Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
A |
12: 71,234,200 (GRCm39) |
C1067S |
possibly damaging |
Het |
AAdacl4fm3 |
T |
C |
4: 144,447,887 (GRCm39) |
T30A |
possibly damaging |
Het |
Agbl3 |
T |
A |
6: 34,834,688 (GRCm39) |
S952R |
possibly damaging |
Het |
Ano9 |
A |
G |
7: 140,686,698 (GRCm39) |
Y429H |
probably damaging |
Het |
Bbs7 |
C |
A |
3: 36,667,415 (GRCm39) |
R7L |
probably damaging |
Het |
Birc2 |
T |
A |
9: 7,849,684 (GRCm39) |
D535V |
possibly damaging |
Het |
Catsper4 |
A |
G |
4: 133,945,240 (GRCm39) |
V206A |
probably damaging |
Het |
Ccdc73 |
T |
G |
2: 104,822,482 (GRCm39) |
S810R |
possibly damaging |
Het |
Cd177 |
A |
T |
7: 24,443,698 (GRCm39) |
L800* |
probably null |
Het |
Cd34 |
T |
C |
1: 194,630,316 (GRCm39) |
|
probably null |
Het |
Cep78 |
G |
A |
19: 15,959,150 (GRCm39) |
R95* |
probably null |
Het |
Cfap69 |
T |
C |
5: 5,713,996 (GRCm39) |
D12G |
probably benign |
Het |
Cpne7 |
A |
G |
8: 123,854,171 (GRCm39) |
D286G |
probably benign |
Het |
Cwc22 |
ATCTCTCTCTCTCTCTCT |
ATCTCTCTCTCTCTCT |
2: 77,759,803 (GRCm39) |
|
probably null |
Het |
Cxcl5 |
A |
T |
5: 90,907,565 (GRCm39) |
I46L |
probably benign |
Het |
Cyp19a1 |
C |
T |
9: 54,087,540 (GRCm39) |
G59D |
probably damaging |
Het |
Dclre1c |
A |
G |
2: 3,438,742 (GRCm39) |
D35G |
probably damaging |
Het |
Defa41 |
A |
G |
8: 21,692,428 (GRCm39) |
N83S |
probably benign |
Het |
Dvl1 |
A |
G |
4: 155,939,409 (GRCm39) |
Y279C |
probably damaging |
Het |
Fes |
A |
G |
7: 80,030,044 (GRCm39) |
L578P |
probably damaging |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Fmn2 |
T |
C |
1: 174,494,229 (GRCm39) |
S1248P |
probably damaging |
Het |
Fmo1 |
T |
G |
1: 162,679,088 (GRCm39) |
S53R |
probably damaging |
Het |
Gabrg1 |
A |
T |
5: 70,931,804 (GRCm39) |
M313K |
probably damaging |
Het |
Galnt10 |
T |
C |
11: 57,675,474 (GRCm39) |
C578R |
probably damaging |
Het |
Gpr39 |
T |
C |
1: 125,800,323 (GRCm39) |
V358A |
probably damaging |
Het |
Gsap |
A |
G |
5: 21,431,323 (GRCm39) |
R216G |
probably damaging |
Het |
Gsap |
A |
T |
5: 21,475,575 (GRCm39) |
T570S |
probably benign |
Het |
Gucy2d |
A |
T |
7: 98,093,030 (GRCm39) |
I136L |
probably benign |
Het |
Hap1 |
A |
T |
11: 100,240,218 (GRCm39) |
V294E |
probably damaging |
Het |
Ipo8 |
A |
G |
6: 148,701,278 (GRCm39) |
V514A |
probably damaging |
Het |
Irf5 |
T |
C |
6: 29,535,958 (GRCm39) |
L324P |
probably damaging |
Het |
Itsn1 |
C |
T |
16: 91,613,740 (GRCm39) |
R251C |
probably damaging |
Het |
Klf11 |
T |
C |
12: 24,701,567 (GRCm39) |
|
probably null |
Het |
Kpna6 |
G |
A |
4: 129,543,099 (GRCm39) |
Q439* |
probably null |
Het |
Mark4 |
A |
T |
7: 19,163,441 (GRCm39) |
S563T |
probably benign |
Het |
Mrpl21 |
A |
T |
19: 3,333,084 (GRCm39) |
I5L |
probably benign |
Het |
Muc4 |
T |
C |
16: 32,753,802 (GRCm38) |
I1226T |
probably benign |
Het |
Myrf |
G |
A |
19: 10,189,839 (GRCm39) |
T815I |
probably damaging |
Het |
Olfr515-ps1 |
A |
T |
7: 108,444,178 (GRCm39) |
|
probably null |
Het |
Or10d4c |
G |
T |
9: 39,558,555 (GRCm39) |
D178Y |
probably damaging |
Het |
Or11g27 |
A |
G |
14: 50,771,778 (GRCm39) |
N303S |
probably benign |
Het |
Or4c15 |
C |
T |
2: 88,760,597 (GRCm39) |
V21I |
probably benign |
Het |
Or52n3 |
A |
G |
7: 104,530,289 (GRCm39) |
Y125C |
possibly damaging |
Het |
Os9 |
T |
C |
10: 126,935,812 (GRCm39) |
D280G |
probably benign |
Het |
Pcdhb14 |
A |
G |
18: 37,582,283 (GRCm39) |
N463S |
probably damaging |
Het |
Pex19 |
G |
A |
1: 171,961,606 (GRCm39) |
E271K |
probably damaging |
Het |
Ppdpf |
G |
A |
2: 180,829,641 (GRCm39) |
S32N |
probably benign |
Het |
Prdm2 |
A |
G |
4: 142,859,477 (GRCm39) |
I1271T |
probably benign |
Het |
Rbbp4 |
T |
C |
4: 129,215,751 (GRCm39) |
T262A |
probably benign |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Spaca9 |
G |
A |
2: 28,583,793 (GRCm39) |
R64W |
probably damaging |
Het |
Sult1e1 |
A |
T |
5: 87,727,770 (GRCm39) |
S171T |
probably damaging |
Het |
Tns1 |
T |
C |
1: 73,992,612 (GRCm39) |
T689A |
probably damaging |
Het |
Vmn2r52 |
T |
C |
7: 9,905,090 (GRCm39) |
I250V |
probably benign |
Het |
Vmn2r55 |
C |
A |
7: 12,402,069 (GRCm39) |
L406F |
probably benign |
Het |
Wdcp |
T |
C |
12: 4,900,621 (GRCm39) |
V159A |
possibly damaging |
Het |
Zbtb3 |
C |
T |
19: 8,781,560 (GRCm39) |
A391V |
probably benign |
Het |
Znhit1 |
A |
T |
5: 137,011,487 (GRCm39) |
S109T |
probably benign |
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 |
R4658:Unc13c
|
UTSW |
9 |
73,840,108 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
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 |
|