Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,244,615 (GRCm39) |
Y2159* |
probably null |
Het |
Abca3 |
A |
G |
17: 24,602,901 (GRCm39) |
T499A |
probably benign |
Het |
Abcb5 |
T |
A |
12: 118,899,702 (GRCm39) |
T322S |
probably damaging |
Het |
Adamts4 |
T |
A |
1: 171,078,419 (GRCm39) |
M1K |
probably null |
Het |
Adamtsl4 |
C |
T |
3: 95,592,765 (GRCm39) |
|
probably null |
Het |
Adh4 |
A |
T |
3: 138,129,950 (GRCm39) |
I259F |
probably damaging |
Het |
Aff3 |
G |
A |
1: 38,220,505 (GRCm39) |
S1135F |
probably damaging |
Het |
Arhgef16 |
T |
C |
4: 154,370,105 (GRCm39) |
D280G |
probably benign |
Het |
Baiap3 |
T |
C |
17: 25,470,707 (GRCm39) |
E71G |
probably damaging |
Het |
Calb2 |
A |
G |
8: 110,879,332 (GRCm39) |
I91T |
possibly damaging |
Het |
Ccr5 |
A |
G |
9: 123,924,697 (GRCm39) |
N100S |
probably benign |
Het |
Cep57 |
G |
T |
9: 13,732,871 (GRCm39) |
R25S |
probably damaging |
Het |
Chadl |
A |
G |
15: 81,580,079 (GRCm39) |
L52P |
probably damaging |
Het |
Clec12b |
T |
C |
6: 129,362,438 (GRCm39) |
T6A |
probably damaging |
Het |
Cnga1 |
T |
A |
5: 72,775,593 (GRCm39) |
N43Y |
probably damaging |
Het |
Col20a1 |
A |
T |
2: 180,628,316 (GRCm39) |
|
probably null |
Het |
Ctps1 |
A |
T |
4: 120,411,300 (GRCm39) |
|
probably null |
Het |
Cyp39a1 |
T |
A |
17: 43,996,099 (GRCm39) |
W224R |
possibly damaging |
Het |
Defb29 |
A |
T |
2: 152,380,848 (GRCm39) |
Y54N |
probably benign |
Het |
Dmbt1 |
A |
T |
7: 130,708,003 (GRCm39) |
D1241V |
probably damaging |
Het |
Dnah1 |
A |
T |
14: 30,996,323 (GRCm39) |
I2671K |
probably benign |
Het |
Dnah2 |
C |
A |
11: 69,407,395 (GRCm39) |
E158* |
probably null |
Het |
Dynlt2b |
A |
G |
16: 32,238,718 (GRCm39) |
Y31C |
probably damaging |
Het |
Edar |
A |
G |
10: 58,464,463 (GRCm39) |
S59P |
possibly damaging |
Het |
Egr2 |
T |
A |
10: 67,376,596 (GRCm39) |
C339* |
probably null |
Het |
Eif5b |
G |
A |
1: 38,084,765 (GRCm39) |
V871I |
possibly damaging |
Het |
Eif5b |
G |
A |
1: 38,090,328 (GRCm39) |
G1169E |
probably damaging |
Het |
Erap1 |
A |
G |
13: 74,810,531 (GRCm39) |
Y290C |
probably damaging |
Het |
Fastkd5 |
T |
A |
2: 130,456,221 (GRCm39) |
T790S |
possibly damaging |
Het |
Fkrp |
C |
T |
7: 16,544,849 (GRCm39) |
V338M |
probably damaging |
Het |
Gabra6 |
T |
C |
11: 42,198,317 (GRCm39) |
T378A |
probably benign |
Het |
Gm4924 |
C |
A |
10: 82,214,475 (GRCm39) |
Q17K |
possibly damaging |
Het |
Gm9847 |
A |
G |
12: 14,545,000 (GRCm39) |
|
noncoding transcript |
Het |
Gpr108 |
A |
G |
17: 57,543,919 (GRCm39) |
F429S |
probably damaging |
Het |
Gpr162 |
G |
A |
6: 124,837,901 (GRCm39) |
R250* |
probably null |
Het |
Gtf2a1 |
A |
T |
12: 91,534,368 (GRCm39) |
D295E |
possibly damaging |
Het |
Gtf2h3 |
C |
T |
5: 124,722,360 (GRCm39) |
T121I |
probably benign |
Het |
Herc1 |
T |
A |
9: 66,372,819 (GRCm39) |
M3125K |
possibly damaging |
Het |
Hoxb6 |
T |
A |
11: 96,191,580 (GRCm39) |
Y167* |
probably null |
Het |
Hrob |
T |
A |
11: 102,146,659 (GRCm39) |
S312T |
probably damaging |
Het |
Htt |
T |
C |
5: 35,006,419 (GRCm39) |
Y1443H |
probably damaging |
Het |
Il21r |
A |
G |
7: 125,224,470 (GRCm39) |
D28G |
probably damaging |
Het |
Impact |
T |
G |
18: 13,107,819 (GRCm39) |
V29G |
probably damaging |
Het |
Itpr3 |
A |
G |
17: 27,334,926 (GRCm39) |
T2147A |
possibly damaging |
Het |
Itsn2 |
T |
A |
12: 4,676,554 (GRCm39) |
L50Q |
probably damaging |
Het |
Jade1 |
A |
G |
3: 41,559,338 (GRCm39) |
D473G |
possibly damaging |
Het |
Kif26a |
T |
G |
12: 112,123,788 (GRCm39) |
L131R |
probably damaging |
Het |
Kif2a |
A |
T |
13: 107,130,432 (GRCm39) |
M1K |
probably null |
Het |
Lrsam1 |
C |
A |
2: 32,831,870 (GRCm39) |
Q368H |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,328,957 (GRCm39) |
Q4592R |
probably damaging |
Het |
Map3k5 |
T |
C |
10: 19,986,465 (GRCm39) |
V893A |
probably damaging |
Het |
Med13l |
G |
T |
5: 118,866,730 (GRCm39) |
V595F |
possibly damaging |
Het |
Mocs1 |
T |
A |
17: 49,761,211 (GRCm39) |
L435Q |
possibly damaging |
Het |
Mtmr4 |
T |
C |
11: 87,495,356 (GRCm39) |
L471P |
probably damaging |
Het |
Myo7a |
T |
C |
7: 97,714,023 (GRCm39) |
E1616G |
possibly damaging |
Het |
Nacad |
T |
A |
11: 6,552,136 (GRCm39) |
S352C |
probably damaging |
Het |
Nfat5 |
T |
A |
8: 108,095,767 (GRCm39) |
M817K |
possibly damaging |
Het |
Ofcc1 |
C |
A |
13: 40,248,129 (GRCm39) |
L668F |
probably damaging |
Het |
Or12j2 |
C |
A |
7: 139,915,980 (GRCm39) |
D68E |
probably damaging |
Het |
Or7e178 |
T |
C |
9: 20,225,265 (GRCm39) |
Q309R |
probably benign |
Het |
Or8j3c |
G |
A |
2: 86,253,721 (GRCm39) |
Q100* |
probably null |
Het |
Plxnb2 |
T |
C |
15: 89,048,223 (GRCm39) |
T696A |
probably benign |
Het |
Prkab2 |
T |
A |
3: 97,569,609 (GRCm39) |
F58L |
probably benign |
Het |
Prpf4 |
G |
T |
4: 62,334,206 (GRCm39) |
L220F |
probably benign |
Het |
Rad18 |
A |
T |
6: 112,658,307 (GRCm39) |
D199E |
probably benign |
Het |
Raet1e |
T |
C |
10: 22,050,304 (GRCm39) |
L29P |
probably damaging |
Het |
Ralgapb |
A |
C |
2: 158,336,630 (GRCm39) |
T1089P |
possibly damaging |
Het |
Rest |
A |
G |
5: 77,430,173 (GRCm39) |
E864G |
probably benign |
Het |
Rgsl1 |
T |
A |
1: 153,669,520 (GRCm39) |
I289F |
probably damaging |
Het |
Rint1 |
T |
C |
5: 24,015,951 (GRCm39) |
Y406H |
probably damaging |
Het |
Rmc1 |
T |
C |
18: 12,313,749 (GRCm39) |
I26T |
possibly damaging |
Het |
Rpl31 |
C |
T |
1: 39,409,108 (GRCm39) |
R41C |
probably benign |
Het |
Scn8a |
T |
C |
15: 100,872,415 (GRCm39) |
S485P |
probably damaging |
Het |
Slamf1 |
T |
A |
1: 171,615,538 (GRCm39) |
V249E |
possibly damaging |
Het |
Slc39a12 |
C |
T |
2: 14,412,414 (GRCm39) |
T362I |
possibly damaging |
Het |
Sos1 |
C |
T |
17: 80,761,319 (GRCm39) |
V126I |
possibly damaging |
Het |
Srcap |
T |
C |
7: 127,124,475 (GRCm39) |
F215S |
probably damaging |
Het |
Supt4a |
T |
A |
11: 87,634,113 (GRCm39) |
S110T |
probably benign |
Het |
Tbc1d30 |
T |
A |
10: 121,138,015 (GRCm39) |
T232S |
probably damaging |
Het |
Tenm3 |
A |
G |
8: 48,732,041 (GRCm39) |
C1288R |
probably damaging |
Het |
Tespa1 |
T |
A |
10: 130,191,356 (GRCm39) |
L100* |
probably null |
Het |
Tgm1 |
C |
A |
14: 55,949,893 (GRCm39) |
R105L |
probably damaging |
Het |
Tgoln1 |
G |
A |
6: 72,593,018 (GRCm39) |
T154I |
possibly damaging |
Het |
Trp53i13 |
G |
A |
11: 77,399,552 (GRCm39) |
T259I |
probably damaging |
Het |
Tubgcp4 |
T |
A |
2: 121,015,251 (GRCm39) |
F320I |
possibly damaging |
Het |
Tut7 |
A |
T |
13: 59,936,443 (GRCm39) |
C817* |
probably null |
Het |
Vmn1r21 |
A |
C |
6: 57,821,079 (GRCm39) |
Y122D |
probably benign |
Het |
Vmn1r75 |
T |
A |
7: 11,614,407 (GRCm39) |
D46E |
probably damaging |
Het |
Vmn2r120 |
A |
T |
17: 57,852,290 (GRCm39) |
L9M |
possibly damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,696,247 (GRCm39) |
I165T |
possibly damaging |
Het |
Vmn2r76 |
A |
T |
7: 85,875,286 (GRCm39) |
Y564N |
probably damaging |
Het |
Wee1 |
G |
T |
7: 109,725,257 (GRCm39) |
E300* |
probably null |
Het |
Xdh |
T |
C |
17: 74,200,617 (GRCm39) |
D1168G |
probably damaging |
Het |
Zfp54 |
A |
G |
17: 21,653,706 (GRCm39) |
T67A |
probably damaging |
Het |
Zfp941 |
G |
T |
7: 140,392,679 (GRCm39) |
H227N |
probably benign |
Het |
Zpr1 |
T |
A |
9: 46,192,373 (GRCm39) |
V399D |
possibly damaging |
Het |
Zzz3 |
A |
G |
3: 152,161,461 (GRCm39) |
E285G |
probably damaging |
Het |
|
Other mutations in Csmd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00519:Csmd2
|
APN |
4 |
128,377,266 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01098:Csmd2
|
APN |
4 |
127,952,845 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01114:Csmd2
|
APN |
4 |
128,262,923 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01364:Csmd2
|
APN |
4 |
128,308,081 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01530:Csmd2
|
APN |
4 |
128,308,094 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01582:Csmd2
|
APN |
4 |
128,457,098 (GRCm39) |
nonsense |
probably null |
|
IGL01670:Csmd2
|
APN |
4 |
128,407,164 (GRCm39) |
splice site |
probably benign |
|
IGL01707:Csmd2
|
APN |
4 |
128,276,798 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01810:Csmd2
|
APN |
4 |
128,374,638 (GRCm39) |
splice site |
probably benign |
|
IGL01837:Csmd2
|
APN |
4 |
128,313,363 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01924:Csmd2
|
APN |
4 |
128,453,740 (GRCm39) |
missense |
unknown |
|
IGL02013:Csmd2
|
APN |
4 |
128,215,116 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02020:Csmd2
|
APN |
4 |
128,453,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02037:Csmd2
|
APN |
4 |
128,371,263 (GRCm39) |
splice site |
probably benign |
|
IGL02303:Csmd2
|
APN |
4 |
128,262,801 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02317:Csmd2
|
APN |
4 |
128,357,520 (GRCm39) |
splice site |
probably benign |
|
IGL02322:Csmd2
|
APN |
4 |
128,357,520 (GRCm39) |
splice site |
probably benign |
|
IGL02338:Csmd2
|
APN |
4 |
128,288,859 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02412:Csmd2
|
APN |
4 |
128,407,165 (GRCm39) |
splice site |
probably benign |
|
IGL02428:Csmd2
|
APN |
4 |
128,368,609 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02491:Csmd2
|
APN |
4 |
128,428,050 (GRCm39) |
missense |
probably benign |
|
IGL02701:Csmd2
|
APN |
4 |
128,389,934 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02801:Csmd2
|
APN |
4 |
128,445,868 (GRCm39) |
splice site |
probably null |
|
IGL02818:Csmd2
|
APN |
4 |
128,103,521 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02863:Csmd2
|
APN |
4 |
128,415,677 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02876:Csmd2
|
APN |
4 |
128,215,128 (GRCm39) |
nonsense |
probably null |
|
IGL02977:Csmd2
|
APN |
4 |
128,387,069 (GRCm39) |
nonsense |
probably null |
|
IGL03006:Csmd2
|
APN |
4 |
128,374,558 (GRCm39) |
splice site |
probably benign |
|
IGL03032:Csmd2
|
APN |
4 |
128,412,834 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03148:Csmd2
|
APN |
4 |
128,278,062 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03157:Csmd2
|
APN |
4 |
128,308,092 (GRCm39) |
nonsense |
probably null |
|
IGL03245:Csmd2
|
APN |
4 |
128,402,915 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03376:Csmd2
|
APN |
4 |
128,411,464 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03014:Csmd2
|
UTSW |
4 |
128,190,222 (GRCm39) |
missense |
probably benign |
0.01 |
R0109:Csmd2
|
UTSW |
4 |
128,438,536 (GRCm39) |
missense |
probably benign |
0.03 |
R0112:Csmd2
|
UTSW |
4 |
128,389,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R0157:Csmd2
|
UTSW |
4 |
128,415,704 (GRCm39) |
missense |
probably benign |
0.02 |
R0390:Csmd2
|
UTSW |
4 |
128,027,466 (GRCm39) |
intron |
probably benign |
|
R0441:Csmd2
|
UTSW |
4 |
128,414,023 (GRCm39) |
missense |
probably benign |
0.00 |
R0519:Csmd2
|
UTSW |
4 |
128,380,798 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0743:Csmd2
|
UTSW |
4 |
128,007,469 (GRCm39) |
missense |
probably benign |
0.00 |
R0746:Csmd2
|
UTSW |
4 |
128,308,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Csmd2
|
UTSW |
4 |
128,389,981 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1019:Csmd2
|
UTSW |
4 |
128,415,807 (GRCm39) |
missense |
probably benign |
0.00 |
R1476:Csmd2
|
UTSW |
4 |
128,380,794 (GRCm39) |
missense |
probably benign |
0.08 |
R1641:Csmd2
|
UTSW |
4 |
128,377,188 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1709:Csmd2
|
UTSW |
4 |
128,389,988 (GRCm39) |
missense |
probably damaging |
0.96 |
R2866:Csmd2
|
UTSW |
4 |
128,308,185 (GRCm39) |
critical splice donor site |
probably null |
|
R2870:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2870:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2871:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2871:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2872:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2872:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2873:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2893:Csmd2
|
UTSW |
4 |
128,432,786 (GRCm39) |
splice site |
probably null |
|
R3796:Csmd2
|
UTSW |
4 |
128,411,388 (GRCm39) |
missense |
probably benign |
0.20 |
R3797:Csmd2
|
UTSW |
4 |
128,411,388 (GRCm39) |
missense |
probably benign |
0.20 |
R3798:Csmd2
|
UTSW |
4 |
128,411,388 (GRCm39) |
missense |
probably benign |
0.20 |
R3914:Csmd2
|
UTSW |
4 |
128,215,117 (GRCm39) |
missense |
probably benign |
0.07 |
R4198:Csmd2
|
UTSW |
4 |
128,404,717 (GRCm39) |
missense |
probably benign |
0.07 |
R4489:Csmd2
|
UTSW |
4 |
128,275,738 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4571:Csmd2
|
UTSW |
4 |
128,373,888 (GRCm39) |
splice site |
probably null |
|
R4581:Csmd2
|
UTSW |
4 |
128,262,881 (GRCm39) |
missense |
probably benign |
0.02 |
R4599:Csmd2
|
UTSW |
4 |
127,881,921 (GRCm39) |
missense |
probably benign |
0.35 |
R4649:Csmd2
|
UTSW |
4 |
128,439,866 (GRCm39) |
missense |
probably benign |
|
R4706:Csmd2
|
UTSW |
4 |
128,438,544 (GRCm39) |
missense |
probably benign |
|
R4776:Csmd2
|
UTSW |
4 |
128,336,685 (GRCm39) |
missense |
probably benign |
0.09 |
R4838:Csmd2
|
UTSW |
4 |
128,411,542 (GRCm39) |
missense |
probably benign |
|
R4900:Csmd2
|
UTSW |
4 |
128,346,318 (GRCm39) |
missense |
probably benign |
0.03 |
R4999:Csmd2
|
UTSW |
4 |
128,415,723 (GRCm39) |
missense |
probably benign |
0.00 |
R5024:Csmd2
|
UTSW |
4 |
128,215,141 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5034:Csmd2
|
UTSW |
4 |
127,952,901 (GRCm39) |
missense |
probably damaging |
0.98 |
R5152:Csmd2
|
UTSW |
4 |
128,445,828 (GRCm39) |
missense |
probably benign |
0.27 |
R5172:Csmd2
|
UTSW |
4 |
128,371,190 (GRCm39) |
missense |
probably benign |
0.10 |
R5231:Csmd2
|
UTSW |
4 |
128,439,842 (GRCm39) |
missense |
probably benign |
0.00 |
R5279:Csmd2
|
UTSW |
4 |
128,350,707 (GRCm39) |
missense |
probably benign |
0.30 |
R5287:Csmd2
|
UTSW |
4 |
128,380,677 (GRCm39) |
missense |
probably benign |
0.01 |
R5403:Csmd2
|
UTSW |
4 |
128,380,677 (GRCm39) |
missense |
probably benign |
0.01 |
R5410:Csmd2
|
UTSW |
4 |
128,442,612 (GRCm39) |
missense |
probably benign |
|
R5551:Csmd2
|
UTSW |
4 |
128,404,741 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5826:Csmd2
|
UTSW |
4 |
128,412,992 (GRCm39) |
splice site |
probably null |
|
R5907:Csmd2
|
UTSW |
4 |
128,091,178 (GRCm39) |
missense |
probably damaging |
0.99 |
R5913:Csmd2
|
UTSW |
4 |
128,445,781 (GRCm39) |
missense |
probably benign |
0.01 |
R5970:Csmd2
|
UTSW |
4 |
128,439,944 (GRCm39) |
missense |
probably benign |
0.00 |
R5977:Csmd2
|
UTSW |
4 |
127,952,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R6027:Csmd2
|
UTSW |
4 |
128,453,739 (GRCm39) |
missense |
unknown |
|
R6075:Csmd2
|
UTSW |
4 |
128,380,658 (GRCm39) |
missense |
probably benign |
0.15 |
R6129:Csmd2
|
UTSW |
4 |
128,387,127 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6363:Csmd2
|
UTSW |
4 |
128,294,172 (GRCm39) |
missense |
probably benign |
0.00 |
R6366:Csmd2
|
UTSW |
4 |
128,377,245 (GRCm39) |
missense |
probably benign |
0.00 |
R6404:Csmd2
|
UTSW |
4 |
128,415,743 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6437:Csmd2
|
UTSW |
4 |
127,881,893 (GRCm39) |
missense |
probably benign |
0.24 |
R6441:Csmd2
|
UTSW |
4 |
128,288,757 (GRCm39) |
missense |
probably benign |
0.03 |
R6643:Csmd2
|
UTSW |
4 |
128,266,390 (GRCm39) |
missense |
probably benign |
0.14 |
R6724:Csmd2
|
UTSW |
4 |
128,457,164 (GRCm39) |
missense |
probably damaging |
0.97 |
R6734:Csmd2
|
UTSW |
4 |
128,357,606 (GRCm39) |
missense |
probably benign |
0.00 |
R6750:Csmd2
|
UTSW |
4 |
128,091,018 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6801:Csmd2
|
UTSW |
4 |
128,277,743 (GRCm39) |
missense |
probably benign |
0.11 |
R6842:Csmd2
|
UTSW |
4 |
128,402,952 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6843:Csmd2
|
UTSW |
4 |
128,357,587 (GRCm39) |
missense |
probably benign |
0.27 |
R6868:Csmd2
|
UTSW |
4 |
128,336,633 (GRCm39) |
missense |
probably benign |
|
R6882:Csmd2
|
UTSW |
4 |
128,343,062 (GRCm39) |
missense |
probably benign |
0.01 |
R7019:Csmd2
|
UTSW |
4 |
128,262,856 (GRCm39) |
missense |
|
|
R7028:Csmd2
|
UTSW |
4 |
128,171,021 (GRCm39) |
missense |
|
|
R7096:Csmd2
|
UTSW |
4 |
128,356,519 (GRCm39) |
missense |
|
|
R7122:Csmd2
|
UTSW |
4 |
128,343,020 (GRCm39) |
missense |
|
|
R7125:Csmd2
|
UTSW |
4 |
128,389,955 (GRCm39) |
missense |
|
|
R7197:Csmd2
|
UTSW |
4 |
128,404,826 (GRCm39) |
missense |
|
|
R7234:Csmd2
|
UTSW |
4 |
128,350,572 (GRCm39) |
missense |
|
|
R7299:Csmd2
|
UTSW |
4 |
128,422,055 (GRCm39) |
missense |
|
|
R7301:Csmd2
|
UTSW |
4 |
128,422,055 (GRCm39) |
missense |
|
|
R7319:Csmd2
|
UTSW |
4 |
128,287,472 (GRCm39) |
missense |
|
|
R7331:Csmd2
|
UTSW |
4 |
128,458,021 (GRCm39) |
splice site |
probably null |
|
R7332:Csmd2
|
UTSW |
4 |
128,313,360 (GRCm39) |
missense |
|
|
R7352:Csmd2
|
UTSW |
4 |
128,451,429 (GRCm39) |
missense |
|
|
R7402:Csmd2
|
UTSW |
4 |
128,215,889 (GRCm39) |
missense |
|
|
R7402:Csmd2
|
UTSW |
4 |
128,215,888 (GRCm39) |
missense |
|
|
R7474:Csmd2
|
UTSW |
4 |
128,439,920 (GRCm39) |
missense |
|
|
R7555:Csmd2
|
UTSW |
4 |
128,346,251 (GRCm39) |
missense |
|
|
R7592:Csmd2
|
UTSW |
4 |
128,357,591 (GRCm39) |
missense |
|
|
R7700:Csmd2
|
UTSW |
4 |
128,439,549 (GRCm39) |
splice site |
probably null |
|
R7714:Csmd2
|
UTSW |
4 |
128,276,743 (GRCm39) |
nonsense |
probably null |
|
R7734:Csmd2
|
UTSW |
4 |
128,445,850 (GRCm39) |
missense |
|
|
R7735:Csmd2
|
UTSW |
4 |
128,350,723 (GRCm39) |
critical splice donor site |
probably null |
|
R7757:Csmd2
|
UTSW |
4 |
128,377,249 (GRCm39) |
missense |
|
|
R7805:Csmd2
|
UTSW |
4 |
128,313,366 (GRCm39) |
missense |
|
|
R7823:Csmd2
|
UTSW |
4 |
128,103,698 (GRCm39) |
missense |
|
|
R7904:Csmd2
|
UTSW |
4 |
128,313,346 (GRCm39) |
missense |
|
|
R7946:Csmd2
|
UTSW |
4 |
128,414,058 (GRCm39) |
missense |
|
|
R7964:Csmd2
|
UTSW |
4 |
128,417,303 (GRCm39) |
missense |
|
|
R7968:Csmd2
|
UTSW |
4 |
128,091,118 (GRCm39) |
missense |
|
|
R8003:Csmd2
|
UTSW |
4 |
128,432,980 (GRCm39) |
nonsense |
probably null |
|
R8071:Csmd2
|
UTSW |
4 |
128,287,331 (GRCm39) |
missense |
|
|
R8504:Csmd2
|
UTSW |
4 |
128,440,483 (GRCm39) |
missense |
|
|
R8511:Csmd2
|
UTSW |
4 |
128,262,692 (GRCm39) |
missense |
|
|
R8517:Csmd2
|
UTSW |
4 |
128,446,479 (GRCm39) |
missense |
|
|
R8704:Csmd2
|
UTSW |
4 |
128,091,147 (GRCm39) |
missense |
|
|
R8722:Csmd2
|
UTSW |
4 |
128,445,743 (GRCm39) |
unclassified |
probably benign |
|
R8729:Csmd2
|
UTSW |
4 |
128,356,638 (GRCm39) |
missense |
|
|
R8801:Csmd2
|
UTSW |
4 |
128,457,195 (GRCm39) |
missense |
probably damaging |
0.97 |
R8803:Csmd2
|
UTSW |
4 |
128,440,477 (GRCm39) |
missense |
|
|
R8839:Csmd2
|
UTSW |
4 |
128,336,681 (GRCm39) |
missense |
|
|
R8867:Csmd2
|
UTSW |
4 |
128,451,469 (GRCm39) |
missense |
|
|
R8913:Csmd2
|
UTSW |
4 |
128,417,351 (GRCm39) |
missense |
|
|
R8928:Csmd2
|
UTSW |
4 |
128,369,582 (GRCm39) |
missense |
|
|
R8974:Csmd2
|
UTSW |
4 |
128,446,380 (GRCm39) |
missense |
|
|
R9001:Csmd2
|
UTSW |
4 |
128,308,079 (GRCm39) |
missense |
|
|
R9132:Csmd2
|
UTSW |
4 |
128,443,007 (GRCm39) |
missense |
|
|
R9245:Csmd2
|
UTSW |
4 |
128,200,168 (GRCm39) |
missense |
|
|
R9249:Csmd2
|
UTSW |
4 |
128,313,323 (GRCm39) |
nonsense |
probably null |
|
R9254:Csmd2
|
UTSW |
4 |
128,091,112 (GRCm39) |
missense |
|
|
R9265:Csmd2
|
UTSW |
4 |
128,294,163 (GRCm39) |
missense |
|
|
R9407:Csmd2
|
UTSW |
4 |
128,442,613 (GRCm39) |
missense |
|
|
R9432:Csmd2
|
UTSW |
4 |
128,171,004 (GRCm39) |
missense |
|
|
R9559:Csmd2
|
UTSW |
4 |
128,438,561 (GRCm39) |
missense |
|
|
R9673:Csmd2
|
UTSW |
4 |
128,308,062 (GRCm39) |
missense |
|
|
R9735:Csmd2
|
UTSW |
4 |
128,402,901 (GRCm39) |
missense |
|
|
R9749:Csmd2
|
UTSW |
4 |
128,389,921 (GRCm39) |
missense |
|
|
R9803:Csmd2
|
UTSW |
4 |
128,262,986 (GRCm39) |
missense |
|
|
Z1177:Csmd2
|
UTSW |
4 |
128,424,590 (GRCm39) |
missense |
|
|
|