Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
C |
T |
7: 45,629,359 (GRCm39) |
V1323I |
probably damaging |
Het |
Adam20 |
G |
A |
8: 41,248,490 (GRCm39) |
R200H |
probably benign |
Het |
Ahnak |
GATCTCTAT |
GAT |
19: 8,984,393 (GRCm39) |
|
probably benign |
Het |
Cbr3 |
A |
G |
16: 93,481,941 (GRCm39) |
D99G |
probably benign |
Het |
Ccdc17 |
T |
A |
4: 116,455,090 (GRCm39) |
L215Q |
probably damaging |
Het |
Cep350 |
A |
G |
1: 155,751,107 (GRCm39) |
Y2022H |
probably benign |
Het |
Cimip2c |
G |
C |
5: 30,641,261 (GRCm39) |
D170H |
possibly damaging |
Het |
Cnbd2 |
T |
C |
2: 156,183,547 (GRCm39) |
S338P |
probably benign |
Het |
D5Ertd579e |
A |
T |
5: 36,787,029 (GRCm39) |
V113D |
possibly damaging |
Het |
Dhx30 |
A |
G |
9: 109,916,718 (GRCm39) |
F570S |
probably damaging |
Het |
Ephb1 |
T |
C |
9: 101,848,384 (GRCm39) |
N679S |
probably damaging |
Het |
Faxc |
T |
C |
4: 21,993,307 (GRCm39) |
I317T |
probably damaging |
Het |
Fgd5 |
T |
C |
6: 91,965,290 (GRCm39) |
Y508H |
possibly damaging |
Het |
Foxd2 |
G |
T |
4: 114,765,195 (GRCm39) |
A275E |
unknown |
Het |
Fut9 |
C |
A |
4: 25,620,679 (GRCm39) |
S45I |
probably benign |
Het |
Gm5148 |
T |
C |
3: 37,768,801 (GRCm39) |
N140D |
unknown |
Het |
Gpr37l1 |
C |
T |
1: 135,089,391 (GRCm39) |
G225S |
probably damaging |
Het |
Gramd1c |
G |
A |
16: 43,825,840 (GRCm39) |
S107L |
possibly damaging |
Het |
Gtpbp2 |
A |
G |
17: 46,478,301 (GRCm39) |
D483G |
|
Het |
Ik |
G |
A |
18: 36,886,566 (GRCm39) |
R346H |
probably benign |
Het |
Ino80e |
A |
T |
7: 126,461,098 (GRCm39) |
Y50N |
unknown |
Het |
Irag1 |
A |
T |
7: 110,470,640 (GRCm39) |
S898T |
possibly damaging |
Het |
Kbtbd2 |
A |
G |
6: 56,756,566 (GRCm39) |
V390A |
probably benign |
Het |
Limch1 |
A |
C |
5: 67,156,360 (GRCm39) |
N276H |
probably damaging |
Het |
Negr1 |
T |
G |
3: 156,774,936 (GRCm39) |
|
probably null |
Het |
Ngef |
G |
A |
1: 87,431,010 (GRCm39) |
P269L |
probably damaging |
Het |
Nlrp14 |
G |
A |
7: 106,781,626 (GRCm39) |
M274I |
probably benign |
Het |
Nr1d1 |
T |
C |
11: 98,662,943 (GRCm39) |
I17V |
probably benign |
Het |
Or10ad1b |
T |
A |
15: 98,124,902 (GRCm39) |
D210V |
probably damaging |
Het |
Or4k35 |
T |
C |
2: 111,100,623 (GRCm39) |
I30V |
probably benign |
Het |
Or5p64 |
A |
G |
7: 107,855,198 (GRCm39) |
I49T |
probably benign |
Het |
Ppip5k2 |
A |
G |
1: 97,677,312 (GRCm39) |
V334A |
|
Het |
Ppp1r9a |
G |
A |
6: 5,045,936 (GRCm39) |
V467I |
probably damaging |
Het |
Ppp2r2c |
A |
G |
5: 37,097,488 (GRCm39) |
I225V |
possibly damaging |
Het |
Ptpro |
A |
T |
6: 137,345,108 (GRCm39) |
N38I |
probably damaging |
Het |
Scn2a |
C |
A |
2: 65,579,149 (GRCm39) |
Q1495K |
possibly damaging |
Het |
Scn7a |
A |
T |
2: 66,519,902 (GRCm39) |
Y1001N |
possibly damaging |
Het |
Sfi1 |
ACA |
ACATCTTCCCAAAGCCAGTCA |
11: 3,103,382 (GRCm39) |
|
probably benign |
Het |
Sh3bgrl2 |
T |
A |
9: 83,430,513 (GRCm39) |
M1K |
probably null |
Het |
Slc25a12 |
C |
T |
2: 71,109,899 (GRCm39) |
V516M |
probably benign |
Het |
Sptbn4 |
A |
G |
7: 27,091,000 (GRCm39) |
L1402P |
probably damaging |
Het |
Styk1 |
CTCTTCATGATTTTCTT |
CTCTT |
6: 131,278,612 (GRCm39) |
|
probably benign |
Het |
Sycp2 |
G |
T |
2: 178,035,957 (GRCm39) |
D243E |
probably damaging |
Het |
Tcerg1 |
T |
C |
18: 42,706,413 (GRCm39) |
F1030S |
probably damaging |
Het |
Tecta |
T |
A |
9: 42,286,596 (GRCm39) |
N687Y |
probably damaging |
Het |
Tep1 |
A |
T |
14: 51,081,759 (GRCm39) |
H1230Q |
|
Het |
Tfap2b |
T |
C |
1: 19,284,373 (GRCm39) |
S94P |
probably damaging |
Het |
Tll2 |
C |
A |
19: 41,092,238 (GRCm39) |
G533V |
probably damaging |
Het |
Vmn2r55 |
A |
G |
7: 12,402,061 (GRCm39) |
V409A |
probably damaging |
Het |
Wdr41 |
A |
G |
13: 95,145,373 (GRCm39) |
E194G |
probably damaging |
Het |
Zan |
G |
T |
5: 137,398,817 (GRCm39) |
S4182R |
unknown |
Het |
Zfpl1 |
T |
C |
19: 6,134,074 (GRCm39) |
Y40C |
probably damaging |
Het |
Znrf3 |
C |
A |
11: 5,232,454 (GRCm39) |
R257L |
possibly damaging |
Het |
|
Other mutations in Svop |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02220:Svop
|
APN |
5 |
114,203,589 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02612:Svop
|
APN |
5 |
114,166,321 (GRCm39) |
makesense |
probably null |
|
R0254:Svop
|
UTSW |
5 |
114,176,600 (GRCm39) |
missense |
probably benign |
|
R1705:Svop
|
UTSW |
5 |
114,180,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Svop
|
UTSW |
5 |
114,198,117 (GRCm39) |
critical splice donor site |
probably null |
|
R3084:Svop
|
UTSW |
5 |
114,180,299 (GRCm39) |
missense |
probably benign |
|
R4494:Svop
|
UTSW |
5 |
114,183,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R4575:Svop
|
UTSW |
5 |
114,203,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Svop
|
UTSW |
5 |
114,203,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R4578:Svop
|
UTSW |
5 |
114,203,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R4725:Svop
|
UTSW |
5 |
114,203,546 (GRCm39) |
unclassified |
probably benign |
|
R5433:Svop
|
UTSW |
5 |
114,198,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R5731:Svop
|
UTSW |
5 |
114,198,124 (GRCm39) |
missense |
probably damaging |
0.99 |
R5783:Svop
|
UTSW |
5 |
114,202,996 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5889:Svop
|
UTSW |
5 |
114,203,692 (GRCm39) |
missense |
probably benign |
0.37 |
R8134:Svop
|
UTSW |
5 |
114,180,992 (GRCm39) |
missense |
probably benign |
0.01 |
R8433:Svop
|
UTSW |
5 |
114,170,822 (GRCm39) |
missense |
probably benign |
0.21 |
R8848:Svop
|
UTSW |
5 |
114,183,687 (GRCm39) |
missense |
|
|
R8851:Svop
|
UTSW |
5 |
114,192,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R8868:Svop
|
UTSW |
5 |
114,170,854 (GRCm39) |
missense |
probably damaging |
0.98 |
R8965:Svop
|
UTSW |
5 |
114,173,271 (GRCm39) |
missense |
probably benign |
0.01 |
R9109:Svop
|
UTSW |
5 |
114,168,231 (GRCm39) |
missense |
probably benign |
0.16 |
R9298:Svop
|
UTSW |
5 |
114,168,231 (GRCm39) |
missense |
probably benign |
0.16 |
R9732:Svop
|
UTSW |
5 |
114,201,142 (GRCm39) |
missense |
probably damaging |
1.00 |
|