Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610318N02Rik |
T |
A |
16: 16,935,446 (GRCm39) |
H214L |
probably benign |
Het |
Abca17 |
T |
C |
17: 24,508,325 (GRCm39) |
E1070G |
possibly damaging |
Het |
Accsl |
A |
T |
2: 93,696,589 (GRCm39) |
|
probably benign |
Het |
Akp3 |
G |
A |
1: 87,055,593 (GRCm39) |
G547R |
unknown |
Het |
Anapc1 |
C |
A |
2: 128,522,108 (GRCm39) |
C150F |
probably damaging |
Het |
Aoc1l3 |
C |
A |
6: 48,967,173 (GRCm39) |
P707H |
probably damaging |
Het |
Arhgef18 |
T |
A |
8: 3,439,023 (GRCm39) |
|
probably benign |
Het |
Borcs5 |
T |
A |
6: 134,687,096 (GRCm39) |
N150K |
probably damaging |
Het |
C9orf72 |
C |
A |
4: 35,218,630 (GRCm39) |
E76D |
probably damaging |
Het |
Cntnap5c |
C |
A |
17: 58,671,241 (GRCm39) |
T1143K |
possibly damaging |
Het |
Col7a1 |
A |
C |
9: 108,784,402 (GRCm39) |
T137P |
unknown |
Het |
Defb8 |
C |
T |
8: 19,495,910 (GRCm39) |
G50E |
probably damaging |
Het |
Dimt1 |
T |
A |
13: 107,086,193 (GRCm39) |
|
probably benign |
Het |
Dnajb11 |
T |
A |
16: 22,689,423 (GRCm39) |
D281E |
probably damaging |
Het |
Eci2 |
G |
T |
13: 35,177,087 (GRCm39) |
N24K |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,236,607 (GRCm39) |
C358S |
probably benign |
Het |
Fbxl13 |
A |
T |
5: 21,825,602 (GRCm39) |
|
probably benign |
Het |
Fbxw11 |
T |
C |
11: 32,661,922 (GRCm39) |
C121R |
probably damaging |
Het |
Fsd2 |
T |
C |
7: 81,209,518 (GRCm39) |
D108G |
probably benign |
Het |
Gab1 |
C |
A |
8: 81,511,471 (GRCm39) |
R458L |
probably damaging |
Het |
Ghrhr |
T |
A |
6: 55,365,254 (GRCm39) |
L416* |
probably null |
Het |
Glipr1l2 |
C |
A |
10: 111,919,371 (GRCm39) |
L31I |
possibly damaging |
Het |
Gm1818 |
A |
G |
12: 48,602,982 (GRCm39) |
|
noncoding transcript |
Het |
Gm19965 |
T |
A |
1: 116,748,550 (GRCm39) |
|
probably benign |
Het |
Gpr149 |
A |
G |
3: 62,511,888 (GRCm39) |
L37P |
probably damaging |
Het |
Hoxa9 |
A |
G |
6: 52,202,693 (GRCm39) |
I131T |
probably damaging |
Het |
Itpkc |
T |
C |
7: 26,927,195 (GRCm39) |
I240V |
probably benign |
Het |
Jakmip3 |
A |
G |
7: 138,629,515 (GRCm39) |
D552G |
probably damaging |
Het |
Kank4 |
T |
C |
4: 98,653,806 (GRCm39) |
Y874C |
probably damaging |
Het |
Kdm3a |
T |
C |
6: 71,577,011 (GRCm39) |
E768G |
possibly damaging |
Het |
Klf6 |
A |
G |
13: 5,911,711 (GRCm39) |
D25G |
probably benign |
Het |
Lamc1 |
T |
C |
1: 153,122,977 (GRCm39) |
|
probably benign |
Het |
Laptm4a |
T |
C |
12: 8,986,716 (GRCm39) |
V258A |
probably damaging |
Het |
Map3k19 |
A |
G |
1: 127,751,617 (GRCm39) |
V578A |
probably benign |
Het |
Mast1 |
T |
C |
8: 85,651,956 (GRCm39) |
E342G |
probably benign |
Het |
Mgat5b |
T |
C |
11: 116,868,622 (GRCm39) |
L515P |
probably damaging |
Het |
Mink1 |
A |
G |
11: 70,502,166 (GRCm39) |
D985G |
probably benign |
Het |
Mphosph9 |
A |
G |
5: 124,453,739 (GRCm39) |
V191A |
possibly damaging |
Het |
Muc6 |
C |
T |
7: 141,234,368 (GRCm39) |
G708S |
probably damaging |
Het |
Pcnt |
A |
T |
10: 76,228,878 (GRCm39) |
|
probably null |
Het |
Psmd8 |
A |
T |
7: 28,875,598 (GRCm39) |
Y174N |
probably damaging |
Het |
Ptgdr2 |
C |
A |
19: 10,918,292 (GRCm39) |
R270S |
possibly damaging |
Het |
Rasal2 |
A |
G |
1: 156,975,218 (GRCm39) |
M1172T |
probably damaging |
Het |
Rif1 |
A |
G |
2: 51,997,640 (GRCm39) |
|
probably benign |
Het |
Rnf123 |
C |
T |
9: 107,954,572 (GRCm39) |
R48H |
probably benign |
Het |
Rsrc1 |
T |
C |
3: 67,263,551 (GRCm39) |
|
probably benign |
Het |
Rxfp2 |
T |
C |
5: 149,975,021 (GRCm39) |
V210A |
probably benign |
Het |
Serpinb9d |
C |
T |
13: 33,384,608 (GRCm39) |
P195L |
probably benign |
Het |
Sis |
A |
G |
3: 72,865,437 (GRCm39) |
|
probably benign |
Het |
Skint4 |
T |
C |
4: 111,981,793 (GRCm39) |
M246T |
probably benign |
Het |
Snrnp200 |
C |
A |
2: 127,070,997 (GRCm39) |
R1093S |
probably damaging |
Het |
Sp100 |
A |
G |
1: 85,629,141 (GRCm39) |
N471D |
possibly damaging |
Het |
Spmip4 |
T |
A |
6: 50,566,121 (GRCm39) |
K118M |
probably damaging |
Het |
Ssxb8 |
T |
G |
X: 8,556,062 (GRCm39) |
H88P |
probably damaging |
Het |
Sufu |
T |
C |
19: 46,389,703 (GRCm39) |
|
probably null |
Het |
Synpo2l |
G |
A |
14: 20,718,235 (GRCm39) |
T10I |
possibly damaging |
Het |
Tdo2 |
A |
T |
3: 81,881,683 (GRCm39) |
S40R |
probably damaging |
Het |
Tent4b |
T |
A |
8: 88,978,635 (GRCm39) |
F445L |
probably damaging |
Het |
Terb1 |
G |
A |
8: 105,210,938 (GRCm39) |
T363I |
probably benign |
Het |
Timd4 |
C |
T |
11: 46,708,498 (GRCm39) |
P175S |
probably damaging |
Het |
Tlr3 |
C |
A |
8: 45,850,171 (GRCm39) |
V833L |
probably damaging |
Het |
Tpst2 |
T |
A |
5: 112,455,911 (GRCm39) |
M150K |
probably damaging |
Het |
Trim67 |
T |
A |
8: 125,543,774 (GRCm39) |
V378E |
probably damaging |
Het |
Tyrp1 |
C |
T |
4: 80,763,105 (GRCm39) |
Q331* |
probably null |
Het |
Ubap2l |
A |
T |
3: 89,930,807 (GRCm39) |
S413T |
probably benign |
Het |
Uimc1 |
G |
A |
13: 55,176,415 (GRCm39) |
T701I |
possibly damaging |
Het |
Vangl2 |
G |
T |
1: 171,832,353 (GRCm39) |
T501N |
probably damaging |
Het |
Vmn1r60 |
A |
G |
7: 5,547,621 (GRCm39) |
S160P |
probably benign |
Het |
Vmn2r66 |
G |
T |
7: 84,654,799 (GRCm39) |
D503E |
probably benign |
Het |
Vmn2r72 |
T |
A |
7: 85,401,152 (GRCm39) |
E89V |
probably damaging |
Het |
Zfp457 |
G |
A |
13: 67,441,748 (GRCm39) |
P180S |
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 |
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 |
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 |
|