Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
T |
C |
10: 79,843,221 (GRCm39) |
L1232P |
probably damaging |
Het |
Akap6 |
A |
T |
12: 53,188,351 (GRCm39) |
I1922F |
possibly damaging |
Het |
Ankdd1a |
C |
T |
9: 65,415,343 (GRCm39) |
A227T |
possibly damaging |
Het |
Arpc5 |
T |
C |
1: 152,647,206 (GRCm39) |
V103A |
possibly damaging |
Het |
Atp9a |
C |
A |
2: 168,510,090 (GRCm39) |
V430F |
probably benign |
Het |
Bod1 |
A |
G |
11: 31,616,932 (GRCm39) |
S110P |
probably damaging |
Het |
Cacna1c |
C |
A |
6: 118,590,914 (GRCm39) |
V1453F |
probably damaging |
Het |
Capn8 |
T |
A |
1: 182,435,264 (GRCm39) |
M414K |
probably damaging |
Het |
Cbl |
A |
T |
9: 44,069,809 (GRCm39) |
|
probably null |
Het |
Ccdc42 |
A |
T |
11: 68,479,106 (GRCm39) |
Q98L |
probably damaging |
Het |
Ccn3 |
T |
C |
15: 54,611,421 (GRCm39) |
|
probably null |
Het |
Cd200 |
C |
A |
16: 45,217,545 (GRCm39) |
V49L |
probably benign |
Het |
Celsr1 |
A |
G |
15: 85,812,531 (GRCm39) |
S2060P |
probably benign |
Het |
Ces1g |
A |
T |
8: 94,057,820 (GRCm39) |
H160Q |
possibly damaging |
Het |
Chrnb2 |
G |
T |
3: 89,668,831 (GRCm39) |
H161Q |
probably damaging |
Het |
Ctns |
G |
A |
11: 73,082,559 (GRCm39) |
T57I |
probably benign |
Het |
Cyp3a25 |
A |
T |
5: 145,931,766 (GRCm39) |
M114K |
possibly damaging |
Het |
D630003M21Rik |
A |
G |
2: 158,057,871 (GRCm39) |
F536L |
probably benign |
Het |
Dcc |
C |
T |
18: 71,943,826 (GRCm39) |
R275Q |
probably benign |
Het |
Dmxl2 |
A |
T |
9: 54,289,990 (GRCm39) |
H2508Q |
possibly damaging |
Het |
Elf5 |
C |
A |
2: 103,269,757 (GRCm39) |
Q113K |
probably damaging |
Het |
Fam83a |
T |
G |
15: 57,849,507 (GRCm39) |
V17G |
possibly damaging |
Het |
Farsa |
T |
C |
8: 85,587,674 (GRCm39) |
|
probably null |
Het |
Fgg |
A |
T |
3: 82,920,283 (GRCm39) |
Q354L |
probably damaging |
Het |
Folh1 |
T |
C |
7: 86,372,517 (GRCm39) |
D679G |
probably damaging |
Het |
Gbp4 |
T |
A |
5: 105,270,975 (GRCm39) |
R83* |
probably null |
Het |
Gm17482 |
T |
A |
6: 115,204,311 (GRCm39) |
|
probably benign |
Het |
Hmgxb4 |
T |
A |
8: 75,749,927 (GRCm39) |
V481D |
possibly damaging |
Het |
Ifi207 |
A |
C |
1: 173,552,619 (GRCm39) |
Y926D |
probably damaging |
Het |
Ikzf5 |
T |
A |
7: 130,993,377 (GRCm39) |
N264Y |
probably damaging |
Het |
Kat6a |
T |
A |
8: 23,430,384 (GRCm39) |
M1913K |
unknown |
Het |
Krt33b |
A |
T |
11: 99,915,694 (GRCm39) |
C351S |
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,427,944 (GRCm39) |
D543G |
probably damaging |
Het |
Lrrfip2 |
C |
T |
9: 111,053,021 (GRCm39) |
R339W |
probably damaging |
Het |
Mapk3 |
T |
G |
7: 126,363,454 (GRCm39) |
M276R |
probably benign |
Het |
Mgst1 |
T |
C |
6: 138,127,827 (GRCm39) |
V137A |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,558,884 (GRCm39) |
T2470A |
unknown |
Het |
Muc4 |
C |
T |
16: 32,575,237 (GRCm39) |
S1274F |
possibly damaging |
Het |
Myo5c |
A |
C |
9: 75,180,198 (GRCm39) |
K713T |
possibly damaging |
Het |
Myzap |
T |
C |
9: 71,466,146 (GRCm39) |
D170G |
possibly damaging |
Het |
Naa50 |
T |
C |
16: 43,979,831 (GRCm39) |
V113A |
probably damaging |
Het |
Neu3 |
T |
C |
7: 99,462,929 (GRCm39) |
T265A |
probably benign |
Het |
Nin |
T |
C |
12: 70,061,631 (GRCm39) |
T2078A |
possibly damaging |
Het |
Nomo1 |
G |
A |
7: 45,683,260 (GRCm39) |
|
probably benign |
Het |
Nprl3 |
A |
G |
11: 32,189,828 (GRCm39) |
L273P |
probably damaging |
Het |
Oaf |
T |
A |
9: 43,136,216 (GRCm39) |
H120L |
possibly damaging |
Het |
Or10s1 |
T |
C |
9: 39,985,824 (GRCm39) |
S78P |
probably damaging |
Het |
Or13p4 |
C |
T |
4: 118,547,145 (GRCm39) |
R168H |
probably benign |
Het |
Or8b36 |
ATTGCTGTTT |
ATTGCTGTTTGCTGTTT |
9: 37,937,836 (GRCm39) |
|
probably null |
Het |
Or8k21 |
T |
C |
2: 86,145,468 (GRCm39) |
H54R |
probably benign |
Het |
Pcdhga3 |
T |
A |
18: 37,809,674 (GRCm39) |
|
probably benign |
Het |
Polq |
G |
A |
16: 36,837,718 (GRCm39) |
|
probably null |
Het |
Prdm8 |
C |
T |
5: 98,333,162 (GRCm39) |
P243L |
possibly damaging |
Het |
Prim2 |
T |
C |
1: 33,701,373 (GRCm39) |
D138G |
probably benign |
Het |
Prl2c5 |
A |
G |
13: 13,365,175 (GRCm39) |
E107G |
probably benign |
Het |
Prr14l |
T |
A |
5: 32,984,869 (GRCm39) |
H1542L |
probably damaging |
Het |
Rab26 |
T |
C |
17: 24,749,072 (GRCm39) |
E203G |
probably damaging |
Het |
Rtkn2 |
A |
T |
10: 67,871,662 (GRCm39) |
H350L |
possibly damaging |
Het |
Scara3 |
T |
C |
14: 66,175,710 (GRCm39) |
D19G |
probably benign |
Het |
Scn3a |
A |
G |
2: 65,302,685 (GRCm39) |
S1254P |
probably damaging |
Het |
Sdcbp |
A |
G |
4: 6,385,059 (GRCm39) |
M93V |
probably benign |
Het |
Sema6a |
C |
A |
18: 47,382,231 (GRCm39) |
R772L |
probably damaging |
Het |
Slc5a7 |
T |
C |
17: 54,584,006 (GRCm39) |
K428R |
probably benign |
Het |
Sptbn2 |
G |
A |
19: 4,774,674 (GRCm39) |
G109D |
probably damaging |
Het |
Tmppe |
T |
C |
9: 114,233,812 (GRCm39) |
L37P |
probably benign |
Het |
Tuba1a |
T |
C |
15: 98,849,410 (GRCm39) |
T56A |
probably benign |
Het |
Tut4 |
T |
A |
4: 108,412,817 (GRCm39) |
I1506N |
probably damaging |
Het |
Vmn2r111 |
A |
G |
17: 22,792,070 (GRCm39) |
I62T |
probably benign |
Het |
Vmn2r73 |
A |
G |
7: 85,506,828 (GRCm39) |
I828T |
probably damaging |
Het |
Vmn2r79 |
T |
A |
7: 86,686,976 (GRCm39) |
W786R |
probably damaging |
Het |
Zp1 |
G |
A |
19: 10,894,084 (GRCm39) |
T405M |
probably null |
Het |
|
Other mutations in Fat2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00720:Fat2
|
APN |
11 |
55,202,070 (GRCm39) |
missense |
probably benign |
|
IGL00897:Fat2
|
APN |
11 |
55,180,078 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01161:Fat2
|
APN |
11 |
55,175,017 (GRCm39) |
missense |
probably benign |
|
IGL01306:Fat2
|
APN |
11 |
55,201,698 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01393:Fat2
|
APN |
11 |
55,160,135 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01529:Fat2
|
APN |
11 |
55,172,982 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01530:Fat2
|
APN |
11 |
55,174,213 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01555:Fat2
|
APN |
11 |
55,169,756 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01758:Fat2
|
APN |
11 |
55,187,035 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01768:Fat2
|
APN |
11 |
55,153,394 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01939:Fat2
|
APN |
11 |
55,174,806 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01941:Fat2
|
APN |
11 |
55,202,831 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01967:Fat2
|
APN |
11 |
55,202,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01978:Fat2
|
APN |
11 |
55,160,972 (GRCm39) |
missense |
probably benign |
0.34 |
IGL01998:Fat2
|
APN |
11 |
55,187,021 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02001:Fat2
|
APN |
11 |
55,203,071 (GRCm39) |
start codon destroyed |
probably null |
0.89 |
IGL02004:Fat2
|
APN |
11 |
55,173,666 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02103:Fat2
|
APN |
11 |
55,180,122 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02131:Fat2
|
APN |
11 |
55,199,868 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02155:Fat2
|
APN |
11 |
55,153,245 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02223:Fat2
|
APN |
11 |
55,163,955 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02231:Fat2
|
APN |
11 |
55,171,918 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02312:Fat2
|
APN |
11 |
55,161,085 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02476:Fat2
|
APN |
11 |
55,201,950 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02539:Fat2
|
APN |
11 |
55,172,619 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02553:Fat2
|
APN |
11 |
55,202,109 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02645:Fat2
|
APN |
11 |
55,173,654 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02664:Fat2
|
APN |
11 |
55,201,922 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02708:Fat2
|
APN |
11 |
55,173,211 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02883:Fat2
|
APN |
11 |
55,147,444 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02894:Fat2
|
APN |
11 |
55,147,479 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02975:Fat2
|
APN |
11 |
55,161,020 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03085:Fat2
|
APN |
11 |
55,174,072 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03106:Fat2
|
APN |
11 |
55,202,727 (GRCm39) |
missense |
probably benign |
0.45 |
IGL03132:Fat2
|
APN |
11 |
55,144,746 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03133:Fat2
|
APN |
11 |
55,176,869 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03194:Fat2
|
APN |
11 |
55,201,821 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03266:Fat2
|
APN |
11 |
55,174,855 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03290:Fat2
|
APN |
11 |
55,147,045 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03291:Fat2
|
APN |
11 |
55,153,421 (GRCm39) |
missense |
probably benign |
|
IGL03325:Fat2
|
APN |
11 |
55,173,168 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03345:Fat2
|
APN |
11 |
55,173,187 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03371:Fat2
|
APN |
11 |
55,201,990 (GRCm39) |
missense |
probably benign |
0.10 |
ANU23:Fat2
|
UTSW |
11 |
55,201,698 (GRCm39) |
missense |
probably benign |
0.28 |
BB001:Fat2
|
UTSW |
11 |
55,153,613 (GRCm39) |
missense |
probably benign |
0.03 |
BB011:Fat2
|
UTSW |
11 |
55,153,613 (GRCm39) |
missense |
probably benign |
0.03 |
P0040:Fat2
|
UTSW |
11 |
55,173,039 (GRCm39) |
missense |
possibly damaging |
0.89 |
PIT4504001:Fat2
|
UTSW |
11 |
55,146,936 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0008:Fat2
|
UTSW |
11 |
55,202,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R0008:Fat2
|
UTSW |
11 |
55,202,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Fat2
|
UTSW |
11 |
55,153,697 (GRCm39) |
missense |
probably benign |
0.16 |
R0012:Fat2
|
UTSW |
11 |
55,153,697 (GRCm39) |
missense |
probably benign |
0.16 |
R0048:Fat2
|
UTSW |
11 |
55,200,865 (GRCm39) |
missense |
probably benign |
0.00 |
R0048:Fat2
|
UTSW |
11 |
55,200,865 (GRCm39) |
missense |
probably benign |
0.00 |
R0098:Fat2
|
UTSW |
11 |
55,189,431 (GRCm39) |
missense |
probably damaging |
0.98 |
R0124:Fat2
|
UTSW |
11 |
55,174,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R0127:Fat2
|
UTSW |
11 |
55,180,112 (GRCm39) |
missense |
probably benign |
0.01 |
R0130:Fat2
|
UTSW |
11 |
55,142,944 (GRCm39) |
missense |
probably benign |
0.26 |
R0131:Fat2
|
UTSW |
11 |
55,164,037 (GRCm39) |
missense |
probably benign |
|
R0158:Fat2
|
UTSW |
11 |
55,187,011 (GRCm39) |
missense |
probably benign |
0.00 |
R0184:Fat2
|
UTSW |
11 |
55,187,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R0367:Fat2
|
UTSW |
11 |
55,182,919 (GRCm39) |
splice site |
probably benign |
|
R0384:Fat2
|
UTSW |
11 |
55,160,291 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0390:Fat2
|
UTSW |
11 |
55,201,603 (GRCm39) |
missense |
probably damaging |
0.99 |
R0403:Fat2
|
UTSW |
11 |
55,161,175 (GRCm39) |
missense |
probably benign |
0.42 |
R0416:Fat2
|
UTSW |
11 |
55,174,960 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0437:Fat2
|
UTSW |
11 |
55,173,625 (GRCm39) |
missense |
probably benign |
0.02 |
R0463:Fat2
|
UTSW |
11 |
55,153,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R0497:Fat2
|
UTSW |
11 |
55,174,228 (GRCm39) |
missense |
probably benign |
0.03 |
R0617:Fat2
|
UTSW |
11 |
55,202,669 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0622:Fat2
|
UTSW |
11 |
55,173,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Fat2
|
UTSW |
11 |
55,200,035 (GRCm39) |
missense |
probably damaging |
0.97 |
R0811:Fat2
|
UTSW |
11 |
55,144,459 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0812:Fat2
|
UTSW |
11 |
55,144,459 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0869:Fat2
|
UTSW |
11 |
55,202,601 (GRCm39) |
missense |
probably benign |
0.08 |
R0870:Fat2
|
UTSW |
11 |
55,202,601 (GRCm39) |
missense |
probably benign |
0.08 |
R0899:Fat2
|
UTSW |
11 |
55,147,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R1278:Fat2
|
UTSW |
11 |
55,159,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R1383:Fat2
|
UTSW |
11 |
55,201,599 (GRCm39) |
missense |
probably benign |
|
R1428:Fat2
|
UTSW |
11 |
55,186,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R1438:Fat2
|
UTSW |
11 |
55,178,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R1495:Fat2
|
UTSW |
11 |
55,153,499 (GRCm39) |
missense |
probably benign |
|
R1506:Fat2
|
UTSW |
11 |
55,175,090 (GRCm39) |
missense |
probably benign |
|
R1547:Fat2
|
UTSW |
11 |
55,143,081 (GRCm39) |
missense |
probably benign |
0.01 |
R1554:Fat2
|
UTSW |
11 |
55,144,490 (GRCm39) |
missense |
probably benign |
0.01 |
R1562:Fat2
|
UTSW |
11 |
55,200,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R1588:Fat2
|
UTSW |
11 |
55,174,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R1592:Fat2
|
UTSW |
11 |
55,182,696 (GRCm39) |
splice site |
probably null |
|
R1601:Fat2
|
UTSW |
11 |
55,172,836 (GRCm39) |
missense |
probably benign |
0.01 |
R1610:Fat2
|
UTSW |
11 |
55,169,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:Fat2
|
UTSW |
11 |
55,175,545 (GRCm39) |
missense |
probably benign |
|
R1634:Fat2
|
UTSW |
11 |
55,158,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1644:Fat2
|
UTSW |
11 |
55,187,007 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1644:Fat2
|
UTSW |
11 |
55,178,609 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1691:Fat2
|
UTSW |
11 |
55,202,678 (GRCm39) |
missense |
probably damaging |
0.99 |
R1734:Fat2
|
UTSW |
11 |
55,172,197 (GRCm39) |
missense |
probably benign |
0.00 |
R1748:Fat2
|
UTSW |
11 |
55,147,473 (GRCm39) |
missense |
probably damaging |
0.97 |
R1771:Fat2
|
UTSW |
11 |
55,201,691 (GRCm39) |
missense |
probably benign |
0.01 |
R1800:Fat2
|
UTSW |
11 |
55,174,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R1807:Fat2
|
UTSW |
11 |
55,180,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R1823:Fat2
|
UTSW |
11 |
55,147,606 (GRCm39) |
missense |
probably benign |
0.29 |
R1848:Fat2
|
UTSW |
11 |
55,202,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Fat2
|
UTSW |
11 |
55,182,840 (GRCm39) |
missense |
probably benign |
0.00 |
R1899:Fat2
|
UTSW |
11 |
55,153,004 (GRCm39) |
missense |
probably benign |
|
R1954:Fat2
|
UTSW |
11 |
55,201,910 (GRCm39) |
missense |
probably benign |
0.06 |
R2010:Fat2
|
UTSW |
11 |
55,144,653 (GRCm39) |
missense |
probably damaging |
0.99 |
R2011:Fat2
|
UTSW |
11 |
55,173,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R2057:Fat2
|
UTSW |
11 |
55,172,686 (GRCm39) |
missense |
possibly damaging |
0.60 |
R2081:Fat2
|
UTSW |
11 |
55,200,503 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2106:Fat2
|
UTSW |
11 |
55,147,390 (GRCm39) |
missense |
probably benign |
0.00 |
R2165:Fat2
|
UTSW |
11 |
55,194,542 (GRCm39) |
missense |
probably benign |
0.00 |
R2176:Fat2
|
UTSW |
11 |
55,158,401 (GRCm39) |
critical splice donor site |
probably null |
|
R2284:Fat2
|
UTSW |
11 |
55,173,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R2338:Fat2
|
UTSW |
11 |
55,202,727 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2340:Fat2
|
UTSW |
11 |
55,160,922 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2427:Fat2
|
UTSW |
11 |
55,201,638 (GRCm39) |
missense |
probably benign |
0.15 |
R2444:Fat2
|
UTSW |
11 |
55,172,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R2858:Fat2
|
UTSW |
11 |
55,174,599 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2882:Fat2
|
UTSW |
11 |
55,202,131 (GRCm39) |
missense |
probably damaging |
0.96 |
R3029:Fat2
|
UTSW |
11 |
55,175,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R3085:Fat2
|
UTSW |
11 |
55,142,997 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3121:Fat2
|
UTSW |
11 |
55,202,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R3418:Fat2
|
UTSW |
11 |
55,169,824 (GRCm39) |
missense |
probably benign |
0.01 |
R3500:Fat2
|
UTSW |
11 |
55,151,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R3607:Fat2
|
UTSW |
11 |
55,172,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R3611:Fat2
|
UTSW |
11 |
55,202,895 (GRCm39) |
missense |
probably benign |
|
R3620:Fat2
|
UTSW |
11 |
55,147,521 (GRCm39) |
missense |
probably damaging |
0.97 |
R3688:Fat2
|
UTSW |
11 |
55,171,927 (GRCm39) |
missense |
probably damaging |
0.99 |
R3704:Fat2
|
UTSW |
11 |
55,200,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Fat2
|
UTSW |
11 |
55,147,012 (GRCm39) |
missense |
probably benign |
|
R3889:Fat2
|
UTSW |
11 |
55,172,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R3951:Fat2
|
UTSW |
11 |
55,187,208 (GRCm39) |
missense |
probably benign |
0.00 |
R4211:Fat2
|
UTSW |
11 |
55,174,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R4249:Fat2
|
UTSW |
11 |
55,175,127 (GRCm39) |
missense |
probably damaging |
0.98 |
R4406:Fat2
|
UTSW |
11 |
55,153,094 (GRCm39) |
missense |
probably benign |
0.00 |
R4433:Fat2
|
UTSW |
11 |
55,200,466 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4436:Fat2
|
UTSW |
11 |
55,187,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R4498:Fat2
|
UTSW |
11 |
55,160,923 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4560:Fat2
|
UTSW |
11 |
55,156,777 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4594:Fat2
|
UTSW |
11 |
55,175,578 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4663:Fat2
|
UTSW |
11 |
55,187,039 (GRCm39) |
nonsense |
probably null |
|
R4669:Fat2
|
UTSW |
11 |
55,202,441 (GRCm39) |
missense |
probably benign |
0.01 |
R4696:Fat2
|
UTSW |
11 |
55,175,841 (GRCm39) |
missense |
probably benign |
0.00 |
R4734:Fat2
|
UTSW |
11 |
55,202,294 (GRCm39) |
missense |
probably benign |
0.01 |
R4749:Fat2
|
UTSW |
11 |
55,202,294 (GRCm39) |
missense |
probably benign |
0.01 |
R4765:Fat2
|
UTSW |
11 |
55,172,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R4803:Fat2
|
UTSW |
11 |
55,175,886 (GRCm39) |
missense |
probably benign |
0.03 |
R4805:Fat2
|
UTSW |
11 |
55,174,805 (GRCm39) |
missense |
probably benign |
0.01 |
R4822:Fat2
|
UTSW |
11 |
55,202,144 (GRCm39) |
missense |
probably benign |
0.02 |
R4840:Fat2
|
UTSW |
11 |
55,169,844 (GRCm39) |
missense |
probably benign |
0.21 |
R4849:Fat2
|
UTSW |
11 |
55,201,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R4943:Fat2
|
UTSW |
11 |
55,169,859 (GRCm39) |
missense |
probably benign |
0.00 |
R4993:Fat2
|
UTSW |
11 |
55,173,918 (GRCm39) |
missense |
probably damaging |
0.99 |
R5097:Fat2
|
UTSW |
11 |
55,201,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R5104:Fat2
|
UTSW |
11 |
55,169,814 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5115:Fat2
|
UTSW |
11 |
55,187,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R5213:Fat2
|
UTSW |
11 |
55,144,658 (GRCm39) |
missense |
probably benign |
0.00 |
R5254:Fat2
|
UTSW |
11 |
55,172,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R5269:Fat2
|
UTSW |
11 |
55,178,704 (GRCm39) |
missense |
probably benign |
0.00 |
R5288:Fat2
|
UTSW |
11 |
55,158,482 (GRCm39) |
missense |
probably benign |
0.00 |
R5355:Fat2
|
UTSW |
11 |
55,172,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R5375:Fat2
|
UTSW |
11 |
55,153,646 (GRCm39) |
missense |
probably benign |
0.00 |
R5379:Fat2
|
UTSW |
11 |
55,194,767 (GRCm39) |
missense |
probably damaging |
0.99 |
R5411:Fat2
|
UTSW |
11 |
55,143,052 (GRCm39) |
missense |
probably benign |
0.23 |
R5416:Fat2
|
UTSW |
11 |
55,194,514 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5480:Fat2
|
UTSW |
11 |
55,200,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R5486:Fat2
|
UTSW |
11 |
55,144,507 (GRCm39) |
missense |
probably benign |
0.00 |
R5526:Fat2
|
UTSW |
11 |
55,160,187 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5532:Fat2
|
UTSW |
11 |
55,153,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R5583:Fat2
|
UTSW |
11 |
55,144,715 (GRCm39) |
missense |
probably benign |
0.00 |
R5588:Fat2
|
UTSW |
11 |
55,173,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R5598:Fat2
|
UTSW |
11 |
55,171,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R5636:Fat2
|
UTSW |
11 |
55,173,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R5653:Fat2
|
UTSW |
11 |
55,201,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R5657:Fat2
|
UTSW |
11 |
55,201,507 (GRCm39) |
nonsense |
probably null |
|
R5660:Fat2
|
UTSW |
11 |
55,175,002 (GRCm39) |
missense |
probably benign |
0.00 |
R5752:Fat2
|
UTSW |
11 |
55,180,063 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5757:Fat2
|
UTSW |
11 |
55,143,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R5792:Fat2
|
UTSW |
11 |
55,153,151 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5872:Fat2
|
UTSW |
11 |
55,161,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R5933:Fat2
|
UTSW |
11 |
55,174,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R6030:Fat2
|
UTSW |
11 |
55,201,129 (GRCm39) |
nonsense |
probably null |
|
R6030:Fat2
|
UTSW |
11 |
55,201,129 (GRCm39) |
nonsense |
probably null |
|
R6032:Fat2
|
UTSW |
11 |
55,144,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:Fat2
|
UTSW |
11 |
55,144,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R6221:Fat2
|
UTSW |
11 |
55,186,898 (GRCm39) |
critical splice donor site |
probably null |
|
R6253:Fat2
|
UTSW |
11 |
55,187,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Fat2
|
UTSW |
11 |
55,153,407 (GRCm39) |
missense |
probably benign |
|
R6450:Fat2
|
UTSW |
11 |
55,180,136 (GRCm39) |
missense |
probably damaging |
0.97 |
R6453:Fat2
|
UTSW |
11 |
55,173,042 (GRCm39) |
missense |
probably benign |
0.29 |
R6455:Fat2
|
UTSW |
11 |
55,161,283 (GRCm39) |
missense |
probably damaging |
0.96 |
R6483:Fat2
|
UTSW |
11 |
55,187,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R6504:Fat2
|
UTSW |
11 |
55,153,223 (GRCm39) |
missense |
probably benign |
0.00 |
R6520:Fat2
|
UTSW |
11 |
55,175,814 (GRCm39) |
missense |
probably damaging |
0.99 |
R6525:Fat2
|
UTSW |
11 |
55,174,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R6617:Fat2
|
UTSW |
11 |
55,186,931 (GRCm39) |
missense |
probably benign |
0.01 |
R6652:Fat2
|
UTSW |
11 |
55,143,088 (GRCm39) |
missense |
probably benign |
|
R6679:Fat2
|
UTSW |
11 |
55,200,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R6680:Fat2
|
UTSW |
11 |
55,201,684 (GRCm39) |
nonsense |
probably null |
|
R6762:Fat2
|
UTSW |
11 |
55,144,308 (GRCm39) |
splice site |
probably null |
|
R6810:Fat2
|
UTSW |
11 |
55,173,067 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6818:Fat2
|
UTSW |
11 |
55,200,167 (GRCm39) |
missense |
probably benign |
0.31 |
R6919:Fat2
|
UTSW |
11 |
55,173,597 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6939:Fat2
|
UTSW |
11 |
55,143,300 (GRCm39) |
nonsense |
probably null |
|
R6941:Fat2
|
UTSW |
11 |
55,152,914 (GRCm39) |
missense |
probably benign |
|
R7023:Fat2
|
UTSW |
11 |
55,201,328 (GRCm39) |
missense |
probably benign |
0.00 |
R7027:Fat2
|
UTSW |
11 |
55,160,259 (GRCm39) |
missense |
probably benign |
0.03 |
R7027:Fat2
|
UTSW |
11 |
55,172,677 (GRCm39) |
nonsense |
probably null |
|
R7095:Fat2
|
UTSW |
11 |
55,202,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Fat2
|
UTSW |
11 |
55,174,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R7116:Fat2
|
UTSW |
11 |
55,173,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Fat2
|
UTSW |
11 |
55,172,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R7167:Fat2
|
UTSW |
11 |
55,175,827 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7213:Fat2
|
UTSW |
11 |
55,171,871 (GRCm39) |
nonsense |
probably null |
|
R7246:Fat2
|
UTSW |
11 |
55,187,208 (GRCm39) |
missense |
probably benign |
0.00 |
R7252:Fat2
|
UTSW |
11 |
55,202,088 (GRCm39) |
missense |
probably damaging |
0.98 |
R7266:Fat2
|
UTSW |
11 |
55,175,856 (GRCm39) |
missense |
probably damaging |
0.99 |
R7316:Fat2
|
UTSW |
11 |
55,176,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Fat2
|
UTSW |
11 |
55,173,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R7355:Fat2
|
UTSW |
11 |
55,147,377 (GRCm39) |
missense |
probably benign |
0.00 |
R7431:Fat2
|
UTSW |
11 |
55,199,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R7459:Fat2
|
UTSW |
11 |
55,194,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R7460:Fat2
|
UTSW |
11 |
55,169,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:Fat2
|
UTSW |
11 |
55,201,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Fat2
|
UTSW |
11 |
55,194,479 (GRCm39) |
missense |
probably benign |
0.31 |
R7678:Fat2
|
UTSW |
11 |
55,173,156 (GRCm39) |
missense |
probably damaging |
0.99 |
R7689:Fat2
|
UTSW |
11 |
55,200,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R7704:Fat2
|
UTSW |
11 |
55,175,173 (GRCm39) |
missense |
probably benign |
0.03 |
R7710:Fat2
|
UTSW |
11 |
55,201,589 (GRCm39) |
missense |
probably benign |
0.35 |
R7724:Fat2
|
UTSW |
11 |
55,175,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R7731:Fat2
|
UTSW |
11 |
55,201,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R7739:Fat2
|
UTSW |
11 |
55,171,957 (GRCm39) |
nonsense |
probably null |
|
R7757:Fat2
|
UTSW |
11 |
55,202,247 (GRCm39) |
missense |
probably benign |
0.00 |
R7876:Fat2
|
UTSW |
11 |
55,202,046 (GRCm39) |
missense |
probably benign |
0.01 |
R7883:Fat2
|
UTSW |
11 |
55,144,190 (GRCm39) |
splice site |
probably null |
|
R7924:Fat2
|
UTSW |
11 |
55,153,613 (GRCm39) |
missense |
probably benign |
0.03 |
R7936:Fat2
|
UTSW |
11 |
55,200,993 (GRCm39) |
missense |
probably benign |
|
R7936:Fat2
|
UTSW |
11 |
55,201,986 (GRCm39) |
nonsense |
probably null |
|
R7938:Fat2
|
UTSW |
11 |
55,163,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R7947:Fat2
|
UTSW |
11 |
55,178,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R8049:Fat2
|
UTSW |
11 |
55,202,892 (GRCm39) |
missense |
probably benign |
0.13 |
R8094:Fat2
|
UTSW |
11 |
55,186,965 (GRCm39) |
missense |
probably benign |
0.06 |
R8157:Fat2
|
UTSW |
11 |
55,142,910 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8170:Fat2
|
UTSW |
11 |
55,161,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R8172:Fat2
|
UTSW |
11 |
55,178,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R8182:Fat2
|
UTSW |
11 |
55,175,223 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8188:Fat2
|
UTSW |
11 |
55,163,997 (GRCm39) |
missense |
probably damaging |
0.98 |
R8204:Fat2
|
UTSW |
11 |
55,175,436 (GRCm39) |
missense |
probably benign |
0.02 |
R8211:Fat2
|
UTSW |
11 |
55,203,035 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8255:Fat2
|
UTSW |
11 |
55,161,101 (GRCm39) |
missense |
probably benign |
0.19 |
R8263:Fat2
|
UTSW |
11 |
55,174,962 (GRCm39) |
missense |
probably benign |
|
R8269:Fat2
|
UTSW |
11 |
55,173,535 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8443:Fat2
|
UTSW |
11 |
55,202,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R8465:Fat2
|
UTSW |
11 |
55,147,530 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8480:Fat2
|
UTSW |
11 |
55,173,794 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8511:Fat2
|
UTSW |
11 |
55,200,063 (GRCm39) |
missense |
probably damaging |
0.99 |
R8680:Fat2
|
UTSW |
11 |
55,144,692 (GRCm39) |
missense |
probably benign |
|
R8704:Fat2
|
UTSW |
11 |
55,172,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R8711:Fat2
|
UTSW |
11 |
55,159,129 (GRCm39) |
missense |
probably benign |
0.22 |
R8724:Fat2
|
UTSW |
11 |
55,173,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R8788:Fat2
|
UTSW |
11 |
55,171,929 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8802:Fat2
|
UTSW |
11 |
55,173,750 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8902:Fat2
|
UTSW |
11 |
55,200,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R8940:Fat2
|
UTSW |
11 |
55,147,636 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8956:Fat2
|
UTSW |
11 |
55,173,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Fat2
|
UTSW |
11 |
55,194,547 (GRCm39) |
missense |
probably damaging |
0.99 |
R9100:Fat2
|
UTSW |
11 |
55,153,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R9132:Fat2
|
UTSW |
11 |
55,189,436 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9173:Fat2
|
UTSW |
11 |
55,169,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R9241:Fat2
|
UTSW |
11 |
55,147,566 (GRCm39) |
missense |
probably benign |
0.00 |
R9253:Fat2
|
UTSW |
11 |
55,201,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R9280:Fat2
|
UTSW |
11 |
55,201,523 (GRCm39) |
missense |
probably benign |
0.36 |
R9351:Fat2
|
UTSW |
11 |
55,172,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R9369:Fat2
|
UTSW |
11 |
55,201,514 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9404:Fat2
|
UTSW |
11 |
55,144,348 (GRCm39) |
critical splice donor site |
probably null |
|
R9431:Fat2
|
UTSW |
11 |
55,142,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R9484:Fat2
|
UTSW |
11 |
55,200,752 (GRCm39) |
missense |
probably damaging |
0.99 |
R9509:Fat2
|
UTSW |
11 |
55,200,713 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9514:Fat2
|
UTSW |
11 |
55,175,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R9606:Fat2
|
UTSW |
11 |
55,180,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R9630:Fat2
|
UTSW |
11 |
55,147,605 (GRCm39) |
missense |
probably benign |
0.29 |
R9727:Fat2
|
UTSW |
11 |
55,159,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R9736:Fat2
|
UTSW |
11 |
55,194,751 (GRCm39) |
missense |
probably damaging |
1.00 |
X0010:Fat2
|
UTSW |
11 |
55,143,086 (GRCm39) |
missense |
probably benign |
0.00 |
X0011:Fat2
|
UTSW |
11 |
55,201,257 (GRCm39) |
missense |
probably damaging |
0.98 |
X0018:Fat2
|
UTSW |
11 |
55,187,036 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Fat2
|
UTSW |
11 |
55,200,240 (GRCm39) |
missense |
possibly damaging |
0.84 |
X0067:Fat2
|
UTSW |
11 |
55,174,060 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1176:Fat2
|
UTSW |
11 |
55,175,817 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fat2
|
UTSW |
11 |
55,173,621 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fat2
|
UTSW |
11 |
55,200,947 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Fat2
|
UTSW |
11 |
55,194,526 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fat2
|
UTSW |
11 |
55,169,792 (GRCm39) |
nonsense |
probably null |
|
Z1186:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1186:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
Z1187:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1187:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
Z1188:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1188:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
Z1189:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1189:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
Z1190:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1190:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
Z1191:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1191:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
Z1192:Fat2
|
UTSW |
11 |
55,200,625 (GRCm39) |
missense |
probably benign |
|
Z1192:Fat2
|
UTSW |
11 |
55,199,796 (GRCm39) |
frame shift |
probably null |
|
|