Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim1 |
T |
G |
19: 57,062,309 (GRCm39) |
N384T |
probably benign |
Het |
Agap3 |
A |
G |
5: 24,706,396 (GRCm39) |
Y843C |
probably damaging |
Het |
Aldh9a1 |
T |
A |
1: 167,182,021 (GRCm39) |
V118E |
probably benign |
Het |
Arhgef26 |
T |
A |
3: 62,252,689 (GRCm39) |
S414T |
possibly damaging |
Het |
Armc9 |
T |
C |
1: 86,087,717 (GRCm39) |
Y18H |
probably damaging |
Het |
Bod1l |
A |
G |
5: 41,970,463 (GRCm39) |
|
probably null |
Het |
Casp1 |
A |
T |
9: 5,299,816 (GRCm39) |
E96D |
probably benign |
Het |
Ccdc171 |
A |
G |
4: 83,611,998 (GRCm39) |
I898V |
probably benign |
Het |
Cd79b |
T |
C |
11: 106,205,365 (GRCm39) |
I42M |
possibly damaging |
Het |
Cdca7 |
G |
A |
2: 72,315,575 (GRCm39) |
R346H |
probably damaging |
Het |
Cdh23 |
T |
A |
10: 60,222,823 (GRCm39) |
D1200V |
probably damaging |
Het |
Cdkn1c |
T |
C |
7: 143,014,326 (GRCm39) |
D40G |
possibly damaging |
Het |
Ckap5 |
G |
A |
2: 91,437,917 (GRCm39) |
R1666H |
probably damaging |
Het |
Cxcl1 |
A |
G |
5: 91,039,182 (GRCm39) |
T5A |
unknown |
Het |
Dnah2 |
A |
C |
11: 69,337,579 (GRCm39) |
|
probably null |
Het |
Dnai3 |
T |
C |
3: 145,803,028 (GRCm39) |
I54M |
probably damaging |
Het |
Ephb3 |
A |
T |
16: 21,037,577 (GRCm39) |
K500* |
probably null |
Het |
Fam13c |
T |
A |
10: 70,390,336 (GRCm39) |
H533Q |
probably benign |
Het |
Fat4 |
T |
A |
3: 39,064,682 (GRCm39) |
D4879E |
probably damaging |
Het |
Grk6 |
G |
T |
13: 55,606,733 (GRCm39) |
W511L |
probably damaging |
Het |
Hivep3 |
G |
C |
4: 119,952,431 (GRCm39) |
S249T |
possibly damaging |
Het |
Iqch |
T |
A |
9: 63,419,599 (GRCm39) |
Y496F |
possibly damaging |
Het |
Itga2 |
T |
C |
13: 115,037,066 (GRCm39) |
I21V |
unknown |
Het |
Itpr2 |
A |
T |
6: 146,226,554 (GRCm39) |
C1397S |
probably damaging |
Het |
Krt86 |
A |
T |
15: 101,374,498 (GRCm39) |
Y297F |
possibly damaging |
Het |
Limch1 |
G |
T |
5: 67,182,519 (GRCm39) |
|
probably null |
Het |
Mfsd6 |
G |
T |
1: 52,748,917 (GRCm39) |
|
probably null |
Het |
Mx1 |
A |
G |
16: 97,256,376 (GRCm39) |
V181A |
probably damaging |
Het |
Nme8 |
G |
A |
13: 19,859,817 (GRCm39) |
R268W |
probably benign |
Het |
Ogfr |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
2: 180,237,059 (GRCm39) |
|
probably benign |
Het |
Or10p1 |
T |
A |
10: 129,443,829 (GRCm39) |
I174F |
possibly damaging |
Het |
Or5d36 |
G |
A |
2: 87,901,000 (GRCm39) |
T242I |
probably damaging |
Het |
Pappa2 |
T |
A |
1: 158,784,096 (GRCm39) |
I305F |
probably benign |
Het |
Pdlim3 |
A |
G |
8: 46,370,539 (GRCm39) |
K232E |
probably damaging |
Het |
Rcn1 |
T |
C |
2: 105,219,359 (GRCm39) |
E278G |
probably damaging |
Het |
Ros1 |
T |
C |
10: 52,057,906 (GRCm39) |
D47G |
probably benign |
Het |
Sema4c |
G |
A |
1: 36,592,160 (GRCm39) |
T229M |
possibly damaging |
Het |
Serpina3j |
T |
A |
12: 104,283,792 (GRCm39) |
W297R |
probably damaging |
Het |
Serpinb11 |
A |
G |
1: 107,304,614 (GRCm39) |
E193G |
probably benign |
Het |
Shank2 |
A |
G |
7: 143,965,289 (GRCm39) |
I966V |
probably benign |
Het |
Siglece |
T |
C |
7: 43,309,327 (GRCm39) |
D77G |
probably damaging |
Het |
Sqstm1 |
G |
T |
11: 50,093,418 (GRCm39) |
Q327K |
probably benign |
Het |
Stip1 |
C |
T |
19: 6,999,178 (GRCm39) |
G467S |
possibly damaging |
Het |
Styxl2 |
T |
C |
1: 165,954,723 (GRCm39) |
E9G |
possibly damaging |
Het |
Svep1 |
A |
T |
4: 58,118,207 (GRCm39) |
D838E |
possibly damaging |
Het |
Tacc2 |
G |
A |
7: 130,330,618 (GRCm39) |
A191T |
probably benign |
Het |
Tnfrsf18 |
T |
A |
4: 156,113,168 (GRCm39) |
W285R |
probably damaging |
Het |
Tspan9 |
T |
C |
6: 127,942,726 (GRCm39) |
D167G |
probably null |
Het |
Uaca |
C |
T |
9: 60,779,120 (GRCm39) |
T1169I |
probably benign |
Het |
Umod |
G |
T |
7: 119,076,369 (GRCm39) |
Y132* |
probably null |
Het |
Vmn2r31 |
A |
G |
7: 7,399,480 (GRCm39) |
F159S |
probably damaging |
Het |
Vmn2r82 |
C |
T |
10: 79,214,605 (GRCm39) |
T196I |
probably benign |
Het |
Wrap53 |
A |
T |
11: 69,453,305 (GRCm39) |
W379R |
probably damaging |
Het |
Zfp866 |
A |
T |
8: 70,219,221 (GRCm39) |
V133D |
probably benign |
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 |
|
R1769:Cdh20
|
UTSW |
1 |
109,980,606 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|