Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
T |
C |
5: 144,982,351 (GRCm39) |
V312A |
probably damaging |
Het |
2810408A11Rik |
A |
G |
11: 69,791,453 (GRCm39) |
V42A |
probably damaging |
Het |
Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
Angpt1 |
T |
A |
15: 42,387,012 (GRCm39) |
Q114L |
probably damaging |
Het |
Apc2 |
T |
C |
10: 80,144,964 (GRCm39) |
I625T |
probably damaging |
Het |
Atg2a |
T |
C |
19: 6,300,628 (GRCm39) |
V735A |
probably benign |
Het |
Birc6 |
T |
A |
17: 74,947,008 (GRCm39) |
I2909N |
probably damaging |
Het |
C7 |
C |
G |
15: 5,041,557 (GRCm39) |
D450H |
probably damaging |
Het |
Cachd1 |
C |
T |
4: 100,821,632 (GRCm39) |
T403I |
probably damaging |
Het |
Cachd1 |
T |
A |
4: 100,824,240 (GRCm39) |
F560L |
probably benign |
Het |
Cacna2d2 |
A |
T |
9: 107,403,350 (GRCm39) |
Y944F |
probably benign |
Het |
Cdkal1 |
C |
T |
13: 30,034,031 (GRCm39) |
D21N |
probably damaging |
Het |
Col18a1 |
T |
C |
10: 76,895,815 (GRCm39) |
R901G |
probably damaging |
Het |
Col27a1 |
C |
T |
4: 63,143,950 (GRCm39) |
P546L |
probably damaging |
Het |
Cps1 |
C |
T |
1: 67,210,041 (GRCm39) |
R624W |
possibly damaging |
Het |
Cyp11a1 |
A |
T |
9: 57,925,643 (GRCm39) |
I93F |
probably benign |
Het |
Cyp2c40 |
G |
C |
19: 39,775,250 (GRCm39) |
T334R |
probably damaging |
Het |
Cyp4f37 |
A |
G |
17: 32,848,864 (GRCm39) |
D244G |
possibly damaging |
Het |
D630003M21Rik |
A |
T |
2: 158,062,390 (GRCm39) |
D43E |
probably damaging |
Het |
Ep400 |
C |
A |
5: 110,833,357 (GRCm39) |
C1955F |
unknown |
Het |
Ethe1 |
G |
A |
7: 24,293,371 (GRCm39) |
V6I |
probably benign |
Het |
Fasn |
T |
C |
11: 120,707,997 (GRCm39) |
Y685C |
probably damaging |
Het |
Gga2 |
T |
G |
7: 121,611,444 (GRCm39) |
D38A |
probably damaging |
Het |
Gm43302 |
T |
A |
5: 105,423,660 (GRCm39) |
I438F |
probably benign |
Het |
Grm1 |
T |
A |
10: 10,955,610 (GRCm39) |
T225S |
possibly damaging |
Het |
Hic2 |
G |
T |
16: 17,076,511 (GRCm39) |
V447L |
probably damaging |
Het |
Hsf2 |
G |
A |
10: 57,388,242 (GRCm39) |
C462Y |
probably damaging |
Het |
Ice1 |
T |
C |
13: 70,752,672 (GRCm39) |
D1138G |
probably damaging |
Het |
Il6 |
A |
G |
5: 30,224,433 (GRCm39) |
T158A |
probably benign |
Het |
Inpp5d |
T |
A |
1: 87,595,611 (GRCm39) |
V120E |
probably benign |
Het |
Iqca1 |
T |
C |
1: 90,008,625 (GRCm39) |
N456S |
probably benign |
Het |
Itgal |
T |
A |
7: 126,908,794 (GRCm39) |
|
probably null |
Het |
Lrrc66 |
G |
C |
5: 73,768,198 (GRCm39) |
Q248E |
probably benign |
Het |
Lrrc7 |
T |
A |
3: 157,865,929 (GRCm39) |
M1271L |
possibly damaging |
Het |
Lrrc74a |
T |
C |
12: 86,795,827 (GRCm39) |
S267P |
probably damaging |
Het |
Map2 |
T |
C |
1: 66,453,233 (GRCm39) |
S550P |
probably damaging |
Het |
Mapk8ip3 |
A |
T |
17: 25,143,119 (GRCm39) |
|
probably null |
Het |
Mdm4 |
A |
C |
1: 132,924,384 (GRCm39) |
S246A |
probably damaging |
Het |
Med23 |
A |
G |
10: 24,779,584 (GRCm39) |
E887G |
probably damaging |
Het |
Mta1 |
C |
T |
12: 113,091,659 (GRCm39) |
A254V |
probably damaging |
Het |
Myh2 |
A |
G |
11: 67,064,300 (GRCm39) |
Y85C |
possibly damaging |
Het |
Myo1g |
A |
G |
11: 6,465,988 (GRCm39) |
Y366H |
probably damaging |
Het |
Nalcn |
G |
A |
14: 123,515,678 (GRCm39) |
P1708S |
probably benign |
Het |
Nlrp9c |
A |
T |
7: 26,093,543 (GRCm39) |
S41T |
probably benign |
Het |
Nptx2 |
T |
A |
5: 144,490,248 (GRCm39) |
S226T |
possibly damaging |
Het |
Nup85 |
T |
A |
11: 115,473,771 (GRCm39) |
S562T |
probably benign |
Het |
Nxpe5 |
T |
C |
5: 138,237,797 (GRCm39) |
V107A |
probably benign |
Het |
Obi1 |
A |
G |
14: 104,717,098 (GRCm39) |
V425A |
possibly damaging |
Het |
Oga |
T |
C |
19: 45,765,423 (GRCm39) |
E128G |
probably benign |
Het |
Or10ac1 |
A |
T |
6: 42,515,453 (GRCm39) |
F168I |
probably damaging |
Het |
Or10al7 |
A |
G |
17: 38,366,328 (GRCm39) |
V43A |
probably benign |
Het |
Or13c3 |
T |
A |
4: 52,855,674 (GRCm39) |
I280F |
probably benign |
Het |
Or6p1 |
A |
G |
1: 174,258,905 (GRCm39) |
T304A |
probably benign |
Het |
Pcdhb12 |
C |
T |
18: 37,569,495 (GRCm39) |
P214S |
possibly damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,455,725 (GRCm39) |
F702I |
probably damaging |
Het |
Pcnx1 |
T |
C |
12: 82,022,094 (GRCm39) |
F1475S |
probably damaging |
Het |
Pde5a |
C |
A |
3: 122,523,013 (GRCm39) |
T40N |
probably benign |
Het |
Pnpla2 |
T |
A |
7: 141,039,481 (GRCm39) |
V398E |
probably damaging |
Het |
Pramel19 |
G |
A |
4: 101,797,655 (GRCm39) |
V18M |
probably benign |
Het |
Pwwp4a |
G |
T |
X: 72,171,261 (GRCm39) |
G218C |
probably damaging |
Het |
Rab20 |
T |
C |
8: 11,504,223 (GRCm39) |
K159R |
probably benign |
Het |
Rfwd3 |
C |
T |
8: 112,014,874 (GRCm39) |
R326Q |
probably damaging |
Het |
Rgs12 |
T |
A |
5: 35,123,747 (GRCm39) |
V510D |
probably benign |
Het |
Slamf6 |
T |
C |
1: 171,770,154 (GRCm39) |
|
probably benign |
Het |
Slc27a5 |
A |
T |
7: 12,731,534 (GRCm39) |
C23* |
probably null |
Het |
Slc35e2 |
T |
C |
4: 155,694,621 (GRCm39) |
V56A |
possibly damaging |
Het |
Slx4ip |
T |
C |
2: 136,909,643 (GRCm39) |
S143P |
probably damaging |
Het |
Stat5a |
C |
T |
11: 100,770,112 (GRCm39) |
S463F |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,146,562 (GRCm39) |
D360G |
possibly damaging |
Het |
Tas2r143 |
A |
T |
6: 42,377,305 (GRCm39) |
D45V |
probably damaging |
Het |
Tdrd5 |
G |
T |
1: 156,105,079 (GRCm39) |
R516S |
probably damaging |
Het |
Thy1 |
A |
G |
9: 43,958,636 (GRCm39) |
D126G |
probably benign |
Het |
Tspear |
C |
T |
10: 77,709,019 (GRCm39) |
T415I |
probably benign |
Het |
Ttll5 |
C |
A |
12: 85,980,176 (GRCm39) |
T920K |
probably benign |
Het |
Tut4 |
T |
C |
4: 108,365,152 (GRCm39) |
F542L |
probably damaging |
Het |
Umod |
T |
C |
7: 119,076,574 (GRCm39) |
E64G |
possibly damaging |
Het |
Usf3 |
A |
G |
16: 44,036,033 (GRCm39) |
N171S |
probably damaging |
Het |
Vmn1r23 |
T |
A |
6: 57,903,675 (GRCm39) |
R34S |
probably damaging |
Het |
Wasf1 |
C |
G |
10: 40,810,475 (GRCm39) |
P239R |
possibly damaging |
Het |
Wdr95 |
C |
T |
5: 149,487,857 (GRCm39) |
R164* |
probably null |
Het |
Zan |
C |
A |
5: 137,418,251 (GRCm39) |
C2949F |
unknown |
Het |
Zbed4 |
T |
C |
15: 88,665,080 (GRCm39) |
S383P |
probably benign |
Het |
Zfand5 |
T |
A |
19: 21,253,895 (GRCm39) |
C33S |
probably damaging |
Het |
Zfp12 |
A |
G |
5: 143,230,984 (GRCm39) |
Y437C |
probably damaging |
Het |
Zfp451 |
A |
C |
1: 33,852,849 (GRCm39) |
S22A |
probably benign |
Het |
|
Other mutations in F5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00840:F5
|
APN |
1 |
164,007,093 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00843:F5
|
APN |
1 |
164,039,360 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00904:F5
|
APN |
1 |
164,021,578 (GRCm39) |
missense |
probably benign |
|
IGL00913:F5
|
APN |
1 |
164,032,465 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01099:F5
|
APN |
1 |
164,021,903 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01134:F5
|
APN |
1 |
164,019,548 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01313:F5
|
APN |
1 |
164,021,181 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01635:F5
|
APN |
1 |
164,035,427 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01697:F5
|
APN |
1 |
164,021,621 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01768:F5
|
APN |
1 |
164,003,914 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01795:F5
|
APN |
1 |
164,021,959 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01835:F5
|
APN |
1 |
164,021,937 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01843:F5
|
APN |
1 |
164,039,395 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01989:F5
|
APN |
1 |
164,003,876 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02036:F5
|
APN |
1 |
164,010,571 (GRCm39) |
splice site |
probably benign |
|
IGL02065:F5
|
APN |
1 |
164,017,695 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02077:F5
|
APN |
1 |
164,026,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02139:F5
|
APN |
1 |
164,020,243 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02210:F5
|
APN |
1 |
164,017,710 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02415:F5
|
APN |
1 |
164,019,498 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02440:F5
|
APN |
1 |
164,034,635 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02471:F5
|
APN |
1 |
164,001,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02535:F5
|
APN |
1 |
164,026,302 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02537:F5
|
APN |
1 |
164,020,686 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02628:F5
|
APN |
1 |
164,021,644 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02638:F5
|
APN |
1 |
164,012,177 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02824:F5
|
APN |
1 |
164,021,916 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02977:F5
|
APN |
1 |
164,021,590 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03028:F5
|
APN |
1 |
164,020,569 (GRCm39) |
nonsense |
probably null |
|
IGL03064:F5
|
APN |
1 |
164,023,163 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03127:F5
|
APN |
1 |
164,021,107 (GRCm39) |
missense |
probably benign |
0.45 |
IGL03131:F5
|
APN |
1 |
163,989,388 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03348:F5
|
APN |
1 |
164,021,721 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03387:F5
|
APN |
1 |
164,020,801 (GRCm39) |
missense |
probably damaging |
1.00 |
James_dean
|
UTSW |
1 |
164,032,389 (GRCm39) |
missense |
probably benign |
0.43 |
BB002:F5
|
UTSW |
1 |
164,003,935 (GRCm39) |
critical splice donor site |
probably null |
|
BB012:F5
|
UTSW |
1 |
164,003,935 (GRCm39) |
critical splice donor site |
probably null |
|
R0002:F5
|
UTSW |
1 |
164,029,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0095:F5
|
UTSW |
1 |
164,019,537 (GRCm39) |
nonsense |
probably null |
|
R0116:F5
|
UTSW |
1 |
164,012,483 (GRCm39) |
missense |
probably benign |
0.01 |
R0359:F5
|
UTSW |
1 |
164,007,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R0426:F5
|
UTSW |
1 |
164,010,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R0452:F5
|
UTSW |
1 |
164,012,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R0457:F5
|
UTSW |
1 |
164,021,769 (GRCm39) |
missense |
probably benign |
0.00 |
R0520:F5
|
UTSW |
1 |
164,037,156 (GRCm39) |
missense |
probably benign |
0.15 |
R0522:F5
|
UTSW |
1 |
164,039,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R0554:F5
|
UTSW |
1 |
164,007,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R0575:F5
|
UTSW |
1 |
164,003,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R0734:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R0739:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1062:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1063:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1149:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1149:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1150:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1151:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1152:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1221:F5
|
UTSW |
1 |
163,989,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1284:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1286:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1358:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1360:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1362:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1383:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:F5
|
UTSW |
1 |
164,026,402 (GRCm39) |
missense |
probably benign |
0.02 |
R1465:F5
|
UTSW |
1 |
164,026,402 (GRCm39) |
missense |
probably benign |
0.02 |
R1545:F5
|
UTSW |
1 |
164,036,529 (GRCm39) |
nonsense |
probably null |
|
R1561:F5
|
UTSW |
1 |
164,014,472 (GRCm39) |
nonsense |
probably null |
|
R1623:F5
|
UTSW |
1 |
164,023,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:F5
|
UTSW |
1 |
164,035,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R1673:F5
|
UTSW |
1 |
164,007,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R1689:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1705:F5
|
UTSW |
1 |
164,045,059 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1732:F5
|
UTSW |
1 |
164,001,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R1763:F5
|
UTSW |
1 |
164,020,104 (GRCm39) |
missense |
probably benign |
0.04 |
R1799:F5
|
UTSW |
1 |
164,021,100 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1800:F5
|
UTSW |
1 |
164,010,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R1842:F5
|
UTSW |
1 |
164,012,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R1915:F5
|
UTSW |
1 |
164,010,486 (GRCm39) |
missense |
probably damaging |
0.97 |
R1926:F5
|
UTSW |
1 |
164,007,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2025:F5
|
UTSW |
1 |
164,037,044 (GRCm39) |
missense |
probably benign |
0.05 |
R2198:F5
|
UTSW |
1 |
164,034,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R2258:F5
|
UTSW |
1 |
164,019,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R2264:F5
|
UTSW |
1 |
164,021,971 (GRCm39) |
missense |
probably benign |
0.32 |
R2281:F5
|
UTSW |
1 |
164,023,289 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2407:F5
|
UTSW |
1 |
164,039,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R2445:F5
|
UTSW |
1 |
164,017,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R2860:F5
|
UTSW |
1 |
164,012,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2861:F5
|
UTSW |
1 |
164,012,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2862:F5
|
UTSW |
1 |
164,012,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2899:F5
|
UTSW |
1 |
164,014,469 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2910:F5
|
UTSW |
1 |
164,032,389 (GRCm39) |
missense |
probably benign |
0.43 |
R2912:F5
|
UTSW |
1 |
164,021,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R2996:F5
|
UTSW |
1 |
164,010,486 (GRCm39) |
missense |
probably damaging |
0.97 |
R3745:F5
|
UTSW |
1 |
164,014,348 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3901:F5
|
UTSW |
1 |
164,003,798 (GRCm39) |
missense |
probably benign |
0.08 |
R3902:F5
|
UTSW |
1 |
164,003,798 (GRCm39) |
missense |
probably benign |
0.08 |
R4365:F5
|
UTSW |
1 |
164,012,519 (GRCm39) |
missense |
probably damaging |
0.98 |
R4448:F5
|
UTSW |
1 |
164,026,468 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4490:F5
|
UTSW |
1 |
164,044,964 (GRCm39) |
missense |
probably benign |
0.40 |
R4514:F5
|
UTSW |
1 |
163,979,566 (GRCm39) |
unclassified |
probably benign |
|
R4598:F5
|
UTSW |
1 |
164,032,366 (GRCm39) |
missense |
probably benign |
0.05 |
R4608:F5
|
UTSW |
1 |
164,036,598 (GRCm39) |
missense |
probably benign |
0.12 |
R4661:F5
|
UTSW |
1 |
164,012,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:F5
|
UTSW |
1 |
164,001,755 (GRCm39) |
missense |
probably benign |
0.00 |
R4689:F5
|
UTSW |
1 |
163,979,542 (GRCm39) |
unclassified |
probably benign |
|
R4716:F5
|
UTSW |
1 |
164,021,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R4732:F5
|
UTSW |
1 |
164,009,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:F5
|
UTSW |
1 |
164,009,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R4854:F5
|
UTSW |
1 |
164,019,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:F5
|
UTSW |
1 |
164,039,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:F5
|
UTSW |
1 |
164,021,755 (GRCm39) |
missense |
probably benign |
|
R5001:F5
|
UTSW |
1 |
164,023,139 (GRCm39) |
missense |
probably benign |
0.00 |
R5042:F5
|
UTSW |
1 |
164,047,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R5056:F5
|
UTSW |
1 |
164,019,601 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5061:F5
|
UTSW |
1 |
164,021,749 (GRCm39) |
missense |
probably benign |
0.00 |
R5143:F5
|
UTSW |
1 |
164,039,397 (GRCm39) |
missense |
probably damaging |
0.98 |
R5622:F5
|
UTSW |
1 |
164,020,134 (GRCm39) |
missense |
probably benign |
0.09 |
R5626:F5
|
UTSW |
1 |
164,036,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R5658:F5
|
UTSW |
1 |
164,019,907 (GRCm39) |
missense |
probably damaging |
0.96 |
R5702:F5
|
UTSW |
1 |
164,022,116 (GRCm39) |
nonsense |
probably null |
|
R5795:F5
|
UTSW |
1 |
163,979,578 (GRCm39) |
missense |
probably benign |
0.09 |
R5884:F5
|
UTSW |
1 |
164,023,215 (GRCm39) |
missense |
probably benign |
0.01 |
R6036:F5
|
UTSW |
1 |
164,012,565 (GRCm39) |
missense |
probably damaging |
0.99 |
R6036:F5
|
UTSW |
1 |
164,012,565 (GRCm39) |
missense |
probably damaging |
0.99 |
R6151:F5
|
UTSW |
1 |
164,017,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:F5
|
UTSW |
1 |
164,009,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R6345:F5
|
UTSW |
1 |
164,019,520 (GRCm39) |
missense |
probably benign |
0.13 |
R6391:F5
|
UTSW |
1 |
164,021,062 (GRCm39) |
missense |
probably damaging |
0.99 |
R6542:F5
|
UTSW |
1 |
164,022,037 (GRCm39) |
missense |
probably benign |
0.32 |
R6620:F5
|
UTSW |
1 |
164,014,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:F5
|
UTSW |
1 |
164,021,076 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6754:F5
|
UTSW |
1 |
164,021,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R6774:F5
|
UTSW |
1 |
164,014,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R6802:F5
|
UTSW |
1 |
164,006,925 (GRCm39) |
missense |
probably damaging |
0.98 |
R6810:F5
|
UTSW |
1 |
164,014,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R6983:F5
|
UTSW |
1 |
164,021,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R7000:F5
|
UTSW |
1 |
164,007,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R7151:F5
|
UTSW |
1 |
164,029,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R7193:F5
|
UTSW |
1 |
164,046,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R7230:F5
|
UTSW |
1 |
164,012,522 (GRCm39) |
missense |
probably benign |
|
R7324:F5
|
UTSW |
1 |
164,021,150 (GRCm39) |
small deletion |
probably benign |
|
R7350:F5
|
UTSW |
1 |
164,020,277 (GRCm39) |
missense |
probably benign |
0.08 |
R7466:F5
|
UTSW |
1 |
164,020,897 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7503:F5
|
UTSW |
1 |
164,019,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R7626:F5
|
UTSW |
1 |
164,014,481 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7742:F5
|
UTSW |
1 |
164,035,453 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7837:F5
|
UTSW |
1 |
164,014,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R7848:F5
|
UTSW |
1 |
163,989,446 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7925:F5
|
UTSW |
1 |
164,003,935 (GRCm39) |
critical splice donor site |
probably null |
|
R8053:F5
|
UTSW |
1 |
164,020,338 (GRCm39) |
missense |
probably benign |
0.26 |
R8094:F5
|
UTSW |
1 |
164,036,509 (GRCm39) |
missense |
probably benign |
0.06 |
R8175:F5
|
UTSW |
1 |
164,019,834 (GRCm39) |
nonsense |
probably null |
|
R8209:F5
|
UTSW |
1 |
164,021,959 (GRCm39) |
missense |
probably benign |
0.00 |
R8226:F5
|
UTSW |
1 |
164,021,959 (GRCm39) |
missense |
probably benign |
0.00 |
R8266:F5
|
UTSW |
1 |
164,012,693 (GRCm39) |
critical splice donor site |
probably null |
|
R8517:F5
|
UTSW |
1 |
164,003,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R8684:F5
|
UTSW |
1 |
164,045,111 (GRCm39) |
missense |
probably benign |
0.01 |
R8941:F5
|
UTSW |
1 |
164,026,440 (GRCm39) |
missense |
probably benign |
0.19 |
R9130:F5
|
UTSW |
1 |
164,001,830 (GRCm39) |
missense |
probably benign |
0.37 |
R9181:F5
|
UTSW |
1 |
164,019,895 (GRCm39) |
missense |
probably benign |
0.00 |
R9186:F5
|
UTSW |
1 |
164,021,470 (GRCm39) |
missense |
probably benign |
|
R9233:F5
|
UTSW |
1 |
164,047,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R9314:F5
|
UTSW |
1 |
164,029,146 (GRCm39) |
missense |
probably benign |
0.01 |
R9631:F5
|
UTSW |
1 |
164,014,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:F5
|
UTSW |
1 |
164,021,730 (GRCm39) |
missense |
probably benign |
0.15 |
X0024:F5
|
UTSW |
1 |
164,020,557 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:F5
|
UTSW |
1 |
163,981,954 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:F5
|
UTSW |
1 |
164,012,085 (GRCm39) |
missense |
probably damaging |
0.97 |
|