Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
A |
T |
17: 9,226,838 (GRCm39) |
Q464H |
probably damaging |
Het |
Abcc5 |
A |
T |
16: 20,224,260 (GRCm39) |
S108T |
probably damaging |
Het |
Acss3 |
T |
C |
10: 106,959,174 (GRCm39) |
S91G |
probably benign |
Het |
Adgrf4 |
T |
A |
17: 42,978,333 (GRCm39) |
I337L |
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,581,648 (GRCm39) |
S4799P |
probably benign |
Het |
Adgrv1 |
T |
C |
13: 81,727,596 (GRCm39) |
D348G |
probably damaging |
Het |
Afdn |
A |
G |
17: 14,109,070 (GRCm39) |
D1546G |
probably benign |
Het |
Agr2 |
A |
T |
12: 36,045,946 (GRCm39) |
R64S |
probably benign |
Het |
Ankrd13a |
T |
A |
5: 114,927,545 (GRCm39) |
|
probably null |
Het |
Apon |
T |
A |
10: 128,090,922 (GRCm39) |
M200K |
possibly damaging |
Het |
Art4 |
T |
C |
6: 136,831,428 (GRCm39) |
S238G |
possibly damaging |
Het |
Atp2a2 |
A |
T |
5: 122,629,847 (GRCm39) |
V74D |
probably benign |
Het |
Atrnl1 |
T |
C |
19: 57,687,955 (GRCm39) |
S807P |
probably damaging |
Het |
C2cd3 |
T |
C |
7: 100,080,022 (GRCm39) |
V936A |
|
Het |
Car15 |
T |
A |
16: 17,654,652 (GRCm39) |
H122L |
probably damaging |
Het |
Cav3 |
A |
T |
6: 112,449,428 (GRCm39) |
R149W |
probably benign |
Het |
Ccdc8 |
A |
T |
7: 16,728,687 (GRCm39) |
I59F |
probably damaging |
Het |
Ccng2 |
G |
A |
5: 93,418,731 (GRCm39) |
V119I |
probably benign |
Het |
Ceacam2 |
A |
G |
7: 25,227,333 (GRCm39) |
I178T |
probably benign |
Het |
Ces2a |
A |
G |
8: 105,467,930 (GRCm39) |
D520G |
probably benign |
Het |
Cln8 |
T |
C |
8: 14,945,057 (GRCm39) |
S124P |
probably benign |
Het |
Coro2a |
T |
A |
4: 46,546,674 (GRCm39) |
D227V |
probably damaging |
Het |
Cpa4 |
A |
C |
6: 30,573,889 (GRCm39) |
R32S |
probably benign |
Het |
Creb3l4 |
G |
T |
3: 90,149,729 (GRCm39) |
D45E |
probably benign |
Het |
Crybb2 |
C |
T |
5: 113,213,759 (GRCm39) |
|
probably null |
Het |
Cul7 |
T |
A |
17: 46,965,521 (GRCm39) |
H566Q |
probably benign |
Het |
Cyp2b10 |
A |
G |
7: 25,614,204 (GRCm39) |
Y226C |
probably damaging |
Het |
Dennd2a |
A |
T |
6: 39,499,743 (GRCm39) |
V274D |
probably benign |
Het |
Drc7 |
T |
C |
8: 95,794,684 (GRCm39) |
I363T |
probably benign |
Het |
Drd3 |
G |
A |
16: 43,643,047 (GRCm39) |
V396I |
probably benign |
Het |
Dync2i1 |
A |
T |
12: 116,218,130 (GRCm39) |
|
probably null |
Het |
Eif2ak4 |
A |
G |
2: 118,280,795 (GRCm39) |
N1054S |
probably benign |
Het |
Epc1 |
A |
C |
18: 6,450,084 (GRCm39) |
V458G |
probably damaging |
Het |
Exoc1 |
T |
A |
5: 76,685,562 (GRCm39) |
D91E |
probably damaging |
Het |
Fat4 |
T |
A |
3: 38,943,485 (GRCm39) |
F793I |
probably damaging |
Het |
Fhod1 |
T |
C |
8: 106,074,469 (GRCm39) |
E6G |
unknown |
Het |
Galnt16 |
G |
A |
12: 80,628,084 (GRCm39) |
|
probably null |
Het |
Ganc |
A |
T |
2: 120,286,582 (GRCm39) |
T804S |
probably benign |
Het |
Gpam |
A |
T |
19: 55,070,062 (GRCm39) |
V398E |
possibly damaging |
Het |
Gpr68 |
A |
G |
12: 100,844,623 (GRCm39) |
V307A |
probably benign |
Het |
Grm7 |
C |
T |
6: 111,335,722 (GRCm39) |
S711L |
probably damaging |
Het |
Hemgn |
T |
A |
4: 46,397,034 (GRCm39) |
R67S |
probably damaging |
Het |
Hmg20b |
T |
C |
10: 81,182,493 (GRCm39) |
D281G |
possibly damaging |
Het |
Ifi211 |
A |
C |
1: 173,729,401 (GRCm39) |
F277V |
probably damaging |
Het |
Ighmbp2 |
T |
C |
19: 3,322,981 (GRCm39) |
I322V |
probably benign |
Het |
Iqce |
A |
T |
5: 140,671,830 (GRCm39) |
L265H |
probably damaging |
Het |
Itgal |
G |
T |
7: 126,898,960 (GRCm39) |
A101S |
probably benign |
Het |
Kif5a |
C |
T |
10: 127,073,248 (GRCm39) |
M647I |
probably benign |
Het |
Kirrel1 |
G |
T |
3: 87,002,988 (GRCm39) |
T135K |
probably damaging |
Het |
Klf16 |
T |
C |
10: 80,412,622 (GRCm39) |
Y138C |
probably benign |
Het |
Klhl7 |
A |
G |
5: 24,331,844 (GRCm39) |
T49A |
probably benign |
Het |
Mr1 |
T |
C |
1: 155,022,474 (GRCm39) |
|
probably benign |
Het |
Mrc1 |
A |
T |
2: 14,330,104 (GRCm39) |
I1238F |
probably damaging |
Het |
Ncoa5 |
C |
T |
2: 164,846,171 (GRCm39) |
M225I |
possibly damaging |
Het |
Nf1 |
A |
T |
11: 79,438,052 (GRCm39) |
T121S |
probably damaging |
Het |
Ngfr |
T |
C |
11: 95,465,147 (GRCm39) |
T234A |
probably benign |
Het |
Ninj1 |
T |
G |
13: 49,347,356 (GRCm39) |
F74V |
probably damaging |
Het |
Npffr1 |
T |
C |
10: 61,462,088 (GRCm39) |
V408A |
probably benign |
Het |
Nsd2 |
T |
C |
5: 34,003,570 (GRCm39) |
V240A |
probably damaging |
Het |
Obi1 |
T |
C |
14: 104,716,814 (GRCm39) |
T520A |
probably damaging |
Het |
Or12d13 |
T |
A |
17: 37,648,062 (GRCm39) |
E20D |
probably benign |
Het |
Or2z2 |
A |
G |
11: 58,345,992 (GRCm39) |
M261T |
probably damaging |
Het |
Or7a35 |
T |
A |
10: 78,853,379 (GRCm39) |
F74L |
probably benign |
Het |
Or8b44 |
G |
A |
9: 38,410,369 (GRCm39) |
V135I |
probably benign |
Het |
Or8g34 |
T |
C |
9: 39,373,173 (GRCm39) |
S146P |
possibly damaging |
Het |
Ovol1 |
T |
C |
19: 5,601,614 (GRCm39) |
H136R |
probably damaging |
Het |
Prag1 |
T |
A |
8: 36,569,760 (GRCm39) |
D114E |
possibly damaging |
Het |
Pramel17 |
T |
C |
4: 101,694,331 (GRCm39) |
N184S |
probably benign |
Het |
Prss3b |
C |
A |
6: 41,010,127 (GRCm39) |
R69L |
probably benign |
Het |
Prss57 |
T |
A |
10: 79,623,234 (GRCm39) |
H71L |
probably benign |
Het |
Ptgs2 |
T |
C |
1: 149,978,448 (GRCm39) |
F187L |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 22,959,779 (GRCm39) |
N92I |
probably damaging |
Het |
Rab23 |
A |
T |
1: 33,773,812 (GRCm39) |
T91S |
possibly damaging |
Het |
Rag1 |
A |
G |
2: 101,474,006 (GRCm39) |
S379P |
probably damaging |
Het |
Ribc2 |
G |
T |
15: 85,027,448 (GRCm39) |
D310Y |
probably damaging |
Het |
Rims1 |
A |
G |
1: 22,507,291 (GRCm39) |
Y620H |
probably damaging |
Het |
Rock1 |
A |
C |
18: 10,090,820 (GRCm39) |
V938G |
probably benign |
Het |
Rsph10b |
A |
G |
5: 143,886,244 (GRCm39) |
N314S |
possibly damaging |
Het |
Sertad1 |
A |
G |
7: 27,189,327 (GRCm39) |
D216G |
possibly damaging |
Het |
Shisal1 |
G |
A |
15: 84,290,914 (GRCm39) |
T131M |
probably benign |
Het |
Slco6d1 |
T |
A |
1: 98,425,252 (GRCm39) |
V600D |
probably damaging |
Het |
Snapc2 |
T |
C |
8: 4,305,314 (GRCm39) |
I232T |
probably damaging |
Het |
Snx13 |
A |
G |
12: 35,136,913 (GRCm39) |
S125G |
probably damaging |
Het |
Srcin1 |
C |
T |
11: 97,425,551 (GRCm39) |
R502H |
probably damaging |
Het |
Tesmin |
A |
G |
19: 3,442,218 (GRCm39) |
E167G |
possibly damaging |
Het |
Tex10 |
T |
C |
4: 48,468,787 (GRCm39) |
I129M |
possibly damaging |
Het |
Tmem235 |
A |
G |
11: 117,754,967 (GRCm39) |
S140G |
probably benign |
Het |
Trim60 |
T |
A |
8: 65,454,177 (GRCm39) |
D24V |
probably damaging |
Het |
Ttc39c |
A |
G |
18: 12,822,936 (GRCm39) |
E148G |
probably benign |
Het |
Vmn2r70 |
G |
T |
7: 85,214,243 (GRCm39) |
T303K |
probably benign |
Het |
Wdr48 |
A |
T |
9: 119,745,894 (GRCm39) |
T426S |
possibly damaging |
Het |
Xirp2 |
A |
T |
2: 67,346,326 (GRCm39) |
T2856S |
probably benign |
Het |
Zswim8 |
A |
G |
14: 20,770,001 (GRCm39) |
N1356S |
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 |
|
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 |
|
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 |
|
|