Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
A |
G |
3: 121,964,592 (GRCm39) |
E925G |
probably damaging |
Het |
Abca9 |
T |
G |
11: 110,006,280 (GRCm39) |
Q1275P |
probably benign |
Het |
Adgrl1 |
T |
A |
8: 84,657,870 (GRCm39) |
M492K |
probably benign |
Het |
Ankrd50 |
T |
A |
3: 38,537,234 (GRCm39) |
K3* |
probably null |
Het |
Arl5b |
T |
C |
2: 15,079,848 (GRCm39) |
S140P |
probably damaging |
Het |
Armc1 |
T |
C |
3: 19,211,840 (GRCm39) |
|
probably benign |
Het |
Ascc1 |
T |
C |
10: 59,840,663 (GRCm39) |
I8T |
probably benign |
Het |
Bche |
A |
G |
3: 73,608,805 (GRCm39) |
V207A |
probably damaging |
Het |
Cacna2d3 |
A |
G |
14: 28,627,259 (GRCm39) |
L1080P |
probably benign |
Het |
Ceacam3 |
C |
A |
7: 16,895,779 (GRCm39) |
A583D |
probably damaging |
Het |
Cep290 |
C |
T |
10: 100,373,299 (GRCm39) |
A1193V |
probably benign |
Het |
Clcn1 |
T |
C |
6: 42,290,046 (GRCm39) |
I827T |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Col28a1 |
T |
C |
6: 8,175,641 (GRCm39) |
D69G |
possibly damaging |
Het |
Cts3 |
A |
G |
13: 61,712,806 (GRCm39) |
W305R |
probably damaging |
Het |
Dmwd |
T |
C |
7: 18,815,084 (GRCm39) |
I578T |
possibly damaging |
Het |
Dnmt3a |
G |
A |
12: 3,949,883 (GRCm39) |
V559M |
probably damaging |
Het |
Dysf |
T |
C |
6: 84,016,549 (GRCm39) |
V70A |
possibly damaging |
Het |
Eml6 |
A |
G |
11: 29,752,434 (GRCm39) |
V993A |
probably benign |
Het |
Etl4 |
T |
A |
2: 20,812,117 (GRCm39) |
L1768* |
probably null |
Het |
F11 |
A |
G |
8: 45,701,675 (GRCm39) |
S353P |
probably damaging |
Het |
Fat3 |
T |
G |
9: 15,881,167 (GRCm39) |
D3235A |
probably damaging |
Het |
Fbxo36 |
T |
A |
1: 84,877,823 (GRCm39) |
F162I |
probably damaging |
Het |
Fgfrl1 |
T |
C |
5: 108,852,897 (GRCm39) |
W200R |
probably damaging |
Het |
Fsip2 |
T |
C |
2: 82,811,064 (GRCm39) |
M2461T |
possibly damaging |
Het |
Fut1 |
A |
G |
7: 45,268,643 (GRCm39) |
Y144C |
probably benign |
Het |
Gprin3 |
G |
A |
6: 59,331,134 (GRCm39) |
A391V |
probably benign |
Het |
H2-Q4 |
A |
G |
17: 35,598,973 (GRCm39) |
E81G |
probably damaging |
Het |
Hacd3 |
A |
G |
9: 64,908,311 (GRCm39) |
S162P |
probably damaging |
Het |
Itga1 |
A |
T |
13: 115,114,150 (GRCm39) |
H918Q |
probably benign |
Het |
Lrp5 |
C |
A |
19: 3,647,430 (GRCm39) |
D1271Y |
probably damaging |
Het |
Lsm8 |
C |
T |
6: 18,849,643 (GRCm39) |
T17I |
probably benign |
Het |
Mup4 |
T |
A |
4: 59,958,145 (GRCm39) |
D141V |
probably damaging |
Het |
Nckap5 |
G |
A |
1: 125,955,146 (GRCm39) |
H405Y |
probably benign |
Het |
Obscn |
T |
C |
11: 59,022,472 (GRCm39) |
R758G |
possibly damaging |
Het |
Or12k8 |
T |
C |
2: 36,974,986 (GRCm39) |
Y258C |
probably benign |
Het |
Ostf1 |
T |
C |
19: 18,562,026 (GRCm39) |
K190R |
probably benign |
Het |
Pnldc1 |
A |
T |
17: 13,118,777 (GRCm39) |
V197E |
probably damaging |
Het |
Ryr3 |
C |
T |
2: 112,516,973 (GRCm39) |
E3318K |
probably damaging |
Het |
Scamp2 |
T |
C |
9: 57,484,995 (GRCm39) |
V67A |
possibly damaging |
Het |
Serpina3g |
C |
A |
12: 104,207,421 (GRCm39) |
L195M |
probably damaging |
Het |
Siglec1 |
G |
T |
2: 130,916,395 (GRCm39) |
T1185N |
possibly damaging |
Het |
Sycp2 |
G |
A |
2: 178,045,528 (GRCm39) |
Q31* |
probably null |
Het |
Tmprss15 |
T |
G |
16: 78,854,578 (GRCm39) |
T277P |
probably damaging |
Het |
Trim34b |
C |
T |
7: 103,978,876 (GRCm39) |
S41L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,557,705 (GRCm39) |
T21507A |
possibly damaging |
Het |
Umad1 |
T |
C |
6: 8,427,161 (GRCm39) |
V138A |
possibly damaging |
Het |
Zfp523 |
A |
G |
17: 28,414,183 (GRCm39) |
I72M |
probably damaging |
Het |
Zfp655 |
C |
T |
5: 145,181,356 (GRCm39) |
R405C |
probably benign |
Het |
Zfp715 |
G |
A |
7: 42,948,692 (GRCm39) |
R423C |
possibly damaging |
Het |
|
Other mutations in Ptprc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
lochy
|
APN |
1 |
138,011,528 (GRCm39) |
splice site |
probably benign |
|
IGL00486:Ptprc
|
APN |
1 |
138,043,359 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00771:Ptprc
|
APN |
1 |
138,041,415 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00833:Ptprc
|
APN |
1 |
138,006,230 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL00919:Ptprc
|
APN |
1 |
138,041,380 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01020:Ptprc
|
APN |
1 |
138,047,911 (GRCm39) |
critical splice acceptor site |
probably null |
0.00 |
IGL01024:Ptprc
|
APN |
1 |
138,008,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01302:Ptprc
|
APN |
1 |
138,027,369 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01548:Ptprc
|
APN |
1 |
138,027,219 (GRCm39) |
critical splice donor site |
probably null |
0.00 |
IGL01620:Ptprc
|
APN |
1 |
137,996,148 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01775:Ptprc
|
APN |
1 |
137,992,497 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01820:Ptprc
|
APN |
1 |
137,993,936 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02340:Ptprc
|
APN |
1 |
137,998,957 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02943:Ptprc
|
APN |
1 |
138,027,251 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03169:Ptprc
|
APN |
1 |
138,041,357 (GRCm39) |
missense |
probably benign |
0.15 |
IGL03308:Ptprc
|
APN |
1 |
138,054,058 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03404:Ptprc
|
APN |
1 |
138,020,739 (GRCm39) |
missense |
probably damaging |
1.00 |
belittle
|
UTSW |
1 |
138,137,493 (GRCm38) |
intron |
probably benign |
|
Benighted
|
UTSW |
1 |
138,054,039 (GRCm39) |
critical splice donor site |
probably null |
|
bletchley
|
UTSW |
1 |
138,045,600 (GRCm39) |
missense |
probably benign |
|
Blush
|
UTSW |
1 |
138,045,458 (GRCm39) |
intron |
probably benign |
|
bruise
|
UTSW |
1 |
137,992,509 (GRCm39) |
missense |
probably damaging |
1.00 |
chor_muang
|
UTSW |
1 |
138,041,300 (GRCm39) |
critical splice donor site |
probably null |
|
crystal
|
UTSW |
1 |
137,999,993 (GRCm39) |
critical splice donor site |
probably null |
|
Dumpling
|
UTSW |
1 |
137,995,628 (GRCm39) |
missense |
probably damaging |
1.00 |
fluorescent
|
UTSW |
1 |
138,028,930 (GRCm39) |
missense |
probably damaging |
0.97 |
fuchsia
|
UTSW |
1 |
138,028,779 (GRCm39) |
critical splice donor site |
probably null |
|
Gentian
|
UTSW |
1 |
137,995,623 (GRCm39) |
critical splice donor site |
probably null |
|
guotie
|
UTSW |
1 |
137,996,139 (GRCm39) |
nonsense |
probably null |
|
guotie2
|
UTSW |
1 |
138,022,037 (GRCm39) |
missense |
probably damaging |
0.97 |
Guotie3
|
UTSW |
1 |
138,006,189 (GRCm39) |
missense |
possibly damaging |
0.92 |
Gyoza
|
UTSW |
1 |
138,011,305 (GRCm39) |
missense |
probably damaging |
1.00 |
Half_measure
|
UTSW |
1 |
137,998,987 (GRCm39) |
missense |
probably damaging |
0.98 |
jirisan
|
UTSW |
1 |
138,041,416 (GRCm39) |
nonsense |
probably null |
|
mauve
|
UTSW |
1 |
138,027,423 (GRCm39) |
missense |
probably benign |
|
Perverse
|
UTSW |
1 |
138,028,782 (GRCm39) |
missense |
probably benign |
0.02 |
petechiae
|
UTSW |
1 |
138,041,446 (GRCm39) |
nonsense |
probably null |
|
ultra
|
UTSW |
1 |
138,006,183 (GRCm39) |
critical splice donor site |
probably null |
|
violaceous
|
UTSW |
1 |
138,011,377 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0013:Ptprc
|
UTSW |
1 |
138,041,297 (GRCm39) |
splice site |
probably null |
|
R0189:Ptprc
|
UTSW |
1 |
138,010,453 (GRCm39) |
missense |
probably benign |
0.10 |
R0390:Ptprc
|
UTSW |
1 |
138,050,313 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0504:Ptprc
|
UTSW |
1 |
138,016,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R0602:Ptprc
|
UTSW |
1 |
138,017,223 (GRCm39) |
splice site |
probably benign |
|
R0627:Ptprc
|
UTSW |
1 |
137,996,058 (GRCm39) |
missense |
probably damaging |
0.99 |
R0632:Ptprc
|
UTSW |
1 |
138,001,348 (GRCm39) |
missense |
probably benign |
0.01 |
R0751:Ptprc
|
UTSW |
1 |
138,020,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R0839:Ptprc
|
UTSW |
1 |
138,028,870 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0942:Ptprc
|
UTSW |
1 |
137,996,139 (GRCm39) |
nonsense |
probably null |
|
R0943:Ptprc
|
UTSW |
1 |
138,038,902 (GRCm39) |
missense |
probably damaging |
0.96 |
R1159:Ptprc
|
UTSW |
1 |
138,000,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Ptprc
|
UTSW |
1 |
138,000,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R1489:Ptprc
|
UTSW |
1 |
138,047,824 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1728:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1728:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1728:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1728:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1728:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1729:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1729:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1729:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1729:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1729:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1730:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1730:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1730:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1730:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1730:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1739:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1739:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1739:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1739:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1739:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1762:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1762:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1762:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1762:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1762:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1783:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1783:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1783:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1783:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1783:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1784:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1784:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1784:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1784:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1784:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1785:Ptprc
|
UTSW |
1 |
138,027,414 (GRCm39) |
missense |
probably benign |
0.05 |
R1785:Ptprc
|
UTSW |
1 |
138,035,561 (GRCm39) |
missense |
probably benign |
0.22 |
R1785:Ptprc
|
UTSW |
1 |
138,039,992 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1785:Ptprc
|
UTSW |
1 |
138,035,575 (GRCm39) |
missense |
probably benign |
0.09 |
R1785:Ptprc
|
UTSW |
1 |
138,035,562 (GRCm39) |
missense |
probably benign |
0.04 |
R1862:Ptprc
|
UTSW |
1 |
138,039,965 (GRCm39) |
missense |
probably benign |
0.13 |
R2145:Ptprc
|
UTSW |
1 |
138,001,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Ptprc
|
UTSW |
1 |
138,038,926 (GRCm39) |
missense |
probably benign |
0.00 |
R2439:Ptprc
|
UTSW |
1 |
137,993,890 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2887:Ptprc
|
UTSW |
1 |
138,007,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R2906:Ptprc
|
UTSW |
1 |
137,992,272 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3774:Ptprc
|
UTSW |
1 |
137,992,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R3775:Ptprc
|
UTSW |
1 |
137,992,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R3776:Ptprc
|
UTSW |
1 |
137,992,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R3834:Ptprc
|
UTSW |
1 |
138,011,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R4019:Ptprc
|
UTSW |
1 |
138,006,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R4377:Ptprc
|
UTSW |
1 |
137,995,663 (GRCm39) |
missense |
probably benign |
0.04 |
R4580:Ptprc
|
UTSW |
1 |
137,998,989 (GRCm39) |
missense |
probably benign |
0.09 |
R4923:Ptprc
|
UTSW |
1 |
138,006,236 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4925:Ptprc
|
UTSW |
1 |
138,027,235 (GRCm39) |
missense |
probably benign |
0.04 |
R4937:Ptprc
|
UTSW |
1 |
138,017,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R4970:Ptprc
|
UTSW |
1 |
138,022,037 (GRCm39) |
missense |
probably damaging |
0.97 |
R5112:Ptprc
|
UTSW |
1 |
138,022,037 (GRCm39) |
missense |
probably damaging |
0.97 |
R5145:Ptprc
|
UTSW |
1 |
138,017,304 (GRCm39) |
missense |
probably benign |
0.07 |
R5158:Ptprc
|
UTSW |
1 |
138,102,822 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5223:Ptprc
|
UTSW |
1 |
138,045,600 (GRCm39) |
missense |
probably benign |
|
R5593:Ptprc
|
UTSW |
1 |
138,045,458 (GRCm39) |
intron |
probably benign |
|
R5689:Ptprc
|
UTSW |
1 |
138,045,515 (GRCm39) |
missense |
probably benign |
0.01 |
R5885:Ptprc
|
UTSW |
1 |
138,016,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R6010:Ptprc
|
UTSW |
1 |
138,028,794 (GRCm39) |
missense |
probably benign |
0.09 |
R6026:Ptprc
|
UTSW |
1 |
137,998,987 (GRCm39) |
missense |
probably damaging |
0.98 |
R6047:Ptprc
|
UTSW |
1 |
138,028,779 (GRCm39) |
critical splice donor site |
probably null |
|
R6173:Ptprc
|
UTSW |
1 |
137,995,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R6328:Ptprc
|
UTSW |
1 |
138,041,416 (GRCm39) |
nonsense |
probably null |
|
R6383:Ptprc
|
UTSW |
1 |
138,006,189 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6436:Ptprc
|
UTSW |
1 |
138,011,377 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6492:Ptprc
|
UTSW |
1 |
138,041,300 (GRCm39) |
critical splice donor site |
probably null |
|
R6520:Ptprc
|
UTSW |
1 |
138,007,881 (GRCm39) |
nonsense |
probably null |
|
R6805:Ptprc
|
UTSW |
1 |
137,995,623 (GRCm39) |
critical splice donor site |
probably null |
|
R6830:Ptprc
|
UTSW |
1 |
137,999,993 (GRCm39) |
critical splice donor site |
probably null |
|
R6847:Ptprc
|
UTSW |
1 |
138,016,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R6960:Ptprc
|
UTSW |
1 |
138,006,183 (GRCm39) |
critical splice donor site |
probably null |
|
R6995:Ptprc
|
UTSW |
1 |
138,016,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R7009:Ptprc
|
UTSW |
1 |
137,992,291 (GRCm39) |
missense |
probably damaging |
0.97 |
R7041:Ptprc
|
UTSW |
1 |
138,054,047 (GRCm39) |
missense |
probably benign |
0.04 |
R7055:Ptprc
|
UTSW |
1 |
138,017,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R7098:Ptprc
|
UTSW |
1 |
138,027,423 (GRCm39) |
missense |
probably benign |
|
R7164:Ptprc
|
UTSW |
1 |
138,045,600 (GRCm39) |
missense |
probably benign |
|
R7188:Ptprc
|
UTSW |
1 |
137,998,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R7191:Ptprc
|
UTSW |
1 |
138,028,782 (GRCm39) |
missense |
probably benign |
0.02 |
R7204:Ptprc
|
UTSW |
1 |
138,045,600 (GRCm39) |
missense |
probably benign |
|
R7316:Ptprc
|
UTSW |
1 |
137,992,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R7644:Ptprc
|
UTSW |
1 |
137,995,645 (GRCm39) |
missense |
probably benign |
0.01 |
R7948:Ptprc
|
UTSW |
1 |
137,992,314 (GRCm39) |
missense |
probably benign |
0.45 |
R8029:Ptprc
|
UTSW |
1 |
138,006,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R8677:Ptprc
|
UTSW |
1 |
138,011,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R8704:Ptprc
|
UTSW |
1 |
138,043,362 (GRCm39) |
missense |
probably benign |
0.34 |
R8824:Ptprc
|
UTSW |
1 |
138,041,446 (GRCm39) |
nonsense |
probably null |
|
R8921:Ptprc
|
UTSW |
1 |
138,054,039 (GRCm39) |
critical splice donor site |
probably null |
|
R8998:Ptprc
|
UTSW |
1 |
138,028,930 (GRCm39) |
missense |
probably damaging |
0.97 |
R8999:Ptprc
|
UTSW |
1 |
138,028,930 (GRCm39) |
missense |
probably damaging |
0.97 |
R9154:Ptprc
|
UTSW |
1 |
138,016,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R9388:Ptprc
|
UTSW |
1 |
138,011,380 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9428:Ptprc
|
UTSW |
1 |
138,041,485 (GRCm39) |
missense |
probably benign |
0.01 |
R9467:Ptprc
|
UTSW |
1 |
137,993,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R9468:Ptprc
|
UTSW |
1 |
138,044,754 (GRCm39) |
missense |
probably benign |
0.01 |
R9479:Ptprc
|
UTSW |
1 |
138,001,388 (GRCm39) |
missense |
probably benign |
0.38 |
R9526:Ptprc
|
UTSW |
1 |
137,996,111 (GRCm39) |
missense |
probably benign |
0.02 |
R9632:Ptprc
|
UTSW |
1 |
138,008,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R9710:Ptprc
|
UTSW |
1 |
138,008,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R9714:Ptprc
|
UTSW |
1 |
138,008,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R9777:Ptprc
|
UTSW |
1 |
138,047,901 (GRCm39) |
missense |
|
|
Z1177:Ptprc
|
UTSW |
1 |
137,995,645 (GRCm39) |
missense |
probably benign |
0.01 |
|