Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
T |
C |
2: 68,494,575 (GRCm39) |
F68S |
unknown |
Het |
Abcb6 |
A |
G |
1: 75,150,248 (GRCm39) |
F637L |
probably damaging |
Het |
Aldh3b3 |
A |
G |
19: 4,014,549 (GRCm39) |
M95V |
probably benign |
Het |
Arhgap45 |
A |
T |
10: 79,858,134 (GRCm39) |
H387L |
possibly damaging |
Het |
Avil |
C |
T |
10: 126,843,460 (GRCm39) |
T130I |
probably benign |
Het |
Bmal2 |
G |
A |
6: 146,720,369 (GRCm39) |
A178T |
not run |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
C3 |
C |
A |
17: 57,527,136 (GRCm39) |
W771L |
probably damaging |
Het |
C6 |
A |
G |
15: 4,844,357 (GRCm39) |
I926M |
|
Het |
Cacna1b |
G |
A |
2: 24,506,874 (GRCm39) |
L1903F |
probably damaging |
Het |
Car3 |
A |
T |
3: 14,928,632 (GRCm39) |
M1L |
probably benign |
Het |
Ccdc175 |
A |
G |
12: 72,202,398 (GRCm39) |
I299T |
probably benign |
Het |
Chd9 |
C |
T |
8: 91,683,066 (GRCm39) |
T502I |
unknown |
Het |
Clec4a1 |
G |
A |
6: 122,904,998 (GRCm39) |
C99Y |
probably damaging |
Het |
Col19a1 |
C |
T |
1: 24,356,788 (GRCm39) |
G632R |
probably damaging |
Het |
Dop1a |
A |
T |
9: 86,417,985 (GRCm39) |
K1951N |
probably damaging |
Het |
Dpf3 |
A |
C |
12: 83,378,701 (GRCm39) |
L122R |
probably damaging |
Het |
Edem3 |
A |
T |
1: 151,683,973 (GRCm39) |
S687C |
probably damaging |
Het |
Edem3 |
G |
A |
1: 151,683,974 (GRCm39) |
S687N |
possibly damaging |
Het |
Fig4 |
A |
G |
10: 41,106,001 (GRCm39) |
|
probably null |
Het |
Fmnl2 |
A |
G |
2: 52,998,443 (GRCm39) |
T603A |
unknown |
Het |
Frmd6 |
T |
A |
12: 70,933,829 (GRCm39) |
L249Q |
probably damaging |
Het |
Glrx3 |
T |
C |
7: 137,046,751 (GRCm39) |
C48R |
probably damaging |
Het |
Gm40460 |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,554 (GRCm39) |
|
probably benign |
Het |
Gm6133 |
A |
T |
18: 78,393,008 (GRCm39) |
M1L |
probably benign |
Het |
Gm9195 |
G |
A |
14: 72,720,116 (GRCm39) |
T105I |
probably benign |
Het |
Hk2 |
G |
A |
6: 82,737,150 (GRCm39) |
T54I |
probably benign |
Het |
Jade1 |
G |
A |
3: 41,559,125 (GRCm39) |
G402D |
probably benign |
Het |
Kmt2a |
T |
C |
9: 44,720,368 (GRCm39) |
D3873G |
unknown |
Het |
Map6 |
A |
T |
7: 98,918,345 (GRCm39) |
T373S |
possibly damaging |
Het |
Megf9 |
T |
C |
4: 70,351,679 (GRCm39) |
T481A |
probably damaging |
Het |
Mtcl3 |
G |
T |
10: 29,072,519 (GRCm39) |
V604L |
probably damaging |
Het |
Mtus1 |
T |
A |
8: 41,537,652 (GRCm39) |
K21N |
probably damaging |
Het |
Muc5b |
C |
T |
7: 141,414,908 (GRCm39) |
T2618I |
unknown |
Het |
Nbas |
A |
G |
12: 13,406,960 (GRCm39) |
I852M |
probably damaging |
Het |
Or14j1 |
T |
A |
17: 38,146,289 (GRCm39) |
M133K |
probably damaging |
Het |
Or4a70 |
C |
T |
2: 89,324,636 (GRCm39) |
V7I |
probably benign |
Het |
Or5b121 |
A |
T |
19: 13,507,817 (GRCm39) |
Q304L |
probably damaging |
Het |
Or5d39 |
A |
G |
2: 87,980,105 (GRCm39) |
I86T |
probably benign |
Het |
Pank4 |
A |
G |
4: 155,054,495 (GRCm39) |
N156S |
probably damaging |
Het |
Pcdhga8 |
A |
G |
18: 37,860,990 (GRCm39) |
E682G |
probably benign |
Het |
Pde10a |
C |
A |
17: 9,168,262 (GRCm39) |
D312E |
possibly damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,376,307 (GRCm39) |
T990A |
probably benign |
Het |
Rab11fip1 |
T |
C |
8: 27,646,609 (GRCm39) |
T156A |
probably damaging |
Het |
Rhbdd2 |
T |
A |
5: 135,665,031 (GRCm39) |
S121T |
possibly damaging |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGGGGCGGCGG |
7: 97,229,124 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
C |
A |
2: 112,508,438 (GRCm39) |
R3418S |
probably benign |
Het |
Ryr3 |
C |
A |
2: 112,508,439 (GRCm39) |
R3418M |
possibly damaging |
Het |
Sbno2 |
G |
A |
10: 79,893,333 (GRCm39) |
P1323S |
probably benign |
Het |
Sec24d |
T |
C |
3: 123,144,412 (GRCm39) |
C630R |
probably damaging |
Het |
Selplg |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
5: 113,957,756 (GRCm39) |
|
probably benign |
Het |
Skp2 |
A |
T |
15: 9,113,905 (GRCm39) |
V371E |
probably damaging |
Het |
Strbp |
A |
T |
2: 37,490,766 (GRCm39) |
S496R |
probably benign |
Het |
Stxbp4 |
G |
A |
11: 90,485,639 (GRCm39) |
T236I |
possibly damaging |
Het |
Terf2 |
C |
T |
8: 107,799,353 (GRCm39) |
|
probably null |
Het |
Thnsl1 |
A |
T |
2: 21,216,599 (GRCm39) |
T118S |
probably benign |
Het |
Tlnrd1 |
A |
T |
7: 83,531,546 (GRCm39) |
V295E |
probably damaging |
Het |
Ttll6 |
A |
G |
11: 96,045,672 (GRCm39) |
T630A |
probably benign |
Het |
Usp9y |
G |
T |
Y: 1,432,180 (GRCm39) |
A435E |
probably benign |
Het |
Vil1 |
A |
C |
1: 74,459,058 (GRCm39) |
R187S |
probably damaging |
Het |
Vmn2r31 |
A |
T |
7: 7,387,579 (GRCm39) |
V664E |
possibly damaging |
Het |
Wdr17 |
T |
C |
8: 55,114,371 (GRCm39) |
I693M |
probably benign |
Het |
Wdr82 |
C |
T |
9: 106,053,865 (GRCm39) |
T72I |
probably damaging |
Het |
Zbtb5 |
A |
G |
4: 44,994,905 (GRCm39) |
S160P |
probably benign |
Het |
Zfat |
G |
A |
15: 68,050,715 (GRCm39) |
Q769* |
probably null |
Het |
Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
Het |
Zfp937 |
T |
A |
2: 150,081,266 (GRCm39) |
I432K |
probably benign |
Het |
Zglp1 |
C |
T |
9: 20,973,903 (GRCm39) |
S261N |
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 |
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 |
|
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 |
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 |
|
|