Other mutations in this stock |
Total: 128 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010B08Rik |
C |
T |
2: 173,561,599 (GRCm39) |
|
probably benign |
Het |
Alpk2 |
G |
A |
18: 65,439,450 (GRCm39) |
H648Y |
possibly damaging |
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 |
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 Myo15a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00845:Myo15a
|
APN |
11 |
60,368,605 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01011:Myo15a
|
APN |
11 |
60,367,818 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01100:Myo15a
|
APN |
11 |
60,401,984 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01357:Myo15a
|
APN |
11 |
60,393,115 (GRCm39) |
splice site |
probably benign |
|
IGL01634:Myo15a
|
APN |
11 |
60,386,298 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01763:Myo15a
|
APN |
11 |
60,412,564 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01901:Myo15a
|
APN |
11 |
60,418,260 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01931:Myo15a
|
APN |
11 |
60,386,964 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02006:Myo15a
|
APN |
11 |
60,401,954 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02041:Myo15a
|
APN |
11 |
60,397,689 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02094:Myo15a
|
APN |
11 |
60,401,473 (GRCm39) |
unclassified |
probably benign |
|
IGL02122:Myo15a
|
APN |
11 |
60,374,292 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02153:Myo15a
|
APN |
11 |
60,389,223 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02328:Myo15a
|
APN |
11 |
60,417,433 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02330:Myo15a
|
APN |
11 |
60,367,987 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02431:Myo15a
|
APN |
11 |
60,401,465 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02639:Myo15a
|
APN |
11 |
60,369,447 (GRCm39) |
missense |
probably benign |
|
IGL02659:Myo15a
|
APN |
11 |
60,382,609 (GRCm39) |
splice site |
probably benign |
|
IGL02800:Myo15a
|
APN |
11 |
60,393,195 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02812:Myo15a
|
APN |
11 |
60,368,005 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02863:Myo15a
|
APN |
11 |
60,368,953 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02873:Myo15a
|
APN |
11 |
60,374,308 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02990:Myo15a
|
APN |
11 |
60,370,266 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03011:Myo15a
|
APN |
11 |
60,400,357 (GRCm39) |
splice site |
probably benign |
|
IGL03243:Myo15a
|
APN |
11 |
60,387,344 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03297:Myo15a
|
APN |
11 |
60,369,967 (GRCm39) |
missense |
probably damaging |
1.00 |
novichok
|
UTSW |
11 |
60,372,566 (GRCm39) |
critical splice donor site |
probably null |
|
parker
|
UTSW |
11 |
60,411,740 (GRCm39) |
critical splice donor site |
probably null |
|
Typhoon
|
UTSW |
11 |
60,378,251 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4131001:Myo15a
|
UTSW |
11 |
60,373,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R0133:Myo15a
|
UTSW |
11 |
60,368,676 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0265:Myo15a
|
UTSW |
11 |
60,405,723 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0389:Myo15a
|
UTSW |
11 |
60,369,364 (GRCm39) |
missense |
probably benign |
|
R0416:Myo15a
|
UTSW |
11 |
60,402,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R0449:Myo15a
|
UTSW |
11 |
60,400,422 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0477:Myo15a
|
UTSW |
11 |
60,411,740 (GRCm39) |
critical splice donor site |
probably null |
|
R0543:Myo15a
|
UTSW |
11 |
60,369,877 (GRCm39) |
missense |
probably benign |
|
R0546:Myo15a
|
UTSW |
11 |
60,397,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R0555:Myo15a
|
UTSW |
11 |
60,412,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R0639:Myo15a
|
UTSW |
11 |
60,370,162 (GRCm39) |
missense |
probably benign |
0.12 |
R0723:Myo15a
|
UTSW |
11 |
60,369,803 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0837:Myo15a
|
UTSW |
11 |
60,378,077 (GRCm39) |
missense |
probably damaging |
0.98 |
R0865:Myo15a
|
UTSW |
11 |
60,382,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R0899:Myo15a
|
UTSW |
11 |
60,368,011 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1022:Myo15a
|
UTSW |
11 |
60,370,442 (GRCm39) |
missense |
probably benign |
0.00 |
R1024:Myo15a
|
UTSW |
11 |
60,370,442 (GRCm39) |
missense |
probably benign |
0.00 |
R1035:Myo15a
|
UTSW |
11 |
60,401,384 (GRCm39) |
unclassified |
probably benign |
|
R1109:Myo15a
|
UTSW |
11 |
60,383,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R1170:Myo15a
|
UTSW |
11 |
60,370,233 (GRCm39) |
missense |
probably benign |
0.04 |
R1241:Myo15a
|
UTSW |
11 |
60,390,256 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1392:Myo15a
|
UTSW |
11 |
60,368,800 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1392:Myo15a
|
UTSW |
11 |
60,368,800 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1434:Myo15a
|
UTSW |
11 |
60,395,157 (GRCm39) |
missense |
probably benign |
0.00 |
R1450:Myo15a
|
UTSW |
11 |
60,386,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R1456:Myo15a
|
UTSW |
11 |
60,399,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Myo15a
|
UTSW |
11 |
60,396,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Myo15a
|
UTSW |
11 |
60,396,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R1548:Myo15a
|
UTSW |
11 |
60,379,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R1551:Myo15a
|
UTSW |
11 |
60,383,791 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1571:Myo15a
|
UTSW |
11 |
60,409,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Myo15a
|
UTSW |
11 |
60,392,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R1777:Myo15a
|
UTSW |
11 |
60,405,762 (GRCm39) |
missense |
probably benign |
|
R1778:Myo15a
|
UTSW |
11 |
60,369,238 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1847:Myo15a
|
UTSW |
11 |
60,390,321 (GRCm39) |
nonsense |
probably null |
|
R1875:Myo15a
|
UTSW |
11 |
60,398,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R1944:Myo15a
|
UTSW |
11 |
60,392,909 (GRCm39) |
missense |
probably damaging |
0.99 |
R1945:Myo15a
|
UTSW |
11 |
60,392,909 (GRCm39) |
missense |
probably damaging |
0.99 |
R2013:Myo15a
|
UTSW |
11 |
60,385,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R2107:Myo15a
|
UTSW |
11 |
60,382,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Myo15a
|
UTSW |
11 |
60,382,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R2112:Myo15a
|
UTSW |
11 |
60,384,994 (GRCm39) |
missense |
probably damaging |
0.99 |
R2147:Myo15a
|
UTSW |
11 |
60,401,055 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2196:Myo15a
|
UTSW |
11 |
60,400,847 (GRCm39) |
nonsense |
probably null |
|
R2207:Myo15a
|
UTSW |
11 |
60,396,860 (GRCm39) |
missense |
probably benign |
0.01 |
R2245:Myo15a
|
UTSW |
11 |
60,399,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R2367:Myo15a
|
UTSW |
11 |
60,408,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R2374:Myo15a
|
UTSW |
11 |
60,369,669 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2438:Myo15a
|
UTSW |
11 |
60,373,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R3154:Myo15a
|
UTSW |
11 |
60,370,186 (GRCm39) |
splice site |
probably null |
|
R3423:Myo15a
|
UTSW |
11 |
60,401,126 (GRCm39) |
critical splice donor site |
probably null |
|
R3551:Myo15a
|
UTSW |
11 |
60,400,489 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3552:Myo15a
|
UTSW |
11 |
60,400,489 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3612:Myo15a
|
UTSW |
11 |
60,368,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R3620:Myo15a
|
UTSW |
11 |
60,369,468 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3713:Myo15a
|
UTSW |
11 |
60,370,057 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3714:Myo15a
|
UTSW |
11 |
60,370,057 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3715:Myo15a
|
UTSW |
11 |
60,370,057 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3783:Myo15a
|
UTSW |
11 |
60,368,398 (GRCm39) |
missense |
probably damaging |
0.97 |
R3784:Myo15a
|
UTSW |
11 |
60,368,398 (GRCm39) |
missense |
probably damaging |
0.97 |
R3785:Myo15a
|
UTSW |
11 |
60,368,398 (GRCm39) |
missense |
probably damaging |
0.97 |
R3786:Myo15a
|
UTSW |
11 |
60,368,398 (GRCm39) |
missense |
probably damaging |
0.97 |
R3787:Myo15a
|
UTSW |
11 |
60,368,398 (GRCm39) |
missense |
probably damaging |
0.97 |
R3894:Myo15a
|
UTSW |
11 |
60,395,145 (GRCm39) |
missense |
probably benign |
0.00 |
R3962:Myo15a
|
UTSW |
11 |
60,370,654 (GRCm39) |
missense |
probably benign |
0.00 |
R4082:Myo15a
|
UTSW |
11 |
60,378,022 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4555:Myo15a
|
UTSW |
11 |
60,387,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4641:Myo15a
|
UTSW |
11 |
60,393,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R4665:Myo15a
|
UTSW |
11 |
60,395,705 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4713:Myo15a
|
UTSW |
11 |
60,370,756 (GRCm39) |
missense |
probably benign |
0.21 |
R4820:Myo15a
|
UTSW |
11 |
60,367,741 (GRCm39) |
missense |
probably damaging |
0.98 |
R5013:Myo15a
|
UTSW |
11 |
60,382,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R5051:Myo15a
|
UTSW |
11 |
60,378,251 (GRCm39) |
critical splice donor site |
probably null |
|
R5187:Myo15a
|
UTSW |
11 |
60,394,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R5230:Myo15a
|
UTSW |
11 |
60,393,674 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5277:Myo15a
|
UTSW |
11 |
60,367,940 (GRCm39) |
nonsense |
probably null |
|
R5345:Myo15a
|
UTSW |
11 |
60,388,364 (GRCm39) |
missense |
probably damaging |
0.99 |
R5349:Myo15a
|
UTSW |
11 |
60,384,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R5356:Myo15a
|
UTSW |
11 |
60,389,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R5445:Myo15a
|
UTSW |
11 |
60,411,603 (GRCm39) |
nonsense |
probably null |
|
R5477:Myo15a
|
UTSW |
11 |
60,368,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R5629:Myo15a
|
UTSW |
11 |
60,370,578 (GRCm39) |
missense |
probably benign |
|
R5728:Myo15a
|
UTSW |
11 |
60,379,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R5818:Myo15a
|
UTSW |
11 |
60,388,777 (GRCm39) |
missense |
probably benign |
0.06 |
R5952:Myo15a
|
UTSW |
11 |
60,370,246 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6338:Myo15a
|
UTSW |
11 |
60,368,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R6467:Myo15a
|
UTSW |
11 |
60,417,487 (GRCm39) |
critical splice donor site |
probably null |
|
R6488:Myo15a
|
UTSW |
11 |
60,369,313 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6521:Myo15a
|
UTSW |
11 |
60,393,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R6645:Myo15a
|
UTSW |
11 |
60,368,118 (GRCm39) |
missense |
probably benign |
0.00 |
R6702:Myo15a
|
UTSW |
11 |
60,383,818 (GRCm39) |
missense |
probably benign |
0.16 |
R6703:Myo15a
|
UTSW |
11 |
60,383,818 (GRCm39) |
missense |
probably benign |
0.16 |
R6821:Myo15a
|
UTSW |
11 |
60,415,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R6882:Myo15a
|
UTSW |
11 |
60,414,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R6908:Myo15a
|
UTSW |
11 |
60,396,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R6932:Myo15a
|
UTSW |
11 |
60,390,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R6958:Myo15a
|
UTSW |
11 |
60,394,451 (GRCm39) |
missense |
probably benign |
0.07 |
R7041:Myo15a
|
UTSW |
11 |
60,396,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R7149:Myo15a
|
UTSW |
11 |
60,400,836 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7163:Myo15a
|
UTSW |
11 |
60,389,195 (GRCm39) |
missense |
|
|
R7229:Myo15a
|
UTSW |
11 |
60,387,321 (GRCm39) |
missense |
probably benign |
0.08 |
R7347:Myo15a
|
UTSW |
11 |
60,368,787 (GRCm39) |
missense |
probably benign |
|
R7368:Myo15a
|
UTSW |
11 |
60,381,741 (GRCm39) |
splice site |
probably null |
|
R7392:Myo15a
|
UTSW |
11 |
60,396,802 (GRCm39) |
missense |
|
|
R7414:Myo15a
|
UTSW |
11 |
60,374,309 (GRCm39) |
missense |
|
|
R7461:Myo15a
|
UTSW |
11 |
60,395,978 (GRCm39) |
missense |
|
|
R7609:Myo15a
|
UTSW |
11 |
60,379,637 (GRCm39) |
missense |
|
|
R7613:Myo15a
|
UTSW |
11 |
60,395,978 (GRCm39) |
missense |
|
|
R7734:Myo15a
|
UTSW |
11 |
60,401,108 (GRCm39) |
missense |
probably benign |
|
R7748:Myo15a
|
UTSW |
11 |
60,395,727 (GRCm39) |
missense |
|
|
R7767:Myo15a
|
UTSW |
11 |
60,392,922 (GRCm39) |
missense |
|
|
R7769:Myo15a
|
UTSW |
11 |
60,399,975 (GRCm39) |
missense |
|
|
R7894:Myo15a
|
UTSW |
11 |
60,381,963 (GRCm39) |
missense |
|
|
R7919:Myo15a
|
UTSW |
11 |
60,417,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R8100:Myo15a
|
UTSW |
11 |
60,408,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R8124:Myo15a
|
UTSW |
11 |
60,398,279 (GRCm39) |
missense |
|
|
R8129:Myo15a
|
UTSW |
11 |
60,399,026 (GRCm39) |
missense |
|
|
R8428:Myo15a
|
UTSW |
11 |
60,387,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R8706:Myo15a
|
UTSW |
11 |
60,370,443 (GRCm39) |
missense |
probably benign |
|
R8735:Myo15a
|
UTSW |
11 |
60,401,679 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8739:Myo15a
|
UTSW |
11 |
60,368,088 (GRCm39) |
missense |
probably benign |
0.06 |
R8790:Myo15a
|
UTSW |
11 |
60,378,047 (GRCm39) |
missense |
|
|
R8790:Myo15a
|
UTSW |
11 |
60,367,362 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8822:Myo15a
|
UTSW |
11 |
60,367,740 (GRCm39) |
missense |
probably damaging |
0.99 |
R8907:Myo15a
|
UTSW |
11 |
60,417,434 (GRCm39) |
missense |
|
|
R8931:Myo15a
|
UTSW |
11 |
60,368,020 (GRCm39) |
missense |
probably benign |
|
R9061:Myo15a
|
UTSW |
11 |
60,393,692 (GRCm39) |
missense |
|
|
R9124:Myo15a
|
UTSW |
11 |
60,369,952 (GRCm39) |
missense |
probably benign |
0.37 |
R9297:Myo15a
|
UTSW |
11 |
60,385,899 (GRCm39) |
missense |
probably null |
|
R9347:Myo15a
|
UTSW |
11 |
60,374,555 (GRCm39) |
missense |
|
|
R9417:Myo15a
|
UTSW |
11 |
60,378,243 (GRCm39) |
missense |
|
|
R9456:Myo15a
|
UTSW |
11 |
60,392,668 (GRCm39) |
missense |
|
|
R9460:Myo15a
|
UTSW |
11 |
60,372,566 (GRCm39) |
critical splice donor site |
probably null |
|
R9615:Myo15a
|
UTSW |
11 |
60,374,320 (GRCm39) |
missense |
|
|
R9630:Myo15a
|
UTSW |
11 |
60,407,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R9746:Myo15a
|
UTSW |
11 |
60,378,234 (GRCm39) |
nonsense |
probably null |
|
X0021:Myo15a
|
UTSW |
11 |
60,373,185 (GRCm39) |
nonsense |
probably null |
|
X0066:Myo15a
|
UTSW |
11 |
60,369,046 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Myo15a
|
UTSW |
11 |
60,369,444 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1176:Myo15a
|
UTSW |
11 |
60,389,229 (GRCm39) |
missense |
|
|
Z1176:Myo15a
|
UTSW |
11 |
60,379,084 (GRCm39) |
missense |
|
|
Z1176:Myo15a
|
UTSW |
11 |
60,415,267 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo15a
|
UTSW |
11 |
60,386,301 (GRCm39) |
missense |
|
|
Z1177:Myo15a
|
UTSW |
11 |
60,379,663 (GRCm39) |
missense |
|
|
Z1177:Myo15a
|
UTSW |
11 |
60,368,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|