Other mutations in this stock |
Total: 129 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010B08Rik |
C |
T |
2: 173,561,599 (GRCm39) |
|
probably benign |
Het |
Ambp |
A |
G |
4: 63,062,502 (GRCm39) |
Y246H |
probably damaging |
Het |
Amz1 |
T |
C |
5: 140,735,088 (GRCm39) |
|
probably null |
Het |
Anks6 |
G |
A |
4: 47,027,109 (GRCm39) |
T703I |
probably damaging |
Het |
Armc2 |
A |
G |
10: 41,823,883 (GRCm39) |
|
probably benign |
Het |
Atp7b |
T |
A |
8: 22,484,672 (GRCm39) |
I1347F |
probably damaging |
Het |
Atp8a1 |
C |
T |
5: 67,779,945 (GRCm39) |
W1149* |
probably null |
Het |
Auh |
A |
G |
13: 52,995,046 (GRCm39) |
I173T |
probably damaging |
Het |
Axin2 |
T |
C |
11: 108,814,829 (GRCm39) |
L239P |
possibly damaging |
Het |
Bbs1 |
A |
T |
19: 4,949,287 (GRCm39) |
F257L |
possibly damaging |
Het |
Cacna2d2 |
C |
T |
9: 107,401,867 (GRCm39) |
P774L |
probably damaging |
Het |
Card6 |
A |
G |
15: 5,137,788 (GRCm39) |
L22P |
probably damaging |
Het |
Ccdc171 |
C |
T |
4: 83,579,946 (GRCm39) |
|
|
Het |
Ccn2 |
T |
C |
10: 24,471,988 (GRCm39) |
V70A |
probably damaging |
Het |
Cdc14a |
T |
A |
3: 116,122,310 (GRCm39) |
N219I |
possibly damaging |
Het |
Cfap65 |
G |
T |
1: 74,967,501 (GRCm39) |
N192K |
probably benign |
Het |
Col14a1 |
T |
C |
15: 55,312,272 (GRCm39) |
|
probably benign |
Het |
Col5a1 |
A |
G |
2: 27,914,665 (GRCm39) |
T94A |
probably benign |
Het |
Col6a5 |
T |
C |
9: 105,759,113 (GRCm39) |
N2031S |
probably damaging |
Het |
Col7a1 |
T |
C |
9: 108,794,989 (GRCm39) |
|
probably benign |
Het |
Cyld |
T |
C |
8: 89,473,543 (GRCm39) |
S739P |
probably damaging |
Het |
Dbr1 |
A |
G |
9: 99,466,072 (GRCm39) |
|
probably null |
Het |
Dip2b |
T |
C |
15: 100,100,233 (GRCm39) |
L1267P |
probably damaging |
Het |
Dolk |
A |
G |
2: 30,175,586 (GRCm39) |
M153T |
probably benign |
Het |
Duxf1 |
C |
T |
10: 58,060,704 (GRCm39) |
E17K |
possibly damaging |
Het |
Duxf1 |
G |
A |
10: 58,060,136 (GRCm39) |
|
probably benign |
Het |
Duxf1 |
A |
G |
10: 58,059,276 (GRCm39) |
C493R |
probably benign |
Het |
Duxf3 |
A |
C |
10: 58,067,498 (GRCm39) |
S27A |
probably benign |
Het |
Eef1d |
C |
T |
15: 75,775,581 (GRCm39) |
R26H |
probably benign |
Homo |
Efcab5 |
C |
T |
11: 77,028,517 (GRCm39) |
|
|
Het |
Epc1 |
T |
C |
18: 6,449,246 (GRCm39) |
D467G |
probably damaging |
Het |
Fancm |
T |
G |
12: 65,152,196 (GRCm39) |
M884R |
probably benign |
Het |
Fbxo24 |
G |
T |
5: 137,620,164 (GRCm39) |
H15N |
probably damaging |
Het |
Frem1 |
A |
G |
4: 82,924,045 (GRCm39) |
F305L |
probably damaging |
Het |
Fstl5 |
A |
G |
3: 76,567,006 (GRCm39) |
D550G |
probably damaging |
Het |
Gcnt3 |
T |
G |
9: 69,941,326 (GRCm39) |
K414T |
possibly damaging |
Het |
Gm10718 |
A |
T |
9: 3,024,417 (GRCm39) |
T134S |
probably benign |
Het |
Gm10722 |
A |
G,C |
9: 3,001,414 (GRCm39) |
|
probably benign |
Het |
Gm10800 |
T |
C |
2: 98,497,163 (GRCm39) |
R152G |
probably benign |
Homo |
Gm10800 |
C |
A |
2: 98,497,250 (GRCm39) |
V123F |
probably benign |
Homo |
Gm10800 |
A |
C |
2: 98,496,893 (GRCm39) |
F220C |
probably benign |
Het |
Gm10801 |
A |
G |
2: 98,492,648 (GRCm39) |
R23G |
probably benign |
Homo |
Gm11168 |
C |
T |
9: 3,004,605 (GRCm39) |
P49S |
probably benign |
Het |
Gm21738 |
G |
A |
14: 19,417,330 (GRCm38) |
S66L |
probably benign |
Het |
Hjurp |
TCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCTG |
T |
1: 88,194,000 (GRCm39) |
|
probably benign |
Het |
Hmgcr |
A |
G |
13: 96,795,562 (GRCm39) |
Y336H |
probably damaging |
Het |
Hoxa13 |
G |
C |
6: 52,260,648 (GRCm38) |
|
probably benign |
Homo |
Hoxa13 |
C |
G |
6: 52,260,647 (GRCm38) |
|
probably benign |
Homo |
Igf2bp3 |
A |
C |
6: 49,094,084 (GRCm39) |
|
probably null |
Het |
Kcnb2 |
A |
T |
1: 15,383,200 (GRCm39) |
K175N |
possibly damaging |
Het |
Kdr |
T |
C |
5: 76,102,631 (GRCm39) |
|
probably benign |
Het |
Kif5c |
A |
G |
2: 49,584,044 (GRCm39) |
K160E |
probably damaging |
Het |
Kif7 |
A |
T |
7: 79,360,817 (GRCm39) |
V186E |
probably damaging |
Het |
Krt16 |
T |
A |
11: 100,139,575 (GRCm39) |
T48S |
unknown |
Het |
Liph |
T |
C |
16: 21,814,119 (GRCm39) |
M1V |
probably null |
Het |
Mctp2 |
A |
G |
7: 71,740,005 (GRCm39) |
F795S |
probably damaging |
Het |
Muc4 |
T |
A |
16: 32,755,699 (GRCm38) |
|
probably benign |
Homo |
Muc4 |
C |
G |
16: 32,755,676 (GRCm38) |
|
probably benign |
Homo |
Muc4 |
T |
A |
16: 32,755,684 (GRCm38) |
|
probably benign |
Homo |
Myo15a |
G |
T |
11: 60,373,953 (GRCm39) |
A1267S |
probably damaging |
Het |
Myo15a |
T |
C |
11: 60,386,280 (GRCm39) |
Y1802H |
probably damaging |
Het |
Myo7b |
G |
A |
18: 32,094,259 (GRCm39) |
T1963I |
probably benign |
Het |
Nadk2 |
TG |
T |
15: 9,100,232 (GRCm39) |
|
probably null |
Homo |
Naip5 |
T |
C |
13: 100,356,268 (GRCm39) |
N1116D |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,356,247 (GRCm39) |
R1123G |
probably benign |
Het |
Nap1l1 |
A |
G |
10: 111,322,583 (GRCm39) |
D61G |
probably null |
Het |
Napsa |
A |
T |
7: 44,230,875 (GRCm39) |
T81S |
probably damaging |
Het |
Ngp |
T |
C |
9: 110,251,337 (GRCm39) |
|
probably benign |
Het |
Nktr |
T |
A |
9: 121,570,687 (GRCm39) |
V143E |
probably damaging |
Het |
Obscn |
A |
G |
11: 58,957,890 (GRCm39) |
|
probably null |
Het |
Or10ag53 |
G |
A |
2: 87,082,973 (GRCm39) |
A231T |
probably benign |
Het |
Or11i1 |
T |
C |
3: 106,729,282 (GRCm39) |
I198V |
probably benign |
Het |
Or4f56 |
G |
A |
2: 111,703,649 (GRCm39) |
L184F |
probably benign |
Het |
Or52ab2 |
C |
T |
7: 102,970,076 (GRCm39) |
R153* |
probably null |
Het |
Or52d3 |
G |
A |
7: 104,229,237 (GRCm39) |
R128Q |
probably damaging |
Het |
Or6p1 |
A |
G |
1: 174,258,390 (GRCm39) |
Y132C |
probably damaging |
Het |
Paip2b |
A |
G |
6: 83,785,823 (GRCm39) |
Y136H |
probably damaging |
Het |
Pde2a |
G |
T |
7: 101,160,361 (GRCm39) |
R845L |
probably damaging |
Het |
Pgap2 |
A |
G |
7: 101,886,405 (GRCm39) |
Y197C |
possibly damaging |
Het |
Phf11b |
A |
G |
14: 59,560,611 (GRCm39) |
|
probably benign |
Het |
Pitpnm2 |
A |
T |
5: 124,269,178 (GRCm39) |
D481E |
probably benign |
Het |
Pxk |
A |
T |
14: 8,152,130 (GRCm38) |
H482L |
probably benign |
Het |
Rad50 |
A |
G |
11: 53,585,726 (GRCm39) |
|
probably null |
Het |
Rbmyf1 |
T |
A |
Y: 2,787,132 (GRCm39) |
N228Y |
probably benign |
Het |
Rbmyf5 |
T |
C |
Y: 3,297,411 (GRCm39) |
H235R |
probably benign |
Het |
Rbmyf6 |
C |
T |
Y: 3,328,944 (GRCm39) |
A241T |
possibly damaging |
Het |
Rnf220 |
A |
G |
4: 117,134,566 (GRCm39) |
|
probably null |
Het |
Saxo5 |
T |
A |
8: 3,526,062 (GRCm39) |
S72T |
possibly damaging |
Het |
Selenbp1 |
C |
T |
3: 94,844,607 (GRCm39) |
T88M |
probably damaging |
Het |
Sft2d1 |
T |
C |
17: 8,609,863 (GRCm39) |
I104T |
possibly damaging |
Het |
Sik1 |
A |
G |
17: 32,070,305 (GRCm39) |
S135P |
probably damaging |
Het |
Slc16a3 |
T |
C |
11: 120,846,172 (GRCm39) |
F34L |
probably damaging |
Het |
Slc6a20b |
T |
C |
9: 123,612,126 (GRCm38) |
N85S |
probably benign |
Homo |
Snrnp27 |
T |
C |
6: 86,659,893 (GRCm39) |
R34G |
unknown |
Het |
Sos2 |
T |
C |
12: 69,664,851 (GRCm39) |
H393R |
probably benign |
Het |
Sp110 |
C |
T |
1: 85,513,971 (GRCm39) |
R262Q |
probably benign |
Het |
Sp110 |
T |
C |
1: 85,513,975 (GRCm39) |
R261G |
probably benign |
Het |
Sp140 |
T |
A |
1: 85,528,893 (GRCm39) |
Y5N |
probably benign |
Het |
Sp140 |
A |
G |
1: 85,570,942 (GRCm39) |
S461G |
probably benign |
Het |
Sp140 |
G |
C |
1: 85,538,603 (GRCm39) |
K113N |
probably benign |
Het |
Sp140l1 |
G |
A |
1: 85,077,341 (GRCm39) |
A75V |
probably benign |
Het |
Sp140l2 |
A |
C |
1: 85,223,395 (GRCm39) |
|
probably benign |
Het |
Speer4a2 |
A |
T |
5: 26,291,485 (GRCm39) |
F107Y |
probably benign |
Het |
Speer4a2 |
C |
G |
5: 26,294,093 (GRCm39) |
W28C |
probably damaging |
Het |
Ssrp1 |
G |
A |
2: 84,868,760 (GRCm39) |
V40M |
probably damaging |
Het |
Tada2a |
T |
C |
11: 83,970,563 (GRCm39) |
E202G |
probably damaging |
Het |
Tcf20 |
C |
A |
15: 82,735,785 (GRCm39) |
A1889S |
probably damaging |
Het |
Tdrd12 |
A |
T |
7: 35,180,528 (GRCm39) |
Y828* |
probably null |
Het |
Tlr2 |
T |
A |
3: 83,745,756 (GRCm39) |
D109V |
probably benign |
Het |
Tomm40 |
G |
A |
7: 19,437,016 (GRCm39) |
T17M |
probably damaging |
Het |
Tsga10ip |
T |
C |
19: 5,440,161 (GRCm39) |
T135A |
possibly damaging |
Het |
Tspan8 |
G |
A |
10: 115,653,515 (GRCm39) |
V4M |
probably damaging |
Het |
Ttc28 |
A |
T |
5: 111,040,719 (GRCm39) |
T36S |
probably benign |
Het |
Ugt1a6b |
G |
A |
1: 88,146,112 (GRCm39) |
R519Q |
probably damaging |
Het |
Ugt1a6b |
TTCA |
T |
1: 88,143,880 (GRCm39) |
|
probably benign |
Het |
Ugt1a6b |
G |
A |
1: 88,143,976 (GRCm39) |
A199T |
probably damaging |
Het |
Unc45a |
A |
G |
7: 79,976,109 (GRCm39) |
M790T |
possibly damaging |
Het |
Vav3 |
T |
C |
3: 109,571,751 (GRCm39) |
|
probably null |
Het |
Vcpkmt |
G |
A |
12: 69,629,552 (GRCm39) |
S70L |
probably benign |
Het |
Vmn1r3 |
C |
T |
4: 3,184,691 (GRCm39) |
M205I |
probably damaging |
Het |
Vmn1r3 |
C |
T |
4: 3,184,774 (GRCm39) |
V178I |
probably benign |
Het |
Vmn2r66 |
T |
C |
7: 84,644,301 (GRCm39) |
Q703R |
probably damaging |
Het |
Vmn2r98 |
G |
T |
17: 19,301,223 (GRCm39) |
V742F |
probably benign |
Het |
Wfdc8 |
A |
G |
2: 164,439,696 (GRCm39) |
S229P |
possibly damaging |
Het |
Xpo4 |
A |
T |
14: 57,822,068 (GRCm39) |
C1083S |
probably null |
Het |
Zbtb38 |
T |
C |
9: 96,568,369 (GRCm39) |
D905G |
probably damaging |
Het |
Zbtb8b |
A |
G |
4: 129,321,308 (GRCm39) |
*518Q |
probably null |
Het |
Zfp600 |
TC |
T |
4: 146,131,802 (GRCm39) |
|
probably null |
Het |
Zfp992 |
C |
T |
4: 146,550,569 (GRCm39) |
P97S |
probably benign |
Het |
|
Other mutations in Alpk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00468:Alpk2
|
APN |
18 |
65,438,894 (GRCm39) |
missense |
probably benign |
0.27 |
IGL00478:Alpk2
|
APN |
18 |
65,440,297 (GRCm39) |
nonsense |
probably null |
|
IGL00898:Alpk2
|
APN |
18 |
65,483,644 (GRCm39) |
missense |
probably benign |
0.29 |
IGL00978:Alpk2
|
APN |
18 |
65,424,605 (GRCm39) |
splice site |
probably benign |
|
IGL01093:Alpk2
|
APN |
18 |
65,482,400 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01094:Alpk2
|
APN |
18 |
65,439,673 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01109:Alpk2
|
APN |
18 |
65,440,211 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01370:Alpk2
|
APN |
18 |
65,483,662 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL01393:Alpk2
|
APN |
18 |
65,440,779 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01629:Alpk2
|
APN |
18 |
65,433,113 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01872:Alpk2
|
APN |
18 |
65,437,824 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01983:Alpk2
|
APN |
18 |
65,483,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02294:Alpk2
|
APN |
18 |
65,439,146 (GRCm39) |
missense |
possibly damaging |
0.45 |
IGL02333:Alpk2
|
APN |
18 |
65,482,551 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02493:Alpk2
|
APN |
18 |
65,483,402 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02551:Alpk2
|
APN |
18 |
65,505,822 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02864:Alpk2
|
APN |
18 |
65,440,670 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02901:Alpk2
|
APN |
18 |
65,439,482 (GRCm39) |
missense |
probably benign |
|
IGL02954:Alpk2
|
APN |
18 |
65,439,207 (GRCm39) |
missense |
probably benign |
|
IGL03257:Alpk2
|
APN |
18 |
65,482,945 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03389:Alpk2
|
APN |
18 |
65,437,937 (GRCm39) |
missense |
possibly damaging |
0.92 |
3-1:Alpk2
|
UTSW |
18 |
65,437,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R0098:Alpk2
|
UTSW |
18 |
65,482,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Alpk2
|
UTSW |
18 |
65,482,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R0414:Alpk2
|
UTSW |
18 |
65,439,230 (GRCm39) |
missense |
probably benign |
0.04 |
R0546:Alpk2
|
UTSW |
18 |
65,439,788 (GRCm39) |
missense |
probably benign |
0.05 |
R0628:Alpk2
|
UTSW |
18 |
65,440,367 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0658:Alpk2
|
UTSW |
18 |
65,482,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R0731:Alpk2
|
UTSW |
18 |
65,438,461 (GRCm39) |
missense |
probably damaging |
0.98 |
R0919:Alpk2
|
UTSW |
18 |
65,440,544 (GRCm39) |
missense |
probably benign |
|
R1069:Alpk2
|
UTSW |
18 |
65,438,085 (GRCm39) |
missense |
probably benign |
0.25 |
R1186:Alpk2
|
UTSW |
18 |
65,427,412 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1508:Alpk2
|
UTSW |
18 |
65,482,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R1535:Alpk2
|
UTSW |
18 |
65,483,275 (GRCm39) |
missense |
probably benign |
|
R1558:Alpk2
|
UTSW |
18 |
65,483,301 (GRCm39) |
missense |
probably benign |
|
R1600:Alpk2
|
UTSW |
18 |
65,511,108 (GRCm39) |
missense |
probably damaging |
0.96 |
R1664:Alpk2
|
UTSW |
18 |
65,482,944 (GRCm39) |
missense |
probably damaging |
0.96 |
R1672:Alpk2
|
UTSW |
18 |
65,414,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R1829:Alpk2
|
UTSW |
18 |
65,427,165 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2110:Alpk2
|
UTSW |
18 |
65,440,151 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2111:Alpk2
|
UTSW |
18 |
65,482,845 (GRCm39) |
missense |
probably benign |
|
R2113:Alpk2
|
UTSW |
18 |
65,438,754 (GRCm39) |
missense |
probably benign |
0.31 |
R2126:Alpk2
|
UTSW |
18 |
65,483,439 (GRCm39) |
nonsense |
probably null |
|
R2198:Alpk2
|
UTSW |
18 |
65,483,255 (GRCm39) |
missense |
probably benign |
0.42 |
R2227:Alpk2
|
UTSW |
18 |
65,511,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R2245:Alpk2
|
UTSW |
18 |
65,438,234 (GRCm39) |
missense |
probably benign |
0.02 |
R2282:Alpk2
|
UTSW |
18 |
65,440,697 (GRCm39) |
missense |
probably benign |
|
R2421:Alpk2
|
UTSW |
18 |
65,439,687 (GRCm39) |
missense |
probably benign |
0.00 |
R2512:Alpk2
|
UTSW |
18 |
65,483,591 (GRCm39) |
missense |
probably damaging |
0.96 |
R3105:Alpk2
|
UTSW |
18 |
65,483,281 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3700:Alpk2
|
UTSW |
18 |
65,438,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R4205:Alpk2
|
UTSW |
18 |
65,438,282 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4239:Alpk2
|
UTSW |
18 |
65,433,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R4353:Alpk2
|
UTSW |
18 |
65,424,523 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4572:Alpk2
|
UTSW |
18 |
65,414,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R4584:Alpk2
|
UTSW |
18 |
65,440,035 (GRCm39) |
missense |
probably damaging |
0.99 |
R4591:Alpk2
|
UTSW |
18 |
65,438,894 (GRCm39) |
missense |
probably benign |
0.27 |
R4595:Alpk2
|
UTSW |
18 |
65,422,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R4648:Alpk2
|
UTSW |
18 |
65,482,953 (GRCm39) |
missense |
probably damaging |
0.99 |
R4815:Alpk2
|
UTSW |
18 |
65,483,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R4828:Alpk2
|
UTSW |
18 |
65,482,184 (GRCm39) |
missense |
probably benign |
|
R4910:Alpk2
|
UTSW |
18 |
65,399,357 (GRCm39) |
nonsense |
probably null |
|
R5042:Alpk2
|
UTSW |
18 |
65,483,579 (GRCm39) |
nonsense |
probably null |
|
R5295:Alpk2
|
UTSW |
18 |
65,438,109 (GRCm39) |
missense |
probably damaging |
0.98 |
R5375:Alpk2
|
UTSW |
18 |
65,505,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R5475:Alpk2
|
UTSW |
18 |
65,440,083 (GRCm39) |
missense |
probably benign |
0.16 |
R5480:Alpk2
|
UTSW |
18 |
65,482,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R5486:Alpk2
|
UTSW |
18 |
65,427,425 (GRCm39) |
splice site |
probably null |
|
R5503:Alpk2
|
UTSW |
18 |
65,439,312 (GRCm39) |
missense |
probably benign |
0.00 |
R5595:Alpk2
|
UTSW |
18 |
65,399,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R5648:Alpk2
|
UTSW |
18 |
65,482,988 (GRCm39) |
missense |
probably damaging |
0.96 |
R5714:Alpk2
|
UTSW |
18 |
65,438,532 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5862:Alpk2
|
UTSW |
18 |
65,440,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R5894:Alpk2
|
UTSW |
18 |
65,414,143 (GRCm39) |
missense |
probably damaging |
0.99 |
R5898:Alpk2
|
UTSW |
18 |
65,440,694 (GRCm39) |
missense |
probably damaging |
0.99 |
R5936:Alpk2
|
UTSW |
18 |
65,483,591 (GRCm39) |
missense |
probably damaging |
0.96 |
R6142:Alpk2
|
UTSW |
18 |
65,438,456 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6291:Alpk2
|
UTSW |
18 |
65,438,972 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6339:Alpk2
|
UTSW |
18 |
65,482,877 (GRCm39) |
missense |
probably benign |
0.00 |
R6407:Alpk2
|
UTSW |
18 |
65,422,809 (GRCm39) |
missense |
probably benign |
0.22 |
R6487:Alpk2
|
UTSW |
18 |
65,399,254 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6667:Alpk2
|
UTSW |
18 |
65,440,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R6786:Alpk2
|
UTSW |
18 |
65,439,705 (GRCm39) |
missense |
probably benign |
|
R6833:Alpk2
|
UTSW |
18 |
65,439,480 (GRCm39) |
missense |
probably benign |
0.08 |
R6984:Alpk2
|
UTSW |
18 |
65,438,749 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6999:Alpk2
|
UTSW |
18 |
65,437,584 (GRCm39) |
missense |
probably damaging |
0.99 |
R7157:Alpk2
|
UTSW |
18 |
65,399,348 (GRCm39) |
nonsense |
probably null |
|
R7167:Alpk2
|
UTSW |
18 |
65,440,049 (GRCm39) |
missense |
probably benign |
0.40 |
R7225:Alpk2
|
UTSW |
18 |
65,438,270 (GRCm39) |
missense |
probably benign |
0.00 |
R7409:Alpk2
|
UTSW |
18 |
65,440,023 (GRCm39) |
missense |
probably benign |
0.01 |
R7533:Alpk2
|
UTSW |
18 |
65,437,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R7576:Alpk2
|
UTSW |
18 |
65,439,887 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7589:Alpk2
|
UTSW |
18 |
65,433,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R7598:Alpk2
|
UTSW |
18 |
65,437,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R7664:Alpk2
|
UTSW |
18 |
65,440,073 (GRCm39) |
missense |
probably benign |
0.03 |
R7711:Alpk2
|
UTSW |
18 |
65,439,555 (GRCm39) |
missense |
probably benign |
|
R7722:Alpk2
|
UTSW |
18 |
65,483,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R7783:Alpk2
|
UTSW |
18 |
65,439,325 (GRCm39) |
nonsense |
probably null |
|
R7806:Alpk2
|
UTSW |
18 |
65,482,487 (GRCm39) |
missense |
probably benign |
|
R7953:Alpk2
|
UTSW |
18 |
65,482,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R8024:Alpk2
|
UTSW |
18 |
65,438,106 (GRCm39) |
missense |
probably benign |
0.01 |
R8043:Alpk2
|
UTSW |
18 |
65,482,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R8063:Alpk2
|
UTSW |
18 |
65,483,417 (GRCm39) |
missense |
probably benign |
0.15 |
R8171:Alpk2
|
UTSW |
18 |
65,439,054 (GRCm39) |
missense |
probably benign |
0.00 |
R8280:Alpk2
|
UTSW |
18 |
65,440,274 (GRCm39) |
missense |
probably benign |
|
R8383:Alpk2
|
UTSW |
18 |
65,438,469 (GRCm39) |
missense |
probably benign |
0.03 |
R8414:Alpk2
|
UTSW |
18 |
65,440,542 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8791:Alpk2
|
UTSW |
18 |
65,438,597 (GRCm39) |
missense |
probably benign |
0.00 |
R8872:Alpk2
|
UTSW |
18 |
65,413,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R9352:Alpk2
|
UTSW |
18 |
65,439,783 (GRCm39) |
missense |
probably benign |
0.01 |
R9449:Alpk2
|
UTSW |
18 |
65,424,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R9525:Alpk2
|
UTSW |
18 |
65,399,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Alpk2
|
UTSW |
18 |
65,439,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R9710:Alpk2
|
UTSW |
18 |
65,482,646 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Alpk2
|
UTSW |
18 |
65,424,471 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Alpk2
|
UTSW |
18 |
65,440,542 (GRCm39) |
missense |
possibly damaging |
0.89 |
X0063:Alpk2
|
UTSW |
18 |
65,440,434 (GRCm39) |
missense |
probably benign |
|
X0064:Alpk2
|
UTSW |
18 |
65,482,755 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Alpk2
|
UTSW |
18 |
65,438,682 (GRCm39) |
missense |
probably damaging |
0.98 |
|