Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430033K04Rik |
A |
G |
5: 138,644,519 (GRCm39) |
I135V |
probably benign |
Het |
Abca1 |
T |
A |
4: 53,074,325 (GRCm39) |
K1119N |
probably damaging |
Het |
Abcb10 |
C |
T |
8: 124,688,791 (GRCm39) |
G495D |
probably damaging |
Het |
Abcc9 |
T |
C |
6: 142,573,194 (GRCm39) |
|
probably benign |
Het |
Akap3 |
A |
G |
6: 126,842,809 (GRCm39) |
E476G |
possibly damaging |
Het |
Aldh3b1 |
A |
G |
19: 3,968,740 (GRCm39) |
F271S |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Ascc3 |
T |
C |
10: 50,576,586 (GRCm39) |
V847A |
probably damaging |
Het |
Best3 |
A |
G |
10: 116,859,883 (GRCm39) |
N381S |
probably benign |
Het |
Blm |
A |
T |
7: 80,163,118 (GRCm39) |
S78T |
probably benign |
Het |
Bmpr2 |
T |
A |
1: 59,907,520 (GRCm39) |
L871Q |
probably damaging |
Het |
Car13 |
T |
A |
3: 14,715,795 (GRCm39) |
H104Q |
probably benign |
Het |
Ccdc39 |
T |
C |
3: 33,880,629 (GRCm39) |
K446R |
probably damaging |
Het |
Ccnb1ip1 |
T |
C |
14: 51,029,568 (GRCm39) |
M165V |
probably benign |
Het |
Cd4 |
A |
T |
6: 124,843,618 (GRCm39) |
M431K |
possibly damaging |
Het |
Ceacam3 |
C |
T |
7: 16,892,301 (GRCm39) |
T348I |
probably damaging |
Het |
Cfap54 |
C |
T |
10: 92,740,125 (GRCm39) |
|
probably null |
Het |
Clcn6 |
A |
T |
4: 148,098,758 (GRCm39) |
|
probably null |
Het |
Csf3 |
A |
G |
11: 98,593,246 (GRCm39) |
Y121C |
probably damaging |
Het |
Csmd3 |
C |
T |
15: 47,567,505 (GRCm39) |
|
probably benign |
Het |
Cyp2c69 |
A |
G |
19: 39,864,815 (GRCm39) |
I221T |
probably benign |
Het |
Dgcr2 |
T |
C |
16: 17,675,115 (GRCm39) |
|
probably benign |
Het |
Dhcr7 |
T |
C |
7: 143,401,250 (GRCm39) |
F474S |
probably damaging |
Het |
Dnah1 |
T |
C |
14: 31,032,839 (GRCm39) |
I399V |
probably null |
Het |
Efcab14 |
T |
A |
4: 115,610,188 (GRCm39) |
L183Q |
probably damaging |
Het |
Evx2 |
A |
G |
2: 74,489,501 (GRCm39) |
V88A |
probably benign |
Het |
Exph5 |
A |
G |
9: 53,285,109 (GRCm39) |
N730S |
probably benign |
Het |
Farsb |
T |
A |
1: 78,443,620 (GRCm39) |
K196I |
probably benign |
Het |
Fbln7 |
C |
T |
2: 128,735,682 (GRCm39) |
|
probably benign |
Het |
Fhdc1 |
A |
G |
3: 84,356,085 (GRCm39) |
F453S |
probably damaging |
Het |
Gast |
T |
A |
11: 100,227,684 (GRCm39) |
W89R |
probably damaging |
Het |
Gata2 |
A |
G |
6: 88,182,237 (GRCm39) |
S402G |
probably benign |
Het |
Gin1 |
T |
A |
1: 97,720,162 (GRCm39) |
S386T |
probably benign |
Het |
Golgb1 |
A |
G |
16: 36,736,363 (GRCm39) |
E1870G |
probably damaging |
Het |
Hivep3 |
T |
A |
4: 119,954,768 (GRCm39) |
V1028E |
possibly damaging |
Het |
Ifi203 |
G |
A |
1: 173,756,326 (GRCm39) |
R486* |
probably null |
Het |
Ifi209 |
G |
A |
1: 173,468,728 (GRCm39) |
S186N |
probably benign |
Het |
Ifih1 |
C |
T |
2: 62,436,738 (GRCm39) |
A562T |
probably damaging |
Het |
Itch |
T |
C |
2: 155,014,481 (GRCm39) |
L106S |
probably damaging |
Het |
Itga4 |
T |
A |
2: 79,146,050 (GRCm39) |
|
probably null |
Het |
Kdm4c |
A |
G |
4: 74,199,234 (GRCm39) |
S141G |
possibly damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Klra3 |
T |
C |
6: 130,307,226 (GRCm39) |
|
probably null |
Het |
Lama2 |
G |
C |
10: 27,084,403 (GRCm39) |
F922L |
probably benign |
Het |
Lama2 |
A |
T |
10: 27,084,402 (GRCm39) |
S923T |
probably damaging |
Het |
Llgl1 |
G |
A |
11: 60,597,873 (GRCm39) |
V331M |
probably damaging |
Het |
Lrrc30 |
T |
C |
17: 67,938,676 (GRCm39) |
*301W |
probably null |
Het |
Map1lc3b |
C |
T |
8: 122,320,226 (GRCm39) |
|
probably benign |
Het |
Mbd2 |
A |
G |
18: 70,749,690 (GRCm39) |
I302V |
probably benign |
Het |
Med27 |
A |
G |
2: 29,390,307 (GRCm39) |
Y78C |
probably damaging |
Het |
Mei1 |
C |
T |
15: 81,996,771 (GRCm39) |
|
probably null |
Het |
Mideas |
G |
A |
12: 84,205,124 (GRCm39) |
|
probably benign |
Het |
Miga1 |
T |
C |
3: 151,993,191 (GRCm39) |
E346G |
probably damaging |
Het |
Myef2 |
A |
G |
2: 124,957,363 (GRCm39) |
S131P |
probably damaging |
Het |
Myocd |
T |
C |
11: 65,069,527 (GRCm39) |
H899R |
probably benign |
Het |
Ncam1 |
A |
G |
9: 49,456,556 (GRCm39) |
|
probably benign |
Het |
Ngf |
T |
A |
3: 102,427,513 (GRCm39) |
N87K |
possibly damaging |
Het |
Nol10 |
T |
A |
12: 17,466,709 (GRCm39) |
|
probably benign |
Het |
Nrip2 |
A |
G |
6: 128,385,231 (GRCm39) |
I221V |
probably benign |
Het |
Nup205 |
G |
A |
6: 35,182,366 (GRCm39) |
G777D |
probably damaging |
Het |
Or5ac17 |
A |
G |
16: 59,036,344 (GRCm39) |
F211L |
probably benign |
Het |
Or5b96 |
A |
G |
19: 12,867,047 (GRCm39) |
V298A |
probably damaging |
Het |
Or6c1 |
T |
A |
10: 129,518,081 (GRCm39) |
T176S |
probably benign |
Het |
Or7g35 |
A |
T |
9: 19,496,682 (GRCm39) |
Q283L |
probably damaging |
Het |
Or8d6 |
G |
T |
9: 39,854,251 (GRCm39) |
D232Y |
probably benign |
Het |
Oxt |
A |
T |
2: 130,418,220 (GRCm39) |
R31W |
probably damaging |
Het |
Pde4dip |
A |
G |
3: 97,603,246 (GRCm39) |
S2248P |
probably benign |
Het |
Pias1 |
A |
G |
9: 62,859,460 (GRCm39) |
V16A |
probably damaging |
Het |
Pkp2 |
T |
C |
16: 16,080,561 (GRCm39) |
S616P |
probably damaging |
Het |
Plch2 |
T |
C |
4: 155,084,540 (GRCm39) |
Y379C |
probably damaging |
Het |
Pnpt1 |
A |
G |
11: 29,104,159 (GRCm39) |
N540D |
probably benign |
Het |
Ptpn23 |
G |
A |
9: 110,220,746 (GRCm39) |
H255Y |
possibly damaging |
Het |
Rad21 |
T |
C |
15: 51,835,703 (GRCm39) |
N237D |
probably benign |
Het |
Ryr3 |
A |
C |
2: 112,582,113 (GRCm39) |
|
probably null |
Het |
Sgk1 |
C |
A |
10: 21,873,007 (GRCm39) |
|
probably benign |
Het |
Slc1a5 |
G |
T |
7: 16,531,464 (GRCm39) |
A490S |
probably damaging |
Het |
Slc5a8 |
T |
C |
10: 88,755,326 (GRCm39) |
Y478H |
probably benign |
Het |
Slc5a8 |
T |
A |
10: 88,755,328 (GRCm39) |
Y478* |
probably null |
Het |
Slc9a3 |
A |
T |
13: 74,311,190 (GRCm39) |
M562L |
probably benign |
Het |
Spmip4 |
A |
G |
6: 50,568,801 (GRCm39) |
|
probably benign |
Het |
Thsd7a |
G |
A |
6: 12,555,714 (GRCm39) |
R57* |
probably null |
Het |
Tiam1 |
T |
C |
16: 89,657,167 (GRCm39) |
R690G |
probably damaging |
Het |
Tmem150b |
A |
G |
7: 4,727,365 (GRCm39) |
S47P |
probably damaging |
Het |
Trim39 |
C |
T |
17: 36,574,832 (GRCm39) |
R190Q |
probably damaging |
Het |
Ttc32 |
A |
T |
12: 9,085,073 (GRCm39) |
I98L |
possibly damaging |
Het |
Vps13c |
A |
G |
9: 67,873,003 (GRCm39) |
T3304A |
probably benign |
Het |
Wdr35 |
A |
C |
12: 9,062,728 (GRCm39) |
D638A |
probably damaging |
Het |
Wwc1 |
G |
T |
11: 35,752,671 (GRCm39) |
P797T |
probably benign |
Het |
Zan |
T |
A |
5: 137,462,780 (GRCm39) |
T800S |
unknown |
Het |
Zbbx |
A |
G |
3: 74,990,926 (GRCm39) |
|
probably benign |
Het |
Zup1 |
T |
C |
10: 33,811,172 (GRCm39) |
M291V |
probably damaging |
Het |
|
Other mutations in Cdh20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00428:Cdh20
|
APN |
1 |
104,881,612 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00742:Cdh20
|
APN |
1 |
109,993,356 (GRCm39) |
missense |
probably benign |
0.22 |
IGL00743:Cdh20
|
APN |
1 |
104,875,153 (GRCm39) |
missense |
probably benign |
0.06 |
IGL00848:Cdh20
|
APN |
1 |
104,861,981 (GRCm39) |
missense |
probably benign |
|
IGL00861:Cdh20
|
APN |
1 |
109,988,718 (GRCm39) |
splice site |
probably benign |
|
IGL01016:Cdh20
|
APN |
1 |
110,036,686 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01393:Cdh20
|
APN |
1 |
104,861,969 (GRCm39) |
missense |
probably benign |
|
IGL01396:Cdh20
|
APN |
1 |
104,875,154 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01485:Cdh20
|
APN |
1 |
104,861,832 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01538:Cdh20
|
APN |
1 |
109,988,870 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01612:Cdh20
|
APN |
1 |
104,921,895 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01763:Cdh20
|
APN |
1 |
109,993,520 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01765:Cdh20
|
APN |
1 |
109,988,836 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01937:Cdh20
|
APN |
1 |
110,065,826 (GRCm39) |
missense |
probably benign |
|
IGL01947:Cdh20
|
APN |
1 |
104,921,649 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01967:Cdh20
|
APN |
1 |
104,868,762 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02020:Cdh20
|
APN |
1 |
110,066,078 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02135:Cdh20
|
APN |
1 |
110,066,004 (GRCm39) |
nonsense |
probably null |
|
IGL02226:Cdh20
|
APN |
1 |
104,881,816 (GRCm39) |
splice site |
probably benign |
|
IGL02285:Cdh20
|
APN |
1 |
110,065,921 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02318:Cdh20
|
APN |
1 |
104,881,764 (GRCm39) |
missense |
probably null |
0.03 |
IGL02326:Cdh20
|
APN |
1 |
104,902,764 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02798:Cdh20
|
APN |
1 |
104,875,190 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02963:Cdh20
|
APN |
1 |
104,861,823 (GRCm39) |
start codon destroyed |
probably null |
0.66 |
IGL03081:Cdh20
|
APN |
1 |
104,868,982 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03237:Cdh20
|
APN |
1 |
110,066,037 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03280:Cdh20
|
APN |
1 |
110,036,498 (GRCm39) |
nonsense |
probably null |
|
IGL03347:Cdh20
|
APN |
1 |
110,065,973 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL03385:Cdh20
|
APN |
1 |
109,993,516 (GRCm39) |
missense |
possibly damaging |
0.90 |
3-1:Cdh20
|
UTSW |
1 |
104,875,145 (GRCm39) |
missense |
possibly damaging |
0.84 |
BB002:Cdh20
|
UTSW |
1 |
104,912,473 (GRCm39) |
missense |
probably damaging |
0.99 |
BB012:Cdh20
|
UTSW |
1 |
104,912,473 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02802:Cdh20
|
UTSW |
1 |
110,065,655 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02991:Cdh20
|
UTSW |
1 |
104,861,972 (GRCm39) |
missense |
probably benign |
|
R0030:Cdh20
|
UTSW |
1 |
110,065,798 (GRCm39) |
nonsense |
probably null |
|
R0070:Cdh20
|
UTSW |
1 |
110,026,102 (GRCm39) |
missense |
probably benign |
0.37 |
R0070:Cdh20
|
UTSW |
1 |
110,026,102 (GRCm39) |
missense |
probably benign |
0.37 |
R0178:Cdh20
|
UTSW |
1 |
104,902,776 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0255:Cdh20
|
UTSW |
1 |
109,922,036 (GRCm39) |
missense |
probably benign |
0.09 |
R0365:Cdh20
|
UTSW |
1 |
110,036,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R0506:Cdh20
|
UTSW |
1 |
110,027,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R0549:Cdh20
|
UTSW |
1 |
110,036,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R0599:Cdh20
|
UTSW |
1 |
109,980,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R0648:Cdh20
|
UTSW |
1 |
109,993,337 (GRCm39) |
splice site |
probably benign |
|
R1033:Cdh20
|
UTSW |
1 |
110,012,783 (GRCm39) |
missense |
probably damaging |
0.96 |
R1114:Cdh20
|
UTSW |
1 |
104,906,739 (GRCm39) |
missense |
probably damaging |
0.96 |
R1173:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1174:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1175:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1401:Cdh20
|
UTSW |
1 |
104,875,222 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1403:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1403:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1406:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1406:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1502:Cdh20
|
UTSW |
1 |
104,881,755 (GRCm39) |
missense |
probably benign |
0.06 |
R1587:Cdh20
|
UTSW |
1 |
110,027,757 (GRCm39) |
missense |
probably damaging |
0.98 |
R1728:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1729:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1730:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1739:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1762:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1764:Cdh20
|
UTSW |
1 |
104,862,070 (GRCm39) |
splice site |
probably benign |
|
R1783:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1785:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1940:Cdh20
|
UTSW |
1 |
109,976,754 (GRCm39) |
missense |
probably benign |
0.09 |
R1972:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1973:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1997:Cdh20
|
UTSW |
1 |
109,976,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Cdh20
|
UTSW |
1 |
109,976,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R2068:Cdh20
|
UTSW |
1 |
110,065,666 (GRCm39) |
nonsense |
probably null |
|
R2069:Cdh20
|
UTSW |
1 |
110,065,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R2137:Cdh20
|
UTSW |
1 |
110,027,836 (GRCm39) |
missense |
probably damaging |
0.97 |
R2155:Cdh20
|
UTSW |
1 |
109,976,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R2198:Cdh20
|
UTSW |
1 |
104,875,047 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2279:Cdh20
|
UTSW |
1 |
104,875,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R2419:Cdh20
|
UTSW |
1 |
104,902,740 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2897:Cdh20
|
UTSW |
1 |
104,875,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R3780:Cdh20
|
UTSW |
1 |
109,976,734 (GRCm39) |
missense |
probably benign |
0.45 |
R3781:Cdh20
|
UTSW |
1 |
109,976,734 (GRCm39) |
missense |
probably benign |
0.45 |
R3782:Cdh20
|
UTSW |
1 |
109,976,734 (GRCm39) |
missense |
probably benign |
0.45 |
R4115:Cdh20
|
UTSW |
1 |
110,066,039 (GRCm39) |
missense |
probably benign |
0.37 |
R4243:Cdh20
|
UTSW |
1 |
104,869,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4244:Cdh20
|
UTSW |
1 |
104,869,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4277:Cdh20
|
UTSW |
1 |
109,993,418 (GRCm39) |
missense |
probably benign |
0.00 |
R4299:Cdh20
|
UTSW |
1 |
109,988,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R4349:Cdh20
|
UTSW |
1 |
104,906,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R4350:Cdh20
|
UTSW |
1 |
104,906,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R4352:Cdh20
|
UTSW |
1 |
104,906,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R4353:Cdh20
|
UTSW |
1 |
104,906,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Cdh20
|
UTSW |
1 |
104,862,035 (GRCm39) |
missense |
probably damaging |
0.97 |
R4754:Cdh20
|
UTSW |
1 |
104,912,410 (GRCm39) |
missense |
probably damaging |
0.99 |
R4777:Cdh20
|
UTSW |
1 |
109,922,055 (GRCm39) |
nonsense |
probably null |
|
R4795:Cdh20
|
UTSW |
1 |
104,868,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R4796:Cdh20
|
UTSW |
1 |
104,868,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R4907:Cdh20
|
UTSW |
1 |
110,066,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R4955:Cdh20
|
UTSW |
1 |
104,912,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Cdh20
|
UTSW |
1 |
110,026,080 (GRCm39) |
missense |
probably benign |
0.01 |
R5056:Cdh20
|
UTSW |
1 |
104,881,722 (GRCm39) |
missense |
probably benign |
0.00 |
R5059:Cdh20
|
UTSW |
1 |
109,993,430 (GRCm39) |
missense |
probably damaging |
0.98 |
R5127:Cdh20
|
UTSW |
1 |
104,875,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R5146:Cdh20
|
UTSW |
1 |
109,922,042 (GRCm39) |
missense |
probably damaging |
0.97 |
R5196:Cdh20
|
UTSW |
1 |
110,065,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R5269:Cdh20
|
UTSW |
1 |
104,861,882 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5304:Cdh20
|
UTSW |
1 |
110,036,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R5496:Cdh20
|
UTSW |
1 |
109,976,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5563:Cdh20
|
UTSW |
1 |
104,875,082 (GRCm39) |
missense |
probably benign |
0.29 |
R5634:Cdh20
|
UTSW |
1 |
104,902,800 (GRCm39) |
missense |
probably damaging |
0.97 |
R5708:Cdh20
|
UTSW |
1 |
104,912,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R5743:Cdh20
|
UTSW |
1 |
110,036,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R5822:Cdh20
|
UTSW |
1 |
104,861,823 (GRCm39) |
start codon destroyed |
probably null |
0.49 |
R5867:Cdh20
|
UTSW |
1 |
109,976,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R5933:Cdh20
|
UTSW |
1 |
104,912,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R6042:Cdh20
|
UTSW |
1 |
110,065,997 (GRCm39) |
missense |
probably damaging |
0.97 |
R6092:Cdh20
|
UTSW |
1 |
110,026,036 (GRCm39) |
missense |
probably benign |
0.00 |
R6109:Cdh20
|
UTSW |
1 |
104,921,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R6497:Cdh20
|
UTSW |
1 |
109,993,528 (GRCm39) |
critical splice donor site |
probably null |
|
R6521:Cdh20
|
UTSW |
1 |
104,869,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R6911:Cdh20
|
UTSW |
1 |
104,912,411 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7111:Cdh20
|
UTSW |
1 |
110,065,638 (GRCm39) |
missense |
|
|
R7169:Cdh20
|
UTSW |
1 |
104,875,078 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7207:Cdh20
|
UTSW |
1 |
104,921,702 (GRCm39) |
missense |
probably damaging |
0.98 |
R7208:Cdh20
|
UTSW |
1 |
104,881,796 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7297:Cdh20
|
UTSW |
1 |
104,898,598 (GRCm39) |
missense |
probably benign |
|
R7511:Cdh20
|
UTSW |
1 |
109,925,583 (GRCm39) |
intron |
probably benign |
|
R7532:Cdh20
|
UTSW |
1 |
110,065,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R7535:Cdh20
|
UTSW |
1 |
104,902,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R7587:Cdh20
|
UTSW |
1 |
104,869,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R7748:Cdh20
|
UTSW |
1 |
104,869,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R7879:Cdh20
|
UTSW |
1 |
109,976,677 (GRCm39) |
missense |
probably benign |
0.01 |
R7879:Cdh20
|
UTSW |
1 |
104,875,047 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7915:Cdh20
|
UTSW |
1 |
104,861,898 (GRCm39) |
missense |
probably benign |
0.15 |
R7925:Cdh20
|
UTSW |
1 |
104,912,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R7978:Cdh20
|
UTSW |
1 |
109,921,835 (GRCm39) |
start gained |
probably benign |
|
R8022:Cdh20
|
UTSW |
1 |
109,988,838 (GRCm39) |
missense |
probably benign |
0.02 |
R8207:Cdh20
|
UTSW |
1 |
109,922,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R8224:Cdh20
|
UTSW |
1 |
109,921,933 (GRCm39) |
missense |
probably benign |
|
R8239:Cdh20
|
UTSW |
1 |
110,027,832 (GRCm39) |
missense |
probably benign |
0.11 |
R8257:Cdh20
|
UTSW |
1 |
104,921,962 (GRCm39) |
missense |
probably benign |
0.25 |
R8444:Cdh20
|
UTSW |
1 |
104,898,583 (GRCm39) |
missense |
probably benign |
0.16 |
R8546:Cdh20
|
UTSW |
1 |
104,861,769 (GRCm39) |
start gained |
probably benign |
|
R8749:Cdh20
|
UTSW |
1 |
110,027,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R8870:Cdh20
|
UTSW |
1 |
104,873,048 (GRCm39) |
missense |
probably damaging |
0.99 |
R8884:Cdh20
|
UTSW |
1 |
110,027,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R9030:Cdh20
|
UTSW |
1 |
110,027,843 (GRCm39) |
missense |
probably benign |
0.21 |
R9310:Cdh20
|
UTSW |
1 |
104,875,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R9498:Cdh20
|
UTSW |
1 |
109,976,635 (GRCm39) |
missense |
probably benign |
0.03 |
R9542:Cdh20
|
UTSW |
1 |
104,875,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R9602:Cdh20
|
UTSW |
1 |
104,868,823 (GRCm39) |
missense |
probably benign |
0.07 |
R9658:Cdh20
|
UTSW |
1 |
109,988,785 (GRCm39) |
missense |
probably damaging |
0.99 |
R9664:Cdh20
|
UTSW |
1 |
104,862,065 (GRCm39) |
missense |
probably benign |
0.10 |
Z1088:Cdh20
|
UTSW |
1 |
110,012,853 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Cdh20
|
UTSW |
1 |
110,036,466 (GRCm39) |
missense |
probably damaging |
1.00 |
|