Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm2 |
A |
G |
7: 119,177,421 (GRCm39) |
H312R |
possibly damaging |
Het |
Aloxe3 |
T |
C |
11: 69,025,114 (GRCm39) |
F409S |
probably damaging |
Het |
Arfgef1 |
T |
A |
1: 10,215,004 (GRCm39) |
N1630I |
probably damaging |
Het |
Catsperd |
G |
A |
17: 56,968,252 (GRCm39) |
D546N |
probably benign |
Het |
Cbl |
A |
G |
9: 44,064,137 (GRCm39) |
S800P |
probably damaging |
Het |
Ccne1 |
A |
T |
7: 37,799,255 (GRCm39) |
S220T |
probably benign |
Het |
Cd177 |
T |
C |
7: 24,443,668 (GRCm39) |
Y810C |
probably benign |
Het |
Cercam |
T |
C |
2: 29,766,033 (GRCm39) |
V304A |
possibly damaging |
Het |
Cfap100 |
T |
C |
6: 90,390,416 (GRCm39) |
T75A |
|
Het |
Clcn4 |
T |
A |
7: 7,287,197 (GRCm39) |
I744F |
possibly damaging |
Het |
Col15a1 |
G |
C |
4: 47,288,200 (GRCm39) |
|
probably benign |
Het |
Col27a1 |
A |
G |
4: 63,246,887 (GRCm39) |
N1670S |
unknown |
Het |
Cps1 |
G |
A |
1: 67,248,831 (GRCm39) |
R1186Q |
probably benign |
Het |
Cr1l |
C |
A |
1: 194,797,053 (GRCm39) |
C328F |
probably damaging |
Het |
Crybg1 |
T |
A |
10: 43,880,091 (GRCm39) |
T366S |
probably benign |
Het |
Ctbp2 |
A |
T |
7: 132,615,712 (GRCm39) |
S408T |
probably damaging |
Het |
Dync1h1 |
T |
C |
12: 110,601,937 (GRCm39) |
S1992P |
probably benign |
Het |
Glyatl3 |
A |
T |
17: 41,225,234 (GRCm39) |
V3E |
probably damaging |
Het |
Gse1 |
T |
C |
8: 121,294,908 (GRCm39) |
M343T |
possibly damaging |
Het |
Gys2 |
T |
C |
6: 142,405,112 (GRCm39) |
D225G |
probably damaging |
Het |
Hecw1 |
T |
C |
13: 14,491,628 (GRCm39) |
S42G |
probably damaging |
Het |
Helz2 |
A |
G |
2: 180,871,883 (GRCm39) |
C2673R |
probably benign |
Het |
Hivep1 |
G |
A |
13: 42,337,975 (GRCm39) |
V2685I |
possibly damaging |
Het |
Icam5 |
A |
G |
9: 20,950,165 (GRCm39) |
E908G |
probably damaging |
Het |
Kcne1 |
A |
T |
16: 92,145,796 (GRCm39) |
L16Q |
possibly damaging |
Het |
Kcnk5 |
G |
T |
14: 20,195,135 (GRCm39) |
Y118* |
probably null |
Het |
Kctd11 |
T |
C |
11: 69,770,676 (GRCm39) |
T121A |
possibly damaging |
Het |
Mier3 |
T |
C |
13: 111,851,260 (GRCm39) |
V414A |
probably benign |
Het |
Mindy4 |
T |
C |
6: 55,295,261 (GRCm39) |
S734P |
possibly damaging |
Het |
Mrps26 |
T |
C |
2: 130,405,769 (GRCm39) |
V24A |
probably benign |
Het |
Mug2 |
C |
G |
6: 122,054,442 (GRCm39) |
Q1074E |
probably benign |
Het |
Myo15b |
T |
C |
11: 115,771,255 (GRCm39) |
S1P |
unknown |
Het |
Ninj1 |
A |
T |
13: 49,344,726 (GRCm39) |
T81S |
probably benign |
Het |
Nod2 |
A |
T |
8: 89,391,880 (GRCm39) |
H729L |
probably damaging |
Het |
Nr1i3 |
G |
A |
1: 171,043,955 (GRCm39) |
V49I |
possibly damaging |
Het |
Olfm5 |
G |
A |
7: 103,810,095 (GRCm39) |
Q89* |
probably null |
Het |
Or10ag52 |
A |
T |
2: 87,044,174 (GRCm39) |
T313S |
probably benign |
Het |
Or2n1b |
A |
T |
17: 38,459,754 (GRCm39) |
I92F |
probably damaging |
Het |
Or2y12 |
T |
C |
11: 49,426,501 (GRCm39) |
V163A |
probably benign |
Het |
Or4e1 |
A |
G |
14: 52,700,984 (GRCm39) |
S161P |
probably benign |
Het |
Or51a25 |
C |
T |
7: 102,373,409 (GRCm39) |
R96H |
possibly damaging |
Het |
Or5aq6 |
A |
C |
2: 86,923,200 (GRCm39) |
D180E |
possibly damaging |
Het |
Or5b124 |
A |
T |
19: 13,610,765 (GRCm39) |
T97S |
probably benign |
Het |
Or8g53 |
T |
A |
9: 39,683,404 (GRCm39) |
T231S |
probably benign |
Het |
Pde4dip |
T |
A |
3: 97,666,132 (GRCm39) |
T371S |
probably benign |
Het |
Pkhd1l1 |
T |
A |
15: 44,453,019 (GRCm39) |
S3981R |
probably benign |
Het |
Plxnd1 |
G |
T |
6: 115,934,526 (GRCm39) |
F1802L |
probably damaging |
Het |
Pramel22 |
T |
C |
4: 143,381,898 (GRCm39) |
N266S |
probably benign |
Het |
Prcp |
A |
G |
7: 92,582,257 (GRCm39) |
H449R |
probably benign |
Het |
Rcvrn |
A |
G |
11: 67,586,480 (GRCm39) |
T80A |
possibly damaging |
Het |
Rhou |
T |
C |
8: 124,387,793 (GRCm39) |
L175P |
probably damaging |
Het |
Sacs |
T |
C |
14: 61,444,115 (GRCm39) |
S2054P |
probably damaging |
Het |
Slc22a30 |
A |
G |
19: 8,321,917 (GRCm39) |
S414P |
probably benign |
Het |
Slc2a13 |
T |
A |
15: 91,227,906 (GRCm39) |
S429C |
probably damaging |
Het |
Slc35b3 |
A |
G |
13: 39,123,958 (GRCm39) |
|
probably benign |
Het |
Smyd3 |
A |
G |
1: 178,877,854 (GRCm39) |
|
probably null |
Het |
Strip1 |
T |
A |
3: 107,535,530 (GRCm39) |
E64D |
probably damaging |
Het |
Sumf2 |
T |
G |
5: 129,875,909 (GRCm39) |
C25G |
possibly damaging |
Het |
Syngap1 |
A |
C |
17: 27,182,057 (GRCm39) |
D1190A |
possibly damaging |
Het |
Tas2r139 |
C |
T |
6: 42,118,099 (GRCm39) |
T77I |
probably benign |
Het |
Tbce |
A |
T |
13: 14,173,027 (GRCm39) |
V468D |
probably damaging |
Het |
Tmem191 |
G |
A |
16: 17,094,302 (GRCm39) |
R42H |
probably damaging |
Het |
Tmem200c |
T |
C |
17: 69,147,633 (GRCm39) |
V72A |
probably damaging |
Het |
Ttc28 |
T |
G |
5: 111,371,342 (GRCm39) |
F628C |
probably benign |
Het |
Wsb2 |
G |
A |
5: 117,501,736 (GRCm39) |
V34M |
possibly damaging |
Het |
Zfand6 |
A |
G |
7: 84,283,558 (GRCm39) |
S15P |
probably damaging |
Het |
Zfp964 |
A |
G |
8: 70,115,873 (GRCm39) |
N158D |
possibly damaging |
Het |
Zic1 |
G |
T |
9: 91,246,542 (GRCm39) |
Q177K |
probably benign |
Het |
Zswim4 |
T |
C |
8: 84,963,633 (GRCm39) |
M1V |
probably null |
Het |
|
Other mutations in Prrc2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00425:Prrc2c
|
APN |
1 |
162,548,182 (GRCm39) |
splice site |
probably null |
|
IGL00577:Prrc2c
|
APN |
1 |
162,525,685 (GRCm39) |
missense |
unknown |
|
IGL00580:Prrc2c
|
APN |
1 |
162,525,685 (GRCm39) |
missense |
unknown |
|
IGL01295:Prrc2c
|
APN |
1 |
162,510,061 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01554:Prrc2c
|
APN |
1 |
162,538,355 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01684:Prrc2c
|
APN |
1 |
162,534,031 (GRCm39) |
unclassified |
probably benign |
|
IGL01745:Prrc2c
|
APN |
1 |
162,552,297 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01770:Prrc2c
|
APN |
1 |
162,532,068 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01905:Prrc2c
|
APN |
1 |
162,532,898 (GRCm39) |
unclassified |
probably benign |
|
IGL02304:Prrc2c
|
APN |
1 |
162,511,705 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02389:Prrc2c
|
APN |
1 |
162,520,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02540:Prrc2c
|
APN |
1 |
162,550,706 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02681:Prrc2c
|
APN |
1 |
162,533,181 (GRCm39) |
unclassified |
probably benign |
|
IGL02686:Prrc2c
|
APN |
1 |
162,535,516 (GRCm39) |
unclassified |
probably benign |
|
IGL02795:Prrc2c
|
APN |
1 |
162,541,868 (GRCm39) |
missense |
probably benign |
|
IGL02894:Prrc2c
|
APN |
1 |
162,505,626 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02957:Prrc2c
|
APN |
1 |
162,534,104 (GRCm39) |
unclassified |
probably benign |
|
IGL02981:Prrc2c
|
APN |
1 |
162,532,748 (GRCm39) |
unclassified |
probably benign |
|
IGL03070:Prrc2c
|
APN |
1 |
162,504,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03096:Prrc2c
|
APN |
1 |
162,529,928 (GRCm39) |
missense |
unknown |
|
R0058:Prrc2c
|
UTSW |
1 |
162,526,453 (GRCm39) |
missense |
unknown |
|
R0058:Prrc2c
|
UTSW |
1 |
162,526,453 (GRCm39) |
missense |
unknown |
|
R0135:Prrc2c
|
UTSW |
1 |
162,543,052 (GRCm39) |
splice site |
probably benign |
|
R0279:Prrc2c
|
UTSW |
1 |
162,543,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R0363:Prrc2c
|
UTSW |
1 |
162,525,380 (GRCm39) |
missense |
unknown |
|
R0436:Prrc2c
|
UTSW |
1 |
162,532,883 (GRCm39) |
unclassified |
probably benign |
|
R0605:Prrc2c
|
UTSW |
1 |
162,509,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R0696:Prrc2c
|
UTSW |
1 |
162,536,421 (GRCm39) |
critical splice donor site |
probably null |
|
R0981:Prrc2c
|
UTSW |
1 |
162,533,550 (GRCm39) |
unclassified |
probably benign |
|
R1693:Prrc2c
|
UTSW |
1 |
162,546,282 (GRCm39) |
missense |
probably damaging |
0.98 |
R1714:Prrc2c
|
UTSW |
1 |
162,504,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R1791:Prrc2c
|
UTSW |
1 |
162,532,551 (GRCm39) |
unclassified |
probably benign |
|
R1794:Prrc2c
|
UTSW |
1 |
162,533,528 (GRCm39) |
unclassified |
probably benign |
|
R1998:Prrc2c
|
UTSW |
1 |
162,532,487 (GRCm39) |
unclassified |
probably benign |
|
R2040:Prrc2c
|
UTSW |
1 |
162,525,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R2168:Prrc2c
|
UTSW |
1 |
162,537,903 (GRCm39) |
unclassified |
probably benign |
|
R2246:Prrc2c
|
UTSW |
1 |
162,535,360 (GRCm39) |
unclassified |
probably benign |
|
R2830:Prrc2c
|
UTSW |
1 |
162,536,485 (GRCm39) |
unclassified |
probably benign |
|
R2926:Prrc2c
|
UTSW |
1 |
162,533,696 (GRCm39) |
unclassified |
probably benign |
|
R3703:Prrc2c
|
UTSW |
1 |
162,538,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R3745:Prrc2c
|
UTSW |
1 |
162,525,754 (GRCm39) |
missense |
unknown |
|
R3760:Prrc2c
|
UTSW |
1 |
162,520,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Prrc2c
|
UTSW |
1 |
162,537,238 (GRCm39) |
unclassified |
probably benign |
|
R3959:Prrc2c
|
UTSW |
1 |
162,536,461 (GRCm39) |
unclassified |
probably benign |
|
R4255:Prrc2c
|
UTSW |
1 |
162,533,895 (GRCm39) |
unclassified |
probably benign |
|
R4276:Prrc2c
|
UTSW |
1 |
162,501,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R4421:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R4593:Prrc2c
|
UTSW |
1 |
162,525,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R4651:Prrc2c
|
UTSW |
1 |
162,550,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R4652:Prrc2c
|
UTSW |
1 |
162,550,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R4660:Prrc2c
|
UTSW |
1 |
162,508,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R4677:Prrc2c
|
UTSW |
1 |
162,532,748 (GRCm39) |
unclassified |
probably benign |
|
R4688:Prrc2c
|
UTSW |
1 |
162,525,256 (GRCm39) |
missense |
unknown |
|
R4753:Prrc2c
|
UTSW |
1 |
162,518,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Prrc2c
|
UTSW |
1 |
162,538,050 (GRCm39) |
missense |
unknown |
|
R4981:Prrc2c
|
UTSW |
1 |
162,520,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R4995:Prrc2c
|
UTSW |
1 |
162,532,879 (GRCm39) |
unclassified |
probably benign |
|
R5119:Prrc2c
|
UTSW |
1 |
162,533,009 (GRCm39) |
unclassified |
probably benign |
|
R5127:Prrc2c
|
UTSW |
1 |
162,525,415 (GRCm39) |
missense |
unknown |
|
R5291:Prrc2c
|
UTSW |
1 |
162,533,151 (GRCm39) |
unclassified |
probably benign |
|
R5474:Prrc2c
|
UTSW |
1 |
162,537,213 (GRCm39) |
unclassified |
probably benign |
|
R5543:Prrc2c
|
UTSW |
1 |
162,501,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R5579:Prrc2c
|
UTSW |
1 |
162,508,327 (GRCm39) |
critical splice donor site |
probably null |
|
R5594:Prrc2c
|
UTSW |
1 |
162,526,600 (GRCm39) |
missense |
unknown |
|
R5620:Prrc2c
|
UTSW |
1 |
162,501,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R5994:Prrc2c
|
UTSW |
1 |
162,501,725 (GRCm39) |
splice site |
probably null |
|
R6142:Prrc2c
|
UTSW |
1 |
162,537,956 (GRCm39) |
missense |
unknown |
|
R6199:Prrc2c
|
UTSW |
1 |
162,510,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Prrc2c
|
UTSW |
1 |
162,541,883 (GRCm39) |
missense |
probably benign |
|
R6504:Prrc2c
|
UTSW |
1 |
162,525,364 (GRCm39) |
missense |
unknown |
|
R6671:Prrc2c
|
UTSW |
1 |
162,525,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R6785:Prrc2c
|
UTSW |
1 |
162,536,670 (GRCm39) |
unclassified |
probably benign |
|
R6799:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6801:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6850:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6851:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6856:Prrc2c
|
UTSW |
1 |
162,509,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R6869:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6882:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6884:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6897:Prrc2c
|
UTSW |
1 |
162,533,075 (GRCm39) |
unclassified |
probably benign |
|
R6934:Prrc2c
|
UTSW |
1 |
162,548,074 (GRCm39) |
missense |
probably benign |
0.10 |
R6976:Prrc2c
|
UTSW |
1 |
162,520,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7132:Prrc2c
|
UTSW |
1 |
162,508,850 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7165:Prrc2c
|
UTSW |
1 |
162,501,086 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7282:Prrc2c
|
UTSW |
1 |
162,507,543 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7467:Prrc2c
|
UTSW |
1 |
162,504,932 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7915:Prrc2c
|
UTSW |
1 |
162,519,977 (GRCm39) |
missense |
probably benign |
0.39 |
R8068:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R8529:Prrc2c
|
UTSW |
1 |
162,536,663 (GRCm39) |
unclassified |
probably benign |
|
R8734:Prrc2c
|
UTSW |
1 |
162,507,081 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8735:Prrc2c
|
UTSW |
1 |
162,537,127 (GRCm39) |
missense |
unknown |
|
R8813:Prrc2c
|
UTSW |
1 |
162,532,812 (GRCm39) |
missense |
unknown |
|
R8946:Prrc2c
|
UTSW |
1 |
162,536,478 (GRCm39) |
unclassified |
probably benign |
|
R8975:Prrc2c
|
UTSW |
1 |
162,533,630 (GRCm39) |
missense |
unknown |
|
R9035:Prrc2c
|
UTSW |
1 |
162,503,295 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9261:Prrc2c
|
UTSW |
1 |
162,505,622 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9287:Prrc2c
|
UTSW |
1 |
162,541,843 (GRCm39) |
missense |
probably benign |
0.34 |
R9289:Prrc2c
|
UTSW |
1 |
162,507,130 (GRCm39) |
missense |
probably benign |
0.33 |
R9466:Prrc2c
|
UTSW |
1 |
162,503,258 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9523:Prrc2c
|
UTSW |
1 |
162,525,298 (GRCm39) |
missense |
unknown |
|
R9542:Prrc2c
|
UTSW |
1 |
162,508,359 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9629:Prrc2c
|
UTSW |
1 |
162,519,959 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9744:Prrc2c
|
UTSW |
1 |
162,505,733 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9748:Prrc2c
|
UTSW |
1 |
162,535,435 (GRCm39) |
missense |
unknown |
|
X0020:Prrc2c
|
UTSW |
1 |
162,535,416 (GRCm39) |
unclassified |
probably benign |
|
X0039:Prrc2c
|
UTSW |
1 |
162,532,362 (GRCm39) |
frame shift |
probably null |
|
|