Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700036A12Rik |
A |
G |
9: 60,677,043 (GRCm39) |
|
noncoding transcript |
Het |
A430110L20Rik |
T |
A |
1: 181,055,423 (GRCm39) |
|
noncoding transcript |
Het |
Abce1 |
T |
C |
8: 80,433,864 (GRCm39) |
K63R |
possibly damaging |
Het |
Acp6 |
A |
G |
3: 97,081,104 (GRCm39) |
|
probably benign |
Het |
Adamts13 |
T |
A |
2: 26,878,366 (GRCm39) |
L579Q |
probably damaging |
Het |
Adamtsl3 |
T |
A |
7: 82,172,528 (GRCm39) |
M497K |
probably damaging |
Het |
Adgrb2 |
T |
A |
4: 129,908,384 (GRCm39) |
M1042K |
possibly damaging |
Het |
Akap12 |
A |
T |
10: 4,303,693 (GRCm39) |
S168C |
probably damaging |
Het |
Akap3 |
A |
T |
6: 126,842,517 (GRCm39) |
M379L |
probably damaging |
Het |
Aldh6a1 |
C |
T |
12: 84,486,437 (GRCm39) |
M135I |
probably null |
Het |
Arhgef12 |
A |
G |
9: 42,900,294 (GRCm39) |
S860P |
probably damaging |
Het |
Atp11b |
A |
C |
3: 35,843,707 (GRCm39) |
T185P |
probably damaging |
Het |
Bcas1 |
T |
C |
2: 170,229,871 (GRCm39) |
D243G |
probably damaging |
Het |
Cdhr2 |
T |
A |
13: 54,865,685 (GRCm39) |
S228T |
probably damaging |
Het |
Cic |
T |
C |
7: 24,979,162 (GRCm39) |
|
probably benign |
Het |
Cimap1d |
A |
T |
10: 79,481,392 (GRCm39) |
|
probably benign |
Het |
Cmya5 |
T |
A |
13: 93,201,835 (GRCm39) |
I3376L |
probably benign |
Het |
Ctrc |
C |
A |
4: 141,573,535 (GRCm39) |
|
probably null |
Het |
Dchs1 |
G |
T |
7: 105,404,451 (GRCm39) |
P2697Q |
probably damaging |
Het |
Drd2 |
G |
A |
9: 49,313,512 (GRCm39) |
R227H |
probably damaging |
Het |
Dscc1 |
C |
A |
15: 54,950,160 (GRCm39) |
C195F |
probably damaging |
Het |
Dzip1 |
T |
A |
14: 119,160,125 (GRCm39) |
M28L |
probably benign |
Het |
Edar |
A |
T |
10: 58,443,188 (GRCm39) |
S313T |
probably benign |
Het |
Eef1e1 |
C |
A |
13: 38,840,099 (GRCm39) |
A69S |
probably damaging |
Het |
Fbn1 |
A |
G |
2: 125,143,849 (GRCm39) |
V2760A |
probably benign |
Het |
Fez1 |
GACAAACA |
GACA |
9: 36,781,845 (GRCm39) |
|
probably null |
Het |
Fgl1 |
C |
G |
8: 41,663,496 (GRCm39) |
A11P |
possibly damaging |
Het |
Fras1 |
T |
C |
5: 96,748,592 (GRCm39) |
V689A |
probably benign |
Het |
Fry |
T |
A |
5: 150,304,324 (GRCm39) |
D571E |
probably damaging |
Het |
Gm11232 |
T |
A |
4: 71,675,450 (GRCm39) |
R104* |
probably null |
Het |
Gm1527 |
A |
G |
3: 28,972,199 (GRCm39) |
I439V |
possibly damaging |
Het |
Gm4922 |
C |
A |
10: 18,659,640 (GRCm39) |
G361* |
probably null |
Het |
Gm7052 |
T |
A |
17: 22,259,447 (GRCm39) |
|
probably benign |
Het |
Gpatch8 |
A |
T |
11: 102,372,055 (GRCm39) |
S494R |
unknown |
Het |
Gria2 |
A |
T |
3: 80,639,352 (GRCm39) |
V220E |
possibly damaging |
Het |
Grik4 |
G |
A |
9: 42,432,418 (GRCm39) |
H860Y |
probably benign |
Het |
Gtpbp1 |
A |
C |
15: 79,591,930 (GRCm39) |
S93R |
probably damaging |
Het |
Gucy2g |
C |
A |
19: 55,203,468 (GRCm39) |
|
probably benign |
Het |
H2ac8 |
C |
A |
13: 23,755,221 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
G |
A |
1: 150,485,451 (GRCm39) |
R4384C |
probably damaging |
Het |
Hspa12b |
G |
C |
2: 130,987,112 (GRCm39) |
A678P |
probably damaging |
Het |
Igsf21 |
T |
A |
4: 139,755,435 (GRCm39) |
N407Y |
probably damaging |
Het |
Insig2 |
A |
G |
1: 121,234,885 (GRCm39) |
Y174H |
probably benign |
Het |
Itpr3 |
T |
A |
17: 27,337,346 (GRCm39) |
M2413K |
probably benign |
Het |
Kalrn |
A |
T |
16: 33,994,857 (GRCm39) |
I1322N |
probably damaging |
Het |
Klk1b24 |
T |
A |
7: 43,840,890 (GRCm39) |
M106K |
possibly damaging |
Het |
Krt81 |
G |
T |
15: 101,358,198 (GRCm39) |
Q352K |
probably benign |
Het |
Lca5l |
A |
T |
16: 95,961,059 (GRCm39) |
S468T |
possibly damaging |
Het |
Lvrn |
T |
C |
18: 47,015,452 (GRCm39) |
|
probably benign |
Het |
Mcpt1 |
T |
A |
14: 56,256,621 (GRCm39) |
|
probably benign |
Het |
Med13l |
T |
C |
5: 118,876,524 (GRCm39) |
M900T |
probably benign |
Het |
Med16 |
A |
G |
10: 79,743,312 (GRCm39) |
|
probably benign |
Het |
Megf6 |
G |
T |
4: 154,261,578 (GRCm39) |
V68L |
probably benign |
Het |
Mep1a |
T |
C |
17: 43,802,563 (GRCm39) |
H154R |
probably damaging |
Het |
Mrc2 |
A |
T |
11: 105,228,598 (GRCm39) |
D659V |
probably benign |
Het |
Mroh8 |
T |
A |
2: 157,063,224 (GRCm39) |
E799V |
probably damaging |
Het |
Mrpl21 |
A |
G |
19: 3,334,808 (GRCm39) |
Y50C |
possibly damaging |
Het |
Msl1 |
A |
G |
11: 98,694,808 (GRCm39) |
|
probably benign |
Het |
Myo1a |
C |
A |
10: 127,555,806 (GRCm39) |
Q932K |
probably benign |
Het |
Nav3 |
A |
C |
10: 109,555,905 (GRCm39) |
S1675R |
probably damaging |
Het |
Neurl2 |
A |
G |
2: 164,674,666 (GRCm39) |
V232A |
possibly damaging |
Het |
Nfatc1 |
T |
A |
18: 80,708,482 (GRCm39) |
|
probably benign |
Het |
Or2w4 |
C |
T |
13: 21,795,992 (GRCm39) |
C49Y |
probably benign |
Het |
Or5k8 |
T |
A |
16: 58,645,039 (GRCm39) |
E11V |
probably null |
Het |
P4hb |
A |
G |
11: 120,453,381 (GRCm39) |
|
probably benign |
Het |
Papss1 |
T |
G |
3: 131,311,615 (GRCm39) |
I281S |
probably damaging |
Het |
Pde10a |
A |
T |
17: 9,183,540 (GRCm39) |
D832V |
probably damaging |
Het |
Pfkfb2 |
A |
T |
1: 130,635,927 (GRCm39) |
Y35N |
possibly damaging |
Het |
Phaf1 |
T |
C |
8: 105,973,188 (GRCm39) |
|
probably null |
Het |
Phf20l1 |
T |
A |
15: 66,476,662 (GRCm39) |
F253Y |
probably damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,379,511 (GRCm39) |
V1046I |
probably benign |
Het |
Plin3 |
C |
T |
17: 56,591,337 (GRCm39) |
A148T |
probably benign |
Het |
Ppp1r8 |
T |
C |
4: 132,567,942 (GRCm39) |
|
probably benign |
Het |
Ppp2r3d |
A |
G |
9: 101,088,511 (GRCm39) |
L604P |
probably damaging |
Het |
Prdm5 |
T |
C |
6: 65,860,585 (GRCm39) |
V239A |
probably damaging |
Het |
Prickle1 |
A |
G |
15: 93,398,519 (GRCm39) |
S770P |
probably damaging |
Het |
Prl2c5 |
T |
A |
13: 13,365,310 (GRCm39) |
I155N |
probably benign |
Het |
Prom1 |
T |
C |
5: 44,190,274 (GRCm39) |
|
probably benign |
Het |
Psg25 |
C |
T |
7: 18,263,512 (GRCm39) |
G104R |
probably damaging |
Het |
Rbm19 |
T |
C |
5: 120,282,094 (GRCm39) |
V817A |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,741,908 (GRCm39) |
Y2091F |
probably damaging |
Het |
Slc16a4 |
A |
G |
3: 107,208,248 (GRCm39) |
T253A |
probably benign |
Het |
Smg7 |
A |
T |
1: 152,731,594 (GRCm39) |
|
probably null |
Het |
Spink5 |
C |
A |
18: 44,140,786 (GRCm39) |
H662N |
probably benign |
Het |
Taf2 |
A |
T |
15: 54,923,311 (GRCm39) |
M322K |
probably damaging |
Het |
Tmc2 |
T |
C |
2: 130,090,682 (GRCm39) |
F676S |
probably damaging |
Het |
Tmem177 |
A |
G |
1: 119,837,915 (GRCm39) |
S255P |
possibly damaging |
Het |
Trim46 |
A |
T |
3: 89,142,375 (GRCm39) |
|
probably null |
Het |
Tubb1 |
T |
A |
2: 174,292,596 (GRCm39) |
|
probably null |
Het |
Upf1 |
T |
C |
8: 70,796,904 (GRCm39) |
T110A |
probably benign |
Het |
Vmn2r9 |
T |
A |
5: 108,996,850 (GRCm39) |
I140L |
probably benign |
Het |
Zfp638 |
T |
A |
6: 83,921,638 (GRCm39) |
H588Q |
probably damaging |
Het |
Zfp780b |
T |
A |
7: 27,664,252 (GRCm39) |
N101I |
probably damaging |
Het |
Zpld2 |
T |
C |
4: 133,924,144 (GRCm39) |
D467G |
probably benign |
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 |
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 |
|
R7296:Dmbt1
|
UTSW |
7 |
130,713,861 (GRCm39) |
missense |
unknown |
|
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 |
|
|