Other mutations in this stock |
Total: 120 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430550D23Rik |
A |
G |
2: 155,845,309 (GRCm39) |
S32P |
possibly damaging |
Het |
Acaca |
T |
C |
11: 84,136,136 (GRCm39) |
V497A |
probably benign |
Het |
Acox1 |
T |
C |
11: 116,071,787 (GRCm39) |
T214A |
probably benign |
Het |
Adgrb2 |
G |
A |
4: 129,908,430 (GRCm39) |
|
probably null |
Het |
Adh1 |
G |
A |
3: 137,995,702 (GRCm39) |
|
probably null |
Het |
Angptl1 |
G |
T |
1: 156,672,421 (GRCm39) |
M82I |
probably benign |
Het |
Arg1 |
A |
G |
10: 24,791,674 (GRCm39) |
L269P |
probably damaging |
Het |
Arid2 |
T |
G |
15: 96,268,605 (GRCm39) |
V906G |
probably benign |
Het |
Arid5b |
A |
T |
10: 68,078,994 (GRCm39) |
H114Q |
probably benign |
Het |
Atad5 |
T |
C |
11: 80,009,969 (GRCm39) |
|
probably null |
Het |
AU040320 |
G |
A |
4: 126,729,493 (GRCm39) |
|
probably null |
Het |
B230104I21Rik |
A |
T |
4: 154,432,185 (GRCm39) |
T44S |
unknown |
Het |
BC024063 |
G |
A |
10: 81,945,991 (GRCm39) |
R537H |
possibly damaging |
Het |
Bfsp2 |
A |
T |
9: 103,330,306 (GRCm39) |
L177Q |
probably damaging |
Het |
Birc5 |
C |
A |
11: 117,743,507 (GRCm39) |
H80Q |
probably damaging |
Het |
Bpifb9a |
T |
C |
2: 154,106,615 (GRCm39) |
L382P |
probably damaging |
Het |
Ces2c |
A |
T |
8: 105,576,302 (GRCm39) |
N105I |
probably benign |
Het |
Cfap91 |
A |
G |
16: 38,141,841 (GRCm39) |
S364P |
possibly damaging |
Het |
Cflar |
G |
A |
1: 58,792,956 (GRCm39) |
V441M |
|
Het |
Ckap4 |
A |
G |
10: 84,364,463 (GRCm39) |
V200A |
probably damaging |
Het |
Clec16a |
C |
A |
16: 10,462,686 (GRCm39) |
T668N |
probably damaging |
Het |
Cntrl |
A |
C |
2: 35,045,421 (GRCm39) |
E1376D |
possibly damaging |
Het |
Coq2 |
T |
C |
5: 100,811,452 (GRCm39) |
Y179C |
probably benign |
Het |
Cpne6 |
A |
G |
14: 55,749,473 (GRCm39) |
E11G |
probably benign |
Het |
Cr2 |
A |
C |
1: 194,847,565 (GRCm39) |
|
probably null |
Het |
Csf2rb2 |
C |
T |
15: 78,169,491 (GRCm39) |
D555N |
probably benign |
Het |
Cyp2j12 |
A |
T |
4: 95,990,363 (GRCm39) |
V401D |
possibly damaging |
Het |
Dbp |
C |
T |
7: 45,355,127 (GRCm39) |
A27V |
probably benign |
Het |
Dll1 |
C |
A |
17: 15,595,151 (GRCm39) |
R42L |
probably benign |
Het |
Dst |
C |
A |
1: 34,230,439 (GRCm39) |
H2677Q |
possibly damaging |
Het |
Efl1 |
G |
T |
7: 82,330,675 (GRCm39) |
V283F |
possibly damaging |
Het |
Enah |
C |
T |
1: 181,789,470 (GRCm39) |
C7Y |
unknown |
Het |
Fam193a |
A |
T |
5: 34,621,460 (GRCm39) |
E1139V |
possibly damaging |
Het |
Fbn1 |
G |
A |
2: 125,162,879 (GRCm39) |
P2136S |
possibly damaging |
Het |
Fggy |
T |
C |
4: 95,485,927 (GRCm39) |
V91A |
probably damaging |
Het |
Fn1 |
T |
A |
1: 71,630,039 (GRCm39) |
D2343V |
probably damaging |
Het |
Galk2 |
T |
C |
2: 125,729,781 (GRCm39) |
V54A |
possibly damaging |
Het |
Glb1l |
T |
A |
1: 75,179,350 (GRCm39) |
Y193F |
probably damaging |
Het |
Gm45861 |
G |
T |
8: 28,031,686 (GRCm39) |
R867L |
unknown |
Het |
Grin2b |
T |
C |
6: 135,717,947 (GRCm39) |
D715G |
possibly damaging |
Het |
Hltf |
A |
T |
3: 20,136,916 (GRCm39) |
R384S |
possibly damaging |
Het |
Hs3st1 |
A |
G |
5: 39,772,310 (GRCm39) |
M111T |
probably damaging |
Het |
Idua |
A |
G |
5: 108,829,362 (GRCm39) |
T388A |
probably benign |
Het |
Kat14 |
T |
C |
2: 144,222,654 (GRCm39) |
S136P |
possibly damaging |
Het |
Kif24 |
A |
C |
4: 41,394,673 (GRCm39) |
C867W |
possibly damaging |
Het |
Klhdc10 |
T |
A |
6: 30,447,989 (GRCm39) |
|
probably null |
Het |
Klra10 |
A |
G |
6: 130,257,327 (GRCm39) |
V59A |
probably damaging |
Het |
Limk1 |
T |
A |
5: 134,698,091 (GRCm39) |
I223F |
probably damaging |
Het |
Lrp10 |
G |
A |
14: 54,705,913 (GRCm39) |
G368S |
probably damaging |
Het |
Lrrc7 |
T |
C |
3: 157,891,046 (GRCm39) |
R374G |
probably benign |
Het |
Lypd1 |
T |
A |
1: 125,801,303 (GRCm39) |
M66L |
probably benign |
Het |
Mast4 |
C |
T |
13: 102,941,149 (GRCm39) |
|
probably null |
Het |
Mbp |
C |
T |
18: 82,572,768 (GRCm39) |
H155Y |
probably damaging |
Het |
Micu3 |
G |
A |
8: 40,788,939 (GRCm39) |
C150Y |
probably benign |
Het |
Mras |
C |
T |
9: 99,271,793 (GRCm39) |
V174I |
probably benign |
Het |
Mroh1 |
T |
A |
15: 76,317,745 (GRCm39) |
I827N |
probably damaging |
Het |
Ms4a12 |
C |
A |
19: 11,203,026 (GRCm39) |
G101* |
probably null |
Het |
Mylk2 |
A |
T |
2: 152,754,353 (GRCm39) |
K149M |
probably damaging |
Het |
Myom3 |
T |
A |
4: 135,528,346 (GRCm39) |
L1064I |
probably damaging |
Het |
Naa30 |
A |
G |
14: 49,425,144 (GRCm39) |
*365W |
probably null |
Het |
Ncoa1 |
C |
T |
12: 4,309,307 (GRCm39) |
G1330R |
probably damaging |
Het |
Nhlh1 |
T |
A |
1: 171,881,846 (GRCm39) |
T7S |
probably benign |
Het |
Nipsnap3a |
A |
G |
4: 52,995,882 (GRCm39) |
Q110R |
probably benign |
Het |
Nostrin |
T |
C |
2: 69,014,240 (GRCm39) |
Y399H |
possibly damaging |
Het |
Nsfl1c |
C |
A |
2: 151,351,431 (GRCm39) |
T263K |
possibly damaging |
Het |
Nup153 |
T |
C |
13: 46,834,657 (GRCm39) |
T1456A |
probably damaging |
Het |
Or14j10 |
G |
T |
17: 37,935,276 (GRCm39) |
D83E |
probably benign |
Het |
Or1o2 |
T |
C |
17: 37,542,871 (GRCm39) |
Y130C |
probably damaging |
Het |
Or51e1 |
T |
A |
7: 102,358,724 (GRCm39) |
I86N |
probably damaging |
Het |
Or52z1 |
T |
A |
7: 103,436,879 (GRCm39) |
I202F |
possibly damaging |
Het |
Or5g26 |
T |
A |
2: 85,494,524 (GRCm39) |
M85L |
probably benign |
Het |
Or8d1b |
A |
T |
9: 38,887,500 (GRCm39) |
H176L |
probably damaging |
Het |
Pan3 |
G |
A |
5: 147,463,491 (GRCm39) |
|
probably null |
Het |
Pcdhgb2 |
C |
T |
18: 37,824,068 (GRCm39) |
T353I |
probably damaging |
Het |
Pcif1 |
A |
T |
2: 164,730,284 (GRCm39) |
H339L |
probably damaging |
Het |
Pcif1 |
A |
G |
2: 164,731,550 (GRCm39) |
H501R |
possibly damaging |
Het |
Pcnt |
T |
C |
10: 76,225,284 (GRCm39) |
H1740R |
probably benign |
Het |
Polr1b |
T |
A |
2: 128,967,583 (GRCm39) |
I992N |
probably damaging |
Het |
Ppfia2 |
C |
T |
10: 106,763,691 (GRCm39) |
T1228M |
possibly damaging |
Het |
Ppp2r5e |
A |
G |
12: 75,509,116 (GRCm39) |
F388L |
probably damaging |
Het |
Ptpre |
G |
T |
7: 135,139,803 (GRCm39) |
R4L |
unknown |
Het |
Pzp |
G |
T |
6: 128,463,879 (GRCm39) |
P1410T |
probably damaging |
Het |
Qrich1 |
A |
C |
9: 108,433,675 (GRCm39) |
K656T |
possibly damaging |
Het |
Rabep1 |
C |
T |
11: 70,808,486 (GRCm39) |
P481S |
probably damaging |
Het |
Rgs9 |
T |
A |
11: 109,118,094 (GRCm39) |
R579W |
probably damaging |
Het |
Rhot1 |
T |
C |
11: 80,139,366 (GRCm39) |
|
probably null |
Het |
Rnf123 |
T |
A |
9: 107,947,607 (GRCm39) |
|
probably null |
Het |
Rreb1 |
T |
G |
13: 38,125,545 (GRCm39) |
C1284G |
probably damaging |
Het |
Rsph4a |
A |
G |
10: 33,785,289 (GRCm39) |
E400G |
probably benign |
Het |
Rufy4 |
T |
A |
1: 74,168,493 (GRCm39) |
|
probably null |
Het |
S100pbp |
A |
G |
4: 129,075,878 (GRCm39) |
L149P |
probably damaging |
Het |
Sall3 |
T |
C |
18: 81,015,255 (GRCm39) |
D891G |
probably benign |
Het |
Scn10a |
C |
T |
9: 119,467,618 (GRCm39) |
V841I |
probably benign |
Het |
Scn5a |
T |
A |
9: 119,351,656 (GRCm39) |
Y775F |
possibly damaging |
Het |
Sec62 |
A |
T |
3: 30,863,945 (GRCm39) |
|
probably null |
Het |
Slc24a1 |
A |
T |
9: 64,856,583 (GRCm39) |
M108K |
unknown |
Het |
Spata22 |
T |
A |
11: 73,226,816 (GRCm39) |
|
probably null |
Het |
Spmap2l |
A |
G |
5: 77,208,633 (GRCm39) |
H387R |
probably damaging |
Het |
Stk4 |
A |
G |
2: 163,928,522 (GRCm39) |
N118S |
probably benign |
Het |
Stt3a |
A |
T |
9: 36,659,266 (GRCm39) |
S358T |
possibly damaging |
Het |
Tbc1d31 |
T |
A |
15: 57,814,391 (GRCm39) |
F531I |
probably damaging |
Het |
Tfrc |
A |
G |
16: 32,437,867 (GRCm39) |
T307A |
probably damaging |
Het |
Tnpo2 |
T |
C |
8: 85,781,651 (GRCm39) |
I811T |
probably damaging |
Het |
Ttc23l |
T |
C |
15: 10,533,853 (GRCm39) |
Y230C |
probably damaging |
Het |
Ttll13 |
A |
G |
7: 79,910,182 (GRCm39) |
D775G |
probably benign |
Het |
Ttn |
T |
C |
2: 76,775,273 (GRCm39) |
K1969R |
unknown |
Het |
Ube2s |
G |
A |
7: 4,813,435 (GRCm39) |
R110* |
probably null |
Het |
Ubxn11 |
G |
A |
4: 133,853,540 (GRCm39) |
R364Q |
probably benign |
Het |
Unc13d |
T |
C |
11: 115,958,697 (GRCm39) |
Q773R |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,285,308 (GRCm39) |
V1948A |
probably damaging |
Het |
Vmn1r205 |
A |
T |
13: 22,776,931 (GRCm39) |
I57N |
probably damaging |
Het |
Vmn2r69 |
GAAAA |
GAAAAA |
7: 85,060,768 (GRCm39) |
|
probably null |
Het |
Vmn2r71 |
A |
T |
7: 85,273,297 (GRCm39) |
T704S |
probably benign |
Het |
Vmn2r93 |
T |
A |
17: 18,533,580 (GRCm39) |
S495T |
probably benign |
Het |
Wiz |
T |
A |
17: 32,598,049 (GRCm39) |
I102F |
probably benign |
Het |
Zan |
A |
C |
5: 137,464,264 (GRCm39) |
L514V |
probably damaging |
Het |
Zfp106 |
T |
A |
2: 120,341,008 (GRCm39) |
N1857I |
probably damaging |
Het |
Zfp106 |
A |
T |
2: 120,376,400 (GRCm39) |
|
probably null |
Het |
Zfp738 |
T |
C |
13: 67,818,474 (GRCm39) |
T506A |
probably benign |
Het |
Zfp934 |
T |
C |
13: 62,666,517 (GRCm39) |
N53S |
probably benign |
Het |
|
Other mutations in Col18a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00952:Col18a1
|
APN |
10 |
76,905,813 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01023:Col18a1
|
APN |
10 |
76,906,809 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01304:Col18a1
|
APN |
10 |
76,911,975 (GRCm39) |
unclassified |
probably benign |
|
IGL01519:Col18a1
|
APN |
10 |
76,895,157 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02217:Col18a1
|
APN |
10 |
76,889,132 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02275:Col18a1
|
APN |
10 |
76,895,217 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02283:Col18a1
|
APN |
10 |
76,948,943 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02492:Col18a1
|
APN |
10 |
76,907,855 (GRCm39) |
splice site |
probably benign |
|
IGL02673:Col18a1
|
APN |
10 |
76,894,997 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02710:Col18a1
|
APN |
10 |
76,949,146 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02850:Col18a1
|
APN |
10 |
76,932,300 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03085:Col18a1
|
APN |
10 |
76,895,015 (GRCm39) |
splice site |
probably benign |
|
IGL03102:Col18a1
|
APN |
10 |
76,903,457 (GRCm39) |
splice site |
probably benign |
|
IGL03139:Col18a1
|
APN |
10 |
76,949,177 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03181:Col18a1
|
APN |
10 |
76,891,532 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03183:Col18a1
|
APN |
10 |
76,909,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R0039:Col18a1
|
UTSW |
10 |
76,913,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R0180:Col18a1
|
UTSW |
10 |
76,932,351 (GRCm39) |
missense |
probably benign |
0.33 |
R0225:Col18a1
|
UTSW |
10 |
76,924,748 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0335:Col18a1
|
UTSW |
10 |
76,895,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R0336:Col18a1
|
UTSW |
10 |
76,894,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Col18a1
|
UTSW |
10 |
76,932,040 (GRCm39) |
missense |
unknown |
|
R1538:Col18a1
|
UTSW |
10 |
76,907,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1594:Col18a1
|
UTSW |
10 |
76,948,870 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1631:Col18a1
|
UTSW |
10 |
76,895,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R1774:Col18a1
|
UTSW |
10 |
76,895,815 (GRCm39) |
missense |
probably damaging |
0.96 |
R1934:Col18a1
|
UTSW |
10 |
76,948,578 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1990:Col18a1
|
UTSW |
10 |
76,916,988 (GRCm39) |
missense |
unknown |
|
R1991:Col18a1
|
UTSW |
10 |
76,916,988 (GRCm39) |
missense |
unknown |
|
R1992:Col18a1
|
UTSW |
10 |
76,916,988 (GRCm39) |
missense |
unknown |
|
R2081:Col18a1
|
UTSW |
10 |
76,890,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R2082:Col18a1
|
UTSW |
10 |
76,895,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R2351:Col18a1
|
UTSW |
10 |
76,948,538 (GRCm39) |
missense |
probably benign |
0.00 |
R2510:Col18a1
|
UTSW |
10 |
76,932,102 (GRCm39) |
missense |
unknown |
|
R3076:Col18a1
|
UTSW |
10 |
76,924,762 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3433:Col18a1
|
UTSW |
10 |
76,932,102 (GRCm39) |
missense |
unknown |
|
R3800:Col18a1
|
UTSW |
10 |
76,903,221 (GRCm39) |
nonsense |
probably null |
|
R3918:Col18a1
|
UTSW |
10 |
76,889,192 (GRCm39) |
missense |
probably benign |
0.05 |
R3981:Col18a1
|
UTSW |
10 |
76,924,721 (GRCm39) |
missense |
probably damaging |
0.99 |
R3983:Col18a1
|
UTSW |
10 |
76,924,721 (GRCm39) |
missense |
probably damaging |
0.99 |
R4182:Col18a1
|
UTSW |
10 |
76,894,675 (GRCm39) |
splice site |
probably null |
|
R4239:Col18a1
|
UTSW |
10 |
76,932,001 (GRCm39) |
missense |
unknown |
|
R5014:Col18a1
|
UTSW |
10 |
76,906,794 (GRCm39) |
critical splice donor site |
probably null |
|
R5107:Col18a1
|
UTSW |
10 |
76,913,057 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5413:Col18a1
|
UTSW |
10 |
76,905,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R5503:Col18a1
|
UTSW |
10 |
76,907,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R5524:Col18a1
|
UTSW |
10 |
76,894,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Col18a1
|
UTSW |
10 |
77,002,177 (GRCm39) |
missense |
unknown |
|
R5958:Col18a1
|
UTSW |
10 |
76,932,231 (GRCm39) |
missense |
probably benign |
0.01 |
R6280:Col18a1
|
UTSW |
10 |
76,948,323 (GRCm39) |
intron |
probably benign |
|
R6309:Col18a1
|
UTSW |
10 |
76,948,576 (GRCm39) |
intron |
probably benign |
|
R6603:Col18a1
|
UTSW |
10 |
76,899,811 (GRCm39) |
critical splice donor site |
probably null |
|
R6608:Col18a1
|
UTSW |
10 |
76,948,628 (GRCm39) |
intron |
probably benign |
|
R6805:Col18a1
|
UTSW |
10 |
76,890,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R6890:Col18a1
|
UTSW |
10 |
76,949,318 (GRCm39) |
intron |
probably benign |
|
R6938:Col18a1
|
UTSW |
10 |
76,948,333 (GRCm39) |
intron |
probably benign |
|
R7002:Col18a1
|
UTSW |
10 |
77,002,177 (GRCm39) |
missense |
unknown |
|
R7154:Col18a1
|
UTSW |
10 |
76,908,799 (GRCm39) |
missense |
probably benign |
0.25 |
R7204:Col18a1
|
UTSW |
10 |
76,921,110 (GRCm39) |
missense |
unknown |
|
R7278:Col18a1
|
UTSW |
10 |
76,932,118 (GRCm39) |
missense |
unknown |
|
R7442:Col18a1
|
UTSW |
10 |
76,932,072 (GRCm39) |
missense |
unknown |
|
R7597:Col18a1
|
UTSW |
10 |
76,949,137 (GRCm39) |
missense |
unknown |
|
R7615:Col18a1
|
UTSW |
10 |
76,902,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R7671:Col18a1
|
UTSW |
10 |
76,921,217 (GRCm39) |
missense |
unknown |
|
R7696:Col18a1
|
UTSW |
10 |
76,921,106 (GRCm39) |
missense |
unknown |
|
R7719:Col18a1
|
UTSW |
10 |
76,913,846 (GRCm39) |
missense |
probably benign |
0.13 |
R7772:Col18a1
|
UTSW |
10 |
76,904,220 (GRCm39) |
splice site |
probably null |
|
R8077:Col18a1
|
UTSW |
10 |
76,916,685 (GRCm39) |
missense |
unknown |
|
R8085:Col18a1
|
UTSW |
10 |
76,924,741 (GRCm39) |
missense |
unknown |
|
R8097:Col18a1
|
UTSW |
10 |
76,948,342 (GRCm39) |
missense |
unknown |
|
R8117:Col18a1
|
UTSW |
10 |
76,895,808 (GRCm39) |
missense |
probably benign |
0.41 |
R8130:Col18a1
|
UTSW |
10 |
76,910,284 (GRCm39) |
missense |
probably benign |
0.03 |
R8151:Col18a1
|
UTSW |
10 |
76,948,418 (GRCm39) |
missense |
unknown |
|
R8379:Col18a1
|
UTSW |
10 |
76,889,072 (GRCm39) |
missense |
probably benign |
0.08 |
R8479:Col18a1
|
UTSW |
10 |
76,916,988 (GRCm39) |
missense |
unknown |
|
R8523:Col18a1
|
UTSW |
10 |
76,890,068 (GRCm39) |
missense |
probably damaging |
0.99 |
R8862:Col18a1
|
UTSW |
10 |
76,949,044 (GRCm39) |
nonsense |
probably null |
|
R9109:Col18a1
|
UTSW |
10 |
76,893,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R9298:Col18a1
|
UTSW |
10 |
76,893,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R9312:Col18a1
|
UTSW |
10 |
76,894,606 (GRCm39) |
missense |
probably damaging |
0.98 |
R9366:Col18a1
|
UTSW |
10 |
76,932,258 (GRCm39) |
missense |
unknown |
|
R9399:Col18a1
|
UTSW |
10 |
76,916,584 (GRCm39) |
missense |
unknown |
|
R9559:Col18a1
|
UTSW |
10 |
76,913,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R9649:Col18a1
|
UTSW |
10 |
76,916,673 (GRCm39) |
missense |
unknown |
|
R9689:Col18a1
|
UTSW |
10 |
76,916,578 (GRCm39) |
nonsense |
probably null |
|
R9719:Col18a1
|
UTSW |
10 |
76,949,432 (GRCm39) |
missense |
unknown |
|
Z1176:Col18a1
|
UTSW |
10 |
76,948,685 (GRCm39) |
missense |
unknown |
|
Z1176:Col18a1
|
UTSW |
10 |
76,891,543 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1177:Col18a1
|
UTSW |
10 |
76,948,672 (GRCm39) |
missense |
unknown |
|
|