Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
A |
11: 110,030,458 (GRCm39) |
Y763F |
probably benign |
Het |
Abcb10 |
C |
T |
8: 124,688,791 (GRCm39) |
G495D |
probably damaging |
Het |
Actl11 |
A |
G |
9: 107,808,682 (GRCm39) |
T1002A |
probably damaging |
Het |
Ampd1 |
T |
A |
3: 102,998,980 (GRCm39) |
N378K |
probably damaging |
Het |
Arhgap42 |
A |
G |
9: 9,033,587 (GRCm39) |
|
probably benign |
Het |
Arhgap6 |
C |
A |
X: 167,579,499 (GRCm39) |
P95T |
possibly damaging |
Het |
Atg14 |
T |
C |
14: 47,798,102 (GRCm39) |
N87S |
probably benign |
Het |
Atp9b |
C |
T |
18: 80,805,353 (GRCm39) |
C735Y |
probably damaging |
Het |
Atp9b |
T |
A |
18: 80,822,122 (GRCm39) |
T110S |
probably benign |
Het |
Birc6 |
T |
G |
17: 74,919,314 (GRCm39) |
L221R |
probably damaging |
Het |
Ces1c |
A |
G |
8: 93,854,233 (GRCm39) |
F101L |
probably benign |
Het |
Cfap91 |
A |
G |
16: 38,141,762 (GRCm39) |
V390A |
probably damaging |
Het |
Chsy1 |
T |
C |
7: 65,821,750 (GRCm39) |
Y662H |
probably damaging |
Het |
Cldn12 |
A |
T |
5: 5,557,900 (GRCm39) |
F176I |
probably benign |
Het |
Col5a2 |
A |
G |
1: 45,450,626 (GRCm39) |
S374P |
probably benign |
Het |
Col6a2 |
A |
T |
10: 76,439,544 (GRCm39) |
V740E |
probably damaging |
Het |
Cpne3 |
A |
T |
4: 19,526,336 (GRCm39) |
I401K |
probably damaging |
Het |
Cspp1 |
T |
A |
1: 10,159,191 (GRCm39) |
|
probably null |
Het |
Ddn |
G |
A |
15: 98,704,647 (GRCm39) |
T215I |
possibly damaging |
Het |
Dync1i1 |
T |
C |
6: 5,769,799 (GRCm39) |
|
probably benign |
Het |
Dync2li1 |
T |
C |
17: 84,954,667 (GRCm39) |
|
probably benign |
Het |
Eif2a |
T |
A |
3: 58,445,005 (GRCm39) |
L50* |
probably null |
Het |
Elavl3 |
G |
A |
9: 21,929,875 (GRCm39) |
A343V |
probably damaging |
Het |
Fastkd1 |
T |
C |
2: 69,538,982 (GRCm39) |
|
probably null |
Het |
Fgf8 |
C |
A |
19: 45,730,786 (GRCm39) |
V80F |
possibly damaging |
Het |
Fras1 |
A |
T |
5: 96,891,046 (GRCm39) |
E2858D |
probably benign |
Het |
Fshr |
A |
T |
17: 89,293,529 (GRCm39) |
L383Q |
probably damaging |
Het |
Glb1 |
A |
G |
9: 114,246,171 (GRCm39) |
K74R |
probably benign |
Het |
Gmeb2 |
T |
G |
2: 180,897,019 (GRCm39) |
M290L |
probably benign |
Het |
Gnptg |
A |
G |
17: 25,454,828 (GRCm39) |
|
probably null |
Het |
Grik2 |
A |
C |
10: 49,008,871 (GRCm39) |
S739A |
probably damaging |
Het |
Grk2 |
T |
A |
19: 4,337,222 (GRCm39) |
Q659L |
probably benign |
Het |
Hdhd5 |
A |
G |
6: 120,491,473 (GRCm39) |
V210A |
probably damaging |
Het |
Hyal1 |
C |
T |
9: 107,455,091 (GRCm39) |
L134F |
probably damaging |
Het |
Itgb2 |
A |
T |
10: 77,381,987 (GRCm39) |
K18N |
possibly damaging |
Het |
Jam3 |
A |
T |
9: 27,017,701 (GRCm39) |
I29K |
possibly damaging |
Het |
Kcnh3 |
C |
A |
15: 99,137,796 (GRCm39) |
D830E |
probably benign |
Het |
Kcnmb4 |
T |
C |
10: 116,309,203 (GRCm39) |
D75G |
possibly damaging |
Het |
Kdm4b |
A |
G |
17: 56,707,025 (GRCm39) |
Y981C |
probably damaging |
Het |
Klk1b26 |
C |
A |
7: 43,665,810 (GRCm39) |
D207E |
probably benign |
Het |
Kmt2a |
G |
T |
9: 44,759,563 (GRCm39) |
T762N |
probably benign |
Het |
Kmt2d |
A |
G |
15: 98,742,819 (GRCm39) |
|
probably benign |
Het |
Lama4 |
T |
C |
10: 38,964,876 (GRCm39) |
S1414P |
possibly damaging |
Het |
Lce1f |
C |
G |
3: 92,626,276 (GRCm39) |
C127S |
unknown |
Het |
Map7d1 |
A |
G |
4: 126,128,558 (GRCm39) |
|
probably null |
Het |
Ninl |
T |
C |
2: 150,822,096 (GRCm39) |
D2G |
possibly damaging |
Het |
Or2w1b |
T |
A |
13: 21,300,303 (GRCm39) |
M147K |
probably benign |
Het |
Or5k3 |
A |
G |
16: 58,969,287 (GRCm39) |
T25A |
probably benign |
Het |
Or5m11b |
C |
T |
2: 85,806,372 (GRCm39) |
P262S |
possibly damaging |
Het |
Or6n1 |
T |
A |
1: 173,916,813 (GRCm39) |
L69* |
probably null |
Het |
Or8g18 |
G |
C |
9: 39,149,547 (GRCm39) |
P58A |
probably benign |
Het |
Pax8 |
A |
G |
2: 24,319,608 (GRCm39) |
Y381H |
possibly damaging |
Het |
Pde7a |
T |
C |
3: 19,314,408 (GRCm39) |
I63V |
possibly damaging |
Het |
Pgm3 |
A |
T |
9: 86,452,340 (GRCm39) |
F40Y |
probably benign |
Het |
Phrf1 |
G |
T |
7: 140,836,564 (GRCm39) |
D78Y |
probably damaging |
Het |
Plekhg1 |
C |
T |
10: 3,890,538 (GRCm39) |
|
probably benign |
Het |
Prss59 |
A |
T |
6: 40,898,652 (GRCm39) |
S199T |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,446,567 (GRCm39) |
S209P |
probably damaging |
Het |
Qtrt2 |
A |
T |
16: 43,689,337 (GRCm39) |
F220L |
probably benign |
Het |
Rgs9 |
A |
G |
11: 109,159,747 (GRCm39) |
|
probably null |
Het |
Rin3 |
A |
G |
12: 102,335,018 (GRCm39) |
T230A |
unknown |
Het |
Ros1 |
A |
T |
10: 51,974,773 (GRCm39) |
V1604E |
possibly damaging |
Het |
Rpp14 |
A |
G |
14: 8,090,528 (GRCm38) |
M151V |
probably benign |
Het |
Sacs |
T |
A |
14: 61,451,153 (GRCm39) |
F4400I |
possibly damaging |
Het |
Scamp1 |
C |
T |
13: 94,361,437 (GRCm39) |
V148I |
probably benign |
Het |
Slc13a5 |
A |
G |
11: 72,141,557 (GRCm39) |
C428R |
probably damaging |
Het |
Slc43a2 |
T |
G |
11: 75,453,733 (GRCm39) |
|
probably null |
Het |
Smarcc2 |
T |
A |
10: 128,299,741 (GRCm39) |
N135K |
probably damaging |
Het |
Snx15 |
G |
C |
19: 6,172,094 (GRCm39) |
S116R |
probably damaging |
Het |
Stag1 |
A |
G |
9: 100,737,885 (GRCm39) |
E414G |
possibly damaging |
Het |
Stag1 |
A |
T |
9: 100,769,426 (GRCm39) |
|
probably benign |
Het |
Tmem106a |
T |
A |
11: 101,481,263 (GRCm39) |
L257Q |
possibly damaging |
Het |
Trim42 |
A |
G |
9: 97,248,138 (GRCm39) |
L186P |
possibly damaging |
Het |
Tshb |
T |
A |
3: 102,685,624 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
A |
2: 76,584,484 (GRCm39) |
D13881V |
probably damaging |
Het |
Uqcrc2 |
T |
C |
7: 120,239,506 (GRCm39) |
V56A |
probably benign |
Het |
Uty |
G |
A |
Y: 1,197,228 (GRCm39) |
T113I |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,864,787 (GRCm39) |
E3032G |
probably benign |
Het |
Wfdc9 |
T |
G |
2: 164,493,729 (GRCm39) |
|
probably benign |
Het |
Zc3h7a |
G |
A |
16: 10,980,520 (GRCm39) |
T31I |
probably damaging |
Het |
Zfp462 |
T |
C |
4: 55,060,046 (GRCm39) |
S1191P |
probably damaging |
Het |
|
Other mutations in Tnc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Tnc
|
APN |
4 |
63,935,061 (GRCm39) |
splice site |
probably benign |
|
IGL00531:Tnc
|
APN |
4 |
63,889,390 (GRCm39) |
splice site |
probably benign |
|
IGL00674:Tnc
|
APN |
4 |
63,883,844 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01015:Tnc
|
APN |
4 |
63,935,571 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01090:Tnc
|
APN |
4 |
63,918,317 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01310:Tnc
|
APN |
4 |
63,931,314 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01331:Tnc
|
APN |
4 |
63,901,112 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01393:Tnc
|
APN |
4 |
63,932,291 (GRCm39) |
splice site |
probably benign |
|
IGL01411:Tnc
|
APN |
4 |
63,918,959 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01472:Tnc
|
APN |
4 |
63,924,656 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01552:Tnc
|
APN |
4 |
63,888,645 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01661:Tnc
|
APN |
4 |
63,888,544 (GRCm39) |
splice site |
probably benign |
|
IGL01669:Tnc
|
APN |
4 |
63,918,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01912:Tnc
|
APN |
4 |
63,926,977 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02028:Tnc
|
APN |
4 |
63,884,909 (GRCm39) |
splice site |
probably benign |
|
IGL02100:Tnc
|
APN |
4 |
63,918,398 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02549:Tnc
|
APN |
4 |
63,933,309 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02642:Tnc
|
APN |
4 |
63,883,816 (GRCm39) |
splice site |
probably benign |
|
IGL02712:Tnc
|
APN |
4 |
63,893,493 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02876:Tnc
|
APN |
4 |
63,933,338 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02886:Tnc
|
APN |
4 |
63,918,344 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02972:Tnc
|
APN |
4 |
63,894,715 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03073:Tnc
|
APN |
4 |
63,889,461 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL03116:Tnc
|
APN |
4 |
63,932,270 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03181:Tnc
|
APN |
4 |
63,885,543 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03358:Tnc
|
APN |
4 |
63,935,852 (GRCm39) |
nonsense |
probably null |
|
tancredo
|
UTSW |
4 |
63,911,534 (GRCm39) |
nonsense |
probably null |
|
BB009:Tnc
|
UTSW |
4 |
63,926,857 (GRCm39) |
missense |
probably benign |
|
BB019:Tnc
|
UTSW |
4 |
63,926,857 (GRCm39) |
missense |
probably benign |
|
P0020:Tnc
|
UTSW |
4 |
63,927,094 (GRCm39) |
missense |
possibly damaging |
0.63 |
PIT4377001:Tnc
|
UTSW |
4 |
63,935,973 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4403001:Tnc
|
UTSW |
4 |
63,882,904 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4468001:Tnc
|
UTSW |
4 |
63,882,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R0243:Tnc
|
UTSW |
4 |
63,888,657 (GRCm39) |
missense |
probably damaging |
0.98 |
R0362:Tnc
|
UTSW |
4 |
63,935,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0410:Tnc
|
UTSW |
4 |
63,925,931 (GRCm39) |
missense |
probably benign |
0.00 |
R0420:Tnc
|
UTSW |
4 |
63,918,396 (GRCm39) |
missense |
probably benign |
0.00 |
R0540:Tnc
|
UTSW |
4 |
63,938,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R0650:Tnc
|
UTSW |
4 |
63,926,971 (GRCm39) |
missense |
probably benign |
0.00 |
R1019:Tnc
|
UTSW |
4 |
63,880,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R1102:Tnc
|
UTSW |
4 |
63,938,705 (GRCm39) |
missense |
probably benign |
0.05 |
R1126:Tnc
|
UTSW |
4 |
63,936,357 (GRCm39) |
missense |
probably damaging |
0.99 |
R1141:Tnc
|
UTSW |
4 |
63,932,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R1142:Tnc
|
UTSW |
4 |
63,932,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R1307:Tnc
|
UTSW |
4 |
63,927,096 (GRCm39) |
missense |
probably damaging |
0.98 |
R1322:Tnc
|
UTSW |
4 |
63,932,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R1414:Tnc
|
UTSW |
4 |
63,883,932 (GRCm39) |
splice site |
probably benign |
|
R1470:Tnc
|
UTSW |
4 |
63,884,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Tnc
|
UTSW |
4 |
63,884,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R1506:Tnc
|
UTSW |
4 |
63,925,921 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1597:Tnc
|
UTSW |
4 |
63,924,621 (GRCm39) |
missense |
probably benign |
|
R1750:Tnc
|
UTSW |
4 |
63,890,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R1765:Tnc
|
UTSW |
4 |
63,932,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Tnc
|
UTSW |
4 |
63,936,333 (GRCm39) |
missense |
probably damaging |
0.98 |
R1808:Tnc
|
UTSW |
4 |
63,918,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Tnc
|
UTSW |
4 |
63,918,299 (GRCm39) |
missense |
probably benign |
0.00 |
R1932:Tnc
|
UTSW |
4 |
63,911,262 (GRCm39) |
critical splice donor site |
probably null |
|
R1941:Tnc
|
UTSW |
4 |
63,933,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Tnc
|
UTSW |
4 |
63,902,867 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2024:Tnc
|
UTSW |
4 |
63,882,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Tnc
|
UTSW |
4 |
63,913,903 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2327:Tnc
|
UTSW |
4 |
63,893,475 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2444:Tnc
|
UTSW |
4 |
63,933,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R2982:Tnc
|
UTSW |
4 |
63,938,756 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3874:Tnc
|
UTSW |
4 |
63,926,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4110:Tnc
|
UTSW |
4 |
63,933,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R4360:Tnc
|
UTSW |
4 |
63,935,161 (GRCm39) |
missense |
probably benign |
0.35 |
R4371:Tnc
|
UTSW |
4 |
63,888,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R4434:Tnc
|
UTSW |
4 |
63,926,066 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4438:Tnc
|
UTSW |
4 |
63,926,066 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4570:Tnc
|
UTSW |
4 |
63,913,909 (GRCm39) |
missense |
probably damaging |
0.99 |
R4595:Tnc
|
UTSW |
4 |
63,913,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R4749:Tnc
|
UTSW |
4 |
63,913,876 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4756:Tnc
|
UTSW |
4 |
63,885,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R4824:Tnc
|
UTSW |
4 |
63,935,857 (GRCm39) |
nonsense |
probably null |
|
R4957:Tnc
|
UTSW |
4 |
63,894,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R4977:Tnc
|
UTSW |
4 |
63,924,485 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5001:Tnc
|
UTSW |
4 |
63,918,299 (GRCm39) |
missense |
probably benign |
0.16 |
R5001:Tnc
|
UTSW |
4 |
63,902,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Tnc
|
UTSW |
4 |
63,924,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R5049:Tnc
|
UTSW |
4 |
63,936,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R5066:Tnc
|
UTSW |
4 |
63,893,466 (GRCm39) |
missense |
probably damaging |
0.96 |
R5073:Tnc
|
UTSW |
4 |
63,938,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R5116:Tnc
|
UTSW |
4 |
63,885,452 (GRCm39) |
critical splice donor site |
probably null |
|
R5195:Tnc
|
UTSW |
4 |
63,885,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5200:Tnc
|
UTSW |
4 |
63,889,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R5221:Tnc
|
UTSW |
4 |
63,911,534 (GRCm39) |
nonsense |
probably null |
|
R5237:Tnc
|
UTSW |
4 |
63,880,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R5265:Tnc
|
UTSW |
4 |
63,911,443 (GRCm39) |
missense |
probably benign |
0.00 |
R5275:Tnc
|
UTSW |
4 |
63,882,967 (GRCm39) |
nonsense |
probably null |
|
R5346:Tnc
|
UTSW |
4 |
63,926,892 (GRCm39) |
missense |
probably benign |
|
R5409:Tnc
|
UTSW |
4 |
63,925,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5409:Tnc
|
UTSW |
4 |
63,884,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R5469:Tnc
|
UTSW |
4 |
63,932,162 (GRCm39) |
splice site |
probably null |
|
R5518:Tnc
|
UTSW |
4 |
63,935,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Tnc
|
UTSW |
4 |
63,926,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R5588:Tnc
|
UTSW |
4 |
63,924,659 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5686:Tnc
|
UTSW |
4 |
63,925,967 (GRCm39) |
splice site |
probably null |
|
R5686:Tnc
|
UTSW |
4 |
63,927,032 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5837:Tnc
|
UTSW |
4 |
63,931,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R5976:Tnc
|
UTSW |
4 |
63,936,403 (GRCm39) |
missense |
probably benign |
0.17 |
R6156:Tnc
|
UTSW |
4 |
63,888,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R6182:Tnc
|
UTSW |
4 |
63,927,033 (GRCm39) |
missense |
probably damaging |
0.99 |
R6360:Tnc
|
UTSW |
4 |
63,918,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R6416:Tnc
|
UTSW |
4 |
63,926,053 (GRCm39) |
missense |
probably benign |
0.05 |
R6778:Tnc
|
UTSW |
4 |
63,913,835 (GRCm39) |
missense |
probably benign |
0.12 |
R6798:Tnc
|
UTSW |
4 |
63,883,841 (GRCm39) |
missense |
probably benign |
0.02 |
R6799:Tnc
|
UTSW |
4 |
63,883,841 (GRCm39) |
missense |
probably benign |
0.02 |
R6943:Tnc
|
UTSW |
4 |
63,900,982 (GRCm39) |
missense |
probably damaging |
0.97 |
R7027:Tnc
|
UTSW |
4 |
63,902,826 (GRCm39) |
missense |
probably benign |
0.02 |
R7183:Tnc
|
UTSW |
4 |
63,931,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R7204:Tnc
|
UTSW |
4 |
63,889,392 (GRCm39) |
splice site |
probably null |
|
R7317:Tnc
|
UTSW |
4 |
63,890,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R7323:Tnc
|
UTSW |
4 |
63,889,469 (GRCm39) |
missense |
probably damaging |
0.96 |
R7327:Tnc
|
UTSW |
4 |
63,882,999 (GRCm39) |
splice site |
probably null |
|
R7382:Tnc
|
UTSW |
4 |
63,932,280 (GRCm39) |
nonsense |
probably null |
|
R7399:Tnc
|
UTSW |
4 |
63,938,894 (GRCm39) |
start gained |
probably benign |
|
R7479:Tnc
|
UTSW |
4 |
63,935,865 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7585:Tnc
|
UTSW |
4 |
63,938,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R7932:Tnc
|
UTSW |
4 |
63,926,857 (GRCm39) |
missense |
probably benign |
|
R7947:Tnc
|
UTSW |
4 |
63,935,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R7974:Tnc
|
UTSW |
4 |
63,918,961 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7991:Tnc
|
UTSW |
4 |
63,926,983 (GRCm39) |
missense |
probably benign |
0.42 |
R8004:Tnc
|
UTSW |
4 |
63,902,894 (GRCm39) |
missense |
probably benign |
0.04 |
R8080:Tnc
|
UTSW |
4 |
63,894,706 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8109:Tnc
|
UTSW |
4 |
63,927,000 (GRCm39) |
missense |
probably benign |
0.11 |
R8145:Tnc
|
UTSW |
4 |
63,935,716 (GRCm39) |
missense |
probably benign |
|
R8340:Tnc
|
UTSW |
4 |
63,926,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R8360:Tnc
|
UTSW |
4 |
63,885,511 (GRCm39) |
missense |
probably benign |
0.00 |
R8671:Tnc
|
UTSW |
4 |
63,935,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R8691:Tnc
|
UTSW |
4 |
63,880,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R8759:Tnc
|
UTSW |
4 |
63,924,501 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8864:Tnc
|
UTSW |
4 |
63,911,296 (GRCm39) |
missense |
probably damaging |
0.98 |
R8927:Tnc
|
UTSW |
4 |
63,925,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Tnc
|
UTSW |
4 |
63,925,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R8949:Tnc
|
UTSW |
4 |
63,927,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R8956:Tnc
|
UTSW |
4 |
63,918,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R9016:Tnc
|
UTSW |
4 |
63,935,331 (GRCm39) |
missense |
probably benign |
0.23 |
R9049:Tnc
|
UTSW |
4 |
63,918,247 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9097:Tnc
|
UTSW |
4 |
63,888,622 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9114:Tnc
|
UTSW |
4 |
63,890,973 (GRCm39) |
missense |
probably benign |
0.03 |
R9151:Tnc
|
UTSW |
4 |
63,938,686 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9488:Tnc
|
UTSW |
4 |
63,913,942 (GRCm39) |
missense |
probably damaging |
0.99 |
R9537:Tnc
|
UTSW |
4 |
63,884,821 (GRCm39) |
missense |
probably damaging |
0.99 |
R9666:Tnc
|
UTSW |
4 |
63,926,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R9700:Tnc
|
UTSW |
4 |
63,933,186 (GRCm39) |
missense |
probably damaging |
0.99 |
R9703:Tnc
|
UTSW |
4 |
63,889,412 (GRCm39) |
missense |
probably benign |
0.00 |
R9771:Tnc
|
UTSW |
4 |
63,925,600 (GRCm39) |
missense |
probably damaging |
1.00 |
S24628:Tnc
|
UTSW |
4 |
63,936,249 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tnc
|
UTSW |
4 |
63,925,663 (GRCm39) |
nonsense |
probably null |
|
Z1177:Tnc
|
UTSW |
4 |
63,878,781 (GRCm39) |
critical splice acceptor site |
probably null |
|
|