Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Add2 |
G |
A |
6: 86,085,002 (GRCm39) |
V543M |
probably benign |
Het |
Agl |
A |
G |
3: 116,552,557 (GRCm39) |
I459T |
possibly damaging |
Het |
Arhgap45 |
G |
A |
10: 79,863,706 (GRCm39) |
A819T |
probably damaging |
Het |
Atg16l2 |
C |
T |
7: 100,945,714 (GRCm39) |
|
probably null |
Het |
Bltp2 |
A |
G |
11: 78,177,457 (GRCm39) |
T1921A |
probably damaging |
Het |
C130073F10Rik |
G |
A |
4: 101,748,031 (GRCm39) |
R48* |
probably null |
Het |
Cdc25b |
C |
T |
2: 131,031,050 (GRCm39) |
T125M |
probably benign |
Het |
Cdc42bpg |
T |
A |
19: 6,356,895 (GRCm39) |
F50L |
probably damaging |
Het |
Chd9 |
T |
A |
8: 91,725,233 (GRCm39) |
D1187E |
unknown |
Het |
Col4a2 |
T |
C |
8: 11,475,542 (GRCm39) |
|
probably null |
Het |
Cped1 |
T |
C |
6: 22,123,587 (GRCm39) |
S447P |
probably benign |
Het |
Def8 |
C |
A |
8: 124,188,215 (GRCm39) |
Y431* |
probably null |
Het |
Gata4 |
A |
G |
14: 63,438,962 (GRCm39) |
S373P |
probably benign |
Het |
Gm9837 |
A |
T |
11: 53,361,136 (GRCm39) |
L26* |
probably null |
Het |
Hspa1b |
A |
T |
17: 35,176,557 (GRCm39) |
V476E |
probably damaging |
Het |
Htr5b |
G |
A |
1: 121,456,108 (GRCm39) |
|
probably benign |
Het |
Hydin |
T |
C |
8: 111,336,277 (GRCm39) |
V5018A |
probably benign |
Het |
Ighv1-85 |
A |
G |
12: 115,963,923 (GRCm39) |
S26P |
probably benign |
Het |
Kics2 |
T |
A |
10: 121,581,247 (GRCm39) |
F83I |
possibly damaging |
Het |
Lrrc2 |
A |
G |
9: 110,789,910 (GRCm39) |
K56E |
possibly damaging |
Het |
Macf1 |
A |
T |
4: 123,266,219 (GRCm39) |
I6793N |
probably damaging |
Het |
Macf1 |
A |
C |
4: 123,275,923 (GRCm39) |
V6215G |
possibly damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Nfxl1 |
A |
G |
5: 72,716,355 (GRCm39) |
|
probably null |
Het |
Odad4 |
A |
G |
11: 100,454,505 (GRCm39) |
D430G |
probably benign |
Het |
Oprk1 |
A |
T |
1: 5,672,540 (GRCm39) |
M226L |
probably benign |
Het |
Or1e1 |
T |
C |
11: 73,245,247 (GRCm39) |
S223P |
possibly damaging |
Het |
Phf2 |
A |
G |
13: 48,961,227 (GRCm39) |
L821P |
unknown |
Het |
Rdh7 |
C |
A |
10: 127,723,284 (GRCm39) |
|
probably null |
Het |
Rpl11 |
A |
G |
4: 135,778,968 (GRCm39) |
V74A |
possibly damaging |
Het |
Safb2 |
G |
A |
17: 56,873,051 (GRCm39) |
R790C |
possibly damaging |
Het |
Sgpp2 |
T |
C |
1: 78,393,609 (GRCm39) |
F204S |
probably benign |
Het |
Sgsm3 |
A |
C |
15: 80,893,643 (GRCm39) |
I426L |
possibly damaging |
Het |
Speer1b |
A |
G |
5: 11,823,926 (GRCm39) |
D158G |
probably damaging |
Het |
Styxl2 |
A |
G |
1: 165,927,648 (GRCm39) |
S655P |
probably damaging |
Het |
Tbccd1 |
A |
G |
16: 22,637,189 (GRCm39) |
L545P |
probably damaging |
Het |
Toporsl |
T |
A |
4: 52,610,489 (GRCm39) |
F127L |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,749,256 (GRCm39) |
Q3931P |
probably damaging |
Het |
Tuba1c |
C |
A |
15: 98,935,396 (GRCm39) |
L286I |
probably benign |
Het |
Usp48 |
A |
G |
4: 137,348,507 (GRCm39) |
R528G |
possibly damaging |
Het |
Utrn |
T |
C |
10: 12,573,867 (GRCm39) |
T1068A |
probably benign |
Het |
Vmn2r103 |
A |
T |
17: 20,032,205 (GRCm39) |
T660S |
probably damaging |
Het |
Vmn2r105 |
G |
T |
17: 20,444,880 (GRCm39) |
Y537* |
probably null |
Het |
Vmn2r88 |
A |
T |
14: 51,656,157 (GRCm39) |
I744F |
|
Het |
Wnt9b |
T |
C |
11: 103,621,601 (GRCm39) |
E352G |
probably damaging |
Het |
Zfp78 |
A |
G |
7: 6,376,228 (GRCm39) |
N46D |
probably damaging |
Het |
|
Other mutations in Ddx19a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00476:Ddx19a
|
APN |
8 |
111,703,102 (GRCm39) |
missense |
probably benign |
|
IGL01395:Ddx19a
|
APN |
8 |
111,717,164 (GRCm39) |
splice site |
probably benign |
|
IGL01676:Ddx19a
|
APN |
8 |
111,707,621 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02243:Ddx19a
|
APN |
8 |
111,703,088 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02677:Ddx19a
|
APN |
8 |
111,716,241 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02870:Ddx19a
|
APN |
8 |
111,710,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R0416:Ddx19a
|
UTSW |
8 |
111,705,689 (GRCm39) |
missense |
probably damaging |
0.96 |
R1574:Ddx19a
|
UTSW |
8 |
111,719,743 (GRCm39) |
splice site |
probably benign |
|
R1664:Ddx19a
|
UTSW |
8 |
111,716,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R4470:Ddx19a
|
UTSW |
8 |
111,703,111 (GRCm39) |
missense |
probably benign |
0.00 |
R4552:Ddx19a
|
UTSW |
8 |
111,705,198 (GRCm39) |
nonsense |
probably null |
|
R4668:Ddx19a
|
UTSW |
8 |
111,705,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R4847:Ddx19a
|
UTSW |
8 |
111,703,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R5390:Ddx19a
|
UTSW |
8 |
111,707,263 (GRCm39) |
nonsense |
probably null |
|
R5815:Ddx19a
|
UTSW |
8 |
111,705,781 (GRCm39) |
nonsense |
probably null |
|
R6842:Ddx19a
|
UTSW |
8 |
111,705,257 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7045:Ddx19a
|
UTSW |
8 |
111,719,706 (GRCm39) |
missense |
probably benign |
|
R7647:Ddx19a
|
UTSW |
8 |
111,703,259 (GRCm39) |
splice site |
probably null |
|
R8716:Ddx19a
|
UTSW |
8 |
111,710,243 (GRCm39) |
missense |
probably damaging |
0.98 |
R8986:Ddx19a
|
UTSW |
8 |
111,705,188 (GRCm39) |
missense |
probably benign |
0.01 |
R9051:Ddx19a
|
UTSW |
8 |
111,710,228 (GRCm39) |
missense |
probably benign |
0.44 |
R9721:Ddx19a
|
UTSW |
8 |
111,705,107 (GRCm39) |
missense |
probably damaging |
1.00 |
|