Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
C |
G |
10: 100,439,390 (GRCm39) |
P187R |
probably damaging |
Het |
Abhd5 |
T |
C |
9: 122,208,079 (GRCm39) |
|
probably null |
Het |
Acadvl |
A |
G |
11: 69,905,617 (GRCm39) |
|
probably null |
Het |
Actn1 |
T |
C |
12: 80,251,852 (GRCm39) |
E75G |
probably damaging |
Het |
Adam4 |
A |
T |
12: 81,467,651 (GRCm39) |
N323K |
possibly damaging |
Het |
Anks6 |
G |
A |
4: 47,027,152 (GRCm39) |
R689W |
probably damaging |
Het |
Anxa2 |
T |
C |
9: 69,392,523 (GRCm39) |
I124T |
probably damaging |
Het |
Aph1c |
T |
C |
9: 66,740,547 (GRCm39) |
T10A |
probably benign |
Het |
Arhgap40 |
T |
A |
2: 158,388,721 (GRCm39) |
W552R |
probably benign |
Het |
Blmh |
A |
G |
11: 76,857,607 (GRCm39) |
Y147C |
probably damaging |
Het |
C1galt1 |
C |
T |
6: 7,866,402 (GRCm39) |
L83F |
probably damaging |
Het |
Ccdc168 |
A |
G |
1: 44,096,130 (GRCm39) |
V1656A |
probably benign |
Het |
Cdh23 |
A |
T |
10: 60,215,122 (GRCm39) |
Y1403N |
possibly damaging |
Het |
Cic |
A |
T |
7: 24,993,235 (GRCm39) |
|
probably null |
Het |
Coro1b |
T |
A |
19: 4,200,583 (GRCm39) |
V200D |
possibly damaging |
Het |
Csl |
T |
A |
10: 99,593,817 (GRCm39) |
E416V |
probably damaging |
Het |
Cyp3a25 |
A |
G |
5: 145,938,257 (GRCm39) |
|
probably null |
Het |
Dennd2d |
T |
A |
3: 106,399,875 (GRCm39) |
F266Y |
probably damaging |
Het |
Dnah10 |
A |
G |
5: 124,838,016 (GRCm39) |
E1072G |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,026,031 (GRCm39) |
K3435N |
probably damaging |
Het |
Dnah9 |
G |
A |
11: 65,772,587 (GRCm39) |
A3715V |
probably damaging |
Het |
Fam186a |
G |
A |
15: 99,845,536 (GRCm39) |
S236L |
unknown |
Het |
Frs3 |
A |
G |
17: 48,013,903 (GRCm39) |
T199A |
probably benign |
Het |
Fsd1 |
A |
G |
17: 56,300,870 (GRCm39) |
N243S |
probably benign |
Het |
Gabra5 |
A |
C |
7: 57,058,641 (GRCm39) |
L369R |
probably benign |
Het |
Gask1b |
A |
G |
3: 79,848,771 (GRCm39) |
N506D |
possibly damaging |
Het |
Gins4 |
A |
G |
8: 23,724,792 (GRCm39) |
V54A |
probably benign |
Het |
Gli1 |
T |
C |
10: 127,170,138 (GRCm39) |
E339G |
possibly damaging |
Het |
Gm12185 |
A |
G |
11: 48,798,594 (GRCm39) |
V633A |
probably damaging |
Het |
Gpr83 |
T |
A |
9: 14,779,493 (GRCm39) |
C182S |
probably null |
Het |
Gspt1 |
A |
G |
16: 11,038,719 (GRCm39) |
V627A |
probably damaging |
Het |
Heatr1 |
T |
C |
13: 12,427,040 (GRCm39) |
C722R |
probably benign |
Het |
Jak1 |
C |
T |
4: 101,020,119 (GRCm39) |
R680Q |
probably damaging |
Het |
Kif2c |
A |
G |
4: 117,027,137 (GRCm39) |
V287A |
probably damaging |
Het |
Kmo |
C |
T |
1: 175,479,184 (GRCm39) |
P240L |
possibly damaging |
Het |
Kmo |
A |
G |
1: 175,484,368 (GRCm39) |
E366G |
probably damaging |
Het |
Lepr |
A |
T |
4: 101,646,541 (GRCm39) |
N824I |
probably damaging |
Het |
Lyrm7 |
T |
A |
11: 54,739,425 (GRCm39) |
H75L |
possibly damaging |
Het |
Map4k1 |
A |
T |
7: 28,690,461 (GRCm39) |
Q351L |
probably benign |
Het |
Matcap2 |
T |
G |
9: 22,341,671 (GRCm39) |
L114R |
probably benign |
Het |
Mgam |
T |
C |
6: 40,638,617 (GRCm39) |
I450T |
probably benign |
Het |
Nbeal2 |
A |
G |
9: 110,465,373 (GRCm39) |
L955P |
probably damaging |
Het |
Nlrp9c |
T |
C |
7: 26,077,526 (GRCm39) |
K752R |
possibly damaging |
Het |
Nsmaf |
A |
T |
4: 6,438,062 (GRCm39) |
I70K |
probably benign |
Het |
Or14a257 |
A |
G |
7: 86,138,333 (GRCm39) |
M142T |
probably damaging |
Het |
Or5ac19 |
C |
T |
16: 59,089,307 (GRCm39) |
C241Y |
probably damaging |
Het |
Otud7a |
A |
G |
7: 63,408,391 (GRCm39) |
Y898C |
probably damaging |
Het |
Pcdhb18 |
A |
C |
18: 37,623,945 (GRCm39) |
D425A |
probably damaging |
Het |
Prdm1 |
A |
T |
10: 44,315,982 (GRCm39) |
L733* |
probably null |
Het |
Prdm2 |
A |
T |
4: 142,862,153 (GRCm39) |
I379N |
probably damaging |
Het |
Ptprg |
A |
T |
14: 12,220,596 (GRCm38) |
Y436F |
probably damaging |
Het |
Riok3 |
A |
G |
18: 12,270,363 (GRCm39) |
D167G |
probably damaging |
Het |
Rnf215 |
G |
T |
11: 4,085,451 (GRCm39) |
R60L |
probably damaging |
Het |
Scart1 |
G |
A |
7: 139,808,069 (GRCm39) |
V747I |
probably benign |
Het |
Sdk1 |
A |
T |
5: 141,985,705 (GRCm39) |
H779L |
probably benign |
Het |
Serpine2 |
A |
G |
1: 79,772,748 (GRCm39) |
F390L |
probably damaging |
Het |
Sh3d21 |
T |
A |
4: 126,045,519 (GRCm39) |
K387* |
probably null |
Het |
Slc13a2 |
T |
C |
11: 78,288,572 (GRCm39) |
Y568C |
possibly damaging |
Het |
Slc27a5 |
T |
C |
7: 12,722,386 (GRCm39) |
|
probably null |
Het |
Slc32a1 |
T |
C |
2: 158,456,497 (GRCm39) |
L384P |
probably damaging |
Het |
Sorcs1 |
T |
C |
19: 50,241,025 (GRCm39) |
N454D |
probably benign |
Het |
Spag8 |
T |
C |
4: 43,652,777 (GRCm39) |
Y228C |
possibly damaging |
Het |
Spata31e4 |
G |
A |
13: 50,854,443 (GRCm39) |
|
probably null |
Het |
Spc25 |
T |
C |
2: 69,030,431 (GRCm39) |
I71V |
probably damaging |
Het |
Tcte1 |
T |
A |
17: 45,846,178 (GRCm39) |
F261I |
probably damaging |
Het |
Thsd7a |
T |
A |
6: 12,471,174 (GRCm39) |
K481N |
probably benign |
Het |
Tll2 |
G |
T |
19: 41,074,839 (GRCm39) |
N908K |
probably benign |
Het |
Tmem236 |
T |
C |
2: 14,197,091 (GRCm39) |
V93A |
probably benign |
Het |
Top2b |
G |
A |
14: 16,408,953 (GRCm38) |
|
probably null |
Het |
Topaz1 |
G |
A |
9: 122,596,076 (GRCm39) |
S949N |
probably benign |
Het |
Triobp |
A |
G |
15: 78,857,938 (GRCm39) |
T1180A |
probably benign |
Het |
Trip11 |
A |
C |
12: 101,852,419 (GRCm39) |
D548E |
probably benign |
Het |
Trpv2 |
T |
A |
11: 62,480,652 (GRCm39) |
|
probably null |
Het |
Ulbp3 |
A |
G |
10: 3,075,230 (GRCm39) |
|
noncoding transcript |
Het |
Vmn1r12 |
T |
A |
6: 57,136,540 (GRCm39) |
H212Q |
probably damaging |
Het |
Vmn2r112 |
A |
G |
17: 22,837,884 (GRCm39) |
T782A |
possibly damaging |
Het |
Vmn2r7 |
A |
G |
3: 64,623,876 (GRCm39) |
V239A |
possibly damaging |
Het |
Vmn2r80 |
T |
A |
10: 79,030,053 (GRCm39) |
N626K |
probably damaging |
Het |
Vmn2r99 |
A |
G |
17: 19,600,322 (GRCm39) |
S449G |
probably benign |
Het |
Wfikkn2 |
T |
C |
11: 94,128,933 (GRCm39) |
T403A |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,346,023 (GRCm39) |
I2755V |
probably benign |
Het |
Yjefn3 |
A |
G |
8: 70,341,729 (GRCm39) |
V153A |
probably benign |
Het |
Zfp677 |
C |
A |
17: 21,617,499 (GRCm39) |
H185Q |
possibly damaging |
Het |
Zfp947 |
C |
T |
17: 22,365,273 (GRCm39) |
V134I |
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 |
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 |
R6276:Baz2b
|
UTSW |
2 |
59,778,567 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|