Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb2 |
T |
G |
4: 129,906,332 (GRCm39) |
I920S |
possibly damaging |
Het |
Afap1l1 |
A |
G |
18: 61,871,786 (GRCm39) |
I556T |
probably benign |
Het |
Ankfy1 |
C |
A |
11: 72,642,931 (GRCm39) |
H665N |
probably benign |
Het |
Aqp9 |
A |
C |
9: 71,069,685 (GRCm39) |
|
probably benign |
Het |
Arhgap21 |
A |
G |
2: 20,854,872 (GRCm39) |
S1497P |
probably benign |
Het |
Armc7 |
A |
G |
11: 115,379,800 (GRCm39) |
D166G |
probably damaging |
Het |
Arrdc1 |
C |
A |
2: 24,816,676 (GRCm39) |
V167F |
possibly damaging |
Het |
Col6a3 |
A |
T |
1: 90,729,164 (GRCm39) |
I1259N |
probably damaging |
Het |
Coq8a |
C |
T |
1: 180,006,168 (GRCm39) |
R207Q |
probably damaging |
Het |
Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
Dcbld1 |
C |
T |
10: 52,196,066 (GRCm39) |
Q425* |
probably null |
Het |
Def8 |
A |
G |
8: 124,188,219 (GRCm39) |
N445D |
probably damaging |
Het |
Dicer1 |
C |
T |
12: 104,679,325 (GRCm39) |
V551I |
probably benign |
Het |
Dst |
A |
T |
1: 34,208,879 (GRCm39) |
T800S |
probably damaging |
Het |
Dtl |
A |
T |
1: 191,300,457 (GRCm39) |
C136S |
probably damaging |
Het |
Duox1 |
T |
A |
2: 122,151,345 (GRCm39) |
Y310N |
probably damaging |
Het |
Duxf1 |
T |
A |
10: 58,059,309 (GRCm39) |
R482* |
probably null |
Het |
Ebf1 |
T |
C |
11: 44,759,996 (GRCm39) |
F211S |
probably damaging |
Het |
Gm44501 |
A |
T |
17: 40,889,884 (GRCm39) |
I133F |
possibly damaging |
Het |
Gm6625 |
T |
C |
8: 89,873,379 (GRCm39) |
|
noncoding transcript |
Het |
Gprc5c |
G |
T |
11: 114,755,093 (GRCm39) |
V257L |
possibly damaging |
Het |
Gtf2a1l |
G |
A |
17: 88,997,471 (GRCm39) |
|
probably null |
Het |
Herc2 |
T |
C |
7: 55,807,234 (GRCm39) |
F2471L |
probably damaging |
Het |
Hfe |
A |
T |
13: 23,892,037 (GRCm39) |
I109N |
probably damaging |
Het |
Hrg |
A |
G |
16: 22,770,000 (GRCm39) |
E43G |
probably benign |
Het |
Hspa1a |
T |
C |
17: 35,189,427 (GRCm39) |
D492G |
probably damaging |
Het |
Itgb8 |
T |
C |
12: 119,134,606 (GRCm39) |
D487G |
probably benign |
Het |
Jag1 |
A |
G |
2: 136,929,062 (GRCm39) |
V798A |
probably damaging |
Het |
Kcnq5 |
A |
G |
1: 21,494,324 (GRCm39) |
V501A |
probably damaging |
Het |
Kntc1 |
T |
C |
5: 123,916,396 (GRCm39) |
V743A |
possibly damaging |
Het |
Ly86 |
G |
T |
13: 37,599,496 (GRCm39) |
V126F |
possibly damaging |
Het |
Med26 |
A |
T |
8: 73,250,691 (GRCm39) |
L136H |
probably damaging |
Het |
Mpp3 |
T |
C |
11: 101,891,413 (GRCm39) |
D575G |
probably benign |
Het |
Myoc |
G |
A |
1: 162,466,994 (GRCm39) |
M54I |
probably benign |
Het |
Nlrp1c-ps |
A |
G |
11: 71,133,454 (GRCm39) |
|
noncoding transcript |
Het |
Or10v9 |
C |
T |
19: 11,833,231 (GRCm39) |
V29M |
possibly damaging |
Het |
Or51t4 |
A |
G |
7: 102,598,272 (GRCm39) |
Y190C |
probably damaging |
Het |
Or5v1b |
A |
G |
17: 37,841,522 (GRCm39) |
Y218C |
probably damaging |
Het |
Pak5 |
A |
T |
2: 135,925,267 (GRCm39) |
D678E |
probably benign |
Het |
Pcdhb12 |
T |
C |
18: 37,570,909 (GRCm39) |
V685A |
possibly damaging |
Het |
Pcdhga2 |
A |
G |
18: 37,802,932 (GRCm39) |
T259A |
possibly damaging |
Het |
Pde6a |
A |
T |
18: 61,398,105 (GRCm39) |
M702L |
probably benign |
Het |
Pigq |
A |
G |
17: 26,150,034 (GRCm39) |
|
probably benign |
Het |
Polrmt |
A |
G |
10: 79,582,385 (GRCm39) |
M1T |
probably null |
Het |
Ptch1 |
A |
C |
13: 63,670,818 (GRCm39) |
I904S |
probably damaging |
Het |
Rflnb |
A |
T |
11: 75,912,964 (GRCm39) |
C141* |
probably null |
Het |
Rilpl1 |
C |
A |
5: 124,652,807 (GRCm39) |
|
probably null |
Het |
Rpgrip1 |
T |
C |
14: 52,358,544 (GRCm39) |
S217P |
possibly damaging |
Het |
Rpgrip1 |
A |
T |
14: 52,397,586 (GRCm39) |
I1292F |
probably damaging |
Het |
Sema3a |
A |
C |
5: 13,631,066 (GRCm39) |
Y534S |
probably damaging |
Het |
Sez6 |
A |
G |
11: 77,866,080 (GRCm39) |
Y736C |
probably damaging |
Het |
Shank1 |
G |
T |
7: 43,983,464 (GRCm39) |
|
probably benign |
Het |
Slc45a4 |
G |
A |
15: 73,458,691 (GRCm39) |
S294F |
probably benign |
Het |
Slc9a8 |
A |
G |
2: 167,313,316 (GRCm39) |
I393V |
possibly damaging |
Het |
Sod1 |
T |
A |
16: 90,019,732 (GRCm39) |
F46Y |
probably damaging |
Het |
Sult1b1 |
T |
C |
5: 87,682,912 (GRCm39) |
D11G |
probably benign |
Het |
Syn3 |
T |
G |
10: 86,302,950 (GRCm39) |
K68N |
possibly damaging |
Het |
Taar8c |
C |
T |
10: 23,977,147 (GRCm39) |
V222I |
probably benign |
Het |
Tbx20 |
T |
C |
9: 24,670,129 (GRCm39) |
K235E |
probably damaging |
Het |
Tcaf3 |
C |
A |
6: 42,570,931 (GRCm39) |
E274* |
probably null |
Het |
Tll1 |
A |
T |
8: 64,523,233 (GRCm39) |
M493K |
probably benign |
Het |
Tmem236 |
T |
A |
2: 14,200,803 (GRCm39) |
S123T |
probably benign |
Het |
Trim33 |
T |
C |
3: 103,238,963 (GRCm39) |
V647A |
possibly damaging |
Het |
Tspear |
T |
A |
10: 77,705,489 (GRCm39) |
Y296N |
possibly damaging |
Het |
Vps13d |
T |
C |
4: 144,882,015 (GRCm39) |
K1187E |
probably damaging |
Het |
Xpot |
C |
T |
10: 121,453,083 (GRCm39) |
V52I |
probably benign |
Het |
Zdhhc3 |
A |
T |
9: 122,929,452 (GRCm39) |
V61E |
probably damaging |
Het |
Zfp955a |
A |
T |
17: 33,461,162 (GRCm39) |
C323* |
probably null |
Het |
|
Other mutations in Golgb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01394:Golgb1
|
APN |
16 |
36,751,926 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01717:Golgb1
|
APN |
16 |
36,735,864 (GRCm39) |
nonsense |
probably null |
|
IGL01965:Golgb1
|
APN |
16 |
36,738,282 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02128:Golgb1
|
APN |
16 |
36,736,666 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02268:Golgb1
|
APN |
16 |
36,733,490 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02383:Golgb1
|
APN |
16 |
36,706,562 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02444:Golgb1
|
APN |
16 |
36,728,178 (GRCm39) |
splice site |
probably benign |
|
IGL02635:Golgb1
|
APN |
16 |
36,735,375 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02655:Golgb1
|
APN |
16 |
36,738,442 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02887:Golgb1
|
APN |
16 |
36,746,211 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02937:Golgb1
|
APN |
16 |
36,736,572 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02973:Golgb1
|
APN |
16 |
36,732,442 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02982:Golgb1
|
APN |
16 |
36,746,172 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03065:Golgb1
|
APN |
16 |
36,733,228 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03109:Golgb1
|
APN |
16 |
36,735,973 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03323:Golgb1
|
APN |
16 |
36,733,815 (GRCm39) |
nonsense |
probably null |
|
I2288:Golgb1
|
UTSW |
16 |
36,718,904 (GRCm39) |
missense |
probably benign |
0.00 |
I2289:Golgb1
|
UTSW |
16 |
36,718,904 (GRCm39) |
missense |
probably benign |
0.00 |
R0071:Golgb1
|
UTSW |
16 |
36,735,865 (GRCm39) |
missense |
probably benign |
0.00 |
R0071:Golgb1
|
UTSW |
16 |
36,735,865 (GRCm39) |
missense |
probably benign |
0.00 |
R0080:Golgb1
|
UTSW |
16 |
36,718,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R0102:Golgb1
|
UTSW |
16 |
36,695,830 (GRCm39) |
intron |
probably benign |
|
R0242:Golgb1
|
UTSW |
16 |
36,695,992 (GRCm39) |
nonsense |
probably null |
|
R0242:Golgb1
|
UTSW |
16 |
36,695,992 (GRCm39) |
nonsense |
probably null |
|
R0276:Golgb1
|
UTSW |
16 |
36,734,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R0394:Golgb1
|
UTSW |
16 |
36,695,941 (GRCm39) |
intron |
probably benign |
|
R0469:Golgb1
|
UTSW |
16 |
36,751,997 (GRCm39) |
missense |
probably benign |
0.41 |
R0522:Golgb1
|
UTSW |
16 |
36,735,567 (GRCm39) |
frame shift |
probably null |
|
R0575:Golgb1
|
UTSW |
16 |
36,739,171 (GRCm39) |
missense |
probably benign |
|
R0600:Golgb1
|
UTSW |
16 |
36,736,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R0608:Golgb1
|
UTSW |
16 |
36,736,692 (GRCm39) |
nonsense |
probably null |
|
R0711:Golgb1
|
UTSW |
16 |
36,739,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R0785:Golgb1
|
UTSW |
16 |
36,719,152 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0893:Golgb1
|
UTSW |
16 |
36,732,639 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1163:Golgb1
|
UTSW |
16 |
36,736,488 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1208:Golgb1
|
UTSW |
16 |
36,735,567 (GRCm39) |
frame shift |
probably null |
|
R1315:Golgb1
|
UTSW |
16 |
36,735,262 (GRCm39) |
missense |
probably benign |
0.40 |
R1429:Golgb1
|
UTSW |
16 |
36,720,925 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1505:Golgb1
|
UTSW |
16 |
36,740,005 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1537:Golgb1
|
UTSW |
16 |
36,719,150 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1610:Golgb1
|
UTSW |
16 |
36,746,463 (GRCm39) |
missense |
probably benign |
0.25 |
R1659:Golgb1
|
UTSW |
16 |
36,707,979 (GRCm39) |
missense |
probably benign |
0.01 |
R1769:Golgb1
|
UTSW |
16 |
36,736,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R2105:Golgb1
|
UTSW |
16 |
36,735,026 (GRCm39) |
missense |
probably benign |
|
R2212:Golgb1
|
UTSW |
16 |
36,707,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R2261:Golgb1
|
UTSW |
16 |
36,713,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R2352:Golgb1
|
UTSW |
16 |
36,718,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R2357:Golgb1
|
UTSW |
16 |
36,732,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R2400:Golgb1
|
UTSW |
16 |
36,738,828 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2513:Golgb1
|
UTSW |
16 |
36,735,513 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3103:Golgb1
|
UTSW |
16 |
36,715,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R3413:Golgb1
|
UTSW |
16 |
36,707,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R3748:Golgb1
|
UTSW |
16 |
36,739,274 (GRCm39) |
missense |
probably benign |
0.00 |
R3847:Golgb1
|
UTSW |
16 |
36,719,095 (GRCm39) |
missense |
probably benign |
0.00 |
R3850:Golgb1
|
UTSW |
16 |
36,719,095 (GRCm39) |
missense |
probably benign |
0.00 |
R3936:Golgb1
|
UTSW |
16 |
36,734,418 (GRCm39) |
nonsense |
probably null |
|
R3975:Golgb1
|
UTSW |
16 |
36,738,933 (GRCm39) |
missense |
probably damaging |
0.99 |
R4025:Golgb1
|
UTSW |
16 |
36,735,706 (GRCm39) |
missense |
probably benign |
0.00 |
R4369:Golgb1
|
UTSW |
16 |
36,737,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R4518:Golgb1
|
UTSW |
16 |
36,749,625 (GRCm39) |
missense |
probably damaging |
0.98 |
R4600:Golgb1
|
UTSW |
16 |
36,738,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Golgb1
|
UTSW |
16 |
36,738,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R4660:Golgb1
|
UTSW |
16 |
36,707,980 (GRCm39) |
missense |
probably damaging |
0.99 |
R4811:Golgb1
|
UTSW |
16 |
36,711,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R4815:Golgb1
|
UTSW |
16 |
36,733,477 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4835:Golgb1
|
UTSW |
16 |
36,711,769 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4916:Golgb1
|
UTSW |
16 |
36,736,480 (GRCm39) |
missense |
probably benign |
0.05 |
R5121:Golgb1
|
UTSW |
16 |
36,739,620 (GRCm39) |
missense |
probably damaging |
0.99 |
R5133:Golgb1
|
UTSW |
16 |
36,711,819 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5143:Golgb1
|
UTSW |
16 |
36,719,051 (GRCm39) |
missense |
probably benign |
0.09 |
R5185:Golgb1
|
UTSW |
16 |
36,695,503 (GRCm39) |
unclassified |
probably benign |
|
R5188:Golgb1
|
UTSW |
16 |
36,738,827 (GRCm39) |
missense |
probably benign |
0.13 |
R5260:Golgb1
|
UTSW |
16 |
36,733,503 (GRCm39) |
missense |
probably benign |
0.00 |
R5297:Golgb1
|
UTSW |
16 |
36,695,978 (GRCm39) |
intron |
probably benign |
|
R5386:Golgb1
|
UTSW |
16 |
36,732,677 (GRCm39) |
nonsense |
probably null |
|
R5438:Golgb1
|
UTSW |
16 |
36,720,870 (GRCm39) |
missense |
probably benign |
0.15 |
R5439:Golgb1
|
UTSW |
16 |
36,720,870 (GRCm39) |
missense |
probably benign |
0.15 |
R5494:Golgb1
|
UTSW |
16 |
36,749,045 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5592:Golgb1
|
UTSW |
16 |
36,746,125 (GRCm39) |
missense |
probably benign |
0.02 |
R5740:Golgb1
|
UTSW |
16 |
36,739,362 (GRCm39) |
missense |
probably damaging |
0.99 |
R5862:Golgb1
|
UTSW |
16 |
36,746,453 (GRCm39) |
splice site |
silent |
|
R5928:Golgb1
|
UTSW |
16 |
36,732,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R6009:Golgb1
|
UTSW |
16 |
36,735,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R6062:Golgb1
|
UTSW |
16 |
36,735,033 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6102:Golgb1
|
UTSW |
16 |
36,733,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R6198:Golgb1
|
UTSW |
16 |
36,713,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R6253:Golgb1
|
UTSW |
16 |
36,735,984 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6254:Golgb1
|
UTSW |
16 |
36,734,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R6321:Golgb1
|
UTSW |
16 |
36,738,559 (GRCm39) |
nonsense |
probably null |
|
R6700:Golgb1
|
UTSW |
16 |
36,695,946 (GRCm39) |
intron |
probably benign |
|
R6870:Golgb1
|
UTSW |
16 |
36,738,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R6882:Golgb1
|
UTSW |
16 |
36,734,352 (GRCm39) |
missense |
probably benign |
|
R6944:Golgb1
|
UTSW |
16 |
36,732,475 (GRCm39) |
missense |
probably benign |
|
R7108:Golgb1
|
UTSW |
16 |
36,734,083 (GRCm39) |
missense |
probably benign |
0.01 |
R7124:Golgb1
|
UTSW |
16 |
36,734,035 (GRCm39) |
missense |
probably benign |
0.01 |
R7125:Golgb1
|
UTSW |
16 |
36,738,325 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7187:Golgb1
|
UTSW |
16 |
36,736,512 (GRCm39) |
missense |
probably benign |
0.43 |
R7205:Golgb1
|
UTSW |
16 |
36,695,663 (GRCm39) |
missense |
unknown |
|
R7206:Golgb1
|
UTSW |
16 |
36,734,111 (GRCm39) |
missense |
probably benign |
0.41 |
R7233:Golgb1
|
UTSW |
16 |
36,735,120 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7320:Golgb1
|
UTSW |
16 |
36,736,313 (GRCm39) |
nonsense |
probably null |
|
R7367:Golgb1
|
UTSW |
16 |
36,718,908 (GRCm39) |
missense |
probably benign |
0.00 |
R7408:Golgb1
|
UTSW |
16 |
36,718,909 (GRCm39) |
missense |
probably damaging |
0.98 |
R7419:Golgb1
|
UTSW |
16 |
36,733,281 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7556:Golgb1
|
UTSW |
16 |
36,736,155 (GRCm39) |
missense |
probably benign |
0.03 |
R7599:Golgb1
|
UTSW |
16 |
36,695,758 (GRCm39) |
missense |
unknown |
|
R7673:Golgb1
|
UTSW |
16 |
36,734,031 (GRCm39) |
missense |
probably benign |
0.05 |
R7789:Golgb1
|
UTSW |
16 |
36,695,761 (GRCm39) |
missense |
unknown |
|
R7792:Golgb1
|
UTSW |
16 |
36,739,092 (GRCm39) |
missense |
probably benign |
0.43 |
R7830:Golgb1
|
UTSW |
16 |
36,719,083 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7847:Golgb1
|
UTSW |
16 |
36,752,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R7905:Golgb1
|
UTSW |
16 |
36,734,047 (GRCm39) |
missense |
probably benign |
|
R7944:Golgb1
|
UTSW |
16 |
36,734,466 (GRCm39) |
missense |
probably benign |
0.02 |
R7945:Golgb1
|
UTSW |
16 |
36,734,466 (GRCm39) |
missense |
probably benign |
0.02 |
R7950:Golgb1
|
UTSW |
16 |
36,735,786 (GRCm39) |
missense |
probably benign |
0.13 |
R8040:Golgb1
|
UTSW |
16 |
36,733,841 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8077:Golgb1
|
UTSW |
16 |
36,738,995 (GRCm39) |
missense |
probably damaging |
0.99 |
R8181:Golgb1
|
UTSW |
16 |
36,737,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R8370:Golgb1
|
UTSW |
16 |
36,732,679 (GRCm39) |
missense |
probably benign |
0.00 |
R8684:Golgb1
|
UTSW |
16 |
36,734,764 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8725:Golgb1
|
UTSW |
16 |
36,739,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R8727:Golgb1
|
UTSW |
16 |
36,739,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R8738:Golgb1
|
UTSW |
16 |
36,736,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R8785:Golgb1
|
UTSW |
16 |
36,740,106 (GRCm39) |
missense |
probably damaging |
0.99 |
R8824:Golgb1
|
UTSW |
16 |
36,736,051 (GRCm39) |
missense |
probably benign |
|
R8825:Golgb1
|
UTSW |
16 |
36,739,809 (GRCm39) |
missense |
probably benign |
0.00 |
R8940:Golgb1
|
UTSW |
16 |
36,736,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Golgb1
|
UTSW |
16 |
36,733,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R9245:Golgb1
|
UTSW |
16 |
36,739,181 (GRCm39) |
nonsense |
probably null |
|
R9365:Golgb1
|
UTSW |
16 |
36,736,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R9612:Golgb1
|
UTSW |
16 |
36,739,967 (GRCm39) |
missense |
probably benign |
0.41 |
R9620:Golgb1
|
UTSW |
16 |
36,739,811 (GRCm39) |
missense |
probably benign |
|
R9691:Golgb1
|
UTSW |
16 |
36,718,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R9747:Golgb1
|
UTSW |
16 |
36,713,769 (GRCm39) |
missense |
probably damaging |
1.00 |
V1662:Golgb1
|
UTSW |
16 |
36,718,904 (GRCm39) |
missense |
probably benign |
0.00 |
X0067:Golgb1
|
UTSW |
16 |
36,734,665 (GRCm39) |
nonsense |
probably null |
|
Z1088:Golgb1
|
UTSW |
16 |
36,740,104 (GRCm39) |
missense |
probably damaging |
1.00 |
|