Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610028H24Rik |
A |
C |
10: 76,285,096 (GRCm39) |
T2P |
possibly damaging |
Het |
2610042L04Rik |
A |
G |
14: 4,348,962 (GRCm38) |
N41S |
probably damaging |
Het |
4933402N03Rik |
T |
C |
7: 130,747,863 (GRCm39) |
D43G |
probably benign |
Het |
Adcy10 |
C |
A |
1: 165,403,297 (GRCm39) |
Y1598* |
probably null |
Het |
Adgrv1 |
G |
A |
13: 81,614,402 (GRCm39) |
T3997M |
probably benign |
Het |
Amfr |
A |
C |
8: 94,726,992 (GRCm39) |
F74V |
probably damaging |
Het |
Ankrd13a |
T |
C |
5: 114,924,787 (GRCm39) |
Y91H |
probably benign |
Het |
Baiap3 |
A |
G |
17: 25,464,732 (GRCm39) |
S767P |
probably benign |
Het |
Car12 |
C |
T |
9: 66,661,008 (GRCm39) |
T124I |
probably damaging |
Het |
Casp9 |
G |
T |
4: 141,534,448 (GRCm39) |
G286V |
probably damaging |
Het |
Cc2d2a |
T |
A |
5: 43,828,577 (GRCm39) |
D18E |
probably benign |
Het |
Cdc27 |
T |
C |
11: 104,419,270 (GRCm39) |
N221D |
probably damaging |
Het |
Cebpz |
A |
G |
17: 79,244,339 (GRCm39) |
S41P |
possibly damaging |
Het |
Cenpo |
T |
A |
12: 4,281,968 (GRCm39) |
S10C |
possibly damaging |
Het |
Chid1 |
A |
G |
7: 141,076,049 (GRCm39) |
V368A |
probably benign |
Het |
Clca3a1 |
C |
A |
3: 144,714,716 (GRCm39) |
V634L |
probably benign |
Het |
Cmtr1 |
A |
G |
17: 29,901,122 (GRCm39) |
D683G |
probably damaging |
Het |
Cpsf3 |
G |
T |
12: 21,350,163 (GRCm39) |
R294L |
probably damaging |
Het |
Ddrgk1 |
G |
A |
2: 130,496,599 (GRCm39) |
T255M |
possibly damaging |
Het |
Dennd6a |
T |
A |
14: 26,337,813 (GRCm39) |
|
probably null |
Het |
Dnah10 |
A |
G |
5: 124,820,743 (GRCm39) |
R526G |
probably damaging |
Het |
Dock3 |
G |
A |
9: 106,790,147 (GRCm39) |
T1484I |
probably benign |
Het |
Efcab10 |
T |
C |
12: 33,448,433 (GRCm39) |
Y89H |
probably damaging |
Het |
Etl4 |
T |
A |
2: 20,806,379 (GRCm39) |
D1200E |
probably damaging |
Het |
Fbn1 |
T |
A |
2: 125,166,865 (GRCm39) |
D2017V |
probably damaging |
Het |
Ftmt |
G |
A |
18: 52,465,307 (GRCm39) |
V208M |
probably damaging |
Het |
Fzd10 |
T |
C |
5: 128,679,995 (GRCm39) |
Y572H |
probably damaging |
Het |
Gcc1 |
T |
C |
6: 28,420,742 (GRCm39) |
K39E |
probably damaging |
Het |
Hydin |
A |
G |
8: 111,118,743 (GRCm39) |
|
probably null |
Het |
Lif |
A |
G |
11: 4,218,940 (GRCm39) |
E73G |
possibly damaging |
Het |
Lrtm1 |
C |
A |
14: 28,749,628 (GRCm39) |
Q357K |
probably benign |
Het |
Mef2d |
T |
A |
3: 88,066,852 (GRCm39) |
L205Q |
probably damaging |
Het |
Naalad2 |
T |
A |
9: 18,296,361 (GRCm39) |
E96D |
probably damaging |
Het |
Nbas |
T |
C |
12: 13,532,596 (GRCm39) |
I1768T |
probably benign |
Het |
Nodal |
T |
C |
10: 61,259,258 (GRCm39) |
S232P |
probably damaging |
Het |
Or52ab7 |
A |
T |
7: 102,978,115 (GRCm39) |
I141F |
possibly damaging |
Het |
Or8b12c |
A |
G |
9: 37,715,317 (GRCm39) |
T37A |
probably benign |
Het |
Parl |
G |
A |
16: 20,120,963 (GRCm39) |
R39C |
possibly damaging |
Het |
Pcdha9 |
G |
A |
18: 37,132,028 (GRCm39) |
V366I |
probably benign |
Het |
Pdzd8 |
A |
G |
19: 59,288,994 (GRCm39) |
V802A |
probably benign |
Het |
Plcl2 |
T |
C |
17: 50,913,873 (GRCm39) |
V294A |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,472,504 (GRCm39) |
S1083T |
probably benign |
Het |
Ptpre |
C |
A |
7: 135,272,909 (GRCm39) |
R468S |
probably damaging |
Het |
Raet1e |
T |
A |
10: 22,056,770 (GRCm39) |
N115K |
probably benign |
Het |
Rfx8 |
C |
A |
1: 39,709,554 (GRCm39) |
S491I |
probably damaging |
Het |
Rpe |
T |
A |
1: 66,740,807 (GRCm39) |
L48* |
probably null |
Het |
Skint5 |
A |
T |
4: 113,800,064 (GRCm39) |
|
probably null |
Het |
Spata24 |
C |
A |
18: 35,793,389 (GRCm39) |
S111I |
possibly damaging |
Het |
Suz12 |
G |
C |
11: 79,893,006 (GRCm39) |
|
probably benign |
Het |
Taf4 |
T |
A |
2: 179,573,832 (GRCm39) |
I679F |
probably damaging |
Het |
Tlr1 |
G |
T |
5: 65,084,472 (GRCm39) |
P35Q |
possibly damaging |
Het |
Tonsl |
T |
C |
15: 76,520,418 (GRCm39) |
|
probably null |
Het |
Tsen54 |
G |
A |
11: 115,711,513 (GRCm39) |
R310H |
probably benign |
Het |
Ttc7b |
A |
G |
12: 100,461,681 (GRCm39) |
S99P |
probably benign |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Uhmk1 |
T |
A |
1: 170,027,563 (GRCm39) |
N378I |
probably damaging |
Het |
Vmn2r107 |
A |
G |
17: 20,565,849 (GRCm39) |
T55A |
probably benign |
Het |
Vmn2r74 |
C |
T |
7: 85,601,280 (GRCm39) |
C786Y |
probably damaging |
Het |
Wdr20rt |
C |
T |
12: 65,272,964 (GRCm39) |
|
probably benign |
Het |
Zfand2a |
T |
A |
5: 139,467,746 (GRCm39) |
H42L |
probably damaging |
Het |
Zfp990 |
T |
A |
4: 145,264,483 (GRCm39) |
C494S |
probably damaging |
Het |
Zkscan4 |
A |
T |
13: 21,668,757 (GRCm39) |
R403W |
possibly damaging |
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 |
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 |
R7112:Polr2a
|
UTSW |
11 |
69,626,135 (GRCm39) |
missense |
unknown |
|
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 |
|