Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb3 |
T |
C |
10: 85,223,947 (GRCm39) |
V252A |
unknown |
Het |
Actn4 |
T |
C |
7: 28,604,044 (GRCm39) |
I406V |
probably benign |
Het |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Ank1 |
T |
A |
8: 23,606,114 (GRCm39) |
F1124I |
probably damaging |
Het |
Arhgap44 |
CTGCT |
CTGCTTGCT |
11: 64,922,910 (GRCm39) |
|
probably null |
Het |
Atp9a |
C |
A |
2: 168,476,790 (GRCm39) |
V1000L |
probably benign |
Het |
Bnip3 |
A |
G |
7: 138,511,033 (GRCm39) |
|
probably benign |
Het |
Btnl6 |
T |
A |
17: 34,727,371 (GRCm39) |
R386S |
probably damaging |
Het |
Calcrl |
A |
G |
2: 84,205,658 (GRCm39) |
V11A |
probably benign |
Het |
Cc2d1a |
G |
T |
8: 84,863,571 (GRCm39) |
A597D |
possibly damaging |
Het |
Celsr3 |
A |
G |
9: 108,714,350 (GRCm39) |
T1960A |
probably benign |
Het |
Cfb |
T |
A |
17: 35,081,078 (GRCm39) |
|
probably null |
Het |
Chd8 |
A |
G |
14: 52,458,528 (GRCm39) |
I860T |
possibly damaging |
Het |
Col28a1 |
A |
G |
6: 8,168,102 (GRCm39) |
|
probably null |
Het |
Crhr2 |
T |
A |
6: 55,068,277 (GRCm39) |
T428S |
probably damaging |
Het |
Crybg2 |
A |
T |
4: 133,819,388 (GRCm39) |
I1753F |
probably damaging |
Het |
Ctsq |
A |
T |
13: 61,186,955 (GRCm39) |
V46E |
probably benign |
Het |
Cxcr1 |
T |
C |
1: 74,231,440 (GRCm39) |
E194G |
probably damaging |
Het |
Dop1a |
A |
T |
9: 86,397,396 (GRCm39) |
H900L |
probably damaging |
Het |
Dpyd |
T |
A |
3: 119,225,224 (GRCm39) |
M999K |
probably benign |
Het |
Gbp3 |
A |
C |
3: 142,273,560 (GRCm39) |
D369A |
possibly damaging |
Het |
Glmp |
A |
G |
3: 88,232,495 (GRCm39) |
E36G |
probably damaging |
Het |
Gm10113 |
T |
C |
13: 46,330,919 (GRCm39) |
|
noncoding transcript |
Het |
Gm6486 |
T |
A |
5: 3,120,846 (GRCm39) |
|
noncoding transcript |
Het |
Gm973 |
T |
G |
1: 59,671,509 (GRCm39) |
L891R |
unknown |
Het |
Heatr3 |
C |
T |
8: 88,866,582 (GRCm39) |
T8M |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,352,831 (GRCm39) |
M2106V |
probably damaging |
Het |
Hfm1 |
A |
T |
5: 107,046,509 (GRCm39) |
|
probably null |
Het |
Hspa14 |
A |
G |
2: 3,490,801 (GRCm39) |
V462A |
possibly damaging |
Het |
Hspa5 |
C |
A |
2: 34,665,761 (GRCm39) |
T535K |
possibly damaging |
Het |
Ift140 |
A |
G |
17: 25,274,563 (GRCm39) |
D745G |
probably benign |
Het |
Ift27 |
A |
T |
15: 78,057,981 (GRCm39) |
C8S |
possibly damaging |
Het |
Irak1bp1 |
G |
A |
9: 82,728,616 (GRCm39) |
W182* |
probably null |
Het |
Itga3 |
A |
G |
11: 94,953,541 (GRCm39) |
I236T |
probably benign |
Het |
Kctd15 |
T |
A |
7: 34,349,547 (GRCm39) |
N26Y |
possibly damaging |
Het |
Kdm1b |
T |
C |
13: 47,232,729 (GRCm39) |
V733A |
possibly damaging |
Het |
Lhx8 |
A |
T |
3: 154,027,340 (GRCm39) |
L234H |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,337,098 (GRCm39) |
T1225S |
probably damaging |
Het |
Lrrn1 |
G |
A |
6: 107,545,488 (GRCm39) |
D429N |
probably benign |
Het |
Mettl3 |
A |
T |
14: 52,536,243 (GRCm39) |
N200K |
possibly damaging |
Het |
Mixl1 |
G |
T |
1: 180,524,336 (GRCm39) |
A81D |
possibly damaging |
Het |
Mroh2b |
T |
C |
15: 4,980,763 (GRCm39) |
I1444T |
probably benign |
Het |
Muc15 |
T |
A |
2: 110,561,786 (GRCm39) |
L74* |
probably null |
Het |
Olfm2 |
T |
A |
9: 20,579,824 (GRCm39) |
Y317F |
probably damaging |
Het |
Or52a33 |
C |
T |
7: 103,288,886 (GRCm39) |
V154M |
probably benign |
Het |
Or5b114-ps1 |
G |
A |
19: 13,352,698 (GRCm39) |
S124N |
probably benign |
Het |
Or5p54 |
T |
A |
7: 107,554,001 (GRCm39) |
I51N |
probably benign |
Het |
Pclo |
A |
T |
5: 14,763,302 (GRCm39) |
Y3925F |
unknown |
Het |
Pik3c2g |
A |
T |
6: 139,599,137 (GRCm39) |
R84S |
probably damaging |
Het |
Pik3c2g |
A |
G |
6: 139,842,518 (GRCm39) |
Q449R |
probably damaging |
Het |
Psg28 |
T |
C |
7: 18,160,305 (GRCm39) |
E297G |
probably damaging |
Het |
Qrich2 |
A |
T |
11: 116,337,832 (GRCm39) |
|
probably benign |
Het |
Rgs9 |
A |
G |
11: 109,130,386 (GRCm39) |
I363T |
probably damaging |
Het |
Rnpepl1 |
A |
G |
1: 92,844,543 (GRCm39) |
D345G |
probably damaging |
Het |
Rtn4 |
T |
A |
11: 29,658,023 (GRCm39) |
F726I |
probably damaging |
Het |
Sart3 |
A |
T |
5: 113,893,507 (GRCm39) |
I330N |
probably damaging |
Het |
Scn5a |
T |
C |
9: 119,391,440 (GRCm39) |
D84G |
probably damaging |
Het |
Sema4a |
T |
C |
3: 88,348,008 (GRCm39) |
T438A |
probably damaging |
Het |
Sfxn1 |
A |
C |
13: 54,242,961 (GRCm39) |
Y73S |
probably benign |
Het |
Slc24a2 |
A |
G |
4: 86,914,882 (GRCm39) |
M585T |
probably damaging |
Het |
Slc26a7 |
A |
G |
4: 14,505,471 (GRCm39) |
V656A |
probably benign |
Het |
Smok2a |
T |
G |
17: 13,445,021 (GRCm39) |
D199E |
probably benign |
Het |
Tbc1d10c |
T |
C |
19: 4,235,030 (GRCm39) |
I344V |
probably benign |
Het |
Tll1 |
A |
T |
8: 64,506,925 (GRCm39) |
Y605* |
probably null |
Het |
Trim75 |
G |
A |
8: 65,435,535 (GRCm39) |
P305L |
probably damaging |
Het |
Vmn2r25 |
A |
T |
6: 123,799,876 (GRCm39) |
I822N |
probably damaging |
Het |
Wasf3 |
T |
G |
5: 146,407,166 (GRCm39) |
D495E |
unknown |
Het |
Wdhd1 |
T |
A |
14: 47,510,667 (GRCm39) |
K119* |
probably null |
Het |
Wnt2b |
T |
A |
3: 104,858,339 (GRCm39) |
D310V |
probably damaging |
Het |
Zfat |
G |
T |
15: 68,052,626 (GRCm39) |
D389E |
probably damaging |
Het |
Zfp282 |
G |
A |
6: 47,857,102 (GRCm39) |
V112M |
probably damaging |
Het |
Zfp617 |
A |
T |
8: 72,687,257 (GRCm39) |
K529I |
probably damaging |
Het |
Zfp866 |
A |
T |
8: 70,218,373 (GRCm39) |
C416S |
probably damaging |
Het |
Zfp991 |
G |
A |
4: 147,264,222 (GRCm39) |
G533D |
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 |
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 |
|