Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd55 |
T |
G |
13: 112,459,677 (GRCm39) |
D90E |
probably damaging |
Het |
Arid1b |
C |
A |
17: 5,045,584 (GRCm39) |
P124Q |
unknown |
Het |
Atxn2 |
C |
T |
5: 121,923,425 (GRCm39) |
P698L |
probably damaging |
Het |
Bend7 |
T |
C |
2: 4,757,531 (GRCm39) |
V191A |
probably benign |
Het |
Bltp1 |
G |
A |
3: 37,104,989 (GRCm39) |
D1485N |
|
Het |
C2cd4a |
T |
G |
9: 67,738,779 (GRCm39) |
H88P |
probably damaging |
Het |
Cacna1s |
C |
T |
1: 136,020,452 (GRCm39) |
Q830* |
probably null |
Het |
Camta1 |
T |
C |
4: 151,228,474 (GRCm39) |
E786G |
possibly damaging |
Het |
Caprin1 |
A |
G |
2: 103,603,390 (GRCm39) |
S443P |
probably benign |
Het |
Cass4 |
T |
G |
2: 172,269,806 (GRCm39) |
F629L |
probably benign |
Het |
Ccdc149 |
T |
A |
5: 52,562,399 (GRCm39) |
D209V |
probably damaging |
Het |
Ccdc150 |
T |
C |
1: 54,316,910 (GRCm39) |
V263A |
probably damaging |
Het |
Cfc1 |
C |
T |
1: 34,576,453 (GRCm39) |
R145C |
probably damaging |
Het |
Cnn1 |
C |
A |
9: 22,019,350 (GRCm39) |
D239E |
probably damaging |
Het |
Cobll1 |
C |
T |
2: 64,933,516 (GRCm39) |
S493N |
probably benign |
Het |
Cox20 |
A |
T |
1: 178,146,771 (GRCm39) |
K13* |
probably null |
Het |
Dclk1 |
G |
A |
3: 55,370,500 (GRCm39) |
S340N |
probably damaging |
Het |
Dennd2c |
T |
A |
3: 103,038,877 (GRCm39) |
D8E |
probably benign |
Het |
Dnajc10 |
A |
T |
2: 80,175,327 (GRCm39) |
K571N |
probably benign |
Het |
Dock7 |
T |
A |
4: 98,896,280 (GRCm39) |
I58F |
|
Het |
Dpy19l4 |
A |
G |
4: 11,304,298 (GRCm39) |
|
probably null |
Het |
Eef2k |
A |
G |
7: 120,483,918 (GRCm39) |
D218G |
probably benign |
Het |
Eya4 |
G |
T |
10: 22,989,845 (GRCm39) |
T504K |
probably damaging |
Het |
Fam222a |
T |
C |
5: 114,749,398 (GRCm39) |
I198T |
probably damaging |
Het |
Fbxw10 |
T |
A |
11: 62,748,585 (GRCm39) |
F404Y |
probably benign |
Het |
Fbxw24 |
A |
T |
9: 109,452,681 (GRCm39) |
Y105N |
probably damaging |
Het |
Fzd10 |
T |
G |
5: 128,678,316 (GRCm39) |
L12R |
possibly damaging |
Het |
Gm14443 |
A |
G |
2: 175,017,610 (GRCm39) |
|
probably benign |
Het |
Gm21028 |
A |
T |
7: 42,227,904 (GRCm39) |
C37S |
probably damaging |
Het |
Gpr179 |
G |
T |
11: 97,229,551 (GRCm39) |
A868E |
probably damaging |
Het |
Grid1 |
A |
T |
14: 35,045,360 (GRCm39) |
Y401F |
probably benign |
Het |
Heatr5a |
G |
A |
12: 51,946,068 (GRCm39) |
T1181I |
probably benign |
Het |
Herc4 |
G |
A |
10: 63,144,125 (GRCm39) |
V753I |
probably damaging |
Het |
Htra1 |
A |
T |
7: 130,563,851 (GRCm39) |
K241* |
probably null |
Het |
Kat6b |
A |
G |
14: 21,720,093 (GRCm39) |
I1482V |
probably benign |
Het |
Kif19a |
G |
T |
11: 114,680,033 (GRCm39) |
R790L |
possibly damaging |
Het |
Lmf2 |
G |
A |
15: 89,239,577 (GRCm39) |
L26F |
probably damaging |
Het |
Lpcat1 |
T |
C |
13: 73,659,462 (GRCm39) |
L408S |
probably damaging |
Het |
Lrrc69 |
T |
A |
4: 14,774,987 (GRCm39) |
R94W |
probably damaging |
Het |
Map4 |
A |
G |
9: 109,864,223 (GRCm39) |
T483A |
probably benign |
Het |
Mettl3 |
C |
A |
14: 52,534,125 (GRCm39) |
C483F |
probably damaging |
Het |
Myh13 |
A |
G |
11: 67,254,109 (GRCm39) |
D1543G |
possibly damaging |
Het |
Myh2 |
G |
A |
11: 67,070,209 (GRCm39) |
V414I |
probably damaging |
Het |
Myh7b |
C |
T |
2: 155,470,722 (GRCm39) |
R1057C |
probably damaging |
Het |
Myo9b |
A |
G |
8: 71,812,246 (GRCm39) |
S2006G |
probably benign |
Het |
Nelfcd |
A |
G |
2: 174,264,978 (GRCm39) |
K239R |
probably benign |
Het |
Nlrp4a |
T |
C |
7: 26,159,077 (GRCm39) |
S786P |
probably damaging |
Het |
Or5g23 |
T |
A |
2: 85,438,331 (GRCm39) |
K308* |
probably null |
Het |
Or6c205 |
A |
G |
10: 129,086,972 (GRCm39) |
T190A |
probably damaging |
Het |
Pdzrn4 |
G |
T |
15: 92,295,216 (GRCm39) |
V141L |
probably benign |
Het |
Phip |
G |
T |
9: 82,757,412 (GRCm39) |
R1587S |
probably damaging |
Het |
Plce1 |
A |
G |
19: 38,726,377 (GRCm39) |
E1448G |
probably damaging |
Het |
Plrg1 |
T |
C |
3: 82,976,308 (GRCm39) |
S326P |
possibly damaging |
Het |
Pom121l2 |
T |
A |
13: 22,165,852 (GRCm39) |
V41E |
probably damaging |
Het |
Pramel17 |
C |
T |
4: 101,695,144 (GRCm39) |
V56M |
probably damaging |
Het |
Preb |
G |
T |
5: 31,113,673 (GRCm39) |
S311* |
probably null |
Het |
Prss33 |
T |
A |
17: 24,053,723 (GRCm39) |
D118V |
probably damaging |
Het |
Pum1 |
C |
A |
4: 130,499,209 (GRCm39) |
Y1008* |
probably null |
Het |
Rassf2 |
G |
A |
2: 131,846,326 (GRCm39) |
R144C |
probably damaging |
Het |
Rnf123 |
A |
T |
9: 107,944,704 (GRCm39) |
M429K |
probably benign |
Het |
Rtl1 |
T |
A |
12: 109,557,291 (GRCm39) |
H1516L |
probably benign |
Het |
Scyl3 |
T |
A |
1: 163,764,007 (GRCm39) |
N124K |
probably damaging |
Het |
Sec24b |
A |
G |
3: 129,801,220 (GRCm39) |
S488P |
probably benign |
Het |
Shc4 |
T |
A |
2: 125,520,618 (GRCm39) |
D277V |
probably damaging |
Het |
Sorl1 |
T |
A |
9: 41,912,814 (GRCm39) |
D1389V |
probably damaging |
Het |
Srcap |
T |
A |
7: 127,158,812 (GRCm39) |
I2896N |
unknown |
Het |
Steap3 |
T |
A |
1: 120,155,564 (GRCm39) |
Y465F |
probably benign |
Het |
Tecta |
C |
A |
9: 42,284,193 (GRCm39) |
C964F |
probably damaging |
Het |
Thap1 |
AGCAGCATCTGCTCG |
AG |
8: 26,650,882 (GRCm39) |
|
probably null |
Het |
Thap1 |
CAGCATCTGCTCGGAGCA |
CAGCA |
8: 26,650,884 (GRCm39) |
|
probably null |
Het |
Tmem178b |
G |
A |
6: 39,981,181 (GRCm39) |
W72* |
probably null |
Het |
Tmem235 |
T |
G |
11: 117,751,665 (GRCm39) |
Y30D |
probably damaging |
Het |
Tpst1 |
C |
A |
5: 130,163,301 (GRCm39) |
T366K |
probably benign |
Het |
Trdv2-1 |
C |
A |
14: 54,183,848 (GRCm39) |
P27T |
probably benign |
Het |
Trim37 |
G |
T |
11: 87,058,328 (GRCm39) |
L335F |
possibly damaging |
Het |
Usp9y |
G |
A |
Y: 1,341,873 (GRCm39) |
R1331W |
probably damaging |
Het |
Vmn1r1 |
T |
G |
1: 181,985,002 (GRCm39) |
H221P |
probably damaging |
Het |
Vmn2r6 |
A |
T |
3: 64,454,671 (GRCm39) |
S543T |
probably benign |
Het |
Wdpcp |
C |
T |
11: 21,661,522 (GRCm39) |
P265S |
probably benign |
Het |
Wdr64 |
T |
C |
1: 175,599,871 (GRCm39) |
L566P |
possibly damaging |
Het |
Zfp248 |
A |
G |
6: 118,405,891 (GRCm39) |
I566T |
possibly damaging |
Het |
Zfp595 |
T |
A |
13: 67,465,463 (GRCm39) |
I270F |
probably damaging |
Het |
Zfp715 |
A |
G |
7: 42,948,847 (GRCm39) |
L371P |
probably damaging |
Het |
|
Other mutations in Greb1l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00485:Greb1l
|
APN |
18 |
10,555,962 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01554:Greb1l
|
APN |
18 |
10,522,144 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01563:Greb1l
|
APN |
18 |
10,469,399 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01944:Greb1l
|
APN |
18 |
10,557,280 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02110:Greb1l
|
APN |
18 |
10,515,271 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02249:Greb1l
|
APN |
18 |
10,532,961 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02318:Greb1l
|
APN |
18 |
10,469,388 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02340:Greb1l
|
APN |
18 |
10,515,200 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02516:Greb1l
|
APN |
18 |
10,537,064 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02566:Greb1l
|
APN |
18 |
10,503,299 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02583:Greb1l
|
APN |
18 |
10,542,362 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02838:Greb1l
|
APN |
18 |
10,560,430 (GRCm39) |
missense |
probably damaging |
1.00 |
A4554:Greb1l
|
UTSW |
18 |
10,532,862 (GRCm39) |
missense |
possibly damaging |
0.58 |
PIT4453001:Greb1l
|
UTSW |
18 |
10,533,032 (GRCm39) |
missense |
probably benign |
0.08 |
PIT4453001:Greb1l
|
UTSW |
18 |
10,533,031 (GRCm39) |
missense |
probably damaging |
0.98 |
R0099:Greb1l
|
UTSW |
18 |
10,509,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Greb1l
|
UTSW |
18 |
10,522,076 (GRCm39) |
intron |
probably benign |
|
R0234:Greb1l
|
UTSW |
18 |
10,560,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Greb1l
|
UTSW |
18 |
10,560,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Greb1l
|
UTSW |
18 |
10,458,567 (GRCm39) |
splice site |
probably benign |
|
R0316:Greb1l
|
UTSW |
18 |
10,547,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R0369:Greb1l
|
UTSW |
18 |
10,469,375 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0394:Greb1l
|
UTSW |
18 |
10,523,374 (GRCm39) |
missense |
probably damaging |
0.99 |
R0478:Greb1l
|
UTSW |
18 |
10,509,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R0555:Greb1l
|
UTSW |
18 |
10,458,781 (GRCm39) |
splice site |
probably benign |
|
R0671:Greb1l
|
UTSW |
18 |
10,474,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R1282:Greb1l
|
UTSW |
18 |
10,547,289 (GRCm39) |
missense |
probably benign |
0.13 |
R1574:Greb1l
|
UTSW |
18 |
10,554,997 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1574:Greb1l
|
UTSW |
18 |
10,554,997 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1607:Greb1l
|
UTSW |
18 |
10,529,703 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1666:Greb1l
|
UTSW |
18 |
10,529,708 (GRCm39) |
critical splice donor site |
probably null |
|
R1666:Greb1l
|
UTSW |
18 |
10,501,080 (GRCm39) |
critical splice donor site |
probably null |
|
R1720:Greb1l
|
UTSW |
18 |
10,553,848 (GRCm39) |
missense |
probably benign |
0.19 |
R1808:Greb1l
|
UTSW |
18 |
10,542,143 (GRCm39) |
missense |
probably benign |
|
R1829:Greb1l
|
UTSW |
18 |
10,509,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R1897:Greb1l
|
UTSW |
18 |
10,498,992 (GRCm39) |
missense |
probably benign |
0.00 |
R1967:Greb1l
|
UTSW |
18 |
10,501,049 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2025:Greb1l
|
UTSW |
18 |
10,515,221 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2086:Greb1l
|
UTSW |
18 |
10,523,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Greb1l
|
UTSW |
18 |
10,511,422 (GRCm39) |
missense |
probably damaging |
0.98 |
R2139:Greb1l
|
UTSW |
18 |
10,555,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R2255:Greb1l
|
UTSW |
18 |
10,554,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R2256:Greb1l
|
UTSW |
18 |
10,503,307 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2257:Greb1l
|
UTSW |
18 |
10,503,307 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2880:Greb1l
|
UTSW |
18 |
10,547,288 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3623:Greb1l
|
UTSW |
18 |
10,542,380 (GRCm39) |
missense |
probably damaging |
0.99 |
R3778:Greb1l
|
UTSW |
18 |
10,469,444 (GRCm39) |
missense |
possibly damaging |
0.60 |
R3975:Greb1l
|
UTSW |
18 |
10,522,247 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4038:Greb1l
|
UTSW |
18 |
10,515,209 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4062:Greb1l
|
UTSW |
18 |
10,522,150 (GRCm39) |
missense |
probably damaging |
0.99 |
R4134:Greb1l
|
UTSW |
18 |
10,529,708 (GRCm39) |
critical splice donor site |
probably null |
|
R4342:Greb1l
|
UTSW |
18 |
10,544,561 (GRCm39) |
missense |
probably benign |
0.12 |
R4409:Greb1l
|
UTSW |
18 |
10,503,182 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4600:Greb1l
|
UTSW |
18 |
10,553,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R4618:Greb1l
|
UTSW |
18 |
10,498,965 (GRCm39) |
missense |
probably benign |
0.00 |
R4683:Greb1l
|
UTSW |
18 |
10,529,563 (GRCm39) |
splice site |
probably null |
|
R4686:Greb1l
|
UTSW |
18 |
10,522,112 (GRCm39) |
missense |
probably damaging |
0.98 |
R4707:Greb1l
|
UTSW |
18 |
10,532,922 (GRCm39) |
missense |
probably benign |
0.02 |
R4780:Greb1l
|
UTSW |
18 |
10,541,792 (GRCm39) |
missense |
probably benign |
0.00 |
R4819:Greb1l
|
UTSW |
18 |
10,458,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R4925:Greb1l
|
UTSW |
18 |
10,547,447 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4960:Greb1l
|
UTSW |
18 |
10,547,306 (GRCm39) |
missense |
probably damaging |
0.99 |
R5150:Greb1l
|
UTSW |
18 |
10,555,950 (GRCm39) |
frame shift |
probably null |
|
R5154:Greb1l
|
UTSW |
18 |
10,458,312 (GRCm39) |
missense |
probably benign |
0.02 |
R5269:Greb1l
|
UTSW |
18 |
10,511,409 (GRCm39) |
missense |
probably benign |
|
R5290:Greb1l
|
UTSW |
18 |
10,542,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5310:Greb1l
|
UTSW |
18 |
10,542,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Greb1l
|
UTSW |
18 |
10,553,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R5337:Greb1l
|
UTSW |
18 |
10,509,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R5393:Greb1l
|
UTSW |
18 |
10,458,312 (GRCm39) |
missense |
probably benign |
0.02 |
R5402:Greb1l
|
UTSW |
18 |
10,537,169 (GRCm39) |
missense |
probably benign |
0.26 |
R5718:Greb1l
|
UTSW |
18 |
10,542,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5719:Greb1l
|
UTSW |
18 |
10,542,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5720:Greb1l
|
UTSW |
18 |
10,542,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5721:Greb1l
|
UTSW |
18 |
10,542,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5902:Greb1l
|
UTSW |
18 |
10,538,302 (GRCm39) |
missense |
probably benign |
0.00 |
R5993:Greb1l
|
UTSW |
18 |
10,544,455 (GRCm39) |
missense |
probably benign |
0.10 |
R6035:Greb1l
|
UTSW |
18 |
10,501,025 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6035:Greb1l
|
UTSW |
18 |
10,501,025 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6045:Greb1l
|
UTSW |
18 |
10,547,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R6063:Greb1l
|
UTSW |
18 |
10,557,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R6297:Greb1l
|
UTSW |
18 |
10,469,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R6405:Greb1l
|
UTSW |
18 |
10,501,076 (GRCm39) |
missense |
probably benign |
0.30 |
R6552:Greb1l
|
UTSW |
18 |
10,541,814 (GRCm39) |
missense |
probably benign |
0.00 |
R6572:Greb1l
|
UTSW |
18 |
10,522,131 (GRCm39) |
missense |
probably benign |
0.07 |
R6575:Greb1l
|
UTSW |
18 |
10,547,347 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6922:Greb1l
|
UTSW |
18 |
10,547,482 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6957:Greb1l
|
UTSW |
18 |
10,558,786 (GRCm39) |
missense |
probably benign |
0.23 |
R6962:Greb1l
|
UTSW |
18 |
10,547,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R7012:Greb1l
|
UTSW |
18 |
10,529,707 (GRCm39) |
critical splice donor site |
probably null |
|
R7179:Greb1l
|
UTSW |
18 |
10,544,576 (GRCm39) |
missense |
probably benign |
0.00 |
R7251:Greb1l
|
UTSW |
18 |
10,515,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R7275:Greb1l
|
UTSW |
18 |
10,544,561 (GRCm39) |
missense |
probably benign |
0.12 |
R7301:Greb1l
|
UTSW |
18 |
10,544,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R7307:Greb1l
|
UTSW |
18 |
10,538,142 (GRCm39) |
missense |
probably damaging |
0.99 |
R7455:Greb1l
|
UTSW |
18 |
10,554,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R7832:Greb1l
|
UTSW |
18 |
10,542,056 (GRCm39) |
missense |
probably benign |
0.38 |
R7934:Greb1l
|
UTSW |
18 |
10,474,371 (GRCm39) |
nonsense |
probably null |
|
R8137:Greb1l
|
UTSW |
18 |
10,474,357 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8138:Greb1l
|
UTSW |
18 |
10,533,060 (GRCm39) |
missense |
probably benign |
0.13 |
R8208:Greb1l
|
UTSW |
18 |
10,510,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R8227:Greb1l
|
UTSW |
18 |
10,515,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R8312:Greb1l
|
UTSW |
18 |
10,511,587 (GRCm39) |
intron |
probably benign |
|
R8331:Greb1l
|
UTSW |
18 |
10,458,706 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8364:Greb1l
|
UTSW |
18 |
10,529,687 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8389:Greb1l
|
UTSW |
18 |
10,529,613 (GRCm39) |
missense |
probably benign |
0.00 |
R8695:Greb1l
|
UTSW |
18 |
10,544,450 (GRCm39) |
missense |
probably benign |
0.01 |
R8795:Greb1l
|
UTSW |
18 |
10,553,739 (GRCm39) |
missense |
probably damaging |
0.98 |
R8836:Greb1l
|
UTSW |
18 |
10,509,257 (GRCm39) |
missense |
probably benign |
0.30 |
R8862:Greb1l
|
UTSW |
18 |
10,555,042 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8872:Greb1l
|
UTSW |
18 |
10,529,684 (GRCm39) |
missense |
probably benign |
0.18 |
R8874:Greb1l
|
UTSW |
18 |
10,544,896 (GRCm39) |
missense |
probably benign |
0.01 |
R8886:Greb1l
|
UTSW |
18 |
10,553,843 (GRCm39) |
missense |
probably benign |
0.21 |
R8921:Greb1l
|
UTSW |
18 |
10,541,825 (GRCm39) |
missense |
probably benign |
0.01 |
R8997:Greb1l
|
UTSW |
18 |
10,510,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R9015:Greb1l
|
UTSW |
18 |
10,541,675 (GRCm39) |
missense |
probably benign |
0.00 |
R9018:Greb1l
|
UTSW |
18 |
10,542,004 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9074:Greb1l
|
UTSW |
18 |
10,558,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R9074:Greb1l
|
UTSW |
18 |
10,532,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R9117:Greb1l
|
UTSW |
18 |
10,542,422 (GRCm39) |
missense |
probably benign |
0.31 |
R9189:Greb1l
|
UTSW |
18 |
10,499,983 (GRCm39) |
missense |
probably benign |
|
R9367:Greb1l
|
UTSW |
18 |
10,522,130 (GRCm39) |
missense |
probably benign |
0.00 |
R9497:Greb1l
|
UTSW |
18 |
10,458,600 (GRCm39) |
missense |
probably benign |
0.00 |
R9796:Greb1l
|
UTSW |
18 |
10,538,233 (GRCm39) |
missense |
possibly damaging |
0.69 |
Z1176:Greb1l
|
UTSW |
18 |
10,515,305 (GRCm39) |
missense |
probably damaging |
1.00 |
|