Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
T |
C |
4: 53,072,924 (GRCm39) |
D1170G |
probably benign |
Het |
Ak7 |
A |
T |
12: 105,676,503 (GRCm39) |
T68S |
probably benign |
Het |
Arhgap12 |
A |
T |
18: 6,111,901 (GRCm39) |
N26K |
probably damaging |
Het |
B3galt1 |
A |
T |
2: 67,949,033 (GRCm39) |
E249D |
probably damaging |
Het |
Catsper4 |
T |
A |
4: 133,954,648 (GRCm39) |
M1L |
probably benign |
Het |
Cc2d2b |
T |
C |
19: 40,773,506 (GRCm39) |
V523A |
possibly damaging |
Het |
Ccn4 |
C |
T |
15: 66,791,047 (GRCm39) |
T283M |
probably benign |
Het |
Cyp11a1 |
T |
C |
9: 57,925,659 (GRCm39) |
F98S |
probably damaging |
Het |
Cyp2d26 |
T |
C |
15: 82,674,446 (GRCm39) |
S479G |
probably damaging |
Het |
Dclre1a |
T |
G |
19: 56,531,141 (GRCm39) |
Y735S |
probably damaging |
Het |
Dio2 |
C |
T |
12: 90,696,671 (GRCm39) |
G106R |
probably damaging |
Het |
Efcab12 |
T |
C |
6: 115,815,273 (GRCm39) |
|
probably benign |
Het |
Ehhadh |
C |
A |
16: 21,581,028 (GRCm39) |
V655L |
probably benign |
Het |
Ercc2 |
G |
A |
7: 19,127,615 (GRCm39) |
R379Q |
probably damaging |
Het |
Fabp4 |
A |
G |
3: 10,273,537 (GRCm39) |
V12A |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,223,980 (GRCm39) |
I590V |
probably benign |
Het |
Grm8 |
C |
A |
6: 27,981,281 (GRCm39) |
V210L |
probably damaging |
Het |
Jakmip3 |
A |
G |
7: 138,625,065 (GRCm39) |
D359G |
probably damaging |
Het |
Lrit1 |
G |
C |
14: 36,782,052 (GRCm39) |
V242L |
probably damaging |
Het |
Ly75 |
A |
T |
2: 60,136,749 (GRCm39) |
Y1493N |
probably benign |
Het |
Lyst |
A |
G |
13: 13,808,663 (GRCm39) |
N111S |
probably benign |
Het |
Lyz2 |
G |
C |
10: 117,114,607 (GRCm39) |
I107M |
possibly damaging |
Het |
Mgat5 |
A |
T |
1: 127,248,371 (GRCm39) |
D91V |
possibly damaging |
Het |
Mical3 |
T |
A |
6: 120,935,504 (GRCm39) |
D1674V |
probably damaging |
Het |
Myom2 |
G |
A |
8: 15,167,741 (GRCm39) |
A1109T |
probably null |
Het |
Naa16 |
A |
G |
14: 79,596,911 (GRCm39) |
Y358H |
possibly damaging |
Het |
Nktr |
T |
A |
9: 121,571,758 (GRCm39) |
H226Q |
probably damaging |
Het |
Ocln |
T |
G |
13: 100,635,380 (GRCm39) |
K503T |
possibly damaging |
Het |
Olfm4 |
T |
C |
14: 80,258,754 (GRCm39) |
L301S |
probably damaging |
Het |
Or4f4b |
G |
A |
2: 111,314,071 (GRCm39) |
V127I |
possibly damaging |
Het |
Or6c74 |
T |
C |
10: 129,869,972 (GRCm39) |
L159P |
probably benign |
Het |
Paqr4 |
G |
A |
17: 23,956,697 (GRCm39) |
A222V |
probably benign |
Het |
Pcdhb13 |
A |
G |
18: 37,576,509 (GRCm39) |
T296A |
probably benign |
Het |
Phka2 |
G |
A |
X: 159,316,044 (GRCm39) |
V230I |
probably damaging |
Het |
Pigg |
T |
C |
5: 108,474,707 (GRCm39) |
V309A |
probably damaging |
Het |
Ptger4 |
T |
C |
15: 5,264,196 (GRCm39) |
R462G |
probably benign |
Het |
Rabggta |
A |
C |
14: 55,959,299 (GRCm39) |
|
probably null |
Het |
Rnf25 |
A |
G |
1: 74,634,403 (GRCm39) |
S207P |
possibly damaging |
Het |
Rsf1 |
G |
GACGGCGGCC |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Rtf1 |
A |
G |
2: 119,541,559 (GRCm39) |
Q264R |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,816,129 (GRCm39) |
V619A |
probably benign |
Het |
Serpinb6d |
A |
G |
13: 33,855,181 (GRCm39) |
N285S |
probably benign |
Het |
Slamf6 |
A |
G |
1: 171,745,320 (GRCm39) |
M16V |
probably damaging |
Het |
Slc22a23 |
A |
G |
13: 34,528,140 (GRCm39) |
|
probably null |
Het |
Slc23a2 |
T |
C |
2: 131,933,173 (GRCm39) |
D95G |
probably damaging |
Het |
Smc3 |
T |
C |
19: 53,617,802 (GRCm39) |
Y600H |
probably damaging |
Het |
Tarbp1 |
G |
A |
8: 127,155,778 (GRCm39) |
T1320M |
possibly damaging |
Het |
Tigd4 |
A |
T |
3: 84,501,423 (GRCm39) |
K113N |
probably damaging |
Het |
Tjp1 |
A |
T |
7: 64,952,763 (GRCm39) |
F1444I |
possibly damaging |
Het |
Tstd3 |
A |
T |
4: 21,767,118 (GRCm39) |
M1K |
probably null |
Het |
Zbtb46 |
T |
C |
2: 181,065,217 (GRCm39) |
D311G |
probably 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 |
R2403:Ptprc
|
UTSW |
1 |
138,016,270 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|