Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak2 |
G |
T |
12: 112,747,747 (GRCm39) |
A1036E |
|
Het |
Baz2b |
A |
T |
2: 59,792,528 (GRCm39) |
H533Q |
possibly damaging |
Het |
Bcl2l11 |
T |
A |
2: 128,000,235 (GRCm39) |
W193R |
probably damaging |
Het |
Bcl2l12 |
C |
T |
7: 44,646,338 (GRCm39) |
G24D |
probably damaging |
Het |
Cacna1b |
A |
G |
2: 24,580,773 (GRCm39) |
V691A |
probably damaging |
Het |
Cdh8 |
T |
C |
8: 99,922,984 (GRCm39) |
D304G |
probably damaging |
Het |
Ces3a |
A |
T |
8: 105,784,594 (GRCm39) |
Q525H |
probably damaging |
Het |
Csmd1 |
C |
A |
8: 16,151,142 (GRCm39) |
C1391F |
probably damaging |
Het |
Cul7 |
G |
T |
17: 46,962,624 (GRCm39) |
G85V |
probably damaging |
Het |
Dnah8 |
G |
A |
17: 31,090,366 (GRCm39) |
V4623I |
possibly damaging |
Het |
Dnhd1 |
T |
A |
7: 105,363,192 (GRCm39) |
L3918Q |
probably damaging |
Het |
Exoc4 |
A |
T |
6: 33,898,423 (GRCm39) |
N881Y |
probably damaging |
Het |
Flt1 |
G |
C |
5: 147,540,379 (GRCm39) |
A770G |
probably damaging |
Het |
Fndc5 |
A |
G |
4: 129,035,915 (GRCm39) |
N184S |
probably benign |
Het |
Folh1 |
A |
G |
7: 86,424,845 (GRCm39) |
|
probably null |
Het |
Frem3 |
A |
T |
8: 81,338,660 (GRCm39) |
T318S |
probably damaging |
Het |
Gba2 |
A |
G |
4: 43,568,453 (GRCm39) |
V671A |
probably benign |
Het |
Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
Jph2 |
G |
A |
2: 163,217,704 (GRCm39) |
T324M |
probably damaging |
Het |
Kank4 |
A |
G |
4: 98,649,758 (GRCm39) |
V937A |
probably damaging |
Het |
Kdm3a |
T |
A |
6: 71,609,154 (GRCm39) |
E24D |
probably benign |
Het |
Kidins220 |
T |
A |
12: 25,054,018 (GRCm39) |
L464Q |
probably damaging |
Het |
Loxhd1 |
T |
A |
18: 77,476,210 (GRCm39) |
V1159E |
probably damaging |
Het |
Malrd1 |
A |
G |
2: 15,929,987 (GRCm39) |
N1498D |
unknown |
Het |
Mplkipl1 |
T |
G |
19: 61,163,997 (GRCm39) |
D146A |
probably damaging |
Het |
Mrgprb5 |
C |
T |
7: 47,818,655 (GRCm39) |
V27I |
probably benign |
Het |
Mtfr2 |
A |
G |
10: 20,233,312 (GRCm39) |
N294D |
probably damaging |
Het |
Muc6 |
A |
T |
7: 141,235,542 (GRCm39) |
L498H |
probably damaging |
Het |
N4bp2 |
A |
G |
5: 65,948,050 (GRCm39) |
T227A |
possibly damaging |
Het |
Nin |
C |
T |
12: 70,149,573 (GRCm39) |
R12Q |
|
Het |
Obscn |
G |
C |
11: 58,920,151 (GRCm39) |
A27G |
|
Het |
Or11h7 |
T |
A |
14: 50,891,583 (GRCm39) |
D296E |
probably benign |
Het |
Or4k5 |
T |
G |
14: 50,385,392 (GRCm39) |
E313A |
probably benign |
Het |
Or52r1b |
G |
A |
7: 102,690,862 (GRCm39) |
D54N |
probably damaging |
Het |
Or8b48 |
T |
A |
9: 38,493,330 (GRCm39) |
Y252* |
probably null |
Het |
Or8s5 |
T |
A |
15: 98,238,421 (GRCm39) |
M150L |
possibly damaging |
Het |
Qprt |
A |
G |
7: 126,707,361 (GRCm39) |
V245A |
probably damaging |
Het |
Rab11fip5 |
T |
A |
6: 85,325,176 (GRCm39) |
E377V |
probably damaging |
Het |
Rere |
A |
G |
4: 150,491,061 (GRCm39) |
T71A |
probably benign |
Het |
Ret |
A |
T |
6: 118,174,063 (GRCm39) |
L11Q |
possibly damaging |
Het |
Rp1 |
C |
T |
1: 4,419,241 (GRCm39) |
V624I |
probably benign |
Het |
Scaf8 |
T |
A |
17: 3,213,304 (GRCm39) |
L131H |
unknown |
Het |
Scgb2a2 |
A |
G |
19: 9,829,021 (GRCm39) |
R58G |
probably benign |
Het |
Scn11a |
A |
G |
9: 119,583,875 (GRCm39) |
I1580T |
probably damaging |
Het |
Slco4c1 |
T |
G |
1: 96,768,866 (GRCm39) |
K332T |
probably damaging |
Het |
Sntg1 |
T |
G |
1: 8,518,289 (GRCm39) |
Y368S |
possibly damaging |
Het |
Stim1 |
A |
G |
7: 102,057,615 (GRCm39) |
T143A |
probably benign |
Het |
Tbr1 |
A |
G |
2: 61,642,160 (GRCm39) |
D475G |
probably benign |
Het |
Tcp1 |
A |
G |
17: 13,136,760 (GRCm39) |
D47G |
probably damaging |
Het |
Tpgs2 |
T |
C |
18: 25,282,194 (GRCm39) |
D119G |
probably damaging |
Het |
Trim40 |
C |
A |
17: 37,193,534 (GRCm39) |
R225M |
probably null |
Het |
Tro |
GCAGTGCTTGGTCCTCCGAAGCCACCTCCAGTGCTTGGTCCTCCGAAGCCACCTCCAGTGCTTGGTCCTCCAAAGCCACCTCCAGTGCTTGGTCCTCCAAAGCCACCTCCAGTATTTGGTCCTCCAAAGCCACCTCCAGTGCTTGGTCC |
GCAGTGCTTGGTCCTCCAAAGCCACCTCCAGTGCTTGGTCCTCCAAAGCCACCTCCAGTATTTGGTCCTCCAAAGCCACCTCCAGTGCTTGGTCC |
X: 149,428,852 (GRCm39) |
|
probably benign |
Het |
Trpm1 |
A |
T |
7: 63,885,593 (GRCm39) |
N870Y |
probably damaging |
Het |
Tsr3 |
A |
G |
17: 25,459,445 (GRCm39) |
D47G |
probably benign |
Het |
Vil1 |
G |
A |
1: 74,455,161 (GRCm39) |
G38R |
probably damaging |
Het |
Vmn2r91 |
A |
T |
17: 18,325,880 (GRCm39) |
Q166L |
possibly damaging |
Het |
Wdr33 |
C |
T |
18: 32,026,056 (GRCm39) |
T919I |
unknown |
Het |
Wdr36 |
T |
C |
18: 32,972,504 (GRCm39) |
V64A |
probably benign |
Het |
Xpnpep1 |
T |
C |
19: 52,998,538 (GRCm39) |
I237V |
probably benign |
Het |
Zfp780b |
A |
T |
7: 27,662,566 (GRCm39) |
I663N |
probably damaging |
Het |
Zfyve9 |
G |
A |
4: 108,507,519 (GRCm39) |
A513V |
probably benign |
Het |
|
Other mutations in Polr2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00987:Polr2a
|
APN |
11 |
69,634,620 (GRCm39) |
splice site |
probably benign |
|
IGL01067:Polr2a
|
APN |
11 |
69,638,840 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01547:Polr2a
|
APN |
11 |
69,635,768 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01589:Polr2a
|
APN |
11 |
69,632,020 (GRCm39) |
missense |
probably benign |
|
IGL01955:Polr2a
|
APN |
11 |
69,632,674 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02457:Polr2a
|
APN |
11 |
69,634,076 (GRCm39) |
splice site |
probably benign |
|
IGL02526:Polr2a
|
APN |
11 |
69,630,293 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02792:Polr2a
|
APN |
11 |
69,636,938 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03058:Polr2a
|
APN |
11 |
69,635,873 (GRCm39) |
splice site |
probably null |
|
IGL03083:Polr2a
|
APN |
11 |
69,635,872 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03198:Polr2a
|
APN |
11 |
69,638,107 (GRCm39) |
splice site |
probably null |
|
IGL03201:Polr2a
|
APN |
11 |
69,636,516 (GRCm39) |
nonsense |
probably null |
|
Leastest
|
UTSW |
11 |
69,638,118 (GRCm39) |
splice site |
probably null |
|
PIT4260001:Polr2a
|
UTSW |
11 |
69,626,793 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0126:Polr2a
|
UTSW |
11 |
69,638,251 (GRCm39) |
missense |
probably damaging |
0.99 |
R0254:Polr2a
|
UTSW |
11 |
69,634,497 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0313:Polr2a
|
UTSW |
11 |
69,625,906 (GRCm39) |
missense |
unknown |
|
R0336:Polr2a
|
UTSW |
11 |
69,627,719 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0453:Polr2a
|
UTSW |
11 |
69,631,845 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0762:Polr2a
|
UTSW |
11 |
69,625,943 (GRCm39) |
missense |
unknown |
|
R1101:Polr2a
|
UTSW |
11 |
69,638,897 (GRCm39) |
missense |
probably benign |
0.23 |
R1509:Polr2a
|
UTSW |
11 |
69,638,039 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1547:Polr2a
|
UTSW |
11 |
69,625,381 (GRCm39) |
missense |
probably benign |
0.39 |
R1567:Polr2a
|
UTSW |
11 |
69,636,857 (GRCm39) |
missense |
probably benign |
0.07 |
R1597:Polr2a
|
UTSW |
11 |
69,630,755 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1614:Polr2a
|
UTSW |
11 |
69,634,199 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1698:Polr2a
|
UTSW |
11 |
69,630,703 (GRCm39) |
critical splice donor site |
probably null |
|
R1735:Polr2a
|
UTSW |
11 |
69,633,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R1743:Polr2a
|
UTSW |
11 |
69,630,329 (GRCm39) |
missense |
probably damaging |
0.96 |
R1899:Polr2a
|
UTSW |
11 |
69,634,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R1900:Polr2a
|
UTSW |
11 |
69,634,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R1931:Polr2a
|
UTSW |
11 |
69,626,201 (GRCm39) |
missense |
unknown |
|
R2217:Polr2a
|
UTSW |
11 |
69,633,511 (GRCm39) |
critical splice donor site |
probably null |
|
R2218:Polr2a
|
UTSW |
11 |
69,633,511 (GRCm39) |
critical splice donor site |
probably null |
|
R2245:Polr2a
|
UTSW |
11 |
69,626,009 (GRCm39) |
missense |
unknown |
|
R3123:Polr2a
|
UTSW |
11 |
69,626,536 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3124:Polr2a
|
UTSW |
11 |
69,626,536 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4018:Polr2a
|
UTSW |
11 |
69,625,885 (GRCm39) |
missense |
unknown |
|
R4025:Polr2a
|
UTSW |
11 |
69,634,485 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4197:Polr2a
|
UTSW |
11 |
69,626,162 (GRCm39) |
missense |
unknown |
|
R4462:Polr2a
|
UTSW |
11 |
69,637,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R4508:Polr2a
|
UTSW |
11 |
69,633,385 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4746:Polr2a
|
UTSW |
11 |
69,626,500 (GRCm39) |
missense |
probably benign |
0.05 |
R5069:Polr2a
|
UTSW |
11 |
69,627,561 (GRCm39) |
splice site |
probably null |
|
R5102:Polr2a
|
UTSW |
11 |
69,637,771 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5195:Polr2a
|
UTSW |
11 |
69,634,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R5234:Polr2a
|
UTSW |
11 |
69,627,666 (GRCm39) |
missense |
probably benign |
0.03 |
R5330:Polr2a
|
UTSW |
11 |
69,638,101 (GRCm39) |
missense |
probably benign |
0.01 |
R5331:Polr2a
|
UTSW |
11 |
69,638,101 (GRCm39) |
missense |
probably benign |
0.01 |
R5896:Polr2a
|
UTSW |
11 |
69,627,086 (GRCm39) |
missense |
probably damaging |
0.99 |
R5910:Polr2a
|
UTSW |
11 |
69,637,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R6128:Polr2a
|
UTSW |
11 |
69,627,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R6238:Polr2a
|
UTSW |
11 |
69,638,047 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6244:Polr2a
|
UTSW |
11 |
69,635,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R6303:Polr2a
|
UTSW |
11 |
69,637,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R6338:Polr2a
|
UTSW |
11 |
69,630,505 (GRCm39) |
splice site |
probably null |
|
R6361:Polr2a
|
UTSW |
11 |
69,634,163 (GRCm39) |
missense |
probably damaging |
0.99 |
R6374:Polr2a
|
UTSW |
11 |
69,627,758 (GRCm39) |
missense |
probably damaging |
0.98 |
R6630:Polr2a
|
UTSW |
11 |
69,626,339 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6631:Polr2a
|
UTSW |
11 |
69,626,339 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6633:Polr2a
|
UTSW |
11 |
69,626,339 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6897:Polr2a
|
UTSW |
11 |
69,626,787 (GRCm39) |
missense |
probably benign |
0.12 |
R6923:Polr2a
|
UTSW |
11 |
69,626,787 (GRCm39) |
missense |
probably benign |
0.12 |
R6933:Polr2a
|
UTSW |
11 |
69,630,293 (GRCm39) |
missense |
probably benign |
0.03 |
R6933:Polr2a
|
UTSW |
11 |
69,627,003 (GRCm39) |
missense |
probably damaging |
0.99 |
R6953:Polr2a
|
UTSW |
11 |
69,632,537 (GRCm39) |
missense |
probably damaging |
0.99 |
R6974:Polr2a
|
UTSW |
11 |
69,638,026 (GRCm39) |
missense |
probably damaging |
0.98 |
R7033:Polr2a
|
UTSW |
11 |
69,638,039 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7085:Polr2a
|
UTSW |
11 |
69,634,706 (GRCm39) |
missense |
probably damaging |
0.99 |
R7124:Polr2a
|
UTSW |
11 |
69,628,288 (GRCm39) |
nonsense |
probably null |
|
R7307:Polr2a
|
UTSW |
11 |
69,638,118 (GRCm39) |
splice site |
probably null |
|
R7319:Polr2a
|
UTSW |
11 |
69,637,196 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7350:Polr2a
|
UTSW |
11 |
69,631,886 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7369:Polr2a
|
UTSW |
11 |
69,636,803 (GRCm39) |
missense |
probably benign |
0.01 |
R7585:Polr2a
|
UTSW |
11 |
69,630,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R7882:Polr2a
|
UTSW |
11 |
69,627,000 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7935:Polr2a
|
UTSW |
11 |
69,638,330 (GRCm39) |
missense |
probably benign |
0.00 |
R8080:Polr2a
|
UTSW |
11 |
69,625,874 (GRCm39) |
missense |
unknown |
|
R8140:Polr2a
|
UTSW |
11 |
69,637,202 (GRCm39) |
missense |
probably benign |
0.12 |
R8221:Polr2a
|
UTSW |
11 |
69,628,344 (GRCm39) |
missense |
probably benign |
0.24 |
R8245:Polr2a
|
UTSW |
11 |
69,630,779 (GRCm39) |
missense |
probably damaging |
0.99 |
R8274:Polr2a
|
UTSW |
11 |
69,638,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R8275:Polr2a
|
UTSW |
11 |
69,638,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R8276:Polr2a
|
UTSW |
11 |
69,638,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R8277:Polr2a
|
UTSW |
11 |
69,638,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R8311:Polr2a
|
UTSW |
11 |
69,628,282 (GRCm39) |
missense |
probably null |
0.20 |
R8477:Polr2a
|
UTSW |
11 |
69,626,312 (GRCm39) |
missense |
probably benign |
0.00 |
R8677:Polr2a
|
UTSW |
11 |
69,626,381 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8976:Polr2a
|
UTSW |
11 |
69,638,037 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9296:Polr2a
|
UTSW |
11 |
69,625,562 (GRCm39) |
missense |
probably benign |
0.39 |
R9659:Polr2a
|
UTSW |
11 |
69,625,654 (GRCm39) |
missense |
unknown |
|
R9731:Polr2a
|
UTSW |
11 |
69,638,043 (GRCm39) |
missense |
possibly damaging |
0.88 |
|