Other mutations in this stock |
Total: 117 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg5 |
T |
G |
17: 84,981,022 (GRCm39) |
Y107S |
possibly damaging |
Het |
Abhd8 |
T |
C |
8: 71,914,499 (GRCm39) |
E43G |
probably damaging |
Het |
Ap1b1 |
T |
G |
11: 4,990,360 (GRCm39) |
L872W |
probably damaging |
Het |
Arid1b |
T |
A |
17: 5,389,518 (GRCm39) |
M1688K |
probably damaging |
Het |
Brca1 |
T |
C |
11: 101,413,248 (GRCm39) |
|
probably benign |
Het |
C4b |
C |
T |
17: 34,952,675 (GRCm39) |
V1151I |
probably benign |
Het |
Card6 |
T |
A |
15: 5,128,113 (GRCm39) |
Q1094H |
unknown |
Het |
Cd22 |
C |
A |
7: 30,577,224 (GRCm39) |
V28F |
possibly damaging |
Het |
Cdc42bpa |
A |
T |
1: 179,859,125 (GRCm39) |
N109I |
probably damaging |
Het |
Ces2b |
T |
C |
8: 105,563,442 (GRCm39) |
Y390H |
probably damaging |
Het |
Clca4a |
T |
C |
3: 144,674,072 (GRCm39) |
Y221C |
probably damaging |
Het |
Cntnap5a |
G |
T |
1: 115,612,686 (GRCm39) |
|
probably benign |
Het |
Cyp4a10 |
C |
A |
4: 115,382,072 (GRCm39) |
H251Q |
probably damaging |
Het |
Dcc |
A |
T |
18: 71,517,297 (GRCm39) |
|
probably null |
Het |
Dnaaf5 |
A |
G |
5: 139,171,273 (GRCm39) |
K812E |
possibly damaging |
Het |
Dnajc13 |
T |
C |
9: 104,115,672 (GRCm39) |
T46A |
probably damaging |
Het |
Duxf1 |
A |
G |
10: 58,059,276 (GRCm39) |
C493R |
probably benign |
Het |
Duxf1 |
C |
T |
10: 58,060,704 (GRCm39) |
E17K |
possibly damaging |
Het |
Duxf1 |
G |
A |
10: 58,060,136 (GRCm39) |
|
probably benign |
Het |
Duxf1 |
G |
C |
10: 58,059,278 (GRCm39) |
P492R |
probably damaging |
Het |
Duxf3 |
C |
A |
10: 58,066,990 (GRCm39) |
C503F |
probably damaging |
Het |
Duxf3 |
C |
A |
10: 58,066,810 (GRCm39) |
R563M |
probably damaging |
Het |
Duxf3 |
A |
C |
10: 58,067,498 (GRCm39) |
S27A |
probably benign |
Het |
Eps8l1 |
G |
A |
7: 4,474,414 (GRCm39) |
S295N |
probably benign |
Het |
Etfdh |
C |
T |
3: 79,517,174 (GRCm39) |
S345N |
probably damaging |
Het |
Fat3 |
A |
G |
9: 15,903,414 (GRCm39) |
|
probably null |
Het |
G530012D18Rik |
T |
G |
1: 85,504,925 (GRCm39) |
|
probably benign |
Het |
Gabra4 |
T |
C |
5: 71,729,106 (GRCm39) |
N558S |
probably damaging |
Het |
Gm10718 |
A |
T |
9: 3,024,417 (GRCm39) |
T134S |
probably benign |
Het |
Gm10722 |
T |
C |
9: 3,001,350 (GRCm39) |
L142S |
probably benign |
Het |
Gm10800 |
T |
C |
2: 98,497,163 (GRCm39) |
R152G |
probably benign |
Het |
Gm10800 |
C |
A |
2: 98,497,250 (GRCm39) |
V123F |
probably benign |
Het |
Gm10800 |
CAAGAAAACTGAAAATCA |
C |
2: 98,497,361 (GRCm39) |
|
probably null |
Het |
Gm10800 |
A |
C |
2: 98,496,893 (GRCm39) |
F220C |
probably benign |
Het |
Gm10801 |
A |
G |
2: 98,492,648 (GRCm39) |
R23G |
probably benign |
Het |
Gm11168 |
C |
T |
9: 3,004,605 (GRCm39) |
P49S |
probably benign |
Het |
Gm21663 |
C |
T |
5: 26,143,767 (GRCm39) |
R185H |
probably benign |
Het |
Gm21738 |
G |
A |
14: 19,417,330 (GRCm38) |
S66L |
probably benign |
Het |
Gpr107 |
T |
A |
2: 31,057,083 (GRCm39) |
D58E |
probably benign |
Het |
Gstm7 |
AAC |
A |
3: 107,838,799 (GRCm39) |
|
probably null |
Het |
Hc |
C |
T |
2: 34,921,833 (GRCm39) |
|
probably benign |
Het |
Hjurp |
TCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCTG |
T |
1: 88,194,000 (GRCm39) |
|
probably benign |
Het |
Hjurp |
A |
G |
1: 88,194,283 (GRCm39) |
|
probably benign |
Het |
Hjurp |
T |
C |
1: 88,194,338 (GRCm39) |
E190G |
probably benign |
Het |
Hjurp |
A |
C |
1: 88,193,768 (GRCm39) |
V380G |
probably damaging |
Het |
Hnrnpa2b1 |
A |
T |
6: 51,441,089 (GRCm39) |
M327K |
probably benign |
Het |
Hoxa13 |
G |
C |
6: 52,260,648 (GRCm38) |
|
probably benign |
Het |
Hoxa13 |
C |
G |
6: 52,260,647 (GRCm38) |
|
probably benign |
Het |
Ifi206 |
A |
G |
1: 173,308,730 (GRCm39) |
V422A |
probably benign |
Het |
Igf2bp3 |
A |
G |
6: 49,094,317 (GRCm39) |
V151A |
probably damaging |
Het |
Ivl |
TTGC |
T |
3: 92,479,608 (GRCm39) |
|
probably benign |
Het |
Kndc1 |
TC |
T |
7: 139,503,692 (GRCm39) |
|
probably null |
Het |
Lig1 |
GC |
G |
7: 13,039,850 (GRCm39) |
|
probably null |
Het |
Lrit1 |
A |
G |
14: 36,783,998 (GRCm39) |
Y442C |
probably damaging |
Het |
Map3k21 |
C |
A |
8: 126,664,047 (GRCm39) |
P536H |
probably damaging |
Het |
Marchf10 |
T |
A |
11: 105,281,346 (GRCm39) |
Y313F |
probably benign |
Het |
Mcm5 |
A |
G |
8: 75,853,864 (GRCm39) |
H706R |
probably benign |
Het |
Mlycd |
T |
G |
8: 120,137,199 (GRCm39) |
I473S |
probably damaging |
Het |
Muc4 |
T |
A |
16: 32,755,684 (GRCm38) |
|
probably benign |
Het |
Muc4 |
C |
A |
16: 32,754,529 (GRCm38) |
H1468N |
probably benign |
Het |
Muc4 |
C |
G |
16: 32,755,676 (GRCm38) |
|
probably benign |
Het |
Myo5c |
T |
C |
9: 75,191,230 (GRCm39) |
V1088A |
probably benign |
Het |
Nadk2 |
TG |
T |
15: 9,100,232 (GRCm39) |
|
probably null |
Het |
Ndufs1 |
A |
G |
1: 63,198,907 (GRCm39) |
|
probably benign |
Het |
Or4n4 |
A |
G |
14: 50,518,784 (GRCm39) |
*309Q |
probably null |
Het |
Pak2 |
A |
T |
16: 31,841,930 (GRCm39) |
Y443N |
probably damaging |
Het |
Pik3r6 |
T |
C |
11: 68,417,931 (GRCm39) |
I73T |
probably damaging |
Het |
Pla2g4c |
A |
G |
7: 13,077,316 (GRCm39) |
E286G |
probably benign |
Het |
Plekhn1 |
G |
A |
4: 156,309,397 (GRCm39) |
R196* |
probably null |
Het |
Pramel41 |
A |
C |
5: 94,594,643 (GRCm39) |
K168Q |
probably benign |
Het |
Prdm10 |
T |
A |
9: 31,237,063 (GRCm39) |
D145E |
probably benign |
Het |
Ptgis |
T |
C |
2: 167,048,750 (GRCm39) |
Y422C |
probably damaging |
Het |
Rasgrf1 |
G |
A |
9: 89,797,626 (GRCm39) |
R168H |
possibly damaging |
Het |
Rbmyf1 |
T |
A |
Y: 2,787,132 (GRCm39) |
N228Y |
probably benign |
Het |
Rpl5 |
T |
C |
5: 108,055,049 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,722,682 (GRCm39) |
K2603E |
probably damaging |
Het |
Sap130 |
T |
C |
18: 31,800,064 (GRCm39) |
|
probably null |
Het |
Scn5a |
C |
A |
9: 119,315,324 (GRCm39) |
D1794Y |
probably damaging |
Het |
Sec31a |
A |
T |
5: 100,555,134 (GRCm39) |
S29T |
probably damaging |
Het |
Selplg |
T |
G |
5: 113,957,689 (GRCm39) |
K206Q |
probably benign |
Het |
Sfmbt1 |
A |
T |
14: 30,538,714 (GRCm39) |
|
probably null |
Het |
Sirpb1a |
A |
T |
3: 15,476,258 (GRCm39) |
F180I |
probably benign |
Het |
Slc44a4 |
A |
G |
17: 35,140,251 (GRCm39) |
I67V |
probably damaging |
Het |
Sp110 |
T |
C |
1: 85,513,975 (GRCm39) |
R261G |
probably benign |
Het |
Sp110 |
C |
T |
1: 85,513,971 (GRCm39) |
R262Q |
probably benign |
Het |
Sp140 |
T |
A |
1: 85,528,893 (GRCm39) |
Y5N |
probably benign |
Het |
Sp140 |
A |
G |
1: 85,570,942 (GRCm39) |
S461G |
probably benign |
Het |
Sp140 |
G |
C |
1: 85,538,603 (GRCm39) |
K113N |
probably benign |
Het |
Sp140l1 |
G |
A |
1: 85,077,341 (GRCm39) |
A75V |
probably benign |
Het |
Sp140l2 |
A |
C |
1: 85,223,395 (GRCm39) |
|
probably benign |
Het |
Speer4a2 |
A |
T |
5: 26,291,485 (GRCm39) |
F107Y |
probably benign |
Het |
Speer4a2 |
C |
G |
5: 26,294,093 (GRCm39) |
W28C |
probably damaging |
Het |
Stab2 |
A |
T |
10: 86,703,039 (GRCm39) |
S1848R |
possibly damaging |
Het |
Stat6 |
T |
C |
10: 127,494,099 (GRCm39) |
V642A |
possibly damaging |
Het |
Tfam |
T |
C |
10: 71,070,813 (GRCm39) |
K63R |
possibly damaging |
Het |
Trim2 |
T |
C |
3: 84,098,164 (GRCm39) |
N379S |
probably benign |
Het |
Trp63 |
C |
T |
16: 25,684,013 (GRCm39) |
T300I |
probably damaging |
Het |
Tymp |
C |
A |
15: 89,260,548 (GRCm39) |
W90L |
probably damaging |
Het |
Ubr5 |
A |
G |
15: 38,042,153 (GRCm39) |
S148P |
|
Het |
Ugt1a10 |
TTCA |
T |
1: 88,143,880 (GRCm39) |
|
probably benign |
Het |
Usp47 |
T |
C |
7: 111,703,548 (GRCm39) |
|
probably benign |
Het |
Uvssa |
C |
T |
5: 33,549,428 (GRCm39) |
A363V |
probably benign |
Het |
Vldlr |
T |
A |
19: 27,212,269 (GRCm39) |
D94E |
probably benign |
Het |
Vmn1r3 |
C |
T |
4: 3,184,691 (GRCm39) |
M205I |
probably damaging |
Het |
Vmn1r3 |
C |
T |
4: 3,184,774 (GRCm39) |
V178I |
probably benign |
Het |
Vmn1r67 |
T |
A |
7: 10,180,877 (GRCm39) |
M47K |
probably benign |
Het |
Vmn1r87 |
A |
T |
7: 12,866,112 (GRCm39) |
H58Q |
probably benign |
Het |
Vmn1r89 |
A |
G |
7: 12,953,515 (GRCm39) |
T84A |
probably benign |
Het |
Vmn2r109 |
T |
C |
17: 20,774,839 (GRCm39) |
|
probably null |
Het |
Xirp2 |
T |
C |
2: 67,349,706 (GRCm39) |
|
probably benign |
Het |
Zbtb2 |
A |
G |
10: 4,319,493 (GRCm39) |
S178P |
probably benign |
Het |
Zfp534 |
C |
A |
4: 147,762,770 (GRCm39) |
D21Y |
probably benign |
Het |
Zfp534 |
C |
T |
4: 147,760,031 (GRCm39) |
E213K |
probably benign |
Het |
Zfp804b |
C |
T |
5: 6,819,422 (GRCm39) |
V1214I |
probably damaging |
Het |
Zfp82 |
G |
T |
7: 29,756,701 (GRCm39) |
T63K |
probably damaging |
Het |
Zfp986 |
C |
T |
4: 145,625,513 (GRCm39) |
R58C |
probably benign |
Het |
Zfp992 |
C |
T |
4: 146,550,569 (GRCm39) |
P97S |
probably benign |
Het |
|
Other mutations in Ralgapb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Ralgapb
|
APN |
2 |
158,262,776 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00534:Ralgapb
|
APN |
2 |
158,272,420 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL01362:Ralgapb
|
APN |
2 |
158,277,385 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01653:Ralgapb
|
APN |
2 |
158,304,079 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01704:Ralgapb
|
APN |
2 |
158,262,795 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02000:Ralgapb
|
APN |
2 |
158,296,034 (GRCm39) |
splice site |
probably benign |
|
IGL02169:Ralgapb
|
APN |
2 |
158,268,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02516:Ralgapb
|
APN |
2 |
158,307,735 (GRCm39) |
splice site |
probably benign |
|
IGL02548:Ralgapb
|
APN |
2 |
158,286,585 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02550:Ralgapb
|
APN |
2 |
158,290,331 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02653:Ralgapb
|
APN |
2 |
158,285,229 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02744:Ralgapb
|
APN |
2 |
158,288,071 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02804:Ralgapb
|
APN |
2 |
158,268,204 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02937:Ralgapb
|
APN |
2 |
158,334,936 (GRCm39) |
splice site |
probably null |
|
IGL02993:Ralgapb
|
APN |
2 |
158,279,314 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03154:Ralgapb
|
APN |
2 |
158,274,786 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03204:Ralgapb
|
APN |
2 |
158,307,832 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03347:Ralgapb
|
APN |
2 |
158,307,880 (GRCm39) |
missense |
possibly damaging |
0.67 |
Chacha
|
UTSW |
2 |
158,334,372 (GRCm39) |
missense |
probably damaging |
0.99 |
Gato
|
UTSW |
2 |
158,286,540 (GRCm39) |
missense |
probably damaging |
1.00 |
Kibble
|
UTSW |
2 |
158,279,060 (GRCm39) |
missense |
probably damaging |
1.00 |
ralston
|
UTSW |
2 |
158,296,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R0037:Ralgapb
|
UTSW |
2 |
158,279,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R0037:Ralgapb
|
UTSW |
2 |
158,279,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R0077:Ralgapb
|
UTSW |
2 |
158,315,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R0581:Ralgapb
|
UTSW |
2 |
158,334,881 (GRCm39) |
missense |
probably benign |
|
R0629:Ralgapb
|
UTSW |
2 |
158,281,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R0839:Ralgapb
|
UTSW |
2 |
158,315,203 (GRCm39) |
critical splice donor site |
probably null |
|
R1331:Ralgapb
|
UTSW |
2 |
158,272,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Ralgapb
|
UTSW |
2 |
158,304,173 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1468:Ralgapb
|
UTSW |
2 |
158,304,173 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1540:Ralgapb
|
UTSW |
2 |
158,307,746 (GRCm39) |
missense |
probably benign |
0.00 |
R1572:Ralgapb
|
UTSW |
2 |
158,288,119 (GRCm39) |
splice site |
probably benign |
|
R1628:Ralgapb
|
UTSW |
2 |
158,272,383 (GRCm39) |
missense |
probably benign |
0.04 |
R1718:Ralgapb
|
UTSW |
2 |
158,285,200 (GRCm39) |
nonsense |
probably null |
|
R1777:Ralgapb
|
UTSW |
2 |
158,304,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Ralgapb
|
UTSW |
2 |
158,334,372 (GRCm39) |
missense |
probably damaging |
0.99 |
R1903:Ralgapb
|
UTSW |
2 |
158,337,483 (GRCm39) |
missense |
probably benign |
0.04 |
R1909:Ralgapb
|
UTSW |
2 |
158,286,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R2157:Ralgapb
|
UTSW |
2 |
158,279,392 (GRCm39) |
missense |
probably benign |
0.15 |
R4524:Ralgapb
|
UTSW |
2 |
158,279,226 (GRCm39) |
missense |
probably benign |
0.00 |
R4946:Ralgapb
|
UTSW |
2 |
158,282,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R4975:Ralgapb
|
UTSW |
2 |
158,277,428 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5014:Ralgapb
|
UTSW |
2 |
158,337,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R5165:Ralgapb
|
UTSW |
2 |
158,307,832 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5465:Ralgapb
|
UTSW |
2 |
158,290,325 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5526:Ralgapb
|
UTSW |
2 |
158,274,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R5566:Ralgapb
|
UTSW |
2 |
158,336,630 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5949:Ralgapb
|
UTSW |
2 |
158,296,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R6140:Ralgapb
|
UTSW |
2 |
158,298,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Ralgapb
|
UTSW |
2 |
158,288,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Ralgapb
|
UTSW |
2 |
158,291,367 (GRCm39) |
splice site |
probably null |
|
R6364:Ralgapb
|
UTSW |
2 |
158,304,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R6458:Ralgapb
|
UTSW |
2 |
158,286,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R6746:Ralgapb
|
UTSW |
2 |
158,318,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R6782:Ralgapb
|
UTSW |
2 |
158,278,486 (GRCm39) |
missense |
probably damaging |
0.99 |
R6788:Ralgapb
|
UTSW |
2 |
158,278,486 (GRCm39) |
missense |
probably damaging |
0.99 |
R7017:Ralgapb
|
UTSW |
2 |
158,290,257 (GRCm39) |
missense |
probably benign |
0.19 |
R7108:Ralgapb
|
UTSW |
2 |
158,336,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R7108:Ralgapb
|
UTSW |
2 |
158,334,380 (GRCm39) |
missense |
probably damaging |
0.98 |
R7236:Ralgapb
|
UTSW |
2 |
158,282,747 (GRCm39) |
missense |
probably benign |
0.34 |
R7454:Ralgapb
|
UTSW |
2 |
158,274,822 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7485:Ralgapb
|
UTSW |
2 |
158,285,275 (GRCm39) |
missense |
probably benign |
0.35 |
R7595:Ralgapb
|
UTSW |
2 |
158,268,085 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7615:Ralgapb
|
UTSW |
2 |
158,292,190 (GRCm39) |
missense |
probably damaging |
0.99 |
R7728:Ralgapb
|
UTSW |
2 |
158,324,423 (GRCm39) |
critical splice donor site |
probably null |
|
R7913:Ralgapb
|
UTSW |
2 |
158,307,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R7953:Ralgapb
|
UTSW |
2 |
158,307,803 (GRCm39) |
missense |
probably benign |
0.10 |
R8245:Ralgapb
|
UTSW |
2 |
158,285,256 (GRCm39) |
missense |
probably damaging |
0.96 |
R8337:Ralgapb
|
UTSW |
2 |
158,292,192 (GRCm39) |
missense |
probably benign |
0.11 |
R8363:Ralgapb
|
UTSW |
2 |
158,268,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R8429:Ralgapb
|
UTSW |
2 |
158,268,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R8673:Ralgapb
|
UTSW |
2 |
158,292,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R8955:Ralgapb
|
UTSW |
2 |
158,337,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R8955:Ralgapb
|
UTSW |
2 |
158,279,264 (GRCm39) |
missense |
probably benign |
0.05 |
R8992:Ralgapb
|
UTSW |
2 |
158,296,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R9013:Ralgapb
|
UTSW |
2 |
158,279,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R9141:Ralgapb
|
UTSW |
2 |
158,262,811 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9166:Ralgapb
|
UTSW |
2 |
158,274,842 (GRCm39) |
critical splice donor site |
probably null |
|
R9242:Ralgapb
|
UTSW |
2 |
158,277,386 (GRCm39) |
missense |
probably benign |
0.13 |
R9274:Ralgapb
|
UTSW |
2 |
158,278,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R9354:Ralgapb
|
UTSW |
2 |
158,279,313 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9454:Ralgapb
|
UTSW |
2 |
158,315,072 (GRCm39) |
missense |
probably benign |
0.30 |
R9489:Ralgapb
|
UTSW |
2 |
158,268,283 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9490:Ralgapb
|
UTSW |
2 |
158,334,350 (GRCm39) |
missense |
probably benign |
0.29 |
R9510:Ralgapb
|
UTSW |
2 |
158,285,856 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Ralgapb
|
UTSW |
2 |
158,277,475 (GRCm39) |
missense |
probably benign |
0.00 |
|