Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810064F22Rik |
T |
A |
9: 22,119,333 (GRCm39) |
|
noncoding transcript |
Het |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Abl1 |
T |
C |
2: 31,669,022 (GRCm39) |
Y110H |
probably damaging |
Het |
Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
Agbl3 |
G |
A |
6: 34,762,219 (GRCm39) |
R73Q |
probably damaging |
Het |
Agl |
C |
T |
3: 116,572,267 (GRCm39) |
|
probably null |
Het |
Amotl1 |
G |
A |
9: 14,504,747 (GRCm39) |
Q191* |
probably null |
Het |
Apbb1ip |
A |
G |
2: 22,743,214 (GRCm39) |
K349E |
possibly damaging |
Het |
Arhgap10 |
G |
A |
8: 78,146,718 (GRCm39) |
Q229* |
probably null |
Het |
Aspm |
C |
T |
1: 139,405,810 (GRCm39) |
Q1566* |
probably null |
Het |
B3gnt3 |
G |
A |
8: 72,145,517 (GRCm39) |
R284C |
probably damaging |
Het |
Bltp3b |
T |
G |
10: 89,630,346 (GRCm39) |
V382G |
probably damaging |
Het |
Brd4 |
A |
G |
17: 32,439,211 (GRCm39) |
V423A |
probably damaging |
Het |
Btbd9 |
A |
T |
17: 30,743,839 (GRCm39) |
I221N |
probably damaging |
Het |
Camp |
A |
G |
9: 109,676,519 (GRCm39) |
V168A |
probably benign |
Het |
Cd1d2 |
T |
A |
3: 86,896,556 (GRCm39) |
|
probably null |
Het |
Cdkn2d |
A |
T |
9: 21,202,223 (GRCm39) |
V8D |
probably benign |
Het |
Cimap1a |
A |
G |
7: 140,429,375 (GRCm39) |
Y168C |
probably damaging |
Het |
Clec4g |
T |
C |
8: 3,766,534 (GRCm39) |
N256D |
probably damaging |
Het |
Clspn |
A |
G |
4: 126,469,743 (GRCm39) |
I771V |
probably benign |
Het |
Cntn6 |
A |
G |
6: 104,836,436 (GRCm39) |
E862G |
possibly damaging |
Het |
Col6a5 |
T |
C |
9: 105,775,950 (GRCm39) |
T1702A |
probably benign |
Het |
Dnah7a |
T |
C |
1: 53,745,888 (GRCm39) |
|
probably benign |
Het |
Dubr |
T |
C |
16: 50,552,886 (GRCm39) |
|
noncoding transcript |
Het |
Dusp26 |
G |
A |
8: 31,584,165 (GRCm39) |
V91M |
probably damaging |
Het |
Edc4 |
A |
T |
8: 106,614,557 (GRCm39) |
|
probably benign |
Het |
F5 |
C |
T |
1: 164,019,715 (GRCm39) |
A730V |
probably damaging |
Het |
Foxf1 |
A |
G |
8: 121,813,553 (GRCm39) |
T358A |
probably benign |
Het |
Frem1 |
A |
T |
4: 82,834,995 (GRCm39) |
N1810K |
possibly damaging |
Het |
Galc |
A |
T |
12: 98,223,136 (GRCm39) |
F87I |
probably damaging |
Het |
Gars1 |
A |
G |
6: 55,023,403 (GRCm39) |
D66G |
probably damaging |
Het |
Gbp11 |
G |
A |
5: 105,473,374 (GRCm39) |
L460F |
probably damaging |
Het |
Gdf7 |
T |
C |
12: 8,348,014 (GRCm39) |
I436V |
probably damaging |
Het |
Gigyf2 |
C |
T |
1: 87,282,135 (GRCm39) |
|
probably benign |
Het |
Gm12239 |
T |
C |
11: 55,906,779 (GRCm39) |
|
noncoding transcript |
Het |
Gm5592 |
A |
C |
7: 40,866,895 (GRCm39) |
|
probably benign |
Het |
Gp2 |
A |
T |
7: 119,051,422 (GRCm39) |
D264E |
possibly damaging |
Het |
Gphn |
G |
A |
12: 78,673,984 (GRCm39) |
V526M |
probably damaging |
Het |
Grid1 |
A |
G |
14: 35,043,598 (GRCm39) |
I318V |
probably benign |
Het |
Grm2 |
C |
A |
9: 106,531,331 (GRCm39) |
V53F |
possibly damaging |
Het |
Gtpbp1 |
T |
C |
15: 79,603,406 (GRCm39) |
S632P |
probably benign |
Het |
H2-M1 |
A |
G |
17: 36,980,950 (GRCm39) |
F329L |
probably benign |
Het |
Hecw1 |
T |
A |
13: 14,491,477 (GRCm39) |
D92V |
probably benign |
Het |
Hgh1 |
T |
C |
15: 76,253,382 (GRCm39) |
L76P |
probably damaging |
Het |
Idi2 |
C |
A |
13: 9,007,879 (GRCm39) |
N63K |
probably benign |
Het |
Ift122 |
A |
G |
6: 115,839,707 (GRCm39) |
T25A |
possibly damaging |
Het |
Itgb2l |
A |
T |
16: 96,227,317 (GRCm39) |
C575* |
probably null |
Het |
Jup |
A |
G |
11: 100,273,867 (GRCm39) |
S225P |
possibly damaging |
Het |
Kcng3 |
A |
T |
17: 83,895,735 (GRCm39) |
C244S |
probably damaging |
Het |
Klhl2 |
T |
A |
8: 65,287,111 (GRCm39) |
M46L |
possibly damaging |
Het |
Ksr1 |
A |
T |
11: 78,918,528 (GRCm39) |
I460N |
probably damaging |
Het |
Lama3 |
T |
A |
18: 12,544,599 (GRCm39) |
F314Y |
probably benign |
Het |
Lbp |
T |
C |
2: 158,169,438 (GRCm39) |
V421A |
possibly damaging |
Het |
Lcp1 |
G |
A |
14: 75,437,929 (GRCm39) |
G113D |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,001,089 (GRCm39) |
L2045H |
probably damaging |
Het |
Mbd2 |
G |
T |
18: 70,701,806 (GRCm39) |
D107Y |
unknown |
Het |
Ms4a14 |
C |
T |
19: 11,287,733 (GRCm39) |
V96I |
possibly damaging |
Het |
N4bp2l2 |
C |
T |
5: 150,585,516 (GRCm39) |
E155K |
probably benign |
Het |
Nbeal2 |
T |
G |
9: 110,460,464 (GRCm39) |
H1790P |
probably damaging |
Het |
Nsg2 |
G |
A |
11: 31,981,806 (GRCm39) |
G84R |
probably benign |
Het |
Or10ad1b |
A |
C |
15: 98,125,425 (GRCm39) |
F34V |
possibly damaging |
Het |
Or12e10 |
A |
G |
2: 87,640,934 (GRCm39) |
T257A |
probably damaging |
Het |
P2rx2 |
T |
C |
5: 110,488,793 (GRCm39) |
N224D |
probably damaging |
Het |
P2rx5 |
A |
T |
11: 73,062,605 (GRCm39) |
E438V |
probably benign |
Het |
Paip1 |
C |
A |
13: 119,586,425 (GRCm39) |
|
probably benign |
Het |
Pik3c2g |
T |
A |
6: 139,714,505 (GRCm39) |
V219E |
probably damaging |
Het |
Ppp1r12b |
T |
C |
1: 134,801,689 (GRCm39) |
E509G |
probably damaging |
Het |
Ppp1r15a |
T |
C |
7: 45,174,797 (GRCm39) |
S4G |
probably benign |
Het |
Ppp5c |
T |
C |
7: 16,742,947 (GRCm39) |
S224G |
probably benign |
Het |
Prr30 |
T |
G |
14: 101,435,879 (GRCm39) |
I228L |
probably benign |
Het |
Purg |
A |
G |
8: 33,877,342 (GRCm39) |
I327V |
possibly damaging |
Het |
Ralb |
T |
C |
1: 119,403,645 (GRCm39) |
T161A |
probably benign |
Het |
Ripor3 |
T |
C |
2: 167,834,733 (GRCm39) |
R253G |
probably benign |
Het |
Scgb2b6 |
T |
C |
7: 31,317,257 (GRCm39) |
|
noncoding transcript |
Het |
Setd5 |
G |
T |
6: 113,128,360 (GRCm39) |
G1438W |
probably damaging |
Het |
Sh3rf3 |
T |
A |
10: 58,649,545 (GRCm39) |
L50Q |
possibly damaging |
Het |
Sipa1l2 |
G |
T |
8: 126,200,340 (GRCm39) |
T662K |
probably damaging |
Het |
Slc22a23 |
T |
C |
13: 34,387,924 (GRCm39) |
S391G |
probably benign |
Het |
Slc4a5 |
G |
A |
6: 83,247,999 (GRCm39) |
V402I |
probably benign |
Het |
Slco4c1 |
G |
A |
1: 96,768,953 (GRCm39) |
P303L |
probably damaging |
Het |
Spink5 |
A |
T |
18: 44,153,908 (GRCm39) |
*1018C |
probably null |
Het |
Stag3 |
T |
A |
5: 138,294,956 (GRCm39) |
|
probably null |
Het |
Tmem117 |
T |
C |
15: 94,992,569 (GRCm39) |
F410L |
probably damaging |
Het |
Tmod1 |
A |
G |
4: 46,090,920 (GRCm39) |
K158E |
possibly damaging |
Het |
Tpsb2 |
GGCTGCTGCTGCTGCTG |
GGCTGCTGCTGCTG |
17: 25,585,536 (GRCm39) |
|
probably benign |
Het |
Traf4 |
G |
A |
11: 78,052,346 (GRCm39) |
Q100* |
probably null |
Het |
Trpc4 |
A |
G |
3: 54,209,639 (GRCm39) |
Y668C |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,597,927 (GRCm39) |
N11335I |
possibly damaging |
Het |
Usp39 |
A |
T |
6: 72,302,665 (GRCm39) |
V463E |
probably benign |
Het |
Vmn1r6 |
A |
C |
6: 56,979,683 (GRCm39) |
Y115S |
probably benign |
Het |
Vmn2r44 |
A |
G |
7: 8,383,300 (GRCm39) |
I98T |
possibly damaging |
Het |
Zfp462 |
A |
G |
4: 55,010,668 (GRCm39) |
Y878C |
probably damaging |
Het |
Zfp474 |
T |
C |
18: 52,771,503 (GRCm39) |
I52T |
possibly damaging |
Het |
|
Other mutations in Skint5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Skint5
|
APN |
4 |
113,400,070 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01288:Skint5
|
APN |
4 |
113,381,332 (GRCm39) |
intron |
probably benign |
|
IGL01313:Skint5
|
APN |
4 |
113,662,361 (GRCm39) |
missense |
unknown |
|
IGL01446:Skint5
|
APN |
4 |
113,800,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01861:Skint5
|
APN |
4 |
113,417,021 (GRCm39) |
splice site |
probably benign |
|
IGL01955:Skint5
|
APN |
4 |
113,480,933 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02150:Skint5
|
APN |
4 |
113,742,988 (GRCm39) |
missense |
unknown |
|
IGL02190:Skint5
|
APN |
4 |
113,797,962 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02271:Skint5
|
APN |
4 |
113,794,778 (GRCm39) |
splice site |
probably null |
|
IGL02426:Skint5
|
APN |
4 |
113,797,981 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02484:Skint5
|
APN |
4 |
113,799,750 (GRCm39) |
nonsense |
probably null |
|
IGL02548:Skint5
|
APN |
4 |
113,588,273 (GRCm39) |
missense |
unknown |
|
IGL02556:Skint5
|
APN |
4 |
113,797,932 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02674:Skint5
|
APN |
4 |
113,487,582 (GRCm39) |
splice site |
probably benign |
|
IGL02697:Skint5
|
APN |
4 |
113,336,910 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02710:Skint5
|
APN |
4 |
113,335,156 (GRCm39) |
missense |
unknown |
|
IGL02721:Skint5
|
APN |
4 |
113,799,746 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02750:Skint5
|
APN |
4 |
113,396,559 (GRCm39) |
missense |
unknown |
|
IGL03121:Skint5
|
APN |
4 |
113,574,284 (GRCm39) |
missense |
unknown |
|
IGL03167:Skint5
|
APN |
4 |
113,751,047 (GRCm39) |
missense |
unknown |
|
IGL03247:Skint5
|
APN |
4 |
113,798,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03264:Skint5
|
APN |
4 |
113,343,854 (GRCm39) |
missense |
unknown |
|
IGL03281:Skint5
|
APN |
4 |
113,524,415 (GRCm39) |
missense |
unknown |
|
IGL03353:Skint5
|
APN |
4 |
113,599,379 (GRCm39) |
missense |
unknown |
|
IGL03377:Skint5
|
APN |
4 |
113,620,735 (GRCm39) |
missense |
unknown |
|
PIT4377001:Skint5
|
UTSW |
4 |
113,454,900 (GRCm39) |
missense |
unknown |
|
R0006:Skint5
|
UTSW |
4 |
113,751,059 (GRCm39) |
splice site |
probably benign |
|
R0026:Skint5
|
UTSW |
4 |
113,403,665 (GRCm39) |
splice site |
probably benign |
|
R0096:Skint5
|
UTSW |
4 |
113,454,965 (GRCm39) |
splice site |
probably benign |
|
R0096:Skint5
|
UTSW |
4 |
113,454,965 (GRCm39) |
splice site |
probably benign |
|
R0277:Skint5
|
UTSW |
4 |
113,794,818 (GRCm39) |
missense |
probably benign |
0.04 |
R0323:Skint5
|
UTSW |
4 |
113,794,818 (GRCm39) |
missense |
probably benign |
0.04 |
R0369:Skint5
|
UTSW |
4 |
113,369,220 (GRCm39) |
critical splice donor site |
probably null |
|
R0375:Skint5
|
UTSW |
4 |
113,562,793 (GRCm39) |
missense |
unknown |
|
R0464:Skint5
|
UTSW |
4 |
113,392,928 (GRCm39) |
missense |
unknown |
|
R0479:Skint5
|
UTSW |
4 |
113,512,869 (GRCm39) |
missense |
unknown |
|
R0507:Skint5
|
UTSW |
4 |
113,425,127 (GRCm39) |
splice site |
probably null |
|
R0533:Skint5
|
UTSW |
4 |
113,685,064 (GRCm39) |
missense |
unknown |
|
R0628:Skint5
|
UTSW |
4 |
113,588,266 (GRCm39) |
nonsense |
probably null |
|
R0645:Skint5
|
UTSW |
4 |
113,620,679 (GRCm39) |
missense |
unknown |
|
R1201:Skint5
|
UTSW |
4 |
113,413,342 (GRCm39) |
missense |
unknown |
|
R1240:Skint5
|
UTSW |
4 |
113,574,304 (GRCm39) |
missense |
unknown |
|
R1270:Skint5
|
UTSW |
4 |
113,799,856 (GRCm39) |
nonsense |
probably null |
|
R1390:Skint5
|
UTSW |
4 |
113,512,881 (GRCm39) |
missense |
unknown |
|
R1398:Skint5
|
UTSW |
4 |
113,636,268 (GRCm39) |
missense |
unknown |
|
R1438:Skint5
|
UTSW |
4 |
113,413,308 (GRCm39) |
splice site |
probably benign |
|
R1591:Skint5
|
UTSW |
4 |
113,856,651 (GRCm39) |
critical splice donor site |
probably null |
|
R1631:Skint5
|
UTSW |
4 |
113,341,123 (GRCm39) |
missense |
probably benign |
0.23 |
R1653:Skint5
|
UTSW |
4 |
113,347,875 (GRCm39) |
missense |
unknown |
|
R1722:Skint5
|
UTSW |
4 |
113,703,508 (GRCm39) |
splice site |
probably null |
|
R1735:Skint5
|
UTSW |
4 |
113,420,656 (GRCm39) |
missense |
unknown |
|
R1765:Skint5
|
UTSW |
4 |
113,434,858 (GRCm39) |
missense |
unknown |
|
R2054:Skint5
|
UTSW |
4 |
113,676,360 (GRCm39) |
critical splice donor site |
probably null |
|
R2058:Skint5
|
UTSW |
4 |
113,727,897 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2197:Skint5
|
UTSW |
4 |
113,798,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R2239:Skint5
|
UTSW |
4 |
113,403,733 (GRCm39) |
missense |
unknown |
|
R2380:Skint5
|
UTSW |
4 |
113,403,733 (GRCm39) |
missense |
unknown |
|
R2406:Skint5
|
UTSW |
4 |
113,799,864 (GRCm39) |
missense |
probably damaging |
0.97 |
R2512:Skint5
|
UTSW |
4 |
113,487,616 (GRCm39) |
missense |
unknown |
|
R2913:Skint5
|
UTSW |
4 |
113,381,289 (GRCm39) |
intron |
probably benign |
|
R3522:Skint5
|
UTSW |
4 |
113,614,102 (GRCm39) |
critical splice donor site |
probably null |
|
R3779:Skint5
|
UTSW |
4 |
113,636,237 (GRCm39) |
splice site |
probably benign |
|
R3815:Skint5
|
UTSW |
4 |
113,703,496 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3815:Skint5
|
UTSW |
4 |
113,486,319 (GRCm39) |
splice site |
probably benign |
|
R3816:Skint5
|
UTSW |
4 |
113,486,319 (GRCm39) |
splice site |
probably benign |
|
R3817:Skint5
|
UTSW |
4 |
113,486,319 (GRCm39) |
splice site |
probably benign |
|
R3818:Skint5
|
UTSW |
4 |
113,486,319 (GRCm39) |
splice site |
probably benign |
|
R3837:Skint5
|
UTSW |
4 |
113,797,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R3943:Skint5
|
UTSW |
4 |
113,799,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R3944:Skint5
|
UTSW |
4 |
113,799,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R4037:Skint5
|
UTSW |
4 |
113,743,011 (GRCm39) |
missense |
unknown |
|
R4038:Skint5
|
UTSW |
4 |
113,743,011 (GRCm39) |
missense |
unknown |
|
R4039:Skint5
|
UTSW |
4 |
113,743,011 (GRCm39) |
missense |
unknown |
|
R4280:Skint5
|
UTSW |
4 |
113,799,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4308:Skint5
|
UTSW |
4 |
113,341,164 (GRCm39) |
missense |
unknown |
|
R4386:Skint5
|
UTSW |
4 |
113,341,090 (GRCm39) |
missense |
probably benign |
0.23 |
R4513:Skint5
|
UTSW |
4 |
113,599,382 (GRCm39) |
missense |
unknown |
|
R4575:Skint5
|
UTSW |
4 |
113,524,390 (GRCm39) |
missense |
unknown |
|
R4631:Skint5
|
UTSW |
4 |
113,486,314 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4722:Skint5
|
UTSW |
4 |
113,751,052 (GRCm39) |
missense |
unknown |
|
R5010:Skint5
|
UTSW |
4 |
113,403,734 (GRCm39) |
missense |
unknown |
|
R5070:Skint5
|
UTSW |
4 |
113,652,735 (GRCm39) |
missense |
unknown |
|
R5158:Skint5
|
UTSW |
4 |
113,599,409 (GRCm39) |
missense |
unknown |
|
R5163:Skint5
|
UTSW |
4 |
113,652,762 (GRCm39) |
missense |
unknown |
|
R5190:Skint5
|
UTSW |
4 |
113,620,711 (GRCm39) |
missense |
unknown |
|
R5232:Skint5
|
UTSW |
4 |
113,434,841 (GRCm39) |
missense |
unknown |
|
R5257:Skint5
|
UTSW |
4 |
113,434,859 (GRCm39) |
missense |
unknown |
|
R5499:Skint5
|
UTSW |
4 |
113,799,700 (GRCm39) |
critical splice donor site |
probably null |
|
R5569:Skint5
|
UTSW |
4 |
113,545,903 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5776:Skint5
|
UTSW |
4 |
113,620,700 (GRCm39) |
missense |
unknown |
|
R5986:Skint5
|
UTSW |
4 |
113,852,845 (GRCm39) |
missense |
probably benign |
0.11 |
R5987:Skint5
|
UTSW |
4 |
113,743,005 (GRCm39) |
missense |
unknown |
|
R5995:Skint5
|
UTSW |
4 |
113,751,029 (GRCm39) |
missense |
unknown |
|
R6063:Skint5
|
UTSW |
4 |
113,347,842 (GRCm39) |
missense |
probably benign |
0.23 |
R6074:Skint5
|
UTSW |
4 |
113,662,397 (GRCm39) |
missense |
unknown |
|
R6111:Skint5
|
UTSW |
4 |
113,562,845 (GRCm39) |
missense |
unknown |
|
R6173:Skint5
|
UTSW |
4 |
113,392,907 (GRCm39) |
missense |
unknown |
|
R6238:Skint5
|
UTSW |
4 |
113,800,064 (GRCm39) |
splice site |
probably null |
|
R6248:Skint5
|
UTSW |
4 |
113,636,286 (GRCm39) |
missense |
unknown |
|
R6318:Skint5
|
UTSW |
4 |
113,374,330 (GRCm39) |
missense |
unknown |
|
R6370:Skint5
|
UTSW |
4 |
113,471,307 (GRCm39) |
missense |
unknown |
|
R6404:Skint5
|
UTSW |
4 |
113,799,806 (GRCm39) |
missense |
probably damaging |
0.97 |
R6499:Skint5
|
UTSW |
4 |
113,396,552 (GRCm39) |
missense |
unknown |
|
R6646:Skint5
|
UTSW |
4 |
113,797,974 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6737:Skint5
|
UTSW |
4 |
113,392,936 (GRCm39) |
missense |
unknown |
|
R6795:Skint5
|
UTSW |
4 |
113,524,420 (GRCm39) |
missense |
unknown |
|
R6815:Skint5
|
UTSW |
4 |
113,574,324 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6935:Skint5
|
UTSW |
4 |
113,799,793 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7028:Skint5
|
UTSW |
4 |
113,798,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R7043:Skint5
|
UTSW |
4 |
113,574,304 (GRCm39) |
missense |
unknown |
|
R7071:Skint5
|
UTSW |
4 |
113,636,277 (GRCm39) |
missense |
unknown |
|
R7142:Skint5
|
UTSW |
4 |
113,428,791 (GRCm39) |
missense |
unknown |
|
R7197:Skint5
|
UTSW |
4 |
113,437,679 (GRCm39) |
critical splice donor site |
probably null |
|
R7208:Skint5
|
UTSW |
4 |
113,396,536 (GRCm39) |
missense |
unknown |
|
R7297:Skint5
|
UTSW |
4 |
113,400,131 (GRCm39) |
missense |
unknown |
|
R7470:Skint5
|
UTSW |
4 |
113,743,000 (GRCm39) |
missense |
unknown |
|
R7470:Skint5
|
UTSW |
4 |
113,614,128 (GRCm39) |
missense |
unknown |
|
R7500:Skint5
|
UTSW |
4 |
113,417,035 (GRCm39) |
missense |
unknown |
|
R7547:Skint5
|
UTSW |
4 |
113,483,785 (GRCm39) |
missense |
unknown |
|
R7556:Skint5
|
UTSW |
4 |
113,425,162 (GRCm39) |
missense |
unknown |
|
R7619:Skint5
|
UTSW |
4 |
113,381,305 (GRCm39) |
missense |
unknown |
|
R7629:Skint5
|
UTSW |
4 |
113,799,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R7646:Skint5
|
UTSW |
4 |
113,620,739 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7725:Skint5
|
UTSW |
4 |
113,685,099 (GRCm39) |
missense |
unknown |
|
R7788:Skint5
|
UTSW |
4 |
113,403,715 (GRCm39) |
missense |
unknown |
|
R7818:Skint5
|
UTSW |
4 |
113,799,923 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7819:Skint5
|
UTSW |
4 |
113,417,032 (GRCm39) |
missense |
unknown |
|
R7958:Skint5
|
UTSW |
4 |
113,480,980 (GRCm39) |
missense |
unknown |
|
R8150:Skint5
|
UTSW |
4 |
113,798,087 (GRCm39) |
missense |
probably benign |
0.21 |
R8214:Skint5
|
UTSW |
4 |
113,662,139 (GRCm39) |
splice site |
probably null |
|
R8413:Skint5
|
UTSW |
4 |
113,572,900 (GRCm39) |
missense |
unknown |
|
R8420:Skint5
|
UTSW |
4 |
113,437,679 (GRCm39) |
critical splice donor site |
probably null |
|
R8459:Skint5
|
UTSW |
4 |
113,703,481 (GRCm39) |
nonsense |
probably null |
|
R8703:Skint5
|
UTSW |
4 |
113,733,207 (GRCm39) |
missense |
unknown |
|
R8710:Skint5
|
UTSW |
4 |
113,483,787 (GRCm39) |
missense |
unknown |
|
R8927:Skint5
|
UTSW |
4 |
113,341,099 (GRCm39) |
missense |
probably benign |
0.23 |
R8928:Skint5
|
UTSW |
4 |
113,341,099 (GRCm39) |
missense |
probably benign |
0.23 |
R8950:Skint5
|
UTSW |
4 |
113,374,349 (GRCm39) |
missense |
unknown |
|
R9047:Skint5
|
UTSW |
4 |
113,512,919 (GRCm39) |
missense |
unknown |
|
R9053:Skint5
|
UTSW |
4 |
113,403,684 (GRCm39) |
missense |
unknown |
|
R9216:Skint5
|
UTSW |
4 |
113,392,955 (GRCm39) |
missense |
unknown |
|
R9441:Skint5
|
UTSW |
4 |
113,347,848 (GRCm39) |
missense |
unknown |
|
R9551:Skint5
|
UTSW |
4 |
113,798,052 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9552:Skint5
|
UTSW |
4 |
113,798,052 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9750:Skint5
|
UTSW |
4 |
113,727,866 (GRCm39) |
missense |
unknown |
|
X0028:Skint5
|
UTSW |
4 |
113,548,306 (GRCm39) |
missense |
unknown |
|
|