Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
T |
A |
11: 58,313,134 (GRCm39) |
|
probably null |
Het |
Acaa2 |
T |
C |
18: 74,926,476 (GRCm39) |
|
probably null |
Het |
Adam7 |
T |
C |
14: 68,748,792 (GRCm39) |
Q485R |
probably benign |
Het |
Adcy4 |
T |
G |
14: 56,006,627 (GRCm39) |
T1069P |
probably benign |
Het |
Arsj |
T |
C |
3: 126,232,337 (GRCm39) |
L361P |
probably damaging |
Het |
Birc2 |
A |
C |
9: 7,826,939 (GRCm39) |
L349R |
probably damaging |
Het |
C1qa |
T |
C |
4: 136,623,727 (GRCm39) |
Y159C |
probably damaging |
Het |
Cdh13 |
A |
G |
8: 119,963,703 (GRCm39) |
K428E |
probably damaging |
Het |
Cenpe |
T |
C |
3: 134,953,235 (GRCm39) |
M1563T |
probably benign |
Het |
Col10a1 |
T |
C |
10: 34,271,696 (GRCm39) |
V556A |
probably benign |
Het |
Creg2 |
G |
A |
1: 39,662,338 (GRCm39) |
L265F |
probably damaging |
Het |
Cyp1a2 |
T |
A |
9: 57,589,433 (GRCm39) |
D127V |
probably damaging |
Het |
Cyp3a44 |
A |
T |
5: 145,740,480 (GRCm39) |
Y53* |
probably null |
Het |
Cyth1 |
C |
T |
11: 118,073,634 (GRCm39) |
R233Q |
probably damaging |
Het |
Dnmbp |
G |
A |
19: 43,890,346 (GRCm39) |
H474Y |
possibly damaging |
Het |
Dvl1 |
G |
A |
4: 155,932,273 (GRCm39) |
V28I |
possibly damaging |
Het |
Ercc2 |
G |
A |
7: 19,120,717 (GRCm39) |
R206H |
possibly damaging |
Het |
Evx2 |
T |
A |
2: 74,486,360 (GRCm39) |
H343L |
probably damaging |
Het |
Fcrl2 |
T |
A |
3: 87,164,648 (GRCm39) |
I293F |
probably benign |
Het |
Gcnt4 |
A |
G |
13: 97,082,974 (GRCm39) |
E90G |
probably damaging |
Het |
Gid8 |
T |
G |
2: 180,358,751 (GRCm39) |
C139G |
probably benign |
Het |
Gm11938 |
C |
A |
11: 99,493,933 (GRCm39) |
C54F |
probably damaging |
Het |
Gm3336 |
G |
A |
8: 71,174,509 (GRCm39) |
V158I |
probably benign |
Het |
Gucy1b1 |
T |
C |
3: 81,968,327 (GRCm39) |
N60D |
probably benign |
Het |
Hdac7 |
T |
C |
15: 97,691,944 (GRCm39) |
K810E |
probably benign |
Het |
Hsp90ab1 |
A |
G |
17: 45,880,629 (GRCm39) |
F361L |
possibly damaging |
Het |
Igf2bp3 |
A |
T |
6: 49,085,858 (GRCm39) |
|
probably null |
Het |
Inpp4b |
T |
A |
8: 82,775,118 (GRCm39) |
I772N |
probably damaging |
Het |
Iqca1 |
A |
G |
1: 90,017,238 (GRCm39) |
L390P |
possibly damaging |
Het |
Itgb2 |
C |
T |
10: 77,396,082 (GRCm39) |
R586W |
probably benign |
Het |
Itih1 |
A |
G |
14: 30,655,432 (GRCm39) |
S588P |
possibly damaging |
Het |
Iyd |
T |
A |
10: 3,497,166 (GRCm39) |
|
probably null |
Het |
Kl |
A |
G |
5: 150,912,425 (GRCm39) |
K725E |
probably benign |
Het |
Layn |
T |
A |
9: 50,968,697 (GRCm39) |
M349L |
probably benign |
Het |
Map3k5 |
T |
C |
10: 19,900,683 (GRCm39) |
Y286H |
probably damaging |
Het |
Med4 |
C |
T |
14: 73,755,472 (GRCm39) |
|
probably benign |
Het |
Mfn1 |
T |
A |
3: 32,588,400 (GRCm39) |
N42K |
possibly damaging |
Het |
Mindy2 |
T |
C |
9: 70,563,874 (GRCm39) |
D152G |
probably benign |
Het |
Mrc2 |
A |
G |
11: 105,238,682 (GRCm39) |
|
probably null |
Het |
Mrpl11 |
C |
A |
19: 5,012,497 (GRCm39) |
A26E |
probably damaging |
Het |
Msh6 |
G |
A |
17: 88,293,568 (GRCm39) |
W774* |
probably null |
Het |
Mtch1 |
A |
T |
17: 29,561,841 (GRCm39) |
V121E |
probably damaging |
Het |
Mtg2 |
G |
T |
2: 179,725,923 (GRCm39) |
E178* |
probably null |
Het |
Ndfip2 |
A |
G |
14: 105,525,204 (GRCm39) |
T65A |
probably benign |
Het |
Ninl |
G |
T |
2: 150,786,503 (GRCm39) |
Q1146K |
probably damaging |
Het |
Notch1 |
T |
C |
2: 26,350,873 (GRCm39) |
D2089G |
possibly damaging |
Het |
Notch3 |
C |
T |
17: 32,366,818 (GRCm39) |
V906M |
probably damaging |
Het |
Or51l14 |
A |
G |
7: 103,101,371 (GRCm39) |
I276V |
probably benign |
Het |
Or6b6 |
A |
G |
7: 106,570,775 (GRCm39) |
Y259H |
probably damaging |
Het |
Osmr |
A |
T |
15: 6,873,891 (GRCm39) |
Y169N |
probably benign |
Het |
Ovgp1 |
T |
C |
3: 105,885,033 (GRCm39) |
V124A |
possibly damaging |
Het |
P2rx1 |
T |
C |
11: 72,904,939 (GRCm39) |
M369T |
probably benign |
Het |
Pde4dip |
T |
C |
3: 97,631,534 (GRCm39) |
Q1125R |
probably damaging |
Het |
Podn |
A |
T |
4: 107,878,892 (GRCm39) |
V180E |
probably damaging |
Het |
Pold1 |
A |
T |
7: 44,188,542 (GRCm39) |
V475E |
probably damaging |
Het |
Polg |
A |
G |
7: 79,111,468 (GRCm39) |
I261T |
possibly damaging |
Het |
Satb1 |
G |
T |
17: 52,047,438 (GRCm39) |
Q595K |
probably benign |
Het |
Scaf8 |
T |
A |
17: 3,214,407 (GRCm39) |
|
probably null |
Het |
Semp2l1 |
T |
A |
1: 32,585,128 (GRCm39) |
M261L |
probably benign |
Het |
Serpinb3a |
C |
T |
1: 106,975,202 (GRCm39) |
|
probably null |
Het |
Slc22a26 |
T |
C |
19: 7,779,480 (GRCm39) |
D112G |
probably damaging |
Het |
Slc25a23 |
A |
G |
17: 57,352,562 (GRCm39) |
F441L |
probably benign |
Het |
Slc25a53 |
T |
C |
X: 135,884,216 (GRCm39) |
T42A |
probably damaging |
Het |
Slc6a15 |
T |
C |
10: 103,229,269 (GRCm39) |
Y103H |
probably damaging |
Het |
Slx4 |
A |
G |
16: 3,804,223 (GRCm39) |
S864P |
probably benign |
Het |
Snap91 |
T |
C |
9: 86,707,130 (GRCm39) |
E220G |
probably damaging |
Het |
Spam1 |
T |
C |
6: 24,796,267 (GRCm39) |
F73L |
probably damaging |
Het |
Sphkap |
C |
T |
1: 83,255,710 (GRCm39) |
V393M |
probably benign |
Het |
Spred2 |
T |
C |
11: 19,971,241 (GRCm39) |
Y370H |
probably damaging |
Het |
Sqle |
T |
C |
15: 59,195,578 (GRCm39) |
|
probably null |
Het |
Srrm2 |
A |
G |
17: 24,037,237 (GRCm39) |
T1390A |
probably benign |
Het |
Tas1r2 |
A |
G |
4: 139,396,352 (GRCm39) |
R564G |
possibly damaging |
Het |
Tbl2 |
G |
T |
5: 135,185,374 (GRCm39) |
|
probably null |
Het |
Tcof1 |
T |
C |
18: 60,964,901 (GRCm39) |
D606G |
possibly damaging |
Het |
Tdpoz3 |
T |
A |
3: 93,734,087 (GRCm39) |
L254H |
probably damaging |
Het |
Trpm1 |
A |
T |
7: 63,884,736 (GRCm39) |
I806F |
probably damaging |
Het |
Ttc22 |
A |
G |
4: 106,496,237 (GRCm39) |
D429G |
probably benign |
Het |
Ube2o |
C |
A |
11: 116,471,972 (GRCm39) |
G90C |
probably damaging |
Het |
Usp34 |
T |
A |
11: 23,332,602 (GRCm39) |
F1110I |
probably damaging |
Het |
Vmn2r82 |
T |
C |
10: 79,214,722 (GRCm39) |
L235P |
probably damaging |
Het |
Vps35 |
A |
G |
8: 86,013,129 (GRCm39) |
V116A |
probably benign |
Het |
Wdfy3 |
A |
G |
5: 102,046,291 (GRCm39) |
|
probably null |
Het |
Zeb2 |
T |
C |
2: 44,878,821 (GRCm39) |
K1138E |
probably benign |
Het |
Zfp513 |
G |
A |
5: 31,357,866 (GRCm39) |
T169I |
probably benign |
Het |
Zfp629 |
T |
C |
7: 127,211,551 (GRCm39) |
D86G |
probably benign |
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 |
|
R2006:Nbas
|
UTSW |
12 |
13,464,742 (GRCm39) |
splice site |
probably null |
|
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 |
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 |
|