Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610318N02Rik |
A |
G |
16: 16,939,260 (GRCm39) |
L41P |
probably damaging |
Het |
Aff4 |
C |
T |
11: 53,290,446 (GRCm39) |
L469F |
probably damaging |
Het |
AI182371 |
G |
A |
2: 34,975,366 (GRCm39) |
H288Y |
probably benign |
Het |
AK157302 |
A |
T |
13: 21,679,827 (GRCm39) |
K118* |
probably null |
Het |
Arhgef2 |
G |
A |
3: 88,543,351 (GRCm39) |
R454Q |
probably damaging |
Het |
Asb17 |
C |
T |
3: 153,550,322 (GRCm39) |
T118M |
probably damaging |
Het |
Atp7b |
A |
G |
8: 22,503,600 (GRCm39) |
V718A |
possibly damaging |
Het |
Cdca2 |
A |
G |
14: 67,952,287 (GRCm39) |
L28S |
probably damaging |
Het |
Cdh20 |
G |
T |
1: 109,976,594 (GRCm39) |
L86F |
probably damaging |
Het |
Cela2a |
A |
T |
4: 141,545,350 (GRCm39) |
|
probably null |
Het |
Cers3 |
T |
A |
7: 66,433,162 (GRCm39) |
Y160N |
probably damaging |
Het |
Chmp2b |
A |
G |
16: 65,343,877 (GRCm39) |
V56A |
probably benign |
Het |
Cryl1 |
A |
G |
14: 57,635,880 (GRCm39) |
V9A |
unknown |
Het |
Dnm1 |
C |
T |
2: 32,204,949 (GRCm39) |
V673M |
probably damaging |
Het |
Dtx4 |
T |
A |
19: 12,462,646 (GRCm39) |
K378* |
probably null |
Het |
Extl1 |
A |
T |
4: 134,090,491 (GRCm39) |
M328K |
possibly damaging |
Het |
Fcgbp |
T |
C |
7: 27,806,628 (GRCm39) |
S2199P |
probably benign |
Het |
Glis3 |
G |
T |
19: 28,508,702 (GRCm39) |
N427K |
probably benign |
Het |
Hdac7 |
T |
C |
15: 97,691,944 (GRCm39) |
K810E |
probably benign |
Het |
Hesx1 |
A |
G |
14: 26,723,434 (GRCm39) |
E88G |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,350,361 (GRCm39) |
Q5086L |
possibly damaging |
Het |
Ier3 |
A |
G |
17: 36,133,101 (GRCm39) |
T128A |
probably benign |
Het |
Igsf10 |
G |
T |
3: 59,239,101 (GRCm39) |
T360K |
probably damaging |
Het |
Ilkap |
A |
C |
1: 91,312,345 (GRCm39) |
C2G |
possibly damaging |
Het |
Itih1 |
A |
G |
14: 30,660,028 (GRCm39) |
F231S |
probably damaging |
Het |
Jrkl |
A |
T |
9: 13,244,913 (GRCm39) |
Y249* |
probably null |
Het |
Kat6a |
AGAGGAGGAGGAGGAGGAGGAGGAG |
AGAGGAGGAGGAGGAGGAGGAG |
8: 23,425,663 (GRCm39) |
|
probably benign |
Het |
Katnal2 |
A |
T |
18: 77,098,637 (GRCm39) |
S184R |
probably benign |
Het |
Kcnh5 |
T |
A |
12: 74,945,230 (GRCm39) |
|
probably null |
Het |
Kcnj11 |
G |
T |
7: 45,748,781 (GRCm39) |
L181I |
probably damaging |
Het |
Klhl2 |
T |
C |
8: 65,202,804 (GRCm39) |
T465A |
probably benign |
Het |
Krt90 |
T |
A |
15: 101,471,046 (GRCm39) |
Y72F |
probably benign |
Het |
Lig4 |
G |
A |
8: 10,022,766 (GRCm39) |
T338I |
probably benign |
Het |
Lrrc37 |
T |
C |
11: 103,511,285 (GRCm39) |
T228A |
unknown |
Het |
Magel2 |
T |
C |
7: 62,030,540 (GRCm39) |
V1148A |
unknown |
Het |
Mak |
C |
A |
13: 41,186,020 (GRCm39) |
E549D |
probably benign |
Het |
Marf1 |
G |
T |
16: 13,950,293 (GRCm39) |
S1001Y |
probably damaging |
Het |
Mcoln1 |
G |
A |
8: 3,561,787 (GRCm39) |
V446I |
probably damaging |
Het |
Meig1 |
T |
C |
2: 3,410,290 (GRCm39) |
N70S |
probably benign |
Het |
Mfsd14a |
G |
A |
3: 116,441,479 (GRCm39) |
T108I |
probably damaging |
Het |
Mocs1 |
G |
A |
17: 49,761,386 (GRCm39) |
M493I |
probably damaging |
Het |
Mrpl11 |
C |
A |
19: 5,012,497 (GRCm39) |
A26E |
probably damaging |
Het |
Myh6 |
A |
T |
14: 55,191,251 (GRCm39) |
D863E |
probably benign |
Het |
Myom2 |
T |
A |
8: 15,134,555 (GRCm39) |
Y453N |
probably damaging |
Het |
Nhlh1 |
A |
G |
1: 171,881,524 (GRCm39) |
I114T |
probably damaging |
Het |
Odr4 |
A |
G |
1: 150,258,086 (GRCm39) |
V183A |
possibly damaging |
Het |
Or12j4 |
A |
C |
7: 140,046,504 (GRCm39) |
H130P |
probably benign |
Het |
Or2y3 |
G |
T |
17: 38,393,071 (GRCm39) |
P266Q |
probably damaging |
Het |
Or4k5 |
A |
T |
14: 50,386,154 (GRCm39) |
M59K |
probably damaging |
Het |
Or5k17 |
G |
T |
16: 58,746,486 (GRCm39) |
F149L |
probably benign |
Het |
Or5p80 |
C |
G |
7: 108,229,984 (GRCm39) |
P262A |
probably damaging |
Het |
Pclo |
T |
C |
5: 14,764,309 (GRCm39) |
S976P |
probably benign |
Het |
Pde3a |
G |
A |
6: 141,429,640 (GRCm39) |
E734K |
possibly damaging |
Het |
Pdzd2 |
A |
T |
15: 12,375,879 (GRCm39) |
S1419T |
probably benign |
Het |
Pdzd8 |
T |
A |
19: 59,288,853 (GRCm39) |
Y849F |
probably damaging |
Het |
Phldb3 |
A |
G |
7: 24,312,070 (GRCm39) |
E128G |
probably damaging |
Het |
Polg |
A |
G |
7: 79,111,468 (GRCm39) |
I261T |
possibly damaging |
Het |
Ppp1r35 |
T |
C |
5: 137,778,267 (GRCm39) |
M254T |
probably benign |
Het |
Ppp3ca |
G |
T |
3: 136,596,211 (GRCm39) |
R292M |
possibly damaging |
Het |
Ptk7 |
T |
A |
17: 46,890,543 (GRCm39) |
T430S |
probably benign |
Het |
Ptrh1 |
T |
A |
2: 32,667,040 (GRCm39) |
N144K |
possibly damaging |
Het |
Rbfox1 |
A |
G |
16: 7,111,946 (GRCm39) |
T211A |
possibly damaging |
Het |
Rbpjl |
A |
G |
2: 164,256,343 (GRCm39) |
D443G |
possibly damaging |
Het |
Rcc1 |
A |
G |
4: 132,065,360 (GRCm39) |
|
probably null |
Het |
Rimbp2 |
G |
T |
5: 128,865,229 (GRCm39) |
S706R |
probably damaging |
Het |
Rsph10b |
G |
C |
5: 143,898,074 (GRCm39) |
E96D |
probably benign |
Het |
Scn10a |
A |
T |
9: 119,438,514 (GRCm39) |
I1784K |
probably benign |
Het |
Sfxn2 |
A |
G |
19: 46,579,985 (GRCm39) |
|
probably null |
Het |
Slamf6 |
T |
A |
1: 171,765,575 (GRCm39) |
L233Q |
probably damaging |
Het |
Slc17a5 |
A |
T |
9: 78,484,455 (GRCm39) |
Y102N |
probably damaging |
Het |
Slc25a53 |
T |
C |
X: 135,884,216 (GRCm39) |
T42A |
probably damaging |
Het |
Slco1a8 |
T |
C |
6: 141,926,670 (GRCm39) |
D552G |
probably damaging |
Het |
Smg7 |
G |
A |
1: 152,716,064 (GRCm39) |
T1057I |
possibly damaging |
Het |
Speer2 |
T |
A |
16: 69,657,485 (GRCm39) |
T53S |
possibly damaging |
Het |
Srm |
A |
C |
4: 148,676,948 (GRCm39) |
I100L |
probably benign |
Het |
Stoml3 |
A |
C |
3: 53,415,008 (GRCm39) |
N267H |
probably damaging |
Het |
Thsd7a |
A |
C |
6: 12,379,632 (GRCm39) |
C931G |
probably damaging |
Het |
Tlr11 |
A |
G |
14: 50,598,139 (GRCm39) |
I42V |
probably benign |
Het |
Tmigd1 |
T |
C |
11: 76,800,999 (GRCm39) |
V162A |
probably benign |
Het |
Tmx3 |
A |
G |
18: 90,528,505 (GRCm39) |
|
probably null |
Het |
Topors |
T |
A |
4: 40,262,790 (GRCm39) |
R165W |
possibly damaging |
Het |
Ttc17 |
A |
T |
2: 94,196,987 (GRCm39) |
S453R |
possibly damaging |
Het |
Vmn1r49 |
G |
T |
6: 90,049,441 (GRCm39) |
T187N |
probably damaging |
Het |
Zbtb49 |
A |
T |
5: 38,371,464 (GRCm39) |
V139E |
possibly damaging |
Het |
Zfp11 |
T |
C |
5: 129,734,216 (GRCm39) |
H415R |
probably damaging |
Het |
Zfp677 |
A |
T |
17: 21,617,970 (GRCm39) |
K342N |
probably benign |
Het |
Zfp979 |
A |
C |
4: 147,697,915 (GRCm39) |
C265G |
possibly damaging |
Het |
Zfpl1 |
T |
C |
19: 6,134,459 (GRCm39) |
R9G |
probably damaging |
Het |
Zkscan8 |
A |
T |
13: 21,704,759 (GRCm39) |
C321* |
probably null |
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 |
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 |
|
|