Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp3 |
T |
A |
9: 104,197,177 (GRCm39) |
Y154F |
probably damaging |
Het |
Acsl6 |
A |
T |
11: 54,241,406 (GRCm39) |
D579V |
probably damaging |
Het |
Adamts18 |
C |
T |
8: 114,465,401 (GRCm39) |
|
probably null |
Het |
Adamts20 |
A |
T |
15: 94,168,257 (GRCm39) |
V1882D |
probably damaging |
Het |
Add3 |
A |
T |
19: 53,225,274 (GRCm39) |
K465* |
probably null |
Het |
Ago1 |
T |
G |
4: 126,333,388 (GRCm39) |
I524L |
probably benign |
Het |
Akr1c18 |
A |
G |
13: 4,187,190 (GRCm39) |
M208T |
probably benign |
Het |
Anapc1 |
C |
A |
2: 128,474,575 (GRCm39) |
L1413F |
probably damaging |
Het |
Arid4b |
A |
T |
13: 14,358,902 (GRCm39) |
D646V |
probably damaging |
Het |
Arnt2 |
T |
C |
7: 83,954,067 (GRCm39) |
E261G |
probably benign |
Het |
Bccip |
C |
T |
7: 133,320,859 (GRCm39) |
T211I |
possibly damaging |
Het |
Cdh26 |
G |
A |
2: 178,108,621 (GRCm39) |
|
probably null |
Het |
Ceacam2 |
A |
G |
7: 25,220,356 (GRCm39) |
F414S |
probably benign |
Het |
Cep43 |
A |
G |
17: 8,410,266 (GRCm39) |
N342S |
possibly damaging |
Het |
Cfb |
T |
C |
17: 35,079,874 (GRCm39) |
R172G |
probably damaging |
Het |
Cntnap5b |
A |
C |
1: 99,700,511 (GRCm39) |
T8P |
probably benign |
Het |
Cpne9 |
A |
T |
6: 113,266,974 (GRCm39) |
I136L |
probably damaging |
Het |
Crtc1 |
A |
T |
8: 70,855,079 (GRCm39) |
|
probably null |
Het |
Dcdc2a |
A |
T |
13: 25,303,369 (GRCm39) |
H300L |
probably benign |
Het |
Dhdh |
C |
T |
7: 45,138,130 (GRCm39) |
V20M |
probably benign |
Het |
Dhx34 |
T |
C |
7: 15,944,462 (GRCm39) |
Q584R |
probably benign |
Het |
Dis3l2 |
A |
G |
1: 86,974,814 (GRCm39) |
Y701C |
probably damaging |
Het |
Dmrt2 |
T |
C |
19: 25,653,019 (GRCm39) |
|
probably null |
Het |
Dnah5 |
A |
G |
15: 28,366,467 (GRCm39) |
T2727A |
probably damaging |
Het |
Dop1a |
A |
G |
9: 86,402,787 (GRCm39) |
E1329G |
probably damaging |
Het |
Evpl |
A |
G |
11: 116,114,117 (GRCm39) |
V1191A |
probably damaging |
Het |
Fhl4 |
T |
C |
10: 84,934,250 (GRCm39) |
D177G |
probably damaging |
Het |
Gask1a |
A |
G |
9: 121,807,418 (GRCm39) |
T521A |
possibly damaging |
Het |
Heg1 |
A |
G |
16: 33,547,126 (GRCm39) |
T662A |
possibly damaging |
Het |
Ifih1 |
A |
G |
2: 62,453,735 (GRCm39) |
|
probably null |
Het |
Il13 |
T |
C |
11: 53,523,345 (GRCm39) |
R87G |
possibly damaging |
Het |
Kcnc3 |
T |
A |
7: 44,245,352 (GRCm39) |
Y547* |
probably null |
Het |
Krt81 |
C |
A |
15: 101,361,508 (GRCm39) |
R24L |
possibly damaging |
Het |
Lama1 |
G |
A |
17: 68,071,693 (GRCm39) |
G860D |
probably benign |
Het |
Lmo7 |
T |
C |
14: 102,124,609 (GRCm39) |
L356P |
probably damaging |
Het |
Lmo7 |
A |
T |
14: 102,133,995 (GRCm39) |
K447I |
probably damaging |
Het |
Lrp2bp |
A |
G |
8: 46,464,995 (GRCm39) |
H38R |
probably damaging |
Het |
Magi3 |
G |
A |
3: 103,922,338 (GRCm39) |
P1460S |
probably damaging |
Het |
Megf8 |
T |
A |
7: 25,063,728 (GRCm39) |
C2695S |
possibly damaging |
Het |
Mrgprb2 |
T |
G |
7: 48,201,718 (GRCm39) |
S336R |
probably benign |
Het |
Mrgprx2 |
C |
T |
7: 48,132,712 (GRCm39) |
M1I |
probably null |
Het |
Mug2 |
T |
C |
6: 122,058,558 (GRCm39) |
L1320P |
probably damaging |
Het |
Noxred1 |
A |
G |
12: 87,273,838 (GRCm39) |
S68P |
probably benign |
Het |
Or51f5 |
T |
A |
7: 102,424,539 (GRCm39) |
H269Q |
probably benign |
Het |
Or56b1b |
T |
A |
7: 108,164,879 (GRCm39) |
Y41F |
probably damaging |
Het |
Os9 |
C |
T |
10: 126,955,508 (GRCm39) |
C123Y |
probably damaging |
Het |
Ostf1 |
T |
A |
19: 18,573,723 (GRCm39) |
T42S |
probably benign |
Het |
Parg |
C |
A |
14: 31,976,517 (GRCm39) |
T186K |
possibly damaging |
Het |
Pcnx1 |
T |
A |
12: 82,041,884 (GRCm39) |
M2172K |
probably benign |
Het |
Pip4k2a |
A |
G |
2: 18,850,747 (GRCm39) |
I360T |
probably damaging |
Het |
Pkn2 |
T |
C |
3: 142,516,219 (GRCm39) |
D568G |
possibly damaging |
Het |
Plch2 |
A |
G |
4: 155,083,343 (GRCm39) |
S431P |
probably damaging |
Het |
Prl8a6 |
A |
T |
13: 27,616,990 (GRCm39) |
C233* |
probably null |
Het |
Prox1 |
G |
A |
1: 189,893,653 (GRCm39) |
T264I |
probably damaging |
Het |
Prr5 |
A |
G |
15: 84,586,967 (GRCm39) |
N248S |
probably benign |
Het |
Psip1 |
A |
C |
4: 83,378,274 (GRCm39) |
S407R |
probably damaging |
Het |
Rab32 |
A |
T |
10: 10,426,640 (GRCm39) |
V102E |
probably damaging |
Het |
Rap1gap2 |
T |
G |
11: 74,279,680 (GRCm39) |
K687Q |
possibly damaging |
Het |
Rbak |
A |
T |
5: 143,159,169 (GRCm39) |
V628E |
probably damaging |
Het |
Rnf148 |
T |
C |
6: 23,654,792 (GRCm39) |
E68G |
possibly damaging |
Het |
Rnf212 |
A |
T |
5: 108,897,308 (GRCm39) |
S3T |
probably damaging |
Het |
Rrad |
T |
G |
8: 105,355,259 (GRCm39) |
I250L |
probably benign |
Het |
Sall4 |
T |
C |
2: 168,597,625 (GRCm39) |
H405R |
probably damaging |
Het |
Scn9a |
T |
C |
2: 66,314,022 (GRCm39) |
R1888G |
probably damaging |
Het |
Setd5 |
G |
T |
6: 113,096,398 (GRCm39) |
E535* |
probably null |
Het |
Slc20a1 |
C |
T |
2: 129,041,811 (GRCm39) |
S58L |
probably damaging |
Het |
Slc31a1 |
A |
G |
4: 62,303,841 (GRCm39) |
|
probably benign |
Het |
Slc38a11 |
G |
T |
2: 65,147,209 (GRCm39) |
Q423K |
probably benign |
Het |
Snrpd1 |
A |
T |
18: 10,626,846 (GRCm39) |
T38S |
possibly damaging |
Het |
Taar4 |
A |
G |
10: 23,836,780 (GRCm39) |
D130G |
probably damaging |
Het |
Tfb2m |
C |
T |
1: 179,358,869 (GRCm39) |
R338H |
probably benign |
Het |
Tm2d2 |
A |
G |
8: 25,512,742 (GRCm39) |
I197V |
possibly damaging |
Het |
Tmem132a |
C |
T |
19: 10,836,355 (GRCm39) |
G725D |
probably damaging |
Het |
Tmem67 |
T |
C |
4: 12,089,317 (GRCm39) |
T38A |
probably benign |
Het |
Tmprss15 |
A |
T |
16: 78,765,155 (GRCm39) |
S816T |
probably benign |
Het |
Tnfrsf11a |
A |
G |
1: 105,754,717 (GRCm39) |
E263G |
probably damaging |
Het |
Tnfrsf17 |
C |
T |
16: 11,133,191 (GRCm39) |
L90F |
probably benign |
Het |
Tpr |
A |
G |
1: 150,278,024 (GRCm39) |
K117E |
possibly damaging |
Het |
Trim43a |
C |
T |
9: 88,466,389 (GRCm39) |
Q5* |
probably null |
Het |
Ubn1 |
A |
T |
16: 4,890,935 (GRCm39) |
D498V |
probably damaging |
Het |
Vipr1 |
T |
A |
9: 121,487,115 (GRCm39) |
C63S |
probably damaging |
Het |
Vmn1r237 |
T |
A |
17: 21,534,932 (GRCm39) |
H218Q |
possibly damaging |
Het |
Vmn2r100 |
C |
A |
17: 19,742,382 (GRCm39) |
P252Q |
possibly damaging |
Het |
Vmn2r95 |
T |
C |
17: 18,671,844 (GRCm39) |
V527A |
probably benign |
Het |
Vmn2r97 |
A |
T |
17: 19,134,734 (GRCm39) |
T51S |
probably benign |
Het |
Vwa8 |
G |
A |
14: 79,184,629 (GRCm39) |
V376I |
probably benign |
Het |
Wdfy4 |
T |
A |
14: 32,802,732 (GRCm39) |
T1838S |
probably benign |
Het |
Zcwpw1 |
A |
T |
5: 137,794,945 (GRCm39) |
E47V |
probably benign |
Het |
Zeb2 |
T |
C |
2: 44,892,659 (GRCm39) |
E130G |
possibly damaging |
Het |
Zfp111 |
A |
G |
7: 23,898,568 (GRCm39) |
Y348H |
probably damaging |
Het |
Zfp53 |
T |
C |
17: 21,729,271 (GRCm39) |
S435P |
probably 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 |
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 |
|
R4585:Bsn
|
UTSW |
9 |
107,987,662 (GRCm39) |
unclassified |
probably benign |
|
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 |
|
|
|