Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700007G11Rik |
A |
T |
5: 98,784,520 (GRCm38) |
D193V |
probably damaging |
Het |
4921517D22Rik |
G |
T |
13: 59,690,810 (GRCm38) |
D69E |
possibly damaging |
Het |
Abat |
A |
C |
16: 8,602,367 (GRCm38) |
M177L |
probably benign |
Het |
Acadvl |
A |
G |
11: 70,014,791 (GRCm38) |
|
probably null |
Het |
Adam5 |
T |
C |
8: 24,806,438 (GRCm38) |
N331S |
probably benign |
Het |
Ager |
A |
G |
17: 34,600,736 (GRCm38) |
E372G |
probably damaging |
Het |
Angpt1 |
T |
A |
15: 42,523,595 (GRCm38) |
Q121L |
possibly damaging |
Het |
Apoa4 |
A |
T |
9: 46,242,880 (GRCm38) |
I260F |
possibly damaging |
Het |
Arhgap32 |
A |
T |
9: 32,245,976 (GRCm38) |
I90F |
probably damaging |
Het |
Arhgap5 |
A |
T |
12: 52,519,639 (GRCm38) |
Q1131L |
probably benign |
Het |
Bach1 |
G |
A |
16: 87,719,291 (GRCm38) |
R240Q |
probably benign |
Het |
Cacna2d3 |
A |
T |
14: 28,969,365 (GRCm38) |
M1K |
probably null |
Het |
Ccdc18 |
G |
A |
5: 108,173,862 (GRCm38) |
|
probably null |
Het |
Ccdc42 |
T |
C |
11: 68,594,616 (GRCm38) |
F267S |
probably damaging |
Het |
Cdh23 |
T |
A |
10: 60,337,306 (GRCm38) |
Y1700F |
probably damaging |
Het |
Cenpe |
G |
A |
3: 135,235,202 (GRCm38) |
S704N |
probably benign |
Het |
Cenpe |
A |
T |
3: 135,235,201 (GRCm38) |
S704C |
probably damaging |
Het |
Cfap54 |
A |
T |
10: 92,875,019 (GRCm38) |
S2727T |
unknown |
Het |
Clu |
T |
A |
14: 65,971,832 (GRCm38) |
V113D |
probably damaging |
Het |
Cnbd2 |
A |
G |
2: 156,320,034 (GRCm38) |
I98V |
probably benign |
Het |
Copa |
G |
T |
1: 172,091,000 (GRCm38) |
R97L |
probably damaging |
Het |
Epb41l1 |
C |
A |
2: 156,534,683 (GRCm38) |
|
probably null |
Het |
Etnk1 |
T |
A |
6: 143,203,154 (GRCm38) |
|
probably null |
Het |
Fnip1 |
A |
T |
11: 54,502,935 (GRCm38) |
K732N |
probably damaging |
Het |
G6pd2 |
A |
G |
5: 61,808,891 (GRCm38) |
E3G |
probably benign |
Het |
Gal3st2 |
A |
G |
1: 93,873,759 (GRCm38) |
T95A |
probably benign |
Het |
Gapvd1 |
A |
G |
2: 34,700,817 (GRCm38) |
S948P |
probably damaging |
Het |
Ggps1 |
A |
T |
13: 14,054,165 (GRCm38) |
Y8* |
probably null |
Het |
Gria2 |
T |
C |
3: 80,706,972 (GRCm38) |
E587G |
probably damaging |
Het |
Hpse |
T |
C |
5: 100,692,279 (GRCm38) |
E324G |
probably benign |
Het |
Il16 |
G |
A |
7: 83,646,388 (GRCm38) |
T493I |
probably benign |
Het |
Ints1 |
T |
C |
5: 139,768,462 (GRCm38) |
T652A |
possibly damaging |
Het |
Ism1 |
A |
G |
2: 139,757,279 (GRCm38) |
I391V |
probably damaging |
Het |
Katnb1 |
A |
G |
8: 95,098,384 (GRCm38) |
D598G |
probably damaging |
Het |
Kif5c |
A |
G |
2: 49,757,429 (GRCm38) |
S880G |
probably benign |
Het |
Klra8 |
T |
C |
6: 130,125,184 (GRCm38) |
N96S |
probably benign |
Het |
Krt79 |
T |
A |
15: 101,931,441 (GRCm38) |
D373V |
probably damaging |
Het |
Lamtor4 |
G |
A |
5: 138,259,112 (GRCm38) |
R92Q |
probably benign |
Het |
Lce1d |
C |
A |
3: 92,686,046 (GRCm38) |
C20F |
unknown |
Het |
Limk1 |
T |
C |
5: 134,672,699 (GRCm38) |
T117A |
probably benign |
Het |
Medag |
A |
T |
5: 149,427,243 (GRCm38) |
K61M |
probably benign |
Het |
Mkrn3 |
T |
C |
7: 62,419,618 (GRCm38) |
M142V |
probably benign |
Het |
Mob3c |
G |
A |
4: 115,831,582 (GRCm38) |
R104H |
probably benign |
Het |
Morc1 |
G |
T |
16: 48,627,070 (GRCm38) |
R903L |
possibly damaging |
Het |
Myh6 |
T |
C |
14: 54,952,292 (GRCm38) |
E1099G |
probably damaging |
Het |
Nphp3 |
T |
G |
9: 104,016,116 (GRCm38) |
C434G |
probably null |
Het |
Npr3 |
C |
T |
15: 11,905,248 (GRCm38) |
C131Y |
probably damaging |
Het |
Oacyl |
C |
A |
18: 65,722,538 (GRCm38) |
Y112* |
probably null |
Het |
Oprl1 |
A |
G |
2: 181,718,381 (GRCm38) |
T77A |
probably damaging |
Het |
Osgep |
A |
G |
14: 50,924,708 (GRCm38) |
V24A |
probably damaging |
Het |
Otx2 |
T |
A |
14: 48,658,797 (GRCm38) |
K260M |
probably damaging |
Het |
Pdcd11 |
T |
C |
19: 47,113,142 (GRCm38) |
L922P |
probably benign |
Het |
Phldb1 |
A |
G |
9: 44,694,408 (GRCm38) |
V375A |
probably damaging |
Het |
Pip5k1b |
C |
T |
19: 24,359,935 (GRCm38) |
|
probably null |
Het |
Psmd3 |
G |
A |
11: 98,682,766 (GRCm38) |
D13N |
probably benign |
Het |
Ranbp3l |
A |
T |
15: 9,062,984 (GRCm38) |
H291L |
probably damaging |
Het |
Rasa4 |
T |
A |
5: 136,101,363 (GRCm38) |
D324E |
probably damaging |
Het |
Rilpl1 |
T |
A |
5: 124,503,692 (GRCm38) |
|
silent |
Het |
Rin2 |
A |
C |
2: 145,883,475 (GRCm38) |
D794A |
probably damaging |
Het |
Ripk1 |
A |
G |
13: 34,030,062 (GRCm38) |
I522M |
probably damaging |
Het |
Rnf31 |
T |
C |
14: 55,592,551 (GRCm38) |
Y143H |
probably benign |
Het |
Rp1 |
T |
G |
1: 4,042,068 (GRCm38) |
I1187L |
unknown |
Het |
Rps6ka5 |
G |
A |
12: 100,619,537 (GRCm38) |
H166Y |
probably damaging |
Het |
Rrm1 |
T |
C |
7: 102,460,334 (GRCm38) |
V455A |
probably damaging |
Het |
Runx2 |
G |
A |
17: 44,814,192 (GRCm38) |
P80L |
probably damaging |
Het |
Scn5a |
T |
G |
9: 119,485,930 (GRCm38) |
E1904A |
probably damaging |
Het |
Sec16a |
G |
T |
2: 26,436,002 (GRCm38) |
S240* |
probably null |
Het |
Slc22a8 |
C |
T |
19: 8,605,417 (GRCm38) |
T154I |
probably benign |
Het |
Slc25a16 |
T |
A |
10: 62,937,454 (GRCm38) |
V156E |
possibly damaging |
Het |
Slc28a3 |
A |
T |
13: 58,610,804 (GRCm38) |
S2T |
probably benign |
Het |
Srd5a3 |
G |
A |
5: 76,149,866 (GRCm38) |
V48I |
probably benign |
Het |
Srebf1 |
A |
C |
11: 60,200,526 (GRCm38) |
H1025Q |
probably damaging |
Het |
Stard9 |
A |
G |
2: 120,697,191 (GRCm38) |
K1310E |
probably benign |
Het |
Swt1 |
A |
G |
1: 151,370,630 (GRCm38) |
V848A |
possibly damaging |
Het |
Tanc2 |
A |
T |
11: 105,840,699 (GRCm38) |
T434S |
possibly damaging |
Het |
Tcf20 |
G |
A |
15: 82,854,682 (GRCm38) |
T856I |
probably benign |
Het |
Tcf7l2 |
T |
C |
19: 55,894,733 (GRCm38) |
|
probably null |
Het |
Tmem246 |
A |
T |
4: 49,586,325 (GRCm38) |
M281K |
probably benign |
Het |
Trim45 |
A |
G |
3: 100,931,879 (GRCm38) |
|
probably benign |
Het |
Tsen2 |
T |
A |
6: 115,547,972 (GRCm38) |
M44K |
possibly damaging |
Het |
Ttc21a |
T |
A |
9: 119,958,073 (GRCm38) |
C715* |
probably null |
Het |
Vmn2r102 |
G |
A |
17: 19,694,194 (GRCm38) |
V674I |
probably damaging |
Het |
Zfp87 |
A |
G |
13: 67,517,054 (GRCm38) |
S430P |
probably damaging |
Het |
|
Other mutations in Ptprc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
lochy
|
APN |
1 |
138,083,790 (GRCm38) |
splice site |
probably benign |
|
IGL00486:Ptprc
|
APN |
1 |
138,115,621 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL00771:Ptprc
|
APN |
1 |
138,113,677 (GRCm38) |
missense |
probably benign |
0.00 |
IGL00833:Ptprc
|
APN |
1 |
138,078,492 (GRCm38) |
missense |
possibly damaging |
0.55 |
IGL00919:Ptprc
|
APN |
1 |
138,113,642 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01020:Ptprc
|
APN |
1 |
138,120,173 (GRCm38) |
critical splice acceptor site |
probably null |
0.00 |
IGL01024:Ptprc
|
APN |
1 |
138,080,912 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01302:Ptprc
|
APN |
1 |
138,099,631 (GRCm38) |
missense |
possibly damaging |
0.82 |
IGL01548:Ptprc
|
APN |
1 |
138,099,481 (GRCm38) |
critical splice donor site |
probably null |
0.00 |
IGL01620:Ptprc
|
APN |
1 |
138,068,410 (GRCm38) |
missense |
possibly damaging |
0.88 |
IGL01775:Ptprc
|
APN |
1 |
138,064,759 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01820:Ptprc
|
APN |
1 |
138,066,198 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02340:Ptprc
|
APN |
1 |
138,071,219 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02943:Ptprc
|
APN |
1 |
138,099,513 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL03169:Ptprc
|
APN |
1 |
138,113,619 (GRCm38) |
missense |
probably benign |
0.15 |
IGL03308:Ptprc
|
APN |
1 |
138,126,320 (GRCm38) |
missense |
possibly damaging |
0.70 |
IGL03404:Ptprc
|
APN |
1 |
138,093,001 (GRCm38) |
missense |
probably damaging |
1.00 |
belittle
|
UTSW |
1 |
138,137,493 (GRCm38) |
intron |
probably benign |
|
Benighted
|
UTSW |
1 |
138,126,301 (GRCm38) |
critical splice donor site |
probably null |
|
bletchley
|
UTSW |
1 |
138,117,862 (GRCm38) |
missense |
probably benign |
|
Blush
|
UTSW |
1 |
138,117,720 (GRCm38) |
intron |
probably benign |
|
bruise
|
UTSW |
1 |
138,064,771 (GRCm38) |
missense |
probably damaging |
1.00 |
chor_muang
|
UTSW |
1 |
138,113,562 (GRCm38) |
critical splice donor site |
probably null |
|
crystal
|
UTSW |
1 |
138,072,255 (GRCm38) |
critical splice donor site |
probably null |
|
Dumpling
|
UTSW |
1 |
138,067,890 (GRCm38) |
missense |
probably damaging |
1.00 |
fluorescent
|
UTSW |
1 |
138,101,192 (GRCm38) |
missense |
probably damaging |
0.97 |
fuchsia
|
UTSW |
1 |
138,101,041 (GRCm38) |
critical splice donor site |
probably null |
|
Gentian
|
UTSW |
1 |
138,067,885 (GRCm38) |
critical splice donor site |
probably null |
|
guotie
|
UTSW |
1 |
138,068,401 (GRCm38) |
nonsense |
probably null |
|
guotie2
|
UTSW |
1 |
138,094,299 (GRCm38) |
missense |
probably damaging |
0.97 |
Guotie3
|
UTSW |
1 |
138,078,451 (GRCm38) |
missense |
possibly damaging |
0.92 |
Gyoza
|
UTSW |
1 |
138,083,567 (GRCm38) |
missense |
probably damaging |
1.00 |
Half_measure
|
UTSW |
1 |
138,071,249 (GRCm38) |
missense |
probably damaging |
0.98 |
jirisan
|
UTSW |
1 |
138,113,678 (GRCm38) |
nonsense |
probably null |
|
mauve
|
UTSW |
1 |
138,099,685 (GRCm38) |
missense |
probably benign |
|
Perverse
|
UTSW |
1 |
138,101,044 (GRCm38) |
missense |
probably benign |
0.02 |
petechiae
|
UTSW |
1 |
138,113,708 (GRCm38) |
nonsense |
probably null |
|
ultra
|
UTSW |
1 |
138,078,445 (GRCm38) |
critical splice donor site |
probably null |
|
violaceous
|
UTSW |
1 |
138,083,639 (GRCm38) |
missense |
possibly damaging |
0.77 |
R0013:Ptprc
|
UTSW |
1 |
138,113,559 (GRCm38) |
splice site |
probably null |
|
R0189:Ptprc
|
UTSW |
1 |
138,082,715 (GRCm38) |
missense |
probably benign |
0.10 |
R0390:Ptprc
|
UTSW |
1 |
138,122,575 (GRCm38) |
missense |
possibly damaging |
0.71 |
R0504:Ptprc
|
UTSW |
1 |
138,088,697 (GRCm38) |
missense |
probably damaging |
1.00 |
R0602:Ptprc
|
UTSW |
1 |
138,089,485 (GRCm38) |
splice site |
probably benign |
|
R0627:Ptprc
|
UTSW |
1 |
138,068,320 (GRCm38) |
missense |
probably damaging |
0.99 |
R0632:Ptprc
|
UTSW |
1 |
138,073,610 (GRCm38) |
missense |
probably benign |
0.01 |
R0751:Ptprc
|
UTSW |
1 |
138,092,930 (GRCm38) |
missense |
probably damaging |
1.00 |
R0839:Ptprc
|
UTSW |
1 |
138,101,132 (GRCm38) |
missense |
possibly damaging |
0.47 |
R0942:Ptprc
|
UTSW |
1 |
138,068,401 (GRCm38) |
nonsense |
probably null |
|
R0943:Ptprc
|
UTSW |
1 |
138,111,164 (GRCm38) |
missense |
probably damaging |
0.96 |
R1159:Ptprc
|
UTSW |
1 |
138,072,319 (GRCm38) |
missense |
probably damaging |
1.00 |
R1442:Ptprc
|
UTSW |
1 |
138,072,312 (GRCm38) |
missense |
probably damaging |
1.00 |
R1489:Ptprc
|
UTSW |
1 |
138,120,086 (GRCm38) |
missense |
possibly damaging |
0.91 |
R1728:Ptprc
|
UTSW |
1 |
138,107,824 (GRCm38) |
missense |
probably benign |
0.04 |
R1728:Ptprc
|
UTSW |
1 |
138,107,823 (GRCm38) |
missense |
probably benign |
0.22 |
R1728:Ptprc
|
UTSW |
1 |
138,099,676 (GRCm38) |
missense |
probably benign |
0.05 |
R1728:Ptprc
|
UTSW |
1 |
138,112,254 (GRCm38) |
missense |
possibly damaging |
0.53 |
R1728:Ptprc
|
UTSW |
1 |
138,107,837 (GRCm38) |
missense |
probably benign |
0.09 |
R1729:Ptprc
|
UTSW |
1 |
138,107,823 (GRCm38) |
missense |
probably benign |
0.22 |
R1729:Ptprc
|
UTSW |
1 |
138,099,676 (GRCm38) |
missense |
probably benign |
0.05 |
R1729:Ptprc
|
UTSW |
1 |
138,112,254 (GRCm38) |
missense |
possibly damaging |
0.53 |
R1729:Ptprc
|
UTSW |
1 |
138,107,837 (GRCm38) |
missense |
probably benign |
0.09 |
R1729:Ptprc
|
UTSW |
1 |
138,107,824 (GRCm38) |
missense |
probably benign |
0.04 |
R1730:Ptprc
|
UTSW |
1 |
138,107,837 (GRCm38) |
missense |
probably benign |
0.09 |
R1730:Ptprc
|
UTSW |
1 |
138,112,254 (GRCm38) |
missense |
possibly damaging |
0.53 |
R1730:Ptprc
|
UTSW |
1 |
138,099,676 (GRCm38) |
missense |
probably benign |
0.05 |
R1730:Ptprc
|
UTSW |
1 |
138,107,823 (GRCm38) |
missense |
probably benign |
0.22 |
R1730:Ptprc
|
UTSW |
1 |
138,107,824 (GRCm38) |
missense |
probably benign |
0.04 |
R1739:Ptprc
|
UTSW |
1 |
138,107,837 (GRCm38) |
missense |
probably benign |
0.09 |
R1739:Ptprc
|
UTSW |
1 |
138,112,254 (GRCm38) |
missense |
possibly damaging |
0.53 |
R1739:Ptprc
|
UTSW |
1 |
138,099,676 (GRCm38) |
missense |
probably benign |
0.05 |
R1739:Ptprc
|
UTSW |
1 |
138,107,823 (GRCm38) |
missense |
probably benign |
0.22 |
R1739:Ptprc
|
UTSW |
1 |
138,107,824 (GRCm38) |
missense |
probably benign |
0.04 |
R1762:Ptprc
|
UTSW |
1 |
138,107,837 (GRCm38) |
missense |
probably benign |
0.09 |
R1762:Ptprc
|
UTSW |
1 |
138,112,254 (GRCm38) |
missense |
possibly damaging |
0.53 |
R1762:Ptprc
|
UTSW |
1 |
138,099,676 (GRCm38) |
missense |
probably benign |
0.05 |
R1762:Ptprc
|
UTSW |
1 |
138,107,823 (GRCm38) |
missense |
probably benign |
0.22 |
R1762:Ptprc
|
UTSW |
1 |
138,107,824 (GRCm38) |
missense |
probably benign |
0.04 |
R1783:Ptprc
|
UTSW |
1 |
138,099,676 (GRCm38) |
missense |
probably benign |
0.05 |
R1783:Ptprc
|
UTSW |
1 |
138,107,823 (GRCm38) |
missense |
probably benign |
0.22 |
R1783:Ptprc
|
UTSW |
1 |
138,107,824 (GRCm38) |
missense |
probably benign |
0.04 |
R1783:Ptprc
|
UTSW |
1 |
138,107,837 (GRCm38) |
missense |
probably benign |
0.09 |
R1783:Ptprc
|
UTSW |
1 |
138,112,254 (GRCm38) |
missense |
possibly damaging |
0.53 |
R1784:Ptprc
|
UTSW |
1 |
138,107,837 (GRCm38) |
missense |
probably benign |
0.09 |
R1784:Ptprc
|
UTSW |
1 |
138,112,254 (GRCm38) |
missense |
possibly damaging |
0.53 |
R1784:Ptprc
|
UTSW |
1 |
138,099,676 (GRCm38) |
missense |
probably benign |
0.05 |
R1784:Ptprc
|
UTSW |
1 |
138,107,823 (GRCm38) |
missense |
probably benign |
0.22 |
R1784:Ptprc
|
UTSW |
1 |
138,107,824 (GRCm38) |
missense |
probably benign |
0.04 |
R1785:Ptprc
|
UTSW |
1 |
138,099,676 (GRCm38) |
missense |
probably benign |
0.05 |
R1785:Ptprc
|
UTSW |
1 |
138,107,823 (GRCm38) |
missense |
probably benign |
0.22 |
R1785:Ptprc
|
UTSW |
1 |
138,112,254 (GRCm38) |
missense |
possibly damaging |
0.53 |
R1785:Ptprc
|
UTSW |
1 |
138,107,837 (GRCm38) |
missense |
probably benign |
0.09 |
R1785:Ptprc
|
UTSW |
1 |
138,107,824 (GRCm38) |
missense |
probably benign |
0.04 |
R1862:Ptprc
|
UTSW |
1 |
138,112,227 (GRCm38) |
missense |
probably benign |
0.13 |
R2145:Ptprc
|
UTSW |
1 |
138,073,681 (GRCm38) |
missense |
probably damaging |
1.00 |
R2290:Ptprc
|
UTSW |
1 |
138,111,188 (GRCm38) |
missense |
probably benign |
0.00 |
R2403:Ptprc
|
UTSW |
1 |
138,088,532 (GRCm38) |
missense |
probably damaging |
1.00 |
R2439:Ptprc
|
UTSW |
1 |
138,066,152 (GRCm38) |
missense |
possibly damaging |
0.67 |
R2887:Ptprc
|
UTSW |
1 |
138,080,178 (GRCm38) |
missense |
probably damaging |
1.00 |
R2906:Ptprc
|
UTSW |
1 |
138,064,534 (GRCm38) |
missense |
possibly damaging |
0.93 |
R3774:Ptprc
|
UTSW |
1 |
138,064,773 (GRCm38) |
missense |
probably damaging |
0.97 |
R3775:Ptprc
|
UTSW |
1 |
138,064,773 (GRCm38) |
missense |
probably damaging |
0.97 |
R3776:Ptprc
|
UTSW |
1 |
138,064,773 (GRCm38) |
missense |
probably damaging |
0.97 |
R3834:Ptprc
|
UTSW |
1 |
138,083,567 (GRCm38) |
missense |
probably damaging |
1.00 |
R4019:Ptprc
|
UTSW |
1 |
138,078,516 (GRCm38) |
missense |
probably damaging |
1.00 |
R4377:Ptprc
|
UTSW |
1 |
138,067,925 (GRCm38) |
missense |
probably benign |
0.04 |
R4580:Ptprc
|
UTSW |
1 |
138,071,251 (GRCm38) |
missense |
probably benign |
0.09 |
R4923:Ptprc
|
UTSW |
1 |
138,078,498 (GRCm38) |
missense |
possibly damaging |
0.93 |
R4925:Ptprc
|
UTSW |
1 |
138,099,497 (GRCm38) |
missense |
probably benign |
0.04 |
R4937:Ptprc
|
UTSW |
1 |
138,089,500 (GRCm38) |
missense |
probably damaging |
1.00 |
R4970:Ptprc
|
UTSW |
1 |
138,094,299 (GRCm38) |
missense |
probably damaging |
0.97 |
R5112:Ptprc
|
UTSW |
1 |
138,094,299 (GRCm38) |
missense |
probably damaging |
0.97 |
R5145:Ptprc
|
UTSW |
1 |
138,089,566 (GRCm38) |
missense |
probably benign |
0.07 |
R5158:Ptprc
|
UTSW |
1 |
138,175,084 (GRCm38) |
missense |
possibly damaging |
0.75 |
R5223:Ptprc
|
UTSW |
1 |
138,117,862 (GRCm38) |
missense |
probably benign |
|
R5593:Ptprc
|
UTSW |
1 |
138,117,720 (GRCm38) |
intron |
probably benign |
|
R5689:Ptprc
|
UTSW |
1 |
138,117,777 (GRCm38) |
missense |
probably benign |
0.01 |
R5885:Ptprc
|
UTSW |
1 |
138,088,508 (GRCm38) |
missense |
probably damaging |
1.00 |
R6010:Ptprc
|
UTSW |
1 |
138,101,056 (GRCm38) |
missense |
probably benign |
0.09 |
R6026:Ptprc
|
UTSW |
1 |
138,071,249 (GRCm38) |
missense |
probably damaging |
0.98 |
R6047:Ptprc
|
UTSW |
1 |
138,101,041 (GRCm38) |
critical splice donor site |
probably null |
|
R6173:Ptprc
|
UTSW |
1 |
138,067,890 (GRCm38) |
missense |
probably damaging |
1.00 |
R6328:Ptprc
|
UTSW |
1 |
138,113,678 (GRCm38) |
nonsense |
probably null |
|
R6383:Ptprc
|
UTSW |
1 |
138,078,451 (GRCm38) |
missense |
possibly damaging |
0.92 |
R6436:Ptprc
|
UTSW |
1 |
138,083,639 (GRCm38) |
missense |
possibly damaging |
0.77 |
R6492:Ptprc
|
UTSW |
1 |
138,113,562 (GRCm38) |
critical splice donor site |
probably null |
|
R6520:Ptprc
|
UTSW |
1 |
138,080,143 (GRCm38) |
nonsense |
probably null |
|
R6805:Ptprc
|
UTSW |
1 |
138,067,885 (GRCm38) |
critical splice donor site |
probably null |
|
R6830:Ptprc
|
UTSW |
1 |
138,072,255 (GRCm38) |
critical splice donor site |
probably null |
|
R6847:Ptprc
|
UTSW |
1 |
138,088,545 (GRCm38) |
missense |
probably damaging |
0.99 |
R6960:Ptprc
|
UTSW |
1 |
138,078,445 (GRCm38) |
critical splice donor site |
probably null |
|
R6995:Ptprc
|
UTSW |
1 |
138,088,744 (GRCm38) |
missense |
probably damaging |
1.00 |
R7041:Ptprc
|
UTSW |
1 |
138,126,309 (GRCm38) |
missense |
probably benign |
0.04 |
R7055:Ptprc
|
UTSW |
1 |
138,089,571 (GRCm38) |
missense |
probably damaging |
1.00 |
R7098:Ptprc
|
UTSW |
1 |
138,099,685 (GRCm38) |
missense |
probably benign |
|
R7164:Ptprc
|
UTSW |
1 |
138,117,862 (GRCm38) |
missense |
probably benign |
|
R7188:Ptprc
|
UTSW |
1 |
138,071,180 (GRCm38) |
missense |
probably damaging |
1.00 |
R7191:Ptprc
|
UTSW |
1 |
138,101,044 (GRCm38) |
missense |
probably benign |
0.02 |
R7204:Ptprc
|
UTSW |
1 |
138,117,862 (GRCm38) |
missense |
probably benign |
|
R7316:Ptprc
|
UTSW |
1 |
138,064,771 (GRCm38) |
missense |
probably damaging |
1.00 |
R7644:Ptprc
|
UTSW |
1 |
138,067,907 (GRCm38) |
missense |
probably benign |
0.01 |
R7948:Ptprc
|
UTSW |
1 |
138,064,576 (GRCm38) |
missense |
probably benign |
0.45 |
R8029:Ptprc
|
UTSW |
1 |
138,078,459 (GRCm38) |
missense |
probably damaging |
1.00 |
R8677:Ptprc
|
UTSW |
1 |
138,083,597 (GRCm38) |
missense |
probably damaging |
1.00 |
R8704:Ptprc
|
UTSW |
1 |
138,115,624 (GRCm38) |
missense |
probably benign |
0.34 |
R8824:Ptprc
|
UTSW |
1 |
138,113,708 (GRCm38) |
nonsense |
probably null |
|
R8921:Ptprc
|
UTSW |
1 |
138,126,301 (GRCm38) |
critical splice donor site |
probably null |
|
R8998:Ptprc
|
UTSW |
1 |
138,101,192 (GRCm38) |
missense |
probably damaging |
0.97 |
R8999:Ptprc
|
UTSW |
1 |
138,101,192 (GRCm38) |
missense |
probably damaging |
0.97 |
R9154:Ptprc
|
UTSW |
1 |
138,088,564 (GRCm38) |
missense |
probably damaging |
1.00 |
R9388:Ptprc
|
UTSW |
1 |
138,083,642 (GRCm38) |
missense |
possibly damaging |
0.87 |
R9428:Ptprc
|
UTSW |
1 |
138,113,747 (GRCm38) |
missense |
probably benign |
0.01 |
R9467:Ptprc
|
UTSW |
1 |
138,066,222 (GRCm38) |
missense |
probably damaging |
1.00 |
R9468:Ptprc
|
UTSW |
1 |
138,117,016 (GRCm38) |
missense |
probably benign |
0.01 |
R9479:Ptprc
|
UTSW |
1 |
138,073,650 (GRCm38) |
missense |
probably benign |
0.38 |
R9526:Ptprc
|
UTSW |
1 |
138,068,373 (GRCm38) |
missense |
probably benign |
0.02 |
R9632:Ptprc
|
UTSW |
1 |
138,080,889 (GRCm38) |
missense |
probably damaging |
1.00 |
R9710:Ptprc
|
UTSW |
1 |
138,080,889 (GRCm38) |
missense |
probably damaging |
1.00 |
R9714:Ptprc
|
UTSW |
1 |
138,080,949 (GRCm38) |
missense |
probably damaging |
1.00 |
R9777:Ptprc
|
UTSW |
1 |
138,120,163 (GRCm38) |
missense |
|
|
Z1177:Ptprc
|
UTSW |
1 |
138,067,907 (GRCm38) |
missense |
probably benign |
0.01 |
|