Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam34 |
T |
C |
8: 44,105,045 (GRCm39) |
E200G |
probably benign |
Het |
Ankfy1 |
C |
T |
11: 72,645,281 (GRCm39) |
Q787* |
probably null |
Het |
Birc6 |
T |
A |
17: 74,855,815 (GRCm39) |
H208Q |
probably damaging |
Het |
Brsk2 |
T |
A |
7: 141,539,157 (GRCm39) |
|
probably null |
Het |
Cabp5 |
T |
A |
7: 13,132,263 (GRCm39) |
F11I |
possibly damaging |
Het |
Ccdc88a |
T |
C |
11: 29,435,964 (GRCm39) |
Y1296H |
probably damaging |
Het |
Ccdc88b |
A |
G |
19: 6,826,454 (GRCm39) |
V1087A |
probably benign |
Het |
Cct3 |
C |
T |
3: 88,228,442 (GRCm39) |
T508I |
probably damaging |
Het |
Ceacam9 |
T |
A |
7: 16,457,658 (GRCm39) |
M57K |
possibly damaging |
Het |
Ces1f |
T |
C |
8: 93,983,546 (GRCm39) |
E487G |
probably damaging |
Het |
Chd5 |
A |
G |
4: 152,443,032 (GRCm39) |
K278E |
probably damaging |
Het |
Cntnap3 |
T |
A |
13: 64,941,122 (GRCm39) |
H286L |
possibly damaging |
Het |
Dnai7 |
T |
G |
6: 145,140,312 (GRCm39) |
D163A |
probably benign |
Het |
Efr3a |
G |
T |
15: 65,659,022 (GRCm39) |
|
probably benign |
Het |
Fastkd2 |
T |
A |
1: 63,770,851 (GRCm39) |
I69N |
possibly damaging |
Het |
Flg2 |
T |
C |
3: 93,107,548 (GRCm39) |
I11T |
possibly damaging |
Het |
Folr2 |
T |
C |
7: 101,490,102 (GRCm39) |
M84V |
possibly damaging |
Het |
Galnt12 |
T |
C |
4: 47,113,786 (GRCm39) |
F360S |
probably damaging |
Het |
Galr2 |
T |
C |
11: 116,173,946 (GRCm39) |
V192A |
probably benign |
Het |
Gas6 |
A |
T |
8: 13,516,809 (GRCm39) |
I563N |
probably damaging |
Het |
Gbe1 |
T |
C |
16: 70,324,085 (GRCm39) |
F567L |
possibly damaging |
Het |
Gm12695 |
G |
A |
4: 96,619,608 (GRCm39) |
H423Y |
probably damaging |
Het |
Gm6902 |
T |
C |
7: 22,973,243 (GRCm39) |
T95A |
probably benign |
Het |
Gpr155 |
G |
T |
2: 73,212,296 (GRCm39) |
A109D |
probably damaging |
Het |
Hsdl1 |
T |
C |
8: 120,294,711 (GRCm39) |
D5G |
probably damaging |
Het |
Hyal1 |
C |
T |
9: 107,455,628 (GRCm39) |
P313S |
probably damaging |
Het |
Igfn1 |
G |
A |
1: 135,902,527 (GRCm39) |
T390M |
probably damaging |
Het |
Irx1 |
C |
A |
13: 72,107,917 (GRCm39) |
R255L |
probably benign |
Het |
Itga2 |
T |
A |
13: 115,002,715 (GRCm39) |
T592S |
probably benign |
Het |
Kit |
C |
A |
5: 75,769,982 (GRCm39) |
S131R |
probably benign |
Het |
Map1b |
T |
C |
13: 99,568,390 (GRCm39) |
T1444A |
unknown |
Het |
Mapk8ip1 |
C |
T |
2: 92,219,496 (GRCm39) |
E112K |
probably benign |
Het |
Marveld3 |
T |
C |
8: 110,681,266 (GRCm39) |
I210V |
probably damaging |
Het |
Masp1 |
T |
A |
16: 23,295,068 (GRCm39) |
I398L |
probably benign |
Het |
Mmrn1 |
T |
C |
6: 60,953,309 (GRCm39) |
I530T |
probably benign |
Het |
Mtss2 |
A |
G |
8: 111,452,833 (GRCm39) |
Y26C |
probably damaging |
Het |
Myo5a |
T |
A |
9: 75,067,747 (GRCm39) |
S600R |
probably benign |
Het |
Myo5a |
A |
G |
9: 75,076,292 (GRCm39) |
I836V |
probably benign |
Het |
Naaladl1 |
A |
G |
19: 6,159,694 (GRCm39) |
D375G |
probably damaging |
Het |
Napepld |
T |
A |
5: 21,888,263 (GRCm39) |
D62V |
possibly damaging |
Het |
Nedd9 |
A |
C |
13: 41,465,483 (GRCm39) |
I719S |
possibly damaging |
Het |
Nes |
T |
A |
3: 87,882,923 (GRCm39) |
M394K |
probably benign |
Het |
Nlrc5 |
A |
T |
8: 95,231,772 (GRCm39) |
Y1288F |
possibly damaging |
Het |
Nlrp14 |
T |
A |
7: 106,791,782 (GRCm39) |
C822* |
probably null |
Het |
Noa1 |
A |
C |
5: 77,457,071 (GRCm39) |
L278R |
probably damaging |
Het |
Nop16 |
A |
G |
13: 54,737,889 (GRCm39) |
|
probably benign |
Het |
Odr4 |
T |
C |
1: 150,268,659 (GRCm39) |
|
probably benign |
Het |
Or11h7 |
A |
T |
14: 50,891,450 (GRCm39) |
Y252F |
probably benign |
Het |
Or5b12 |
A |
G |
19: 12,897,229 (GRCm39) |
V148A |
probably benign |
Het |
Osbpl10 |
C |
T |
9: 114,890,962 (GRCm39) |
H117Y |
probably benign |
Het |
Oxct1 |
A |
T |
15: 4,077,058 (GRCm39) |
E130D |
probably benign |
Het |
Padi2 |
A |
G |
4: 140,676,575 (GRCm39) |
E571G |
possibly damaging |
Het |
Pcdhac2 |
G |
A |
18: 37,278,717 (GRCm39) |
V566M |
probably benign |
Het |
Pdcd11 |
G |
A |
19: 47,086,659 (GRCm39) |
E222K |
possibly damaging |
Het |
Pira12 |
C |
A |
7: 3,897,204 (GRCm39) |
C544F |
probably damaging |
Het |
Plekha2 |
A |
G |
8: 25,578,356 (GRCm39) |
|
probably null |
Het |
Pogz |
T |
C |
3: 94,777,418 (GRCm39) |
L366P |
probably benign |
Het |
Ppp4r3b |
A |
G |
11: 29,138,086 (GRCm39) |
I145V |
probably benign |
Het |
Prkcd |
A |
G |
14: 30,320,407 (GRCm39) |
|
probably null |
Het |
Ptprk |
T |
A |
10: 28,468,853 (GRCm39) |
H1438Q |
probably damaging |
Het |
Rbm4 |
A |
T |
19: 4,842,650 (GRCm39) |
V63E |
possibly damaging |
Het |
Sbk2 |
T |
A |
7: 4,961,938 (GRCm39) |
H116L |
probably damaging |
Het |
Septin9 |
T |
A |
11: 117,250,264 (GRCm39) |
C529* |
probably null |
Het |
Setx |
T |
A |
2: 29,038,663 (GRCm39) |
V1716D |
probably benign |
Het |
Slc19a3 |
C |
T |
1: 82,997,162 (GRCm39) |
V349I |
probably benign |
Het |
Slc27a4 |
C |
A |
2: 29,695,722 (GRCm39) |
R86S |
probably benign |
Het |
Slc4a8 |
A |
G |
15: 100,696,059 (GRCm39) |
H613R |
possibly damaging |
Het |
Smoc2 |
A |
G |
17: 14,545,884 (GRCm39) |
R58G |
probably damaging |
Het |
Sphkap |
T |
A |
1: 83,254,021 (GRCm39) |
N1243Y |
probably damaging |
Het |
Srsf5 |
T |
C |
12: 80,996,720 (GRCm39) |
S261P |
unknown |
Het |
Tab1 |
A |
T |
15: 80,042,999 (GRCm39) |
T398S |
possibly damaging |
Het |
Tas2r131 |
T |
A |
6: 132,934,705 (GRCm39) |
T35S |
probably benign |
Het |
Tasor2 |
T |
C |
13: 3,625,714 (GRCm39) |
K1412R |
possibly damaging |
Het |
Tigd4 |
T |
A |
3: 84,502,310 (GRCm39) |
V409E |
possibly damaging |
Het |
Tlr12 |
T |
C |
4: 128,510,501 (GRCm39) |
Q583R |
probably benign |
Het |
Tmprss9 |
T |
A |
10: 80,733,145 (GRCm39) |
C894S |
unknown |
Het |
Topaz1 |
T |
A |
9: 122,578,250 (GRCm39) |
S387T |
probably benign |
Het |
Tsfm |
T |
C |
10: 126,847,558 (GRCm39) |
R178G |
probably benign |
Het |
Ttll13 |
T |
C |
7: 79,902,875 (GRCm39) |
I181T |
probably damaging |
Het |
Ttyh3 |
T |
A |
5: 140,610,896 (GRCm39) |
K97N |
|
Het |
Ubr4 |
A |
G |
4: 139,142,394 (GRCm39) |
E38G |
|
Het |
Ugt2b37 |
T |
C |
5: 87,402,118 (GRCm39) |
Y171C |
probably damaging |
Het |
Unc5b |
C |
A |
10: 60,601,020 (GRCm39) |
M935I |
probably benign |
Het |
Usp34 |
T |
C |
11: 23,362,314 (GRCm39) |
S1606P |
|
Het |
Vmn1r195 |
T |
C |
13: 22,463,244 (GRCm39) |
L238P |
probably damaging |
Het |
Vmn2r85 |
T |
A |
10: 130,261,081 (GRCm39) |
M419L |
probably benign |
Het |
Washc2 |
G |
T |
6: 116,236,020 (GRCm39) |
A1164S |
probably benign |
Het |
Wdfy3 |
A |
T |
5: 102,042,940 (GRCm39) |
M1937K |
probably benign |
Het |
Wdfy3 |
A |
T |
5: 102,099,265 (GRCm39) |
L261* |
probably null |
Het |
Wdr64 |
A |
T |
1: 175,559,092 (GRCm39) |
Y285F |
probably benign |
Het |
Wtap |
A |
G |
17: 13,199,797 (GRCm39) |
L62P |
probably damaging |
Het |
Zfp1007 |
A |
C |
5: 109,825,170 (GRCm39) |
Y93* |
probably null |
Het |
Zfp94 |
C |
A |
7: 24,002,498 (GRCm39) |
V315F |
probably benign |
Het |
Zhx1 |
A |
T |
15: 57,911,798 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Sdk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00498:Sdk1
|
APN |
5 |
142,071,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00945:Sdk1
|
APN |
5 |
142,070,368 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00946:Sdk1
|
APN |
5 |
142,070,368 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01394:Sdk1
|
APN |
5 |
141,598,970 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01398:Sdk1
|
APN |
5 |
141,923,332 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01410:Sdk1
|
APN |
5 |
142,197,875 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01525:Sdk1
|
APN |
5 |
141,985,675 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01548:Sdk1
|
APN |
5 |
142,071,520 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01672:Sdk1
|
APN |
5 |
142,170,930 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01676:Sdk1
|
APN |
5 |
142,113,591 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01679:Sdk1
|
APN |
5 |
142,031,919 (GRCm39) |
missense |
probably benign |
|
IGL01929:Sdk1
|
APN |
5 |
141,938,785 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01970:Sdk1
|
APN |
5 |
142,071,437 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02016:Sdk1
|
APN |
5 |
142,020,184 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02060:Sdk1
|
APN |
5 |
141,938,767 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02457:Sdk1
|
APN |
5 |
141,938,771 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02634:Sdk1
|
APN |
5 |
141,595,787 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02637:Sdk1
|
APN |
5 |
142,080,327 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02731:Sdk1
|
APN |
5 |
142,158,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03180:Sdk1
|
APN |
5 |
142,071,497 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03259:Sdk1
|
APN |
5 |
141,938,788 (GRCm39) |
nonsense |
probably null |
|
PIT4453001:Sdk1
|
UTSW |
5 |
142,197,793 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4544001:Sdk1
|
UTSW |
5 |
141,941,987 (GRCm39) |
missense |
probably benign |
0.08 |
R0149:Sdk1
|
UTSW |
5 |
141,842,809 (GRCm39) |
intron |
probably benign |
|
R0173:Sdk1
|
UTSW |
5 |
142,159,564 (GRCm39) |
splice site |
probably benign |
|
R0240:Sdk1
|
UTSW |
5 |
141,984,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Sdk1
|
UTSW |
5 |
141,984,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Sdk1
|
UTSW |
5 |
142,129,677 (GRCm39) |
splice site |
probably benign |
|
R0245:Sdk1
|
UTSW |
5 |
141,940,713 (GRCm39) |
missense |
probably benign |
0.02 |
R0270:Sdk1
|
UTSW |
5 |
142,070,321 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0398:Sdk1
|
UTSW |
5 |
141,948,476 (GRCm39) |
missense |
probably benign |
0.05 |
R0401:Sdk1
|
UTSW |
5 |
142,031,916 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0501:Sdk1
|
UTSW |
5 |
141,923,473 (GRCm39) |
missense |
probably benign |
|
R0558:Sdk1
|
UTSW |
5 |
142,117,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Sdk1
|
UTSW |
5 |
141,940,713 (GRCm39) |
missense |
probably benign |
0.02 |
R0834:Sdk1
|
UTSW |
5 |
141,227,779 (GRCm39) |
missense |
probably benign |
|
R0962:Sdk1
|
UTSW |
5 |
142,147,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R1424:Sdk1
|
UTSW |
5 |
142,147,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1438:Sdk1
|
UTSW |
5 |
142,024,078 (GRCm39) |
missense |
probably damaging |
0.96 |
R1517:Sdk1
|
UTSW |
5 |
142,113,591 (GRCm39) |
missense |
probably damaging |
0.99 |
R1519:Sdk1
|
UTSW |
5 |
141,985,705 (GRCm39) |
missense |
probably benign |
0.00 |
R1539:Sdk1
|
UTSW |
5 |
142,080,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Sdk1
|
UTSW |
5 |
141,984,634 (GRCm39) |
missense |
probably benign |
0.03 |
R1574:Sdk1
|
UTSW |
5 |
141,984,634 (GRCm39) |
missense |
probably benign |
0.03 |
R1673:Sdk1
|
UTSW |
5 |
141,934,261 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1686:Sdk1
|
UTSW |
5 |
142,020,292 (GRCm39) |
missense |
probably benign |
0.00 |
R1806:Sdk1
|
UTSW |
5 |
142,147,681 (GRCm39) |
missense |
probably benign |
|
R1806:Sdk1
|
UTSW |
5 |
141,598,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R1925:Sdk1
|
UTSW |
5 |
142,171,040 (GRCm39) |
missense |
probably benign |
0.09 |
R1956:Sdk1
|
UTSW |
5 |
142,080,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R1976:Sdk1
|
UTSW |
5 |
142,129,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R2124:Sdk1
|
UTSW |
5 |
142,170,943 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2152:Sdk1
|
UTSW |
5 |
141,778,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R2186:Sdk1
|
UTSW |
5 |
142,032,047 (GRCm39) |
missense |
probably benign |
0.00 |
R2187:Sdk1
|
UTSW |
5 |
142,100,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R2306:Sdk1
|
UTSW |
5 |
141,948,455 (GRCm39) |
missense |
probably benign |
0.00 |
R2520:Sdk1
|
UTSW |
5 |
142,071,526 (GRCm39) |
missense |
probably benign |
0.19 |
R2698:Sdk1
|
UTSW |
5 |
142,197,805 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2763:Sdk1
|
UTSW |
5 |
142,070,306 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3023:Sdk1
|
UTSW |
5 |
142,031,991 (GRCm39) |
missense |
probably benign |
|
R3500:Sdk1
|
UTSW |
5 |
141,992,371 (GRCm39) |
splice site |
probably benign |
|
R3613:Sdk1
|
UTSW |
5 |
142,105,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R3824:Sdk1
|
UTSW |
5 |
141,921,804 (GRCm39) |
missense |
probably benign |
|
R3916:Sdk1
|
UTSW |
5 |
142,036,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R3917:Sdk1
|
UTSW |
5 |
142,036,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R4158:Sdk1
|
UTSW |
5 |
142,100,154 (GRCm39) |
missense |
probably benign |
0.00 |
R4160:Sdk1
|
UTSW |
5 |
142,100,154 (GRCm39) |
missense |
probably benign |
0.00 |
R4161:Sdk1
|
UTSW |
5 |
142,100,154 (GRCm39) |
missense |
probably benign |
0.00 |
R4386:Sdk1
|
UTSW |
5 |
142,080,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R4649:Sdk1
|
UTSW |
5 |
141,992,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R4701:Sdk1
|
UTSW |
5 |
142,170,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R4780:Sdk1
|
UTSW |
5 |
141,944,993 (GRCm39) |
missense |
probably damaging |
0.97 |
R4787:Sdk1
|
UTSW |
5 |
141,568,168 (GRCm39) |
missense |
probably benign |
|
R4825:Sdk1
|
UTSW |
5 |
141,568,049 (GRCm39) |
missense |
probably benign |
0.11 |
R4853:Sdk1
|
UTSW |
5 |
142,132,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Sdk1
|
UTSW |
5 |
142,147,531 (GRCm39) |
missense |
probably benign |
0.01 |
R4928:Sdk1
|
UTSW |
5 |
141,842,758 (GRCm39) |
intron |
probably benign |
|
R5111:Sdk1
|
UTSW |
5 |
142,113,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R5188:Sdk1
|
UTSW |
5 |
141,942,015 (GRCm39) |
critical splice donor site |
probably null |
|
R5246:Sdk1
|
UTSW |
5 |
142,100,317 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5273:Sdk1
|
UTSW |
5 |
141,984,583 (GRCm39) |
missense |
probably damaging |
0.99 |
R5484:Sdk1
|
UTSW |
5 |
142,085,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R5525:Sdk1
|
UTSW |
5 |
142,171,020 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5578:Sdk1
|
UTSW |
5 |
141,598,880 (GRCm39) |
nonsense |
probably null |
|
R5593:Sdk1
|
UTSW |
5 |
141,941,879 (GRCm39) |
missense |
probably damaging |
0.98 |
R5654:Sdk1
|
UTSW |
5 |
141,921,853 (GRCm39) |
missense |
probably damaging |
0.96 |
R5672:Sdk1
|
UTSW |
5 |
142,173,900 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5768:Sdk1
|
UTSW |
5 |
142,129,626 (GRCm39) |
missense |
probably benign |
0.00 |
R5781:Sdk1
|
UTSW |
5 |
141,921,803 (GRCm39) |
missense |
probably benign |
0.00 |
R5846:Sdk1
|
UTSW |
5 |
142,100,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R5851:Sdk1
|
UTSW |
5 |
141,948,424 (GRCm39) |
missense |
probably benign |
0.00 |
R6164:Sdk1
|
UTSW |
5 |
142,117,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R6235:Sdk1
|
UTSW |
5 |
142,020,181 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6364:Sdk1
|
UTSW |
5 |
141,948,464 (GRCm39) |
missense |
probably benign |
0.00 |
R6453:Sdk1
|
UTSW |
5 |
142,082,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R6892:Sdk1
|
UTSW |
5 |
142,032,053 (GRCm39) |
missense |
probably benign |
0.00 |
R6996:Sdk1
|
UTSW |
5 |
142,197,769 (GRCm39) |
missense |
probably benign |
0.16 |
R7003:Sdk1
|
UTSW |
5 |
142,082,489 (GRCm39) |
missense |
probably benign |
0.01 |
R7022:Sdk1
|
UTSW |
5 |
142,080,412 (GRCm39) |
splice site |
probably null |
|
R7027:Sdk1
|
UTSW |
5 |
142,082,481 (GRCm39) |
splice site |
probably null |
|
R7098:Sdk1
|
UTSW |
5 |
142,082,625 (GRCm39) |
missense |
probably damaging |
0.96 |
R7107:Sdk1
|
UTSW |
5 |
142,067,471 (GRCm39) |
missense |
probably damaging |
0.99 |
R7203:Sdk1
|
UTSW |
5 |
142,031,931 (GRCm39) |
missense |
probably benign |
0.08 |
R7313:Sdk1
|
UTSW |
5 |
141,923,377 (GRCm39) |
missense |
probably damaging |
0.97 |
R7363:Sdk1
|
UTSW |
5 |
142,173,897 (GRCm39) |
missense |
probably benign |
0.05 |
R7375:Sdk1
|
UTSW |
5 |
141,984,598 (GRCm39) |
missense |
probably benign |
0.01 |
R7446:Sdk1
|
UTSW |
5 |
142,130,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R7527:Sdk1
|
UTSW |
5 |
141,778,731 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7598:Sdk1
|
UTSW |
5 |
141,595,753 (GRCm39) |
nonsense |
probably null |
|
R7747:Sdk1
|
UTSW |
5 |
142,070,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R7985:Sdk1
|
UTSW |
5 |
142,113,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R8129:Sdk1
|
UTSW |
5 |
142,177,648 (GRCm39) |
missense |
probably benign |
0.10 |
R8217:Sdk1
|
UTSW |
5 |
142,197,713 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8249:Sdk1
|
UTSW |
5 |
142,173,770 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8376:Sdk1
|
UTSW |
5 |
142,144,376 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8779:Sdk1
|
UTSW |
5 |
141,948,457 (GRCm39) |
missense |
probably benign |
0.00 |
R8807:Sdk1
|
UTSW |
5 |
142,071,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R8907:Sdk1
|
UTSW |
5 |
142,070,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R8942:Sdk1
|
UTSW |
5 |
142,082,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R8945:Sdk1
|
UTSW |
5 |
141,598,935 (GRCm39) |
missense |
probably benign |
|
R9006:Sdk1
|
UTSW |
5 |
141,923,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R9249:Sdk1
|
UTSW |
5 |
142,129,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R9275:Sdk1
|
UTSW |
5 |
141,941,953 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9345:Sdk1
|
UTSW |
5 |
142,147,708 (GRCm39) |
missense |
probably benign |
|
R9463:Sdk1
|
UTSW |
5 |
141,948,548 (GRCm39) |
missense |
probably benign |
0.31 |
R9549:Sdk1
|
UTSW |
5 |
141,940,657 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9572:Sdk1
|
UTSW |
5 |
141,595,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R9602:Sdk1
|
UTSW |
5 |
142,071,353 (GRCm39) |
missense |
probably damaging |
0.99 |
R9703:Sdk1
|
UTSW |
5 |
142,100,283 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9720:Sdk1
|
UTSW |
5 |
142,197,796 (GRCm39) |
missense |
probably damaging |
0.96 |
R9771:Sdk1
|
UTSW |
5 |
142,082,624 (GRCm39) |
missense |
probably damaging |
0.99 |
X0017:Sdk1
|
UTSW |
5 |
141,984,535 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Sdk1
|
UTSW |
5 |
141,945,065 (GRCm39) |
missense |
probably null |
0.58 |
Z1177:Sdk1
|
UTSW |
5 |
141,948,463 (GRCm39) |
missense |
possibly damaging |
0.87 |
|