Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AI837181 |
CGG |
CGGTGG |
19: 5,475,262 (GRCm39) |
|
probably benign |
Het |
Ankrd44 |
T |
C |
1: 54,817,471 (GRCm39) |
H79R |
probably damaging |
Het |
Atg9a |
T |
A |
1: 75,159,273 (GRCm39) |
E826V |
probably damaging |
Het |
Atrnl1 |
T |
C |
19: 57,630,905 (GRCm39) |
V224A |
probably benign |
Het |
Bltp1 |
TTATTATTATTAT |
TTATTATTATTATTAATATTATTATTAT |
3: 37,104,897 (GRCm39) |
|
probably benign |
Het |
Cpn2 |
G |
A |
16: 30,078,156 (GRCm39) |
A515V |
probably benign |
Het |
Cyp2a12 |
T |
C |
7: 26,734,785 (GRCm39) |
F402S |
possibly damaging |
Het |
Defb22 |
TGCGGCA |
TGCGGCAGAGCTGGGCGTTGCGGCA |
2: 152,327,752 (GRCm39) |
|
probably benign |
Het |
Dnah10 |
G |
T |
5: 124,854,971 (GRCm39) |
V2016F |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,542,290 (GRCm39) |
|
probably null |
Het |
Efhd2 |
GCC |
GCCGCCCCC |
4: 141,602,084 (GRCm39) |
|
probably benign |
Het |
Fam131a |
A |
C |
16: 20,513,690 (GRCm39) |
|
probably benign |
Het |
Gm7247 |
AGACCAGACC |
A |
14: 51,601,781 (GRCm39) |
|
probably benign |
Het |
Gna13 |
T |
C |
11: 109,283,218 (GRCm39) |
V186A |
probably benign |
Het |
Grk3 |
T |
A |
5: 113,089,554 (GRCm39) |
I333L |
probably benign |
Het |
Gstp1 |
A |
T |
19: 4,085,507 (GRCm39) |
V200E |
probably benign |
Het |
Gtf2h1 |
T |
G |
7: 46,453,289 (GRCm39) |
V74G |
possibly damaging |
Het |
Kcnh8 |
G |
A |
17: 53,285,267 (GRCm39) |
R1079H |
probably benign |
Het |
Kiz |
A |
G |
2: 146,712,750 (GRCm39) |
D138G |
possibly damaging |
Het |
Kmt2b |
TTCTCCT |
TTCTCCTTCTCCT |
7: 30,285,782 (GRCm39) |
|
probably benign |
Het |
Lats1 |
A |
G |
10: 7,586,372 (GRCm39) |
T912A |
probably damaging |
Het |
Lce1m |
GCTGCCACC |
GCTGCCACCACTTCTGCCACC |
3: 92,925,576 (GRCm39) |
|
probably benign |
Het |
Lce1m |
TGCC |
TGCCGCCGCTGCCGCC |
3: 92,925,602 (GRCm39) |
|
probably benign |
Het |
Lrrc2 |
TTGATTCGGTTCACC |
T |
9: 110,810,744 (GRCm39) |
|
probably null |
Het |
Med12l |
T |
C |
3: 58,980,711 (GRCm39) |
F359S |
probably benign |
Het |
Mmut |
A |
G |
17: 41,262,649 (GRCm39) |
I444V |
probably benign |
Het |
Ncoa2 |
CTTAAAA |
C |
1: 13,219,333 (GRCm39) |
|
probably benign |
Het |
Ngp |
A |
G |
9: 110,250,824 (GRCm39) |
T114A |
possibly damaging |
Het |
Nlrc5 |
A |
T |
8: 95,203,516 (GRCm39) |
T539S |
probably benign |
Het |
Nxf1 |
A |
G |
19: 8,749,673 (GRCm39) |
D190G |
probably damaging |
Het |
Or6c2b |
A |
T |
10: 128,948,211 (GRCm39) |
F28I |
probably damaging |
Het |
Or8g2 |
A |
T |
9: 39,821,341 (GRCm39) |
M81L |
probably benign |
Het |
Pramel16 |
C |
G |
4: 143,675,478 (GRCm39) |
Q449H |
probably damaging |
Het |
Prdm15 |
G |
A |
16: 97,609,956 (GRCm39) |
H563Y |
probably damaging |
Het |
Rbm12 |
CAGG |
CAGGGATTGCGGGACCTGGTATTGCGGGACCAGG |
2: 155,938,026 (GRCm39) |
|
probably benign |
Het |
Sema3g |
C |
T |
14: 30,949,798 (GRCm39) |
H660Y |
probably damaging |
Het |
Slco1a8 |
A |
T |
6: 141,954,440 (GRCm39) |
V31E |
probably damaging |
Het |
Smarca2 |
AGCAGCAGCAGCAGCAGCAGCA |
AGCAGCAGCAGCAGCAGCAGCAGCAGCA |
19: 26,608,397 (GRCm39) |
|
probably benign |
Het |
Stpg2 |
A |
T |
3: 138,918,011 (GRCm39) |
|
probably null |
Het |
Taar7f |
C |
T |
10: 23,926,321 (GRCm39) |
T305M |
possibly damaging |
Het |
Tbcb |
C |
T |
7: 29,923,771 (GRCm39) |
V208M |
probably damaging |
Het |
Tenm2 |
T |
A |
11: 35,915,030 (GRCm39) |
Q2169L |
possibly damaging |
Het |
Tln1 |
A |
G |
4: 43,555,890 (GRCm39) |
V108A |
probably damaging |
Het |
Tmc8 |
T |
C |
11: 117,674,060 (GRCm39) |
M42T |
probably benign |
Het |
Trdc |
T |
C |
14: 54,381,660 (GRCm39) |
V115A |
|
Het |
Ttbk2 |
A |
G |
2: 120,579,115 (GRCm39) |
V669A |
probably benign |
Het |
Tusc1 |
GCC |
GCCACCACC |
4: 93,223,553 (GRCm39) |
|
probably benign |
Het |
Utp25 |
A |
G |
1: 192,802,974 (GRCm39) |
F248L |
probably benign |
Het |
Vps16 |
A |
G |
2: 130,280,129 (GRCm39) |
H118R |
probably benign |
Het |
Wdpcp |
T |
A |
11: 21,661,587 (GRCm39) |
C286* |
probably null |
Het |
Zbed4 |
C |
A |
15: 88,665,439 (GRCm39) |
Y502* |
probably null |
Het |
Zdbf2 |
T |
A |
1: 63,341,811 (GRCm39) |
N63K |
possibly damaging |
Het |
|
Other mutations in A030005L19Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
RF001:A030005L19Rik
|
UTSW |
1 |
82,891,311 (GRCm39) |
small insertion |
probably benign |
|
RF005:A030005L19Rik
|
UTSW |
1 |
82,891,306 (GRCm39) |
small insertion |
probably benign |
|
RF011:A030005L19Rik
|
UTSW |
1 |
82,891,307 (GRCm39) |
small insertion |
probably benign |
|
RF011:A030005L19Rik
|
UTSW |
1 |
82,891,294 (GRCm39) |
small insertion |
probably benign |
|
RF011:A030005L19Rik
|
UTSW |
1 |
82,891,290 (GRCm39) |
small insertion |
probably benign |
|
RF016:A030005L19Rik
|
UTSW |
1 |
82,891,298 (GRCm39) |
small insertion |
probably benign |
|
RF018:A030005L19Rik
|
UTSW |
1 |
82,891,293 (GRCm39) |
small insertion |
probably benign |
|
RF023:A030005L19Rik
|
UTSW |
1 |
82,891,117 (GRCm39) |
small deletion |
probably benign |
|
RF028:A030005L19Rik
|
UTSW |
1 |
82,891,301 (GRCm39) |
small insertion |
probably benign |
|
RF028:A030005L19Rik
|
UTSW |
1 |
82,891,299 (GRCm39) |
small insertion |
probably benign |
|
RF034:A030005L19Rik
|
UTSW |
1 |
82,891,301 (GRCm39) |
small insertion |
probably benign |
|
RF035:A030005L19Rik
|
UTSW |
1 |
82,891,310 (GRCm39) |
small insertion |
probably benign |
|
RF038:A030005L19Rik
|
UTSW |
1 |
82,891,301 (GRCm39) |
small insertion |
probably benign |
|
RF040:A030005L19Rik
|
UTSW |
1 |
82,891,311 (GRCm39) |
small insertion |
probably benign |
|
RF040:A030005L19Rik
|
UTSW |
1 |
82,891,298 (GRCm39) |
small insertion |
probably benign |
|
RF042:A030005L19Rik
|
UTSW |
1 |
82,891,305 (GRCm39) |
small insertion |
probably benign |
|
RF044:A030005L19Rik
|
UTSW |
1 |
82,891,310 (GRCm39) |
small insertion |
probably benign |
|
RF053:A030005L19Rik
|
UTSW |
1 |
82,891,294 (GRCm39) |
small insertion |
probably benign |
|
RF059:A030005L19Rik
|
UTSW |
1 |
82,891,300 (GRCm39) |
small insertion |
probably benign |
|
RF060:A030005L19Rik
|
UTSW |
1 |
82,891,308 (GRCm39) |
small insertion |
probably benign |
|
RF060:A030005L19Rik
|
UTSW |
1 |
82,891,300 (GRCm39) |
nonsense |
probably null |
|
RF060:A030005L19Rik
|
UTSW |
1 |
82,891,117 (GRCm39) |
small deletion |
probably benign |
|
|