Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700066M21Rik |
T |
A |
1: 57,422,302 (GRCm39) |
M226K |
probably benign |
Het |
4921524L21Rik |
T |
G |
18: 6,626,385 (GRCm39) |
S132R |
probably damaging |
Het |
A4gnt |
T |
G |
9: 99,502,335 (GRCm39) |
I165S |
probably damaging |
Het |
Abca14 |
G |
A |
7: 119,877,534 (GRCm39) |
D1061N |
probably benign |
Het |
Abcc9 |
G |
A |
6: 142,617,319 (GRCm39) |
P582S |
probably damaging |
Het |
Abhd5 |
G |
A |
9: 122,208,638 (GRCm39) |
V343I |
probably benign |
Het |
Adam6a |
C |
T |
12: 113,509,192 (GRCm39) |
R522C |
probably damaging |
Het |
Ankle2 |
G |
A |
5: 110,385,590 (GRCm39) |
R313H |
probably damaging |
Het |
Aplf |
G |
A |
6: 87,623,197 (GRCm39) |
T315I |
probably damaging |
Het |
Asic5 |
C |
T |
3: 81,928,383 (GRCm39) |
P491S |
probably benign |
Het |
Atp5f1b |
T |
C |
10: 127,921,391 (GRCm39) |
Y230H |
probably benign |
Het |
B4galt6 |
A |
T |
18: 20,861,099 (GRCm39) |
I51N |
probably damaging |
Het |
Bmal2 |
G |
A |
6: 146,723,632 (GRCm39) |
V321I |
not run |
Het |
C4b |
A |
G |
17: 34,962,633 (GRCm39) |
L23S |
probably damaging |
Het |
Cables2 |
A |
G |
2: 179,902,129 (GRCm39) |
V410A |
|
Het |
Ccdc168 |
T |
A |
1: 44,100,076 (GRCm39) |
K341* |
probably null |
Het |
Cdyl |
A |
G |
13: 36,047,378 (GRCm39) |
M489V |
probably damaging |
Het |
Clip4 |
T |
C |
17: 72,096,996 (GRCm39) |
M40T |
probably damaging |
Het |
Col12a1 |
T |
C |
9: 79,589,348 (GRCm39) |
Y1069C |
probably damaging |
Het |
Col6a3 |
T |
C |
1: 90,755,708 (GRCm39) |
M194V |
probably benign |
Het |
Colec11 |
T |
A |
12: 28,644,714 (GRCm39) |
D260V |
probably damaging |
Het |
Cracdl |
T |
C |
1: 37,653,699 (GRCm39) |
T1036A |
possibly damaging |
Het |
Cux2 |
T |
C |
5: 121,999,319 (GRCm39) |
D1207G |
probably benign |
Het |
Cyp2d34 |
G |
T |
15: 82,501,436 (GRCm39) |
N297K |
possibly damaging |
Het |
Dnmt3c |
A |
G |
2: 153,556,946 (GRCm39) |
T288A |
probably benign |
Het |
Dock8 |
T |
A |
19: 25,162,245 (GRCm39) |
F1842I |
probably benign |
Het |
Dysf |
A |
G |
6: 84,083,880 (GRCm39) |
I740V |
probably benign |
Het |
Epha6 |
T |
A |
16: 59,736,201 (GRCm39) |
M778L |
probably benign |
Het |
Eri2 |
A |
T |
7: 119,385,739 (GRCm39) |
L254* |
probably null |
Het |
Fam43b |
A |
G |
4: 138,123,152 (GRCm39) |
F56S |
probably damaging |
Het |
Fat4 |
C |
A |
3: 38,943,294 (GRCm39) |
S729* |
probably null |
Het |
Fbxw22 |
C |
A |
9: 109,211,143 (GRCm39) |
W386L |
probably benign |
Het |
Fgd6 |
T |
A |
10: 93,879,909 (GRCm39) |
C254* |
probably null |
Het |
Fgd6 |
C |
A |
10: 93,975,743 (GRCm39) |
T1386K |
probably benign |
Het |
Fkbp7 |
G |
T |
2: 76,502,108 (GRCm39) |
D98E |
possibly damaging |
Het |
Hectd1 |
C |
T |
12: 51,832,635 (GRCm39) |
C913Y |
possibly damaging |
Het |
Hgf |
T |
A |
5: 16,769,841 (GRCm39) |
M105K |
probably benign |
Het |
Icam1 |
A |
C |
9: 20,930,311 (GRCm39) |
D55A |
probably benign |
Het |
Itga2 |
A |
C |
13: 114,993,930 (GRCm39) |
|
probably null |
Het |
Kcnj5 |
A |
C |
9: 32,234,045 (GRCm39) |
L90R |
probably damaging |
Het |
Klra17 |
T |
A |
6: 129,808,555 (GRCm39) |
N226I |
possibly damaging |
Het |
Krt1 |
T |
A |
15: 101,759,064 (GRCm39) |
R33S |
unknown |
Het |
L3mbtl3 |
T |
A |
10: 26,158,728 (GRCm39) |
D615V |
unknown |
Het |
Lrp2 |
T |
A |
2: 69,312,725 (GRCm39) |
Y2521F |
probably benign |
Het |
Megf10 |
A |
T |
18: 57,408,825 (GRCm39) |
N589I |
probably damaging |
Het |
Metap1d |
G |
C |
2: 71,337,129 (GRCm39) |
G14A |
probably benign |
Het |
Mfap5 |
T |
A |
6: 122,505,381 (GRCm39) |
D162E |
probably benign |
Het |
Mixl1 |
T |
C |
1: 180,524,523 (GRCm39) |
I19V |
probably benign |
Het |
Mtrr |
G |
T |
13: 68,716,979 (GRCm39) |
Y411* |
probably null |
Het |
Myh7 |
T |
C |
14: 55,227,482 (GRCm39) |
T318A |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,349,383 (GRCm39) |
Y2348* |
probably null |
Het |
Nhsl3 |
A |
G |
4: 129,119,211 (GRCm39) |
Y170H |
probably damaging |
Het |
Niban2 |
T |
C |
2: 32,812,654 (GRCm39) |
S468P |
possibly damaging |
Het |
Nlrc3 |
T |
C |
16: 3,781,454 (GRCm39) |
S668G |
probably damaging |
Het |
Nutm1 |
G |
A |
2: 112,080,401 (GRCm39) |
R505C |
probably damaging |
Het |
Or10ag59 |
T |
A |
2: 87,406,052 (GRCm39) |
V208E |
probably damaging |
Het |
Or12j2 |
A |
T |
7: 139,916,654 (GRCm39) |
D293V |
possibly damaging |
Het |
Or4c117 |
C |
A |
2: 88,955,180 (GRCm39) |
R298S |
probably benign |
Het |
Pcna |
A |
G |
2: 132,094,797 (GRCm39) |
S54P |
probably benign |
Het |
Pde6a |
A |
G |
18: 61,391,364 (GRCm39) |
T570A |
probably damaging |
Het |
Phf21b |
A |
T |
15: 84,739,918 (GRCm39) |
M1K |
probably null |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Prob1 |
A |
G |
18: 35,786,352 (GRCm39) |
F634S |
possibly damaging |
Het |
Prss50 |
A |
G |
9: 110,690,357 (GRCm39) |
T167A |
probably damaging |
Het |
Ptpn1 |
T |
C |
2: 167,816,692 (GRCm39) |
V249A |
probably damaging |
Het |
Rai1 |
G |
A |
11: 60,079,499 (GRCm39) |
V1188I |
probably benign |
Het |
Ric1 |
G |
A |
19: 29,561,978 (GRCm39) |
|
probably null |
Het |
Robo1 |
C |
T |
16: 72,786,519 (GRCm39) |
Q844* |
probably null |
Het |
Rpn1 |
A |
G |
6: 88,061,619 (GRCm39) |
D36G |
possibly damaging |
Het |
Serpinb1b |
A |
T |
13: 33,277,810 (GRCm39) |
M348L |
probably benign |
Het |
Setd4 |
T |
C |
16: 93,380,830 (GRCm39) |
|
probably null |
Het |
Setd5 |
T |
G |
6: 113,124,518 (GRCm39) |
S1124A |
probably benign |
Het |
Slc35c1 |
C |
A |
2: 92,289,084 (GRCm39) |
V154F |
probably damaging |
Het |
Slc7a6os |
G |
T |
8: 106,937,121 (GRCm39) |
S113* |
probably null |
Het |
Syne2 |
T |
A |
12: 76,149,810 (GRCm39) |
D1787E |
probably benign |
Het |
Tas2r144 |
A |
C |
6: 42,192,373 (GRCm39) |
I38L |
probably damaging |
Het |
Tepsin |
G |
T |
11: 119,982,534 (GRCm39) |
T512K |
possibly damaging |
Het |
Utp20 |
A |
G |
10: 88,606,586 (GRCm39) |
V1662A |
probably benign |
Het |
Vmn1r201 |
C |
T |
13: 22,659,509 (GRCm39) |
A241V |
possibly damaging |
Het |
Vmn2r60 |
T |
A |
7: 41,785,826 (GRCm39) |
S210T |
probably benign |
Het |
Wdr6 |
G |
T |
9: 108,451,784 (GRCm39) |
H700N |
probably damaging |
Het |
Zdhhc8 |
T |
C |
16: 18,052,790 (GRCm39) |
T29A |
probably benign |
Het |
Zfp335 |
A |
G |
2: 164,742,052 (GRCm39) |
I614T |
probably damaging |
Het |
Zfp54 |
T |
A |
17: 21,653,844 (GRCm39) |
S113T |
probably benign |
Het |
Zfp873 |
T |
A |
10: 81,897,071 (GRCm39) |
C601S |
probably damaging |
Het |
Zfyve26 |
T |
C |
12: 79,325,146 (GRCm39) |
|
probably null |
Het |
Zmynd8 |
T |
C |
2: 165,681,929 (GRCm39) |
T201A |
probably damaging |
Het |
|
Other mutations in Dmbt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Dmbt1
|
APN |
7 |
130,681,270 (GRCm39) |
intron |
probably benign |
|
IGL00161:Dmbt1
|
APN |
7 |
130,711,357 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00331:Dmbt1
|
APN |
7 |
130,701,020 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL00769:Dmbt1
|
APN |
7 |
130,684,230 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00792:Dmbt1
|
APN |
7 |
130,699,337 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL00823:Dmbt1
|
APN |
7 |
130,659,888 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01072:Dmbt1
|
APN |
7 |
130,687,098 (GRCm39) |
splice site |
probably benign |
|
IGL01317:Dmbt1
|
APN |
7 |
130,642,921 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01335:Dmbt1
|
APN |
7 |
130,690,497 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01372:Dmbt1
|
APN |
7 |
130,705,409 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01511:Dmbt1
|
APN |
7 |
130,718,457 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL01627:Dmbt1
|
APN |
7 |
130,682,915 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01890:Dmbt1
|
APN |
7 |
130,676,149 (GRCm39) |
intron |
probably benign |
|
IGL02160:Dmbt1
|
APN |
7 |
130,684,418 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02186:Dmbt1
|
APN |
7 |
130,694,986 (GRCm39) |
splice site |
probably benign |
|
IGL02197:Dmbt1
|
APN |
7 |
130,687,152 (GRCm39) |
splice site |
probably benign |
|
IGL02332:Dmbt1
|
APN |
7 |
130,668,343 (GRCm39) |
intron |
probably benign |
|
IGL02427:Dmbt1
|
APN |
7 |
130,689,815 (GRCm39) |
splice site |
probably null |
|
IGL02726:Dmbt1
|
APN |
7 |
130,676,140 (GRCm39) |
intron |
probably benign |
|
IGL02967:Dmbt1
|
APN |
7 |
130,672,919 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03003:Dmbt1
|
APN |
7 |
130,684,409 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03089:Dmbt1
|
APN |
7 |
130,712,778 (GRCm39) |
missense |
probably damaging |
0.99 |
cavity
|
UTSW |
7 |
130,713,965 (GRCm39) |
missense |
unknown |
|
lacunar
|
UTSW |
7 |
130,699,361 (GRCm39) |
missense |
probably damaging |
0.97 |
BB005:Dmbt1
|
UTSW |
7 |
130,639,620 (GRCm39) |
missense |
probably benign |
0.16 |
BB015:Dmbt1
|
UTSW |
7 |
130,639,620 (GRCm39) |
missense |
probably benign |
0.16 |
H8562:Dmbt1
|
UTSW |
7 |
130,713,805 (GRCm39) |
nonsense |
probably null |
|
K3955:Dmbt1
|
UTSW |
7 |
130,721,293 (GRCm39) |
missense |
probably damaging |
0.98 |
R0051:Dmbt1
|
UTSW |
7 |
130,721,225 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0051:Dmbt1
|
UTSW |
7 |
130,721,225 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0257:Dmbt1
|
UTSW |
7 |
130,708,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R0388:Dmbt1
|
UTSW |
7 |
130,697,779 (GRCm39) |
splice site |
probably benign |
|
R0427:Dmbt1
|
UTSW |
7 |
130,642,632 (GRCm39) |
nonsense |
probably null |
|
R0478:Dmbt1
|
UTSW |
7 |
130,642,917 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0502:Dmbt1
|
UTSW |
7 |
130,699,403 (GRCm39) |
splice site |
probably null |
|
R0538:Dmbt1
|
UTSW |
7 |
130,651,631 (GRCm39) |
splice site |
probably benign |
|
R0626:Dmbt1
|
UTSW |
7 |
130,703,811 (GRCm39) |
missense |
probably damaging |
0.97 |
R0631:Dmbt1
|
UTSW |
7 |
130,699,383 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0948:Dmbt1
|
UTSW |
7 |
130,694,847 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1169:Dmbt1
|
UTSW |
7 |
130,676,254 (GRCm39) |
critical splice donor site |
probably null |
|
R1413:Dmbt1
|
UTSW |
7 |
130,651,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R1458:Dmbt1
|
UTSW |
7 |
130,646,217 (GRCm39) |
splice site |
probably benign |
|
R1463:Dmbt1
|
UTSW |
7 |
130,711,366 (GRCm39) |
critical splice donor site |
probably null |
|
R1509:Dmbt1
|
UTSW |
7 |
130,676,061 (GRCm39) |
intron |
probably benign |
|
R1990:Dmbt1
|
UTSW |
7 |
130,660,018 (GRCm39) |
missense |
probably damaging |
0.98 |
R2018:Dmbt1
|
UTSW |
7 |
130,712,718 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2019:Dmbt1
|
UTSW |
7 |
130,712,718 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2042:Dmbt1
|
UTSW |
7 |
130,708,089 (GRCm39) |
missense |
probably damaging |
0.99 |
R2056:Dmbt1
|
UTSW |
7 |
130,707,900 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2057:Dmbt1
|
UTSW |
7 |
130,707,900 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2058:Dmbt1
|
UTSW |
7 |
130,707,900 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2059:Dmbt1
|
UTSW |
7 |
130,707,900 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2061:Dmbt1
|
UTSW |
7 |
130,700,863 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2092:Dmbt1
|
UTSW |
7 |
130,651,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R2102:Dmbt1
|
UTSW |
7 |
130,703,762 (GRCm39) |
missense |
probably damaging |
0.97 |
R2155:Dmbt1
|
UTSW |
7 |
130,699,305 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2243:Dmbt1
|
UTSW |
7 |
130,648,292 (GRCm39) |
missense |
probably benign |
0.03 |
R2256:Dmbt1
|
UTSW |
7 |
130,692,224 (GRCm39) |
missense |
probably benign |
0.01 |
R2391:Dmbt1
|
UTSW |
7 |
130,708,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R2394:Dmbt1
|
UTSW |
7 |
130,696,464 (GRCm39) |
nonsense |
probably null |
|
R3014:Dmbt1
|
UTSW |
7 |
130,633,827 (GRCm39) |
intron |
probably benign |
|
R3155:Dmbt1
|
UTSW |
7 |
130,651,887 (GRCm39) |
nonsense |
probably null |
|
R3176:Dmbt1
|
UTSW |
7 |
130,689,801 (GRCm39) |
missense |
probably benign |
0.19 |
R3276:Dmbt1
|
UTSW |
7 |
130,689,801 (GRCm39) |
missense |
probably benign |
0.19 |
R3442:Dmbt1
|
UTSW |
7 |
130,707,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Dmbt1
|
UTSW |
7 |
130,713,819 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4060:Dmbt1
|
UTSW |
7 |
130,675,932 (GRCm39) |
intron |
probably benign |
|
R4396:Dmbt1
|
UTSW |
7 |
130,718,361 (GRCm39) |
missense |
probably damaging |
0.98 |
R4453:Dmbt1
|
UTSW |
7 |
130,642,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R5001:Dmbt1
|
UTSW |
7 |
130,651,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R5051:Dmbt1
|
UTSW |
7 |
130,696,472 (GRCm39) |
missense |
probably benign |
0.01 |
R5156:Dmbt1
|
UTSW |
7 |
130,699,400 (GRCm39) |
critical splice donor site |
probably null |
|
R5225:Dmbt1
|
UTSW |
7 |
130,696,465 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5281:Dmbt1
|
UTSW |
7 |
130,684,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R5308:Dmbt1
|
UTSW |
7 |
130,642,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R5447:Dmbt1
|
UTSW |
7 |
130,721,240 (GRCm39) |
missense |
probably damaging |
0.99 |
R5467:Dmbt1
|
UTSW |
7 |
130,642,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R5497:Dmbt1
|
UTSW |
7 |
130,665,133 (GRCm39) |
intron |
probably benign |
|
R5526:Dmbt1
|
UTSW |
7 |
130,642,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R5554:Dmbt1
|
UTSW |
7 |
130,701,030 (GRCm39) |
nonsense |
probably null |
|
R5566:Dmbt1
|
UTSW |
7 |
130,708,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R5595:Dmbt1
|
UTSW |
7 |
130,655,797 (GRCm39) |
missense |
probably benign |
0.17 |
R6154:Dmbt1
|
UTSW |
7 |
130,711,370 (GRCm39) |
splice site |
probably null |
|
R6188:Dmbt1
|
UTSW |
7 |
130,699,361 (GRCm39) |
missense |
probably damaging |
0.97 |
R6214:Dmbt1
|
UTSW |
7 |
130,668,463 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6215:Dmbt1
|
UTSW |
7 |
130,668,463 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6391:Dmbt1
|
UTSW |
7 |
130,659,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6397:Dmbt1
|
UTSW |
7 |
130,705,308 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6436:Dmbt1
|
UTSW |
7 |
130,718,370 (GRCm39) |
missense |
probably benign |
0.01 |
R6603:Dmbt1
|
UTSW |
7 |
130,648,240 (GRCm39) |
splice site |
probably null |
|
R6719:Dmbt1
|
UTSW |
7 |
130,721,332 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6781:Dmbt1
|
UTSW |
7 |
130,648,291 (GRCm39) |
missense |
probably benign |
0.16 |
R7148:Dmbt1
|
UTSW |
7 |
130,668,464 (GRCm39) |
nonsense |
probably null |
|
R7191:Dmbt1
|
UTSW |
7 |
130,646,250 (GRCm39) |
missense |
unknown |
|
R7269:Dmbt1
|
UTSW |
7 |
130,668,351 (GRCm39) |
missense |
unknown |
|
R7288:Dmbt1
|
UTSW |
7 |
130,685,519 (GRCm39) |
nonsense |
probably null |
|
R7349:Dmbt1
|
UTSW |
7 |
130,642,854 (GRCm39) |
missense |
unknown |
|
R7386:Dmbt1
|
UTSW |
7 |
130,713,965 (GRCm39) |
missense |
unknown |
|
R7428:Dmbt1
|
UTSW |
7 |
130,710,192 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7481:Dmbt1
|
UTSW |
7 |
130,681,241 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7486:Dmbt1
|
UTSW |
7 |
130,668,192 (GRCm39) |
missense |
unknown |
|
R7513:Dmbt1
|
UTSW |
7 |
130,692,242 (GRCm39) |
missense |
unknown |
|
R7553:Dmbt1
|
UTSW |
7 |
130,706,597 (GRCm39) |
missense |
unknown |
|
R7567:Dmbt1
|
UTSW |
7 |
130,663,093 (GRCm39) |
splice site |
probably null |
|
R7584:Dmbt1
|
UTSW |
7 |
130,690,481 (GRCm39) |
nonsense |
probably null |
|
R7736:Dmbt1
|
UTSW |
7 |
130,718,625 (GRCm39) |
missense |
unknown |
|
R7758:Dmbt1
|
UTSW |
7 |
130,722,926 (GRCm39) |
missense |
unknown |
|
R7928:Dmbt1
|
UTSW |
7 |
130,639,620 (GRCm39) |
missense |
probably benign |
0.16 |
R8080:Dmbt1
|
UTSW |
7 |
130,690,500 (GRCm39) |
missense |
unknown |
|
R8098:Dmbt1
|
UTSW |
7 |
130,710,188 (GRCm39) |
nonsense |
probably null |
|
R8125:Dmbt1
|
UTSW |
7 |
130,700,953 (GRCm39) |
missense |
unknown |
|
R8177:Dmbt1
|
UTSW |
7 |
130,708,162 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8350:Dmbt1
|
UTSW |
7 |
130,687,147 (GRCm39) |
critical splice donor site |
probably null |
|
R8366:Dmbt1
|
UTSW |
7 |
130,668,330 (GRCm39) |
missense |
unknown |
|
R8378:Dmbt1
|
UTSW |
7 |
130,708,195 (GRCm39) |
missense |
probably damaging |
0.96 |
R8399:Dmbt1
|
UTSW |
7 |
130,684,317 (GRCm39) |
missense |
unknown |
|
R8400:Dmbt1
|
UTSW |
7 |
130,684,317 (GRCm39) |
missense |
unknown |
|
R8445:Dmbt1
|
UTSW |
7 |
130,692,110 (GRCm39) |
missense |
unknown |
|
R8450:Dmbt1
|
UTSW |
7 |
130,687,147 (GRCm39) |
critical splice donor site |
probably null |
|
R8511:Dmbt1
|
UTSW |
7 |
130,703,742 (GRCm39) |
missense |
unknown |
|
R8688:Dmbt1
|
UTSW |
7 |
130,659,984 (GRCm39) |
missense |
unknown |
|
R8850:Dmbt1
|
UTSW |
7 |
130,692,134 (GRCm39) |
missense |
unknown |
|
R8852:Dmbt1
|
UTSW |
7 |
130,642,853 (GRCm39) |
missense |
unknown |
|
R8871:Dmbt1
|
UTSW |
7 |
130,718,597 (GRCm39) |
missense |
unknown |
|
R8943:Dmbt1
|
UTSW |
7 |
130,721,372 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8978:Dmbt1
|
UTSW |
7 |
130,639,611 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9004:Dmbt1
|
UTSW |
7 |
130,713,798 (GRCm39) |
missense |
unknown |
|
R9020:Dmbt1
|
UTSW |
7 |
130,712,787 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9088:Dmbt1
|
UTSW |
7 |
130,718,418 (GRCm39) |
missense |
unknown |
|
R9230:Dmbt1
|
UTSW |
7 |
130,639,642 (GRCm39) |
missense |
probably benign |
0.01 |
R9304:Dmbt1
|
UTSW |
7 |
130,700,855 (GRCm39) |
missense |
unknown |
|
R9377:Dmbt1
|
UTSW |
7 |
130,694,832 (GRCm39) |
missense |
unknown |
|
R9428:Dmbt1
|
UTSW |
7 |
130,668,208 (GRCm39) |
missense |
unknown |
|
R9474:Dmbt1
|
UTSW |
7 |
130,675,987 (GRCm39) |
missense |
unknown |
|
R9573:Dmbt1
|
UTSW |
7 |
130,657,910 (GRCm39) |
critical splice donor site |
probably null |
|
R9675:Dmbt1
|
UTSW |
7 |
130,712,652 (GRCm39) |
missense |
probably damaging |
0.98 |
R9689:Dmbt1
|
UTSW |
7 |
130,660,015 (GRCm39) |
missense |
unknown |
|
R9781:Dmbt1
|
UTSW |
7 |
130,639,599 (GRCm39) |
missense |
probably benign |
0.00 |
X0024:Dmbt1
|
UTSW |
7 |
130,713,977 (GRCm39) |
nonsense |
probably null |
|
X0062:Dmbt1
|
UTSW |
7 |
130,696,581 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1176:Dmbt1
|
UTSW |
7 |
130,690,542 (GRCm39) |
missense |
unknown |
|
Z1177:Dmbt1
|
UTSW |
7 |
130,684,215 (GRCm39) |
critical splice acceptor site |
probably null |
|
|