Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
A |
T |
7: 29,274,326 (GRCm39) |
|
noncoding transcript |
Het |
4933434E20Rik |
A |
G |
3: 89,970,516 (GRCm39) |
N17D |
probably benign |
Het |
A1bg |
T |
C |
15: 60,792,100 (GRCm39) |
D176G |
probably benign |
Het |
Abcg5 |
A |
T |
17: 84,966,076 (GRCm39) |
M428K |
possibly damaging |
Het |
Adam1a |
A |
T |
5: 121,657,752 (GRCm39) |
C514S |
probably damaging |
Het |
Angptl3 |
A |
G |
4: 98,925,649 (GRCm39) |
Q325R |
probably benign |
Het |
Ankrd26 |
C |
T |
6: 118,525,811 (GRCm39) |
W378* |
probably null |
Het |
Apob |
T |
C |
12: 8,065,391 (GRCm39) |
V4087A |
possibly damaging |
Het |
Auts2 |
A |
G |
5: 131,494,931 (GRCm39) |
I117T |
probably damaging |
Het |
AW146154 |
T |
A |
7: 41,129,892 (GRCm39) |
E408V |
probably damaging |
Het |
Bicd1 |
A |
T |
6: 149,385,588 (GRCm39) |
N107I |
probably benign |
Het |
Blm |
T |
C |
7: 80,159,294 (GRCm39) |
S281G |
probably benign |
Het |
Btaf1 |
T |
A |
19: 36,979,858 (GRCm39) |
D1542E |
probably benign |
Het |
C2cd2l |
A |
G |
9: 44,226,442 (GRCm39) |
|
probably null |
Het |
Capn8 |
C |
A |
1: 182,432,116 (GRCm39) |
N362K |
probably damaging |
Het |
Ccdc14 |
T |
G |
16: 34,525,408 (GRCm39) |
S186A |
probably damaging |
Het |
Cdca4 |
A |
G |
12: 112,785,167 (GRCm39) |
L187P |
probably damaging |
Het |
Chil6 |
T |
A |
3: 106,313,290 (GRCm39) |
K20* |
probably null |
Het |
Cmss1 |
A |
T |
16: 57,136,545 (GRCm39) |
L109* |
probably null |
Het |
Cmtm6 |
G |
T |
9: 114,560,410 (GRCm39) |
W36L |
probably benign |
Het |
Cnksr3 |
T |
G |
10: 7,110,757 (GRCm39) |
I35L |
possibly damaging |
Het |
Col4a2 |
G |
T |
8: 11,473,570 (GRCm39) |
G534* |
probably null |
Het |
Col5a1 |
T |
G |
2: 27,915,656 (GRCm39) |
V180G |
probably damaging |
Het |
Ctnna3 |
T |
C |
10: 63,417,723 (GRCm39) |
F154L |
probably benign |
Het |
Fabp7 |
G |
A |
10: 57,661,676 (GRCm39) |
V50M |
possibly damaging |
Het |
Fam170a |
T |
A |
18: 50,415,050 (GRCm39) |
V232D |
probably damaging |
Het |
Fam186a |
T |
G |
15: 99,843,689 (GRCm39) |
T852P |
unknown |
Het |
Fam20a |
T |
C |
11: 109,564,389 (GRCm39) |
I455V |
probably benign |
Het |
Fbxl6 |
C |
T |
15: 76,421,004 (GRCm39) |
V324M |
probably damaging |
Het |
Galnt18 |
T |
C |
7: 111,378,730 (GRCm39) |
T9A |
probably damaging |
Het |
Gpld1 |
A |
G |
13: 25,166,699 (GRCm39) |
T650A |
probably benign |
Het |
Gprc5d |
A |
G |
6: 135,093,515 (GRCm39) |
F131L |
probably benign |
Het |
H2az2 |
C |
T |
11: 6,389,437 (GRCm39) |
G7E |
unknown |
Het |
Haus4 |
A |
T |
14: 54,783,292 (GRCm39) |
|
probably null |
Het |
Helq |
A |
G |
5: 100,922,029 (GRCm39) |
I725T |
possibly damaging |
Het |
Igsf23 |
T |
A |
7: 19,675,755 (GRCm39) |
D117V |
possibly damaging |
Het |
Kiz |
A |
T |
2: 146,784,008 (GRCm39) |
S514C |
probably damaging |
Het |
Klhl6 |
A |
T |
16: 19,775,783 (GRCm39) |
N258K |
probably benign |
Het |
Krt72 |
G |
C |
15: 101,689,508 (GRCm39) |
|
probably null |
Het |
Large1 |
A |
T |
8: 73,774,975 (GRCm39) |
I245N |
probably damaging |
Het |
Lrrc31 |
T |
C |
3: 30,733,306 (GRCm39) |
I469M |
probably damaging |
Het |
Lypd4 |
T |
A |
7: 24,566,121 (GRCm39) |
I68F |
probably benign |
Het |
Mast1 |
A |
G |
8: 85,650,408 (GRCm39) |
S442P |
probably damaging |
Het |
Mmp20 |
T |
A |
9: 7,645,300 (GRCm39) |
H283Q |
probably benign |
Het |
Mrps5 |
G |
A |
2: 127,445,627 (GRCm39) |
V385M |
possibly damaging |
Het |
Ms4a15 |
T |
C |
19: 10,956,590 (GRCm39) |
K241E |
possibly damaging |
Het |
Myt1 |
A |
G |
2: 181,439,255 (GRCm39) |
E259G |
probably damaging |
Het |
Myt1l |
C |
A |
12: 29,945,304 (GRCm39) |
T1023K |
unknown |
Het |
Ncapd3 |
T |
C |
9: 26,997,342 (GRCm39) |
L1221P |
probably damaging |
Het |
Ncoa6 |
A |
G |
2: 155,249,053 (GRCm39) |
V1417A |
possibly damaging |
Het |
Nmnat1 |
A |
G |
4: 149,557,802 (GRCm39) |
V80A |
possibly damaging |
Het |
Nwd2 |
A |
G |
5: 63,965,189 (GRCm39) |
E1591G |
probably benign |
Het |
Or10ac1 |
A |
G |
6: 42,515,770 (GRCm39) |
F62S |
probably damaging |
Het |
Or8j3b |
A |
G |
2: 86,204,853 (GRCm39) |
L301S |
possibly damaging |
Het |
Osbpl1a |
A |
T |
18: 12,901,593 (GRCm39) |
|
probably null |
Het |
Papln |
T |
C |
12: 83,821,194 (GRCm39) |
I204T |
probably damaging |
Het |
Phf1 |
A |
G |
17: 27,153,652 (GRCm39) |
T97A |
probably benign |
Het |
Plxnb1 |
A |
G |
9: 108,934,442 (GRCm39) |
D890G |
probably damaging |
Het |
Ppp1r12b |
G |
T |
1: 134,883,471 (GRCm39) |
A17E |
probably benign |
Het |
Ptgir |
A |
G |
7: 16,640,794 (GRCm39) |
M29V |
possibly damaging |
Het |
Rbp2 |
G |
A |
9: 98,389,876 (GRCm39) |
C96Y |
probably damaging |
Het |
Rgmb |
A |
T |
17: 16,027,624 (GRCm39) |
M365K |
possibly damaging |
Het |
Ric1 |
A |
G |
19: 29,572,936 (GRCm39) |
N792S |
possibly damaging |
Het |
Ruvbl1 |
T |
C |
6: 88,474,211 (GRCm39) |
Y405H |
possibly damaging |
Het |
Scaf4 |
A |
G |
16: 90,047,195 (GRCm39) |
M394T |
unknown |
Het |
Siglech |
T |
A |
7: 55,418,177 (GRCm39) |
C48* |
probably null |
Het |
Skic2 |
A |
G |
17: 35,061,897 (GRCm39) |
V695A |
possibly damaging |
Het |
Slc2a5 |
A |
G |
4: 150,224,462 (GRCm39) |
T320A |
probably benign |
Het |
Slc6a7 |
T |
C |
18: 61,135,277 (GRCm39) |
Y417C |
probably benign |
Het |
Sox21 |
A |
G |
14: 118,472,336 (GRCm39) |
C238R |
possibly damaging |
Het |
Tbata |
A |
T |
10: 61,019,132 (GRCm39) |
K109N |
probably damaging |
Het |
Tecpr2 |
T |
G |
12: 110,921,164 (GRCm39) |
S1246A |
probably benign |
Het |
Tekt3 |
A |
G |
11: 62,972,085 (GRCm39) |
D247G |
probably benign |
Het |
Tenm3 |
A |
T |
8: 48,766,271 (GRCm39) |
|
probably null |
Het |
Thada |
A |
T |
17: 84,748,532 (GRCm39) |
|
probably null |
Het |
Tpcn2 |
C |
T |
7: 144,826,088 (GRCm39) |
G204R |
probably damaging |
Het |
Tpm2 |
T |
C |
4: 43,519,220 (GRCm39) |
|
probably null |
Het |
Trbv24 |
T |
C |
6: 41,195,026 (GRCm39) |
|
probably benign |
Het |
Tyw1 |
A |
G |
5: 130,305,899 (GRCm39) |
R341G |
probably benign |
Het |
Vmn1r183 |
T |
G |
7: 23,754,564 (GRCm39) |
N122K |
probably benign |
Het |
Vmn2r61 |
T |
A |
7: 41,916,459 (GRCm39) |
H357Q |
possibly damaging |
Het |
Vps13b |
C |
T |
15: 35,869,518 (GRCm39) |
T2674I |
probably damaging |
Het |
Vps13b |
T |
C |
15: 35,910,439 (GRCm39) |
L3401P |
probably benign |
Het |
Vps16 |
T |
G |
2: 130,280,220 (GRCm39) |
|
probably benign |
Het |
Vrtn |
T |
A |
12: 84,696,468 (GRCm39) |
I406N |
probably damaging |
Het |
Vwa8 |
A |
T |
14: 79,172,053 (GRCm39) |
Y278F |
probably benign |
Het |
Washc4 |
A |
T |
10: 83,415,376 (GRCm39) |
I789F |
possibly damaging |
Het |
Zbtb20 |
C |
A |
16: 43,438,761 (GRCm39) |
T627K |
probably damaging |
Het |
Zfyve16 |
A |
T |
13: 92,658,693 (GRCm39) |
I406K |
probably benign |
Het |
Zfyve9 |
A |
C |
4: 108,575,195 (GRCm39) |
S629A |
possibly damaging |
Het |
Zpld1 |
A |
T |
16: 55,068,618 (GRCm39) |
N164K |
probably damaging |
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 |
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 |
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 |
|