Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap8l |
A |
G |
17: 32,551,900 (GRCm39) |
|
probably benign |
Het |
Alk |
T |
C |
17: 72,181,171 (GRCm39) |
Q1373R |
probably damaging |
Het |
Atf7ip2 |
T |
G |
16: 10,028,911 (GRCm39) |
S148A |
probably benign |
Het |
Bpi |
C |
T |
2: 158,116,734 (GRCm39) |
S377F |
probably damaging |
Het |
Ccni |
A |
T |
5: 93,336,034 (GRCm39) |
C122S |
possibly damaging |
Het |
Cd5l |
A |
G |
3: 87,273,300 (GRCm39) |
R90G |
probably benign |
Het |
Ceacam3 |
C |
T |
7: 16,897,026 (GRCm39) |
S664F |
probably damaging |
Het |
Clca3a2 |
A |
T |
3: 144,512,133 (GRCm39) |
D534E |
probably damaging |
Het |
Ep400 |
A |
T |
5: 110,822,826 (GRCm39) |
S2524R |
probably damaging |
Het |
Fhdc1 |
G |
A |
3: 84,352,042 (GRCm39) |
A1061V |
possibly damaging |
Het |
Gart |
A |
G |
16: 91,418,725 (GRCm39) |
|
probably benign |
Het |
Gsdmc4 |
A |
G |
15: 63,767,113 (GRCm39) |
V219A |
probably benign |
Het |
Hus1 |
T |
C |
11: 8,946,915 (GRCm39) |
T261A |
probably benign |
Het |
Lman2l |
A |
G |
1: 36,482,624 (GRCm39) |
I84T |
probably damaging |
Het |
Megf8 |
G |
A |
7: 25,037,325 (GRCm39) |
V742M |
probably damaging |
Het |
Myo1d |
A |
G |
11: 80,567,679 (GRCm39) |
V267A |
probably benign |
Het |
Notch2 |
A |
G |
3: 98,048,870 (GRCm39) |
T1803A |
probably benign |
Het |
Or1e17 |
T |
A |
11: 73,831,894 (GRCm39) |
M274K |
possibly damaging |
Het |
Or4f54 |
T |
A |
2: 111,123,042 (GRCm39) |
M143K |
probably benign |
Het |
Or6c70 |
A |
G |
10: 129,709,948 (GRCm39) |
F226S |
probably damaging |
Het |
Pate11 |
T |
C |
9: 36,388,483 (GRCm39) |
|
probably benign |
Het |
Pde5a |
G |
A |
3: 122,554,534 (GRCm39) |
R208Q |
probably damaging |
Het |
Pla2r1 |
T |
C |
2: 60,282,780 (GRCm39) |
N745S |
probably benign |
Het |
Ptgdr2 |
T |
A |
19: 10,917,573 (GRCm39) |
I30N |
possibly damaging |
Het |
Rap1gap2 |
G |
A |
11: 74,298,195 (GRCm39) |
T415I |
probably damaging |
Het |
Slc6a6 |
T |
C |
6: 91,703,037 (GRCm39) |
Y137H |
probably benign |
Het |
Stk39 |
T |
C |
2: 68,042,306 (GRCm39) |
D543G |
probably damaging |
Het |
Trpc4 |
G |
A |
3: 54,198,653 (GRCm39) |
V526M |
probably damaging |
Het |
Trrap |
A |
G |
5: 144,714,727 (GRCm39) |
I100V |
probably benign |
Het |
Vmn1r-ps123 |
A |
C |
13: 23,180,527 (GRCm39) |
|
noncoding transcript |
Het |
Vwa5b2 |
G |
A |
16: 20,423,540 (GRCm39) |
G1151D |
probably damaging |
Het |
Zfp358 |
T |
A |
8: 3,546,858 (GRCm39) |
I480N |
probably benign |
Het |
Zfp423 |
T |
C |
8: 88,508,202 (GRCm39) |
D714G |
probably damaging |
Het |
|
Other mutations in Sptbn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00227:Sptbn1
|
APN |
11 |
30,060,818 (GRCm39) |
nonsense |
probably null |
|
IGL01098:Sptbn1
|
APN |
11 |
30,109,385 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01843:Sptbn1
|
APN |
11 |
30,054,623 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02070:Sptbn1
|
APN |
11 |
30,095,979 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02075:Sptbn1
|
APN |
11 |
30,088,496 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02094:Sptbn1
|
APN |
11 |
30,050,659 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02102:Sptbn1
|
APN |
11 |
30,087,427 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02189:Sptbn1
|
APN |
11 |
30,067,871 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02256:Sptbn1
|
APN |
11 |
30,070,990 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02354:Sptbn1
|
APN |
11 |
30,060,783 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02361:Sptbn1
|
APN |
11 |
30,060,783 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02377:Sptbn1
|
APN |
11 |
30,069,491 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02504:Sptbn1
|
APN |
11 |
30,092,293 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02672:Sptbn1
|
APN |
11 |
30,087,239 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02733:Sptbn1
|
APN |
11 |
30,147,747 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02755:Sptbn1
|
APN |
11 |
30,092,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Sptbn1
|
UTSW |
11 |
30,073,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Sptbn1
|
UTSW |
11 |
30,073,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Sptbn1
|
UTSW |
11 |
30,064,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0139:Sptbn1
|
UTSW |
11 |
30,092,289 (GRCm39) |
missense |
probably benign |
0.00 |
R0370:Sptbn1
|
UTSW |
11 |
30,071,545 (GRCm39) |
missense |
probably benign |
|
R0389:Sptbn1
|
UTSW |
11 |
30,089,250 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0415:Sptbn1
|
UTSW |
11 |
30,099,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R0552:Sptbn1
|
UTSW |
11 |
30,095,985 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0601:Sptbn1
|
UTSW |
11 |
30,100,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Sptbn1
|
UTSW |
11 |
30,088,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Sptbn1
|
UTSW |
11 |
30,067,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R0708:Sptbn1
|
UTSW |
11 |
30,064,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0711:Sptbn1
|
UTSW |
11 |
30,064,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Sptbn1
|
UTSW |
11 |
30,060,902 (GRCm39) |
missense |
probably damaging |
0.96 |
R0755:Sptbn1
|
UTSW |
11 |
30,089,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R0892:Sptbn1
|
UTSW |
11 |
30,092,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R0927:Sptbn1
|
UTSW |
11 |
30,071,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R1102:Sptbn1
|
UTSW |
11 |
30,070,785 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1460:Sptbn1
|
UTSW |
11 |
30,088,637 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1479:Sptbn1
|
UTSW |
11 |
30,063,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Sptbn1
|
UTSW |
11 |
30,071,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R1649:Sptbn1
|
UTSW |
11 |
30,087,301 (GRCm39) |
missense |
probably damaging |
0.97 |
R1663:Sptbn1
|
UTSW |
11 |
30,070,783 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1671:Sptbn1
|
UTSW |
11 |
30,092,245 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1680:Sptbn1
|
UTSW |
11 |
30,109,371 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1695:Sptbn1
|
UTSW |
11 |
30,086,124 (GRCm39) |
missense |
probably benign |
0.13 |
R1868:Sptbn1
|
UTSW |
11 |
30,064,781 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1918:Sptbn1
|
UTSW |
11 |
30,092,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R1921:Sptbn1
|
UTSW |
11 |
30,054,469 (GRCm39) |
missense |
probably damaging |
0.98 |
R2026:Sptbn1
|
UTSW |
11 |
30,054,559 (GRCm39) |
missense |
probably benign |
0.02 |
R2038:Sptbn1
|
UTSW |
11 |
30,109,293 (GRCm39) |
critical splice donor site |
probably null |
|
R2047:Sptbn1
|
UTSW |
11 |
30,088,360 (GRCm39) |
splice site |
probably benign |
|
R2312:Sptbn1
|
UTSW |
11 |
30,104,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Sptbn1
|
UTSW |
11 |
30,169,686 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3624:Sptbn1
|
UTSW |
11 |
30,090,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R3723:Sptbn1
|
UTSW |
11 |
30,087,335 (GRCm39) |
missense |
possibly damaging |
0.59 |
R3862:Sptbn1
|
UTSW |
11 |
30,092,329 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4446:Sptbn1
|
UTSW |
11 |
30,089,114 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4582:Sptbn1
|
UTSW |
11 |
30,169,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R4705:Sptbn1
|
UTSW |
11 |
30,050,660 (GRCm39) |
missense |
probably benign |
|
R4707:Sptbn1
|
UTSW |
11 |
30,087,197 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4718:Sptbn1
|
UTSW |
11 |
30,104,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R4789:Sptbn1
|
UTSW |
11 |
30,067,759 (GRCm39) |
missense |
probably benign |
|
R4824:Sptbn1
|
UTSW |
11 |
30,068,295 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4855:Sptbn1
|
UTSW |
11 |
30,092,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R5009:Sptbn1
|
UTSW |
11 |
30,074,016 (GRCm39) |
missense |
probably benign |
0.05 |
R5071:Sptbn1
|
UTSW |
11 |
30,063,854 (GRCm39) |
critical splice donor site |
probably null |
|
R5153:Sptbn1
|
UTSW |
11 |
30,071,510 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5334:Sptbn1
|
UTSW |
11 |
30,087,364 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5462:Sptbn1
|
UTSW |
11 |
30,050,520 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5523:Sptbn1
|
UTSW |
11 |
30,087,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R5707:Sptbn1
|
UTSW |
11 |
30,093,174 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5724:Sptbn1
|
UTSW |
11 |
30,094,113 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5738:Sptbn1
|
UTSW |
11 |
30,095,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R5864:Sptbn1
|
UTSW |
11 |
30,095,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R5895:Sptbn1
|
UTSW |
11 |
30,073,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R5932:Sptbn1
|
UTSW |
11 |
30,086,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R5966:Sptbn1
|
UTSW |
11 |
30,074,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R5984:Sptbn1
|
UTSW |
11 |
30,068,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R6155:Sptbn1
|
UTSW |
11 |
30,087,403 (GRCm39) |
missense |
probably damaging |
0.99 |
R6163:Sptbn1
|
UTSW |
11 |
30,109,443 (GRCm39) |
nonsense |
probably null |
|
R6226:Sptbn1
|
UTSW |
11 |
30,086,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R6271:Sptbn1
|
UTSW |
11 |
30,050,660 (GRCm39) |
missense |
probably benign |
0.00 |
R6443:Sptbn1
|
UTSW |
11 |
30,089,429 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6591:Sptbn1
|
UTSW |
11 |
30,063,984 (GRCm39) |
missense |
probably damaging |
0.99 |
R6616:Sptbn1
|
UTSW |
11 |
30,074,030 (GRCm39) |
missense |
probably benign |
0.08 |
R6691:Sptbn1
|
UTSW |
11 |
30,063,984 (GRCm39) |
missense |
probably damaging |
0.99 |
R6751:Sptbn1
|
UTSW |
11 |
30,067,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R6823:Sptbn1
|
UTSW |
11 |
30,064,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R6863:Sptbn1
|
UTSW |
11 |
30,096,777 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6885:Sptbn1
|
UTSW |
11 |
30,088,634 (GRCm39) |
missense |
probably benign |
0.26 |
R6892:Sptbn1
|
UTSW |
11 |
30,092,187 (GRCm39) |
missense |
probably benign |
0.27 |
R6998:Sptbn1
|
UTSW |
11 |
30,050,633 (GRCm39) |
missense |
probably damaging |
0.97 |
R7043:Sptbn1
|
UTSW |
11 |
30,053,323 (GRCm39) |
missense |
probably benign |
0.02 |
R7092:Sptbn1
|
UTSW |
11 |
30,087,119 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7272:Sptbn1
|
UTSW |
11 |
30,064,859 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7301:Sptbn1
|
UTSW |
11 |
30,067,798 (GRCm39) |
nonsense |
probably null |
|
R7379:Sptbn1
|
UTSW |
11 |
30,089,292 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7774:Sptbn1
|
UTSW |
11 |
30,092,142 (GRCm39) |
missense |
probably damaging |
0.99 |
R7813:Sptbn1
|
UTSW |
11 |
30,088,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R7837:Sptbn1
|
UTSW |
11 |
30,088,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R7843:Sptbn1
|
UTSW |
11 |
30,104,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R7846:Sptbn1
|
UTSW |
11 |
30,092,153 (GRCm39) |
missense |
probably damaging |
0.98 |
R7877:Sptbn1
|
UTSW |
11 |
30,079,601 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7902:Sptbn1
|
UTSW |
11 |
30,086,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R8060:Sptbn1
|
UTSW |
11 |
30,051,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R8116:Sptbn1
|
UTSW |
11 |
30,089,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R8169:Sptbn1
|
UTSW |
11 |
30,147,783 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8208:Sptbn1
|
UTSW |
11 |
30,074,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Sptbn1
|
UTSW |
11 |
30,063,906 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8412:Sptbn1
|
UTSW |
11 |
30,088,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R8470:Sptbn1
|
UTSW |
11 |
30,070,758 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8544:Sptbn1
|
UTSW |
11 |
30,169,750 (GRCm39) |
start gained |
probably benign |
|
R8674:Sptbn1
|
UTSW |
11 |
30,089,352 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8846:Sptbn1
|
UTSW |
11 |
30,075,009 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8889:Sptbn1
|
UTSW |
11 |
30,067,800 (GRCm39) |
missense |
probably benign |
0.03 |
R8892:Sptbn1
|
UTSW |
11 |
30,067,800 (GRCm39) |
missense |
probably benign |
0.03 |
R8927:Sptbn1
|
UTSW |
11 |
30,088,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Sptbn1
|
UTSW |
11 |
30,088,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R8975:Sptbn1
|
UTSW |
11 |
30,073,869 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9115:Sptbn1
|
UTSW |
11 |
30,087,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R9127:Sptbn1
|
UTSW |
11 |
30,104,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R9193:Sptbn1
|
UTSW |
11 |
30,087,551 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9237:Sptbn1
|
UTSW |
11 |
30,096,803 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Sptbn1
|
UTSW |
11 |
30,147,787 (GRCm39) |
missense |
probably benign |
0.13 |
Z1176:Sptbn1
|
UTSW |
11 |
30,087,439 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sptbn1
|
UTSW |
11 |
30,070,659 (GRCm39) |
missense |
probably benign |
0.27 |
Z1177:Sptbn1
|
UTSW |
11 |
30,064,734 (GRCm39) |
missense |
probably damaging |
1.00 |
|