Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
A |
T |
14: 118,553,288 (GRCm38) |
I844N |
possibly damaging |
Het |
Bend7 |
A |
T |
2: 4,744,244 (GRCm38) |
K57N |
probably damaging |
Het |
Cacna2d4 |
C |
T |
6: 119,307,286 (GRCm38) |
R745W |
probably damaging |
Het |
Cyp2a12 |
T |
C |
7: 27,032,542 (GRCm38) |
I236T |
probably benign |
Het |
Dnase1l2 |
A |
G |
17: 24,441,880 (GRCm38) |
V170A |
possibly damaging |
Het |
Dnm2 |
T |
A |
9: 21,500,265 (GRCm38) |
Y597N |
probably damaging |
Het |
Epsti1 |
A |
T |
14: 77,931,275 (GRCm38) |
R117S |
probably damaging |
Het |
Gabarapl2 |
A |
T |
8: 111,942,505 (GRCm38) |
I32F |
probably damaging |
Het |
Glrb |
T |
A |
3: 80,879,680 (GRCm38) |
I59F |
probably damaging |
Het |
Gm13089 |
A |
T |
4: 143,698,564 (GRCm38) |
I103N |
probably damaging |
Het |
Gm17689 |
T |
C |
9: 36,581,301 (GRCm38) |
S103G |
probably benign |
Het |
Gosr1 |
A |
G |
11: 76,730,146 (GRCm38) |
I239T |
probably benign |
Het |
Kif5b |
G |
T |
18: 6,209,192 (GRCm38) |
R857S |
probably damaging |
Het |
Kmt5a |
C |
A |
5: 124,447,219 (GRCm38) |
N44K |
probably damaging |
Het |
Ksr1 |
A |
T |
11: 79,021,503 (GRCm38) |
H675Q |
possibly damaging |
Het |
Maats1 |
A |
G |
16: 38,335,634 (GRCm38) |
F76L |
probably damaging |
Het |
Mep1b |
A |
G |
18: 21,080,458 (GRCm38) |
D68G |
possibly damaging |
Het |
Nebl |
A |
C |
2: 17,411,118 (GRCm38) |
S327A |
probably benign |
Het |
Nfat5 |
G |
A |
8: 107,368,066 (GRCm38) |
E962K |
probably damaging |
Het |
Nfatc4 |
A |
C |
14: 55,826,644 (GRCm38) |
D126A |
probably damaging |
Het |
Nmt2 |
A |
T |
2: 3,314,785 (GRCm38) |
R271* |
probably null |
Het |
Nol7 |
G |
A |
13: 43,400,615 (GRCm38) |
V133I |
probably benign |
Het |
Npepps |
A |
G |
11: 97,206,058 (GRCm38) |
|
probably benign |
Het |
Nphp3 |
GCATCATCATCATCATC |
GCATCATCATCATC |
9: 104,022,768 (GRCm38) |
|
probably benign |
Het |
Olfr1100 |
G |
A |
2: 86,978,499 (GRCm38) |
T99I |
probably benign |
Het |
Olfr376 |
A |
T |
11: 73,374,889 (GRCm38) |
I47F |
probably benign |
Het |
Olfr610 |
C |
T |
7: 103,506,862 (GRCm38) |
W28* |
probably null |
Het |
Olfr798 |
T |
A |
10: 129,625,843 (GRCm38) |
T73S |
probably benign |
Het |
Ovgp1 |
T |
A |
3: 105,974,932 (GRCm38) |
L37H |
probably damaging |
Het |
Padi3 |
G |
T |
4: 140,786,429 (GRCm38) |
A646D |
probably benign |
Het |
Pamr1 |
A |
G |
2: 102,609,907 (GRCm38) |
E142G |
probably damaging |
Het |
Papolg |
A |
T |
11: 23,870,818 (GRCm38) |
|
probably null |
Het |
Pfkl |
C |
T |
10: 77,995,243 (GRCm38) |
|
probably null |
Het |
Plrg1 |
T |
C |
3: 83,059,917 (GRCm38) |
S132P |
probably benign |
Het |
Prr14l |
C |
A |
5: 32,831,194 (GRCm38) |
C319F |
possibly damaging |
Het |
Prtn3 |
T |
A |
10: 79,879,677 (GRCm38) |
M1K |
probably null |
Het |
Ptpn22 |
T |
C |
3: 103,902,171 (GRCm38) |
F700S |
probably damaging |
Het |
Ptprz1 |
C |
T |
6: 23,044,367 (GRCm38) |
Q1273* |
probably null |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,110,324 (GRCm38) |
|
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,554,529 (GRCm38) |
D4963G |
probably damaging |
Het |
Sec16a |
G |
A |
2: 26,419,722 (GRCm38) |
L2091F |
possibly damaging |
Het |
Senp6 |
C |
T |
9: 80,093,589 (GRCm38) |
R27C |
probably damaging |
Het |
Shcbp1 |
T |
A |
8: 4,764,906 (GRCm38) |
M191L |
probably benign |
Het |
Sirt4 |
T |
C |
5: 115,482,955 (GRCm38) |
K53E |
probably benign |
Het |
Slc10a2 |
A |
G |
8: 5,089,132 (GRCm38) |
S271P |
probably damaging |
Het |
Slc35b2 |
T |
A |
17: 45,566,825 (GRCm38) |
F293I |
probably damaging |
Het |
Slc38a10 |
C |
T |
11: 120,140,643 (GRCm38) |
V103M |
probably damaging |
Het |
St5 |
A |
G |
7: 109,557,345 (GRCm38) |
L66P |
probably damaging |
Het |
Stab2 |
T |
A |
10: 86,887,895 (GRCm38) |
I1479F |
probably damaging |
Het |
Synpo2 |
A |
G |
3: 123,112,706 (GRCm38) |
V987A |
probably benign |
Het |
Syt9 |
A |
G |
7: 107,436,561 (GRCm38) |
I262V |
probably damaging |
Het |
Taf2 |
GCTTCTTCTTCTTCTTCTT |
GCTTCTTCTTCTTCTT |
15: 55,016,461 (GRCm38) |
|
probably benign |
Het |
Tmem39a |
A |
T |
16: 38,585,402 (GRCm38) |
I200F |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,749,269 (GRCm38) |
T23760M |
probably damaging |
Het |
Uqcrc1 |
C |
T |
9: 108,944,705 (GRCm38) |
Q22* |
probably null |
Het |
Wdtc1 |
A |
G |
4: 133,300,661 (GRCm38) |
W377R |
probably damaging |
Het |
Zfp454 |
A |
G |
11: 50,873,937 (GRCm38) |
S223P |
probably benign |
Het |
|
Other mutations in Csmd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00519:Csmd2
|
APN |
4 |
128,483,473 (GRCm38) |
missense |
probably benign |
0.03 |
IGL01098:Csmd2
|
APN |
4 |
128,059,052 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01114:Csmd2
|
APN |
4 |
128,369,130 (GRCm38) |
missense |
probably benign |
0.04 |
IGL01364:Csmd2
|
APN |
4 |
128,414,288 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01530:Csmd2
|
APN |
4 |
128,414,301 (GRCm38) |
missense |
possibly damaging |
0.66 |
IGL01582:Csmd2
|
APN |
4 |
128,563,305 (GRCm38) |
nonsense |
probably null |
|
IGL01670:Csmd2
|
APN |
4 |
128,513,371 (GRCm38) |
splice site |
probably benign |
|
IGL01707:Csmd2
|
APN |
4 |
128,383,005 (GRCm38) |
missense |
possibly damaging |
0.81 |
IGL01810:Csmd2
|
APN |
4 |
128,480,845 (GRCm38) |
splice site |
probably benign |
|
IGL01837:Csmd2
|
APN |
4 |
128,419,570 (GRCm38) |
missense |
possibly damaging |
0.92 |
IGL01924:Csmd2
|
APN |
4 |
128,559,947 (GRCm38) |
missense |
unknown |
|
IGL02013:Csmd2
|
APN |
4 |
128,321,323 (GRCm38) |
missense |
possibly damaging |
0.47 |
IGL02020:Csmd2
|
APN |
4 |
128,559,879 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02037:Csmd2
|
APN |
4 |
128,477,470 (GRCm38) |
splice site |
probably benign |
|
IGL02303:Csmd2
|
APN |
4 |
128,369,008 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02317:Csmd2
|
APN |
4 |
128,463,727 (GRCm38) |
splice site |
probably benign |
|
IGL02322:Csmd2
|
APN |
4 |
128,463,727 (GRCm38) |
splice site |
probably benign |
|
IGL02338:Csmd2
|
APN |
4 |
128,395,066 (GRCm38) |
missense |
possibly damaging |
0.79 |
IGL02412:Csmd2
|
APN |
4 |
128,513,372 (GRCm38) |
splice site |
probably benign |
|
IGL02428:Csmd2
|
APN |
4 |
128,474,816 (GRCm38) |
missense |
possibly damaging |
0.82 |
IGL02491:Csmd2
|
APN |
4 |
128,534,257 (GRCm38) |
missense |
probably benign |
|
IGL02701:Csmd2
|
APN |
4 |
128,496,141 (GRCm38) |
missense |
probably benign |
0.17 |
IGL02801:Csmd2
|
APN |
4 |
128,552,075 (GRCm38) |
splice site |
probably null |
|
IGL02818:Csmd2
|
APN |
4 |
128,209,728 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02863:Csmd2
|
APN |
4 |
128,521,884 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02876:Csmd2
|
APN |
4 |
128,321,335 (GRCm38) |
nonsense |
probably null |
|
IGL02977:Csmd2
|
APN |
4 |
128,493,276 (GRCm38) |
nonsense |
probably null |
|
IGL03006:Csmd2
|
APN |
4 |
128,480,765 (GRCm38) |
splice site |
probably benign |
|
IGL03032:Csmd2
|
APN |
4 |
128,519,041 (GRCm38) |
missense |
probably benign |
0.03 |
IGL03148:Csmd2
|
APN |
4 |
128,384,269 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03157:Csmd2
|
APN |
4 |
128,414,299 (GRCm38) |
nonsense |
probably null |
|
IGL03245:Csmd2
|
APN |
4 |
128,509,122 (GRCm38) |
missense |
probably benign |
0.12 |
IGL03376:Csmd2
|
APN |
4 |
128,517,671 (GRCm38) |
missense |
probably benign |
0.03 |
IGL03014:Csmd2
|
UTSW |
4 |
128,296,429 (GRCm38) |
missense |
probably benign |
0.01 |
R0109:Csmd2
|
UTSW |
4 |
128,544,743 (GRCm38) |
missense |
probably benign |
0.03 |
R0112:Csmd2
|
UTSW |
4 |
128,496,029 (GRCm38) |
missense |
probably damaging |
1.00 |
R0157:Csmd2
|
UTSW |
4 |
128,521,911 (GRCm38) |
missense |
probably benign |
0.02 |
R0390:Csmd2
|
UTSW |
4 |
128,133,673 (GRCm38) |
intron |
probably benign |
|
R0441:Csmd2
|
UTSW |
4 |
128,520,230 (GRCm38) |
missense |
probably benign |
0.00 |
R0519:Csmd2
|
UTSW |
4 |
128,487,005 (GRCm38) |
missense |
possibly damaging |
0.95 |
R0746:Csmd2
|
UTSW |
4 |
128,414,297 (GRCm38) |
missense |
probably damaging |
1.00 |
R0973:Csmd2
|
UTSW |
4 |
128,496,188 (GRCm38) |
missense |
possibly damaging |
0.91 |
R1019:Csmd2
|
UTSW |
4 |
128,522,014 (GRCm38) |
missense |
probably benign |
0.00 |
R1476:Csmd2
|
UTSW |
4 |
128,487,001 (GRCm38) |
missense |
probably benign |
0.08 |
R1641:Csmd2
|
UTSW |
4 |
128,483,395 (GRCm38) |
missense |
possibly damaging |
0.68 |
R1709:Csmd2
|
UTSW |
4 |
128,496,195 (GRCm38) |
missense |
probably damaging |
0.96 |
R2866:Csmd2
|
UTSW |
4 |
128,414,392 (GRCm38) |
critical splice donor site |
probably null |
|
R2870:Csmd2
|
UTSW |
4 |
128,557,718 (GRCm38) |
missense |
unknown |
|
R2870:Csmd2
|
UTSW |
4 |
128,557,718 (GRCm38) |
missense |
unknown |
|
R2871:Csmd2
|
UTSW |
4 |
128,557,718 (GRCm38) |
missense |
unknown |
|
R2871:Csmd2
|
UTSW |
4 |
128,557,718 (GRCm38) |
missense |
unknown |
|
R2872:Csmd2
|
UTSW |
4 |
128,557,718 (GRCm38) |
missense |
unknown |
|
R2872:Csmd2
|
UTSW |
4 |
128,557,718 (GRCm38) |
missense |
unknown |
|
R2873:Csmd2
|
UTSW |
4 |
128,557,718 (GRCm38) |
missense |
unknown |
|
R2893:Csmd2
|
UTSW |
4 |
128,538,993 (GRCm38) |
splice site |
probably null |
|
R3796:Csmd2
|
UTSW |
4 |
128,517,595 (GRCm38) |
missense |
probably benign |
0.20 |
R3797:Csmd2
|
UTSW |
4 |
128,517,595 (GRCm38) |
missense |
probably benign |
0.20 |
R3798:Csmd2
|
UTSW |
4 |
128,517,595 (GRCm38) |
missense |
probably benign |
0.20 |
R3914:Csmd2
|
UTSW |
4 |
128,321,324 (GRCm38) |
missense |
probably benign |
0.07 |
R4198:Csmd2
|
UTSW |
4 |
128,510,924 (GRCm38) |
missense |
probably benign |
0.07 |
R4489:Csmd2
|
UTSW |
4 |
128,381,945 (GRCm38) |
missense |
possibly damaging |
0.68 |
R4571:Csmd2
|
UTSW |
4 |
128,480,095 (GRCm38) |
splice site |
probably null |
|
R4581:Csmd2
|
UTSW |
4 |
128,369,088 (GRCm38) |
missense |
probably benign |
0.02 |
R4599:Csmd2
|
UTSW |
4 |
127,988,128 (GRCm38) |
missense |
probably benign |
0.35 |
R4649:Csmd2
|
UTSW |
4 |
128,546,073 (GRCm38) |
missense |
probably benign |
|
R4706:Csmd2
|
UTSW |
4 |
128,544,751 (GRCm38) |
missense |
probably benign |
|
R4776:Csmd2
|
UTSW |
4 |
128,442,892 (GRCm38) |
missense |
probably benign |
0.09 |
R4838:Csmd2
|
UTSW |
4 |
128,517,749 (GRCm38) |
missense |
probably benign |
|
R4900:Csmd2
|
UTSW |
4 |
128,452,525 (GRCm38) |
missense |
probably benign |
0.03 |
R4999:Csmd2
|
UTSW |
4 |
128,521,930 (GRCm38) |
missense |
probably benign |
0.00 |
R5024:Csmd2
|
UTSW |
4 |
128,321,348 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5034:Csmd2
|
UTSW |
4 |
128,059,108 (GRCm38) |
missense |
probably damaging |
0.98 |
R5152:Csmd2
|
UTSW |
4 |
128,552,035 (GRCm38) |
missense |
probably benign |
0.27 |
R5172:Csmd2
|
UTSW |
4 |
128,477,397 (GRCm38) |
missense |
probably benign |
0.10 |
R5231:Csmd2
|
UTSW |
4 |
128,546,049 (GRCm38) |
missense |
probably benign |
0.00 |
R5279:Csmd2
|
UTSW |
4 |
128,456,914 (GRCm38) |
missense |
probably benign |
0.30 |
R5287:Csmd2
|
UTSW |
4 |
128,486,884 (GRCm38) |
missense |
probably benign |
0.01 |
R5403:Csmd2
|
UTSW |
4 |
128,486,884 (GRCm38) |
missense |
probably benign |
0.01 |
R5410:Csmd2
|
UTSW |
4 |
128,548,819 (GRCm38) |
missense |
probably benign |
|
R5551:Csmd2
|
UTSW |
4 |
128,510,948 (GRCm38) |
missense |
possibly damaging |
0.83 |
R5566:Csmd2
|
UTSW |
4 |
128,462,889 (GRCm38) |
critical splice donor site |
probably null |
|
R5826:Csmd2
|
UTSW |
4 |
128,519,199 (GRCm38) |
splice site |
probably null |
|
R5907:Csmd2
|
UTSW |
4 |
128,197,385 (GRCm38) |
missense |
probably damaging |
0.99 |
R5913:Csmd2
|
UTSW |
4 |
128,551,988 (GRCm38) |
missense |
probably benign |
0.01 |
R5970:Csmd2
|
UTSW |
4 |
128,546,151 (GRCm38) |
missense |
probably benign |
0.00 |
R5977:Csmd2
|
UTSW |
4 |
128,059,034 (GRCm38) |
missense |
probably damaging |
1.00 |
R6027:Csmd2
|
UTSW |
4 |
128,559,946 (GRCm38) |
missense |
unknown |
|
R6075:Csmd2
|
UTSW |
4 |
128,486,865 (GRCm38) |
missense |
probably benign |
0.15 |
R6129:Csmd2
|
UTSW |
4 |
128,493,334 (GRCm38) |
missense |
possibly damaging |
0.79 |
R6363:Csmd2
|
UTSW |
4 |
128,400,379 (GRCm38) |
missense |
probably benign |
0.00 |
R6366:Csmd2
|
UTSW |
4 |
128,483,452 (GRCm38) |
missense |
probably benign |
0.00 |
R6404:Csmd2
|
UTSW |
4 |
128,521,950 (GRCm38) |
missense |
possibly damaging |
0.90 |
R6437:Csmd2
|
UTSW |
4 |
127,988,100 (GRCm38) |
missense |
probably benign |
0.24 |
R6441:Csmd2
|
UTSW |
4 |
128,394,964 (GRCm38) |
missense |
probably benign |
0.03 |
R6643:Csmd2
|
UTSW |
4 |
128,372,597 (GRCm38) |
missense |
probably benign |
0.14 |
R6724:Csmd2
|
UTSW |
4 |
128,563,371 (GRCm38) |
missense |
probably damaging |
0.97 |
R6734:Csmd2
|
UTSW |
4 |
128,463,813 (GRCm38) |
missense |
probably benign |
0.00 |
R6750:Csmd2
|
UTSW |
4 |
128,197,225 (GRCm38) |
missense |
possibly damaging |
0.91 |
R6801:Csmd2
|
UTSW |
4 |
128,383,950 (GRCm38) |
missense |
probably benign |
0.11 |
R6842:Csmd2
|
UTSW |
4 |
128,509,159 (GRCm38) |
missense |
possibly damaging |
0.72 |
R6843:Csmd2
|
UTSW |
4 |
128,463,794 (GRCm38) |
missense |
probably benign |
0.27 |
R6868:Csmd2
|
UTSW |
4 |
128,442,840 (GRCm38) |
missense |
probably benign |
|
R6882:Csmd2
|
UTSW |
4 |
128,449,269 (GRCm38) |
missense |
probably benign |
0.01 |
R7019:Csmd2
|
UTSW |
4 |
128,369,063 (GRCm38) |
missense |
|
|
R7028:Csmd2
|
UTSW |
4 |
128,277,228 (GRCm38) |
missense |
|
|
R7096:Csmd2
|
UTSW |
4 |
128,462,726 (GRCm38) |
missense |
|
|
R7122:Csmd2
|
UTSW |
4 |
128,449,227 (GRCm38) |
missense |
|
|
R7125:Csmd2
|
UTSW |
4 |
128,496,162 (GRCm38) |
missense |
|
|
R7197:Csmd2
|
UTSW |
4 |
128,511,033 (GRCm38) |
missense |
|
|
R7234:Csmd2
|
UTSW |
4 |
128,456,779 (GRCm38) |
missense |
|
|
R7299:Csmd2
|
UTSW |
4 |
128,528,262 (GRCm38) |
missense |
|
|
R7301:Csmd2
|
UTSW |
4 |
128,528,262 (GRCm38) |
missense |
|
|
R7319:Csmd2
|
UTSW |
4 |
128,393,679 (GRCm38) |
missense |
|
|
R7331:Csmd2
|
UTSW |
4 |
128,564,228 (GRCm38) |
splice site |
probably null |
|
R7332:Csmd2
|
UTSW |
4 |
128,419,567 (GRCm38) |
missense |
|
|
R7352:Csmd2
|
UTSW |
4 |
128,557,636 (GRCm38) |
missense |
|
|
R7402:Csmd2
|
UTSW |
4 |
128,322,096 (GRCm38) |
missense |
|
|
R7402:Csmd2
|
UTSW |
4 |
128,322,095 (GRCm38) |
missense |
|
|
R7474:Csmd2
|
UTSW |
4 |
128,546,127 (GRCm38) |
missense |
|
|
R7555:Csmd2
|
UTSW |
4 |
128,452,458 (GRCm38) |
missense |
|
|
R7592:Csmd2
|
UTSW |
4 |
128,463,798 (GRCm38) |
missense |
|
|
R7700:Csmd2
|
UTSW |
4 |
128,545,756 (GRCm38) |
splice site |
probably null |
|
R7714:Csmd2
|
UTSW |
4 |
128,382,950 (GRCm38) |
nonsense |
probably null |
|
R7734:Csmd2
|
UTSW |
4 |
128,552,057 (GRCm38) |
missense |
|
|
R7735:Csmd2
|
UTSW |
4 |
128,456,930 (GRCm38) |
critical splice donor site |
probably null |
|
R7757:Csmd2
|
UTSW |
4 |
128,483,456 (GRCm38) |
missense |
|
|
R7805:Csmd2
|
UTSW |
4 |
128,419,573 (GRCm38) |
missense |
|
|
R7823:Csmd2
|
UTSW |
4 |
128,209,905 (GRCm38) |
missense |
|
|
R7904:Csmd2
|
UTSW |
4 |
128,419,553 (GRCm38) |
missense |
|
|
R7946:Csmd2
|
UTSW |
4 |
128,520,265 (GRCm38) |
missense |
|
|
R7964:Csmd2
|
UTSW |
4 |
128,523,510 (GRCm38) |
missense |
|
|
R7968:Csmd2
|
UTSW |
4 |
128,197,325 (GRCm38) |
missense |
|
|
R8003:Csmd2
|
UTSW |
4 |
128,539,187 (GRCm38) |
nonsense |
probably null |
|
R8071:Csmd2
|
UTSW |
4 |
128,393,538 (GRCm38) |
missense |
|
|
R8504:Csmd2
|
UTSW |
4 |
128,546,690 (GRCm38) |
missense |
|
|
R8511:Csmd2
|
UTSW |
4 |
128,368,899 (GRCm38) |
missense |
|
|
R8517:Csmd2
|
UTSW |
4 |
128,552,686 (GRCm38) |
missense |
|
|
R8704:Csmd2
|
UTSW |
4 |
128,197,354 (GRCm38) |
missense |
|
|
R8722:Csmd2
|
UTSW |
4 |
128,551,950 (GRCm38) |
unclassified |
probably benign |
|
R8729:Csmd2
|
UTSW |
4 |
128,462,845 (GRCm38) |
missense |
|
|
R8801:Csmd2
|
UTSW |
4 |
128,563,402 (GRCm38) |
missense |
probably damaging |
0.97 |
R8803:Csmd2
|
UTSW |
4 |
128,546,684 (GRCm38) |
missense |
|
|
R8839:Csmd2
|
UTSW |
4 |
128,442,888 (GRCm38) |
missense |
|
|
R8867:Csmd2
|
UTSW |
4 |
128,557,676 (GRCm38) |
missense |
|
|
R8913:Csmd2
|
UTSW |
4 |
128,523,558 (GRCm38) |
missense |
|
|
R8928:Csmd2
|
UTSW |
4 |
128,475,789 (GRCm38) |
missense |
|
|
R8974:Csmd2
|
UTSW |
4 |
128,552,587 (GRCm38) |
missense |
|
|
R9001:Csmd2
|
UTSW |
4 |
128,414,286 (GRCm38) |
missense |
|
|
R9132:Csmd2
|
UTSW |
4 |
128,549,214 (GRCm38) |
missense |
|
|
R9245:Csmd2
|
UTSW |
4 |
128,306,375 (GRCm38) |
missense |
|
|
R9249:Csmd2
|
UTSW |
4 |
128,419,530 (GRCm38) |
nonsense |
probably null |
|
R9254:Csmd2
|
UTSW |
4 |
128,197,319 (GRCm38) |
missense |
|
|
R9265:Csmd2
|
UTSW |
4 |
128,400,370 (GRCm38) |
missense |
|
|
R9407:Csmd2
|
UTSW |
4 |
128,548,820 (GRCm38) |
missense |
|
|
R9432:Csmd2
|
UTSW |
4 |
128,277,211 (GRCm38) |
missense |
|
|
R9559:Csmd2
|
UTSW |
4 |
128,544,768 (GRCm38) |
missense |
|
|
R9673:Csmd2
|
UTSW |
4 |
128,414,269 (GRCm38) |
missense |
|
|
R9735:Csmd2
|
UTSW |
4 |
128,509,108 (GRCm38) |
missense |
|
|
R9749:Csmd2
|
UTSW |
4 |
128,496,128 (GRCm38) |
missense |
|
|
R9803:Csmd2
|
UTSW |
4 |
128,369,193 (GRCm38) |
missense |
|
|
Z1177:Csmd2
|
UTSW |
4 |
128,530,797 (GRCm38) |
missense |
|
|
|