Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
T |
11: 110,204,275 (GRCm39) |
F333L |
probably benign |
Het |
Abcc2 |
T |
A |
19: 43,793,500 (GRCm39) |
F384Y |
probably damaging |
Het |
Acr |
C |
T |
15: 89,458,404 (GRCm39) |
P362S |
probably benign |
Het |
Acss3 |
T |
C |
10: 106,798,871 (GRCm39) |
D484G |
possibly damaging |
Het |
Actrt1 |
A |
G |
X: 45,418,593 (GRCm39) |
T203A |
probably benign |
Het |
Agtpbp1 |
A |
T |
13: 59,648,135 (GRCm39) |
C562S |
probably benign |
Het |
Ahnak |
A |
G |
19: 8,984,439 (GRCm39) |
K1908E |
probably damaging |
Het |
Amph |
G |
A |
13: 19,326,198 (GRCm39) |
V643M |
probably damaging |
Het |
Apaf1 |
A |
T |
10: 90,897,634 (GRCm39) |
I283N |
probably damaging |
Het |
Bbx |
G |
A |
16: 50,044,758 (GRCm39) |
T493M |
possibly damaging |
Het |
Best2 |
C |
T |
8: 85,739,818 (GRCm39) |
|
probably null |
Het |
C4bp |
C |
A |
1: 130,575,769 (GRCm39) |
E75* |
probably null |
Het |
Calr3 |
A |
T |
8: 73,188,695 (GRCm39) |
V144D |
probably damaging |
Het |
Capn1 |
C |
T |
19: 6,041,613 (GRCm39) |
G632D |
probably damaging |
Het |
Catsper2 |
C |
A |
2: 121,236,838 (GRCm39) |
E270* |
probably null |
Het |
Ccdc110 |
A |
T |
8: 46,396,349 (GRCm39) |
I747F |
probably damaging |
Het |
Ccdc15 |
T |
A |
9: 37,226,768 (GRCm39) |
D389V |
possibly damaging |
Het |
Cd226 |
A |
G |
18: 89,265,435 (GRCm39) |
I125V |
probably benign |
Het |
Crb2 |
A |
T |
2: 37,673,446 (GRCm39) |
D114V |
probably damaging |
Het |
Crebbp |
TTGCTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTG |
16: 3,902,617 (GRCm39) |
|
probably benign |
Het |
Crebrf |
T |
C |
17: 26,961,857 (GRCm39) |
V318A |
possibly damaging |
Het |
Dab1 |
T |
C |
4: 104,462,522 (GRCm39) |
I32T |
probably damaging |
Het |
Daw1 |
T |
C |
1: 83,169,066 (GRCm39) |
V181A |
probably damaging |
Het |
Dlg2 |
G |
A |
7: 91,614,825 (GRCm39) |
E255K |
possibly damaging |
Het |
Dnah10 |
T |
A |
5: 124,906,651 (GRCm39) |
D4170E |
possibly damaging |
Het |
Dnah12 |
A |
G |
14: 26,536,416 (GRCm39) |
T2111A |
possibly damaging |
Het |
Dock10 |
T |
C |
1: 80,527,506 (GRCm39) |
Y1081C |
possibly damaging |
Het |
Dscam |
T |
C |
16: 96,621,112 (GRCm39) |
Y532C |
probably damaging |
Het |
Fam83c |
T |
C |
2: 155,672,223 (GRCm39) |
D404G |
probably benign |
Het |
Fam83g |
A |
G |
11: 61,593,801 (GRCm39) |
N445S |
possibly damaging |
Het |
Ghr |
C |
T |
15: 3,357,464 (GRCm39) |
C268Y |
probably damaging |
Het |
Gm8444 |
T |
C |
15: 81,727,775 (GRCm39) |
|
probably benign |
Het |
Gp6 |
T |
A |
7: 4,387,988 (GRCm39) |
K160N |
probably benign |
Het |
Grm3 |
T |
C |
5: 9,639,793 (GRCm39) |
Y84C |
possibly damaging |
Het |
Gtf3c2 |
C |
A |
5: 31,325,440 (GRCm39) |
G450C |
probably damaging |
Het |
Icosl |
A |
T |
10: 77,907,787 (GRCm39) |
M116L |
possibly damaging |
Het |
Il31ra |
T |
G |
13: 112,666,890 (GRCm39) |
Y396S |
probably damaging |
Het |
Insig1 |
A |
G |
5: 28,276,464 (GRCm39) |
N10S |
probably benign |
Het |
Kcnh2 |
C |
A |
5: 24,531,568 (GRCm39) |
G448C |
probably damaging |
Het |
L1td1 |
C |
T |
4: 98,621,726 (GRCm39) |
S96L |
possibly damaging |
Het |
Mapre3 |
A |
T |
5: 31,019,168 (GRCm39) |
N4I |
probably damaging |
Het |
Mblac2 |
T |
A |
13: 81,859,860 (GRCm39) |
D70E |
probably benign |
Het |
Mki67 |
T |
A |
7: 135,300,238 (GRCm39) |
K1599* |
probably null |
Het |
Mpg |
A |
G |
11: 32,181,840 (GRCm39) |
I283V |
probably benign |
Het |
Mrtfb |
G |
T |
16: 13,199,440 (GRCm39) |
E98* |
probably null |
Het |
Mybpc1 |
C |
A |
10: 88,381,921 (GRCm39) |
A576S |
probably damaging |
Het |
Myo1h |
T |
G |
5: 114,499,140 (GRCm39) |
V129G |
probably damaging |
Het |
Nars1 |
A |
T |
18: 64,638,099 (GRCm39) |
V285E |
probably damaging |
Het |
Neb |
T |
C |
2: 52,089,456 (GRCm39) |
D5172G |
probably null |
Het |
Npbwr1 |
T |
A |
1: 5,986,570 (GRCm39) |
S315C |
probably damaging |
Het |
Nyap1 |
T |
C |
5: 137,733,953 (GRCm39) |
H360R |
possibly damaging |
Het |
Nyx |
A |
G |
X: 13,352,974 (GRCm39) |
E276G |
probably damaging |
Het |
Or10ag59 |
T |
A |
2: 87,405,536 (GRCm39) |
M36K |
probably benign |
Het |
Or1e1 |
G |
T |
11: 73,245,518 (GRCm39) |
C313F |
probably benign |
Het |
Or2l13b |
A |
G |
16: 19,349,455 (GRCm39) |
Y72H |
probably benign |
Het |
Or2w6 |
T |
C |
13: 21,842,642 (GRCm39) |
T284A |
possibly damaging |
Het |
Or4c1 |
A |
G |
2: 89,133,160 (GRCm39) |
Y259H |
possibly damaging |
Het |
Or4c118 |
A |
T |
2: 88,975,241 (GRCm39) |
V42E |
probably benign |
Het |
Or5v1b |
C |
T |
17: 37,841,597 (GRCm39) |
S243F |
probably damaging |
Het |
Or7e174 |
A |
T |
9: 20,012,165 (GRCm39) |
M37L |
probably benign |
Het |
Or7g16 |
G |
A |
9: 18,726,801 (GRCm39) |
S263L |
probably benign |
Het |
Or8g23 |
T |
A |
9: 38,971,729 (GRCm39) |
T78S |
probably damaging |
Het |
Paf1 |
C |
A |
7: 28,095,193 (GRCm39) |
|
probably null |
Het |
Pcsk5 |
T |
C |
19: 17,455,280 (GRCm39) |
D1050G |
probably benign |
Het |
Pgap1 |
A |
G |
1: 54,590,220 (GRCm39) |
S73P |
possibly damaging |
Het |
Phtf1 |
G |
A |
3: 103,911,799 (GRCm39) |
|
probably null |
Het |
Pik3c2b |
G |
T |
1: 132,994,282 (GRCm39) |
R82L |
probably damaging |
Het |
Pik3ca |
T |
C |
3: 32,504,206 (GRCm39) |
L632P |
probably damaging |
Het |
Plau |
G |
T |
14: 20,888,760 (GRCm39) |
|
probably null |
Het |
Pld4 |
A |
T |
12: 112,734,923 (GRCm39) |
Q460L |
possibly damaging |
Het |
Prdm2 |
T |
A |
4: 142,858,447 (GRCm39) |
Q1614H |
possibly damaging |
Het |
Ptprq |
C |
T |
10: 107,502,407 (GRCm39) |
G837D |
probably damaging |
Het |
Rad9b |
A |
G |
5: 122,477,842 (GRCm39) |
V178A |
possibly damaging |
Het |
Rfc1 |
G |
T |
5: 65,468,397 (GRCm39) |
Y105* |
probably null |
Het |
Sardh |
G |
A |
2: 27,118,351 (GRCm39) |
R460C |
probably damaging |
Het |
Scn5a |
C |
A |
9: 119,365,546 (GRCm39) |
R367L |
probably damaging |
Het |
Sdcbp |
A |
T |
4: 6,386,536 (GRCm39) |
I137L |
probably benign |
Het |
Shmt2 |
A |
G |
10: 127,355,029 (GRCm39) |
V273A |
probably benign |
Het |
Slc5a9 |
G |
T |
4: 111,737,423 (GRCm39) |
P612H |
probably benign |
Het |
Slitrk4 |
TTGT |
TT |
X: 63,314,294 (GRCm39) |
|
probably null |
Het |
Slitrk4 |
TG |
T |
X: 63,314,295 (GRCm39) |
|
probably null |
Het |
Spata1 |
A |
T |
3: 146,199,438 (GRCm39) |
S9T |
probably benign |
Het |
Syn3 |
T |
C |
10: 85,909,097 (GRCm39) |
T328A |
probably benign |
Het |
Tdrd6 |
A |
G |
17: 43,939,546 (GRCm39) |
F501L |
probably damaging |
Het |
Tekt5 |
T |
C |
16: 10,213,070 (GRCm39) |
I72V |
probably benign |
Het |
Ticrr |
T |
C |
7: 79,343,821 (GRCm39) |
S1229P |
possibly damaging |
Het |
Tlr6 |
T |
C |
5: 65,110,748 (GRCm39) |
S720G |
probably damaging |
Het |
Tmem156 |
T |
A |
5: 65,237,294 (GRCm39) |
D87V |
probably damaging |
Het |
Togaram1 |
T |
A |
12: 65,065,914 (GRCm39) |
D1639E |
probably damaging |
Het |
Ucn2 |
A |
G |
9: 108,815,430 (GRCm39) |
K64R |
probably benign |
Het |
Vmn2r57 |
T |
A |
7: 41,098,001 (GRCm39) |
Y22F |
probably benign |
Het |
Vwa1 |
T |
C |
4: 155,855,307 (GRCm39) |
T269A |
probably benign |
Het |
Washc5 |
A |
G |
15: 59,213,004 (GRCm39) |
L892P |
possibly damaging |
Het |
Wdr20 |
T |
C |
12: 110,760,002 (GRCm39) |
V296A |
probably damaging |
Het |
Xxylt1 |
A |
T |
16: 30,869,586 (GRCm39) |
H171Q |
probably damaging |
Het |
Yju2 |
C |
T |
17: 56,271,543 (GRCm39) |
Q155* |
probably null |
Het |
Zfp275 |
A |
G |
X: 72,396,841 (GRCm39) |
T118A |
possibly damaging |
Het |
|
Other mutations in Nbas |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00486:Nbas
|
APN |
12 |
13,503,076 (GRCm39) |
missense |
probably benign |
0.19 |
IGL00712:Nbas
|
APN |
12 |
13,412,626 (GRCm39) |
splice site |
probably benign |
|
IGL00808:Nbas
|
APN |
12 |
13,616,121 (GRCm39) |
splice site |
probably benign |
|
IGL00915:Nbas
|
APN |
12 |
13,424,753 (GRCm39) |
nonsense |
probably null |
|
IGL00923:Nbas
|
APN |
12 |
13,386,285 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01152:Nbas
|
APN |
12 |
13,410,959 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01633:Nbas
|
APN |
12 |
13,533,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01672:Nbas
|
APN |
12 |
13,429,650 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01799:Nbas
|
APN |
12 |
13,374,401 (GRCm39) |
splice site |
probably benign |
|
IGL01812:Nbas
|
APN |
12 |
13,503,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01934:Nbas
|
APN |
12 |
13,339,880 (GRCm39) |
splice site |
probably benign |
|
IGL02093:Nbas
|
APN |
12 |
13,610,963 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02115:Nbas
|
APN |
12 |
13,367,693 (GRCm39) |
splice site |
probably benign |
|
IGL02175:Nbas
|
APN |
12 |
13,616,260 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02268:Nbas
|
APN |
12 |
13,455,398 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02483:Nbas
|
APN |
12 |
13,374,295 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02539:Nbas
|
APN |
12 |
13,322,704 (GRCm39) |
splice site |
probably benign |
|
IGL02557:Nbas
|
APN |
12 |
13,411,029 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02815:Nbas
|
APN |
12 |
13,360,267 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Nbas
|
APN |
12 |
13,412,542 (GRCm39) |
missense |
probably benign |
|
IGL03131:Nbas
|
APN |
12 |
13,329,417 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03214:Nbas
|
APN |
12 |
13,381,111 (GRCm39) |
splice site |
probably benign |
|
IGL03308:Nbas
|
APN |
12 |
13,374,349 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03368:Nbas
|
APN |
12 |
13,378,452 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03372:Nbas
|
APN |
12 |
13,584,473 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03391:Nbas
|
APN |
12 |
13,533,750 (GRCm39) |
missense |
probably benign |
0.28 |
medvedev
|
UTSW |
12 |
13,584,578 (GRCm39) |
critical splice donor site |
probably null |
|
oligarchs
|
UTSW |
12 |
13,570,751 (GRCm39) |
missense |
possibly damaging |
0.75 |
putin
|
UTSW |
12 |
13,371,756 (GRCm39) |
missense |
probably damaging |
1.00 |
1mM(1):Nbas
|
UTSW |
12 |
13,338,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R0057:Nbas
|
UTSW |
12 |
13,440,958 (GRCm39) |
missense |
probably benign |
0.00 |
R0076:Nbas
|
UTSW |
12 |
13,374,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R0153:Nbas
|
UTSW |
12 |
13,323,877 (GRCm39) |
splice site |
probably benign |
|
R0371:Nbas
|
UTSW |
12 |
13,381,096 (GRCm39) |
missense |
probably damaging |
0.97 |
R0449:Nbas
|
UTSW |
12 |
13,569,109 (GRCm39) |
missense |
probably benign |
0.18 |
R0791:Nbas
|
UTSW |
12 |
13,532,634 (GRCm39) |
missense |
probably benign |
0.28 |
R0931:Nbas
|
UTSW |
12 |
13,381,115 (GRCm39) |
splice site |
probably benign |
|
R1236:Nbas
|
UTSW |
12 |
13,319,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R1371:Nbas
|
UTSW |
12 |
13,532,379 (GRCm39) |
splice site |
probably benign |
|
R1567:Nbas
|
UTSW |
12 |
13,335,279 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1587:Nbas
|
UTSW |
12 |
13,608,686 (GRCm39) |
missense |
probably benign |
|
R1719:Nbas
|
UTSW |
12 |
13,610,978 (GRCm39) |
critical splice donor site |
probably null |
|
R1747:Nbas
|
UTSW |
12 |
13,385,899 (GRCm39) |
missense |
probably benign |
0.00 |
R1777:Nbas
|
UTSW |
12 |
13,563,563 (GRCm39) |
missense |
probably benign |
0.16 |
R1848:Nbas
|
UTSW |
12 |
13,463,598 (GRCm39) |
missense |
probably damaging |
0.97 |
R1856:Nbas
|
UTSW |
12 |
13,524,230 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1891:Nbas
|
UTSW |
12 |
13,440,973 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1911:Nbas
|
UTSW |
12 |
13,616,145 (GRCm39) |
missense |
probably benign |
|
R1912:Nbas
|
UTSW |
12 |
13,616,145 (GRCm39) |
missense |
probably benign |
|
R2054:Nbas
|
UTSW |
12 |
13,524,207 (GRCm39) |
missense |
probably benign |
0.36 |
R2065:Nbas
|
UTSW |
12 |
13,616,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R2089:Nbas
|
UTSW |
12 |
13,411,046 (GRCm39) |
missense |
probably benign |
0.03 |
R2091:Nbas
|
UTSW |
12 |
13,411,046 (GRCm39) |
missense |
probably benign |
0.03 |
R2091:Nbas
|
UTSW |
12 |
13,411,046 (GRCm39) |
missense |
probably benign |
0.03 |
R2156:Nbas
|
UTSW |
12 |
13,491,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R2164:Nbas
|
UTSW |
12 |
13,380,647 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2339:Nbas
|
UTSW |
12 |
13,412,593 (GRCm39) |
missense |
probably benign |
0.12 |
R2398:Nbas
|
UTSW |
12 |
13,482,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R3806:Nbas
|
UTSW |
12 |
13,532,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R3855:Nbas
|
UTSW |
12 |
13,329,415 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4019:Nbas
|
UTSW |
12 |
13,532,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4083:Nbas
|
UTSW |
12 |
13,524,192 (GRCm39) |
missense |
probably damaging |
0.96 |
R4201:Nbas
|
UTSW |
12 |
13,424,827 (GRCm39) |
missense |
probably benign |
0.00 |
R4231:Nbas
|
UTSW |
12 |
13,443,344 (GRCm39) |
missense |
probably damaging |
0.98 |
R4552:Nbas
|
UTSW |
12 |
13,385,938 (GRCm39) |
critical splice donor site |
probably null |
|
R4560:Nbas
|
UTSW |
12 |
13,633,528 (GRCm39) |
missense |
probably benign |
0.00 |
R4728:Nbas
|
UTSW |
12 |
13,338,740 (GRCm39) |
missense |
probably damaging |
0.98 |
R4752:Nbas
|
UTSW |
12 |
13,532,538 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4832:Nbas
|
UTSW |
12 |
13,533,740 (GRCm39) |
missense |
probably benign |
0.00 |
R4874:Nbas
|
UTSW |
12 |
13,371,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R4988:Nbas
|
UTSW |
12 |
13,458,266 (GRCm39) |
missense |
probably benign |
0.45 |
R5020:Nbas
|
UTSW |
12 |
13,424,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R5079:Nbas
|
UTSW |
12 |
13,424,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R5129:Nbas
|
UTSW |
12 |
13,440,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R5239:Nbas
|
UTSW |
12 |
13,491,519 (GRCm39) |
missense |
probably benign |
0.31 |
R5299:Nbas
|
UTSW |
12 |
13,491,926 (GRCm39) |
nonsense |
probably null |
|
R5351:Nbas
|
UTSW |
12 |
13,610,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R5389:Nbas
|
UTSW |
12 |
13,584,578 (GRCm39) |
critical splice donor site |
probably null |
|
R5436:Nbas
|
UTSW |
12 |
13,424,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R5654:Nbas
|
UTSW |
12 |
13,633,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R5690:Nbas
|
UTSW |
12 |
13,386,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R5842:Nbas
|
UTSW |
12 |
13,319,267 (GRCm39) |
critical splice donor site |
probably null |
|
R5959:Nbas
|
UTSW |
12 |
13,338,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R5982:Nbas
|
UTSW |
12 |
13,443,431 (GRCm39) |
missense |
probably benign |
0.00 |
R6238:Nbas
|
UTSW |
12 |
13,532,596 (GRCm39) |
missense |
probably benign |
|
R6270:Nbas
|
UTSW |
12 |
13,374,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R6363:Nbas
|
UTSW |
12 |
13,532,577 (GRCm39) |
missense |
probably benign |
|
R6424:Nbas
|
UTSW |
12 |
13,465,734 (GRCm39) |
critical splice donor site |
probably null |
|
R6458:Nbas
|
UTSW |
12 |
13,338,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R6526:Nbas
|
UTSW |
12 |
13,455,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6654:Nbas
|
UTSW |
12 |
13,533,875 (GRCm39) |
nonsense |
probably null |
|
R7085:Nbas
|
UTSW |
12 |
13,335,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R7179:Nbas
|
UTSW |
12 |
13,455,398 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7197:Nbas
|
UTSW |
12 |
13,570,751 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7378:Nbas
|
UTSW |
12 |
13,324,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R7393:Nbas
|
UTSW |
12 |
13,443,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R7425:Nbas
|
UTSW |
12 |
13,519,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R7446:Nbas
|
UTSW |
12 |
13,443,499 (GRCm39) |
missense |
probably benign |
0.02 |
R7481:Nbas
|
UTSW |
12 |
13,406,960 (GRCm39) |
missense |
probably damaging |
0.97 |
R7535:Nbas
|
UTSW |
12 |
13,329,390 (GRCm39) |
missense |
probably damaging |
0.97 |
R7626:Nbas
|
UTSW |
12 |
13,608,661 (GRCm39) |
missense |
probably benign |
0.00 |
R7678:Nbas
|
UTSW |
12 |
13,465,662 (GRCm39) |
missense |
probably damaging |
0.97 |
R7912:Nbas
|
UTSW |
12 |
13,455,458 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7964:Nbas
|
UTSW |
12 |
13,406,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R8193:Nbas
|
UTSW |
12 |
13,483,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R8325:Nbas
|
UTSW |
12 |
13,338,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R8405:Nbas
|
UTSW |
12 |
13,329,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R8437:Nbas
|
UTSW |
12 |
13,616,251 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8559:Nbas
|
UTSW |
12 |
13,402,809 (GRCm39) |
missense |
probably benign |
0.00 |
R8684:Nbas
|
UTSW |
12 |
13,386,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R8826:Nbas
|
UTSW |
12 |
13,402,875 (GRCm39) |
splice site |
probably benign |
|
R8921:Nbas
|
UTSW |
12 |
13,463,590 (GRCm39) |
missense |
probably benign |
|
R8956:Nbas
|
UTSW |
12 |
13,482,923 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9083:Nbas
|
UTSW |
12 |
13,385,856 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9172:Nbas
|
UTSW |
12 |
13,424,751 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9430:Nbas
|
UTSW |
12 |
13,371,654 (GRCm39) |
missense |
probably benign |
0.35 |
R9627:Nbas
|
UTSW |
12 |
13,350,203 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9649:Nbas
|
UTSW |
12 |
13,633,417 (GRCm39) |
missense |
probably damaging |
1.00 |
RF013:Nbas
|
UTSW |
12 |
13,329,409 (GRCm39) |
missense |
possibly damaging |
0.54 |
T0722:Nbas
|
UTSW |
12 |
13,402,809 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Nbas
|
UTSW |
12 |
13,533,877 (GRCm39) |
missense |
probably benign |
0.06 |
|