Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
A |
T |
5: 114,338,625 (GRCm39) |
R778S |
probably damaging |
Het |
Adam17 |
A |
G |
12: 21,382,161 (GRCm39) |
C567R |
probably damaging |
Het |
Ankrd28 |
G |
A |
14: 31,432,825 (GRCm39) |
A758V |
probably damaging |
Het |
Atrn |
T |
C |
2: 130,775,349 (GRCm39) |
Y151H |
probably damaging |
Het |
B3gat3 |
A |
G |
19: 8,902,996 (GRCm39) |
T118A |
possibly damaging |
Het |
Camta1 |
A |
G |
4: 151,228,367 (GRCm39) |
C822R |
probably damaging |
Het |
Capn15 |
G |
T |
17: 26,179,742 (GRCm39) |
Q807K |
probably benign |
Het |
Clec12a |
T |
C |
6: 129,331,493 (GRCm39) |
Y145H |
probably damaging |
Het |
Clk1 |
T |
C |
1: 58,452,146 (GRCm39) |
I393V |
probably benign |
Het |
Cpm |
A |
G |
10: 117,503,956 (GRCm39) |
I121V |
probably benign |
Het |
Cux1 |
A |
G |
5: 136,279,448 (GRCm39) |
I405T |
possibly damaging |
Het |
Dnah3 |
A |
G |
7: 119,549,874 (GRCm39) |
S3471P |
probably damaging |
Het |
Dok6 |
A |
G |
18: 89,491,971 (GRCm39) |
|
probably benign |
Het |
Eif4g1 |
A |
T |
16: 20,504,684 (GRCm39) |
D1124V |
possibly damaging |
Het |
Eif4g3 |
A |
G |
4: 137,933,443 (GRCm39) |
E1756G |
probably damaging |
Het |
Exo5 |
A |
G |
4: 120,779,748 (GRCm39) |
V39A |
probably benign |
Het |
Fmnl1 |
A |
T |
11: 103,088,520 (GRCm39) |
I90F |
probably damaging |
Het |
Fryl |
G |
T |
5: 73,238,396 (GRCm39) |
T1450K |
probably damaging |
Het |
Gde1 |
T |
C |
7: 118,293,751 (GRCm39) |
M91V |
probably benign |
Het |
Gimd1 |
T |
C |
3: 132,350,343 (GRCm39) |
I84T |
probably damaging |
Het |
Gm13889 |
C |
T |
2: 93,787,453 (GRCm39) |
|
probably benign |
Het |
Gm6445 |
T |
A |
19: 9,585,561 (GRCm39) |
|
noncoding transcript |
Het |
Gm8113 |
T |
C |
14: 44,169,867 (GRCm39) |
S483P |
probably damaging |
Het |
Grik2 |
T |
C |
10: 49,399,888 (GRCm39) |
I281V |
possibly damaging |
Het |
Grik5 |
T |
C |
7: 24,760,152 (GRCm39) |
|
probably benign |
Het |
Herc1 |
A |
T |
9: 66,386,773 (GRCm39) |
I3796F |
possibly damaging |
Het |
Hoxb13 |
A |
T |
11: 96,085,309 (GRCm39) |
D14V |
probably benign |
Het |
Hspg2 |
A |
G |
4: 137,261,041 (GRCm39) |
Y1645C |
probably damaging |
Het |
Igkv8-16 |
G |
T |
6: 70,363,762 (GRCm39) |
R87S |
probably damaging |
Het |
Ints1 |
A |
T |
5: 139,760,054 (GRCm39) |
V140E |
possibly damaging |
Het |
Kbtbd11 |
C |
A |
8: 15,078,917 (GRCm39) |
D505E |
possibly damaging |
Het |
Kcnu1 |
G |
A |
8: 26,427,583 (GRCm39) |
C300Y |
probably damaging |
Het |
Kmt2d |
G |
C |
15: 98,750,410 (GRCm39) |
|
probably benign |
Het |
Lats1 |
T |
C |
10: 7,578,493 (GRCm39) |
V539A |
probably benign |
Het |
Lipo5 |
C |
T |
19: 33,441,922 (GRCm39) |
G200D |
unknown |
Het |
Lmo7 |
C |
A |
14: 102,124,393 (GRCm39) |
A284D |
probably damaging |
Het |
Lyst |
G |
A |
13: 13,809,968 (GRCm39) |
R546H |
probably damaging |
Het |
Mcpt8 |
T |
C |
14: 56,321,285 (GRCm39) |
M60V |
possibly damaging |
Het |
Mdn1 |
A |
G |
4: 32,730,749 (GRCm39) |
|
probably null |
Het |
Mphosph10 |
A |
G |
7: 64,038,722 (GRCm39) |
|
probably null |
Het |
Muc5b |
G |
A |
7: 141,395,135 (GRCm39) |
S47N |
unknown |
Het |
Notch3 |
A |
T |
17: 32,373,737 (GRCm39) |
N490K |
probably damaging |
Het |
Nr1d1 |
G |
A |
11: 98,662,738 (GRCm39) |
S85L |
possibly damaging |
Het |
Obscn |
T |
A |
11: 58,945,114 (GRCm39) |
R4635* |
probably null |
Het |
Or10al5 |
G |
T |
17: 38,063,054 (GRCm39) |
C103F |
probably damaging |
Het |
Or13f5 |
T |
C |
4: 52,826,240 (GRCm39) |
L281P |
probably damaging |
Het |
Or9i16 |
T |
C |
19: 13,864,912 (GRCm39) |
I221V |
probably benign |
Het |
Pappa |
G |
A |
4: 65,233,033 (GRCm39) |
|
probably null |
Het |
Pcdhb17 |
G |
A |
18: 37,619,652 (GRCm39) |
G481S |
probably damaging |
Het |
Pde1a |
TCC |
TC |
2: 79,728,525 (GRCm39) |
|
probably benign |
Het |
Phf3 |
A |
T |
1: 30,902,169 (GRCm39) |
M48K |
probably damaging |
Het |
Pira2 |
A |
T |
7: 3,843,933 (GRCm39) |
V613E |
probably damaging |
Het |
Poc1a |
T |
C |
9: 106,226,887 (GRCm39) |
S327P |
possibly damaging |
Het |
Ptpn9 |
A |
G |
9: 56,927,321 (GRCm39) |
H66R |
probably benign |
Het |
Rabgap1 |
C |
T |
2: 37,377,561 (GRCm39) |
R353* |
probably null |
Het |
Rcc1l |
G |
T |
5: 134,200,729 (GRCm39) |
N134K |
probably damaging |
Het |
Rims1 |
G |
A |
1: 22,497,793 (GRCm39) |
T787I |
probably damaging |
Het |
Rreb1 |
T |
G |
13: 38,132,777 (GRCm39) |
S1651A |
probably damaging |
Het |
Rsl1d1 |
T |
C |
16: 11,019,238 (GRCm39) |
D100G |
probably damaging |
Het |
Samd4 |
C |
T |
14: 47,301,703 (GRCm39) |
R147C |
probably damaging |
Het |
Serpinb6e |
T |
C |
13: 34,025,299 (GRCm39) |
|
probably benign |
Het |
Ska1 |
T |
C |
18: 74,330,111 (GRCm39) |
I210V |
probably benign |
Het |
Slc17a1 |
A |
G |
13: 24,062,543 (GRCm39) |
I237V |
probably benign |
Het |
Slc22a4 |
A |
T |
11: 53,888,336 (GRCm39) |
S231T |
probably benign |
Het |
Slc7a4 |
T |
A |
16: 17,393,797 (GRCm39) |
M66L |
probably damaging |
Het |
Snapc1 |
A |
G |
12: 74,030,642 (GRCm39) |
T381A |
possibly damaging |
Het |
St6galnac2 |
C |
T |
11: 116,575,351 (GRCm39) |
|
probably benign |
Het |
Taar2 |
C |
T |
10: 23,817,401 (GRCm39) |
L314F |
probably benign |
Het |
Tmem74b |
A |
G |
2: 151,548,561 (GRCm39) |
D96G |
probably damaging |
Het |
Tnfrsf17 |
T |
C |
16: 11,131,833 (GRCm39) |
F6S |
probably benign |
Het |
Tpp2 |
G |
T |
1: 43,993,870 (GRCm39) |
G252W |
probably damaging |
Het |
Trf |
A |
G |
9: 103,100,807 (GRCm39) |
F209L |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,728,935 (GRCm39) |
|
probably benign |
Het |
Uhmk1 |
A |
T |
1: 170,034,774 (GRCm39) |
H311Q |
probably damaging |
Het |
Uqcrc2 |
A |
G |
7: 120,250,144 (GRCm39) |
Y253C |
probably damaging |
Het |
Vmn2r117 |
A |
G |
17: 23,697,390 (GRCm39) |
F101L |
probably benign |
Het |
Vmn2r43 |
T |
C |
7: 8,258,070 (GRCm39) |
N381S |
probably benign |
Het |
Zfp879 |
T |
A |
11: 50,724,024 (GRCm39) |
Y271F |
probably damaging |
Het |
|
Other mutations in Unc13c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00420:Unc13c
|
APN |
9 |
73,643,985 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00693:Unc13c
|
APN |
9 |
73,665,884 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01022:Unc13c
|
APN |
9 |
73,424,610 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01088:Unc13c
|
APN |
9 |
73,839,563 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01123:Unc13c
|
APN |
9 |
73,840,479 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01131:Unc13c
|
APN |
9 |
73,471,335 (GRCm39) |
missense |
probably benign |
|
IGL01135:Unc13c
|
APN |
9 |
73,392,175 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01393:Unc13c
|
APN |
9 |
73,447,552 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01752:Unc13c
|
APN |
9 |
73,839,093 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01893:Unc13c
|
APN |
9 |
73,600,648 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01897:Unc13c
|
APN |
9 |
73,453,309 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01936:Unc13c
|
APN |
9 |
73,600,524 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02122:Unc13c
|
APN |
9 |
73,641,679 (GRCm39) |
splice site |
probably benign |
|
IGL02341:Unc13c
|
APN |
9 |
73,840,492 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02434:Unc13c
|
APN |
9 |
73,839,910 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02545:Unc13c
|
APN |
9 |
73,388,357 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02709:Unc13c
|
APN |
9 |
73,466,238 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02815:Unc13c
|
APN |
9 |
73,447,545 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02904:Unc13c
|
APN |
9 |
73,388,349 (GRCm39) |
nonsense |
probably null |
|
IGL03117:Unc13c
|
APN |
9 |
73,441,307 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03260:Unc13c
|
APN |
9 |
73,838,626 (GRCm39) |
missense |
probably benign |
0.11 |
Feeling
|
UTSW |
9 |
73,600,553 (GRCm39) |
missense |
possibly damaging |
0.46 |
Inkling
|
UTSW |
9 |
73,839,126 (GRCm39) |
missense |
probably damaging |
1.00 |
notion
|
UTSW |
9 |
73,643,844 (GRCm39) |
missense |
probably damaging |
1.00 |
BB001:Unc13c
|
UTSW |
9 |
73,641,690 (GRCm39) |
missense |
probably benign |
0.05 |
BB011:Unc13c
|
UTSW |
9 |
73,641,690 (GRCm39) |
missense |
probably benign |
0.05 |
PIT4431001:Unc13c
|
UTSW |
9 |
73,656,829 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4651001:Unc13c
|
UTSW |
9 |
73,391,021 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0017:Unc13c
|
UTSW |
9 |
73,600,583 (GRCm39) |
missense |
probably benign |
0.07 |
R0039:Unc13c
|
UTSW |
9 |
73,576,847 (GRCm39) |
splice site |
probably benign |
|
R0164:Unc13c
|
UTSW |
9 |
73,602,174 (GRCm39) |
missense |
probably benign |
0.01 |
R0164:Unc13c
|
UTSW |
9 |
73,602,174 (GRCm39) |
missense |
probably benign |
0.01 |
R0308:Unc13c
|
UTSW |
9 |
73,388,400 (GRCm39) |
missense |
probably benign |
0.04 |
R0344:Unc13c
|
UTSW |
9 |
73,838,067 (GRCm39) |
missense |
probably benign |
0.39 |
R0421:Unc13c
|
UTSW |
9 |
73,840,492 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0606:Unc13c
|
UTSW |
9 |
73,438,265 (GRCm39) |
splice site |
probably benign |
|
R0655:Unc13c
|
UTSW |
9 |
73,838,235 (GRCm39) |
missense |
probably damaging |
0.96 |
R1013:Unc13c
|
UTSW |
9 |
73,840,614 (GRCm39) |
missense |
probably benign |
0.45 |
R1293:Unc13c
|
UTSW |
9 |
73,481,356 (GRCm39) |
missense |
probably benign |
0.06 |
R1493:Unc13c
|
UTSW |
9 |
73,546,350 (GRCm39) |
missense |
probably benign |
0.27 |
R1675:Unc13c
|
UTSW |
9 |
73,546,332 (GRCm39) |
critical splice donor site |
probably null |
|
R1789:Unc13c
|
UTSW |
9 |
73,663,621 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2001:Unc13c
|
UTSW |
9 |
73,390,897 (GRCm39) |
splice site |
probably null |
|
R2055:Unc13c
|
UTSW |
9 |
73,643,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Unc13c
|
UTSW |
9 |
73,572,938 (GRCm39) |
missense |
probably damaging |
0.99 |
R2420:Unc13c
|
UTSW |
9 |
73,838,829 (GRCm39) |
missense |
probably damaging |
0.97 |
R2421:Unc13c
|
UTSW |
9 |
73,838,829 (GRCm39) |
missense |
probably damaging |
0.97 |
R2422:Unc13c
|
UTSW |
9 |
73,838,829 (GRCm39) |
missense |
probably damaging |
0.97 |
R3415:Unc13c
|
UTSW |
9 |
73,839,868 (GRCm39) |
missense |
probably benign |
0.00 |
R3423:Unc13c
|
UTSW |
9 |
73,837,935 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3820:Unc13c
|
UTSW |
9 |
73,838,240 (GRCm39) |
missense |
probably benign |
0.00 |
R3857:Unc13c
|
UTSW |
9 |
73,606,390 (GRCm39) |
nonsense |
probably null |
|
R3859:Unc13c
|
UTSW |
9 |
73,606,390 (GRCm39) |
nonsense |
probably null |
|
R3895:Unc13c
|
UTSW |
9 |
73,840,805 (GRCm39) |
missense |
probably benign |
|
R4038:Unc13c
|
UTSW |
9 |
73,441,188 (GRCm39) |
critical splice donor site |
probably null |
|
R4077:Unc13c
|
UTSW |
9 |
73,643,821 (GRCm39) |
nonsense |
probably null |
|
R4125:Unc13c
|
UTSW |
9 |
73,481,289 (GRCm39) |
critical splice donor site |
probably null |
|
R4128:Unc13c
|
UTSW |
9 |
73,641,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R4235:Unc13c
|
UTSW |
9 |
73,438,234 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4295:Unc13c
|
UTSW |
9 |
73,641,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R4307:Unc13c
|
UTSW |
9 |
73,600,649 (GRCm39) |
missense |
probably benign |
0.06 |
R4694:Unc13c
|
UTSW |
9 |
73,479,636 (GRCm39) |
missense |
probably benign |
0.00 |
R4735:Unc13c
|
UTSW |
9 |
73,600,620 (GRCm39) |
missense |
probably benign |
0.00 |
R4744:Unc13c
|
UTSW |
9 |
73,839,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Unc13c
|
UTSW |
9 |
73,839,469 (GRCm39) |
missense |
probably damaging |
0.97 |
R4827:Unc13c
|
UTSW |
9 |
73,838,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R4838:Unc13c
|
UTSW |
9 |
73,839,354 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4869:Unc13c
|
UTSW |
9 |
73,587,716 (GRCm39) |
missense |
probably benign |
0.02 |
R4873:Unc13c
|
UTSW |
9 |
73,424,566 (GRCm39) |
missense |
probably damaging |
0.98 |
R4875:Unc13c
|
UTSW |
9 |
73,424,566 (GRCm39) |
missense |
probably damaging |
0.98 |
R4876:Unc13c
|
UTSW |
9 |
73,656,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R4905:Unc13c
|
UTSW |
9 |
73,587,674 (GRCm39) |
missense |
probably benign |
|
R4912:Unc13c
|
UTSW |
9 |
73,481,304 (GRCm39) |
missense |
probably damaging |
0.99 |
R5026:Unc13c
|
UTSW |
9 |
73,838,185 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5127:Unc13c
|
UTSW |
9 |
73,840,654 (GRCm39) |
missense |
probably benign |
0.26 |
R5151:Unc13c
|
UTSW |
9 |
73,838,757 (GRCm39) |
missense |
probably benign |
0.02 |
R5171:Unc13c
|
UTSW |
9 |
73,665,236 (GRCm39) |
missense |
probably benign |
|
R5244:Unc13c
|
UTSW |
9 |
73,433,233 (GRCm39) |
critical splice donor site |
probably null |
|
R5342:Unc13c
|
UTSW |
9 |
73,838,105 (GRCm39) |
missense |
probably benign |
0.00 |
R5399:Unc13c
|
UTSW |
9 |
73,656,970 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5409:Unc13c
|
UTSW |
9 |
73,485,672 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5460:Unc13c
|
UTSW |
9 |
73,453,271 (GRCm39) |
missense |
probably benign |
|
R5680:Unc13c
|
UTSW |
9 |
73,839,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R5681:Unc13c
|
UTSW |
9 |
73,453,357 (GRCm39) |
splice site |
probably null |
|
R5728:Unc13c
|
UTSW |
9 |
73,466,238 (GRCm39) |
missense |
probably benign |
0.01 |
R5762:Unc13c
|
UTSW |
9 |
73,719,649 (GRCm39) |
missense |
probably benign |
0.00 |
R5764:Unc13c
|
UTSW |
9 |
73,441,185 (GRCm39) |
splice site |
probably null |
|
R5829:Unc13c
|
UTSW |
9 |
73,600,650 (GRCm39) |
missense |
probably benign |
0.15 |
R5894:Unc13c
|
UTSW |
9 |
73,600,486 (GRCm39) |
critical splice donor site |
probably null |
|
R5936:Unc13c
|
UTSW |
9 |
73,485,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R6043:Unc13c
|
UTSW |
9 |
73,643,933 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6046:Unc13c
|
UTSW |
9 |
73,838,166 (GRCm39) |
missense |
probably benign |
|
R6148:Unc13c
|
UTSW |
9 |
73,600,648 (GRCm39) |
missense |
probably benign |
0.15 |
R6207:Unc13c
|
UTSW |
9 |
73,665,910 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6277:Unc13c
|
UTSW |
9 |
73,606,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R6338:Unc13c
|
UTSW |
9 |
73,641,729 (GRCm39) |
missense |
probably damaging |
0.99 |
R6615:Unc13c
|
UTSW |
9 |
73,837,890 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6978:Unc13c
|
UTSW |
9 |
73,839,259 (GRCm39) |
missense |
probably benign |
0.39 |
R7053:Unc13c
|
UTSW |
9 |
73,839,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R7223:Unc13c
|
UTSW |
9 |
73,536,473 (GRCm39) |
missense |
probably benign |
0.44 |
R7259:Unc13c
|
UTSW |
9 |
73,424,645 (GRCm39) |
missense |
probably benign |
0.00 |
R7353:Unc13c
|
UTSW |
9 |
73,481,355 (GRCm39) |
missense |
probably benign |
0.00 |
R7357:Unc13c
|
UTSW |
9 |
73,840,811 (GRCm39) |
small insertion |
probably benign |
|
R7357:Unc13c
|
UTSW |
9 |
73,840,810 (GRCm39) |
small insertion |
probably benign |
|
R7607:Unc13c
|
UTSW |
9 |
73,576,817 (GRCm39) |
missense |
probably damaging |
0.98 |
R7626:Unc13c
|
UTSW |
9 |
73,641,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R7639:Unc13c
|
UTSW |
9 |
73,840,450 (GRCm39) |
missense |
probably damaging |
0.99 |
R7657:Unc13c
|
UTSW |
9 |
73,441,185 (GRCm39) |
splice site |
probably null |
|
R7665:Unc13c
|
UTSW |
9 |
73,587,756 (GRCm39) |
missense |
probably benign |
0.28 |
R7704:Unc13c
|
UTSW |
9 |
73,606,494 (GRCm39) |
missense |
probably benign |
0.27 |
R7776:Unc13c
|
UTSW |
9 |
73,602,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R7811:Unc13c
|
UTSW |
9 |
73,600,553 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7833:Unc13c
|
UTSW |
9 |
73,388,391 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7839:Unc13c
|
UTSW |
9 |
73,840,596 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7869:Unc13c
|
UTSW |
9 |
73,602,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R7924:Unc13c
|
UTSW |
9 |
73,641,690 (GRCm39) |
missense |
probably benign |
0.05 |
R8047:Unc13c
|
UTSW |
9 |
73,719,636 (GRCm39) |
nonsense |
probably null |
|
R8167:Unc13c
|
UTSW |
9 |
73,643,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R8202:Unc13c
|
UTSW |
9 |
73,643,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R8210:Unc13c
|
UTSW |
9 |
73,392,220 (GRCm39) |
missense |
probably benign |
0.13 |
R8352:Unc13c
|
UTSW |
9 |
73,838,290 (GRCm39) |
missense |
probably damaging |
0.99 |
R8368:Unc13c
|
UTSW |
9 |
73,838,070 (GRCm39) |
missense |
probably benign |
0.15 |
R8452:Unc13c
|
UTSW |
9 |
73,838,290 (GRCm39) |
missense |
probably damaging |
0.99 |
R8535:Unc13c
|
UTSW |
9 |
73,447,653 (GRCm39) |
missense |
probably benign |
|
R8677:Unc13c
|
UTSW |
9 |
73,840,243 (GRCm39) |
missense |
probably benign |
0.00 |
R8700:Unc13c
|
UTSW |
9 |
73,479,679 (GRCm39) |
missense |
probably benign |
0.44 |
R8848:Unc13c
|
UTSW |
9 |
73,433,263 (GRCm39) |
missense |
probably benign |
|
R8902:Unc13c
|
UTSW |
9 |
73,656,830 (GRCm39) |
missense |
probably damaging |
0.97 |
R8953:Unc13c
|
UTSW |
9 |
73,840,044 (GRCm39) |
missense |
probably benign |
0.00 |
R8961:Unc13c
|
UTSW |
9 |
73,839,524 (GRCm39) |
missense |
probably benign |
0.06 |
R9015:Unc13c
|
UTSW |
9 |
73,453,322 (GRCm39) |
missense |
probably benign |
|
R9114:Unc13c
|
UTSW |
9 |
73,719,665 (GRCm39) |
missense |
probably benign |
0.02 |
R9217:Unc13c
|
UTSW |
9 |
73,485,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R9252:Unc13c
|
UTSW |
9 |
73,424,553 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9273:Unc13c
|
UTSW |
9 |
73,839,862 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9317:Unc13c
|
UTSW |
9 |
73,447,662 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9412:Unc13c
|
UTSW |
9 |
73,839,772 (GRCm39) |
missense |
probably benign |
|
R9505:Unc13c
|
UTSW |
9 |
73,838,824 (GRCm39) |
missense |
probably benign |
0.22 |
R9516:Unc13c
|
UTSW |
9 |
73,392,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R9528:Unc13c
|
UTSW |
9 |
73,837,960 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9567:Unc13c
|
UTSW |
9 |
73,536,485 (GRCm39) |
missense |
probably damaging |
0.99 |
R9756:Unc13c
|
UTSW |
9 |
73,839,526 (GRCm39) |
missense |
probably benign |
0.23 |
R9783:Unc13c
|
UTSW |
9 |
73,392,227 (GRCm39) |
missense |
probably benign |
0.09 |
|