Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9330160F10Rik |
C |
T |
11: 68,951,013 (GRCm39) |
|
silent |
Het |
Adck1 |
G |
T |
12: 88,413,480 (GRCm39) |
V271F |
probably damaging |
Het |
Aggf1 |
T |
C |
13: 95,507,437 (GRCm39) |
D116G |
probably benign |
Het |
Anapc1 |
A |
T |
2: 128,505,853 (GRCm39) |
V661E |
probably damaging |
Het |
Apoa5 |
T |
C |
9: 46,180,437 (GRCm39) |
|
probably null |
Het |
Atp8a2 |
C |
T |
14: 60,264,369 (GRCm39) |
|
probably null |
Het |
Bnipl |
A |
T |
3: 95,157,577 (GRCm39) |
|
probably benign |
Het |
Cbs |
T |
G |
17: 31,834,519 (GRCm39) |
D490A |
probably benign |
Het |
Chrdl1 |
G |
T |
X: 142,086,510 (GRCm39) |
H199N |
possibly damaging |
Het |
Dcaf1 |
C |
T |
9: 106,740,310 (GRCm39) |
T1232I |
probably benign |
Het |
Ephb4 |
A |
G |
5: 137,369,024 (GRCm39) |
K805E |
probably damaging |
Het |
Ergic3 |
A |
G |
2: 155,852,395 (GRCm39) |
N135D |
probably benign |
Het |
Fbxw18 |
C |
T |
9: 109,530,390 (GRCm39) |
V74I |
probably benign |
Het |
Fmo4 |
G |
T |
1: 162,626,649 (GRCm39) |
T299N |
probably benign |
Het |
Gmeb1 |
T |
C |
4: 131,953,147 (GRCm39) |
K540E |
probably damaging |
Het |
H60c |
T |
A |
10: 3,209,826 (GRCm39) |
S154C |
possibly damaging |
Het |
Herc1 |
T |
C |
9: 66,388,151 (GRCm39) |
L3812S |
probably damaging |
Het |
Hipk3 |
T |
C |
2: 104,261,724 (GRCm39) |
D937G |
probably damaging |
Het |
Ift122 |
A |
G |
6: 115,902,398 (GRCm39) |
D1079G |
probably benign |
Het |
Il6st |
T |
C |
13: 112,631,774 (GRCm39) |
W438R |
probably benign |
Het |
Lypla2 |
C |
T |
4: 135,696,932 (GRCm39) |
V117I |
probably benign |
Het |
Mapk8ip1 |
T |
C |
2: 92,216,220 (GRCm39) |
Y516C |
probably damaging |
Het |
Mmp24 |
G |
A |
2: 155,654,213 (GRCm39) |
G397D |
probably damaging |
Het |
Muc4 |
G |
A |
16: 32,570,131 (GRCm39) |
S397N |
possibly damaging |
Het |
Muc5b |
T |
G |
7: 141,416,987 (GRCm39) |
V3311G |
probably benign |
Het |
Naca |
A |
G |
10: 127,872,358 (GRCm39) |
|
probably benign |
Het |
Nrxn1 |
A |
G |
17: 91,395,829 (GRCm39) |
V109A |
probably benign |
Het |
Nup210 |
T |
G |
6: 91,053,680 (GRCm39) |
D279A |
probably benign |
Het |
Or10g6 |
A |
T |
9: 39,934,066 (GRCm39) |
I126F |
probably damaging |
Het |
Or8h7 |
A |
G |
2: 86,721,460 (GRCm39) |
S20P |
possibly damaging |
Het |
Pappa |
T |
A |
4: 65,074,361 (GRCm39) |
V305E |
possibly damaging |
Het |
Pcdh19 |
A |
T |
X: 132,489,245 (GRCm39) |
M977K |
probably benign |
Het |
Pdzph1 |
T |
A |
17: 59,274,334 (GRCm39) |
I837F |
possibly damaging |
Het |
Phip |
A |
T |
9: 82,753,372 (GRCm39) |
L1791M |
probably damaging |
Het |
Pkdrej |
C |
T |
15: 85,700,489 (GRCm39) |
V1816I |
possibly damaging |
Het |
Ptprz1 |
G |
A |
6: 23,033,447 (GRCm39) |
V1063M |
probably damaging |
Het |
Qprt |
A |
T |
7: 126,707,528 (GRCm39) |
M220K |
probably damaging |
Het |
R3hcc1 |
T |
C |
14: 69,937,475 (GRCm39) |
K391E |
possibly damaging |
Het |
Rbbp7 |
C |
A |
X: 161,554,052 (GRCm39) |
P162Q |
probably benign |
Het |
Rev3l |
A |
T |
10: 39,701,095 (GRCm39) |
N1864I |
probably damaging |
Het |
Rims1 |
A |
G |
1: 22,669,556 (GRCm39) |
I84T |
possibly damaging |
Het |
Rnase2b |
A |
T |
14: 51,400,240 (GRCm39) |
K107I |
probably benign |
Het |
Sbf1 |
C |
A |
15: 89,186,708 (GRCm39) |
E864* |
probably null |
Het |
Strip2 |
G |
A |
6: 29,917,179 (GRCm39) |
|
probably benign |
Het |
Stx4a |
T |
C |
7: 127,447,570 (GRCm39) |
I238T |
probably damaging |
Het |
Tbc1d2b |
C |
T |
9: 90,104,412 (GRCm39) |
V577I |
possibly damaging |
Het |
Tex38 |
T |
C |
4: 115,637,591 (GRCm39) |
T71A |
possibly damaging |
Het |
Usp38 |
T |
C |
8: 81,712,343 (GRCm39) |
E564G |
possibly damaging |
Het |
Vmn2r72 |
A |
T |
7: 85,387,374 (GRCm39) |
V730E |
probably benign |
Het |
Wwp2 |
T |
A |
8: 108,280,689 (GRCm39) |
L644Q |
probably damaging |
Het |
Zfp267 |
T |
C |
3: 36,218,877 (GRCm39) |
F300S |
possibly damaging |
Het |
Zpld1 |
A |
G |
16: 55,071,974 (GRCm39) |
I95T |
probably benign |
Het |
|
Other mutations in Ddx19b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01452:Ddx19b
|
APN |
8 |
111,747,620 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02445:Ddx19b
|
APN |
8 |
111,735,456 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02756:Ddx19b
|
APN |
8 |
111,737,910 (GRCm39) |
splice site |
probably benign |
|
R0411:Ddx19b
|
UTSW |
8 |
111,750,596 (GRCm39) |
critical splice donor site |
probably null |
|
R0483:Ddx19b
|
UTSW |
8 |
111,735,310 (GRCm39) |
missense |
probably benign |
0.07 |
R1510:Ddx19b
|
UTSW |
8 |
111,742,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R1797:Ddx19b
|
UTSW |
8 |
111,739,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Ddx19b
|
UTSW |
8 |
111,734,890 (GRCm39) |
missense |
probably benign |
0.00 |
R1981:Ddx19b
|
UTSW |
8 |
111,735,975 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1982:Ddx19b
|
UTSW |
8 |
111,735,975 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3771:Ddx19b
|
UTSW |
8 |
111,747,613 (GRCm39) |
missense |
probably benign |
0.03 |
R4190:Ddx19b
|
UTSW |
8 |
111,737,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R4191:Ddx19b
|
UTSW |
8 |
111,737,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R4193:Ddx19b
|
UTSW |
8 |
111,737,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R5132:Ddx19b
|
UTSW |
8 |
111,749,040 (GRCm39) |
missense |
probably benign |
|
R5435:Ddx19b
|
UTSW |
8 |
111,735,458 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7980:Ddx19b
|
UTSW |
8 |
111,738,077 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8062:Ddx19b
|
UTSW |
8 |
111,747,611 (GRCm39) |
missense |
probably benign |
0.00 |
R8265:Ddx19b
|
UTSW |
8 |
111,735,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R8899:Ddx19b
|
UTSW |
8 |
111,737,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R9136:Ddx19b
|
UTSW |
8 |
111,734,906 (GRCm39) |
missense |
probably benign |
|
R9598:Ddx19b
|
UTSW |
8 |
111,747,673 (GRCm39) |
missense |
probably benign |
|
Z1088:Ddx19b
|
UTSW |
8 |
111,742,207 (GRCm39) |
missense |
probably benign |
0.37 |
|