Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310039H08Rik |
T |
C |
17: 47,083,872 (GRCm39) |
V45A |
probably benign |
Het |
4921509C19Rik |
A |
G |
2: 151,313,791 (GRCm39) |
I629T |
unknown |
Het |
4933402N03Rik |
T |
C |
7: 130,740,413 (GRCm39) |
R268G |
probably damaging |
Het |
Abca13 |
A |
T |
11: 9,384,193 (GRCm39) |
R3882* |
probably null |
Het |
Adamts3 |
T |
G |
5: 89,850,866 (GRCm39) |
T558P |
probably damaging |
Het |
Ano2 |
A |
G |
6: 125,767,304 (GRCm39) |
N214S |
probably benign |
Het |
Arhgef4 |
A |
T |
1: 34,850,866 (GRCm39) |
|
probably null |
Het |
Boc |
C |
T |
16: 44,320,743 (GRCm39) |
A306T |
probably benign |
Het |
Capn10 |
T |
C |
1: 92,871,503 (GRCm39) |
F367S |
probably damaging |
Het |
Ccdc6 |
T |
C |
10: 70,025,086 (GRCm39) |
|
probably benign |
Het |
Cobll1 |
G |
T |
2: 64,929,372 (GRCm39) |
S688R |
possibly damaging |
Het |
Cpxm2 |
G |
T |
7: 131,650,767 (GRCm39) |
P631Q |
possibly damaging |
Het |
Cyp2c68 |
A |
G |
19: 39,687,779 (GRCm39) |
V406A |
possibly damaging |
Het |
Cyp4a30b |
T |
A |
4: 115,312,200 (GRCm39) |
Y118N |
probably damaging |
Het |
Dgki |
A |
T |
6: 37,276,781 (GRCm39) |
|
probably benign |
Het |
Disp2 |
A |
G |
2: 118,623,237 (GRCm39) |
N1323S |
probably damaging |
Het |
Eps8l1 |
C |
A |
7: 4,476,944 (GRCm39) |
P471Q |
probably damaging |
Het |
Fam20a |
A |
C |
11: 109,612,513 (GRCm39) |
L10R |
unknown |
Het |
Fpr-rs4 |
T |
A |
17: 18,242,446 (GRCm39) |
I151K |
probably damaging |
Het |
Gga1 |
C |
A |
15: 78,769,509 (GRCm39) |
P161T |
probably damaging |
Het |
Gm9923 |
T |
A |
10: 72,145,306 (GRCm39) |
Y52* |
probably null |
Het |
Gucy2g |
A |
G |
19: 55,194,688 (GRCm39) |
F910L |
probably damaging |
Het |
H2-T5 |
A |
T |
17: 36,476,750 (GRCm39) |
H241Q |
possibly damaging |
Het |
Helz |
T |
C |
11: 107,539,971 (GRCm39) |
V315A |
probably damaging |
Het |
Hk2 |
T |
C |
6: 82,716,629 (GRCm39) |
Y301C |
probably damaging |
Het |
Htt |
C |
T |
5: 35,010,109 (GRCm39) |
P1521S |
probably damaging |
Het |
Iah1 |
T |
C |
12: 21,366,434 (GRCm39) |
M1T |
probably null |
Het |
Ik |
T |
C |
18: 36,885,467 (GRCm39) |
S287P |
probably damaging |
Het |
Itga1 |
T |
A |
13: 115,185,906 (GRCm39) |
D32V |
probably damaging |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
Klk14 |
A |
G |
7: 43,341,392 (GRCm39) |
I15V |
probably benign |
Het |
Kng2 |
T |
C |
16: 22,806,391 (GRCm39) |
I603V |
possibly damaging |
Het |
Lama1 |
T |
C |
17: 68,080,773 (GRCm39) |
I1267T |
possibly damaging |
Het |
Lrp1b |
A |
C |
2: 40,812,316 (GRCm39) |
L2430V |
probably benign |
Het |
Lrrn3 |
T |
G |
12: 41,504,243 (GRCm39) |
K25Q |
possibly damaging |
Het |
Lta4h |
T |
A |
10: 93,304,678 (GRCm39) |
N233K |
probably benign |
Het |
Mapk13 |
T |
C |
17: 28,989,023 (GRCm39) |
I53T |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,666,430 (GRCm39) |
F123L |
probably damaging |
Het |
Myh4 |
G |
C |
11: 67,136,637 (GRCm39) |
D472H |
probably damaging |
Het |
Nipa2 |
A |
T |
7: 55,585,574 (GRCm39) |
N121K |
probably benign |
Het |
Nostrin |
C |
T |
2: 69,014,268 (GRCm39) |
T408M |
probably benign |
Het |
Oosp2 |
C |
T |
19: 11,627,017 (GRCm39) |
R102H |
probably damaging |
Het |
Or1j18 |
A |
G |
2: 36,624,686 (GRCm39) |
M118V |
probably damaging |
Het |
Or4k15b |
T |
C |
14: 50,272,287 (GRCm39) |
D191G |
probably damaging |
Het |
Osgin2 |
T |
A |
4: 16,001,946 (GRCm39) |
I202L |
probably benign |
Het |
Pbld2 |
C |
A |
10: 62,893,476 (GRCm39) |
R271S |
probably damaging |
Het |
Pex6 |
C |
T |
17: 47,023,027 (GRCm39) |
T201I |
probably benign |
Het |
Pilra |
T |
C |
5: 137,833,777 (GRCm39) |
I96M |
probably damaging |
Het |
Pllp |
T |
A |
8: 95,403,906 (GRCm39) |
D47V |
possibly damaging |
Het |
Plxna2 |
A |
G |
1: 194,444,902 (GRCm39) |
S765G |
probably benign |
Het |
Prkca |
A |
T |
11: 107,852,434 (GRCm39) |
Y100N |
probably damaging |
Het |
Prkg1 |
T |
A |
19: 31,641,579 (GRCm39) |
K35* |
probably null |
Het |
Psmc2 |
A |
G |
5: 22,008,263 (GRCm39) |
D389G |
possibly damaging |
Het |
Rnf213 |
A |
G |
11: 119,331,951 (GRCm39) |
T2387A |
probably damaging |
Het |
Ros1 |
T |
C |
10: 52,005,192 (GRCm39) |
N914S |
probably damaging |
Het |
Ruvbl1 |
C |
A |
6: 88,468,581 (GRCm39) |
T367K |
probably benign |
Het |
Scube2 |
C |
T |
7: 109,409,920 (GRCm39) |
R525H |
probably damaging |
Het |
Sec14l4 |
T |
C |
11: 3,985,200 (GRCm39) |
|
probably null |
Het |
Secisbp2l |
T |
C |
2: 125,587,862 (GRCm39) |
D751G |
probably damaging |
Het |
Setd3 |
T |
C |
12: 108,074,949 (GRCm39) |
D402G |
probably benign |
Het |
Slc15a2 |
T |
A |
16: 36,578,211 (GRCm39) |
K359N |
probably damaging |
Het |
Slc25a21 |
A |
G |
12: 57,243,721 (GRCm39) |
S2P |
probably benign |
Het |
Slfn8 |
A |
T |
11: 82,908,332 (GRCm39) |
H70Q |
probably benign |
Het |
Spef2 |
T |
C |
15: 9,647,576 (GRCm39) |
I944V |
probably benign |
Het |
Spg11 |
A |
G |
2: 121,895,557 (GRCm39) |
F1887S |
probably damaging |
Het |
Sptbn4 |
A |
T |
7: 27,066,160 (GRCm39) |
D649E |
possibly damaging |
Het |
Sptbn4 |
T |
C |
7: 27,063,844 (GRCm39) |
E879G |
probably damaging |
Het |
Stx5a |
C |
A |
19: 8,720,725 (GRCm39) |
R121S |
probably damaging |
Het |
Tbcd |
T |
C |
11: 121,384,597 (GRCm39) |
L26P |
probably damaging |
Het |
Tecpr1 |
T |
C |
5: 144,144,255 (GRCm39) |
D649G |
probably benign |
Het |
Tfam |
A |
G |
10: 71,073,677 (GRCm39) |
S32P |
probably benign |
Het |
Tmt1b |
G |
T |
10: 128,796,571 (GRCm39) |
C79* |
probably null |
Het |
Trmt44 |
C |
T |
5: 35,715,387 (GRCm39) |
R642H |
probably benign |
Het |
Trpm3 |
G |
A |
19: 22,965,145 (GRCm39) |
A1547T |
probably benign |
Het |
Ttll6 |
T |
C |
11: 96,044,003 (GRCm39) |
V519A |
probably benign |
Het |
Umodl1 |
T |
C |
17: 31,217,088 (GRCm39) |
F1107L |
probably benign |
Het |
Usp5 |
A |
T |
6: 124,794,919 (GRCm39) |
V677E |
probably damaging |
Het |
Utp20 |
A |
T |
10: 88,643,307 (GRCm39) |
L605* |
probably null |
Het |
Utrn |
T |
C |
10: 12,620,984 (GRCm39) |
D229G |
probably damaging |
Het |
Uty |
A |
T |
Y: 1,176,502 (GRCm39) |
L178* |
probably null |
Het |
Vmn2r88 |
A |
T |
14: 51,650,791 (GRCm39) |
D168V |
possibly damaging |
Het |
Vps13b |
T |
C |
15: 35,646,324 (GRCm39) |
V1476A |
probably damaging |
Het |
Vps13b |
C |
A |
15: 35,879,967 (GRCm39) |
T3014K |
probably benign |
Het |
Vps13b |
C |
T |
15: 35,841,487 (GRCm39) |
H2506Y |
probably benign |
Het |
Vps37c |
T |
C |
19: 10,690,132 (GRCm39) |
V198A |
probably benign |
Het |
Zfc3h1 |
T |
C |
10: 115,259,290 (GRCm39) |
Y1621H |
probably benign |
Het |
Zfp251 |
T |
C |
15: 76,738,607 (GRCm39) |
D162G |
possibly damaging |
Het |
Zfp292 |
T |
C |
4: 34,807,078 (GRCm39) |
T1994A |
probably benign |
Het |
Zfp791 |
A |
G |
8: 85,837,559 (GRCm39) |
Y102H |
probably benign |
Het |
|
Other mutations in Dock1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00484:Dock1
|
APN |
7 |
134,748,260 (GRCm39) |
splice site |
probably benign |
|
IGL01319:Dock1
|
APN |
7 |
134,391,007 (GRCm39) |
missense |
probably benign |
|
IGL01390:Dock1
|
APN |
7 |
134,346,776 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01394:Dock1
|
APN |
7 |
134,367,945 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01489:Dock1
|
APN |
7 |
134,601,050 (GRCm39) |
splice site |
probably benign |
|
IGL01505:Dock1
|
APN |
7 |
134,760,239 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01586:Dock1
|
APN |
7 |
134,355,106 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01637:Dock1
|
APN |
7 |
134,739,542 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01649:Dock1
|
APN |
7 |
134,379,139 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01652:Dock1
|
APN |
7 |
134,379,226 (GRCm39) |
splice site |
probably benign |
|
IGL01859:Dock1
|
APN |
7 |
134,678,890 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02068:Dock1
|
APN |
7 |
134,373,277 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02168:Dock1
|
APN |
7 |
134,678,860 (GRCm39) |
splice site |
probably benign |
|
IGL02200:Dock1
|
APN |
7 |
134,346,000 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02244:Dock1
|
APN |
7 |
134,379,174 (GRCm39) |
nonsense |
probably null |
|
IGL02285:Dock1
|
APN |
7 |
134,683,649 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02319:Dock1
|
APN |
7 |
134,374,178 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02334:Dock1
|
APN |
7 |
134,747,294 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02338:Dock1
|
APN |
7 |
134,734,804 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02351:Dock1
|
APN |
7 |
134,710,548 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02358:Dock1
|
APN |
7 |
134,710,548 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02607:Dock1
|
APN |
7 |
134,453,242 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02638:Dock1
|
APN |
7 |
134,748,209 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02724:Dock1
|
APN |
7 |
134,765,082 (GRCm39) |
missense |
probably benign |
|
IGL02820:Dock1
|
APN |
7 |
134,768,944 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02950:Dock1
|
APN |
7 |
134,331,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02993:Dock1
|
APN |
7 |
134,346,027 (GRCm39) |
missense |
probably benign |
|
IGL03000:Dock1
|
APN |
7 |
134,390,969 (GRCm39) |
missense |
probably benign |
0.17 |
IGL03092:Dock1
|
APN |
7 |
134,366,945 (GRCm39) |
splice site |
probably benign |
|
IGL03131:Dock1
|
APN |
7 |
134,475,912 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03136:Dock1
|
APN |
7 |
134,770,118 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03210:Dock1
|
APN |
7 |
134,358,668 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03220:Dock1
|
APN |
7 |
134,710,251 (GRCm39) |
critical splice donor site |
probably null |
|
P0028:Dock1
|
UTSW |
7 |
134,601,053 (GRCm39) |
splice site |
probably benign |
|
PIT4453001:Dock1
|
UTSW |
7 |
134,754,029 (GRCm39) |
missense |
probably benign |
|
R0003:Dock1
|
UTSW |
7 |
134,331,793 (GRCm39) |
splice site |
probably benign |
|
R0058:Dock1
|
UTSW |
7 |
134,710,490 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0058:Dock1
|
UTSW |
7 |
134,710,490 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0062:Dock1
|
UTSW |
7 |
134,379,224 (GRCm39) |
splice site |
probably null |
|
R0062:Dock1
|
UTSW |
7 |
134,379,224 (GRCm39) |
splice site |
probably null |
|
R0179:Dock1
|
UTSW |
7 |
134,700,566 (GRCm39) |
missense |
probably damaging |
0.99 |
R0180:Dock1
|
UTSW |
7 |
134,700,566 (GRCm39) |
missense |
probably damaging |
0.99 |
R0347:Dock1
|
UTSW |
7 |
134,365,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R0399:Dock1
|
UTSW |
7 |
134,765,171 (GRCm39) |
missense |
probably benign |
0.00 |
R0457:Dock1
|
UTSW |
7 |
134,739,874 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0480:Dock1
|
UTSW |
7 |
134,339,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R0521:Dock1
|
UTSW |
7 |
134,745,507 (GRCm39) |
missense |
probably benign |
0.21 |
R0792:Dock1
|
UTSW |
7 |
134,475,879 (GRCm39) |
missense |
probably benign |
0.02 |
R1136:Dock1
|
UTSW |
7 |
134,449,902 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1224:Dock1
|
UTSW |
7 |
134,710,548 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1267:Dock1
|
UTSW |
7 |
134,348,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R1373:Dock1
|
UTSW |
7 |
134,768,904 (GRCm39) |
missense |
probably benign |
0.01 |
R1401:Dock1
|
UTSW |
7 |
134,735,665 (GRCm39) |
nonsense |
probably null |
|
R1454:Dock1
|
UTSW |
7 |
134,453,338 (GRCm39) |
splice site |
probably benign |
|
R1465:Dock1
|
UTSW |
7 |
134,384,138 (GRCm39) |
missense |
probably benign |
0.00 |
R1465:Dock1
|
UTSW |
7 |
134,384,138 (GRCm39) |
missense |
probably benign |
0.00 |
R1523:Dock1
|
UTSW |
7 |
134,345,976 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1643:Dock1
|
UTSW |
7 |
134,700,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R1659:Dock1
|
UTSW |
7 |
134,390,972 (GRCm39) |
missense |
probably damaging |
0.98 |
R1793:Dock1
|
UTSW |
7 |
134,700,456 (GRCm39) |
splice site |
probably null |
|
R1864:Dock1
|
UTSW |
7 |
134,748,236 (GRCm39) |
missense |
probably benign |
0.07 |
R1911:Dock1
|
UTSW |
7 |
134,601,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R2567:Dock1
|
UTSW |
7 |
134,747,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R3816:Dock1
|
UTSW |
7 |
134,346,015 (GRCm39) |
nonsense |
probably null |
|
R3971:Dock1
|
UTSW |
7 |
134,348,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R4063:Dock1
|
UTSW |
7 |
134,717,021 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4163:Dock1
|
UTSW |
7 |
134,346,051 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4271:Dock1
|
UTSW |
7 |
134,335,783 (GRCm39) |
missense |
probably damaging |
0.99 |
R4717:Dock1
|
UTSW |
7 |
134,449,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R4725:Dock1
|
UTSW |
7 |
134,346,743 (GRCm39) |
nonsense |
probably null |
|
R4788:Dock1
|
UTSW |
7 |
134,747,213 (GRCm39) |
missense |
probably damaging |
0.98 |
R4869:Dock1
|
UTSW |
7 |
134,335,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4889:Dock1
|
UTSW |
7 |
134,346,705 (GRCm39) |
missense |
probably benign |
0.02 |
R4953:Dock1
|
UTSW |
7 |
134,754,017 (GRCm39) |
missense |
probably benign |
0.34 |
R5031:Dock1
|
UTSW |
7 |
134,753,975 (GRCm39) |
missense |
probably benign |
0.02 |
R5161:Dock1
|
UTSW |
7 |
134,335,791 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5168:Dock1
|
UTSW |
7 |
134,720,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R5212:Dock1
|
UTSW |
7 |
134,390,923 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5648:Dock1
|
UTSW |
7 |
134,348,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R5685:Dock1
|
UTSW |
7 |
134,374,091 (GRCm39) |
missense |
probably benign |
0.19 |
R5834:Dock1
|
UTSW |
7 |
134,365,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R6181:Dock1
|
UTSW |
7 |
134,760,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R6334:Dock1
|
UTSW |
7 |
134,453,305 (GRCm39) |
missense |
probably benign |
0.01 |
R6406:Dock1
|
UTSW |
7 |
134,747,215 (GRCm39) |
missense |
probably benign |
0.26 |
R6425:Dock1
|
UTSW |
7 |
134,765,110 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6489:Dock1
|
UTSW |
7 |
134,592,270 (GRCm39) |
missense |
probably damaging |
0.99 |
R6616:Dock1
|
UTSW |
7 |
134,710,221 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6706:Dock1
|
UTSW |
7 |
134,735,615 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6766:Dock1
|
UTSW |
7 |
134,358,522 (GRCm39) |
splice site |
probably null |
|
R6861:Dock1
|
UTSW |
7 |
134,373,207 (GRCm39) |
missense |
probably benign |
0.00 |
R6985:Dock1
|
UTSW |
7 |
134,765,132 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7259:Dock1
|
UTSW |
7 |
134,384,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R7285:Dock1
|
UTSW |
7 |
134,346,737 (GRCm39) |
missense |
probably benign |
0.01 |
R7471:Dock1
|
UTSW |
7 |
134,765,072 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7497:Dock1
|
UTSW |
7 |
134,367,003 (GRCm39) |
missense |
probably benign |
|
R7691:Dock1
|
UTSW |
7 |
134,739,886 (GRCm39) |
critical splice donor site |
probably null |
|
R7732:Dock1
|
UTSW |
7 |
134,346,699 (GRCm39) |
missense |
probably benign |
0.01 |
R7818:Dock1
|
UTSW |
7 |
134,365,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R7918:Dock1
|
UTSW |
7 |
134,747,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R7960:Dock1
|
UTSW |
7 |
134,678,917 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7961:Dock1
|
UTSW |
7 |
134,346,786 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7985:Dock1
|
UTSW |
7 |
134,348,683 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8009:Dock1
|
UTSW |
7 |
134,346,786 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8060:Dock1
|
UTSW |
7 |
134,592,358 (GRCm39) |
splice site |
probably benign |
|
R8060:Dock1
|
UTSW |
7 |
134,770,132 (GRCm39) |
missense |
probably benign |
|
R8061:Dock1
|
UTSW |
7 |
134,374,052 (GRCm39) |
missense |
probably benign |
0.00 |
R8101:Dock1
|
UTSW |
7 |
134,601,017 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8405:Dock1
|
UTSW |
7 |
134,379,192 (GRCm39) |
missense |
probably benign |
0.04 |
R8508:Dock1
|
UTSW |
7 |
134,384,138 (GRCm39) |
missense |
probably benign |
0.00 |
R8803:Dock1
|
UTSW |
7 |
134,475,816 (GRCm39) |
missense |
probably benign |
0.28 |
R9007:Dock1
|
UTSW |
7 |
134,500,825 (GRCm39) |
intron |
probably benign |
|
R9026:Dock1
|
UTSW |
7 |
134,720,746 (GRCm39) |
missense |
probably damaging |
0.97 |
R9111:Dock1
|
UTSW |
7 |
134,601,017 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9359:Dock1
|
UTSW |
7 |
134,770,125 (GRCm39) |
missense |
probably benign |
|
R9398:Dock1
|
UTSW |
7 |
134,774,228 (GRCm39) |
missense |
probably damaging |
0.99 |
R9403:Dock1
|
UTSW |
7 |
134,770,125 (GRCm39) |
missense |
probably benign |
|
R9408:Dock1
|
UTSW |
7 |
134,717,065 (GRCm39) |
missense |
probably damaging |
0.99 |
R9476:Dock1
|
UTSW |
7 |
134,592,279 (GRCm39) |
missense |
probably benign |
0.10 |
R9478:Dock1
|
UTSW |
7 |
134,367,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R9510:Dock1
|
UTSW |
7 |
134,592,279 (GRCm39) |
missense |
probably benign |
0.10 |
R9544:Dock1
|
UTSW |
7 |
134,348,186 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9605:Dock1
|
UTSW |
7 |
134,384,141 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9657:Dock1
|
UTSW |
7 |
134,339,429 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9767:Dock1
|
UTSW |
7 |
134,342,796 (GRCm39) |
missense |
possibly damaging |
0.68 |
X0062:Dock1
|
UTSW |
7 |
134,710,180 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dock1
|
UTSW |
7 |
134,406,276 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Dock1
|
UTSW |
7 |
134,384,129 (GRCm39) |
nonsense |
probably null |
|
|