Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap9 |
T |
C |
5: 4,026,151 (GRCm39) |
S1269P |
probably benign |
Het |
Akr7a5 |
G |
T |
4: 139,038,238 (GRCm39) |
R58L |
probably benign |
Het |
Art2a |
A |
T |
7: 101,203,956 (GRCm39) |
L194* |
probably null |
Het |
Aurkaip1 |
C |
A |
4: 155,917,091 (GRCm39) |
A113D |
possibly damaging |
Het |
Ccdc175 |
T |
G |
12: 72,221,953 (GRCm39) |
D123A |
possibly damaging |
Het |
Ccdc7b |
A |
G |
8: 129,837,401 (GRCm39) |
T131A |
probably benign |
Het |
Ccnt2 |
T |
C |
1: 127,730,766 (GRCm39) |
S548P |
probably damaging |
Het |
Cep126 |
T |
C |
9: 8,103,338 (GRCm39) |
Q224R |
probably damaging |
Het |
Cic |
A |
T |
7: 24,972,203 (GRCm39) |
I645L |
probably benign |
Het |
Cngb1 |
C |
T |
8: 96,023,756 (GRCm39) |
|
probably null |
Het |
Col13a1 |
T |
C |
10: 61,723,024 (GRCm39) |
|
probably null |
Het |
Corin |
A |
T |
5: 72,487,042 (GRCm39) |
V706D |
probably damaging |
Het |
Crebrf |
A |
G |
17: 26,981,229 (GRCm39) |
K535R |
probably damaging |
Het |
Cuzd1 |
G |
A |
7: 130,916,529 (GRCm39) |
P310L |
probably damaging |
Het |
Cxcr5 |
T |
A |
9: 44,425,442 (GRCm39) |
I72F |
probably benign |
Het |
Dapp1 |
T |
C |
3: 137,644,932 (GRCm39) |
Q148R |
probably benign |
Het |
Dcaf17 |
T |
A |
2: 70,918,924 (GRCm39) |
S499R |
probably benign |
Het |
Defb3 |
A |
T |
8: 19,345,172 (GRCm39) |
I43F |
possibly damaging |
Het |
Dlgap2 |
G |
A |
8: 14,777,999 (GRCm39) |
|
probably null |
Het |
Dnah8 |
A |
G |
17: 30,970,541 (GRCm39) |
D2684G |
probably benign |
Het |
Dnajc10 |
T |
G |
2: 80,178,122 (GRCm39) |
F710V |
probably damaging |
Het |
Ep400 |
G |
A |
5: 110,901,725 (GRCm39) |
T464I |
probably damaging |
Het |
Epc1 |
G |
A |
18: 6,441,157 (GRCm39) |
Q14* |
probably null |
Het |
Eral1 |
A |
T |
11: 77,969,130 (GRCm39) |
N123K |
probably damaging |
Het |
Ercc5 |
G |
A |
1: 44,198,017 (GRCm39) |
V145I |
probably benign |
Het |
Evc |
A |
G |
5: 37,481,057 (GRCm39) |
S263P |
probably damaging |
Het |
Fancc |
A |
T |
13: 63,495,378 (GRCm39) |
M182K |
probably benign |
Het |
Fbxl3 |
G |
T |
14: 103,320,526 (GRCm39) |
A355E |
probably damaging |
Het |
Glra3 |
C |
A |
8: 56,542,028 (GRCm39) |
T257K |
probably damaging |
Het |
Gm12789 |
A |
G |
4: 101,847,159 (GRCm39) |
Y148C |
possibly damaging |
Het |
Gm14393 |
C |
A |
2: 174,904,497 (GRCm39) |
|
probably benign |
Het |
Gm19965 |
T |
A |
1: 116,749,508 (GRCm39) |
N396K |
probably benign |
Het |
Gm27013 |
A |
T |
6: 130,498,003 (GRCm39) |
|
noncoding transcript |
Het |
Gmcl1 |
A |
G |
6: 86,699,605 (GRCm39) |
S141P |
probably damaging |
Het |
Gsdmd |
T |
A |
15: 75,737,600 (GRCm39) |
|
probably null |
Het |
Gtf2a1 |
C |
T |
12: 91,529,700 (GRCm39) |
V338I |
possibly damaging |
Het |
H2ac15 |
T |
C |
13: 21,937,882 (GRCm39) |
N39S |
possibly damaging |
Het |
Hap1 |
G |
A |
11: 100,245,550 (GRCm39) |
T138M |
probably benign |
Het |
Ints2 |
G |
T |
11: 86,140,101 (GRCm39) |
R244S |
probably damaging |
Het |
Itgb4 |
T |
C |
11: 115,884,151 (GRCm39) |
V945A |
probably damaging |
Het |
Itih2 |
C |
T |
2: 10,115,211 (GRCm39) |
S387N |
probably benign |
Het |
Klra2 |
T |
A |
6: 131,207,120 (GRCm39) |
D163V |
probably benign |
Het |
Lctl |
T |
C |
9: 64,038,882 (GRCm39) |
S324P |
probably damaging |
Het |
Lrrc24 |
C |
A |
15: 76,607,889 (GRCm39) |
R43L |
probably damaging |
Het |
Mogs |
G |
T |
6: 83,095,619 (GRCm39) |
R812L |
possibly damaging |
Het |
Mroh5 |
T |
A |
15: 73,661,120 (GRCm39) |
T467S |
probably benign |
Het |
Mtap |
G |
A |
4: 89,090,511 (GRCm39) |
V194I |
probably benign |
Het |
Myoz1 |
A |
G |
14: 20,700,663 (GRCm39) |
W185R |
probably damaging |
Het |
Nufip2 |
T |
C |
11: 77,632,554 (GRCm39) |
V690A |
unknown |
Het |
Obox1 |
A |
T |
7: 15,290,152 (GRCm39) |
N165I |
possibly damaging |
Het |
Or1j1 |
C |
T |
2: 36,702,537 (GRCm39) |
C189Y |
probably damaging |
Het |
Or4b1d |
T |
A |
2: 89,968,558 (GRCm39) |
E308D |
probably benign |
Het |
Or4c113 |
T |
G |
2: 88,885,498 (GRCm39) |
I91L |
possibly damaging |
Het |
Or6c35 |
A |
G |
10: 129,169,142 (GRCm39) |
T131A |
probably benign |
Het |
Pabpc6 |
A |
G |
17: 9,888,002 (GRCm39) |
L183P |
probably damaging |
Het |
Pcdh15 |
C |
T |
10: 74,460,116 (GRCm39) |
R1355W |
probably damaging |
Het |
Pcdhgb8 |
C |
A |
18: 37,895,413 (GRCm39) |
A161E |
probably benign |
Het |
Pex1 |
A |
G |
5: 3,683,885 (GRCm39) |
Y1127C |
probably damaging |
Het |
Phc2 |
A |
T |
4: 128,637,303 (GRCm39) |
H563L |
probably damaging |
Het |
Plekha2 |
C |
A |
8: 25,533,685 (GRCm39) |
E291* |
probably null |
Het |
Qser1 |
C |
A |
2: 104,617,138 (GRCm39) |
V1225L |
probably benign |
Het |
Ralgapa2 |
A |
T |
2: 146,156,944 (GRCm39) |
D1882E |
probably damaging |
Het |
Rgs17 |
T |
C |
10: 5,792,596 (GRCm39) |
D70G |
probably benign |
Het |
Runx1t1 |
A |
T |
4: 13,889,864 (GRCm39) |
T598S |
unknown |
Het |
Scn2a |
T |
A |
2: 65,573,395 (GRCm39) |
|
probably null |
Het |
Serpinb10 |
T |
A |
1: 107,474,779 (GRCm39) |
C314S |
probably benign |
Het |
Setbp1 |
A |
C |
18: 79,130,164 (GRCm39) |
S23A |
probably benign |
Het |
Sh3pxd2b |
A |
G |
11: 32,346,479 (GRCm39) |
D116G |
possibly damaging |
Het |
Slc4a1 |
G |
T |
11: 102,252,245 (GRCm39) |
|
probably benign |
Het |
Snx19 |
T |
C |
9: 30,351,491 (GRCm39) |
L155P |
probably damaging |
Het |
Sox2 |
A |
G |
3: 34,705,193 (GRCm39) |
N210S |
probably benign |
Het |
Spag6 |
T |
C |
2: 18,736,958 (GRCm39) |
|
probably null |
Het |
Speer4b |
A |
T |
5: 27,703,036 (GRCm39) |
L154Q |
probably null |
Het |
Strn3 |
T |
A |
12: 51,696,953 (GRCm39) |
E259D |
probably benign |
Het |
Tenm1 |
G |
A |
X: 41,626,856 (GRCm39) |
Q1931* |
probably null |
Het |
Trp53bp1 |
C |
G |
2: 121,038,432 (GRCm39) |
G1469R |
probably damaging |
Het |
Ttc8 |
C |
A |
12: 98,948,789 (GRCm39) |
Q492K |
probably benign |
Het |
Ttn |
T |
C |
2: 76,798,747 (GRCm39) |
H509R |
probably benign |
Het |
Utrn |
T |
A |
10: 12,564,050 (GRCm39) |
H1270L |
probably benign |
Het |
Vopp1 |
G |
A |
6: 57,731,533 (GRCm39) |
P153S |
probably damaging |
Het |
Wdfy4 |
T |
A |
14: 32,809,912 (GRCm39) |
I1770F |
possibly damaging |
Het |
Zfp14 |
G |
T |
7: 29,738,341 (GRCm39) |
Q215K |
probably damaging |
Het |
Zfp473 |
A |
T |
7: 44,382,376 (GRCm39) |
Y651* |
probably null |
Het |
Zfp735 |
G |
T |
11: 73,580,550 (GRCm39) |
E16D |
possibly damaging |
Het |
|
Other mutations in Bsn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Bsn
|
APN |
9 |
107,992,309 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00330:Bsn
|
APN |
9 |
107,992,539 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00863:Bsn
|
APN |
9 |
107,992,521 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01123:Bsn
|
APN |
9 |
107,993,185 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01330:Bsn
|
APN |
9 |
107,988,112 (GRCm39) |
unclassified |
probably benign |
|
IGL01336:Bsn
|
APN |
9 |
107,988,984 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01399:Bsn
|
APN |
9 |
107,984,386 (GRCm39) |
missense |
unknown |
|
IGL01683:Bsn
|
APN |
9 |
107,992,095 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02022:Bsn
|
APN |
9 |
107,987,617 (GRCm39) |
unclassified |
probably benign |
|
IGL02396:Bsn
|
APN |
9 |
107,993,245 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02538:Bsn
|
APN |
9 |
107,982,435 (GRCm39) |
missense |
unknown |
|
IGL02565:Bsn
|
APN |
9 |
107,990,487 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02661:Bsn
|
APN |
9 |
107,984,135 (GRCm39) |
nonsense |
probably null |
|
IGL02739:Bsn
|
APN |
9 |
107,989,745 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02951:Bsn
|
APN |
9 |
107,992,812 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02987:Bsn
|
APN |
9 |
108,003,503 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03033:Bsn
|
APN |
9 |
107,993,192 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03069:Bsn
|
APN |
9 |
107,991,462 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03076:Bsn
|
APN |
9 |
107,982,581 (GRCm39) |
missense |
unknown |
|
R0068:Bsn
|
UTSW |
9 |
107,989,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Bsn
|
UTSW |
9 |
107,989,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R0167:Bsn
|
UTSW |
9 |
108,003,185 (GRCm39) |
missense |
probably benign |
0.01 |
R0234:Bsn
|
UTSW |
9 |
107,993,595 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0234:Bsn
|
UTSW |
9 |
107,993,595 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0359:Bsn
|
UTSW |
9 |
107,989,045 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0514:Bsn
|
UTSW |
9 |
108,002,981 (GRCm39) |
missense |
probably benign |
0.07 |
R0593:Bsn
|
UTSW |
9 |
107,987,505 (GRCm39) |
missense |
unknown |
|
R0617:Bsn
|
UTSW |
9 |
107,984,439 (GRCm39) |
missense |
unknown |
|
R0636:Bsn
|
UTSW |
9 |
107,985,033 (GRCm39) |
missense |
unknown |
|
R0652:Bsn
|
UTSW |
9 |
107,982,941 (GRCm39) |
missense |
unknown |
|
R0718:Bsn
|
UTSW |
9 |
107,988,559 (GRCm39) |
unclassified |
probably benign |
|
R0730:Bsn
|
UTSW |
9 |
107,984,011 (GRCm39) |
missense |
unknown |
|
R0905:Bsn
|
UTSW |
9 |
107,982,834 (GRCm39) |
missense |
unknown |
|
R0963:Bsn
|
UTSW |
9 |
107,989,006 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0992:Bsn
|
UTSW |
9 |
107,991,553 (GRCm39) |
nonsense |
probably null |
|
R1101:Bsn
|
UTSW |
9 |
107,993,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R1393:Bsn
|
UTSW |
9 |
107,987,716 (GRCm39) |
unclassified |
probably benign |
|
R1490:Bsn
|
UTSW |
9 |
107,991,193 (GRCm39) |
missense |
probably benign |
0.03 |
R1566:Bsn
|
UTSW |
9 |
108,003,184 (GRCm39) |
missense |
probably benign |
0.35 |
R1582:Bsn
|
UTSW |
9 |
107,982,291 (GRCm39) |
missense |
unknown |
|
R1738:Bsn
|
UTSW |
9 |
107,984,133 (GRCm39) |
missense |
unknown |
|
R1867:Bsn
|
UTSW |
9 |
107,983,918 (GRCm39) |
missense |
unknown |
|
R1918:Bsn
|
UTSW |
9 |
107,984,772 (GRCm39) |
missense |
unknown |
|
R1933:Bsn
|
UTSW |
9 |
107,993,643 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1946:Bsn
|
UTSW |
9 |
107,991,850 (GRCm39) |
missense |
probably damaging |
0.99 |
R1978:Bsn
|
UTSW |
9 |
107,991,748 (GRCm39) |
missense |
probably benign |
0.35 |
R2068:Bsn
|
UTSW |
9 |
108,003,749 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2068:Bsn
|
UTSW |
9 |
107,987,883 (GRCm39) |
unclassified |
probably benign |
|
R2113:Bsn
|
UTSW |
9 |
107,992,085 (GRCm39) |
missense |
probably benign |
0.14 |
R2136:Bsn
|
UTSW |
9 |
107,990,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R2172:Bsn
|
UTSW |
9 |
107,987,191 (GRCm39) |
intron |
probably benign |
|
R2266:Bsn
|
UTSW |
9 |
107,992,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R2293:Bsn
|
UTSW |
9 |
107,990,266 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2294:Bsn
|
UTSW |
9 |
107,990,266 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2368:Bsn
|
UTSW |
9 |
107,988,229 (GRCm39) |
nonsense |
probably null |
|
R2442:Bsn
|
UTSW |
9 |
107,984,119 (GRCm39) |
missense |
unknown |
|
R2507:Bsn
|
UTSW |
9 |
107,993,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R2880:Bsn
|
UTSW |
9 |
107,990,266 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2881:Bsn
|
UTSW |
9 |
107,990,266 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2922:Bsn
|
UTSW |
9 |
107,992,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R2922:Bsn
|
UTSW |
9 |
107,985,385 (GRCm39) |
missense |
unknown |
|
R3618:Bsn
|
UTSW |
9 |
107,994,760 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3742:Bsn
|
UTSW |
9 |
107,982,938 (GRCm39) |
missense |
unknown |
|
R3825:Bsn
|
UTSW |
9 |
107,984,055 (GRCm39) |
missense |
unknown |
|
R3982:Bsn
|
UTSW |
9 |
107,984,365 (GRCm39) |
missense |
unknown |
|
R4094:Bsn
|
UTSW |
9 |
107,991,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R4158:Bsn
|
UTSW |
9 |
107,990,145 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4225:Bsn
|
UTSW |
9 |
107,983,932 (GRCm39) |
missense |
unknown |
|
R4261:Bsn
|
UTSW |
9 |
107,987,883 (GRCm39) |
unclassified |
probably benign |
|
R4482:Bsn
|
UTSW |
9 |
107,991,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R4515:Bsn
|
UTSW |
9 |
107,981,277 (GRCm39) |
splice site |
probably null |
|
R4628:Bsn
|
UTSW |
9 |
107,990,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R4636:Bsn
|
UTSW |
9 |
107,992,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R4679:Bsn
|
UTSW |
9 |
107,987,329 (GRCm39) |
missense |
unknown |
|
R4723:Bsn
|
UTSW |
9 |
107,989,854 (GRCm39) |
missense |
probably benign |
0.03 |
R4843:Bsn
|
UTSW |
9 |
107,984,388 (GRCm39) |
missense |
unknown |
|
R4885:Bsn
|
UTSW |
9 |
107,984,726 (GRCm39) |
nonsense |
probably null |
|
R4936:Bsn
|
UTSW |
9 |
107,988,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R4942:Bsn
|
UTSW |
9 |
107,983,678 (GRCm39) |
missense |
unknown |
|
R4972:Bsn
|
UTSW |
9 |
107,992,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Bsn
|
UTSW |
9 |
107,992,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R5067:Bsn
|
UTSW |
9 |
107,989,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R5206:Bsn
|
UTSW |
9 |
107,982,572 (GRCm39) |
missense |
unknown |
|
R5286:Bsn
|
UTSW |
9 |
107,988,123 (GRCm39) |
unclassified |
probably benign |
|
R5492:Bsn
|
UTSW |
9 |
107,989,714 (GRCm39) |
missense |
probably damaging |
0.98 |
R5553:Bsn
|
UTSW |
9 |
107,987,620 (GRCm39) |
unclassified |
probably benign |
|
R5561:Bsn
|
UTSW |
9 |
107,982,710 (GRCm39) |
missense |
unknown |
|
R5597:Bsn
|
UTSW |
9 |
107,992,131 (GRCm39) |
missense |
probably benign |
0.06 |
R5646:Bsn
|
UTSW |
9 |
107,987,631 (GRCm39) |
unclassified |
probably benign |
|
R5796:Bsn
|
UTSW |
9 |
108,003,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R5801:Bsn
|
UTSW |
9 |
107,990,208 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5802:Bsn
|
UTSW |
9 |
107,990,208 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5850:Bsn
|
UTSW |
9 |
107,992,149 (GRCm39) |
missense |
probably damaging |
0.99 |
R5938:Bsn
|
UTSW |
9 |
107,990,208 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6221:Bsn
|
UTSW |
9 |
107,982,765 (GRCm39) |
missense |
unknown |
|
R6243:Bsn
|
UTSW |
9 |
107,984,760 (GRCm39) |
missense |
unknown |
|
R6254:Bsn
|
UTSW |
9 |
107,989,065 (GRCm39) |
missense |
probably damaging |
0.96 |
R6263:Bsn
|
UTSW |
9 |
107,990,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R6345:Bsn
|
UTSW |
9 |
107,984,554 (GRCm39) |
missense |
unknown |
|
R6368:Bsn
|
UTSW |
9 |
107,988,513 (GRCm39) |
unclassified |
probably benign |
|
R6574:Bsn
|
UTSW |
9 |
107,991,153 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6793:Bsn
|
UTSW |
9 |
107,991,814 (GRCm39) |
nonsense |
probably null |
|
R6802:Bsn
|
UTSW |
9 |
107,987,823 (GRCm39) |
unclassified |
probably benign |
|
R6943:Bsn
|
UTSW |
9 |
107,985,016 (GRCm39) |
missense |
unknown |
|
R6999:Bsn
|
UTSW |
9 |
107,990,632 (GRCm39) |
missense |
probably benign |
0.00 |
R7149:Bsn
|
UTSW |
9 |
107,993,520 (GRCm39) |
nonsense |
probably null |
|
R7199:Bsn
|
UTSW |
9 |
107,992,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Bsn
|
UTSW |
9 |
108,003,620 (GRCm39) |
nonsense |
probably null |
|
R7349:Bsn
|
UTSW |
9 |
107,987,982 (GRCm39) |
missense |
unknown |
|
R7372:Bsn
|
UTSW |
9 |
107,987,718 (GRCm39) |
missense |
unknown |
|
R7373:Bsn
|
UTSW |
9 |
107,990,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R7413:Bsn
|
UTSW |
9 |
108,016,690 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7473:Bsn
|
UTSW |
9 |
107,989,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R7482:Bsn
|
UTSW |
9 |
107,990,728 (GRCm39) |
missense |
probably damaging |
0.98 |
R7530:Bsn
|
UTSW |
9 |
107,989,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R7549:Bsn
|
UTSW |
9 |
107,992,014 (GRCm39) |
missense |
probably benign |
0.05 |
R7570:Bsn
|
UTSW |
9 |
107,990,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R7635:Bsn
|
UTSW |
9 |
107,988,189 (GRCm39) |
missense |
unknown |
|
R7696:Bsn
|
UTSW |
9 |
107,991,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R7757:Bsn
|
UTSW |
9 |
107,991,939 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7868:Bsn
|
UTSW |
9 |
107,992,098 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7897:Bsn
|
UTSW |
9 |
107,989,065 (GRCm39) |
missense |
probably damaging |
0.98 |
R7960:Bsn
|
UTSW |
9 |
107,992,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R8022:Bsn
|
UTSW |
9 |
107,991,603 (GRCm39) |
missense |
probably benign |
0.01 |
R8056:Bsn
|
UTSW |
9 |
107,982,506 (GRCm39) |
missense |
|
|
R8158:Bsn
|
UTSW |
9 |
107,987,232 (GRCm39) |
missense |
unknown |
|
R8161:Bsn
|
UTSW |
9 |
108,016,729 (GRCm39) |
missense |
probably benign |
0.20 |
R8225:Bsn
|
UTSW |
9 |
107,984,305 (GRCm39) |
missense |
|
|
R8282:Bsn
|
UTSW |
9 |
107,984,890 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8296:Bsn
|
UTSW |
9 |
107,994,578 (GRCm39) |
missense |
probably benign |
0.00 |
R8415:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8417:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8426:Bsn
|
UTSW |
9 |
108,003,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R8437:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8438:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8439:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8440:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8441:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8442:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8513:Bsn
|
UTSW |
9 |
107,991,709 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8529:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8535:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8546:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8548:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8549:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8682:Bsn
|
UTSW |
9 |
107,983,368 (GRCm39) |
missense |
|
|
R8773:Bsn
|
UTSW |
9 |
107,987,704 (GRCm39) |
missense |
unknown |
|
R8883:Bsn
|
UTSW |
9 |
107,990,227 (GRCm39) |
missense |
probably damaging |
0.98 |
R8906:Bsn
|
UTSW |
9 |
107,984,752 (GRCm39) |
missense |
unknown |
|
R9018:Bsn
|
UTSW |
9 |
107,994,488 (GRCm39) |
missense |
probably benign |
0.06 |
R9070:Bsn
|
UTSW |
9 |
107,987,295 (GRCm39) |
missense |
|
|
R9094:Bsn
|
UTSW |
9 |
107,988,052 (GRCm39) |
missense |
unknown |
|
R9098:Bsn
|
UTSW |
9 |
107,990,173 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9128:Bsn
|
UTSW |
9 |
107,993,349 (GRCm39) |
missense |
probably benign |
0.21 |
R9162:Bsn
|
UTSW |
9 |
107,987,883 (GRCm39) |
missense |
unknown |
|
R9224:Bsn
|
UTSW |
9 |
107,982,686 (GRCm39) |
missense |
|
|
R9230:Bsn
|
UTSW |
9 |
107,989,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R9233:Bsn
|
UTSW |
9 |
107,994,289 (GRCm39) |
missense |
probably benign |
0.28 |
R9245:Bsn
|
UTSW |
9 |
107,993,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R9275:Bsn
|
UTSW |
9 |
107,988,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R9307:Bsn
|
UTSW |
9 |
107,992,993 (GRCm39) |
missense |
probably benign |
0.01 |
R9343:Bsn
|
UTSW |
9 |
107,992,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R9377:Bsn
|
UTSW |
9 |
107,993,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R9377:Bsn
|
UTSW |
9 |
107,990,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R9378:Bsn
|
UTSW |
9 |
107,984,854 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9408:Bsn
|
UTSW |
9 |
108,016,652 (GRCm39) |
nonsense |
probably null |
|
R9455:Bsn
|
UTSW |
9 |
107,988,531 (GRCm39) |
missense |
unknown |
|
R9563:Bsn
|
UTSW |
9 |
107,984,616 (GRCm39) |
missense |
|
|
R9615:Bsn
|
UTSW |
9 |
107,984,430 (GRCm39) |
missense |
|
|
R9656:Bsn
|
UTSW |
9 |
107,994,407 (GRCm39) |
missense |
probably benign |
0.09 |
R9698:Bsn
|
UTSW |
9 |
107,993,170 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Bsn
|
UTSW |
9 |
107,990,703 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Bsn
|
UTSW |
9 |
108,016,409 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Bsn
|
UTSW |
9 |
108,016,394 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Bsn
|
UTSW |
9 |
107,982,698 (GRCm39) |
missense |
|
|
|