Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
C |
T |
1: 130,743,772 (GRCm38) |
P577L |
probably damaging |
Het |
Aff3 |
A |
T |
1: 38,209,570 (GRCm38) |
S819T |
probably damaging |
Het |
Aftph |
G |
T |
11: 20,726,982 (GRCm38) |
S209* |
probably null |
Het |
Astn1 |
T |
A |
1: 158,612,395 (GRCm38) |
D844E |
probably benign |
Het |
Cc2d2a |
A |
G |
5: 43,671,266 (GRCm38) |
K29E |
probably benign |
Het |
Ccdc93 |
T |
C |
1: 121,463,117 (GRCm38) |
S273P |
possibly damaging |
Het |
Cd200r3 |
C |
A |
16: 44,943,776 (GRCm38) |
H2N |
probably benign |
Het |
Cd200r3 |
G |
T |
16: 44,943,775 (GRCm38) |
M1I |
probably null |
Het |
Col7a1 |
G |
A |
9: 108,974,956 (GRCm38) |
|
probably null |
Het |
Cyp3a41a |
T |
A |
5: 145,705,830 (GRCm38) |
M240L |
probably benign |
Het |
D430042O09Rik |
A |
T |
7: 125,851,960 (GRCm38) |
I1088F |
probably damaging |
Het |
Dcstamp |
T |
C |
15: 39,754,510 (GRCm38) |
V105A |
possibly damaging |
Het |
Dmbt1 |
C |
A |
7: 131,082,679 (GRCm38) |
P635Q |
probably benign |
Het |
Dsg1a |
T |
A |
18: 20,336,819 (GRCm38) |
M634K |
probably benign |
Het |
Farp2 |
T |
C |
1: 93,567,418 (GRCm38) |
Y138H |
probably damaging |
Het |
Fga |
T |
C |
3: 83,032,730 (GRCm38) |
S564P |
probably damaging |
Het |
Gbf1 |
T |
C |
19: 46,255,655 (GRCm38) |
L142S |
probably damaging |
Het |
Gm5422 |
T |
C |
10: 31,250,844 (GRCm38) |
|
noncoding transcript |
Het |
Helz2 |
A |
G |
2: 181,240,253 (GRCm38) |
V249A |
probably damaging |
Het |
Ift81 |
T |
C |
5: 122,594,662 (GRCm38) |
I270V |
probably benign |
Het |
Kif6 |
C |
T |
17: 49,753,871 (GRCm38) |
R411* |
probably null |
Het |
Klhl35 |
T |
A |
7: 99,470,343 (GRCm38) |
V345D |
probably damaging |
Het |
Mcm3ap |
C |
A |
10: 76,504,697 (GRCm38) |
D1531E |
probably benign |
Het |
Muc5b |
C |
A |
7: 141,863,614 (GRCm38) |
D3432E |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,350,314 (GRCm38) |
V998D |
probably damaging |
Het |
Nlrc3 |
C |
A |
16: 3,964,862 (GRCm38) |
V228L |
probably benign |
Het |
Nrap |
T |
C |
19: 56,321,952 (GRCm38) |
H1456R |
probably damaging |
Het |
Nt5c1b |
C |
T |
12: 10,374,910 (GRCm38) |
A210V |
possibly damaging |
Het |
Olfr364-ps1 |
T |
C |
2: 37,146,452 (GRCm38) |
V80A |
probably benign |
Het |
Olfr46 |
A |
G |
7: 140,610,370 (GRCm38) |
Y60C |
probably damaging |
Het |
Osbpl7 |
T |
C |
11: 97,050,695 (GRCm38) |
Y15H |
probably benign |
Het |
Pde8b |
T |
A |
13: 95,041,957 (GRCm38) |
N552Y |
probably damaging |
Het |
Pi4kb |
T |
A |
3: 94,984,812 (GRCm38) |
S280T |
probably benign |
Het |
Pkd1 |
T |
A |
17: 24,593,603 (GRCm38) |
|
probably null |
Het |
Polh |
A |
T |
17: 46,194,366 (GRCm38) |
V108E |
possibly damaging |
Het |
Prob1 |
A |
G |
18: 35,653,375 (GRCm38) |
S609P |
possibly damaging |
Het |
Ptprz1 |
T |
A |
6: 23,002,583 (GRCm38) |
N1557K |
probably damaging |
Het |
Rev1 |
A |
C |
1: 38,088,073 (GRCm38) |
F369V |
possibly damaging |
Het |
Rgma |
A |
G |
7: 73,417,440 (GRCm38) |
N148D |
probably damaging |
Het |
Robo3 |
A |
G |
9: 37,419,291 (GRCm38) |
L1003S |
probably damaging |
Het |
Sdhb |
T |
C |
4: 140,973,000 (GRCm38) |
V137A |
probably damaging |
Het |
Sema6c |
T |
C |
3: 95,169,614 (GRCm38) |
L337P |
probably damaging |
Het |
Shc4 |
A |
T |
2: 125,723,333 (GRCm38) |
Y15* |
probably null |
Het |
Slc4a9 |
T |
C |
18: 36,536,893 (GRCm38) |
S722P |
probably damaging |
Het |
Smarcc1 |
A |
G |
9: 110,206,100 (GRCm38) |
N864D |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,455,087 (GRCm38) |
L745P |
probably damaging |
Het |
Syce1l |
A |
G |
8: 113,654,067 (GRCm38) |
D137G |
probably damaging |
Het |
Tbc1d1 |
G |
T |
5: 64,316,438 (GRCm38) |
W768L |
probably damaging |
Het |
Tmbim7 |
A |
G |
5: 3,661,887 (GRCm38) |
D7G |
probably benign |
Het |
Tmem109 |
A |
C |
19: 10,874,331 (GRCm38) |
S64A |
probably benign |
Het |
Tnfrsf21 |
A |
G |
17: 43,039,943 (GRCm38) |
R333G |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,781,611 (GRCm38) |
S17316R |
probably damaging |
Het |
Usp10 |
A |
G |
8: 119,954,810 (GRCm38) |
T668A |
possibly damaging |
Het |
Xirp2 |
T |
A |
2: 67,515,562 (GRCm38) |
F2716I |
possibly damaging |
Het |
|
Other mutations in Hmcn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00965:Hmcn2
|
APN |
2 |
31,343,096 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00966:Hmcn2
|
APN |
2 |
31,428,994 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL00973:Hmcn2
|
APN |
2 |
31,383,821 (GRCm38) |
intron |
probably benign |
|
IGL01364:Hmcn2
|
APN |
2 |
31,361,814 (GRCm38) |
nonsense |
probably null |
|
IGL01486:Hmcn2
|
APN |
2 |
31,336,621 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01530:Hmcn2
|
APN |
2 |
31,354,264 (GRCm38) |
missense |
possibly damaging |
0.85 |
IGL01550:Hmcn2
|
APN |
2 |
31,424,252 (GRCm38) |
missense |
possibly damaging |
0.84 |
IGL01710:Hmcn2
|
APN |
2 |
31,343,102 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01764:Hmcn2
|
APN |
2 |
31,405,630 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL01924:Hmcn2
|
APN |
2 |
31,398,917 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02003:Hmcn2
|
APN |
2 |
31,428,982 (GRCm38) |
missense |
possibly damaging |
0.90 |
IGL02117:Hmcn2
|
APN |
2 |
31,457,173 (GRCm38) |
missense |
possibly damaging |
0.75 |
IGL02205:Hmcn2
|
APN |
2 |
31,400,127 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02273:Hmcn2
|
APN |
2 |
31,424,377 (GRCm38) |
missense |
probably benign |
0.06 |
IGL02313:Hmcn2
|
APN |
2 |
31,453,605 (GRCm38) |
missense |
possibly damaging |
0.68 |
IGL02326:Hmcn2
|
APN |
2 |
31,450,952 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02486:Hmcn2
|
APN |
2 |
31,420,095 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02551:Hmcn2
|
APN |
2 |
31,454,811 (GRCm38) |
missense |
possibly damaging |
0.83 |
IGL02695:Hmcn2
|
APN |
2 |
31,408,973 (GRCm38) |
missense |
possibly damaging |
0.87 |
IGL02725:Hmcn2
|
APN |
2 |
31,405,528 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02792:Hmcn2
|
APN |
2 |
31,346,590 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02882:Hmcn2
|
APN |
2 |
31,413,367 (GRCm38) |
nonsense |
probably null |
|
IGL03067:Hmcn2
|
APN |
2 |
31,346,630 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03137:Hmcn2
|
APN |
2 |
31,362,230 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL03220:Hmcn2
|
APN |
2 |
31,346,621 (GRCm38) |
missense |
possibly damaging |
0.94 |
IGL03411:Hmcn2
|
APN |
2 |
31,346,637 (GRCm38) |
missense |
possibly damaging |
0.83 |
PIT4544001:Hmcn2
|
UTSW |
2 |
31,428,250 (GRCm38) |
missense |
probably damaging |
0.98 |
R0044:Hmcn2
|
UTSW |
2 |
31,412,508 (GRCm38) |
missense |
probably damaging |
0.98 |
R0044:Hmcn2
|
UTSW |
2 |
31,412,508 (GRCm38) |
missense |
probably damaging |
0.98 |
R0048:Hmcn2
|
UTSW |
2 |
31,428,237 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0048:Hmcn2
|
UTSW |
2 |
31,428,237 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0078:Hmcn2
|
UTSW |
2 |
31,388,344 (GRCm38) |
missense |
probably damaging |
1.00 |
R0090:Hmcn2
|
UTSW |
2 |
31,426,198 (GRCm38) |
missense |
probably damaging |
1.00 |
R0173:Hmcn2
|
UTSW |
2 |
31,438,331 (GRCm38) |
critical splice donor site |
probably null |
|
R0257:Hmcn2
|
UTSW |
2 |
31,369,164 (GRCm38) |
splice site |
probably benign |
|
R0266:Hmcn2
|
UTSW |
2 |
31,445,353 (GRCm38) |
splice site |
probably benign |
|
R0266:Hmcn2
|
UTSW |
2 |
31,394,827 (GRCm38) |
missense |
probably benign |
0.03 |
R0326:Hmcn2
|
UTSW |
2 |
31,423,225 (GRCm38) |
nonsense |
probably null |
|
R0366:Hmcn2
|
UTSW |
2 |
31,424,206 (GRCm38) |
missense |
possibly damaging |
0.88 |
R0400:Hmcn2
|
UTSW |
2 |
31,400,129 (GRCm38) |
missense |
probably damaging |
0.98 |
R0412:Hmcn2
|
UTSW |
2 |
31,388,247 (GRCm38) |
missense |
probably damaging |
0.98 |
R0436:Hmcn2
|
UTSW |
2 |
31,405,612 (GRCm38) |
missense |
probably damaging |
1.00 |
R0457:Hmcn2
|
UTSW |
2 |
31,415,284 (GRCm38) |
critical splice donor site |
probably null |
|
R0487:Hmcn2
|
UTSW |
2 |
31,386,677 (GRCm38) |
missense |
possibly damaging |
0.60 |
R0568:Hmcn2
|
UTSW |
2 |
31,415,236 (GRCm38) |
missense |
probably benign |
0.02 |
R0755:Hmcn2
|
UTSW |
2 |
31,453,160 (GRCm38) |
missense |
probably damaging |
0.99 |
R0811:Hmcn2
|
UTSW |
2 |
31,420,371 (GRCm38) |
missense |
probably damaging |
0.99 |
R0812:Hmcn2
|
UTSW |
2 |
31,420,371 (GRCm38) |
missense |
probably damaging |
0.99 |
R0964:Hmcn2
|
UTSW |
2 |
31,391,511 (GRCm38) |
missense |
probably benign |
0.23 |
R0988:Hmcn2
|
UTSW |
2 |
31,335,451 (GRCm38) |
missense |
probably damaging |
1.00 |
R1484:Hmcn2
|
UTSW |
2 |
31,346,495 (GRCm38) |
missense |
probably damaging |
1.00 |
R1509:Hmcn2
|
UTSW |
2 |
31,314,479 (GRCm38) |
missense |
possibly damaging |
0.86 |
R1535:Hmcn2
|
UTSW |
2 |
31,420,407 (GRCm38) |
missense |
possibly damaging |
0.91 |
R1574:Hmcn2
|
UTSW |
2 |
31,404,887 (GRCm38) |
missense |
probably damaging |
0.97 |
R1574:Hmcn2
|
UTSW |
2 |
31,404,887 (GRCm38) |
missense |
probably damaging |
0.97 |
R1600:Hmcn2
|
UTSW |
2 |
31,430,787 (GRCm38) |
missense |
probably damaging |
0.98 |
R1623:Hmcn2
|
UTSW |
2 |
31,458,039 (GRCm38) |
missense |
possibly damaging |
0.84 |
R1692:Hmcn2
|
UTSW |
2 |
31,450,844 (GRCm38) |
missense |
possibly damaging |
0.47 |
R1719:Hmcn2
|
UTSW |
2 |
31,354,721 (GRCm38) |
missense |
probably damaging |
1.00 |
R1747:Hmcn2
|
UTSW |
2 |
31,457,985 (GRCm38) |
missense |
probably benign |
0.00 |
R1756:Hmcn2
|
UTSW |
2 |
31,396,120 (GRCm38) |
missense |
probably damaging |
0.99 |
R1763:Hmcn2
|
UTSW |
2 |
31,314,590 (GRCm38) |
missense |
probably damaging |
1.00 |
R1815:Hmcn2
|
UTSW |
2 |
31,393,043 (GRCm38) |
missense |
probably damaging |
0.97 |
R1822:Hmcn2
|
UTSW |
2 |
31,383,692 (GRCm38) |
missense |
probably damaging |
0.99 |
R1858:Hmcn2
|
UTSW |
2 |
31,415,283 (GRCm38) |
critical splice donor site |
probably null |
|
R1895:Hmcn2
|
UTSW |
2 |
31,405,635 (GRCm38) |
missense |
probably damaging |
0.99 |
R1908:Hmcn2
|
UTSW |
2 |
31,411,910 (GRCm38) |
critical splice donor site |
probably null |
|
R1946:Hmcn2
|
UTSW |
2 |
31,405,635 (GRCm38) |
missense |
probably damaging |
0.99 |
R1966:Hmcn2
|
UTSW |
2 |
31,389,329 (GRCm38) |
missense |
probably damaging |
0.99 |
R2007:Hmcn2
|
UTSW |
2 |
31,438,255 (GRCm38) |
missense |
possibly damaging |
0.91 |
R2050:Hmcn2
|
UTSW |
2 |
31,335,436 (GRCm38) |
missense |
probably damaging |
1.00 |
R2055:Hmcn2
|
UTSW |
2 |
31,378,282 (GRCm38) |
missense |
probably benign |
0.33 |
R2097:Hmcn2
|
UTSW |
2 |
31,380,419 (GRCm38) |
missense |
probably damaging |
1.00 |
R2145:Hmcn2
|
UTSW |
2 |
31,333,931 (GRCm38) |
splice site |
probably benign |
|
R2155:Hmcn2
|
UTSW |
2 |
31,460,349 (GRCm38) |
missense |
possibly damaging |
0.68 |
R2170:Hmcn2
|
UTSW |
2 |
31,380,281 (GRCm38) |
missense |
probably benign |
0.08 |
R2188:Hmcn2
|
UTSW |
2 |
31,419,935 (GRCm38) |
missense |
probably benign |
0.14 |
R2208:Hmcn2
|
UTSW |
2 |
31,380,297 (GRCm38) |
missense |
probably damaging |
1.00 |
R2217:Hmcn2
|
UTSW |
2 |
31,350,574 (GRCm38) |
missense |
probably benign |
0.02 |
R2407:Hmcn2
|
UTSW |
2 |
31,335,412 (GRCm38) |
critical splice acceptor site |
probably null |
|
R2764:Hmcn2
|
UTSW |
2 |
31,388,298 (GRCm38) |
missense |
probably damaging |
0.98 |
R2913:Hmcn2
|
UTSW |
2 |
31,460,210 (GRCm38) |
missense |
possibly damaging |
0.68 |
R2986:Hmcn2
|
UTSW |
2 |
31,360,998 (GRCm38) |
missense |
probably damaging |
1.00 |
R3157:Hmcn2
|
UTSW |
2 |
31,400,255 (GRCm38) |
missense |
probably damaging |
0.99 |
R3406:Hmcn2
|
UTSW |
2 |
31,433,272 (GRCm38) |
splice site |
probably benign |
|
R3429:Hmcn2
|
UTSW |
2 |
31,409,144 (GRCm38) |
missense |
possibly damaging |
0.87 |
R3737:Hmcn2
|
UTSW |
2 |
31,336,612 (GRCm38) |
nonsense |
probably null |
|
R3739:Hmcn2
|
UTSW |
2 |
31,336,612 (GRCm38) |
nonsense |
probably null |
|
R3771:Hmcn2
|
UTSW |
2 |
31,360,896 (GRCm38) |
missense |
probably damaging |
0.99 |
R3772:Hmcn2
|
UTSW |
2 |
31,360,896 (GRCm38) |
missense |
probably damaging |
0.99 |
R3773:Hmcn2
|
UTSW |
2 |
31,360,896 (GRCm38) |
missense |
probably damaging |
0.99 |
R3804:Hmcn2
|
UTSW |
2 |
31,352,885 (GRCm38) |
splice site |
probably null |
|
R3837:Hmcn2
|
UTSW |
2 |
31,413,407 (GRCm38) |
missense |
probably damaging |
0.99 |
R3838:Hmcn2
|
UTSW |
2 |
31,413,407 (GRCm38) |
missense |
probably damaging |
0.99 |
R3846:Hmcn2
|
UTSW |
2 |
31,430,350 (GRCm38) |
missense |
possibly damaging |
0.51 |
R3925:Hmcn2
|
UTSW |
2 |
31,453,157 (GRCm38) |
missense |
probably benign |
0.00 |
R3934:Hmcn2
|
UTSW |
2 |
31,380,484 (GRCm38) |
critical splice donor site |
probably null |
|
R3946:Hmcn2
|
UTSW |
2 |
31,382,394 (GRCm38) |
missense |
possibly damaging |
0.91 |
R4035:Hmcn2
|
UTSW |
2 |
31,336,612 (GRCm38) |
nonsense |
probably null |
|
R4057:Hmcn2
|
UTSW |
2 |
31,400,238 (GRCm38) |
missense |
probably damaging |
1.00 |
R4583:Hmcn2
|
UTSW |
2 |
31,413,265 (GRCm38) |
missense |
possibly damaging |
0.84 |
R4623:Hmcn2
|
UTSW |
2 |
31,396,710 (GRCm38) |
missense |
probably damaging |
1.00 |
R4647:Hmcn2
|
UTSW |
2 |
31,399,019 (GRCm38) |
missense |
possibly damaging |
0.82 |
R4668:Hmcn2
|
UTSW |
2 |
31,435,792 (GRCm38) |
missense |
probably benign |
0.40 |
R4669:Hmcn2
|
UTSW |
2 |
31,435,792 (GRCm38) |
missense |
probably benign |
0.40 |
R4687:Hmcn2
|
UTSW |
2 |
31,438,285 (GRCm38) |
missense |
probably benign |
0.14 |
R4735:Hmcn2
|
UTSW |
2 |
31,383,775 (GRCm38) |
missense |
probably benign |
0.06 |
R4772:Hmcn2
|
UTSW |
2 |
31,445,314 (GRCm38) |
missense |
probably benign |
0.02 |
R4866:Hmcn2
|
UTSW |
2 |
31,389,391 (GRCm38) |
missense |
possibly damaging |
0.88 |
R4916:Hmcn2
|
UTSW |
2 |
31,360,980 (GRCm38) |
missense |
probably damaging |
0.98 |
R4943:Hmcn2
|
UTSW |
2 |
31,335,492 (GRCm38) |
missense |
probably damaging |
1.00 |
R4967:Hmcn2
|
UTSW |
2 |
31,354,164 (GRCm38) |
critical splice acceptor site |
probably null |
|
R4973:Hmcn2
|
UTSW |
2 |
31,344,096 (GRCm38) |
missense |
probably benign |
0.15 |
R4975:Hmcn2
|
UTSW |
2 |
31,393,025 (GRCm38) |
missense |
possibly damaging |
0.88 |
R4994:Hmcn2
|
UTSW |
2 |
31,458,055 (GRCm38) |
critical splice donor site |
probably null |
|
R4997:Hmcn2
|
UTSW |
2 |
31,401,708 (GRCm38) |
missense |
probably damaging |
1.00 |
R5045:Hmcn2
|
UTSW |
2 |
31,409,081 (GRCm38) |
missense |
probably damaging |
1.00 |
R5117:Hmcn2
|
UTSW |
2 |
31,458,049 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5151:Hmcn2
|
UTSW |
2 |
31,389,443 (GRCm38) |
missense |
probably null |
|
R5232:Hmcn2
|
UTSW |
2 |
31,457,748 (GRCm38) |
missense |
probably damaging |
0.99 |
R5237:Hmcn2
|
UTSW |
2 |
31,414,716 (GRCm38) |
missense |
probably benign |
0.01 |
R5288:Hmcn2
|
UTSW |
2 |
31,460,321 (GRCm38) |
missense |
probably benign |
0.11 |
R5375:Hmcn2
|
UTSW |
2 |
31,430,441 (GRCm38) |
missense |
possibly damaging |
0.92 |
R5379:Hmcn2
|
UTSW |
2 |
31,409,011 (GRCm38) |
missense |
probably damaging |
0.99 |
R5385:Hmcn2
|
UTSW |
2 |
31,460,321 (GRCm38) |
missense |
probably benign |
0.11 |
R5412:Hmcn2
|
UTSW |
2 |
31,346,617 (GRCm38) |
missense |
possibly damaging |
0.77 |
R5426:Hmcn2
|
UTSW |
2 |
31,336,544 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5434:Hmcn2
|
UTSW |
2 |
31,420,363 (GRCm38) |
missense |
probably damaging |
1.00 |
R5441:Hmcn2
|
UTSW |
2 |
31,406,416 (GRCm38) |
missense |
possibly damaging |
0.82 |
R5484:Hmcn2
|
UTSW |
2 |
31,393,054 (GRCm38) |
nonsense |
probably null |
|
R5492:Hmcn2
|
UTSW |
2 |
31,420,306 (GRCm38) |
missense |
probably benign |
0.03 |
R5572:Hmcn2
|
UTSW |
2 |
31,414,526 (GRCm38) |
critical splice acceptor site |
probably null |
|
R5572:Hmcn2
|
UTSW |
2 |
31,414,525 (GRCm38) |
critical splice acceptor site |
probably null |
|
R5591:Hmcn2
|
UTSW |
2 |
31,344,047 (GRCm38) |
missense |
probably damaging |
1.00 |
R5614:Hmcn2
|
UTSW |
2 |
31,428,303 (GRCm38) |
missense |
probably damaging |
0.99 |
R5634:Hmcn2
|
UTSW |
2 |
31,333,881 (GRCm38) |
missense |
probably damaging |
1.00 |
R5645:Hmcn2
|
UTSW |
2 |
31,420,812 (GRCm38) |
missense |
possibly damaging |
0.92 |
R5716:Hmcn2
|
UTSW |
2 |
31,458,738 (GRCm38) |
missense |
possibly damaging |
0.68 |
R5716:Hmcn2
|
UTSW |
2 |
31,336,567 (GRCm38) |
missense |
probably damaging |
1.00 |
R5725:Hmcn2
|
UTSW |
2 |
31,383,815 (GRCm38) |
critical splice donor site |
probably null |
|
R5760:Hmcn2
|
UTSW |
2 |
31,414,568 (GRCm38) |
missense |
possibly damaging |
0.91 |
R5774:Hmcn2
|
UTSW |
2 |
31,409,135 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5838:Hmcn2
|
UTSW |
2 |
31,457,807 (GRCm38) |
missense |
probably damaging |
0.99 |
R5899:Hmcn2
|
UTSW |
2 |
31,354,673 (GRCm38) |
missense |
possibly damaging |
0.93 |
R5916:Hmcn2
|
UTSW |
2 |
31,396,139 (GRCm38) |
missense |
probably damaging |
1.00 |
R5973:Hmcn2
|
UTSW |
2 |
31,420,323 (GRCm38) |
missense |
probably damaging |
0.99 |
R6002:Hmcn2
|
UTSW |
2 |
31,420,309 (GRCm38) |
missense |
probably damaging |
0.99 |
R6018:Hmcn2
|
UTSW |
2 |
31,370,792 (GRCm38) |
missense |
probably benign |
0.13 |
R6063:Hmcn2
|
UTSW |
2 |
31,434,713 (GRCm38) |
missense |
probably benign |
0.06 |
R6161:Hmcn2
|
UTSW |
2 |
31,356,254 (GRCm38) |
missense |
probably benign |
|
R6166:Hmcn2
|
UTSW |
2 |
31,369,262 (GRCm38) |
missense |
probably damaging |
1.00 |
R6177:Hmcn2
|
UTSW |
2 |
31,420,106 (GRCm38) |
nonsense |
probably null |
|
R6191:Hmcn2
|
UTSW |
2 |
31,458,746 (GRCm38) |
missense |
probably damaging |
0.99 |
R6195:Hmcn2
|
UTSW |
2 |
31,384,115 (GRCm38) |
missense |
probably damaging |
0.96 |
R6273:Hmcn2
|
UTSW |
2 |
31,411,834 (GRCm38) |
missense |
probably damaging |
0.99 |
R6293:Hmcn2
|
UTSW |
2 |
31,335,451 (GRCm38) |
missense |
probably damaging |
1.00 |
R6349:Hmcn2
|
UTSW |
2 |
31,388,373 (GRCm38) |
missense |
probably damaging |
1.00 |
R6395:Hmcn2
|
UTSW |
2 |
31,369,257 (GRCm38) |
missense |
probably damaging |
1.00 |
R6448:Hmcn2
|
UTSW |
2 |
31,420,820 (GRCm38) |
missense |
probably benign |
0.02 |
R6450:Hmcn2
|
UTSW |
2 |
31,361,800 (GRCm38) |
missense |
probably benign |
0.11 |
R6479:Hmcn2
|
UTSW |
2 |
31,425,468 (GRCm38) |
missense |
probably damaging |
0.99 |
R6502:Hmcn2
|
UTSW |
2 |
31,382,478 (GRCm38) |
missense |
probably damaging |
0.99 |
R6511:Hmcn2
|
UTSW |
2 |
31,356,342 (GRCm38) |
missense |
possibly damaging |
0.79 |
R6537:Hmcn2
|
UTSW |
2 |
31,415,268 (GRCm38) |
missense |
probably benign |
0.00 |
R6880:Hmcn2
|
UTSW |
2 |
31,343,056 (GRCm38) |
missense |
probably damaging |
1.00 |
R6924:Hmcn2
|
UTSW |
2 |
31,350,505 (GRCm38) |
splice site |
probably null |
|
R6971:Hmcn2
|
UTSW |
2 |
31,432,321 (GRCm38) |
missense |
probably benign |
0.02 |
R7057:Hmcn2
|
UTSW |
2 |
31,422,649 (GRCm38) |
missense |
probably damaging |
0.99 |
R7141:Hmcn2
|
UTSW |
2 |
31,360,896 (GRCm38) |
missense |
probably benign |
0.17 |
R7268:Hmcn2
|
UTSW |
2 |
31,457,966 (GRCm38) |
missense |
possibly damaging |
0.48 |
R7307:Hmcn2
|
UTSW |
2 |
31,343,081 (GRCm38) |
missense |
probably damaging |
0.96 |
R7322:Hmcn2
|
UTSW |
2 |
31,459,081 (GRCm38) |
missense |
probably damaging |
0.99 |
R7334:Hmcn2
|
UTSW |
2 |
31,453,135 (GRCm38) |
missense |
possibly damaging |
0.82 |
R7334:Hmcn2
|
UTSW |
2 |
31,435,794 (GRCm38) |
missense |
probably damaging |
0.98 |
R7335:Hmcn2
|
UTSW |
2 |
31,392,157 (GRCm38) |
missense |
possibly damaging |
0.88 |
R7358:Hmcn2
|
UTSW |
2 |
31,416,812 (GRCm38) |
missense |
probably damaging |
1.00 |
R7359:Hmcn2
|
UTSW |
2 |
31,388,383 (GRCm38) |
missense |
probably benign |
0.13 |
R7488:Hmcn2
|
UTSW |
2 |
31,420,830 (GRCm38) |
missense |
probably damaging |
1.00 |
R7498:Hmcn2
|
UTSW |
2 |
31,383,475 (GRCm38) |
splice site |
probably null |
|
R7560:Hmcn2
|
UTSW |
2 |
31,457,173 (GRCm38) |
missense |
probably benign |
|
R7566:Hmcn2
|
UTSW |
2 |
31,454,857 (GRCm38) |
missense |
probably damaging |
0.96 |
R7570:Hmcn2
|
UTSW |
2 |
31,423,911 (GRCm38) |
missense |
probably benign |
|
R7574:Hmcn2
|
UTSW |
2 |
31,455,519 (GRCm38) |
missense |
possibly damaging |
0.68 |
R7599:Hmcn2
|
UTSW |
2 |
31,356,286 (GRCm38) |
missense |
possibly damaging |
0.93 |
R7654:Hmcn2
|
UTSW |
2 |
31,346,569 (GRCm38) |
missense |
probably benign |
0.00 |
R7662:Hmcn2
|
UTSW |
2 |
31,382,345 (GRCm38) |
missense |
probably benign |
0.01 |
R7666:Hmcn2
|
UTSW |
2 |
31,380,233 (GRCm38) |
missense |
probably damaging |
1.00 |
R7698:Hmcn2
|
UTSW |
2 |
31,423,153 (GRCm38) |
missense |
probably damaging |
0.98 |
R7722:Hmcn2
|
UTSW |
2 |
31,382,500 (GRCm38) |
nonsense |
probably null |
|
R7739:Hmcn2
|
UTSW |
2 |
31,458,026 (GRCm38) |
missense |
possibly damaging |
0.48 |
R7749:Hmcn2
|
UTSW |
2 |
31,453,033 (GRCm38) |
splice site |
probably null |
|
R7828:Hmcn2
|
UTSW |
2 |
31,405,875 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7912:Hmcn2
|
UTSW |
2 |
31,420,299 (GRCm38) |
missense |
probably benign |
0.00 |
R7978:Hmcn2
|
UTSW |
2 |
31,389,347 (GRCm38) |
missense |
probably benign |
0.40 |
R8075:Hmcn2
|
UTSW |
2 |
31,389,391 (GRCm38) |
missense |
possibly damaging |
0.88 |
R8088:Hmcn2
|
UTSW |
2 |
31,426,903 (GRCm38) |
nonsense |
probably null |
|
R8101:Hmcn2
|
UTSW |
2 |
31,350,070 (GRCm38) |
missense |
probably benign |
0.08 |
R8124:Hmcn2
|
UTSW |
2 |
31,400,124 (GRCm38) |
missense |
probably benign |
0.01 |
R8145:Hmcn2
|
UTSW |
2 |
31,423,105 (GRCm38) |
missense |
probably damaging |
1.00 |
R8230:Hmcn2
|
UTSW |
2 |
31,344,473 (GRCm38) |
missense |
possibly damaging |
0.91 |
R8267:Hmcn2
|
UTSW |
2 |
31,459,179 (GRCm38) |
missense |
probably benign |
|
R8277:Hmcn2
|
UTSW |
2 |
31,369,177 (GRCm38) |
missense |
probably benign |
0.16 |
R8307:Hmcn2
|
UTSW |
2 |
31,396,115 (GRCm38) |
missense |
probably damaging |
0.99 |
R8353:Hmcn2
|
UTSW |
2 |
31,385,341 (GRCm38) |
splice site |
probably null |
|
R8415:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8416:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8437:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8438:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8440:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8442:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8497:Hmcn2
|
UTSW |
2 |
31,423,345 (GRCm38) |
missense |
possibly damaging |
0.92 |
R8520:Hmcn2
|
UTSW |
2 |
31,354,714 (GRCm38) |
missense |
probably damaging |
1.00 |
R8530:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8537:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8550:Hmcn2
|
UTSW |
2 |
31,350,642 (GRCm38) |
critical splice donor site |
probably null |
|
R8721:Hmcn2
|
UTSW |
2 |
31,425,177 (GRCm38) |
missense |
probably damaging |
1.00 |
R8795:Hmcn2
|
UTSW |
2 |
31,425,381 (GRCm38) |
missense |
probably benign |
0.01 |
R8802:Hmcn2
|
UTSW |
2 |
31,411,276 (GRCm38) |
missense |
probably damaging |
0.97 |
R8804:Hmcn2
|
UTSW |
2 |
31,425,381 (GRCm38) |
missense |
probably benign |
0.01 |
R8805:Hmcn2
|
UTSW |
2 |
31,425,381 (GRCm38) |
missense |
probably benign |
0.01 |
R8904:Hmcn2
|
UTSW |
2 |
31,433,392 (GRCm38) |
missense |
possibly damaging |
0.92 |
R8937:Hmcn2
|
UTSW |
2 |
31,314,415 (GRCm38) |
start codon destroyed |
probably benign |
0.01 |
R8947:Hmcn2
|
UTSW |
2 |
31,388,208 (GRCm38) |
missense |
probably damaging |
0.99 |
R8948:Hmcn2
|
UTSW |
2 |
31,354,729 (GRCm38) |
missense |
probably damaging |
1.00 |
R8950:Hmcn2
|
UTSW |
2 |
31,354,729 (GRCm38) |
missense |
probably damaging |
1.00 |
R8959:Hmcn2
|
UTSW |
2 |
31,392,147 (GRCm38) |
missense |
probably damaging |
1.00 |
R9025:Hmcn2
|
UTSW |
2 |
31,457,955 (GRCm38) |
missense |
possibly damaging |
0.56 |
R9039:Hmcn2
|
UTSW |
2 |
31,354,634 (GRCm38) |
missense |
probably damaging |
0.97 |
R9068:Hmcn2
|
UTSW |
2 |
31,413,673 (GRCm38) |
missense |
probably benign |
0.01 |
R9161:Hmcn2
|
UTSW |
2 |
31,352,746 (GRCm38) |
missense |
probably benign |
0.02 |
R9178:Hmcn2
|
UTSW |
2 |
31,391,509 (GRCm38) |
missense |
possibly damaging |
0.77 |
R9204:Hmcn2
|
UTSW |
2 |
31,388,365 (GRCm38) |
missense |
probably damaging |
0.98 |
R9317:Hmcn2
|
UTSW |
2 |
31,460,316 (GRCm38) |
missense |
possibly damaging |
0.91 |
R9341:Hmcn2
|
UTSW |
2 |
31,389,347 (GRCm38) |
missense |
probably benign |
0.40 |
R9343:Hmcn2
|
UTSW |
2 |
31,389,347 (GRCm38) |
missense |
probably benign |
0.40 |
R9355:Hmcn2
|
UTSW |
2 |
31,438,290 (GRCm38) |
missense |
probably benign |
0.18 |
R9371:Hmcn2
|
UTSW |
2 |
31,411,905 (GRCm38) |
missense |
probably damaging |
1.00 |
R9450:Hmcn2
|
UTSW |
2 |
31,426,833 (GRCm38) |
missense |
probably damaging |
1.00 |
R9477:Hmcn2
|
UTSW |
2 |
31,396,019 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9483:Hmcn2
|
UTSW |
2 |
31,430,363 (GRCm38) |
missense |
|
|
R9536:Hmcn2
|
UTSW |
2 |
31,445,118 (GRCm38) |
missense |
possibly damaging |
0.86 |
R9580:Hmcn2
|
UTSW |
2 |
31,404,863 (GRCm38) |
missense |
probably benign |
0.16 |
R9593:Hmcn2
|
UTSW |
2 |
31,354,730 (GRCm38) |
missense |
probably damaging |
0.99 |
R9649:Hmcn2
|
UTSW |
2 |
31,402,438 (GRCm38) |
missense |
possibly damaging |
0.95 |
R9706:Hmcn2
|
UTSW |
2 |
31,415,267 (GRCm38) |
missense |
probably benign |
0.00 |
X0066:Hmcn2
|
UTSW |
2 |
31,454,811 (GRCm38) |
missense |
possibly damaging |
0.83 |
X0067:Hmcn2
|
UTSW |
2 |
31,405,867 (GRCm38) |
missense |
possibly damaging |
0.82 |
Z1088:Hmcn2
|
UTSW |
2 |
31,459,064 (GRCm38) |
splice site |
probably null |
|
Z1088:Hmcn2
|
UTSW |
2 |
31,381,067 (GRCm38) |
missense |
probably benign |
0.01 |
Z1176:Hmcn2
|
UTSW |
2 |
31,429,091 (GRCm38) |
missense |
probably damaging |
0.97 |
Z1176:Hmcn2
|
UTSW |
2 |
31,425,416 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Hmcn2
|
UTSW |
2 |
31,344,029 (GRCm38) |
missense |
possibly damaging |
0.95 |
Z1177:Hmcn2
|
UTSW |
2 |
31,426,824 (GRCm38) |
missense |
probably damaging |
0.99 |
Z1177:Hmcn2
|
UTSW |
2 |
31,344,506 (GRCm38) |
missense |
probably damaging |
1.00 |
|