Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr3 |
A |
T |
1: 125,322,874 (GRCm39) |
D364E |
probably benign |
Het |
Adra2c |
C |
T |
5: 35,437,423 (GRCm39) |
T65I |
probably damaging |
Het |
Agap2 |
T |
A |
10: 126,925,229 (GRCm39) |
|
probably null |
Het |
Ager |
T |
C |
17: 34,817,728 (GRCm39) |
V126A |
possibly damaging |
Het |
Arhgap39 |
T |
C |
15: 76,621,736 (GRCm39) |
I288M |
probably benign |
Het |
Arhgap45 |
A |
T |
10: 79,862,068 (GRCm39) |
S541C |
probably benign |
Het |
Asb4 |
A |
G |
6: 5,431,043 (GRCm39) |
Y426C |
probably damaging |
Het |
Azi2 |
C |
T |
9: 117,878,406 (GRCm39) |
T82I |
probably damaging |
Het |
Ccdc146 |
A |
C |
5: 21,506,338 (GRCm39) |
I701S |
probably damaging |
Het |
Ccnq |
T |
C |
11: 78,642,056 (GRCm39) |
K145E |
probably damaging |
Het |
Cd55b |
T |
A |
1: 130,345,903 (GRCm39) |
I172F |
probably damaging |
Het |
Cdk11b |
A |
G |
4: 155,718,647 (GRCm39) |
E199G |
probably benign |
Het |
Cntnap4 |
A |
T |
8: 113,478,921 (GRCm39) |
T216S |
possibly damaging |
Het |
D5Ertd579e |
A |
T |
5: 36,761,858 (GRCm39) |
N1336K |
possibly damaging |
Het |
Dlg5 |
T |
C |
14: 24,214,636 (GRCm39) |
N649S |
probably damaging |
Het |
Dmxl1 |
A |
G |
18: 49,979,653 (GRCm39) |
E96G |
probably benign |
Het |
Dscaml1 |
C |
T |
9: 45,579,458 (GRCm39) |
T335I |
possibly damaging |
Het |
Epb41l2 |
G |
T |
10: 25,378,022 (GRCm39) |
G695C |
probably damaging |
Het |
Erbb4 |
C |
T |
1: 68,599,735 (GRCm39) |
R114H |
probably damaging |
Het |
F2rl1 |
G |
T |
13: 95,650,446 (GRCm39) |
Y145* |
probably null |
Het |
Fsip2 |
A |
T |
2: 82,810,785 (GRCm39) |
Y2368F |
possibly damaging |
Het |
Galnt7 |
C |
T |
8: 57,989,612 (GRCm39) |
|
probably null |
Het |
Garre1 |
A |
T |
7: 33,941,802 (GRCm39) |
Y627* |
probably null |
Het |
Gm6811 |
T |
A |
17: 21,314,245 (GRCm39) |
|
noncoding transcript |
Het |
Gm6811 |
T |
G |
17: 21,314,952 (GRCm39) |
|
noncoding transcript |
Het |
H2-M1 |
G |
A |
17: 36,982,602 (GRCm39) |
T86M |
possibly damaging |
Het |
Hk2 |
T |
C |
6: 82,720,347 (GRCm39) |
D170G |
probably benign |
Het |
Hmcn1 |
C |
T |
1: 150,614,432 (GRCm39) |
A1325T |
possibly damaging |
Het |
Insrr |
T |
A |
3: 87,707,826 (GRCm39) |
Y89* |
probably null |
Het |
Itga1 |
T |
C |
13: 115,117,388 (GRCm39) |
E871G |
probably benign |
Het |
Kat6a |
T |
C |
8: 23,429,421 (GRCm39) |
L1592P |
possibly damaging |
Het |
Kndc1 |
C |
A |
7: 139,500,979 (GRCm39) |
A756E |
probably benign |
Het |
Krt12 |
A |
T |
11: 99,312,728 (GRCm39) |
C105* |
probably null |
Het |
Lama1 |
G |
A |
17: 68,091,083 (GRCm39) |
|
probably null |
Het |
Lama3 |
A |
G |
18: 12,640,006 (GRCm39) |
N67S |
probably benign |
Het |
Lrrk1 |
A |
G |
7: 65,956,587 (GRCm39) |
|
probably null |
Het |
Lypd9 |
T |
A |
11: 58,337,192 (GRCm39) |
I94L |
possibly damaging |
Het |
Map2 |
T |
C |
1: 66,438,578 (GRCm39) |
V34A |
probably damaging |
Het |
Mroh6 |
A |
G |
15: 75,757,549 (GRCm39) |
L487P |
probably damaging |
Het |
Myo18b |
A |
T |
5: 112,959,508 (GRCm39) |
S1430T |
probably benign |
Het |
Notch3 |
G |
A |
17: 32,373,723 (GRCm39) |
T495I |
probably benign |
Het |
Or1e31 |
A |
T |
11: 73,690,229 (GRCm39) |
M118K |
probably damaging |
Het |
Palld |
C |
T |
8: 61,966,457 (GRCm39) |
A980T |
probably damaging |
Het |
Paxip1 |
A |
T |
5: 27,966,666 (GRCm39) |
I620N |
probably damaging |
Het |
Pcdha6 |
A |
G |
18: 37,102,820 (GRCm39) |
|
probably null |
Het |
Pcdhb11 |
G |
A |
18: 37,554,813 (GRCm39) |
V48M |
probably benign |
Het |
Pcdhga6 |
A |
G |
18: 37,840,697 (GRCm39) |
E139G |
probably benign |
Het |
Pck1 |
T |
C |
2: 172,999,112 (GRCm39) |
V426A |
probably damaging |
Het |
Pck2 |
T |
A |
14: 55,780,081 (GRCm39) |
I110N |
probably damaging |
Het |
Peg10 |
GAT |
GATCAT |
6: 4,756,449 (GRCm39) |
|
probably benign |
Het |
Phactr3 |
G |
A |
2: 177,920,812 (GRCm39) |
E222K |
probably damaging |
Het |
Ppip5k1 |
A |
T |
2: 121,153,684 (GRCm39) |
|
probably benign |
Het |
Prodh2 |
A |
G |
7: 30,206,076 (GRCm39) |
H278R |
probably benign |
Het |
Rspry1 |
T |
A |
8: 95,349,886 (GRCm39) |
H91Q |
probably damaging |
Het |
Slc13a2 |
CGTTATCTGT |
CGT |
11: 78,294,306 (GRCm39) |
|
probably benign |
Het |
Smn1 |
A |
G |
13: 100,264,503 (GRCm39) |
N78S |
possibly damaging |
Het |
Spta1 |
T |
A |
1: 174,046,078 (GRCm39) |
I1614N |
probably damaging |
Het |
Syt17 |
T |
C |
7: 118,033,513 (GRCm39) |
D165G |
probably damaging |
Het |
Tbck |
A |
G |
3: 132,448,766 (GRCm39) |
Y593C |
probably damaging |
Het |
Tcaf2 |
G |
C |
6: 42,606,687 (GRCm39) |
F422L |
probably benign |
Het |
Tex15 |
T |
A |
8: 34,067,217 (GRCm39) |
F2216I |
possibly damaging |
Het |
Trpc4 |
A |
G |
3: 54,225,441 (GRCm39) |
E846G |
probably benign |
Het |
Ttc41 |
T |
C |
10: 86,580,313 (GRCm39) |
I753T |
probably benign |
Het |
Vdac1 |
C |
T |
11: 52,267,309 (GRCm39) |
T70M |
possibly damaging |
Het |
Vmn1r124 |
A |
C |
7: 20,994,104 (GRCm39) |
F147V |
probably benign |
Het |
Vmn1r220 |
T |
C |
13: 23,368,465 (GRCm39) |
D77G |
probably damaging |
Het |
Vmn2r28 |
T |
C |
7: 5,493,730 (GRCm39) |
H72R |
probably benign |
Het |
Vmn2r78 |
A |
T |
7: 86,570,318 (GRCm39) |
I279L |
probably benign |
Het |
Vmn2r95 |
G |
T |
17: 18,671,732 (GRCm39) |
A490S |
possibly damaging |
Het |
Wdfy4 |
C |
T |
14: 32,831,482 (GRCm39) |
A915T |
possibly damaging |
Het |
Zmiz2 |
G |
T |
11: 6,345,604 (GRCm39) |
|
probably null |
Het |
Zscan2 |
A |
G |
7: 80,525,557 (GRCm39) |
N426S |
probably benign |
Het |
|
Other mutations in Baz2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00430:Baz2b
|
APN |
2 |
59,743,139 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00476:Baz2b
|
APN |
2 |
59,744,083 (GRCm39) |
missense |
probably benign |
0.06 |
IGL00489:Baz2b
|
APN |
2 |
59,788,019 (GRCm39) |
nonsense |
probably null |
|
IGL00514:Baz2b
|
APN |
2 |
59,792,821 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00678:Baz2b
|
APN |
2 |
59,836,527 (GRCm39) |
missense |
unknown |
|
IGL01348:Baz2b
|
APN |
2 |
59,764,031 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01354:Baz2b
|
APN |
2 |
59,799,233 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01924:Baz2b
|
APN |
2 |
59,765,615 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02125:Baz2b
|
APN |
2 |
59,798,984 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02314:Baz2b
|
APN |
2 |
59,792,571 (GRCm39) |
missense |
probably benign |
|
IGL02370:Baz2b
|
APN |
2 |
59,753,933 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02473:Baz2b
|
APN |
2 |
59,790,407 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02499:Baz2b
|
APN |
2 |
59,731,840 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02609:Baz2b
|
APN |
2 |
59,747,713 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02705:Baz2b
|
APN |
2 |
59,778,604 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02711:Baz2b
|
APN |
2 |
59,747,849 (GRCm39) |
unclassified |
probably benign |
|
IGL02716:Baz2b
|
APN |
2 |
59,792,868 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02724:Baz2b
|
APN |
2 |
59,807,718 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02750:Baz2b
|
APN |
2 |
59,799,002 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02869:Baz2b
|
APN |
2 |
59,807,872 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02886:Baz2b
|
APN |
2 |
59,788,087 (GRCm39) |
splice site |
probably null |
|
IGL02892:Baz2b
|
APN |
2 |
59,731,080 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03132:Baz2b
|
APN |
2 |
59,738,097 (GRCm39) |
splice site |
probably benign |
|
IGL03183:Baz2b
|
APN |
2 |
59,733,640 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03197:Baz2b
|
APN |
2 |
59,731,898 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0054:Baz2b
|
UTSW |
2 |
59,762,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R0054:Baz2b
|
UTSW |
2 |
59,762,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R0122:Baz2b
|
UTSW |
2 |
59,743,963 (GRCm39) |
splice site |
probably null |
|
R0136:Baz2b
|
UTSW |
2 |
59,732,298 (GRCm39) |
missense |
probably benign |
0.22 |
R0144:Baz2b
|
UTSW |
2 |
59,737,839 (GRCm39) |
missense |
probably damaging |
0.98 |
R0403:Baz2b
|
UTSW |
2 |
59,799,721 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0498:Baz2b
|
UTSW |
2 |
59,732,340 (GRCm39) |
unclassified |
probably benign |
|
R0528:Baz2b
|
UTSW |
2 |
59,767,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R1025:Baz2b
|
UTSW |
2 |
59,792,826 (GRCm39) |
missense |
probably benign |
0.06 |
R1470:Baz2b
|
UTSW |
2 |
59,808,890 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1470:Baz2b
|
UTSW |
2 |
59,808,890 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1510:Baz2b
|
UTSW |
2 |
59,752,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R1511:Baz2b
|
UTSW |
2 |
59,792,368 (GRCm39) |
missense |
probably benign |
0.12 |
R1514:Baz2b
|
UTSW |
2 |
59,792,670 (GRCm39) |
missense |
probably benign |
0.13 |
R1519:Baz2b
|
UTSW |
2 |
59,778,598 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1523:Baz2b
|
UTSW |
2 |
59,798,981 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1630:Baz2b
|
UTSW |
2 |
59,836,474 (GRCm39) |
missense |
unknown |
|
R1641:Baz2b
|
UTSW |
2 |
59,743,234 (GRCm39) |
missense |
probably damaging |
0.99 |
R1674:Baz2b
|
UTSW |
2 |
59,743,336 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1778:Baz2b
|
UTSW |
2 |
59,836,480 (GRCm39) |
missense |
unknown |
|
R1826:Baz2b
|
UTSW |
2 |
59,799,077 (GRCm39) |
missense |
probably benign |
0.12 |
R1835:Baz2b
|
UTSW |
2 |
59,732,163 (GRCm39) |
missense |
probably benign |
0.02 |
R1954:Baz2b
|
UTSW |
2 |
59,799,087 (GRCm39) |
missense |
probably benign |
0.12 |
R1981:Baz2b
|
UTSW |
2 |
59,754,024 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2029:Baz2b
|
UTSW |
2 |
59,743,067 (GRCm39) |
unclassified |
probably benign |
|
R2567:Baz2b
|
UTSW |
2 |
59,744,255 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2842:Baz2b
|
UTSW |
2 |
59,743,348 (GRCm39) |
missense |
probably benign |
0.27 |
R2848:Baz2b
|
UTSW |
2 |
59,755,010 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3809:Baz2b
|
UTSW |
2 |
59,799,240 (GRCm39) |
missense |
probably benign |
0.12 |
R3935:Baz2b
|
UTSW |
2 |
59,743,105 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3936:Baz2b
|
UTSW |
2 |
59,743,105 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4072:Baz2b
|
UTSW |
2 |
59,742,917 (GRCm39) |
splice site |
probably null |
|
R4182:Baz2b
|
UTSW |
2 |
59,928,801 (GRCm39) |
intron |
probably benign |
|
R4255:Baz2b
|
UTSW |
2 |
59,750,916 (GRCm39) |
unclassified |
probably benign |
|
R4359:Baz2b
|
UTSW |
2 |
59,731,957 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4716:Baz2b
|
UTSW |
2 |
59,799,599 (GRCm39) |
missense |
probably benign |
0.06 |
R4743:Baz2b
|
UTSW |
2 |
59,744,255 (GRCm39) |
missense |
probably benign |
0.01 |
R4772:Baz2b
|
UTSW |
2 |
59,788,795 (GRCm39) |
missense |
probably damaging |
0.96 |
R4858:Baz2b
|
UTSW |
2 |
59,738,087 (GRCm39) |
missense |
probably benign |
|
R4868:Baz2b
|
UTSW |
2 |
59,755,226 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4872:Baz2b
|
UTSW |
2 |
59,773,103 (GRCm39) |
splice site |
probably null |
|
R4889:Baz2b
|
UTSW |
2 |
59,767,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R4890:Baz2b
|
UTSW |
2 |
59,756,383 (GRCm39) |
missense |
probably damaging |
0.99 |
R4914:Baz2b
|
UTSW |
2 |
59,744,387 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4915:Baz2b
|
UTSW |
2 |
59,744,387 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4918:Baz2b
|
UTSW |
2 |
59,744,387 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5027:Baz2b
|
UTSW |
2 |
59,928,988 (GRCm39) |
intron |
probably benign |
|
R5031:Baz2b
|
UTSW |
2 |
59,743,151 (GRCm39) |
missense |
probably benign |
0.00 |
R5082:Baz2b
|
UTSW |
2 |
59,731,835 (GRCm39) |
nonsense |
probably null |
|
R5133:Baz2b
|
UTSW |
2 |
59,792,368 (GRCm39) |
missense |
probably benign |
0.12 |
R5276:Baz2b
|
UTSW |
2 |
59,792,958 (GRCm39) |
missense |
probably benign |
0.40 |
R5279:Baz2b
|
UTSW |
2 |
59,762,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R5294:Baz2b
|
UTSW |
2 |
59,808,946 (GRCm39) |
missense |
probably benign |
0.11 |
R5447:Baz2b
|
UTSW |
2 |
59,744,332 (GRCm39) |
missense |
probably damaging |
0.99 |
R5903:Baz2b
|
UTSW |
2 |
59,790,233 (GRCm39) |
missense |
probably damaging |
0.99 |
R5910:Baz2b
|
UTSW |
2 |
59,807,770 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6140:Baz2b
|
UTSW |
2 |
59,742,871 (GRCm39) |
missense |
probably damaging |
0.99 |
R6195:Baz2b
|
UTSW |
2 |
59,737,855 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6199:Baz2b
|
UTSW |
2 |
59,809,019 (GRCm39) |
missense |
probably benign |
0.00 |
R6208:Baz2b
|
UTSW |
2 |
59,755,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R6233:Baz2b
|
UTSW |
2 |
59,737,855 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6324:Baz2b
|
UTSW |
2 |
59,737,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6490:Baz2b
|
UTSW |
2 |
59,732,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R6578:Baz2b
|
UTSW |
2 |
59,799,623 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6720:Baz2b
|
UTSW |
2 |
59,755,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R6760:Baz2b
|
UTSW |
2 |
59,792,776 (GRCm39) |
missense |
probably benign |
0.40 |
R6836:Baz2b
|
UTSW |
2 |
59,747,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R6859:Baz2b
|
UTSW |
2 |
59,731,874 (GRCm39) |
missense |
probably benign |
0.01 |
R6880:Baz2b
|
UTSW |
2 |
59,743,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R6916:Baz2b
|
UTSW |
2 |
59,799,120 (GRCm39) |
missense |
probably benign |
|
R6978:Baz2b
|
UTSW |
2 |
59,738,059 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7037:Baz2b
|
UTSW |
2 |
59,764,014 (GRCm39) |
critical splice donor site |
probably null |
|
R7112:Baz2b
|
UTSW |
2 |
59,792,528 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7117:Baz2b
|
UTSW |
2 |
59,742,841 (GRCm39) |
missense |
|
|
R7198:Baz2b
|
UTSW |
2 |
59,792,550 (GRCm39) |
missense |
probably benign |
0.00 |
R7270:Baz2b
|
UTSW |
2 |
59,792,836 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7282:Baz2b
|
UTSW |
2 |
59,750,781 (GRCm39) |
missense |
probably benign |
0.17 |
R7464:Baz2b
|
UTSW |
2 |
59,807,792 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7609:Baz2b
|
UTSW |
2 |
59,792,817 (GRCm39) |
missense |
probably benign |
0.40 |
R7703:Baz2b
|
UTSW |
2 |
59,747,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R7850:Baz2b
|
UTSW |
2 |
59,767,060 (GRCm39) |
missense |
probably damaging |
0.98 |
R7851:Baz2b
|
UTSW |
2 |
59,767,060 (GRCm39) |
missense |
probably damaging |
0.98 |
R7988:Baz2b
|
UTSW |
2 |
59,792,485 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8079:Baz2b
|
UTSW |
2 |
59,731,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R8084:Baz2b
|
UTSW |
2 |
59,792,580 (GRCm39) |
missense |
probably benign |
|
R8343:Baz2b
|
UTSW |
2 |
59,731,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R8348:Baz2b
|
UTSW |
2 |
59,742,137 (GRCm39) |
missense |
|
|
R8438:Baz2b
|
UTSW |
2 |
59,747,828 (GRCm39) |
nonsense |
probably null |
|
R8448:Baz2b
|
UTSW |
2 |
59,742,137 (GRCm39) |
missense |
|
|
R8511:Baz2b
|
UTSW |
2 |
59,732,158 (GRCm39) |
missense |
probably benign |
|
R8893:Baz2b
|
UTSW |
2 |
59,755,149 (GRCm39) |
missense |
probably damaging |
0.96 |
R8947:Baz2b
|
UTSW |
2 |
59,778,583 (GRCm39) |
missense |
probably benign |
0.06 |
R8998:Baz2b
|
UTSW |
2 |
59,799,608 (GRCm39) |
missense |
probably benign |
0.02 |
R9241:Baz2b
|
UTSW |
2 |
59,743,993 (GRCm39) |
missense |
probably benign |
0.01 |
R9245:Baz2b
|
UTSW |
2 |
59,743,331 (GRCm39) |
missense |
probably benign |
|
R9577:Baz2b
|
UTSW |
2 |
59,809,031 (GRCm39) |
missense |
probably benign |
0.06 |
R9581:Baz2b
|
UTSW |
2 |
59,799,300 (GRCm39) |
missense |
probably benign |
|
R9601:Baz2b
|
UTSW |
2 |
59,731,847 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9613:Baz2b
|
UTSW |
2 |
59,731,824 (GRCm39) |
missense |
probably benign |
0.09 |
R9639:Baz2b
|
UTSW |
2 |
59,731,828 (GRCm39) |
missense |
probably benign |
0.01 |
X0011:Baz2b
|
UTSW |
2 |
59,807,705 (GRCm39) |
missense |
possibly damaging |
0.53 |
X0053:Baz2b
|
UTSW |
2 |
59,731,019 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Baz2b
|
UTSW |
2 |
59,799,626 (GRCm39) |
missense |
probably benign |
|
Z1088:Baz2b
|
UTSW |
2 |
59,790,359 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Baz2b
|
UTSW |
2 |
59,807,864 (GRCm39) |
missense |
probably benign |
0.01 |
Z1188:Baz2b
|
UTSW |
2 |
59,807,749 (GRCm39) |
missense |
probably benign |
|
|