Other mutations in this stock |
Total: 129 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010B08Rik |
C |
T |
2: 173,561,599 (GRCm39) |
|
probably benign |
Het |
Alpk2 |
G |
A |
18: 65,439,450 (GRCm39) |
H648Y |
possibly damaging |
Het |
Ambp |
A |
G |
4: 63,062,502 (GRCm39) |
Y246H |
probably damaging |
Het |
Amz1 |
T |
C |
5: 140,735,088 (GRCm39) |
|
probably null |
Het |
Anks6 |
G |
A |
4: 47,027,109 (GRCm39) |
T703I |
probably damaging |
Het |
Armc2 |
A |
G |
10: 41,823,883 (GRCm39) |
|
probably benign |
Het |
Atp7b |
T |
A |
8: 22,484,672 (GRCm39) |
I1347F |
probably damaging |
Het |
Atp8a1 |
C |
T |
5: 67,779,945 (GRCm39) |
W1149* |
probably null |
Het |
Auh |
A |
G |
13: 52,995,046 (GRCm39) |
I173T |
probably damaging |
Het |
Axin2 |
T |
C |
11: 108,814,829 (GRCm39) |
L239P |
possibly damaging |
Het |
Bbs1 |
A |
T |
19: 4,949,287 (GRCm39) |
F257L |
possibly damaging |
Het |
Cacna2d2 |
C |
T |
9: 107,401,867 (GRCm39) |
P774L |
probably damaging |
Het |
Card6 |
A |
G |
15: 5,137,788 (GRCm39) |
L22P |
probably damaging |
Het |
Ccdc171 |
C |
T |
4: 83,579,946 (GRCm39) |
|
|
Het |
Ccn2 |
T |
C |
10: 24,471,988 (GRCm39) |
V70A |
probably damaging |
Het |
Cdc14a |
T |
A |
3: 116,122,310 (GRCm39) |
N219I |
possibly damaging |
Het |
Cfap65 |
G |
T |
1: 74,967,501 (GRCm39) |
N192K |
probably benign |
Het |
Col14a1 |
T |
C |
15: 55,312,272 (GRCm39) |
|
probably benign |
Het |
Col5a1 |
A |
G |
2: 27,914,665 (GRCm39) |
T94A |
probably benign |
Het |
Col6a5 |
T |
C |
9: 105,759,113 (GRCm39) |
N2031S |
probably damaging |
Het |
Col7a1 |
T |
C |
9: 108,794,989 (GRCm39) |
|
probably benign |
Het |
Cyld |
T |
C |
8: 89,473,543 (GRCm39) |
S739P |
probably damaging |
Het |
Dbr1 |
A |
G |
9: 99,466,072 (GRCm39) |
|
probably null |
Het |
Dip2b |
T |
C |
15: 100,100,233 (GRCm39) |
L1267P |
probably damaging |
Het |
Dolk |
A |
G |
2: 30,175,586 (GRCm39) |
M153T |
probably benign |
Het |
Duxf1 |
C |
T |
10: 58,060,704 (GRCm39) |
E17K |
possibly damaging |
Het |
Duxf1 |
G |
A |
10: 58,060,136 (GRCm39) |
|
probably benign |
Het |
Duxf1 |
A |
G |
10: 58,059,276 (GRCm39) |
C493R |
probably benign |
Het |
Duxf3 |
A |
C |
10: 58,067,498 (GRCm39) |
S27A |
probably benign |
Het |
Eef1d |
C |
T |
15: 75,775,581 (GRCm39) |
R26H |
probably benign |
Homo |
Efcab5 |
C |
T |
11: 77,028,517 (GRCm39) |
|
|
Het |
Epc1 |
T |
C |
18: 6,449,246 (GRCm39) |
D467G |
probably damaging |
Het |
Fancm |
T |
G |
12: 65,152,196 (GRCm39) |
M884R |
probably benign |
Het |
Fbxo24 |
G |
T |
5: 137,620,164 (GRCm39) |
H15N |
probably damaging |
Het |
Frem1 |
A |
G |
4: 82,924,045 (GRCm39) |
F305L |
probably damaging |
Het |
Fstl5 |
A |
G |
3: 76,567,006 (GRCm39) |
D550G |
probably damaging |
Het |
Gcnt3 |
T |
G |
9: 69,941,326 (GRCm39) |
K414T |
possibly damaging |
Het |
Gm10718 |
A |
T |
9: 3,024,417 (GRCm39) |
T134S |
probably benign |
Het |
Gm10722 |
A |
G,C |
9: 3,001,414 (GRCm39) |
|
probably benign |
Het |
Gm10800 |
T |
C |
2: 98,497,163 (GRCm39) |
R152G |
probably benign |
Homo |
Gm10800 |
C |
A |
2: 98,497,250 (GRCm39) |
V123F |
probably benign |
Homo |
Gm10800 |
A |
C |
2: 98,496,893 (GRCm39) |
F220C |
probably benign |
Het |
Gm10801 |
A |
G |
2: 98,492,648 (GRCm39) |
R23G |
probably benign |
Homo |
Gm11168 |
C |
T |
9: 3,004,605 (GRCm39) |
P49S |
probably benign |
Het |
Gm21738 |
G |
A |
14: 19,417,330 (GRCm38) |
S66L |
probably benign |
Het |
Hjurp |
TCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCTG |
T |
1: 88,194,000 (GRCm39) |
|
probably benign |
Het |
Hmgcr |
A |
G |
13: 96,795,562 (GRCm39) |
Y336H |
probably damaging |
Het |
Hoxa13 |
G |
C |
6: 52,260,648 (GRCm38) |
|
probably benign |
Homo |
Hoxa13 |
C |
G |
6: 52,260,647 (GRCm38) |
|
probably benign |
Homo |
Igf2bp3 |
A |
C |
6: 49,094,084 (GRCm39) |
|
probably null |
Het |
Kcnb2 |
A |
T |
1: 15,383,200 (GRCm39) |
K175N |
possibly damaging |
Het |
Kdr |
T |
C |
5: 76,102,631 (GRCm39) |
|
probably benign |
Het |
Kif5c |
A |
G |
2: 49,584,044 (GRCm39) |
K160E |
probably damaging |
Het |
Kif7 |
A |
T |
7: 79,360,817 (GRCm39) |
V186E |
probably damaging |
Het |
Krt16 |
T |
A |
11: 100,139,575 (GRCm39) |
T48S |
unknown |
Het |
Liph |
T |
C |
16: 21,814,119 (GRCm39) |
M1V |
probably null |
Het |
Mctp2 |
A |
G |
7: 71,740,005 (GRCm39) |
F795S |
probably damaging |
Het |
Muc4 |
T |
A |
16: 32,755,699 (GRCm38) |
|
probably benign |
Homo |
Muc4 |
C |
G |
16: 32,755,676 (GRCm38) |
|
probably benign |
Homo |
Muc4 |
T |
A |
16: 32,755,684 (GRCm38) |
|
probably benign |
Homo |
Myo15a |
G |
T |
11: 60,373,953 (GRCm39) |
A1267S |
probably damaging |
Het |
Myo15a |
T |
C |
11: 60,386,280 (GRCm39) |
Y1802H |
probably damaging |
Het |
Myo7b |
G |
A |
18: 32,094,259 (GRCm39) |
T1963I |
probably benign |
Het |
Nadk2 |
TG |
T |
15: 9,100,232 (GRCm39) |
|
probably null |
Homo |
Naip5 |
T |
C |
13: 100,356,268 (GRCm39) |
N1116D |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,356,247 (GRCm39) |
R1123G |
probably benign |
Het |
Nap1l1 |
A |
G |
10: 111,322,583 (GRCm39) |
D61G |
probably null |
Het |
Napsa |
A |
T |
7: 44,230,875 (GRCm39) |
T81S |
probably damaging |
Het |
Ngp |
T |
C |
9: 110,251,337 (GRCm39) |
|
probably benign |
Het |
Nktr |
T |
A |
9: 121,570,687 (GRCm39) |
V143E |
probably damaging |
Het |
Obscn |
A |
G |
11: 58,957,890 (GRCm39) |
|
probably null |
Het |
Or10ag53 |
G |
A |
2: 87,082,973 (GRCm39) |
A231T |
probably benign |
Het |
Or11i1 |
T |
C |
3: 106,729,282 (GRCm39) |
I198V |
probably benign |
Het |
Or4f56 |
G |
A |
2: 111,703,649 (GRCm39) |
L184F |
probably benign |
Het |
Or52ab2 |
C |
T |
7: 102,970,076 (GRCm39) |
R153* |
probably null |
Het |
Or52d3 |
G |
A |
7: 104,229,237 (GRCm39) |
R128Q |
probably damaging |
Het |
Or6p1 |
A |
G |
1: 174,258,390 (GRCm39) |
Y132C |
probably damaging |
Het |
Paip2b |
A |
G |
6: 83,785,823 (GRCm39) |
Y136H |
probably damaging |
Het |
Pde2a |
G |
T |
7: 101,160,361 (GRCm39) |
R845L |
probably damaging |
Het |
Pgap2 |
A |
G |
7: 101,886,405 (GRCm39) |
Y197C |
possibly damaging |
Het |
Phf11b |
A |
G |
14: 59,560,611 (GRCm39) |
|
probably benign |
Het |
Pitpnm2 |
A |
T |
5: 124,269,178 (GRCm39) |
D481E |
probably benign |
Het |
Pxk |
A |
T |
14: 8,152,130 (GRCm38) |
H482L |
probably benign |
Het |
Rad50 |
A |
G |
11: 53,585,726 (GRCm39) |
|
probably null |
Het |
Rbmyf1 |
T |
A |
Y: 2,787,132 (GRCm39) |
N228Y |
probably benign |
Het |
Rbmyf5 |
T |
C |
Y: 3,297,411 (GRCm39) |
H235R |
probably benign |
Het |
Rbmyf6 |
C |
T |
Y: 3,328,944 (GRCm39) |
A241T |
possibly damaging |
Het |
Rnf220 |
A |
G |
4: 117,134,566 (GRCm39) |
|
probably null |
Het |
Saxo5 |
T |
A |
8: 3,526,062 (GRCm39) |
S72T |
possibly damaging |
Het |
Selenbp1 |
C |
T |
3: 94,844,607 (GRCm39) |
T88M |
probably damaging |
Het |
Sft2d1 |
T |
C |
17: 8,609,863 (GRCm39) |
I104T |
possibly damaging |
Het |
Sik1 |
A |
G |
17: 32,070,305 (GRCm39) |
S135P |
probably damaging |
Het |
Slc16a3 |
T |
C |
11: 120,846,172 (GRCm39) |
F34L |
probably damaging |
Het |
Slc6a20b |
T |
C |
9: 123,612,126 (GRCm38) |
N85S |
probably benign |
Homo |
Snrnp27 |
T |
C |
6: 86,659,893 (GRCm39) |
R34G |
unknown |
Het |
Sos2 |
T |
C |
12: 69,664,851 (GRCm39) |
H393R |
probably benign |
Het |
Sp110 |
C |
T |
1: 85,513,971 (GRCm39) |
R262Q |
probably benign |
Het |
Sp110 |
T |
C |
1: 85,513,975 (GRCm39) |
R261G |
probably benign |
Het |
Sp140 |
T |
A |
1: 85,528,893 (GRCm39) |
Y5N |
probably benign |
Het |
Sp140 |
A |
G |
1: 85,570,942 (GRCm39) |
S461G |
probably benign |
Het |
Sp140 |
G |
C |
1: 85,538,603 (GRCm39) |
K113N |
probably benign |
Het |
Sp140l1 |
G |
A |
1: 85,077,341 (GRCm39) |
A75V |
probably benign |
Het |
Sp140l2 |
A |
C |
1: 85,223,395 (GRCm39) |
|
probably benign |
Het |
Speer4a2 |
C |
G |
5: 26,294,093 (GRCm39) |
W28C |
probably damaging |
Het |
Speer4a2 |
A |
T |
5: 26,291,485 (GRCm39) |
F107Y |
probably benign |
Het |
Ssrp1 |
G |
A |
2: 84,868,760 (GRCm39) |
V40M |
probably damaging |
Het |
Tada2a |
T |
C |
11: 83,970,563 (GRCm39) |
E202G |
probably damaging |
Het |
Tcf20 |
C |
A |
15: 82,735,785 (GRCm39) |
A1889S |
probably damaging |
Het |
Tdrd12 |
A |
T |
7: 35,180,528 (GRCm39) |
Y828* |
probably null |
Het |
Tlr2 |
T |
A |
3: 83,745,756 (GRCm39) |
D109V |
probably benign |
Het |
Tomm40 |
G |
A |
7: 19,437,016 (GRCm39) |
T17M |
probably damaging |
Het |
Tsga10ip |
T |
C |
19: 5,440,161 (GRCm39) |
T135A |
possibly damaging |
Het |
Tspan8 |
G |
A |
10: 115,653,515 (GRCm39) |
V4M |
probably damaging |
Het |
Ttc28 |
A |
T |
5: 111,040,719 (GRCm39) |
T36S |
probably benign |
Het |
Ugt1a6b |
G |
A |
1: 88,146,112 (GRCm39) |
R519Q |
probably damaging |
Het |
Ugt1a6b |
TTCA |
T |
1: 88,143,880 (GRCm39) |
|
probably benign |
Het |
Ugt1a6b |
G |
A |
1: 88,143,976 (GRCm39) |
A199T |
probably damaging |
Het |
Unc45a |
A |
G |
7: 79,976,109 (GRCm39) |
M790T |
possibly damaging |
Het |
Vav3 |
T |
C |
3: 109,571,751 (GRCm39) |
|
probably null |
Het |
Vcpkmt |
G |
A |
12: 69,629,552 (GRCm39) |
S70L |
probably benign |
Het |
Vmn1r3 |
C |
T |
4: 3,184,691 (GRCm39) |
M205I |
probably damaging |
Het |
Vmn1r3 |
C |
T |
4: 3,184,774 (GRCm39) |
V178I |
probably benign |
Het |
Vmn2r66 |
T |
C |
7: 84,644,301 (GRCm39) |
Q703R |
probably damaging |
Het |
Wfdc8 |
A |
G |
2: 164,439,696 (GRCm39) |
S229P |
possibly damaging |
Het |
Xpo4 |
A |
T |
14: 57,822,068 (GRCm39) |
C1083S |
probably null |
Het |
Zbtb38 |
T |
C |
9: 96,568,369 (GRCm39) |
D905G |
probably damaging |
Het |
Zbtb8b |
A |
G |
4: 129,321,308 (GRCm39) |
*518Q |
probably null |
Het |
Zfp600 |
TC |
T |
4: 146,131,802 (GRCm39) |
|
probably null |
Het |
Zfp992 |
C |
T |
4: 146,550,569 (GRCm39) |
P97S |
probably benign |
Het |
|
Other mutations in Vmn2r98 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00897:Vmn2r98
|
APN |
17 |
19,286,007 (GRCm39) |
splice site |
probably benign |
|
IGL01296:Vmn2r98
|
APN |
17 |
19,285,447 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01363:Vmn2r98
|
APN |
17 |
19,286,020 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01618:Vmn2r98
|
APN |
17 |
19,285,521 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01746:Vmn2r98
|
APN |
17 |
19,286,713 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01747:Vmn2r98
|
APN |
17 |
19,286,702 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01770:Vmn2r98
|
APN |
17 |
19,286,702 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01868:Vmn2r98
|
APN |
17 |
19,286,548 (GRCm39) |
missense |
probably benign |
|
IGL02123:Vmn2r98
|
APN |
17 |
19,300,941 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02323:Vmn2r98
|
APN |
17 |
19,286,113 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02543:Vmn2r98
|
APN |
17 |
19,286,083 (GRCm39) |
missense |
probably benign |
|
IGL02650:Vmn2r98
|
APN |
17 |
19,301,223 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02676:Vmn2r98
|
APN |
17 |
19,285,521 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02803:Vmn2r98
|
APN |
17 |
19,286,275 (GRCm39) |
missense |
probably benign |
|
IGL02807:Vmn2r98
|
APN |
17 |
19,301,283 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03307:Vmn2r98
|
APN |
17 |
19,286,242 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03396:Vmn2r98
|
APN |
17 |
19,290,107 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0122:Vmn2r98
|
UTSW |
17 |
19,286,662 (GRCm39) |
missense |
probably benign |
0.06 |
R0329:Vmn2r98
|
UTSW |
17 |
19,286,609 (GRCm39) |
missense |
probably benign |
0.21 |
R0330:Vmn2r98
|
UTSW |
17 |
19,286,609 (GRCm39) |
missense |
probably benign |
0.21 |
R0368:Vmn2r98
|
UTSW |
17 |
19,286,089 (GRCm39) |
nonsense |
probably null |
|
R0545:Vmn2r98
|
UTSW |
17 |
19,273,875 (GRCm39) |
missense |
probably benign |
0.15 |
R0635:Vmn2r98
|
UTSW |
17 |
19,300,759 (GRCm39) |
missense |
probably benign |
0.00 |
R0689:Vmn2r98
|
UTSW |
17 |
19,300,782 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1035:Vmn2r98
|
UTSW |
17 |
19,301,011 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1243:Vmn2r98
|
UTSW |
17 |
19,286,210 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1421:Vmn2r98
|
UTSW |
17 |
19,285,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R1629:Vmn2r98
|
UTSW |
17 |
19,287,645 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1643:Vmn2r98
|
UTSW |
17 |
19,301,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1795:Vmn2r98
|
UTSW |
17 |
19,286,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R1958:Vmn2r98
|
UTSW |
17 |
19,286,680 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1962:Vmn2r98
|
UTSW |
17 |
19,285,595 (GRCm39) |
nonsense |
probably null |
|
R2165:Vmn2r98
|
UTSW |
17 |
19,301,553 (GRCm39) |
missense |
unknown |
|
R2238:Vmn2r98
|
UTSW |
17 |
19,286,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R2252:Vmn2r98
|
UTSW |
17 |
19,300,698 (GRCm39) |
missense |
probably benign |
0.00 |
R2323:Vmn2r98
|
UTSW |
17 |
19,286,081 (GRCm39) |
missense |
probably benign |
0.18 |
R2887:Vmn2r98
|
UTSW |
17 |
19,301,439 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2909:Vmn2r98
|
UTSW |
17 |
19,287,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R3001:Vmn2r98
|
UTSW |
17 |
19,286,125 (GRCm39) |
missense |
probably benign |
0.01 |
R3002:Vmn2r98
|
UTSW |
17 |
19,286,125 (GRCm39) |
missense |
probably benign |
0.01 |
R3003:Vmn2r98
|
UTSW |
17 |
19,286,125 (GRCm39) |
missense |
probably benign |
0.01 |
R3788:Vmn2r98
|
UTSW |
17 |
19,300,887 (GRCm39) |
missense |
probably benign |
0.31 |
R4570:Vmn2r98
|
UTSW |
17 |
19,286,354 (GRCm39) |
missense |
probably benign |
0.11 |
R4706:Vmn2r98
|
UTSW |
17 |
19,290,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R4723:Vmn2r98
|
UTSW |
17 |
19,286,602 (GRCm39) |
missense |
probably benign |
0.01 |
R5036:Vmn2r98
|
UTSW |
17 |
19,286,419 (GRCm39) |
missense |
probably benign |
0.00 |
R5072:Vmn2r98
|
UTSW |
17 |
19,286,306 (GRCm39) |
missense |
probably benign |
0.07 |
R5121:Vmn2r98
|
UTSW |
17 |
19,273,815 (GRCm39) |
missense |
probably benign |
0.13 |
R5283:Vmn2r98
|
UTSW |
17 |
19,300,981 (GRCm39) |
missense |
probably benign |
0.05 |
R5294:Vmn2r98
|
UTSW |
17 |
19,290,016 (GRCm39) |
nonsense |
probably null |
|
R5371:Vmn2r98
|
UTSW |
17 |
19,290,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R5532:Vmn2r98
|
UTSW |
17 |
19,287,645 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5598:Vmn2r98
|
UTSW |
17 |
19,301,161 (GRCm39) |
missense |
probably benign |
0.37 |
R5800:Vmn2r98
|
UTSW |
17 |
19,286,260 (GRCm39) |
missense |
probably benign |
0.17 |
R6089:Vmn2r98
|
UTSW |
17 |
19,286,336 (GRCm39) |
missense |
probably benign |
0.29 |
R6155:Vmn2r98
|
UTSW |
17 |
19,286,143 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6853:Vmn2r98
|
UTSW |
17 |
19,286,063 (GRCm39) |
missense |
probably benign |
0.00 |
R6920:Vmn2r98
|
UTSW |
17 |
19,285,510 (GRCm39) |
missense |
probably damaging |
0.98 |
R7012:Vmn2r98
|
UTSW |
17 |
19,286,530 (GRCm39) |
missense |
probably benign |
0.06 |
R7042:Vmn2r98
|
UTSW |
17 |
19,301,184 (GRCm39) |
missense |
probably benign |
|
R7068:Vmn2r98
|
UTSW |
17 |
19,285,575 (GRCm39) |
missense |
probably benign |
|
R7607:Vmn2r98
|
UTSW |
17 |
19,287,570 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7763:Vmn2r98
|
UTSW |
17 |
19,300,797 (GRCm39) |
missense |
probably benign |
0.00 |
R7771:Vmn2r98
|
UTSW |
17 |
19,287,460 (GRCm39) |
splice site |
probably null |
|
R7915:Vmn2r98
|
UTSW |
17 |
19,287,493 (GRCm39) |
missense |
probably benign |
0.10 |
R8028:Vmn2r98
|
UTSW |
17 |
19,273,912 (GRCm39) |
missense |
probably benign |
0.00 |
R8205:Vmn2r98
|
UTSW |
17 |
19,301,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R8241:Vmn2r98
|
UTSW |
17 |
19,301,031 (GRCm39) |
missense |
probably damaging |
0.99 |
R8906:Vmn2r98
|
UTSW |
17 |
19,286,532 (GRCm39) |
missense |
probably benign |
|
R8952:Vmn2r98
|
UTSW |
17 |
19,285,531 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9147:Vmn2r98
|
UTSW |
17 |
19,286,383 (GRCm39) |
missense |
probably benign |
0.04 |
R9148:Vmn2r98
|
UTSW |
17 |
19,286,383 (GRCm39) |
missense |
probably benign |
0.04 |
R9187:Vmn2r98
|
UTSW |
17 |
19,301,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R9344:Vmn2r98
|
UTSW |
17 |
19,286,777 (GRCm39) |
missense |
probably benign |
0.14 |
R9467:Vmn2r98
|
UTSW |
17 |
19,287,517 (GRCm39) |
missense |
probably benign |
0.01 |
R9487:Vmn2r98
|
UTSW |
17 |
19,301,496 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9753:Vmn2r98
|
UTSW |
17 |
19,285,665 (GRCm39) |
missense |
probably benign |
0.27 |
Z1177:Vmn2r98
|
UTSW |
17 |
19,287,685 (GRCm39) |
nonsense |
probably null |
|
Z1177:Vmn2r98
|
UTSW |
17 |
19,285,398 (GRCm39) |
critical splice acceptor site |
probably null |
|
|