Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd8 |
C |
A |
8: 71,916,157 (GRCm39) |
|
probably benign |
Het |
Adam5 |
A |
T |
8: 25,236,755 (GRCm39) |
D648E |
probably benign |
Het |
Akr1d1 |
A |
G |
6: 37,535,336 (GRCm39) |
D240G |
probably damaging |
Het |
Ankmy2 |
A |
G |
12: 36,207,363 (GRCm39) |
H3R |
possibly damaging |
Het |
Anpep |
A |
C |
7: 79,490,605 (GRCm39) |
|
probably null |
Het |
Apobr |
A |
G |
7: 126,186,903 (GRCm39) |
T20A |
possibly damaging |
Het |
Atp2a2 |
A |
T |
5: 122,604,899 (GRCm39) |
Y427N |
probably benign |
Het |
Camkk2 |
A |
C |
5: 122,902,190 (GRCm39) |
S40A |
possibly damaging |
Het |
Camp |
T |
C |
9: 109,677,497 (GRCm39) |
N112S |
probably benign |
Het |
Cbx7 |
A |
G |
15: 79,802,591 (GRCm39) |
S229P |
probably damaging |
Het |
Cnot2 |
T |
C |
10: 116,363,781 (GRCm39) |
N41S |
probably damaging |
Het |
Dchs1 |
A |
G |
7: 105,421,605 (GRCm39) |
F272L |
possibly damaging |
Het |
Dct |
T |
C |
14: 118,273,954 (GRCm39) |
K318E |
probably benign |
Het |
Dhrs11 |
A |
C |
11: 84,719,633 (GRCm39) |
L31V |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,543,093 (GRCm39) |
D2359G |
probably benign |
Het |
Dnajc7 |
A |
G |
11: 100,481,718 (GRCm39) |
S305P |
probably benign |
Het |
Dscc1 |
CTGAATGAAT |
CTGAAT |
15: 54,943,572 (GRCm39) |
|
probably benign |
Het |
Flnc |
A |
G |
6: 29,444,415 (GRCm39) |
|
probably benign |
Het |
Garin3 |
T |
C |
11: 46,298,693 (GRCm39) |
*666Q |
probably null |
Het |
Gm7535 |
A |
G |
17: 18,131,800 (GRCm39) |
|
probably benign |
Het |
Grtp1 |
A |
G |
8: 13,229,376 (GRCm39) |
F313L |
probably damaging |
Het |
Haus6 |
T |
C |
4: 86,511,846 (GRCm39) |
Y425C |
possibly damaging |
Het |
Hdac1 |
T |
A |
4: 129,422,753 (GRCm39) |
N83Y |
possibly damaging |
Het |
Hdlbp |
A |
G |
1: 93,358,840 (GRCm39) |
I237T |
probably damaging |
Het |
Hfm1 |
A |
T |
5: 107,046,442 (GRCm39) |
D481E |
probably damaging |
Het |
Hipk3 |
T |
C |
2: 104,264,780 (GRCm39) |
I737V |
probably benign |
Het |
Il23r |
T |
A |
6: 67,467,652 (GRCm39) |
|
probably null |
Het |
Il24 |
G |
A |
1: 130,810,268 (GRCm39) |
T196I |
probably benign |
Het |
Ints3 |
C |
T |
3: 90,307,610 (GRCm39) |
|
probably null |
Het |
Kcna6 |
T |
C |
6: 126,715,473 (GRCm39) |
E472G |
probably benign |
Het |
Kcnj16 |
C |
T |
11: 110,916,409 (GRCm39) |
T357M |
probably benign |
Het |
Kdm4b |
T |
A |
17: 56,708,302 (GRCm39) |
V957E |
probably damaging |
Het |
Kif21b |
G |
A |
1: 136,075,284 (GRCm39) |
D166N |
probably damaging |
Het |
Klhl11 |
G |
T |
11: 100,354,070 (GRCm39) |
Q584K |
probably benign |
Het |
Krt9 |
A |
T |
11: 100,080,817 (GRCm39) |
M345K |
probably benign |
Het |
Lgr5 |
T |
C |
10: 115,331,150 (GRCm39) |
|
probably benign |
Het |
Lilrb4b |
A |
T |
10: 51,357,831 (GRCm39) |
Q80L |
possibly damaging |
Het |
Lrrc69 |
T |
C |
4: 14,708,669 (GRCm39) |
E225G |
possibly damaging |
Het |
Ly9 |
A |
G |
1: 171,427,341 (GRCm39) |
S405P |
probably damaging |
Het |
Myh2 |
A |
G |
11: 67,071,740 (GRCm39) |
D519G |
possibly damaging |
Het |
Nav3 |
G |
A |
10: 109,606,045 (GRCm39) |
|
probably benign |
Het |
Nfkb1 |
G |
A |
3: 135,321,110 (GRCm39) |
T215I |
possibly damaging |
Het |
Ninj2 |
A |
T |
6: 120,175,600 (GRCm39) |
|
probably benign |
Het |
Obsl1 |
A |
G |
1: 75,482,244 (GRCm39) |
C209R |
probably damaging |
Het |
Or13a25 |
G |
A |
7: 140,247,734 (GRCm39) |
C171Y |
probably damaging |
Het |
Or2d4 |
A |
G |
7: 106,544,133 (GRCm39) |
I25T |
probably benign |
Het |
Or2j6 |
A |
T |
7: 139,980,713 (GRCm39) |
M82K |
possibly damaging |
Het |
Or2t44 |
A |
C |
11: 58,677,210 (GRCm39) |
D50A |
probably damaging |
Het |
Or2y1g |
T |
C |
11: 49,171,110 (GRCm39) |
I45T |
probably damaging |
Het |
Or52z14 |
A |
T |
7: 103,252,879 (GRCm39) |
Y6F |
probably benign |
Het |
Otud4 |
G |
C |
8: 80,366,641 (GRCm39) |
R36P |
probably damaging |
Het |
Pgbd5 |
T |
A |
8: 125,097,331 (GRCm39) |
M491L |
probably benign |
Het |
Pitrm1 |
A |
T |
13: 6,608,220 (GRCm39) |
D316V |
probably damaging |
Het |
Plod3 |
A |
G |
5: 137,019,707 (GRCm39) |
|
probably null |
Het |
Plppr3 |
A |
T |
10: 79,703,294 (GRCm39) |
Y63* |
probably null |
Het |
Pramel52-ps |
A |
T |
5: 94,531,931 (GRCm39) |
I272L |
probably benign |
Het |
Prickle2 |
T |
C |
6: 92,388,433 (GRCm39) |
D323G |
probably damaging |
Het |
Psmd11 |
A |
T |
11: 80,336,089 (GRCm39) |
I114F |
probably damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Rbp3 |
C |
T |
14: 33,677,975 (GRCm39) |
T641M |
probably damaging |
Het |
Rbp3 |
T |
G |
14: 33,678,418 (GRCm39) |
S789A |
probably benign |
Het |
Rfxap |
C |
A |
3: 54,714,747 (GRCm39) |
R117L |
probably damaging |
Het |
Rims2 |
T |
A |
15: 39,208,710 (GRCm39) |
M171K |
probably damaging |
Het |
Scin |
A |
G |
12: 40,183,907 (GRCm39) |
|
probably null |
Het |
Scn11a |
A |
G |
9: 119,583,744 (GRCm39) |
S1624P |
probably benign |
Het |
Slc41a3 |
G |
A |
6: 90,619,210 (GRCm39) |
V330M |
probably damaging |
Het |
Slc9c1 |
A |
G |
16: 45,370,469 (GRCm39) |
I237V |
probably benign |
Het |
Spag6 |
A |
G |
2: 18,736,930 (GRCm39) |
I218V |
probably benign |
Het |
Stam2 |
T |
C |
2: 52,599,638 (GRCm39) |
T257A |
possibly damaging |
Het |
Tbc1d24 |
G |
A |
17: 24,426,938 (GRCm39) |
R318* |
probably null |
Het |
Tedc2 |
T |
A |
17: 24,435,291 (GRCm39) |
E366V |
probably damaging |
Het |
Tedc2 |
C |
A |
17: 24,435,292 (GRCm39) |
E366* |
probably null |
Het |
Trpm3 |
T |
A |
19: 22,903,446 (GRCm39) |
Y1069N |
possibly damaging |
Het |
Tuba8 |
A |
G |
6: 121,197,479 (GRCm39) |
D47G |
probably benign |
Het |
Tulp3 |
A |
T |
6: 128,303,769 (GRCm39) |
S277T |
probably benign |
Het |
Uqcc6 |
T |
A |
10: 82,456,051 (GRCm39) |
T37S |
possibly damaging |
Het |
Wdr7 |
GTT |
GT |
18: 63,893,654 (GRCm39) |
|
probably null |
Het |
Ybx2 |
A |
G |
11: 69,827,294 (GRCm39) |
|
probably null |
Het |
Zfp407 |
C |
T |
18: 84,577,898 (GRCm39) |
A1072T |
probably benign |
Het |
Zfp788 |
T |
A |
7: 41,299,905 (GRCm39) |
I795N |
probably damaging |
Het |
|
Other mutations in Pcnt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01075:Pcnt
|
APN |
10 |
76,258,738 (GRCm39) |
nonsense |
probably null |
|
IGL01307:Pcnt
|
APN |
10 |
76,247,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01549:Pcnt
|
APN |
10 |
76,203,320 (GRCm39) |
splice site |
probably null |
|
IGL01576:Pcnt
|
APN |
10 |
76,204,656 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01611:Pcnt
|
APN |
10 |
76,272,258 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01630:Pcnt
|
APN |
10 |
76,256,080 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01647:Pcnt
|
APN |
10 |
76,205,835 (GRCm39) |
nonsense |
probably null |
|
IGL01689:Pcnt
|
APN |
10 |
76,247,487 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01690:Pcnt
|
APN |
10 |
76,228,609 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01723:Pcnt
|
APN |
10 |
76,254,333 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01920:Pcnt
|
APN |
10 |
76,240,362 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01958:Pcnt
|
APN |
10 |
76,269,513 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02210:Pcnt
|
APN |
10 |
76,225,053 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02225:Pcnt
|
APN |
10 |
76,225,308 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02228:Pcnt
|
APN |
10 |
76,225,308 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02237:Pcnt
|
APN |
10 |
76,188,818 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02279:Pcnt
|
APN |
10 |
76,239,599 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02303:Pcnt
|
APN |
10 |
76,278,393 (GRCm39) |
splice site |
probably benign |
|
IGL02355:Pcnt
|
APN |
10 |
76,210,996 (GRCm39) |
nonsense |
probably null |
|
IGL02362:Pcnt
|
APN |
10 |
76,210,996 (GRCm39) |
nonsense |
probably null |
|
IGL02428:Pcnt
|
APN |
10 |
76,265,090 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02536:Pcnt
|
APN |
10 |
76,216,063 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02715:Pcnt
|
APN |
10 |
76,204,556 (GRCm39) |
splice site |
probably benign |
|
IGL02800:Pcnt
|
APN |
10 |
76,248,417 (GRCm39) |
nonsense |
probably null |
|
IGL03395:Pcnt
|
APN |
10 |
76,272,325 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02799:Pcnt
|
UTSW |
10 |
76,248,417 (GRCm39) |
nonsense |
probably null |
|
PIT4520001:Pcnt
|
UTSW |
10 |
76,256,069 (GRCm39) |
missense |
probably damaging |
0.99 |
R0049:Pcnt
|
UTSW |
10 |
76,205,655 (GRCm39) |
unclassified |
probably benign |
|
R0049:Pcnt
|
UTSW |
10 |
76,205,655 (GRCm39) |
unclassified |
probably benign |
|
R0109:Pcnt
|
UTSW |
10 |
76,225,030 (GRCm39) |
missense |
probably benign |
0.00 |
R0117:Pcnt
|
UTSW |
10 |
76,244,561 (GRCm39) |
nonsense |
probably null |
|
R0254:Pcnt
|
UTSW |
10 |
76,228,414 (GRCm39) |
missense |
probably benign |
0.10 |
R0392:Pcnt
|
UTSW |
10 |
76,220,660 (GRCm39) |
missense |
probably benign |
|
R0511:Pcnt
|
UTSW |
10 |
76,240,429 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0570:Pcnt
|
UTSW |
10 |
76,247,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Pcnt
|
UTSW |
10 |
76,256,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R0635:Pcnt
|
UTSW |
10 |
76,240,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R0707:Pcnt
|
UTSW |
10 |
76,256,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R0749:Pcnt
|
UTSW |
10 |
76,217,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0969:Pcnt
|
UTSW |
10 |
76,263,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R1172:Pcnt
|
UTSW |
10 |
76,228,878 (GRCm39) |
splice site |
probably null |
|
R1174:Pcnt
|
UTSW |
10 |
76,228,878 (GRCm39) |
splice site |
probably null |
|
R1175:Pcnt
|
UTSW |
10 |
76,228,878 (GRCm39) |
splice site |
probably null |
|
R1512:Pcnt
|
UTSW |
10 |
76,240,496 (GRCm39) |
splice site |
probably null |
|
R1542:Pcnt
|
UTSW |
10 |
76,237,220 (GRCm39) |
missense |
probably benign |
0.02 |
R1542:Pcnt
|
UTSW |
10 |
76,225,221 (GRCm39) |
missense |
probably benign |
0.08 |
R1558:Pcnt
|
UTSW |
10 |
76,258,756 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1562:Pcnt
|
UTSW |
10 |
76,203,164 (GRCm39) |
missense |
probably benign |
0.02 |
R1762:Pcnt
|
UTSW |
10 |
76,190,971 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1779:Pcnt
|
UTSW |
10 |
76,244,630 (GRCm39) |
missense |
probably damaging |
0.99 |
R1869:Pcnt
|
UTSW |
10 |
76,215,740 (GRCm39) |
missense |
probably null |
0.94 |
R1911:Pcnt
|
UTSW |
10 |
76,204,650 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1995:Pcnt
|
UTSW |
10 |
76,228,633 (GRCm39) |
nonsense |
probably null |
|
R2073:Pcnt
|
UTSW |
10 |
76,216,214 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2111:Pcnt
|
UTSW |
10 |
76,256,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R2112:Pcnt
|
UTSW |
10 |
76,256,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R2309:Pcnt
|
UTSW |
10 |
76,278,460 (GRCm39) |
start gained |
probably benign |
|
R2902:Pcnt
|
UTSW |
10 |
76,211,064 (GRCm39) |
missense |
probably damaging |
0.98 |
R3623:Pcnt
|
UTSW |
10 |
76,269,584 (GRCm39) |
missense |
probably benign |
0.23 |
R4088:Pcnt
|
UTSW |
10 |
76,263,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R4300:Pcnt
|
UTSW |
10 |
76,203,225 (GRCm39) |
missense |
probably benign |
0.40 |
R4402:Pcnt
|
UTSW |
10 |
76,228,227 (GRCm39) |
missense |
probably benign |
0.00 |
R4407:Pcnt
|
UTSW |
10 |
76,210,704 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4483:Pcnt
|
UTSW |
10 |
76,237,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Pcnt
|
UTSW |
10 |
76,190,047 (GRCm39) |
missense |
probably benign |
0.01 |
R4734:Pcnt
|
UTSW |
10 |
76,273,040 (GRCm39) |
missense |
probably benign |
0.25 |
R4747:Pcnt
|
UTSW |
10 |
76,272,299 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4782:Pcnt
|
UTSW |
10 |
76,245,411 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4795:Pcnt
|
UTSW |
10 |
76,205,858 (GRCm39) |
missense |
probably benign |
0.21 |
R4831:Pcnt
|
UTSW |
10 |
76,248,335 (GRCm39) |
missense |
probably damaging |
0.96 |
R4873:Pcnt
|
UTSW |
10 |
76,205,688 (GRCm39) |
missense |
probably benign |
0.03 |
R4875:Pcnt
|
UTSW |
10 |
76,205,688 (GRCm39) |
missense |
probably benign |
0.03 |
R4946:Pcnt
|
UTSW |
10 |
76,192,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Pcnt
|
UTSW |
10 |
76,190,911 (GRCm39) |
missense |
probably benign |
0.00 |
R5033:Pcnt
|
UTSW |
10 |
76,235,779 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5106:Pcnt
|
UTSW |
10 |
76,237,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R5118:Pcnt
|
UTSW |
10 |
76,248,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R5167:Pcnt
|
UTSW |
10 |
76,256,258 (GRCm39) |
missense |
probably damaging |
0.97 |
R5199:Pcnt
|
UTSW |
10 |
76,254,378 (GRCm39) |
missense |
probably benign |
0.09 |
R5223:Pcnt
|
UTSW |
10 |
76,216,106 (GRCm39) |
missense |
probably damaging |
0.99 |
R5241:Pcnt
|
UTSW |
10 |
76,269,451 (GRCm39) |
missense |
probably benign |
0.26 |
R5308:Pcnt
|
UTSW |
10 |
76,192,159 (GRCm39) |
nonsense |
probably null |
|
R5328:Pcnt
|
UTSW |
10 |
76,247,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R5454:Pcnt
|
UTSW |
10 |
76,225,381 (GRCm39) |
splice site |
probably null |
|
R5543:Pcnt
|
UTSW |
10 |
76,247,886 (GRCm39) |
missense |
probably benign |
0.01 |
R5588:Pcnt
|
UTSW |
10 |
76,278,445 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5647:Pcnt
|
UTSW |
10 |
76,221,675 (GRCm39) |
missense |
probably benign |
0.17 |
R5668:Pcnt
|
UTSW |
10 |
76,245,334 (GRCm39) |
missense |
probably benign |
0.16 |
R5712:Pcnt
|
UTSW |
10 |
76,265,105 (GRCm39) |
missense |
probably damaging |
0.96 |
R5714:Pcnt
|
UTSW |
10 |
76,256,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R5797:Pcnt
|
UTSW |
10 |
76,228,590 (GRCm39) |
missense |
probably benign |
0.00 |
R5946:Pcnt
|
UTSW |
10 |
76,217,897 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5955:Pcnt
|
UTSW |
10 |
76,247,456 (GRCm39) |
missense |
possibly damaging |
0.45 |
R6024:Pcnt
|
UTSW |
10 |
76,255,871 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6267:Pcnt
|
UTSW |
10 |
76,221,632 (GRCm39) |
missense |
probably benign |
0.02 |
R6485:Pcnt
|
UTSW |
10 |
76,225,164 (GRCm39) |
nonsense |
probably null |
|
R6605:Pcnt
|
UTSW |
10 |
76,265,032 (GRCm39) |
critical splice donor site |
probably null |
|
R6877:Pcnt
|
UTSW |
10 |
76,269,851 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6882:Pcnt
|
UTSW |
10 |
76,263,662 (GRCm39) |
missense |
probably benign |
0.00 |
R6919:Pcnt
|
UTSW |
10 |
76,221,632 (GRCm39) |
missense |
probably benign |
0.02 |
R7025:Pcnt
|
UTSW |
10 |
76,239,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R7098:Pcnt
|
UTSW |
10 |
76,220,673 (GRCm39) |
missense |
probably benign |
|
R7109:Pcnt
|
UTSW |
10 |
76,205,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R7121:Pcnt
|
UTSW |
10 |
76,263,761 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7143:Pcnt
|
UTSW |
10 |
76,224,894 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7152:Pcnt
|
UTSW |
10 |
76,247,194 (GRCm39) |
splice site |
probably null |
|
R7213:Pcnt
|
UTSW |
10 |
76,244,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R7368:Pcnt
|
UTSW |
10 |
76,235,835 (GRCm39) |
missense |
probably benign |
|
R7453:Pcnt
|
UTSW |
10 |
76,225,284 (GRCm39) |
missense |
probably benign |
|
R7486:Pcnt
|
UTSW |
10 |
76,254,271 (GRCm39) |
missense |
probably benign |
|
R7486:Pcnt
|
UTSW |
10 |
76,254,270 (GRCm39) |
missense |
probably benign |
0.03 |
R7538:Pcnt
|
UTSW |
10 |
76,235,773 (GRCm39) |
missense |
probably benign |
|
R7575:Pcnt
|
UTSW |
10 |
76,225,086 (GRCm39) |
missense |
probably benign |
0.32 |
R7662:Pcnt
|
UTSW |
10 |
76,223,356 (GRCm39) |
missense |
probably benign |
0.27 |
R7685:Pcnt
|
UTSW |
10 |
76,258,642 (GRCm39) |
missense |
probably benign |
0.14 |
R7764:Pcnt
|
UTSW |
10 |
76,190,082 (GRCm39) |
missense |
probably benign |
0.33 |
R7802:Pcnt
|
UTSW |
10 |
76,211,137 (GRCm39) |
splice site |
probably null |
|
R8432:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8439:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8493:Pcnt
|
UTSW |
10 |
76,239,457 (GRCm39) |
critical splice donor site |
probably null |
|
R8530:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8535:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8830:Pcnt
|
UTSW |
10 |
76,218,008 (GRCm39) |
missense |
probably benign |
0.03 |
R8878:Pcnt
|
UTSW |
10 |
76,244,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R8911:Pcnt
|
UTSW |
10 |
76,223,359 (GRCm39) |
missense |
probably damaging |
0.98 |
R8988:Pcnt
|
UTSW |
10 |
76,245,407 (GRCm39) |
nonsense |
probably null |
|
R9084:Pcnt
|
UTSW |
10 |
76,235,826 (GRCm39) |
missense |
probably benign |
0.09 |
R9169:Pcnt
|
UTSW |
10 |
76,221,572 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9372:Pcnt
|
UTSW |
10 |
76,258,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R9411:Pcnt
|
UTSW |
10 |
76,258,896 (GRCm39) |
missense |
probably damaging |
0.96 |
R9448:Pcnt
|
UTSW |
10 |
76,256,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R9459:Pcnt
|
UTSW |
10 |
76,228,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R9479:Pcnt
|
UTSW |
10 |
76,217,963 (GRCm39) |
missense |
probably benign |
0.00 |
R9503:Pcnt
|
UTSW |
10 |
76,263,882 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9561:Pcnt
|
UTSW |
10 |
76,217,128 (GRCm39) |
nonsense |
probably null |
|
R9618:Pcnt
|
UTSW |
10 |
76,188,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R9648:Pcnt
|
UTSW |
10 |
76,190,089 (GRCm39) |
missense |
probably benign |
0.32 |
R9733:Pcnt
|
UTSW |
10 |
76,237,314 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Pcnt
|
UTSW |
10 |
76,217,991 (GRCm39) |
nonsense |
probably null |
|
Z1177:Pcnt
|
UTSW |
10 |
76,235,802 (GRCm39) |
missense |
probably benign |
0.00 |
|