Other mutations in this stock |
Total: 109 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930533L02Rik |
A |
G |
7: 124,917,815 (GRCm39) |
K69R |
unknown |
Het |
Abca13 |
A |
C |
11: 9,244,701 (GRCm39) |
D2188A |
probably benign |
Het |
Acad11 |
T |
C |
9: 104,001,224 (GRCm39) |
M708T |
probably damaging |
Het |
Adam7 |
T |
C |
14: 68,748,306 (GRCm39) |
|
probably null |
Het |
Adgre1 |
T |
A |
17: 57,751,060 (GRCm39) |
I578N |
probably benign |
Het |
Agbl4 |
T |
C |
4: 111,474,419 (GRCm39) |
S403P |
probably damaging |
Het |
Ak3 |
A |
G |
19: 29,025,192 (GRCm39) |
M13T |
possibly damaging |
Het |
Ap2s1 |
T |
C |
7: 16,481,305 (GRCm39) |
|
probably benign |
Het |
Arhgef1 |
A |
T |
7: 24,623,224 (GRCm39) |
|
probably benign |
Het |
Arsk |
T |
C |
13: 76,223,051 (GRCm39) |
N182S |
probably benign |
Het |
Aspscr1 |
G |
A |
11: 120,569,246 (GRCm39) |
V15I |
probably damaging |
Het |
Asxl2 |
A |
G |
12: 3,492,487 (GRCm39) |
Y24C |
probably damaging |
Het |
Atp8b1 |
A |
G |
18: 64,701,323 (GRCm39) |
F345S |
possibly damaging |
Het |
Atp8b3 |
T |
C |
10: 80,362,743 (GRCm39) |
K672E |
probably benign |
Het |
Bltp1 |
T |
A |
3: 36,997,331 (GRCm39) |
C1129* |
probably null |
Het |
Bmp2k |
A |
G |
5: 97,235,682 (GRCm39) |
|
probably benign |
Het |
Casp6 |
T |
A |
3: 129,704,172 (GRCm39) |
V86E |
probably benign |
Het |
Cdca5 |
A |
G |
19: 6,140,742 (GRCm39) |
E260G |
unknown |
Het |
Cpb2 |
T |
A |
14: 75,502,898 (GRCm39) |
V159D |
probably damaging |
Het |
Cylc2 |
T |
A |
4: 51,228,477 (GRCm39) |
S183T |
unknown |
Het |
Dhtkd1 |
T |
A |
2: 5,919,699 (GRCm39) |
M561L |
probably benign |
Het |
Dync2h1 |
T |
C |
9: 7,129,046 (GRCm39) |
D1823G |
probably benign |
Het |
Efcab5 |
G |
A |
11: 77,031,749 (GRCm39) |
R42W |
probably damaging |
Het |
Erc1 |
T |
C |
6: 119,597,289 (GRCm39) |
K1003E |
probably damaging |
Het |
Ezr |
G |
A |
17: 7,022,164 (GRCm39) |
Q105* |
probably null |
Het |
Fam83d |
T |
A |
2: 158,627,467 (GRCm39) |
D385E |
probably benign |
Het |
Fbn2 |
A |
G |
18: 58,178,389 (GRCm39) |
C1950R |
probably damaging |
Het |
Fbxo32 |
A |
T |
15: 58,047,605 (GRCm39) |
I236N |
probably damaging |
Het |
Fcgbp |
G |
T |
7: 27,784,918 (GRCm39) |
|
probably null |
Het |
Foxe3 |
T |
C |
4: 114,782,805 (GRCm39) |
N136D |
probably damaging |
Het |
Fscn2 |
A |
T |
11: 120,258,837 (GRCm39) |
I461F |
probably damaging |
Het |
Gldc |
A |
G |
19: 30,093,851 (GRCm39) |
I722T |
possibly damaging |
Het |
Gm10717 |
T |
G |
9: 3,025,619 (GRCm39) |
V68G |
possibly damaging |
Het |
Gm4841 |
A |
G |
18: 60,403,718 (GRCm39) |
L125S |
possibly damaging |
Het |
Gnl3 |
A |
C |
14: 30,735,384 (GRCm39) |
|
probably null |
Het |
Gsto1 |
A |
T |
19: 47,846,416 (GRCm39) |
I88F |
probably damaging |
Het |
Gucy1b1 |
T |
A |
3: 81,945,463 (GRCm39) |
|
probably null |
Het |
Hhla1 |
C |
A |
15: 65,820,352 (GRCm39) |
V133F |
probably benign |
Het |
Hipk3 |
T |
A |
2: 104,271,593 (GRCm39) |
L446F |
probably damaging |
Het |
Hscb |
T |
C |
5: 110,982,556 (GRCm39) |
E177G |
possibly damaging |
Het |
Hsd17b6 |
T |
C |
10: 127,827,274 (GRCm39) |
D266G |
probably benign |
Het |
Ipo4 |
T |
C |
14: 55,869,572 (GRCm39) |
S363G |
probably benign |
Het |
Kcnip3 |
A |
G |
2: 127,301,899 (GRCm39) |
|
probably benign |
Het |
Klhl41 |
A |
G |
2: 69,501,640 (GRCm39) |
Y367C |
probably damaging |
Het |
Klk1b4 |
C |
G |
7: 43,861,053 (GRCm39) |
P232R |
possibly damaging |
Het |
Lcp2 |
A |
G |
11: 34,004,322 (GRCm39) |
D53G |
probably damaging |
Het |
Llgl2 |
A |
G |
11: 115,741,546 (GRCm39) |
K559E |
probably damaging |
Het |
Lrrc59 |
A |
C |
11: 94,534,248 (GRCm39) |
T269P |
probably damaging |
Het |
Mark1 |
A |
G |
1: 184,677,149 (GRCm39) |
S34P |
possibly damaging |
Het |
Megf11 |
G |
A |
9: 64,598,632 (GRCm39) |
|
probably null |
Het |
Mplkip |
A |
G |
13: 17,871,565 (GRCm39) |
I159V |
possibly damaging |
Het |
Muc4 |
C |
A |
16: 32,755,690 (GRCm38) |
|
probably benign |
Het |
Myo9b |
T |
C |
8: 71,808,596 (GRCm39) |
|
probably benign |
Het |
Napg |
C |
T |
18: 63,120,034 (GRCm39) |
R149C |
probably damaging |
Het |
Ndrg3 |
A |
G |
2: 156,776,855 (GRCm39) |
|
probably benign |
Het |
Nfe2l3 |
T |
A |
6: 51,434,448 (GRCm39) |
M336K |
probably benign |
Het |
Nrxn1 |
A |
C |
17: 91,008,170 (GRCm39) |
|
probably null |
Het |
Nsun3 |
A |
T |
16: 62,597,007 (GRCm39) |
|
probably benign |
Het |
Nuak1 |
T |
C |
10: 84,210,315 (GRCm39) |
E591G |
probably benign |
Het |
Or10g1b |
T |
C |
14: 52,627,846 (GRCm39) |
Y128C |
probably damaging |
Het |
Or10s1 |
G |
A |
9: 39,986,010 (GRCm39) |
V140I |
probably benign |
Het |
Or1e17 |
A |
T |
11: 73,831,773 (GRCm39) |
I234F |
probably benign |
Het |
Or4k2 |
T |
C |
14: 50,423,789 (GRCm39) |
N296S |
probably null |
Het |
Or6c70 |
T |
A |
10: 129,709,936 (GRCm39) |
Q230L |
probably damaging |
Het |
Or6d15 |
A |
T |
6: 116,559,562 (GRCm39) |
V115E |
probably damaging |
Het |
Or6z6 |
T |
A |
7: 6,491,433 (GRCm39) |
M147L |
probably benign |
Het |
Orc4 |
A |
T |
2: 48,827,479 (GRCm39) |
V38E |
possibly damaging |
Het |
Ovgp1 |
T |
C |
3: 105,887,208 (GRCm39) |
|
probably benign |
Het |
Palm3 |
T |
A |
8: 84,755,349 (GRCm39) |
V287D |
probably damaging |
Het |
Pde4dip |
T |
A |
3: 97,751,028 (GRCm39) |
H62L |
probably benign |
Het |
Pdk4 |
G |
T |
6: 5,491,620 (GRCm39) |
P100Q |
probably damaging |
Het |
Pdss2 |
T |
A |
10: 43,248,172 (GRCm39) |
H225Q |
probably benign |
Het |
Pkhd1 |
A |
T |
1: 20,345,762 (GRCm39) |
D2755E |
probably benign |
Het |
Prune2 |
A |
T |
19: 17,098,753 (GRCm39) |
D1419V |
probably damaging |
Het |
Pth2r |
A |
C |
1: 65,427,775 (GRCm39) |
I483L |
probably benign |
Het |
Qrsl1 |
A |
G |
10: 43,772,003 (GRCm39) |
|
probably null |
Het |
Rab11fip4 |
A |
G |
11: 79,577,455 (GRCm39) |
H403R |
possibly damaging |
Het |
Ralgapa1 |
A |
T |
12: 55,724,023 (GRCm39) |
I1548N |
probably damaging |
Het |
Ric8a |
T |
G |
7: 140,437,813 (GRCm39) |
|
probably benign |
Het |
Rsbn1 |
T |
C |
3: 103,821,897 (GRCm39) |
F44S |
possibly damaging |
Het |
Serpinc1 |
T |
A |
1: 160,817,272 (GRCm39) |
M1K |
probably null |
Het |
Sf3b1 |
T |
C |
1: 55,058,416 (GRCm39) |
I58V |
probably damaging |
Het |
Sh3d19 |
T |
A |
3: 86,033,978 (GRCm39) |
M777K |
probably benign |
Het |
Sipa1 |
A |
T |
19: 5,704,093 (GRCm39) |
M743K |
probably benign |
Het |
Skint5 |
T |
C |
4: 113,794,818 (GRCm39) |
H255R |
probably benign |
Het |
Slco6b1 |
A |
T |
1: 96,916,398 (GRCm39) |
|
noncoding transcript |
Het |
Slfn4 |
A |
T |
11: 83,077,777 (GRCm39) |
R188S |
probably damaging |
Het |
Sort1 |
T |
C |
3: 108,231,908 (GRCm39) |
|
probably benign |
Het |
Spg21 |
A |
T |
9: 65,372,629 (GRCm39) |
K20N |
possibly damaging |
Het |
Sptbn2 |
A |
T |
19: 4,795,173 (GRCm39) |
I1544F |
probably benign |
Het |
Srf |
T |
C |
17: 46,860,415 (GRCm39) |
T456A |
possibly damaging |
Het |
Ssbp2 |
T |
A |
13: 91,712,715 (GRCm39) |
|
probably benign |
Het |
Stx2 |
C |
T |
5: 129,065,967 (GRCm39) |
V230I |
probably benign |
Het |
Sv2b |
A |
T |
7: 74,856,187 (GRCm39) |
D34E |
possibly damaging |
Het |
Synpo2l |
A |
G |
14: 20,711,856 (GRCm39) |
S255P |
probably damaging |
Het |
Tbx15 |
C |
T |
3: 99,259,707 (GRCm39) |
P526L |
probably damaging |
Het |
Tenm4 |
C |
A |
7: 96,344,157 (GRCm39) |
P250Q |
possibly damaging |
Het |
Tgm1 |
C |
A |
14: 55,948,384 (GRCm39) |
|
probably benign |
Het |
Tgm1 |
T |
C |
14: 55,950,109 (GRCm39) |
|
probably benign |
Het |
Thsd7b |
A |
G |
1: 130,123,000 (GRCm39) |
I1540V |
probably benign |
Het |
Tnrc6c |
A |
G |
11: 117,630,707 (GRCm39) |
K1023E |
probably damaging |
Het |
Ube2l6 |
A |
T |
2: 84,636,771 (GRCm39) |
|
probably null |
Het |
Uty |
T |
A |
Y: 1,169,979 (GRCm39) |
I326F |
probably damaging |
Het |
Wdfy4 |
T |
C |
14: 32,805,742 (GRCm39) |
D1735G |
possibly damaging |
Het |
Wnt11 |
A |
G |
7: 98,496,590 (GRCm39) |
K177E |
probably damaging |
Het |
Wnt5a |
A |
T |
14: 28,235,225 (GRCm39) |
M70L |
possibly damaging |
Het |
Wwc1 |
T |
A |
11: 35,743,175 (GRCm39) |
E882V |
probably damaging |
Het |
Zfp455 |
G |
T |
13: 67,346,728 (GRCm39) |
|
probably null |
Het |
Zmpste24 |
A |
G |
4: 120,940,050 (GRCm39) |
Y199H |
probably damaging |
Het |
|
Other mutations in Myo18b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Myo18b
|
APN |
5 |
113,021,997 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00847:Myo18b
|
APN |
5 |
112,978,255 (GRCm39) |
splice site |
probably benign |
|
IGL00848:Myo18b
|
APN |
5 |
113,019,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00969:Myo18b
|
APN |
5 |
113,022,873 (GRCm39) |
unclassified |
probably benign |
|
IGL01018:Myo18b
|
APN |
5 |
112,957,613 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01448:Myo18b
|
APN |
5 |
112,959,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01490:Myo18b
|
APN |
5 |
112,957,566 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01556:Myo18b
|
APN |
5 |
112,905,315 (GRCm39) |
splice site |
probably benign |
|
IGL01637:Myo18b
|
APN |
5 |
112,988,495 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01819:Myo18b
|
APN |
5 |
113,025,916 (GRCm39) |
missense |
unknown |
|
IGL02007:Myo18b
|
APN |
5 |
113,022,838 (GRCm39) |
unclassified |
probably benign |
|
IGL02146:Myo18b
|
APN |
5 |
112,991,151 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02229:Myo18b
|
APN |
5 |
113,025,976 (GRCm39) |
missense |
unknown |
|
IGL02319:Myo18b
|
APN |
5 |
112,939,005 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02398:Myo18b
|
APN |
5 |
112,978,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02420:Myo18b
|
APN |
5 |
112,975,852 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02626:Myo18b
|
APN |
5 |
113,025,951 (GRCm39) |
missense |
unknown |
|
IGL02815:Myo18b
|
APN |
5 |
112,957,601 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02822:Myo18b
|
APN |
5 |
112,923,211 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02852:Myo18b
|
APN |
5 |
112,863,377 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02995:Myo18b
|
APN |
5 |
112,923,279 (GRCm39) |
splice site |
probably benign |
|
IGL03019:Myo18b
|
APN |
5 |
112,840,263 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03039:Myo18b
|
APN |
5 |
112,988,637 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03112:Myo18b
|
APN |
5 |
113,021,856 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03123:Myo18b
|
APN |
5 |
113,022,804 (GRCm39) |
unclassified |
probably benign |
|
IGL03288:Myo18b
|
APN |
5 |
112,937,863 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03391:Myo18b
|
APN |
5 |
113,022,345 (GRCm39) |
unclassified |
probably benign |
|
klippel
|
UTSW |
5 |
112,905,319 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4651001:Myo18b
|
UTSW |
5 |
112,982,301 (GRCm39) |
missense |
probably benign |
0.01 |
R0271:Myo18b
|
UTSW |
5 |
112,957,551 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0352:Myo18b
|
UTSW |
5 |
113,022,389 (GRCm39) |
unclassified |
probably benign |
|
R0504:Myo18b
|
UTSW |
5 |
113,021,442 (GRCm39) |
unclassified |
probably benign |
|
R0539:Myo18b
|
UTSW |
5 |
112,871,734 (GRCm39) |
missense |
probably damaging |
0.99 |
R0599:Myo18b
|
UTSW |
5 |
113,013,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R0627:Myo18b
|
UTSW |
5 |
112,946,700 (GRCm39) |
missense |
probably benign |
0.38 |
R0659:Myo18b
|
UTSW |
5 |
112,908,193 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0671:Myo18b
|
UTSW |
5 |
112,840,632 (GRCm39) |
missense |
probably benign |
0.00 |
R0847:Myo18b
|
UTSW |
5 |
113,022,354 (GRCm39) |
unclassified |
probably benign |
|
R1082:Myo18b
|
UTSW |
5 |
112,908,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R1116:Myo18b
|
UTSW |
5 |
112,951,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R1264:Myo18b
|
UTSW |
5 |
112,978,185 (GRCm39) |
missense |
probably benign |
0.12 |
R1280:Myo18b
|
UTSW |
5 |
112,871,671 (GRCm39) |
critical splice donor site |
probably null |
|
R1444:Myo18b
|
UTSW |
5 |
112,923,117 (GRCm39) |
critical splice donor site |
probably null |
|
R1446:Myo18b
|
UTSW |
5 |
112,905,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Myo18b
|
UTSW |
5 |
112,840,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Myo18b
|
UTSW |
5 |
112,840,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1590:Myo18b
|
UTSW |
5 |
113,023,132 (GRCm39) |
nonsense |
probably null |
|
R1601:Myo18b
|
UTSW |
5 |
113,019,364 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1903:Myo18b
|
UTSW |
5 |
112,840,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Myo18b
|
UTSW |
5 |
112,908,222 (GRCm39) |
missense |
probably benign |
0.04 |
R1936:Myo18b
|
UTSW |
5 |
112,908,222 (GRCm39) |
missense |
probably benign |
0.04 |
R2008:Myo18b
|
UTSW |
5 |
113,021,423 (GRCm39) |
missense |
probably benign |
|
R2127:Myo18b
|
UTSW |
5 |
112,978,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Myo18b
|
UTSW |
5 |
112,978,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Myo18b
|
UTSW |
5 |
113,021,892 (GRCm39) |
missense |
probably benign |
0.01 |
R2170:Myo18b
|
UTSW |
5 |
112,871,724 (GRCm39) |
missense |
probably benign |
0.23 |
R2258:Myo18b
|
UTSW |
5 |
113,022,529 (GRCm39) |
unclassified |
probably benign |
|
R2265:Myo18b
|
UTSW |
5 |
112,930,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R2483:Myo18b
|
UTSW |
5 |
113,006,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R2931:Myo18b
|
UTSW |
5 |
112,840,993 (GRCm39) |
missense |
probably benign |
0.01 |
R3160:Myo18b
|
UTSW |
5 |
112,840,594 (GRCm39) |
missense |
probably damaging |
0.99 |
R3162:Myo18b
|
UTSW |
5 |
112,840,594 (GRCm39) |
missense |
probably damaging |
0.99 |
R3777:Myo18b
|
UTSW |
5 |
112,905,462 (GRCm39) |
missense |
probably damaging |
0.99 |
R4240:Myo18b
|
UTSW |
5 |
112,951,053 (GRCm39) |
critical splice donor site |
probably null |
|
R4243:Myo18b
|
UTSW |
5 |
112,840,261 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4245:Myo18b
|
UTSW |
5 |
112,840,261 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4533:Myo18b
|
UTSW |
5 |
112,840,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Myo18b
|
UTSW |
5 |
112,994,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R4661:Myo18b
|
UTSW |
5 |
113,023,041 (GRCm39) |
unclassified |
probably benign |
|
R4755:Myo18b
|
UTSW |
5 |
113,022,340 (GRCm39) |
nonsense |
probably null |
|
R4771:Myo18b
|
UTSW |
5 |
112,840,093 (GRCm39) |
nonsense |
probably null |
|
R4812:Myo18b
|
UTSW |
5 |
112,957,584 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4840:Myo18b
|
UTSW |
5 |
113,021,895 (GRCm39) |
missense |
probably benign |
0.02 |
R4888:Myo18b
|
UTSW |
5 |
113,022,346 (GRCm39) |
unclassified |
probably benign |
|
R4995:Myo18b
|
UTSW |
5 |
112,908,258 (GRCm39) |
missense |
probably damaging |
0.99 |
R5001:Myo18b
|
UTSW |
5 |
112,909,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R5015:Myo18b
|
UTSW |
5 |
112,937,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Myo18b
|
UTSW |
5 |
113,023,083 (GRCm39) |
unclassified |
probably benign |
|
R5070:Myo18b
|
UTSW |
5 |
112,909,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5105:Myo18b
|
UTSW |
5 |
112,988,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R5121:Myo18b
|
UTSW |
5 |
113,022,346 (GRCm39) |
unclassified |
probably benign |
|
R5130:Myo18b
|
UTSW |
5 |
113,021,769 (GRCm39) |
missense |
probably benign |
0.06 |
R5186:Myo18b
|
UTSW |
5 |
113,019,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R5437:Myo18b
|
UTSW |
5 |
112,905,439 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5535:Myo18b
|
UTSW |
5 |
112,937,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Myo18b
|
UTSW |
5 |
113,016,161 (GRCm39) |
missense |
probably damaging |
0.96 |
R5810:Myo18b
|
UTSW |
5 |
112,982,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R5898:Myo18b
|
UTSW |
5 |
112,950,196 (GRCm39) |
splice site |
probably null |
|
R6065:Myo18b
|
UTSW |
5 |
112,840,647 (GRCm39) |
missense |
probably benign |
0.00 |
R6104:Myo18b
|
UTSW |
5 |
113,022,157 (GRCm39) |
unclassified |
probably benign |
|
R6113:Myo18b
|
UTSW |
5 |
113,014,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Myo18b
|
UTSW |
5 |
113,022,038 (GRCm39) |
missense |
probably benign |
0.01 |
R6167:Myo18b
|
UTSW |
5 |
113,020,373 (GRCm39) |
splice site |
probably null |
|
R6220:Myo18b
|
UTSW |
5 |
112,905,373 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6276:Myo18b
|
UTSW |
5 |
112,959,508 (GRCm39) |
missense |
probably benign |
0.31 |
R6290:Myo18b
|
UTSW |
5 |
113,013,601 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6291:Myo18b
|
UTSW |
5 |
113,013,601 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6795:Myo18b
|
UTSW |
5 |
112,994,230 (GRCm39) |
missense |
probably damaging |
0.99 |
R6798:Myo18b
|
UTSW |
5 |
112,909,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R6817:Myo18b
|
UTSW |
5 |
112,978,104 (GRCm39) |
missense |
probably benign |
0.00 |
R6937:Myo18b
|
UTSW |
5 |
112,950,258 (GRCm39) |
missense |
probably benign |
0.12 |
R7034:Myo18b
|
UTSW |
5 |
112,871,770 (GRCm39) |
nonsense |
probably null |
|
R7097:Myo18b
|
UTSW |
5 |
113,022,271 (GRCm39) |
missense |
unknown |
|
R7145:Myo18b
|
UTSW |
5 |
112,965,545 (GRCm39) |
nonsense |
probably null |
|
R7201:Myo18b
|
UTSW |
5 |
112,863,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Myo18b
|
UTSW |
5 |
112,923,154 (GRCm39) |
missense |
probably benign |
0.01 |
R7265:Myo18b
|
UTSW |
5 |
112,959,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R7409:Myo18b
|
UTSW |
5 |
113,021,971 (GRCm39) |
missense |
probably benign |
0.25 |
R7466:Myo18b
|
UTSW |
5 |
112,871,758 (GRCm39) |
missense |
probably benign |
0.02 |
R7487:Myo18b
|
UTSW |
5 |
112,982,299 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7571:Myo18b
|
UTSW |
5 |
112,978,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7600:Myo18b
|
UTSW |
5 |
113,025,969 (GRCm39) |
missense |
unknown |
|
R7612:Myo18b
|
UTSW |
5 |
113,013,168 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7617:Myo18b
|
UTSW |
5 |
112,905,319 (GRCm39) |
critical splice donor site |
probably null |
|
R7696:Myo18b
|
UTSW |
5 |
112,840,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R7710:Myo18b
|
UTSW |
5 |
113,022,891 (GRCm39) |
missense |
unknown |
|
R8047:Myo18b
|
UTSW |
5 |
112,871,681 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8070:Myo18b
|
UTSW |
5 |
112,938,986 (GRCm39) |
missense |
probably benign |
0.01 |
R8088:Myo18b
|
UTSW |
5 |
113,027,376 (GRCm39) |
start gained |
probably benign |
|
R8247:Myo18b
|
UTSW |
5 |
112,840,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R8276:Myo18b
|
UTSW |
5 |
112,943,273 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8313:Myo18b
|
UTSW |
5 |
113,023,045 (GRCm39) |
missense |
unknown |
|
R8375:Myo18b
|
UTSW |
5 |
112,908,259 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8432:Myo18b
|
UTSW |
5 |
112,912,378 (GRCm39) |
missense |
probably benign |
0.00 |
R8475:Myo18b
|
UTSW |
5 |
113,021,422 (GRCm39) |
nonsense |
probably null |
|
R8482:Myo18b
|
UTSW |
5 |
113,019,489 (GRCm39) |
nonsense |
probably null |
|
R8671:Myo18b
|
UTSW |
5 |
113,022,609 (GRCm39) |
missense |
unknown |
|
R8681:Myo18b
|
UTSW |
5 |
113,021,429 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8918:Myo18b
|
UTSW |
5 |
113,022,873 (GRCm39) |
unclassified |
probably benign |
|
R8941:Myo18b
|
UTSW |
5 |
113,022,795 (GRCm39) |
unclassified |
probably benign |
|
R8962:Myo18b
|
UTSW |
5 |
113,006,346 (GRCm39) |
missense |
probably benign |
0.24 |
R8972:Myo18b
|
UTSW |
5 |
112,841,164 (GRCm39) |
missense |
probably benign |
0.00 |
R9116:Myo18b
|
UTSW |
5 |
112,975,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R9209:Myo18b
|
UTSW |
5 |
113,022,927 (GRCm39) |
missense |
unknown |
|
R9358:Myo18b
|
UTSW |
5 |
112,943,269 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9469:Myo18b
|
UTSW |
5 |
112,994,247 (GRCm39) |
missense |
probably benign |
0.15 |
R9607:Myo18b
|
UTSW |
5 |
113,022,544 (GRCm39) |
missense |
unknown |
|
R9659:Myo18b
|
UTSW |
5 |
113,022,382 (GRCm39) |
missense |
unknown |
|
Z1088:Myo18b
|
UTSW |
5 |
112,905,350 (GRCm39) |
missense |
probably benign |
0.25 |
Z1088:Myo18b
|
UTSW |
5 |
112,840,809 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1176:Myo18b
|
UTSW |
5 |
112,979,056 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Myo18b
|
UTSW |
5 |
112,957,604 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1176:Myo18b
|
UTSW |
5 |
112,910,587 (GRCm39) |
missense |
not run |
|
Z1177:Myo18b
|
UTSW |
5 |
113,021,407 (GRCm39) |
nonsense |
probably null |
|
Z1177:Myo18b
|
UTSW |
5 |
112,910,587 (GRCm39) |
missense |
not run |
|
Z1177:Myo18b
|
UTSW |
5 |
112,840,765 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo18b
|
UTSW |
5 |
113,023,018 (GRCm39) |
nonsense |
probably null |
|
|