UTSW |
13 |
102,872,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R8248:Mast4
|
UTSW |
13 |
102,875,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R8283:Mast4
|
UTSW |
13 |
102,895,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R8346:Mast4
|
UTSW |
13 |
102,887,986 (GRCm39) |
missense |
probably damaging |
0.99 |
R8434:Mast4
|
UTSW |
13 |
102,897,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R8796:Mast4
|
UTSW |
13 |
102,919,899 (GRCm39) |
missense |
probably benign |
0.07 |
R8850:Mast4
|
UTSW |
13 |
102,895,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R9012:Mast4
|
UTSW |
13 |
102,934,606 (GRCm39) |
missense |
probably benign |
0.05 |
R9375:Mast4
|
UTSW |
13 |
102,917,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R9389:Mast4
|
UTSW |
13 |
103,470,438 (GRCm39) |
missense |
probably benign |
0.00 |
R9404:Mast4
|
UTSW |
13 |
102,887,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R9520:Mast4
|
UTSW |
13 |
102,925,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R9525:Mast4
|
UTSW |
13 |
102,872,944 (GRCm39) |
missense |
probably benign |
0.00 |
R9526:Mast4
|
UTSW |
13 |
102,873,593 (GRCm39) |
missense |
probably benign |
0.00 |
R9709:Mast4
|
UTSW |
13 |
102,910,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R9790:Mast4
|
UTSW |
13 |
102,890,705 (GRCm39) |
missense |
probably benign |
0.01 |
R9791:Mast4
|
UTSW |
13 |
102,890,705 (GRCm39) |
missense |
probably benign |
0.01 |
RF005:Mast4
|
UTSW |
13 |
102,872,815 (GRCm39) |
small insertion |
probably benign |
|
RF015:Mast4
|
UTSW |
13 |
102,875,755 (GRCm39) |
frame shift |
probably null |
|
RF019:Mast4
|
UTSW |
13 |
102,872,815 (GRCm39) |
small insertion |
probably benign |
|
RF037:Mast4
|
UTSW |
13 |
102,875,749 (GRCm39) |
small deletion |
probably benign |
|
RF039:Mast4
|
UTSW |
13 |
102,875,749 (GRCm39) |
small deletion |
probably benign |
|
RF040:Mast4
|
UTSW |
13 |
102,875,749 (GRCm39) |
small deletion |
probably benign |
|
Z1088:Mast4
|
UTSW |
13 |
102,875,027 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mast4
|
UTSW |
13 |
102,874,968 (GRCm39) |
missense |
probably damaging |
1.00 |
|