Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933436I01Rik |
T |
A |
X: 66,964,308 (GRCm39) |
I184L |
probably benign |
Het |
Abcb5 |
A |
T |
12: 118,904,303 (GRCm39) |
C162* |
probably null |
Het |
Akr1c19 |
A |
T |
13: 4,288,391 (GRCm39) |
|
probably null |
Het |
Akt3 |
A |
G |
1: 176,930,551 (GRCm39) |
S136P |
possibly damaging |
Het |
Alox12e |
G |
A |
11: 70,206,828 (GRCm39) |
R620W |
probably damaging |
Het |
Ascc2 |
A |
T |
11: 4,631,496 (GRCm39) |
M646L |
probably benign |
Het |
Btnl9 |
T |
C |
11: 49,060,390 (GRCm39) |
T453A |
probably damaging |
Het |
C6 |
G |
T |
15: 4,820,552 (GRCm39) |
C521F |
probably damaging |
Het |
Ccnt1 |
A |
T |
15: 98,449,823 (GRCm39) |
H156Q |
probably benign |
Het |
Cdh20 |
A |
T |
1: 110,065,666 (GRCm39) |
R647* |
probably null |
Het |
Clptm1l |
C |
T |
13: 73,755,842 (GRCm39) |
Q153* |
probably null |
Het |
Cmya5 |
T |
A |
13: 93,227,032 (GRCm39) |
K2685N |
possibly damaging |
Het |
Cnksr2 |
A |
C |
X: 156,728,302 (GRCm39) |
S224R |
possibly damaging |
Het |
Cntn1 |
T |
C |
15: 92,215,943 (GRCm39) |
V992A |
possibly damaging |
Het |
Dapk1 |
G |
A |
13: 60,899,022 (GRCm39) |
D831N |
probably damaging |
Het |
Dnaaf3 |
T |
C |
7: 4,526,798 (GRCm39) |
I426M |
possibly damaging |
Het |
Dnah6 |
A |
G |
6: 72,998,165 (GRCm39) |
Y4034H |
probably benign |
Het |
Dtx2 |
C |
T |
5: 136,059,431 (GRCm39) |
S493F |
probably damaging |
Het |
Ehd1 |
T |
C |
19: 6,348,108 (GRCm39) |
L362P |
probably benign |
Het |
Endov |
T |
C |
11: 119,390,408 (GRCm39) |
F12S |
probably damaging |
Het |
Eps8 |
A |
T |
6: 137,499,172 (GRCm39) |
W239R |
probably benign |
Het |
Fance |
T |
C |
17: 28,539,799 (GRCm39) |
F83S |
possibly damaging |
Het |
Fn1 |
A |
G |
1: 71,639,598 (GRCm39) |
V1731A |
probably damaging |
Het |
Gak |
G |
T |
5: 108,718,091 (GRCm39) |
T1244K |
probably benign |
Het |
Gas8 |
T |
A |
8: 124,253,276 (GRCm39) |
I208N |
probably damaging |
Het |
Gm9830 |
A |
T |
9: 44,375,579 (GRCm39) |
|
noncoding transcript |
Het |
Gm9837 |
T |
A |
11: 53,361,092 (GRCm39) |
|
probably benign |
Het |
Gtf2f2 |
A |
G |
14: 76,155,136 (GRCm39) |
S142P |
possibly damaging |
Het |
Hdac3 |
C |
A |
18: 38,076,569 (GRCm39) |
G257V |
probably damaging |
Het |
Heg1 |
A |
G |
16: 33,547,960 (GRCm39) |
T916A |
probably benign |
Het |
Herc2 |
G |
T |
7: 55,782,245 (GRCm39) |
G1311C |
probably damaging |
Het |
Htt |
C |
T |
5: 34,983,326 (GRCm39) |
T975I |
probably benign |
Het |
Il2rg |
A |
G |
X: 100,311,416 (GRCm39) |
L57P |
possibly damaging |
Het |
Itm2b |
T |
C |
14: 73,600,575 (GRCm39) |
K242E |
probably damaging |
Het |
Itpr3 |
G |
A |
17: 27,317,050 (GRCm39) |
M768I |
probably benign |
Het |
Klrg2 |
G |
A |
6: 38,613,928 (GRCm39) |
T25I |
probably benign |
Het |
Lcn5 |
G |
A |
2: 25,548,053 (GRCm39) |
V21M |
probably damaging |
Het |
Liat1 |
T |
C |
11: 75,891,077 (GRCm39) |
S64P |
possibly damaging |
Het |
Lonp2 |
A |
G |
8: 87,392,403 (GRCm39) |
T490A |
probably damaging |
Het |
Lrrn3 |
A |
T |
12: 41,502,995 (GRCm39) |
S441T |
probably damaging |
Het |
Mpdz |
G |
A |
4: 81,254,067 (GRCm39) |
R1W |
probably null |
Het |
Mpp4 |
G |
A |
1: 59,182,941 (GRCm39) |
P322L |
possibly damaging |
Het |
Mpzl2 |
G |
A |
9: 44,955,169 (GRCm39) |
|
probably null |
Het |
Naf1 |
A |
G |
8: 67,340,432 (GRCm39) |
D414G |
probably damaging |
Het |
Notch3 |
A |
G |
17: 32,354,482 (GRCm39) |
C1748R |
probably benign |
Het |
Nup133 |
C |
A |
8: 124,641,314 (GRCm39) |
D869Y |
probably damaging |
Het |
Oasl2 |
A |
C |
5: 115,049,298 (GRCm39) |
D466A |
probably benign |
Het |
Opa3 |
T |
C |
7: 18,978,739 (GRCm39) |
I68T |
possibly damaging |
Het |
Or2ab1 |
A |
G |
11: 58,488,396 (GRCm39) |
N58S |
probably damaging |
Het |
Or2ag1 |
T |
A |
7: 106,313,373 (GRCm39) |
R172W |
probably benign |
Het |
Or2d3c |
T |
G |
7: 106,526,162 (GRCm39) |
Y168S |
probably damaging |
Het |
Or5p63 |
T |
C |
7: 107,811,547 (GRCm39) |
Y63C |
probably damaging |
Het |
Or8g37 |
T |
C |
9: 39,731,846 (GRCm39) |
F304L |
probably benign |
Het |
Pcdh8 |
A |
T |
14: 80,005,651 (GRCm39) |
S912R |
probably damaging |
Het |
Pdzrn3 |
T |
C |
6: 101,127,660 (GRCm39) |
E1002G |
probably damaging |
Het |
Pik3c2a |
A |
T |
7: 115,972,126 (GRCm39) |
L768* |
probably null |
Het |
Plxna4 |
A |
G |
6: 32,494,551 (GRCm39) |
S22P |
possibly damaging |
Het |
Plxnb3 |
T |
A |
X: 72,815,357 (GRCm39) |
Y1845* |
probably null |
Het |
Pramel11 |
T |
C |
4: 143,623,482 (GRCm39) |
M231V |
probably damaging |
Het |
Prl7a2 |
T |
A |
13: 27,844,870 (GRCm39) |
Y172F |
probably damaging |
Het |
Pum1 |
A |
G |
4: 130,501,745 (GRCm39) |
T845A |
probably benign |
Het |
Rad21l |
T |
C |
2: 151,509,927 (GRCm39) |
H58R |
probably damaging |
Het |
Rgma |
A |
C |
7: 73,059,379 (GRCm39) |
D161A |
probably damaging |
Het |
Scai |
T |
C |
2: 39,013,025 (GRCm39) |
Y135C |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,582,417 (GRCm39) |
H1588Q |
probably benign |
Het |
Sdha |
A |
T |
13: 74,472,087 (GRCm39) |
|
probably null |
Het |
Slc12a3 |
A |
G |
8: 95,072,456 (GRCm39) |
D658G |
probably damaging |
Het |
Slc5a3 |
A |
G |
16: 91,874,128 (GRCm39) |
S62G |
probably damaging |
Het |
Spata13 |
GTTAGGCT |
GT |
14: 60,998,320 (GRCm39) |
|
probably benign |
Het |
Sulf1 |
A |
G |
1: 12,910,627 (GRCm39) |
I649V |
probably damaging |
Het |
Thbs1 |
C |
T |
2: 117,954,018 (GRCm39) |
Q1090* |
probably null |
Het |
Tjp2 |
C |
A |
19: 24,099,687 (GRCm39) |
R400L |
probably benign |
Het |
Tle4 |
A |
T |
19: 14,427,113 (GRCm39) |
Y769* |
probably null |
Het |
Trmt5 |
A |
T |
12: 73,331,444 (GRCm39) |
|
probably null |
Het |
Troap |
T |
C |
15: 98,980,344 (GRCm39) |
L508P |
probably benign |
Het |
Ubac2 |
T |
A |
14: 122,145,691 (GRCm39) |
Y116* |
probably null |
Het |
Ugt2b36 |
T |
C |
5: 87,240,100 (GRCm39) |
E95G |
probably benign |
Het |
Ush1c |
T |
C |
7: 45,878,905 (GRCm39) |
Y74C |
probably damaging |
Het |
Usp36 |
T |
C |
11: 118,165,844 (GRCm39) |
T160A |
possibly damaging |
Het |
Usp54 |
G |
T |
14: 20,627,273 (GRCm39) |
P462T |
probably damaging |
Het |
Vmn1r55 |
A |
G |
7: 5,150,048 (GRCm39) |
V125A |
possibly damaging |
Het |
Vps11 |
A |
G |
9: 44,269,613 (GRCm39) |
S213P |
probably damaging |
Het |
Zfp668 |
C |
T |
7: 127,465,837 (GRCm39) |
G449D |
probably benign |
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 |
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 |
|
|
|