Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
G |
A |
17: 24,483,318 (GRCm39) |
R1713C |
unknown |
Het |
Ano6 |
C |
T |
15: 95,846,298 (GRCm39) |
T512I |
probably damaging |
Het |
Ap3s1 |
T |
C |
18: 46,887,505 (GRCm39) |
V46A |
probably benign |
Het |
Art2a |
C |
A |
7: 101,204,413 (GRCm39) |
V42F |
probably damaging |
Het |
Asph |
C |
T |
4: 9,531,960 (GRCm39) |
V386M |
probably benign |
Het |
B4galnt4 |
T |
A |
7: 140,644,643 (GRCm39) |
D179E |
probably benign |
Het |
Bbx |
T |
C |
16: 50,071,730 (GRCm39) |
I232V |
probably benign |
Het |
C1ql2 |
A |
G |
1: 120,269,321 (GRCm39) |
I159V |
probably benign |
Het |
Ccar1 |
A |
G |
10: 62,612,496 (GRCm39) |
V223A |
possibly damaging |
Het |
Cd2ap |
A |
T |
17: 43,136,802 (GRCm39) |
L277I |
probably benign |
Het |
Cfap44 |
G |
A |
16: 44,250,255 (GRCm39) |
E778K |
probably benign |
Het |
Chd3 |
A |
T |
11: 69,240,063 (GRCm39) |
D1626E |
probably benign |
Het |
Crocc |
C |
T |
4: 140,769,032 (GRCm39) |
G505S |
probably benign |
Het |
Crocc |
T |
A |
4: 140,773,851 (GRCm39) |
Q72L |
probably damaging |
Het |
Drosha |
T |
C |
15: 12,834,156 (GRCm39) |
|
probably benign |
Het |
Eps8l1 |
T |
A |
7: 4,474,296 (GRCm39) |
S256T |
possibly damaging |
Het |
F830045P16Rik |
A |
G |
2: 129,316,310 (GRCm39) |
V133A |
probably damaging |
Het |
Fermt2 |
A |
T |
14: 45,697,338 (GRCm39) |
M671K |
possibly damaging |
Het |
Fhdc1 |
G |
A |
3: 84,353,336 (GRCm39) |
L630F |
probably benign |
Het |
Gon4l |
T |
C |
3: 88,807,306 (GRCm39) |
S1667P |
probably damaging |
Het |
H2-Q10 |
C |
T |
17: 35,781,026 (GRCm39) |
T8M |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,324,725 (GRCm39) |
T4215S |
probably benign |
Het |
I0C0044D17Rik |
G |
A |
4: 98,708,576 (GRCm39) |
|
probably benign |
Het |
Ifi204 |
A |
G |
1: 173,579,223 (GRCm39) |
F541L |
probably benign |
Het |
Igkv6-17 |
C |
T |
6: 70,348,764 (GRCm39) |
A45V |
probably damaging |
Het |
Intu |
G |
A |
3: 40,608,524 (GRCm39) |
A161T |
probably damaging |
Het |
Kcnmb2 |
A |
G |
3: 32,233,141 (GRCm39) |
Y73C |
probably damaging |
Het |
Lrit1 |
T |
C |
14: 36,776,945 (GRCm39) |
F22L |
probably benign |
Het |
Lrp1b |
A |
T |
2: 41,174,156 (GRCm39) |
C699* |
probably null |
Het |
Lrrc8d |
A |
G |
5: 105,959,992 (GRCm39) |
D134G |
probably benign |
Het |
Map1b |
T |
C |
13: 99,567,645 (GRCm39) |
D1692G |
unknown |
Het |
Met |
C |
T |
6: 17,491,967 (GRCm39) |
S243F |
probably damaging |
Het |
Mlph |
C |
A |
1: 90,855,882 (GRCm39) |
H96Q |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,372,582 (GRCm39) |
V4088D |
probably damaging |
Het |
Nampt |
T |
A |
12: 32,898,658 (GRCm39) |
S425T |
probably damaging |
Het |
Nts |
G |
A |
10: 102,320,856 (GRCm39) |
H78Y |
probably benign |
Het |
Nxf1 |
A |
G |
19: 8,745,151 (GRCm39) |
E467G |
possibly damaging |
Het |
Olfml2a |
C |
A |
2: 38,841,155 (GRCm39) |
D230E |
probably benign |
Het |
Or4b13 |
C |
A |
2: 90,082,771 (GRCm39) |
C187F |
probably benign |
Het |
Or52n2c |
C |
T |
7: 104,574,599 (GRCm39) |
R124H |
probably benign |
Het |
Pcsk5 |
A |
G |
19: 17,432,045 (GRCm39) |
|
probably null |
Het |
Pde5a |
C |
A |
3: 122,618,574 (GRCm39) |
T629K |
probably benign |
Het |
Plcb3 |
G |
T |
19: 6,940,202 (GRCm39) |
R462S |
possibly damaging |
Het |
Pnpla6 |
T |
A |
8: 3,574,156 (GRCm39) |
M469K |
probably benign |
Het |
Pram1 |
A |
T |
17: 33,860,386 (GRCm39) |
K318* |
probably null |
Het |
Prkd1 |
T |
C |
12: 50,388,826 (GRCm39) |
R906G |
probably benign |
Het |
Ptprh |
T |
A |
7: 4,576,361 (GRCm39) |
T300S |
possibly damaging |
Het |
Rdh16f2 |
A |
G |
10: 127,712,743 (GRCm39) |
Y247C |
probably benign |
Het |
Rimbp3 |
A |
G |
16: 17,028,781 (GRCm39) |
E735G |
probably damaging |
Het |
Sall3 |
G |
A |
18: 81,017,470 (GRCm39) |
P153S |
possibly damaging |
Het |
Samd4b |
T |
A |
7: 28,123,056 (GRCm39) |
M1L |
possibly damaging |
Het |
Septin12 |
T |
C |
16: 4,810,127 (GRCm39) |
E136G |
probably damaging |
Het |
Shpk |
A |
T |
11: 73,104,270 (GRCm39) |
K140* |
probably null |
Het |
Sidt1 |
G |
T |
16: 44,079,829 (GRCm39) |
F608L |
probably benign |
Het |
Skint5 |
A |
G |
4: 113,347,842 (GRCm39) |
Y1300H |
probably benign |
Het |
Slc22a28 |
G |
A |
19: 8,094,386 (GRCm39) |
P212S |
probably benign |
Het |
Slc22a5 |
A |
T |
11: 53,758,359 (GRCm39) |
F480L |
possibly damaging |
Het |
Slc35e2 |
C |
T |
4: 155,694,483 (GRCm39) |
P10L |
probably benign |
Het |
Slc3a1 |
C |
T |
17: 85,335,951 (GRCm39) |
P31L |
probably benign |
Het |
Slc4a7 |
T |
C |
14: 14,793,964 (GRCm38) |
V1074A |
possibly damaging |
Het |
Snx2 |
C |
T |
18: 53,342,697 (GRCm39) |
Q254* |
probably null |
Het |
Sox30 |
G |
A |
11: 45,882,769 (GRCm39) |
V600I |
probably benign |
Het |
Svil |
T |
G |
18: 5,106,724 (GRCm39) |
V1855G |
probably damaging |
Het |
Tdpoz9 |
A |
G |
3: 93,957,408 (GRCm39) |
F7L |
probably benign |
Het |
Tdrd7 |
A |
G |
4: 46,005,486 (GRCm39) |
T431A |
probably benign |
Het |
Tenm2 |
A |
T |
11: 36,054,544 (GRCm39) |
|
probably null |
Het |
Tigar |
A |
G |
6: 127,068,164 (GRCm39) |
S85P |
probably benign |
Het |
Tnr |
A |
C |
1: 159,740,254 (GRCm39) |
M1143L |
probably benign |
Het |
Trio |
G |
T |
15: 27,891,465 (GRCm39) |
Q429K |
possibly damaging |
Het |
Urb1 |
T |
C |
16: 90,585,985 (GRCm39) |
I452M |
probably benign |
Het |
Uroc1 |
A |
T |
6: 90,324,910 (GRCm39) |
E461V |
probably benign |
Het |
Vax1 |
C |
A |
19: 59,157,036 (GRCm39) |
R99L |
unknown |
Het |
Xab2 |
A |
T |
8: 3,663,051 (GRCm39) |
I510N |
possibly damaging |
Het |
Zbtb34 |
A |
T |
2: 33,301,842 (GRCm39) |
I233K |
possibly damaging |
Het |
Zbtb47 |
A |
G |
9: 121,592,598 (GRCm39) |
E306G |
probably benign |
Het |
Zfp27 |
A |
G |
7: 29,593,727 (GRCm39) |
F746S |
probably damaging |
Het |
Zfp719 |
C |
T |
7: 43,239,050 (GRCm39) |
Q213* |
probably null |
Het |
Zswim6 |
T |
C |
13: 107,865,112 (GRCm39) |
|
noncoding transcript |
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 |
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 |
|
R9332:Greb1l
|
UTSW |
18 |
10,532,796 (GRCm39) |
missense |
possibly damaging |
0.92 |
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 |
|