Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
T |
C |
9: 53,325,685 (GRCm39) |
L74S |
probably damaging |
Het |
5730409E04Rik |
A |
G |
4: 126,505,525 (GRCm39) |
S18G |
probably benign |
Het |
Adam29 |
A |
G |
8: 56,325,659 (GRCm39) |
I265T |
probably benign |
Het |
Aff4 |
C |
T |
11: 53,297,466 (GRCm39) |
S896L |
probably benign |
Het |
Ankrd27 |
T |
C |
7: 35,318,822 (GRCm39) |
I571T |
probably damaging |
Het |
Bdp1 |
C |
A |
13: 100,186,478 (GRCm39) |
R1658I |
probably damaging |
Het |
Carm1 |
C |
T |
9: 21,458,323 (GRCm39) |
T7M |
unknown |
Het |
Ccdc183 |
A |
G |
2: 25,506,296 (GRCm39) |
V100A |
probably damaging |
Het |
Cd86 |
CA |
CAA |
16: 36,426,917 (GRCm39) |
|
probably null |
Het |
Ceacam2 |
T |
G |
7: 25,220,341 (GRCm39) |
D239A |
probably benign |
Het |
Cfap96 |
T |
A |
8: 46,423,444 (GRCm39) |
E89D |
possibly damaging |
Het |
Cimap1c |
T |
A |
9: 56,757,262 (GRCm39) |
M139L |
possibly damaging |
Het |
Cmya5 |
T |
C |
13: 93,231,836 (GRCm39) |
D1084G |
probably benign |
Het |
Cog5 |
T |
A |
12: 31,810,888 (GRCm39) |
I194K |
probably damaging |
Het |
Col20a1 |
C |
T |
2: 180,636,007 (GRCm39) |
Q211* |
probably null |
Het |
Col9a1 |
T |
A |
1: 24,234,498 (GRCm39) |
L13Q |
unknown |
Het |
Cracr2a |
A |
T |
6: 127,585,669 (GRCm39) |
M156L |
probably benign |
Het |
Cts8 |
C |
T |
13: 61,399,505 (GRCm39) |
M151I |
possibly damaging |
Het |
Cyp2ab1 |
A |
T |
16: 20,135,469 (GRCm39) |
L11Q |
probably null |
Het |
Dhrs13 |
T |
A |
11: 77,925,208 (GRCm39) |
C160S |
probably benign |
Het |
Enthd1 |
T |
A |
15: 80,358,415 (GRCm39) |
E368D |
probably damaging |
Het |
Fbh1 |
A |
G |
2: 11,760,522 (GRCm39) |
I676T |
probably damaging |
Het |
Fcgrt |
T |
C |
7: 44,751,421 (GRCm39) |
R176G |
probably benign |
Het |
Gatd1 |
A |
G |
7: 140,990,947 (GRCm39) |
F67L |
possibly damaging |
Het |
Gm4353 |
G |
A |
7: 115,683,727 (GRCm39) |
P23S |
probably damaging |
Het |
Gm6882 |
T |
A |
7: 21,161,677 (GRCm39) |
I64F |
possibly damaging |
Het |
Grwd1 |
A |
T |
7: 45,480,204 (GRCm39) |
M1K |
probably null |
Het |
Hook2 |
T |
A |
8: 85,718,046 (GRCm39) |
S58T |
probably benign |
Het |
Iqch |
T |
G |
9: 63,329,117 (GRCm39) |
*1072C |
probably null |
Het |
Kmt2d |
G |
A |
15: 98,748,267 (GRCm39) |
T3019I |
unknown |
Het |
Lmx1a |
T |
C |
1: 167,674,247 (GRCm39) |
S356P |
probably benign |
Het |
Lrig3 |
A |
G |
10: 125,842,712 (GRCm39) |
M546V |
probably benign |
Het |
Lrrc1 |
C |
A |
9: 77,379,504 (GRCm39) |
E96* |
probably null |
Het |
Lrtm2 |
C |
A |
6: 119,294,113 (GRCm39) |
M339I |
probably damaging |
Het |
Map10 |
T |
C |
8: 126,398,584 (GRCm39) |
V659A |
probably benign |
Het |
Map7d1 |
A |
G |
4: 126,130,778 (GRCm39) |
C384R |
probably damaging |
Het |
Mcur1 |
T |
C |
13: 43,698,012 (GRCm39) |
D296G |
probably damaging |
Het |
Mettl24 |
A |
T |
10: 40,686,508 (GRCm39) |
H295L |
probably damaging |
Het |
Mgat4f |
T |
C |
1: 134,318,163 (GRCm39) |
S312P |
probably benign |
Het |
Mpl |
A |
G |
4: 118,305,741 (GRCm39) |
|
probably null |
Het |
Mrps5 |
T |
C |
2: 127,437,617 (GRCm39) |
V148A |
probably benign |
Het |
N4bp2 |
T |
C |
5: 65,964,891 (GRCm39) |
V980A |
probably damaging |
Het |
Ncaph |
A |
T |
2: 126,958,506 (GRCm39) |
D504E |
probably damaging |
Het |
Nxph1 |
A |
G |
6: 9,247,497 (GRCm39) |
N156S |
probably damaging |
Het |
Or2t26 |
T |
A |
11: 49,040,012 (GRCm39) |
C309* |
probably null |
Het |
Or4f14b |
T |
A |
2: 111,775,501 (GRCm39) |
Q100L |
probably damaging |
Het |
Pafah1b3 |
T |
A |
7: 24,994,657 (GRCm39) |
I186L |
probably benign |
Het |
Papola |
C |
A |
12: 105,775,790 (GRCm39) |
N235K |
possibly damaging |
Het |
Pcnx3 |
A |
T |
19: 5,737,527 (GRCm39) |
M98K |
probably benign |
Het |
Pip4p1 |
A |
C |
14: 51,167,634 (GRCm39) |
M104R |
possibly damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,330,800 (GRCm39) |
N125S |
probably damaging |
Het |
Pls1 |
T |
A |
9: 95,655,612 (GRCm39) |
H380L |
probably benign |
Het |
Plxna1 |
T |
C |
6: 89,300,311 (GRCm39) |
T1591A |
possibly damaging |
Het |
Pparg |
T |
G |
6: 115,418,581 (GRCm39) |
S147A |
probably benign |
Het |
Prdm10 |
T |
C |
9: 31,279,003 (GRCm39) |
S1025P |
probably benign |
Het |
Prkcd |
T |
A |
14: 30,321,664 (GRCm39) |
H510L |
probably damaging |
Het |
Ptprh |
T |
A |
7: 4,572,480 (GRCm39) |
E499D |
possibly damaging |
Het |
Rad51ap1 |
A |
G |
6: 126,901,983 (GRCm39) |
S256P |
probably benign |
Het |
Rnf207 |
A |
G |
4: 152,396,634 (GRCm39) |
I459T |
probably benign |
Het |
Runx2 |
G |
A |
17: 45,125,079 (GRCm39) |
P80L |
probably damaging |
Het |
Ryr3 |
A |
T |
2: 112,731,188 (GRCm39) |
D727E |
probably damaging |
Het |
Sdk2 |
C |
T |
11: 113,720,795 (GRCm39) |
R1378H |
possibly damaging |
Het |
Slc7a11 |
A |
G |
3: 50,397,680 (GRCm39) |
S11P |
probably benign |
Het |
Sox4 |
A |
G |
13: 29,137,000 (GRCm39) |
V2A |
probably damaging |
Het |
Srf |
A |
G |
17: 46,866,318 (GRCm39) |
F146S |
probably damaging |
Het |
Srrm2 |
T |
C |
17: 24,035,747 (GRCm39) |
V797A |
unknown |
Het |
Stk32c |
T |
C |
7: 138,684,218 (GRCm39) |
D463G |
possibly damaging |
Het |
Syne2 |
C |
A |
12: 76,018,654 (GRCm39) |
Y3384* |
probably null |
Het |
Tektl1 |
T |
C |
10: 78,588,324 (GRCm39) |
D162G |
probably damaging |
Het |
Traip |
T |
A |
9: 107,838,184 (GRCm39) |
M139K |
possibly damaging |
Het |
Trappc2l |
T |
A |
8: 123,341,051 (GRCm39) |
F100Y |
probably damaging |
Het |
Ush1c |
T |
C |
7: 45,878,643 (GRCm39) |
D124G |
probably damaging |
Het |
Uty |
A |
G |
Y: 1,099,691 (GRCm39) |
V1168A |
probably benign |
Het |
Vmn2r25 |
T |
C |
6: 123,816,882 (GRCm39) |
D233G |
possibly damaging |
Het |
Zdbf2 |
C |
T |
1: 63,334,120 (GRCm39) |
R31C |
possibly damaging |
Het |
|
Other mutations in Rad54b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00770:Rad54b
|
APN |
4 |
11,593,765 (GRCm39) |
missense |
probably benign |
|
IGL00774:Rad54b
|
APN |
4 |
11,593,765 (GRCm39) |
missense |
probably benign |
|
IGL00956:Rad54b
|
APN |
4 |
11,597,833 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00961:Rad54b
|
APN |
4 |
11,599,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01064:Rad54b
|
APN |
4 |
11,604,866 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02150:Rad54b
|
APN |
4 |
11,610,502 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02326:Rad54b
|
APN |
4 |
11,612,713 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03105:Rad54b
|
APN |
4 |
11,615,569 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03143:Rad54b
|
APN |
4 |
11,599,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03288:Rad54b
|
APN |
4 |
11,569,833 (GRCm39) |
missense |
possibly damaging |
0.83 |
kerplunk
|
UTSW |
4 |
11,612,655 (GRCm39) |
missense |
probably damaging |
1.00 |
Schnipfel
|
UTSW |
4 |
11,583,689 (GRCm39) |
unclassified |
probably benign |
|
P0033:Rad54b
|
UTSW |
4 |
11,609,285 (GRCm39) |
unclassified |
probably benign |
|
R0076:Rad54b
|
UTSW |
4 |
11,609,480 (GRCm39) |
unclassified |
probably benign |
|
R0094:Rad54b
|
UTSW |
4 |
11,599,681 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0391:Rad54b
|
UTSW |
4 |
11,601,702 (GRCm39) |
missense |
probably damaging |
0.98 |
R0441:Rad54b
|
UTSW |
4 |
11,563,394 (GRCm39) |
missense |
probably benign |
0.08 |
R0442:Rad54b
|
UTSW |
4 |
11,610,362 (GRCm39) |
missense |
probably benign |
0.02 |
R0442:Rad54b
|
UTSW |
4 |
11,609,480 (GRCm39) |
unclassified |
probably benign |
|
R0449:Rad54b
|
UTSW |
4 |
11,606,131 (GRCm39) |
missense |
probably benign |
0.43 |
R0519:Rad54b
|
UTSW |
4 |
11,599,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R0843:Rad54b
|
UTSW |
4 |
11,609,471 (GRCm39) |
critical splice donor site |
probably null |
|
R1118:Rad54b
|
UTSW |
4 |
11,563,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R1439:Rad54b
|
UTSW |
4 |
11,606,152 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1763:Rad54b
|
UTSW |
4 |
11,604,989 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1812:Rad54b
|
UTSW |
4 |
11,612,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R1854:Rad54b
|
UTSW |
4 |
11,601,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Rad54b
|
UTSW |
4 |
11,601,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R1918:Rad54b
|
UTSW |
4 |
11,601,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Rad54b
|
UTSW |
4 |
11,601,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R2057:Rad54b
|
UTSW |
4 |
11,606,088 (GRCm39) |
missense |
probably benign |
0.08 |
R2386:Rad54b
|
UTSW |
4 |
11,597,874 (GRCm39) |
missense |
probably benign |
|
R2437:Rad54b
|
UTSW |
4 |
11,606,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R4299:Rad54b
|
UTSW |
4 |
11,597,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R4391:Rad54b
|
UTSW |
4 |
11,615,570 (GRCm39) |
missense |
probably benign |
0.00 |
R4672:Rad54b
|
UTSW |
4 |
11,609,449 (GRCm39) |
missense |
probably benign |
0.05 |
R4673:Rad54b
|
UTSW |
4 |
11,609,449 (GRCm39) |
missense |
probably benign |
0.05 |
R4826:Rad54b
|
UTSW |
4 |
11,599,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R4930:Rad54b
|
UTSW |
4 |
11,615,579 (GRCm39) |
missense |
probably damaging |
0.99 |
R5796:Rad54b
|
UTSW |
4 |
11,615,446 (GRCm39) |
missense |
probably benign |
0.01 |
R5901:Rad54b
|
UTSW |
4 |
11,595,919 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6185:Rad54b
|
UTSW |
4 |
11,593,804 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6355:Rad54b
|
UTSW |
4 |
11,604,989 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6576:Rad54b
|
UTSW |
4 |
11,601,577 (GRCm39) |
missense |
probably benign |
|
R6684:Rad54b
|
UTSW |
4 |
11,583,689 (GRCm39) |
unclassified |
probably benign |
|
R6821:Rad54b
|
UTSW |
4 |
11,612,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R6947:Rad54b
|
UTSW |
4 |
11,569,859 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7361:Rad54b
|
UTSW |
4 |
11,599,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R7483:Rad54b
|
UTSW |
4 |
11,610,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R7511:Rad54b
|
UTSW |
4 |
11,578,956 (GRCm39) |
splice site |
probably null |
|
R7847:Rad54b
|
UTSW |
4 |
11,612,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R7908:Rad54b
|
UTSW |
4 |
11,595,868 (GRCm39) |
missense |
probably null |
0.01 |
R8198:Rad54b
|
UTSW |
4 |
11,612,440 (GRCm39) |
critical splice donor site |
probably null |
|
R9140:Rad54b
|
UTSW |
4 |
11,610,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R9213:Rad54b
|
UTSW |
4 |
11,609,321 (GRCm39) |
nonsense |
probably null |
|
|