Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057M21Rik |
A |
G |
7: 130,959,389 (GRCm39) |
S150P |
probably damaging |
Het |
5530400C23Rik |
T |
G |
6: 133,270,174 (GRCm39) |
|
probably benign |
Het |
Ahctf1 |
A |
C |
1: 179,591,033 (GRCm39) |
|
probably null |
Het |
Ang5 |
T |
C |
14: 44,200,206 (GRCm39) |
V90A |
probably benign |
Het |
Ano9 |
C |
T |
7: 140,684,623 (GRCm39) |
G442R |
probably damaging |
Het |
Apaf1 |
G |
A |
10: 90,895,914 (GRCm39) |
T386I |
probably damaging |
Het |
Apob |
C |
A |
12: 8,056,440 (GRCm39) |
H1608N |
probably damaging |
Het |
Arhgap12 |
C |
A |
18: 6,064,433 (GRCm39) |
|
probably benign |
Het |
Asxl1 |
T |
A |
2: 153,241,824 (GRCm39) |
D791E |
probably benign |
Het |
Avl9 |
T |
C |
6: 56,713,891 (GRCm39) |
V383A |
probably benign |
Het |
Btbd1 |
A |
C |
7: 81,465,754 (GRCm39) |
D197E |
probably damaging |
Het |
Camta2 |
T |
C |
11: 70,564,785 (GRCm39) |
I938V |
possibly damaging |
Het |
Ccn5 |
G |
A |
2: 163,667,233 (GRCm39) |
C78Y |
probably damaging |
Het |
Cdca7 |
C |
A |
2: 72,313,811 (GRCm39) |
A200D |
possibly damaging |
Het |
Cep104 |
A |
T |
4: 154,091,249 (GRCm39) |
Y923F |
possibly damaging |
Het |
Cep135 |
G |
C |
5: 76,769,152 (GRCm39) |
V601L |
probably benign |
Het |
Ces2b |
G |
A |
8: 105,562,542 (GRCm39) |
G291S |
probably benign |
Het |
Col6a6 |
C |
T |
9: 105,638,639 (GRCm39) |
G1400D |
probably damaging |
Het |
Cyth2 |
T |
C |
7: 45,462,541 (GRCm39) |
E1G |
probably damaging |
Het |
Dand5 |
A |
T |
8: 85,542,921 (GRCm39) |
L185Q |
probably damaging |
Het |
Dck |
T |
C |
5: 88,929,080 (GRCm39) |
V253A |
probably benign |
Het |
Ddx20 |
A |
G |
3: 105,586,396 (GRCm39) |
S650P |
probably damaging |
Het |
Dicer1 |
G |
A |
12: 104,673,123 (GRCm39) |
P799S |
probably damaging |
Het |
Dst |
C |
T |
1: 34,228,200 (GRCm39) |
P1606L |
probably damaging |
Het |
Eya2 |
G |
A |
2: 165,611,157 (GRCm39) |
C477Y |
probably damaging |
Het |
Fip1l1 |
T |
A |
5: 74,756,503 (GRCm39) |
N498K |
probably damaging |
Het |
Flt4 |
C |
T |
11: 49,527,166 (GRCm39) |
|
probably benign |
Het |
Galntl6 |
T |
C |
8: 58,290,217 (GRCm39) |
|
probably null |
Het |
Gda |
A |
T |
19: 21,411,667 (GRCm39) |
F44I |
possibly damaging |
Het |
Gli2 |
G |
A |
1: 118,768,119 (GRCm39) |
R703C |
probably damaging |
Het |
Gramd1b |
T |
C |
9: 40,219,651 (GRCm39) |
D341G |
probably damaging |
Het |
Grid2 |
G |
T |
6: 63,480,419 (GRCm39) |
A78S |
probably benign |
Het |
Hao2 |
A |
T |
3: 98,790,876 (GRCm39) |
|
probably benign |
Het |
Hook3 |
A |
G |
8: 26,609,014 (GRCm39) |
V10A |
probably benign |
Het |
Kif20a |
A |
G |
18: 34,762,262 (GRCm39) |
E425G |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,403,252 (GRCm39) |
D2107G |
probably benign |
Het |
Lrriq3 |
T |
C |
3: 154,893,373 (GRCm39) |
I358T |
possibly damaging |
Het |
Mad2l2 |
A |
G |
4: 148,225,381 (GRCm39) |
D17G |
possibly damaging |
Het |
Mastl |
G |
T |
2: 23,023,358 (GRCm39) |
T455K |
probably benign |
Het |
Mkln1 |
G |
T |
6: 31,409,862 (GRCm39) |
|
probably benign |
Het |
Mmp1b |
A |
T |
9: 7,387,947 (GRCm39) |
Y16N |
possibly damaging |
Het |
Mmp24 |
C |
T |
2: 155,634,517 (GRCm39) |
A79V |
probably benign |
Het |
Mrps35 |
T |
A |
6: 146,972,232 (GRCm39) |
C292S |
possibly damaging |
Het |
Myom1 |
T |
C |
17: 71,427,643 (GRCm39) |
F1435L |
possibly damaging |
Het |
Nars2 |
C |
T |
7: 96,689,130 (GRCm39) |
H351Y |
probably damaging |
Het |
Nat2 |
A |
T |
8: 67,953,919 (GRCm39) |
I10F |
probably damaging |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Olfm5 |
A |
T |
7: 103,803,076 (GRCm39) |
Y462* |
probably null |
Het |
Or13p5 |
C |
T |
4: 118,591,986 (GRCm39) |
H87Y |
probably damaging |
Het |
Or1j12 |
C |
A |
2: 36,342,660 (GRCm39) |
A21E |
probably benign |
Het |
Or2w3 |
C |
A |
11: 58,556,986 (GRCm39) |
F200L |
probably damaging |
Het |
Or4c122 |
C |
A |
2: 89,079,742 (GRCm39) |
E87* |
probably null |
Het |
Or4e1 |
T |
C |
14: 52,700,966 (GRCm39) |
I167V |
probably benign |
Het |
Or5p70 |
T |
A |
7: 107,994,438 (GRCm39) |
I37N |
probably damaging |
Het |
Or7g35 |
T |
C |
9: 19,496,600 (GRCm39) |
S256P |
possibly damaging |
Het |
Or8d2b |
T |
A |
9: 38,789,111 (GRCm39) |
I213N |
probably damaging |
Het |
Or8g20 |
A |
T |
9: 39,396,284 (GRCm39) |
F85L |
probably benign |
Het |
Otog |
A |
T |
7: 45,900,819 (GRCm39) |
|
probably benign |
Het |
Pdcd2l |
A |
T |
7: 33,892,232 (GRCm39) |
D212E |
possibly damaging |
Het |
Pex5 |
T |
C |
6: 124,381,596 (GRCm39) |
N213S |
probably benign |
Het |
Pkn3 |
C |
T |
2: 29,971,146 (GRCm39) |
P238S |
probably benign |
Het |
Pramel32 |
A |
T |
4: 88,547,536 (GRCm39) |
I45K |
probably damaging |
Het |
Prl2b1 |
A |
T |
13: 27,574,723 (GRCm39) |
|
probably null |
Het |
Ptprb |
A |
T |
10: 116,204,712 (GRCm39) |
I1849L |
possibly damaging |
Het |
Rasal3 |
G |
T |
17: 32,612,500 (GRCm39) |
S787Y |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,532,177 (GRCm39) |
D596E |
possibly damaging |
Het |
Sdhd |
A |
T |
9: 50,515,064 (GRCm39) |
V9D |
possibly damaging |
Het |
Serinc5 |
T |
C |
13: 92,844,565 (GRCm39) |
S436P |
probably damaging |
Het |
Slc27a1 |
C |
T |
8: 72,036,808 (GRCm39) |
P348L |
probably damaging |
Het |
Slc28a2b |
A |
T |
2: 122,344,879 (GRCm39) |
I162F |
probably damaging |
Het |
Smg1 |
G |
A |
7: 117,759,606 (GRCm39) |
|
probably benign |
Het |
Sorl1 |
A |
T |
9: 41,955,196 (GRCm39) |
|
probably benign |
Het |
Sprtn |
T |
A |
8: 125,626,957 (GRCm39) |
H112Q |
probably damaging |
Het |
Tasor2 |
A |
T |
13: 3,626,054 (GRCm39) |
F1299I |
probably benign |
Het |
Tet2 |
A |
G |
3: 133,173,363 (GRCm39) |
M1633T |
probably benign |
Het |
Tet2 |
T |
A |
3: 133,173,486 (GRCm39) |
D1592V |
probably benign |
Het |
Tmem68 |
A |
T |
4: 3,569,667 (GRCm39) |
C8S |
probably damaging |
Het |
Tnrc6a |
T |
A |
7: 122,771,039 (GRCm39) |
I943N |
probably benign |
Het |
Trib2 |
A |
T |
12: 15,844,069 (GRCm39) |
V191D |
probably damaging |
Het |
Tsc22d4 |
T |
C |
5: 137,760,917 (GRCm39) |
S113P |
probably damaging |
Het |
Ttc21b |
T |
C |
2: 66,069,914 (GRCm39) |
R250G |
probably damaging |
Het |
Ubr2 |
T |
C |
17: 47,278,174 (GRCm39) |
Y721C |
probably damaging |
Het |
Ubtfl1 |
A |
T |
9: 18,320,660 (GRCm39) |
I63F |
probably damaging |
Het |
Ush1c |
G |
A |
7: 45,874,332 (GRCm39) |
P171S |
probably benign |
Het |
Utp20 |
A |
T |
10: 88,603,323 (GRCm39) |
N1843K |
probably damaging |
Het |
Vangl1 |
A |
G |
3: 102,074,253 (GRCm39) |
Y285H |
probably damaging |
Het |
Virma |
A |
G |
4: 11,498,769 (GRCm39) |
D70G |
probably damaging |
Het |
Vmn2r102 |
T |
C |
17: 19,898,277 (GRCm39) |
F431L |
probably benign |
Het |
Wdr17 |
A |
G |
8: 55,114,530 (GRCm39) |
I662T |
probably damaging |
Het |
Wdr87-ps |
T |
A |
7: 29,232,690 (GRCm39) |
|
noncoding transcript |
Het |
Zfp160 |
G |
A |
17: 21,247,268 (GRCm39) |
R606H |
probably benign |
Het |
Zfp369 |
C |
T |
13: 65,444,248 (GRCm39) |
R464C |
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 |
|
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 |
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 |
|