Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930512M02Rik |
A |
G |
11: 11,539,365 (GRCm39) |
|
probably benign |
Het |
Apba1 |
A |
C |
19: 23,912,194 (GRCm39) |
N558T |
probably damaging |
Het |
Arfgef2 |
T |
A |
2: 166,702,320 (GRCm39) |
|
probably null |
Het |
Arsb |
T |
C |
13: 94,077,135 (GRCm39) |
S501P |
probably benign |
Het |
Atp10b |
A |
G |
11: 43,145,141 (GRCm39) |
T1295A |
probably benign |
Het |
Atp8b5 |
G |
T |
4: 43,361,898 (GRCm39) |
R648L |
probably damaging |
Het |
Bcl2a1b |
T |
C |
9: 89,081,789 (GRCm39) |
I126T |
possibly damaging |
Het |
Brd9 |
T |
C |
13: 74,090,802 (GRCm39) |
|
probably benign |
Het |
Cd93 |
T |
C |
2: 148,283,430 (GRCm39) |
|
probably benign |
Het |
Chd5 |
A |
G |
4: 152,467,778 (GRCm39) |
K1692R |
probably benign |
Het |
Clcn4 |
T |
C |
7: 7,299,791 (GRCm39) |
T13A |
probably damaging |
Het |
Clec14a |
A |
G |
12: 58,315,580 (GRCm39) |
F14S |
possibly damaging |
Het |
Clec4g |
A |
G |
8: 3,768,440 (GRCm39) |
V97A |
probably benign |
Het |
Col24a1 |
G |
A |
3: 145,229,897 (GRCm39) |
R1483K |
possibly damaging |
Het |
Crem |
A |
T |
18: 3,299,226 (GRCm39) |
V82D |
probably damaging |
Het |
Ctnna2 |
T |
A |
6: 77,618,423 (GRCm39) |
T180S |
probably benign |
Het |
Cybrd1 |
T |
C |
2: 70,960,099 (GRCm39) |
I99T |
probably benign |
Het |
Cyp4a32 |
G |
A |
4: 115,478,671 (GRCm39) |
V468M |
probably damaging |
Het |
Dlk1 |
A |
G |
12: 109,420,985 (GRCm39) |
|
probably benign |
Het |
Dnaaf9 |
C |
T |
2: 130,627,466 (GRCm39) |
|
probably benign |
Het |
Dnah7b |
A |
T |
1: 46,179,336 (GRCm39) |
Y1003F |
probably benign |
Het |
Egfem1 |
A |
C |
3: 29,722,399 (GRCm39) |
E376A |
possibly damaging |
Het |
Etl4 |
T |
A |
2: 20,812,165 (GRCm39) |
I1416K |
probably damaging |
Het |
Fbxl4 |
A |
G |
4: 22,386,106 (GRCm39) |
T238A |
probably benign |
Het |
Fer1l6 |
A |
G |
15: 58,420,187 (GRCm39) |
I33M |
probably benign |
Het |
Fndc3a |
A |
G |
14: 72,794,049 (GRCm39) |
S830P |
probably damaging |
Het |
Fras1 |
C |
T |
5: 96,903,368 (GRCm39) |
R3082* |
probably null |
Het |
Galnt13 |
T |
C |
2: 54,950,504 (GRCm39) |
V395A |
possibly damaging |
Het |
Gpd2 |
C |
T |
2: 57,235,275 (GRCm39) |
T335I |
probably damaging |
Het |
Gucy2d |
C |
A |
7: 98,108,209 (GRCm39) |
|
probably null |
Het |
Hydin |
A |
G |
8: 111,235,759 (GRCm39) |
|
probably benign |
Het |
Ints5 |
G |
T |
19: 8,874,497 (GRCm39) |
V819L |
possibly damaging |
Het |
Klhdc10 |
C |
G |
6: 30,450,669 (GRCm39) |
Q292E |
possibly damaging |
Het |
Lmbrd2 |
G |
A |
15: 9,149,566 (GRCm39) |
A67T |
probably benign |
Het |
Lrp1 |
T |
G |
10: 127,430,838 (GRCm39) |
T404P |
probably damaging |
Het |
Marchf7 |
T |
C |
2: 60,064,470 (GRCm39) |
S249P |
probably benign |
Het |
Mcm10 |
T |
A |
2: 5,013,434 (GRCm39) |
K66M |
probably benign |
Het |
Mtmr7 |
C |
A |
8: 41,004,642 (GRCm39) |
D645Y |
probably damaging |
Het |
Muc6 |
T |
A |
7: 141,216,868 (GRCm39) |
I2602F |
possibly damaging |
Het |
Myh13 |
G |
A |
11: 67,260,121 (GRCm39) |
|
probably benign |
Het |
Myo18a |
G |
A |
11: 77,741,632 (GRCm39) |
V1776I |
possibly damaging |
Het |
Ncapg2 |
T |
C |
12: 116,406,695 (GRCm39) |
L957S |
probably damaging |
Het |
Ncoa3 |
T |
C |
2: 165,896,422 (GRCm39) |
S442P |
probably damaging |
Het |
Or5t5 |
G |
A |
2: 86,616,079 (GRCm39) |
E2K |
probably benign |
Het |
Or6x1 |
G |
A |
9: 40,098,729 (GRCm39) |
G106D |
probably damaging |
Het |
Or7g32 |
T |
A |
9: 19,388,776 (GRCm39) |
T257S |
possibly damaging |
Het |
Pdcd6 |
G |
T |
13: 74,457,831 (GRCm39) |
N113K |
possibly damaging |
Het |
Pfkfb4 |
C |
T |
9: 108,856,810 (GRCm39) |
|
probably benign |
Het |
Pfkm |
A |
G |
15: 98,024,195 (GRCm39) |
H401R |
probably benign |
Het |
Phldb2 |
C |
A |
16: 45,601,814 (GRCm39) |
D754Y |
probably damaging |
Het |
Plekhb2 |
T |
A |
1: 34,902,195 (GRCm39) |
M49K |
probably damaging |
Het |
Polrmt |
A |
G |
10: 79,573,445 (GRCm39) |
S1057P |
possibly damaging |
Het |
Prps1l1 |
A |
G |
12: 35,035,077 (GRCm39) |
N64S |
probably benign |
Het |
Prss3l |
T |
G |
6: 41,422,190 (GRCm39) |
|
probably benign |
Het |
Psg16 |
T |
C |
7: 16,864,583 (GRCm39) |
S393P |
probably benign |
Het |
Rundc1 |
C |
T |
11: 101,315,973 (GRCm39) |
T15I |
probably benign |
Het |
Scaf11 |
A |
G |
15: 96,329,697 (GRCm39) |
L143S |
probably damaging |
Het |
Sephs1 |
A |
G |
2: 4,904,371 (GRCm39) |
T250A |
probably benign |
Het |
Serpinf1 |
T |
G |
11: 75,304,771 (GRCm39) |
I197L |
probably benign |
Het |
Siglec1 |
C |
T |
2: 130,916,445 (GRCm39) |
|
probably benign |
Het |
Slc28a1 |
G |
A |
7: 80,787,925 (GRCm39) |
V271I |
probably benign |
Het |
Sntg1 |
T |
C |
1: 8,853,048 (GRCm39) |
D34G |
probably damaging |
Het |
Sptbn4 |
A |
T |
7: 27,059,161 (GRCm39) |
|
probably benign |
Het |
Suclg1 |
T |
C |
6: 73,233,211 (GRCm39) |
I51T |
possibly damaging |
Het |
Syne1 |
C |
T |
10: 5,491,989 (GRCm39) |
R9Q |
probably damaging |
Het |
Trim47 |
T |
A |
11: 115,997,344 (GRCm39) |
H470L |
probably damaging |
Het |
Ttc41 |
T |
A |
10: 86,548,841 (GRCm39) |
Y12N |
possibly damaging |
Het |
Tubgcp2 |
T |
C |
7: 139,612,105 (GRCm39) |
E69G |
probably damaging |
Het |
Tubgcp3 |
G |
A |
8: 12,691,116 (GRCm39) |
T474M |
probably damaging |
Het |
Ush2a |
T |
C |
1: 188,184,016 (GRCm39) |
L1440P |
probably damaging |
Het |
Usp28 |
A |
C |
9: 48,935,367 (GRCm39) |
D458A |
possibly damaging |
Het |
Vcan |
A |
T |
13: 89,851,665 (GRCm39) |
D1098E |
probably damaging |
Het |
Vmn1r73 |
C |
T |
7: 11,490,773 (GRCm39) |
T197I |
probably benign |
Het |
Vmn2r15 |
T |
C |
5: 109,434,344 (GRCm39) |
S787G |
probably damaging |
Het |
Vmn2r90 |
T |
A |
17: 17,948,401 (GRCm39) |
I549N |
probably damaging |
Het |
Vps33b |
T |
A |
7: 79,933,162 (GRCm39) |
|
probably null |
Het |
Zfp516 |
A |
T |
18: 83,005,795 (GRCm39) |
K900* |
probably null |
Het |
Zfp974 |
T |
A |
7: 27,610,357 (GRCm39) |
N456I |
probably damaging |
Het |
|
Other mutations in Ubr5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Ubr5
|
APN |
15 |
37,984,280 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00548:Ubr5
|
APN |
15 |
38,004,565 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00675:Ubr5
|
APN |
15 |
38,018,528 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL00770:Ubr5
|
APN |
15 |
38,006,785 (GRCm39) |
missense |
probably benign |
0.27 |
IGL00774:Ubr5
|
APN |
15 |
38,006,785 (GRCm39) |
missense |
probably benign |
0.27 |
IGL00919:Ubr5
|
APN |
15 |
38,041,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00962:Ubr5
|
APN |
15 |
37,986,178 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01328:Ubr5
|
APN |
15 |
37,981,767 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01359:Ubr5
|
APN |
15 |
37,973,250 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01394:Ubr5
|
APN |
15 |
38,009,875 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01674:Ubr5
|
APN |
15 |
37,998,623 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01981:Ubr5
|
APN |
15 |
37,996,842 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01993:Ubr5
|
APN |
15 |
37,973,256 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02159:Ubr5
|
APN |
15 |
37,991,623 (GRCm39) |
splice site |
probably benign |
|
IGL02252:Ubr5
|
APN |
15 |
38,025,138 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02442:Ubr5
|
APN |
15 |
38,038,145 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02502:Ubr5
|
APN |
15 |
38,030,933 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02503:Ubr5
|
APN |
15 |
38,018,558 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02503:Ubr5
|
APN |
15 |
38,018,564 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02546:Ubr5
|
APN |
15 |
38,008,991 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02556:Ubr5
|
APN |
15 |
38,002,692 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02647:Ubr5
|
APN |
15 |
37,992,326 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02679:Ubr5
|
APN |
15 |
38,002,558 (GRCm39) |
missense |
probably benign |
0.36 |
IGL02726:Ubr5
|
APN |
15 |
38,000,806 (GRCm39) |
splice site |
probably benign |
|
IGL02884:Ubr5
|
APN |
15 |
37,998,620 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02972:Ubr5
|
APN |
15 |
38,042,196 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03000:Ubr5
|
APN |
15 |
38,025,096 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03028:Ubr5
|
APN |
15 |
38,047,837 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03057:Ubr5
|
APN |
15 |
38,041,150 (GRCm39) |
splice site |
probably benign |
|
IGL03085:Ubr5
|
APN |
15 |
38,029,812 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03198:Ubr5
|
APN |
15 |
38,045,964 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03368:Ubr5
|
APN |
15 |
37,998,560 (GRCm39) |
missense |
probably damaging |
0.96 |
Anchovy
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
P0016:Ubr5
|
UTSW |
15 |
38,000,822 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4142001:Ubr5
|
UTSW |
15 |
38,042,153 (GRCm39) |
missense |
|
|
R0133:Ubr5
|
UTSW |
15 |
37,996,815 (GRCm39) |
missense |
probably damaging |
0.98 |
R0173:Ubr5
|
UTSW |
15 |
38,004,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Ubr5
|
UTSW |
15 |
37,968,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Ubr5
|
UTSW |
15 |
37,968,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R0314:Ubr5
|
UTSW |
15 |
37,997,431 (GRCm39) |
missense |
probably damaging |
0.99 |
R0390:Ubr5
|
UTSW |
15 |
38,030,916 (GRCm39) |
missense |
probably benign |
0.19 |
R0415:Ubr5
|
UTSW |
15 |
37,973,224 (GRCm39) |
missense |
probably damaging |
0.98 |
R0531:Ubr5
|
UTSW |
15 |
37,991,588 (GRCm39) |
missense |
probably benign |
0.34 |
R0650:Ubr5
|
UTSW |
15 |
38,031,051 (GRCm39) |
splice site |
probably benign |
|
R0720:Ubr5
|
UTSW |
15 |
37,973,235 (GRCm39) |
missense |
probably damaging |
0.98 |
R1183:Ubr5
|
UTSW |
15 |
37,997,419 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1302:Ubr5
|
UTSW |
15 |
38,041,723 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1442:Ubr5
|
UTSW |
15 |
38,015,168 (GRCm39) |
splice site |
probably benign |
|
R1507:Ubr5
|
UTSW |
15 |
37,981,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R1575:Ubr5
|
UTSW |
15 |
38,041,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R1577:Ubr5
|
UTSW |
15 |
38,030,974 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1622:Ubr5
|
UTSW |
15 |
38,009,357 (GRCm39) |
unclassified |
probably benign |
|
R1721:Ubr5
|
UTSW |
15 |
38,042,090 (GRCm39) |
missense |
probably benign |
0.18 |
R1799:Ubr5
|
UTSW |
15 |
37,989,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Ubr5
|
UTSW |
15 |
37,981,161 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1867:Ubr5
|
UTSW |
15 |
38,042,090 (GRCm39) |
missense |
probably benign |
0.18 |
R1868:Ubr5
|
UTSW |
15 |
38,042,090 (GRCm39) |
missense |
probably benign |
0.18 |
R2065:Ubr5
|
UTSW |
15 |
38,041,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R2107:Ubr5
|
UTSW |
15 |
37,989,546 (GRCm39) |
missense |
probably benign |
0.00 |
R2201:Ubr5
|
UTSW |
15 |
38,002,543 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2261:Ubr5
|
UTSW |
15 |
37,988,528 (GRCm39) |
missense |
probably damaging |
0.99 |
R2441:Ubr5
|
UTSW |
15 |
37,989,589 (GRCm39) |
missense |
probably damaging |
0.99 |
R2512:Ubr5
|
UTSW |
15 |
38,002,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R3008:Ubr5
|
UTSW |
15 |
38,031,089 (GRCm39) |
missense |
probably benign |
|
R3412:Ubr5
|
UTSW |
15 |
38,004,479 (GRCm39) |
splice site |
probably benign |
|
R3898:Ubr5
|
UTSW |
15 |
37,997,983 (GRCm39) |
missense |
probably benign |
0.02 |
R3900:Ubr5
|
UTSW |
15 |
38,019,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4032:Ubr5
|
UTSW |
15 |
38,025,081 (GRCm39) |
missense |
|
|
R4352:Ubr5
|
UTSW |
15 |
38,041,817 (GRCm39) |
missense |
probably benign |
0.31 |
R4362:Ubr5
|
UTSW |
15 |
38,078,647 (GRCm39) |
missense |
probably damaging |
0.99 |
R4467:Ubr5
|
UTSW |
15 |
38,004,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R4507:Ubr5
|
UTSW |
15 |
38,013,786 (GRCm39) |
missense |
probably damaging |
0.96 |
R4683:Ubr5
|
UTSW |
15 |
38,038,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:Ubr5
|
UTSW |
15 |
38,018,541 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4878:Ubr5
|
UTSW |
15 |
38,006,808 (GRCm39) |
missense |
probably benign |
0.01 |
R4999:Ubr5
|
UTSW |
15 |
38,009,912 (GRCm39) |
missense |
probably benign |
0.06 |
R5057:Ubr5
|
UTSW |
15 |
38,004,353 (GRCm39) |
missense |
probably damaging |
0.98 |
R5177:Ubr5
|
UTSW |
15 |
38,006,761 (GRCm39) |
missense |
probably benign |
0.22 |
R5186:Ubr5
|
UTSW |
15 |
37,998,160 (GRCm39) |
missense |
probably damaging |
0.99 |
R5378:Ubr5
|
UTSW |
15 |
37,989,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R5486:Ubr5
|
UTSW |
15 |
38,008,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5494:Ubr5
|
UTSW |
15 |
38,019,525 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5617:Ubr5
|
UTSW |
15 |
38,030,901 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5636:Ubr5
|
UTSW |
15 |
37,984,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Ubr5
|
UTSW |
15 |
38,015,337 (GRCm39) |
missense |
probably damaging |
0.99 |
R5715:Ubr5
|
UTSW |
15 |
38,002,477 (GRCm39) |
missense |
probably benign |
0.06 |
R5781:Ubr5
|
UTSW |
15 |
38,006,785 (GRCm39) |
missense |
probably benign |
0.27 |
R6645:Ubr5
|
UTSW |
15 |
38,029,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R6774:Ubr5
|
UTSW |
15 |
38,015,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R6823:Ubr5
|
UTSW |
15 |
37,989,842 (GRCm39) |
missense |
probably benign |
0.08 |
R6877:Ubr5
|
UTSW |
15 |
38,002,814 (GRCm39) |
missense |
probably damaging |
0.98 |
R7105:Ubr5
|
UTSW |
15 |
38,009,019 (GRCm39) |
missense |
|
|
R7166:Ubr5
|
UTSW |
15 |
37,976,389 (GRCm39) |
missense |
|
|
R7514:Ubr5
|
UTSW |
15 |
37,988,481 (GRCm39) |
missense |
|
|
R7523:Ubr5
|
UTSW |
15 |
38,004,299 (GRCm39) |
missense |
|
|
R7631:Ubr5
|
UTSW |
15 |
38,029,751 (GRCm39) |
missense |
|
|
R7709:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7710:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7712:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7803:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7816:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7817:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7821:Ubr5
|
UTSW |
15 |
37,997,431 (GRCm39) |
missense |
probably damaging |
0.96 |
R7824:Ubr5
|
UTSW |
15 |
37,991,566 (GRCm39) |
missense |
probably damaging |
0.97 |
R7841:Ubr5
|
UTSW |
15 |
37,981,150 (GRCm39) |
missense |
|
|
R7869:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7896:Ubr5
|
UTSW |
15 |
38,041,817 (GRCm39) |
missense |
probably benign |
0.31 |
R8191:Ubr5
|
UTSW |
15 |
38,006,751 (GRCm39) |
missense |
|
|
R8342:Ubr5
|
UTSW |
15 |
38,025,081 (GRCm39) |
missense |
|
|
R8745:Ubr5
|
UTSW |
15 |
38,025,039 (GRCm39) |
missense |
|
|
R8811:Ubr5
|
UTSW |
15 |
38,041,123 (GRCm39) |
missense |
|
|
R8904:Ubr5
|
UTSW |
15 |
38,042,153 (GRCm39) |
missense |
|
|
R8955:Ubr5
|
UTSW |
15 |
38,029,825 (GRCm39) |
missense |
|
|
R8956:Ubr5
|
UTSW |
15 |
38,015,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Ubr5
|
UTSW |
15 |
38,002,503 (GRCm39) |
missense |
|
|
R9102:Ubr5
|
UTSW |
15 |
38,018,596 (GRCm39) |
missense |
|
|
R9183:Ubr5
|
UTSW |
15 |
37,997,420 (GRCm39) |
missense |
|
|
R9235:Ubr5
|
UTSW |
15 |
38,045,982 (GRCm39) |
missense |
|
|
R9392:Ubr5
|
UTSW |
15 |
37,984,251 (GRCm39) |
missense |
|
|
R9473:Ubr5
|
UTSW |
15 |
38,002,617 (GRCm39) |
missense |
|
|
R9596:Ubr5
|
UTSW |
15 |
37,986,213 (GRCm39) |
missense |
|
|
R9659:Ubr5
|
UTSW |
15 |
37,984,254 (GRCm39) |
missense |
|
|
R9683:Ubr5
|
UTSW |
15 |
37,978,271 (GRCm39) |
missense |
|
|
RF024:Ubr5
|
UTSW |
15 |
38,028,896 (GRCm39) |
missense |
|
|
X0024:Ubr5
|
UTSW |
15 |
37,992,304 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ubr5
|
UTSW |
15 |
38,040,999 (GRCm39) |
missense |
|
|
|