Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
A |
C |
3: 124,208,042 (GRCm39) |
S212R |
probably benign |
Het |
4930562C15Rik |
T |
C |
16: 4,682,196 (GRCm39) |
S170P |
probably benign |
Het |
9330182O14Rik |
G |
A |
15: 40,008,303 (GRCm39) |
C59Y |
unknown |
Het |
AA986860 |
A |
G |
1: 130,670,624 (GRCm39) |
E282G |
possibly damaging |
Het |
Adam1a |
G |
T |
5: 121,657,397 (GRCm39) |
T632K |
probably benign |
Het |
Aspg |
G |
T |
12: 112,089,417 (GRCm39) |
A402S |
probably damaging |
Het |
Capn7 |
C |
T |
14: 31,058,642 (GRCm39) |
|
probably benign |
Het |
Card9 |
C |
T |
2: 26,246,896 (GRCm39) |
|
probably null |
Het |
Cdh13 |
T |
C |
8: 119,694,912 (GRCm39) |
V254A |
probably damaging |
Het |
Colec10 |
T |
C |
15: 54,325,767 (GRCm39) |
V199A |
probably damaging |
Het |
Copb2 |
T |
C |
9: 98,459,106 (GRCm39) |
S283P |
probably damaging |
Het |
Csmd1 |
G |
T |
8: 15,953,202 (GRCm39) |
S3426R |
probably damaging |
Het |
Cyp4f14 |
A |
G |
17: 33,133,562 (GRCm39) |
V98A |
probably benign |
Het |
Disp1 |
C |
A |
1: 182,869,030 (GRCm39) |
R1130L |
probably damaging |
Het |
Dysf |
A |
G |
6: 84,167,883 (GRCm39) |
|
probably null |
Het |
Efcab3 |
T |
C |
11: 104,629,100 (GRCm39) |
F926S |
probably benign |
Het |
Eif4ebp1 |
T |
C |
8: 27,763,447 (GRCm39) |
V80A |
probably damaging |
Het |
Eloa |
T |
A |
4: 135,736,452 (GRCm39) |
I565F |
probably damaging |
Het |
Espn |
G |
T |
4: 152,215,721 (GRCm39) |
H513N |
probably benign |
Het |
Fam83c |
C |
T |
2: 155,671,491 (GRCm39) |
S648N |
probably benign |
Het |
Fdxr |
C |
T |
11: 115,160,403 (GRCm39) |
V351M |
probably benign |
Het |
Fras1 |
A |
T |
5: 96,862,260 (GRCm39) |
D2213V |
probably damaging |
Het |
Gbp4 |
T |
A |
5: 105,267,825 (GRCm39) |
I474F |
possibly damaging |
Het |
Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
Hipk2 |
A |
T |
6: 38,795,413 (GRCm39) |
Y285* |
probably null |
Het |
Ifi27l2b |
T |
C |
12: 103,417,579 (GRCm39) |
I203V |
probably damaging |
Het |
Itga10 |
T |
A |
3: 96,559,081 (GRCm39) |
M390K |
probably damaging |
Het |
Itgb8 |
G |
T |
12: 119,166,159 (GRCm39) |
S124* |
probably null |
Het |
Klhdc10 |
T |
A |
6: 30,441,826 (GRCm39) |
F173I |
probably damaging |
Het |
Kng2 |
T |
G |
16: 22,830,805 (GRCm39) |
N168T |
probably damaging |
Het |
Krtap24-1 |
T |
C |
16: 88,408,434 (GRCm39) |
T231A |
probably damaging |
Het |
Lbx2 |
A |
T |
6: 83,065,045 (GRCm39) |
D194V |
probably damaging |
Het |
Lrrc39 |
C |
A |
3: 116,359,562 (GRCm39) |
Q36K |
probably benign |
Het |
Madd |
T |
C |
2: 90,992,393 (GRCm39) |
E1093G |
possibly damaging |
Het |
Mfap3l |
A |
G |
8: 61,124,303 (GRCm39) |
T182A |
probably damaging |
Het |
Myo9b |
T |
A |
8: 71,786,345 (GRCm39) |
Y670* |
probably null |
Het |
Nbea |
A |
G |
3: 55,899,865 (GRCm39) |
L1428P |
probably damaging |
Het |
Nkx2-3 |
T |
C |
19: 43,603,245 (GRCm39) |
Y284H |
possibly damaging |
Het |
Nphp4 |
A |
G |
4: 152,640,141 (GRCm39) |
D1009G |
probably benign |
Het |
Npy2r |
G |
A |
3: 82,448,490 (GRCm39) |
A95V |
probably damaging |
Het |
Nuggc |
A |
G |
14: 65,846,251 (GRCm39) |
E70G |
probably damaging |
Het |
Or5ap2 |
T |
C |
2: 85,680,254 (GRCm39) |
S153P |
probably benign |
Het |
Or5m11 |
T |
A |
2: 85,781,817 (GRCm39) |
S137T |
possibly damaging |
Het |
Palld |
A |
T |
8: 61,969,679 (GRCm39) |
V1215D |
unknown |
Het |
Pard6g |
T |
C |
18: 80,160,340 (GRCm39) |
I151T |
possibly damaging |
Het |
Parp12 |
T |
C |
6: 39,088,670 (GRCm39) |
I189V |
probably benign |
Het |
Parp4 |
A |
G |
14: 56,840,256 (GRCm39) |
I554V |
probably benign |
Het |
Pcnx2 |
G |
A |
8: 126,480,356 (GRCm39) |
P1984S |
probably damaging |
Het |
Piwil4 |
T |
C |
9: 14,648,196 (GRCm39) |
M128V |
probably benign |
Het |
Polr2a |
C |
A |
11: 69,628,288 (GRCm39) |
E1302* |
probably null |
Het |
Psg17 |
C |
A |
7: 18,548,421 (GRCm39) |
G450V |
probably damaging |
Het |
Psg17 |
C |
G |
7: 18,548,422 (GRCm39) |
G450R |
probably damaging |
Het |
Rag1 |
T |
C |
2: 101,474,128 (GRCm39) |
E338G |
probably damaging |
Het |
Rev3l |
A |
T |
10: 39,698,163 (GRCm39) |
K887* |
probably null |
Het |
Rragd |
T |
C |
4: 32,996,027 (GRCm39) |
F124S |
possibly damaging |
Het |
Scube1 |
A |
T |
15: 83,513,712 (GRCm39) |
|
probably null |
Het |
Sfpq |
A |
T |
4: 126,919,725 (GRCm39) |
D490V |
possibly damaging |
Het |
Smc1b |
G |
T |
15: 84,955,798 (GRCm39) |
Q1034K |
probably damaging |
Het |
Smg7 |
T |
C |
1: 152,753,831 (GRCm39) |
N5S |
probably benign |
Het |
Spata31d1a |
A |
C |
13: 59,850,301 (GRCm39) |
L609R |
probably damaging |
Het |
Ssh2 |
A |
G |
11: 77,345,164 (GRCm39) |
K1050E |
probably benign |
Het |
Stab1 |
G |
A |
14: 30,882,824 (GRCm39) |
T393I |
possibly damaging |
Het |
Sult2a4 |
C |
T |
7: 13,722,320 (GRCm39) |
W49* |
probably null |
Het |
Thrap3 |
A |
T |
4: 126,074,231 (GRCm39) |
S172T |
unknown |
Het |
Tmem130 |
A |
G |
5: 144,687,721 (GRCm39) |
V205A |
probably damaging |
Het |
Ube2d2b |
A |
G |
5: 107,978,717 (GRCm39) |
I123V |
probably benign |
Het |
Unc79 |
G |
T |
12: 103,027,652 (GRCm39) |
L414F |
probably damaging |
Het |
Vmn2r30 |
C |
T |
7: 7,337,183 (GRCm39) |
S151N |
probably benign |
Het |
Vmn2r54 |
T |
A |
7: 12,356,078 (GRCm39) |
T443S |
probably benign |
Het |
Zfp229 |
T |
A |
17: 21,961,597 (GRCm39) |
S51T |
probably damaging |
Het |
Zfp617 |
T |
C |
8: 72,686,384 (GRCm39) |
L238P |
probably damaging |
Het |
Zfp707 |
T |
A |
15: 75,845,398 (GRCm39) |
C87* |
probably null |
Het |
Zfp853 |
T |
C |
5: 143,275,362 (GRCm39) |
K101R |
unknown |
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 |
R4904:Golgb1
|
UTSW |
16 |
36,713,748 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|