Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810055G02Rik |
A |
C |
19: 3,766,686 (GRCm39) |
N91T |
possibly damaging |
Het |
2510009E07Rik |
CCGGAAGGGGAGGAGCAGTGACCCAGTTTCGGA |
CCGGA |
16: 21,472,148 (GRCm39) |
|
probably null |
Het |
4932414N04Rik |
A |
G |
2: 68,562,498 (GRCm39) |
D375G |
possibly damaging |
Het |
Adad2 |
C |
A |
8: 120,339,725 (GRCm39) |
P69Q |
probably benign |
Het |
Adamts3 |
G |
A |
5: 89,825,575 (GRCm39) |
T1088I |
probably damaging |
Het |
Ank2 |
A |
G |
3: 126,726,720 (GRCm39) |
V858A |
probably benign |
Het |
Ankrd13a |
A |
G |
5: 114,939,798 (GRCm39) |
N475S |
probably benign |
Het |
Barhl2 |
G |
A |
5: 106,603,352 (GRCm39) |
T269I |
probably benign |
Het |
Boc |
G |
A |
16: 44,323,931 (GRCm39) |
R157W |
|
Het |
Catsperb |
C |
A |
12: 101,486,904 (GRCm39) |
A477E |
possibly damaging |
Het |
Ccser1 |
T |
A |
6: 61,787,842 (GRCm39) |
I220K |
probably benign |
Het |
Cd200r3 |
A |
T |
16: 44,778,102 (GRCm39) |
I242F |
possibly damaging |
Het |
Cdc34b |
A |
C |
11: 94,632,911 (GRCm39) |
D37A |
probably damaging |
Het |
Chek2 |
A |
G |
5: 111,013,458 (GRCm39) |
|
probably benign |
Het |
Cngb1 |
A |
T |
8: 95,989,736 (GRCm39) |
V792D |
probably damaging |
Het |
Cops7a |
T |
C |
6: 124,939,371 (GRCm39) |
K93E |
possibly damaging |
Het |
Crispld1 |
T |
C |
1: 17,820,995 (GRCm39) |
I345T |
possibly damaging |
Het |
Dgkd |
A |
G |
1: 87,869,157 (GRCm39) |
D1170G |
probably damaging |
Het |
Dhx35 |
A |
G |
2: 158,648,918 (GRCm39) |
T115A |
possibly damaging |
Het |
Dnai1 |
G |
A |
4: 41,625,125 (GRCm39) |
R363H |
probably benign |
Het |
Dnmbp |
T |
A |
19: 43,878,681 (GRCm39) |
Q130L |
probably benign |
Het |
Egfr |
A |
G |
11: 16,861,635 (GRCm39) |
Y1138C |
probably damaging |
Het |
Elf3 |
A |
T |
1: 135,182,678 (GRCm39) |
L329Q |
probably damaging |
Het |
Enkur |
A |
G |
2: 21,201,568 (GRCm39) |
M39T |
probably benign |
Het |
Epha7 |
T |
C |
4: 28,821,615 (GRCm39) |
I260T |
probably damaging |
Het |
Fbxo28 |
A |
T |
1: 182,144,634 (GRCm39) |
I310K |
probably damaging |
Het |
Fga |
C |
A |
3: 82,939,111 (GRCm39) |
N495K |
probably benign |
Het |
Galnt6 |
T |
C |
15: 100,601,247 (GRCm39) |
D344G |
probably damaging |
Het |
Gm572 |
A |
G |
4: 148,751,290 (GRCm39) |
Q221R |
probably benign |
Het |
Gpa33 |
G |
A |
1: 165,974,216 (GRCm39) |
A18T |
probably benign |
Het |
Gpatch11 |
C |
T |
17: 79,145,289 (GRCm39) |
T6I |
probably benign |
Het |
Gpr84 |
T |
A |
15: 103,217,625 (GRCm39) |
S151C |
probably damaging |
Het |
H2-M11 |
T |
A |
17: 36,859,851 (GRCm39) |
Y281* |
probably null |
Het |
Hadh |
T |
C |
3: 131,038,891 (GRCm39) |
N155S |
probably benign |
Het |
Hoxd13 |
A |
G |
2: 74,500,266 (GRCm39) |
Y269C |
|
Het |
Iars1 |
T |
A |
13: 49,882,177 (GRCm39) |
C1074S |
probably benign |
Het |
Ibtk |
G |
T |
9: 85,625,457 (GRCm39) |
H98N |
possibly damaging |
Het |
Igsf10 |
C |
T |
3: 59,233,739 (GRCm39) |
G1665R |
probably benign |
Het |
Inpp5d |
A |
G |
1: 87,625,337 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
C |
1: 135,321,951 (GRCm39) |
V593G |
probably damaging |
Het |
Irx3 |
T |
C |
8: 92,526,915 (GRCm39) |
D263G |
possibly damaging |
Het |
Kif13a |
A |
G |
13: 46,927,154 (GRCm39) |
V1179A |
probably benign |
Het |
Lrrc4c |
T |
C |
2: 97,460,393 (GRCm39) |
Y340H |
probably benign |
Het |
Lysmd1 |
A |
G |
3: 95,045,219 (GRCm39) |
D155G |
probably damaging |
Het |
Mical2 |
T |
A |
7: 111,980,671 (GRCm39) |
I105N |
probably damaging |
Het |
Mob2 |
A |
T |
7: 141,563,261 (GRCm39) |
L66Q |
probably damaging |
Het |
Myh1 |
A |
G |
11: 67,096,739 (GRCm39) |
S337G |
probably benign |
Het |
Neb |
T |
C |
2: 52,096,259 (GRCm39) |
D1002G |
probably benign |
Het |
Nebl |
A |
T |
2: 17,382,928 (GRCm39) |
N116K |
probably benign |
Het |
Nkx2-6 |
T |
C |
14: 69,412,623 (GRCm39) |
S264P |
probably benign |
Het |
Nlgn3 |
T |
C |
X: 100,352,390 (GRCm39) |
V179A |
probably damaging |
Het |
Nlrp4e |
A |
G |
7: 23,020,556 (GRCm39) |
T348A |
possibly damaging |
Het |
Nomo1 |
A |
T |
7: 45,722,004 (GRCm39) |
I982F |
probably benign |
Het |
Or10j5 |
A |
G |
1: 172,784,186 (GRCm39) |
|
probably benign |
Het |
Or11g24 |
T |
G |
14: 50,662,291 (GRCm39) |
F105C |
probably damaging |
Het |
Or1j19 |
A |
T |
2: 36,676,621 (GRCm39) |
Y28F |
probably benign |
Het |
Or8g22 |
A |
G |
9: 38,958,077 (GRCm39) |
F213L |
possibly damaging |
Het |
Palld |
A |
G |
8: 62,003,198 (GRCm39) |
|
probably null |
Het |
Pcdh7 |
A |
G |
5: 57,879,154 (GRCm39) |
Y903C |
probably damaging |
Het |
Pknox2 |
G |
A |
9: 36,804,167 (GRCm39) |
T460M |
possibly damaging |
Het |
Ppm1h |
C |
T |
10: 122,714,451 (GRCm39) |
T330I |
probably damaging |
Het |
Ppp2r2b |
C |
T |
18: 42,821,399 (GRCm39) |
R253H |
probably damaging |
Het |
Pramel58 |
G |
T |
5: 94,831,413 (GRCm39) |
R140L |
possibly damaging |
Het |
Prr18 |
G |
A |
17: 8,560,476 (GRCm39) |
A211T |
probably benign |
Het |
Ptgs2 |
A |
G |
1: 149,979,859 (GRCm39) |
I321M |
|
Het |
Rara |
G |
T |
11: 98,860,989 (GRCm39) |
R159L |
probably damaging |
Het |
Rasa4 |
T |
A |
5: 136,133,446 (GRCm39) |
I635N |
probably benign |
Het |
Rxfp2 |
A |
T |
5: 149,989,888 (GRCm39) |
H423L |
possibly damaging |
Het |
Scn4b |
A |
G |
9: 45,059,169 (GRCm39) |
I147V |
possibly damaging |
Het |
Scrn3 |
G |
A |
2: 73,161,352 (GRCm39) |
V313I |
probably benign |
Het |
Scrn3 |
C |
A |
2: 73,161,355 (GRCm39) |
P314T |
possibly damaging |
Het |
Sh2b1 |
A |
G |
7: 126,070,292 (GRCm39) |
|
probably null |
Het |
Slc26a10 |
T |
C |
10: 127,016,459 (GRCm39) |
Q3R |
probably benign |
Het |
Slitrk1 |
A |
G |
14: 109,149,139 (GRCm39) |
I524T |
probably damaging |
Het |
Smcp |
T |
A |
3: 92,491,530 (GRCm39) |
N106Y |
unknown |
Het |
Spata31h1 |
T |
C |
10: 82,122,379 (GRCm39) |
T3544A |
probably benign |
Het |
St8sia5 |
G |
A |
18: 77,336,172 (GRCm39) |
V202M |
probably damaging |
Het |
Stxbp5l |
A |
T |
16: 37,028,526 (GRCm39) |
D512E |
probably damaging |
Het |
Tas1r2 |
A |
G |
4: 139,397,046 (GRCm39) |
E795G |
probably damaging |
Het |
Tdrd1 |
T |
A |
19: 56,831,145 (GRCm39) |
V320D |
probably damaging |
Het |
Tmem71 |
T |
A |
15: 66,404,606 (GRCm39) |
I261L |
probably benign |
Het |
Tns2 |
T |
C |
15: 102,020,039 (GRCm39) |
L643P |
probably damaging |
Het |
Upf1 |
G |
A |
8: 70,786,815 (GRCm39) |
Q890* |
probably null |
Het |
Usp43 |
A |
T |
11: 67,782,307 (GRCm39) |
H370Q |
possibly damaging |
Het |
Vmn1r236 |
T |
A |
17: 21,507,356 (GRCm39) |
I158N |
possibly damaging |
Het |
Vmn2r98 |
T |
A |
17: 19,286,532 (GRCm39) |
N343K |
probably benign |
Het |
Vwa8 |
T |
C |
14: 79,329,815 (GRCm39) |
S1216P |
probably benign |
Het |
Yars1 |
A |
C |
4: 129,090,747 (GRCm39) |
D97A |
probably damaging |
Het |
Zer1 |
G |
A |
2: 30,001,035 (GRCm39) |
H129Y |
probably benign |
Het |
Zfat |
C |
T |
15: 67,956,404 (GRCm39) |
D1143N |
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 |
|
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 |
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 |
|
|
|