Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ano2 |
A |
G |
6: 125,992,943 (GRCm38) |
T741A |
possibly damaging |
Het |
Aox4 |
T |
C |
1: 58,250,219 (GRCm38) |
M767T |
probably damaging |
Het |
Arhgap39 |
C |
A |
15: 76,765,491 (GRCm38) |
S27I |
probably benign |
Het |
AU018091 |
T |
A |
7: 3,159,513 (GRCm38) |
M296L |
probably benign |
Het |
Axin1 |
A |
G |
17: 26,187,968 (GRCm38) |
T512A |
probably benign |
Het |
B4galnt3 |
A |
T |
6: 120,214,968 (GRCm38) |
D602E |
probably benign |
Het |
Bcl6 |
G |
A |
16: 23,966,226 (GRCm38) |
R675* |
probably null |
Het |
Bsnd |
A |
T |
4: 106,492,033 (GRCm38) |
D3E |
probably benign |
Het |
Btbd18 |
C |
T |
2: 84,666,428 (GRCm38) |
R137* |
probably null |
Het |
C2cd5 |
A |
G |
6: 143,019,409 (GRCm38) |
S871P |
probably benign |
Het |
Cobl |
G |
T |
11: 12,254,128 (GRCm38) |
P858Q |
probably damaging |
Het |
Col6a1 |
C |
T |
10: 76,710,341 (GRCm38) |
|
probably null |
Het |
Crb2 |
A |
T |
2: 37,787,408 (GRCm38) |
H304L |
probably benign |
Het |
Crybg1 |
T |
A |
10: 43,964,666 (GRCm38) |
Y1812F |
possibly damaging |
Het |
Ddx60 |
A |
T |
8: 61,988,108 (GRCm38) |
K1070N |
possibly damaging |
Het |
Defb22 |
T |
C |
2: 152,485,920 (GRCm38) |
K115R |
unknown |
Het |
Dhx8 |
C |
T |
11: 101,740,175 (GRCm38) |
|
probably null |
Het |
Dnah5 |
T |
A |
15: 28,365,522 (GRCm38) |
|
probably null |
Het |
Dnah7b |
T |
A |
1: 46,126,804 (GRCm38) |
F543Y |
probably benign |
Het |
Ehhadh |
A |
G |
16: 21,766,321 (GRCm38) |
F270S |
probably damaging |
Het |
Esyt2 |
A |
G |
12: 116,346,508 (GRCm38) |
M397V |
probably benign |
Het |
Fanca |
A |
T |
8: 123,316,425 (GRCm38) |
L74H |
probably damaging |
Het |
Fbxl17 |
C |
A |
17: 63,060,351 (GRCm38) |
V676F |
probably benign |
Het |
Fndc1 |
A |
G |
17: 7,801,645 (GRCm38) |
V102A |
probably damaging |
Het |
Gpalpp1 |
T |
C |
14: 76,095,011 (GRCm38) |
Y273C |
probably damaging |
Het |
Gpatch8 |
TTCCTCCTCCTCCTCTTCCTCCTCCTC |
TTCCTCCTCCTCCTCCTCTTCCTCCTCCTC |
11: 102,480,188 (GRCm38) |
|
probably benign |
Het |
Grik2 |
T |
C |
10: 49,535,367 (GRCm38) |
H225R |
probably benign |
Het |
Helz2 |
A |
T |
2: 181,231,285 (GRCm38) |
S2411T |
probably benign |
Het |
Hnmt |
C |
T |
2: 24,014,341 (GRCm38) |
A103T |
probably damaging |
Het |
Ighv15-2 |
G |
T |
12: 114,564,590 (GRCm38) |
Y114* |
probably null |
Het |
Irak2 |
A |
G |
6: 113,678,709 (GRCm38) |
H357R |
probably benign |
Het |
Kcp |
T |
C |
6: 29,499,015 (GRCm38) |
E320G |
probably damaging |
Het |
Kpna4 |
A |
G |
3: 69,089,798 (GRCm38) |
L352S |
probably damaging |
Het |
Krt36 |
G |
A |
11: 100,105,146 (GRCm38) |
Q151* |
probably null |
Het |
Krt77 |
G |
A |
15: 101,865,496 (GRCm38) |
T241M |
probably benign |
Het |
Lca5l |
T |
A |
16: 96,173,809 (GRCm38) |
N305I |
probably damaging |
Het |
Lefty1 |
T |
A |
1: 180,937,767 (GRCm38) |
L300Q |
probably benign |
Het |
Mertk |
A |
G |
2: 128,736,649 (GRCm38) |
Y185C |
probably damaging |
Het |
Mmp14 |
T |
C |
14: 54,436,251 (GRCm38) |
I124T |
possibly damaging |
Het |
Nlrc4 |
T |
C |
17: 74,447,103 (GRCm38) |
E95G |
possibly damaging |
Het |
Npc1 |
A |
G |
18: 12,213,291 (GRCm38) |
F283L |
possibly damaging |
Het |
Olfr1180 |
A |
C |
2: 88,412,118 (GRCm38) |
L180W |
probably damaging |
Het |
Olfr1282 |
A |
T |
2: 111,335,901 (GRCm38) |
M59K |
probably damaging |
Het |
Pcdha11 |
T |
C |
18: 37,011,225 (GRCm38) |
V123A |
probably damaging |
Het |
Pcdhga2 |
T |
C |
18: 37,669,208 (GRCm38) |
V35A |
probably damaging |
Het |
Pgd |
G |
T |
4: 149,161,678 (GRCm38) |
T94K |
probably benign |
Het |
Pik3c2a |
T |
C |
7: 116,342,252 (GRCm38) |
N1593S |
probably damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 109,624,195 (GRCm38) |
|
probably benign |
Het |
Plcb3 |
A |
G |
19: 6,958,084 (GRCm38) |
|
probably null |
Het |
Prkd3 |
C |
T |
17: 78,966,355 (GRCm38) |
D491N |
probably benign |
Het |
Ptprf |
T |
C |
4: 118,231,543 (GRCm38) |
T688A |
probably damaging |
Het |
Pycr2 |
T |
A |
1: 180,906,682 (GRCm38) |
L210M |
probably damaging |
Het |
Rpl36 |
T |
C |
17: 56,614,137 (GRCm38) |
I81T |
probably benign |
Het |
Rraga |
C |
T |
4: 86,576,016 (GRCm38) |
A33V |
probably damaging |
Het |
Slc29a1 |
G |
A |
17: 45,585,762 (GRCm38) |
A429V |
probably damaging |
Het |
Synj1 |
C |
T |
16: 90,948,090 (GRCm38) |
G1189R |
probably benign |
Het |
Synpo2 |
A |
G |
3: 123,112,404 (GRCm38) |
*1088Q |
probably null |
Het |
Tbc1d21 |
T |
C |
9: 58,363,093 (GRCm38) |
D133G |
probably damaging |
Het |
Tenm2 |
A |
G |
11: 36,024,182 (GRCm38) |
V2176A |
probably damaging |
Het |
Tff1 |
A |
G |
17: 31,162,798 (GRCm38) |
I35T |
probably benign |
Het |
Thnsl1 |
T |
C |
2: 21,212,953 (GRCm38) |
V506A |
possibly damaging |
Het |
Timm10b |
A |
G |
7: 105,640,880 (GRCm38) |
Q50R |
unknown |
Het |
Tjp2 |
A |
T |
19: 24,101,981 (GRCm38) |
N843K |
probably benign |
Het |
Tle1 |
A |
T |
4: 72,139,061 (GRCm38) |
F101I |
probably benign |
Het |
Tmem225 |
T |
C |
9: 40,148,368 (GRCm38) |
F15L |
probably benign |
Het |
Trav12-3 |
T |
C |
14: 53,622,161 (GRCm38) |
L88P |
probably benign |
Het |
Ttc7b |
A |
T |
12: 100,355,034 (GRCm38) |
W613R |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,945,316 (GRCm38) |
D1840G |
unknown |
Het |
Ttn |
T |
A |
2: 76,778,504 (GRCm38) |
M17723L |
probably benign |
Het |
Tubgcp2 |
T |
C |
7: 140,001,036 (GRCm38) |
H668R |
probably benign |
Het |
Ush2a |
C |
A |
1: 188,728,484 (GRCm38) |
N2647K |
possibly damaging |
Het |
Vmn1r14 |
C |
T |
6: 57,233,866 (GRCm38) |
S143F |
probably benign |
Het |
Vmn2r70 |
A |
G |
7: 85,565,054 (GRCm38) |
S297P |
probably damaging |
Het |
Ywhab |
T |
C |
2: 164,014,060 (GRCm38) |
F119L |
probably damaging |
Het |
Zmym2 |
T |
A |
14: 56,950,202 (GRCm38) |
D1108E |
probably benign |
Het |
|
Other mutations in Stab1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Stab1
|
APN |
14 |
31,161,357 (GRCm38) |
missense |
probably benign |
0.01 |
IGL00323:Stab1
|
APN |
14 |
31,139,306 (GRCm38) |
missense |
probably benign |
0.04 |
IGL00515:Stab1
|
APN |
14 |
31,159,729 (GRCm38) |
missense |
probably benign |
0.20 |
IGL00844:Stab1
|
APN |
14 |
31,147,066 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01374:Stab1
|
APN |
14 |
31,147,075 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01384:Stab1
|
APN |
14 |
31,150,408 (GRCm38) |
missense |
probably benign |
|
IGL01431:Stab1
|
APN |
14 |
31,148,995 (GRCm38) |
missense |
probably benign |
0.06 |
IGL01787:Stab1
|
APN |
14 |
31,139,808 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02128:Stab1
|
APN |
14 |
31,150,441 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02138:Stab1
|
APN |
14 |
31,143,513 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02256:Stab1
|
APN |
14 |
31,141,592 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02340:Stab1
|
APN |
14 |
31,140,410 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL02507:Stab1
|
APN |
14 |
31,139,210 (GRCm38) |
unclassified |
probably benign |
|
IGL02695:Stab1
|
APN |
14 |
31,159,271 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02755:Stab1
|
APN |
14 |
31,139,638 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02870:Stab1
|
APN |
14 |
31,139,397 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02884:Stab1
|
APN |
14 |
31,150,143 (GRCm38) |
splice site |
probably null |
|
IGL03035:Stab1
|
APN |
14 |
31,147,769 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03267:Stab1
|
APN |
14 |
31,142,729 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03286:Stab1
|
APN |
14 |
31,159,326 (GRCm38) |
splice site |
probably benign |
|
IGL03366:Stab1
|
APN |
14 |
31,150,263 (GRCm38) |
missense |
possibly damaging |
0.58 |
IGL03412:Stab1
|
APN |
14 |
31,154,407 (GRCm38) |
missense |
probably benign |
0.42 |
R0906_Stab1_335
|
UTSW |
14 |
31,145,249 (GRCm38) |
missense |
probably benign |
0.19 |
R5086_Stab1_467
|
UTSW |
14 |
31,159,304 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02835:Stab1
|
UTSW |
14 |
31,146,024 (GRCm38) |
critical splice donor site |
probably null |
|
K7371:Stab1
|
UTSW |
14 |
31,150,249 (GRCm38) |
missense |
probably damaging |
1.00 |
R0053:Stab1
|
UTSW |
14 |
31,140,687 (GRCm38) |
missense |
possibly damaging |
0.57 |
R0053:Stab1
|
UTSW |
14 |
31,140,687 (GRCm38) |
missense |
possibly damaging |
0.57 |
R0066:Stab1
|
UTSW |
14 |
31,157,070 (GRCm38) |
splice site |
probably benign |
|
R0066:Stab1
|
UTSW |
14 |
31,157,070 (GRCm38) |
splice site |
probably benign |
|
R0363:Stab1
|
UTSW |
14 |
31,159,008 (GRCm38) |
splice site |
probably benign |
|
R0387:Stab1
|
UTSW |
14 |
31,148,101 (GRCm38) |
missense |
probably benign |
0.00 |
R0391:Stab1
|
UTSW |
14 |
31,143,418 (GRCm38) |
missense |
probably benign |
0.21 |
R0513:Stab1
|
UTSW |
14 |
31,148,945 (GRCm38) |
missense |
probably benign |
0.08 |
R0546:Stab1
|
UTSW |
14 |
31,139,550 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0825:Stab1
|
UTSW |
14 |
31,152,600 (GRCm38) |
missense |
probably benign |
0.16 |
R0906:Stab1
|
UTSW |
14 |
31,145,249 (GRCm38) |
missense |
probably benign |
0.19 |
R0963:Stab1
|
UTSW |
14 |
31,147,274 (GRCm38) |
missense |
probably damaging |
0.97 |
R1219:Stab1
|
UTSW |
14 |
31,140,621 (GRCm38) |
splice site |
probably null |
|
R1234:Stab1
|
UTSW |
14 |
31,150,236 (GRCm38) |
missense |
probably damaging |
1.00 |
R1260:Stab1
|
UTSW |
14 |
31,151,889 (GRCm38) |
missense |
probably damaging |
1.00 |
R1400:Stab1
|
UTSW |
14 |
31,139,830 (GRCm38) |
missense |
possibly damaging |
0.92 |
R1405:Stab1
|
UTSW |
14 |
31,149,001 (GRCm38) |
missense |
probably benign |
0.19 |
R1405:Stab1
|
UTSW |
14 |
31,149,001 (GRCm38) |
missense |
probably benign |
0.19 |
R1440:Stab1
|
UTSW |
14 |
31,151,690 (GRCm38) |
nonsense |
probably null |
|
R1472:Stab1
|
UTSW |
14 |
31,141,586 (GRCm38) |
missense |
probably benign |
0.01 |
R1474:Stab1
|
UTSW |
14 |
31,149,861 (GRCm38) |
missense |
probably benign |
0.45 |
R1475:Stab1
|
UTSW |
14 |
31,163,828 (GRCm38) |
missense |
probably benign |
|
R1509:Stab1
|
UTSW |
14 |
31,151,584 (GRCm38) |
splice site |
probably benign |
|
R1551:Stab1
|
UTSW |
14 |
31,160,499 (GRCm38) |
missense |
probably benign |
0.00 |
R1572:Stab1
|
UTSW |
14 |
31,150,823 (GRCm38) |
missense |
probably damaging |
1.00 |
R1633:Stab1
|
UTSW |
14 |
31,150,380 (GRCm38) |
splice site |
probably null |
|
R1719:Stab1
|
UTSW |
14 |
31,146,028 (GRCm38) |
nonsense |
probably null |
|
R1733:Stab1
|
UTSW |
14 |
31,145,303 (GRCm38) |
missense |
probably damaging |
1.00 |
R1763:Stab1
|
UTSW |
14 |
31,168,416 (GRCm38) |
missense |
probably benign |
0.04 |
R1808:Stab1
|
UTSW |
14 |
31,141,144 (GRCm38) |
missense |
possibly damaging |
0.80 |
R1816:Stab1
|
UTSW |
14 |
31,157,465 (GRCm38) |
missense |
probably benign |
0.03 |
R1853:Stab1
|
UTSW |
14 |
31,140,463 (GRCm38) |
missense |
probably damaging |
1.00 |
R1891:Stab1
|
UTSW |
14 |
31,141,330 (GRCm38) |
missense |
probably benign |
0.07 |
R1984:Stab1
|
UTSW |
14 |
31,150,648 (GRCm38) |
missense |
probably benign |
0.20 |
R1998:Stab1
|
UTSW |
14 |
31,162,153 (GRCm38) |
nonsense |
probably null |
|
R2165:Stab1
|
UTSW |
14 |
31,168,435 (GRCm38) |
missense |
probably benign |
0.20 |
R2191:Stab1
|
UTSW |
14 |
31,159,270 (GRCm38) |
missense |
probably damaging |
1.00 |
R2191:Stab1
|
UTSW |
14 |
31,142,800 (GRCm38) |
missense |
probably benign |
0.03 |
R2233:Stab1
|
UTSW |
14 |
31,161,880 (GRCm38) |
missense |
probably benign |
0.08 |
R2303:Stab1
|
UTSW |
14 |
31,146,070 (GRCm38) |
missense |
probably damaging |
1.00 |
R2496:Stab1
|
UTSW |
14 |
31,161,463 (GRCm38) |
missense |
probably damaging |
1.00 |
R2504:Stab1
|
UTSW |
14 |
31,163,040 (GRCm38) |
critical splice donor site |
probably null |
|
R2519:Stab1
|
UTSW |
14 |
31,154,872 (GRCm38) |
missense |
probably damaging |
1.00 |
R2926:Stab1
|
UTSW |
14 |
31,161,799 (GRCm38) |
missense |
probably damaging |
1.00 |
R4025:Stab1
|
UTSW |
14 |
31,154,952 (GRCm38) |
missense |
possibly damaging |
0.46 |
R4113:Stab1
|
UTSW |
14 |
31,168,479 (GRCm38) |
missense |
probably damaging |
0.98 |
R4258:Stab1
|
UTSW |
14 |
31,154,672 (GRCm38) |
missense |
possibly damaging |
0.92 |
R4588:Stab1
|
UTSW |
14 |
31,157,445 (GRCm38) |
missense |
probably benign |
0.01 |
R4644:Stab1
|
UTSW |
14 |
31,140,487 (GRCm38) |
unclassified |
probably benign |
|
R4660:Stab1
|
UTSW |
14 |
31,154,915 (GRCm38) |
missense |
possibly damaging |
0.91 |
R4801:Stab1
|
UTSW |
14 |
31,141,371 (GRCm38) |
nonsense |
probably null |
|
R4802:Stab1
|
UTSW |
14 |
31,141,371 (GRCm38) |
nonsense |
probably null |
|
R4870:Stab1
|
UTSW |
14 |
31,142,043 (GRCm38) |
missense |
probably benign |
0.13 |
R4872:Stab1
|
UTSW |
14 |
31,140,393 (GRCm38) |
missense |
probably damaging |
1.00 |
R4881:Stab1
|
UTSW |
14 |
31,143,672 (GRCm38) |
missense |
probably benign |
0.32 |
R4941:Stab1
|
UTSW |
14 |
31,151,571 (GRCm38) |
missense |
probably benign |
0.00 |
R5061:Stab1
|
UTSW |
14 |
31,163,099 (GRCm38) |
missense |
probably damaging |
1.00 |
R5086:Stab1
|
UTSW |
14 |
31,159,304 (GRCm38) |
missense |
probably damaging |
1.00 |
R5086:Stab1
|
UTSW |
14 |
31,143,624 (GRCm38) |
missense |
probably damaging |
1.00 |
R5087:Stab1
|
UTSW |
14 |
31,159,304 (GRCm38) |
missense |
probably damaging |
1.00 |
R5092:Stab1
|
UTSW |
14 |
31,145,855 (GRCm38) |
missense |
probably benign |
0.01 |
R5102:Stab1
|
UTSW |
14 |
31,148,017 (GRCm38) |
critical splice donor site |
probably null |
|
R5107:Stab1
|
UTSW |
14 |
31,163,795 (GRCm38) |
splice site |
probably null |
|
R5195:Stab1
|
UTSW |
14 |
31,140,521 (GRCm38) |
unclassified |
probably benign |
|
R5217:Stab1
|
UTSW |
14 |
31,159,519 (GRCm38) |
missense |
probably benign |
0.25 |
R5285:Stab1
|
UTSW |
14 |
31,143,476 (GRCm38) |
unclassified |
probably benign |
|
R5327:Stab1
|
UTSW |
14 |
31,161,836 (GRCm38) |
nonsense |
probably null |
|
R5647:Stab1
|
UTSW |
14 |
31,157,440 (GRCm38) |
nonsense |
probably null |
|
R5696:Stab1
|
UTSW |
14 |
31,160,221 (GRCm38) |
missense |
probably benign |
|
R5996:Stab1
|
UTSW |
14 |
31,139,551 (GRCm38) |
missense |
probably benign |
0.39 |
R6016:Stab1
|
UTSW |
14 |
31,158,993 (GRCm38) |
missense |
probably damaging |
1.00 |
R6017:Stab1
|
UTSW |
14 |
31,141,544 (GRCm38) |
missense |
probably benign |
0.00 |
R6174:Stab1
|
UTSW |
14 |
31,162,519 (GRCm38) |
nonsense |
probably null |
|
R6366:Stab1
|
UTSW |
14 |
31,141,438 (GRCm38) |
missense |
probably benign |
0.10 |
R6754:Stab1
|
UTSW |
14 |
31,141,081 (GRCm38) |
missense |
probably benign |
|
R6788:Stab1
|
UTSW |
14 |
31,139,160 (GRCm38) |
missense |
probably damaging |
1.00 |
R6898:Stab1
|
UTSW |
14 |
31,158,963 (GRCm38) |
missense |
probably benign |
0.00 |
R7124:Stab1
|
UTSW |
14 |
31,160,867 (GRCm38) |
missense |
possibly damaging |
0.94 |
R7145:Stab1
|
UTSW |
14 |
31,145,073 (GRCm38) |
critical splice donor site |
probably null |
|
R7213:Stab1
|
UTSW |
14 |
31,143,673 (GRCm38) |
missense |
probably benign |
|
R7215:Stab1
|
UTSW |
14 |
31,160,797 (GRCm38) |
missense |
possibly damaging |
0.93 |
R7319:Stab1
|
UTSW |
14 |
31,140,826 (GRCm38) |
missense |
probably damaging |
1.00 |
R7389:Stab1
|
UTSW |
14 |
31,147,239 (GRCm38) |
missense |
probably benign |
0.00 |
R7400:Stab1
|
UTSW |
14 |
31,157,384 (GRCm38) |
missense |
probably null |
1.00 |
R7427:Stab1
|
UTSW |
14 |
31,159,259 (GRCm38) |
missense |
probably benign |
0.00 |
R7428:Stab1
|
UTSW |
14 |
31,159,259 (GRCm38) |
missense |
probably benign |
0.00 |
R7484:Stab1
|
UTSW |
14 |
31,160,317 (GRCm38) |
missense |
probably benign |
0.00 |
R7568:Stab1
|
UTSW |
14 |
31,152,595 (GRCm38) |
missense |
probably damaging |
1.00 |
R7574:Stab1
|
UTSW |
14 |
31,154,665 (GRCm38) |
missense |
probably benign |
|
R7619:Stab1
|
UTSW |
14 |
31,145,237 (GRCm38) |
missense |
probably benign |
|
R7623:Stab1
|
UTSW |
14 |
31,140,621 (GRCm38) |
missense |
probably benign |
0.03 |
R7721:Stab1
|
UTSW |
14 |
31,141,456 (GRCm38) |
missense |
possibly damaging |
0.48 |
R7869:Stab1
|
UTSW |
14 |
31,154,472 (GRCm38) |
missense |
probably benign |
0.01 |
R7936:Stab1
|
UTSW |
14 |
31,157,415 (GRCm38) |
missense |
possibly damaging |
0.88 |
R7956:Stab1
|
UTSW |
14 |
31,160,024 (GRCm38) |
missense |
probably benign |
0.02 |
R7973:Stab1
|
UTSW |
14 |
31,159,633 (GRCm38) |
critical splice donor site |
probably null |
|
R8059:Stab1
|
UTSW |
14 |
31,160,241 (GRCm38) |
missense |
probably benign |
0.02 |
R8116:Stab1
|
UTSW |
14 |
31,158,953 (GRCm38) |
missense |
possibly damaging |
0.80 |
R8304:Stab1
|
UTSW |
14 |
31,148,954 (GRCm38) |
missense |
probably benign |
0.14 |
R8368:Stab1
|
UTSW |
14 |
31,148,411 (GRCm38) |
missense |
possibly damaging |
0.91 |
R8495:Stab1
|
UTSW |
14 |
31,155,833 (GRCm38) |
missense |
probably damaging |
1.00 |
R8513:Stab1
|
UTSW |
14 |
31,149,790 (GRCm38) |
critical splice donor site |
probably null |
|
R8544:Stab1
|
UTSW |
14 |
31,163,051 (GRCm38) |
nonsense |
probably null |
|
R8671:Stab1
|
UTSW |
14 |
31,157,408 (GRCm38) |
missense |
probably damaging |
1.00 |
R8885:Stab1
|
UTSW |
14 |
31,161,814 (GRCm38) |
missense |
possibly damaging |
0.79 |
R8974:Stab1
|
UTSW |
14 |
31,160,822 (GRCm38) |
missense |
probably benign |
|
R9022:Stab1
|
UTSW |
14 |
31,160,269 (GRCm38) |
missense |
probably benign |
0.01 |
R9059:Stab1
|
UTSW |
14 |
31,154,848 (GRCm38) |
missense |
probably benign |
0.01 |
R9226:Stab1
|
UTSW |
14 |
31,145,855 (GRCm38) |
missense |
probably benign |
0.00 |
R9272:Stab1
|
UTSW |
14 |
31,145,341 (GRCm38) |
missense |
probably benign |
0.05 |
R9388:Stab1
|
UTSW |
14 |
31,154,355 (GRCm38) |
missense |
probably damaging |
1.00 |
R9401:Stab1
|
UTSW |
14 |
31,161,112 (GRCm38) |
missense |
probably benign |
|
R9433:Stab1
|
UTSW |
14 |
31,143,574 (GRCm38) |
missense |
probably benign |
0.00 |
R9450:Stab1
|
UTSW |
14 |
31,162,939 (GRCm38) |
missense |
possibly damaging |
0.62 |
R9505:Stab1
|
UTSW |
14 |
31,155,765 (GRCm38) |
missense |
probably damaging |
1.00 |
R9570:Stab1
|
UTSW |
14 |
31,142,681 (GRCm38) |
missense |
probably benign |
0.01 |
R9624:Stab1
|
UTSW |
14 |
31,141,388 (GRCm38) |
missense |
|
|
R9694:Stab1
|
UTSW |
14 |
31,154,944 (GRCm38) |
missense |
probably benign |
0.06 |
R9723:Stab1
|
UTSW |
14 |
31,163,891 (GRCm38) |
missense |
probably benign |
0.10 |
X0026:Stab1
|
UTSW |
14 |
31,162,191 (GRCm38) |
missense |
possibly damaging |
0.91 |
Z1176:Stab1
|
UTSW |
14 |
31,150,660 (GRCm38) |
missense |
probably benign |
0.00 |
Z1176:Stab1
|
UTSW |
14 |
31,142,038 (GRCm38) |
missense |
probably benign |
0.00 |
|