Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam15 |
A |
G |
3: 89,253,135 (GRCm39) |
Y230H |
probably benign |
Het |
Ano7 |
G |
T |
1: 93,312,641 (GRCm39) |
|
probably null |
Het |
Arap2 |
T |
C |
5: 62,834,506 (GRCm39) |
Y792C |
probably damaging |
Het |
Art3 |
C |
A |
5: 92,560,100 (GRCm39) |
|
probably benign |
Het |
Atad2 |
C |
T |
15: 57,963,250 (GRCm39) |
G1085D |
probably benign |
Het |
Birc6 |
C |
A |
17: 74,953,497 (GRCm39) |
A3253E |
probably damaging |
Het |
C9 |
C |
T |
15: 6,526,607 (GRCm39) |
P547L |
probably benign |
Het |
Cecr2 |
T |
C |
6: 120,739,169 (GRCm39) |
S1271P |
probably damaging |
Het |
Ces1e |
T |
A |
8: 93,948,305 (GRCm39) |
K105* |
probably null |
Het |
Cpsf4 |
A |
G |
5: 145,115,683 (GRCm39) |
N204S |
probably benign |
Het |
Cracd |
A |
G |
5: 77,006,275 (GRCm39) |
T879A |
unknown |
Het |
Dgkz |
T |
C |
2: 91,769,733 (GRCm39) |
D615G |
possibly damaging |
Het |
Disp1 |
G |
T |
1: 182,869,974 (GRCm39) |
N815K |
probably damaging |
Het |
Enah |
A |
G |
1: 181,758,750 (GRCm39) |
|
probably benign |
Het |
Fcgbp |
A |
G |
7: 27,800,919 (GRCm39) |
T1322A |
possibly damaging |
Het |
Frem1 |
A |
G |
4: 82,918,395 (GRCm39) |
F516L |
probably damaging |
Het |
Fyco1 |
T |
C |
9: 123,660,413 (GRCm39) |
Y190C |
probably damaging |
Het |
Gfra1 |
T |
C |
19: 58,227,687 (GRCm39) |
D417G |
probably benign |
Het |
Gigyf2 |
T |
C |
1: 87,368,485 (GRCm39) |
I1055T |
probably damaging |
Het |
Invs |
A |
G |
4: 48,398,146 (GRCm39) |
E444G |
probably damaging |
Het |
Itga10 |
A |
G |
3: 96,559,901 (GRCm39) |
T519A |
probably benign |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Kdm2b |
A |
G |
5: 123,009,931 (GRCm39) |
S727P |
probably benign |
Het |
Kidins220 |
A |
T |
12: 25,107,139 (GRCm39) |
K1531* |
probably null |
Het |
Ksr1 |
C |
T |
11: 78,929,024 (GRCm39) |
V266M |
probably damaging |
Het |
Lin9 |
T |
A |
1: 180,496,763 (GRCm39) |
L351I |
probably benign |
Het |
Lipi |
T |
C |
16: 75,370,798 (GRCm39) |
R140G |
possibly damaging |
Het |
Lrrc32 |
T |
C |
7: 98,147,618 (GRCm39) |
S133P |
probably damaging |
Het |
Map3k7 |
T |
A |
4: 31,964,318 (GRCm39) |
I19N |
probably damaging |
Het |
Marf1 |
A |
G |
16: 13,970,449 (GRCm39) |
V90A |
probably benign |
Het |
Mark3 |
T |
C |
12: 111,621,877 (GRCm39) |
L673P |
probably damaging |
Het |
Meis1 |
T |
C |
11: 18,966,229 (GRCm39) |
H48R |
probably benign |
Het |
Mettl26 |
G |
A |
17: 26,094,995 (GRCm39) |
V87M |
probably damaging |
Het |
Mknk2 |
T |
C |
10: 80,511,696 (GRCm39) |
R5G |
probably benign |
Het |
Mtcl3 |
G |
T |
10: 29,026,240 (GRCm39) |
V441F |
probably damaging |
Het |
Mterf1b |
T |
C |
5: 4,246,956 (GRCm39) |
V199A |
possibly damaging |
Het |
Ncs1 |
T |
A |
2: 31,170,666 (GRCm39) |
|
probably null |
Het |
Nek10 |
T |
C |
14: 14,986,704 (GRCm38) |
V1014A |
probably benign |
Het |
Notch2 |
A |
G |
3: 98,042,744 (GRCm39) |
N1370D |
probably benign |
Het |
Nr2e3 |
TCCATCGGAGTGTTCCC |
TC |
9: 59,850,701 (GRCm39) |
|
probably benign |
Het |
Opn5 |
C |
G |
17: 42,903,897 (GRCm39) |
R146T |
probably damaging |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or5m3 |
T |
C |
2: 85,838,636 (GRCm39) |
I172T |
probably damaging |
Het |
Or8b55 |
T |
A |
9: 38,726,952 (GRCm39) |
M51K |
probably benign |
Het |
Or8g33 |
A |
G |
9: 39,338,032 (GRCm39) |
C112R |
probably damaging |
Het |
Pcdhb18 |
G |
A |
18: 37,623,537 (GRCm39) |
R289Q |
probably benign |
Het |
Pcyox1l |
C |
T |
18: 61,832,359 (GRCm39) |
|
probably null |
Het |
Plxnb2 |
T |
C |
15: 89,044,962 (GRCm39) |
T1128A |
possibly damaging |
Het |
Prex1 |
T |
C |
2: 166,425,127 (GRCm39) |
T960A |
probably benign |
Het |
Prkaa2 |
A |
C |
4: 104,893,291 (GRCm39) |
*553G |
probably null |
Het |
Rasgrp4 |
A |
G |
7: 28,844,639 (GRCm39) |
D297G |
probably damaging |
Het |
Sdf4 |
G |
A |
4: 156,083,856 (GRCm39) |
V109I |
probably benign |
Het |
Serpinb3d |
T |
C |
1: 107,007,027 (GRCm39) |
K227R |
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,398,822 (GRCm39) |
I750N |
probably damaging |
Het |
Shtn1 |
T |
A |
19: 59,020,673 (GRCm39) |
K183M |
probably damaging |
Het |
Skic3 |
A |
G |
13: 76,303,852 (GRCm39) |
T1257A |
probably benign |
Het |
Slc22a30 |
T |
C |
19: 8,381,945 (GRCm39) |
T109A |
probably benign |
Het |
Slco1c1 |
A |
G |
6: 141,487,929 (GRCm39) |
D99G |
probably damaging |
Het |
Tcf25 |
T |
A |
8: 124,122,354 (GRCm39) |
|
probably null |
Het |
Tex10 |
A |
G |
4: 48,452,928 (GRCm39) |
V677A |
probably benign |
Het |
Tmem131l |
A |
G |
3: 83,847,879 (GRCm39) |
S329P |
probably benign |
Het |
Trappc10 |
T |
A |
10: 78,058,573 (GRCm39) |
N136I |
probably damaging |
Het |
Trpt1 |
T |
C |
19: 6,975,906 (GRCm39) |
F173L |
probably benign |
Het |
Ube4b |
G |
A |
4: 149,421,925 (GRCm39) |
R955C |
probably damaging |
Het |
Usp34 |
C |
A |
11: 23,371,340 (GRCm39) |
P1840T |
probably benign |
Het |
Vmn1r27 |
A |
T |
6: 58,192,985 (GRCm39) |
N6K |
possibly damaging |
Het |
Wdr25 |
T |
C |
12: 108,993,347 (GRCm39) |
V521A |
possibly damaging |
Het |
Wdr64 |
G |
A |
1: 175,639,623 (GRCm39) |
E1031K |
possibly damaging |
Het |
Wnt10a |
A |
G |
1: 74,839,755 (GRCm39) |
N147S |
probably damaging |
Het |
Zbed5 |
T |
C |
5: 129,931,059 (GRCm39) |
I336T |
possibly damaging |
Het |
Zfp758 |
T |
A |
17: 22,594,796 (GRCm39) |
H427Q |
probably damaging |
Het |
Zfp961 |
C |
A |
8: 72,722,070 (GRCm39) |
H194Q |
probably damaging |
Het |
|
Other mutations in Fry |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00327:Fry
|
APN |
5 |
150,263,869 (GRCm39) |
nonsense |
probably null |
|
IGL00328:Fry
|
APN |
5 |
150,263,869 (GRCm39) |
nonsense |
probably null |
|
IGL00841:Fry
|
APN |
5 |
150,346,189 (GRCm39) |
missense |
probably benign |
|
IGL00938:Fry
|
APN |
5 |
150,293,645 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01015:Fry
|
APN |
5 |
150,346,252 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01401:Fry
|
APN |
5 |
150,362,253 (GRCm39) |
missense |
probably benign |
|
IGL01616:Fry
|
APN |
5 |
150,323,064 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01616:Fry
|
APN |
5 |
150,362,276 (GRCm39) |
splice site |
probably null |
|
IGL01748:Fry
|
APN |
5 |
150,269,116 (GRCm39) |
splice site |
probably benign |
|
IGL01965:Fry
|
APN |
5 |
150,305,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02030:Fry
|
APN |
5 |
150,395,083 (GRCm39) |
splice site |
probably benign |
|
IGL02079:Fry
|
APN |
5 |
150,323,089 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02087:Fry
|
APN |
5 |
150,327,059 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02113:Fry
|
APN |
5 |
150,323,070 (GRCm39) |
missense |
probably benign |
|
IGL02209:Fry
|
APN |
5 |
150,360,491 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02250:Fry
|
APN |
5 |
150,326,899 (GRCm39) |
splice site |
probably benign |
|
IGL02265:Fry
|
APN |
5 |
150,360,618 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02486:Fry
|
APN |
5 |
150,414,642 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02552:Fry
|
APN |
5 |
150,304,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02881:Fry
|
APN |
5 |
150,282,516 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03008:Fry
|
APN |
5 |
150,269,021 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03140:Fry
|
APN |
5 |
150,419,166 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03171:Fry
|
APN |
5 |
150,304,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03389:Fry
|
APN |
5 |
150,317,696 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03404:Fry
|
APN |
5 |
150,249,633 (GRCm39) |
missense |
probably damaging |
1.00 |
Brook
|
UTSW |
5 |
150,249,597 (GRCm39) |
missense |
probably damaging |
1.00 |
haydn
|
UTSW |
5 |
150,341,929 (GRCm39) |
missense |
possibly damaging |
0.94 |
miracle
|
UTSW |
5 |
150,360,624 (GRCm39) |
missense |
probably damaging |
0.99 |
quickening
|
UTSW |
5 |
150,358,241 (GRCm39) |
missense |
probably damaging |
1.00 |
seasons
|
UTSW |
5 |
150,389,902 (GRCm39) |
missense |
probably benign |
0.06 |
Vivaldi
|
UTSW |
5 |
150,317,603 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0023:Fry
|
UTSW |
5 |
150,374,563 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0024:Fry
|
UTSW |
5 |
150,304,268 (GRCm39) |
missense |
probably benign |
0.03 |
R0030:Fry
|
UTSW |
5 |
150,296,034 (GRCm39) |
nonsense |
probably null |
|
R0053:Fry
|
UTSW |
5 |
150,384,842 (GRCm39) |
splice site |
probably benign |
|
R0089:Fry
|
UTSW |
5 |
150,263,892 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0212:Fry
|
UTSW |
5 |
150,419,862 (GRCm39) |
missense |
probably damaging |
0.99 |
R0241:Fry
|
UTSW |
5 |
150,183,811 (GRCm39) |
intron |
probably benign |
|
R0265:Fry
|
UTSW |
5 |
150,358,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R0317:Fry
|
UTSW |
5 |
150,394,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R0532:Fry
|
UTSW |
5 |
150,402,226 (GRCm39) |
splice site |
probably benign |
|
R0532:Fry
|
UTSW |
5 |
150,357,172 (GRCm39) |
unclassified |
probably benign |
|
R0599:Fry
|
UTSW |
5 |
150,360,624 (GRCm39) |
missense |
probably damaging |
0.99 |
R0631:Fry
|
UTSW |
5 |
150,419,817 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0723:Fry
|
UTSW |
5 |
150,419,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Fry
|
UTSW |
5 |
150,326,897 (GRCm39) |
splice site |
probably benign |
|
R0790:Fry
|
UTSW |
5 |
150,389,902 (GRCm39) |
missense |
probably benign |
0.06 |
R0928:Fry
|
UTSW |
5 |
150,360,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R1104:Fry
|
UTSW |
5 |
150,419,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R1144:Fry
|
UTSW |
5 |
150,341,929 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1172:Fry
|
UTSW |
5 |
150,404,959 (GRCm39) |
nonsense |
probably null |
|
R1312:Fry
|
UTSW |
5 |
150,326,897 (GRCm39) |
splice site |
probably benign |
|
R1347:Fry
|
UTSW |
5 |
150,419,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R1347:Fry
|
UTSW |
5 |
150,419,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R1437:Fry
|
UTSW |
5 |
150,233,890 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1458:Fry
|
UTSW |
5 |
150,304,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R1542:Fry
|
UTSW |
5 |
150,328,431 (GRCm39) |
missense |
probably benign |
0.13 |
R1692:Fry
|
UTSW |
5 |
150,293,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Fry
|
UTSW |
5 |
150,360,174 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1874:Fry
|
UTSW |
5 |
150,269,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R1875:Fry
|
UTSW |
5 |
150,249,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R1881:Fry
|
UTSW |
5 |
150,401,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R1884:Fry
|
UTSW |
5 |
150,326,985 (GRCm39) |
missense |
probably benign |
0.00 |
R1929:Fry
|
UTSW |
5 |
150,324,389 (GRCm39) |
missense |
probably null |
0.02 |
R2066:Fry
|
UTSW |
5 |
150,293,584 (GRCm39) |
splice site |
probably benign |
|
R2270:Fry
|
UTSW |
5 |
150,324,389 (GRCm39) |
missense |
probably null |
0.02 |
R2356:Fry
|
UTSW |
5 |
150,394,897 (GRCm39) |
missense |
probably benign |
|
R3720:Fry
|
UTSW |
5 |
150,378,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Fry
|
UTSW |
5 |
150,321,663 (GRCm39) |
missense |
probably damaging |
0.96 |
R3824:Fry
|
UTSW |
5 |
150,419,884 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3902:Fry
|
UTSW |
5 |
150,269,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Fry
|
UTSW |
5 |
150,336,814 (GRCm39) |
missense |
probably benign |
|
R4250:Fry
|
UTSW |
5 |
150,233,825 (GRCm39) |
missense |
probably damaging |
0.99 |
R4332:Fry
|
UTSW |
5 |
150,305,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R4495:Fry
|
UTSW |
5 |
150,233,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Fry
|
UTSW |
5 |
150,309,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R4682:Fry
|
UTSW |
5 |
150,346,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Fry
|
UTSW |
5 |
150,309,472 (GRCm39) |
missense |
|
|
R4733:Fry
|
UTSW |
5 |
150,309,472 (GRCm39) |
missense |
|
|
R4755:Fry
|
UTSW |
5 |
150,321,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R4788:Fry
|
UTSW |
5 |
150,323,101 (GRCm39) |
missense |
probably benign |
0.00 |
R4803:Fry
|
UTSW |
5 |
150,322,998 (GRCm39) |
missense |
probably benign |
0.31 |
R4858:Fry
|
UTSW |
5 |
150,325,108 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4872:Fry
|
UTSW |
5 |
150,317,704 (GRCm39) |
critical splice donor site |
probably null |
|
R4902:Fry
|
UTSW |
5 |
150,419,168 (GRCm39) |
missense |
probably benign |
0.43 |
R4915:Fry
|
UTSW |
5 |
150,402,328 (GRCm39) |
missense |
probably benign |
0.30 |
R4938:Fry
|
UTSW |
5 |
150,401,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4983:Fry
|
UTSW |
5 |
150,321,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Fry
|
UTSW |
5 |
150,357,069 (GRCm39) |
missense |
probably benign |
0.16 |
R5040:Fry
|
UTSW |
5 |
150,312,319 (GRCm39) |
missense |
probably damaging |
0.99 |
R5145:Fry
|
UTSW |
5 |
150,293,689 (GRCm39) |
missense |
probably damaging |
0.98 |
R5170:Fry
|
UTSW |
5 |
150,353,319 (GRCm39) |
missense |
probably benign |
0.03 |
R5233:Fry
|
UTSW |
5 |
150,393,185 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5428:Fry
|
UTSW |
5 |
150,328,824 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5468:Fry
|
UTSW |
5 |
150,323,053 (GRCm39) |
missense |
probably benign |
0.44 |
R5481:Fry
|
UTSW |
5 |
150,183,784 (GRCm39) |
missense |
probably benign |
0.01 |
R5494:Fry
|
UTSW |
5 |
150,314,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R5538:Fry
|
UTSW |
5 |
150,419,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R5638:Fry
|
UTSW |
5 |
150,282,546 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5645:Fry
|
UTSW |
5 |
150,304,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5716:Fry
|
UTSW |
5 |
150,293,686 (GRCm39) |
nonsense |
probably null |
|
R5812:Fry
|
UTSW |
5 |
150,323,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R5873:Fry
|
UTSW |
5 |
150,302,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R5933:Fry
|
UTSW |
5 |
150,314,265 (GRCm39) |
intron |
probably benign |
|
R6037:Fry
|
UTSW |
5 |
150,351,644 (GRCm39) |
missense |
probably benign |
0.03 |
R6037:Fry
|
UTSW |
5 |
150,351,644 (GRCm39) |
missense |
probably benign |
0.03 |
R6158:Fry
|
UTSW |
5 |
150,378,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6178:Fry
|
UTSW |
5 |
150,377,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R6481:Fry
|
UTSW |
5 |
150,309,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R6562:Fry
|
UTSW |
5 |
150,249,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R6676:Fry
|
UTSW |
5 |
150,304,387 (GRCm39) |
missense |
probably benign |
0.22 |
R6717:Fry
|
UTSW |
5 |
150,419,777 (GRCm39) |
missense |
probably benign |
0.00 |
R6828:Fry
|
UTSW |
5 |
150,389,911 (GRCm39) |
splice site |
probably null |
|
R6874:Fry
|
UTSW |
5 |
150,360,768 (GRCm39) |
missense |
probably benign |
0.00 |
R6930:Fry
|
UTSW |
5 |
150,351,695 (GRCm39) |
missense |
probably benign |
0.00 |
R6963:Fry
|
UTSW |
5 |
150,381,309 (GRCm39) |
missense |
probably benign |
0.17 |
R6965:Fry
|
UTSW |
5 |
150,339,685 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7051:Fry
|
UTSW |
5 |
150,318,634 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7085:Fry
|
UTSW |
5 |
150,362,214 (GRCm39) |
missense |
probably benign |
0.02 |
R7108:Fry
|
UTSW |
5 |
150,414,555 (GRCm39) |
missense |
|
|
R7108:Fry
|
UTSW |
5 |
150,319,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R7115:Fry
|
UTSW |
5 |
150,309,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R7116:Fry
|
UTSW |
5 |
150,319,334 (GRCm39) |
critical splice donor site |
probably null |
|
R7197:Fry
|
UTSW |
5 |
150,393,232 (GRCm39) |
missense |
|
|
R7256:Fry
|
UTSW |
5 |
150,390,251 (GRCm39) |
missense |
|
|
R7318:Fry
|
UTSW |
5 |
150,360,458 (GRCm39) |
missense |
probably damaging |
0.98 |
R7323:Fry
|
UTSW |
5 |
150,419,814 (GRCm39) |
missense |
|
|
R7358:Fry
|
UTSW |
5 |
150,339,788 (GRCm39) |
missense |
probably benign |
|
R7361:Fry
|
UTSW |
5 |
150,360,312 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7395:Fry
|
UTSW |
5 |
150,304,348 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7487:Fry
|
UTSW |
5 |
150,338,039 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7491:Fry
|
UTSW |
5 |
150,389,791 (GRCm39) |
missense |
|
|
R7574:Fry
|
UTSW |
5 |
150,304,359 (GRCm39) |
missense |
probably benign |
0.00 |
R7582:Fry
|
UTSW |
5 |
150,419,847 (GRCm39) |
missense |
|
|
R7586:Fry
|
UTSW |
5 |
150,349,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R7650:Fry
|
UTSW |
5 |
150,336,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Fry
|
UTSW |
5 |
150,328,792 (GRCm39) |
missense |
probably damaging |
0.98 |
R7700:Fry
|
UTSW |
5 |
150,328,792 (GRCm39) |
missense |
probably damaging |
0.98 |
R7972:Fry
|
UTSW |
5 |
150,233,861 (GRCm39) |
missense |
probably benign |
0.05 |
R8058:Fry
|
UTSW |
5 |
150,419,232 (GRCm39) |
missense |
|
|
R8070:Fry
|
UTSW |
5 |
150,401,472 (GRCm39) |
missense |
|
|
R8159:Fry
|
UTSW |
5 |
150,322,998 (GRCm39) |
missense |
probably benign |
0.31 |
R8202:Fry
|
UTSW |
5 |
150,355,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R8261:Fry
|
UTSW |
5 |
150,369,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R8279:Fry
|
UTSW |
5 |
150,419,726 (GRCm39) |
missense |
|
|
R8338:Fry
|
UTSW |
5 |
150,282,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R8370:Fry
|
UTSW |
5 |
150,319,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R8673:Fry
|
UTSW |
5 |
150,318,576 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8786:Fry
|
UTSW |
5 |
150,317,501 (GRCm39) |
missense |
probably benign |
0.00 |
R8815:Fry
|
UTSW |
5 |
150,317,603 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8847:Fry
|
UTSW |
5 |
150,309,472 (GRCm39) |
missense |
|
|
R9023:Fry
|
UTSW |
5 |
150,360,768 (GRCm39) |
missense |
probably benign |
0.00 |
R9025:Fry
|
UTSW |
5 |
150,219,273 (GRCm39) |
intron |
probably benign |
|
R9125:Fry
|
UTSW |
5 |
150,269,525 (GRCm39) |
missense |
probably damaging |
0.97 |
R9172:Fry
|
UTSW |
5 |
150,336,793 (GRCm39) |
missense |
probably benign |
|
R9262:Fry
|
UTSW |
5 |
150,305,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R9263:Fry
|
UTSW |
5 |
150,322,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R9293:Fry
|
UTSW |
5 |
150,419,297 (GRCm39) |
missense |
|
|
R9368:Fry
|
UTSW |
5 |
150,401,403 (GRCm39) |
missense |
|
|
R9401:Fry
|
UTSW |
5 |
150,302,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R9402:Fry
|
UTSW |
5 |
150,360,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R9402:Fry
|
UTSW |
5 |
150,357,161 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9420:Fry
|
UTSW |
5 |
150,356,994 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9557:Fry
|
UTSW |
5 |
150,389,781 (GRCm39) |
missense |
|
|
R9647:Fry
|
UTSW |
5 |
150,292,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9650:Fry
|
UTSW |
5 |
150,369,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:Fry
|
UTSW |
5 |
150,362,251 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9664:Fry
|
UTSW |
5 |
150,282,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R9668:Fry
|
UTSW |
5 |
150,282,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R9732:Fry
|
UTSW |
5 |
150,328,758 (GRCm39) |
missense |
probably benign |
0.00 |
R9773:Fry
|
UTSW |
5 |
150,322,728 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fry
|
UTSW |
5 |
150,233,902 (GRCm39) |
missense |
possibly damaging |
0.80 |
|