Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
T |
C |
6: 146,855,034 (GRCm39) |
T3A |
unknown |
Het |
4933412E24Rik |
T |
C |
15: 59,888,422 (GRCm39) |
E6G |
probably damaging |
Het |
Abca6 |
A |
G |
11: 110,087,523 (GRCm39) |
L1135P |
possibly damaging |
Het |
Agps |
A |
G |
2: 75,681,876 (GRCm39) |
D113G |
probably damaging |
Het |
Ankhd1 |
G |
T |
18: 36,780,881 (GRCm39) |
V1978L |
probably benign |
Het |
Ankrd31 |
T |
A |
13: 96,957,966 (GRCm39) |
|
probably null |
Het |
Arhgap5 |
T |
A |
12: 52,565,480 (GRCm39) |
M817K |
possibly damaging |
Het |
Bdp1 |
C |
A |
13: 100,235,637 (GRCm39) |
V105F |
probably damaging |
Het |
Brdt |
A |
G |
5: 107,496,454 (GRCm39) |
N189D |
possibly damaging |
Het |
Ccdc180 |
A |
T |
4: 45,909,428 (GRCm39) |
N532I |
probably benign |
Het |
Ccnc |
A |
C |
4: 21,730,480 (GRCm39) |
K39T |
probably damaging |
Het |
Cfap251 |
T |
C |
5: 123,392,487 (GRCm39) |
V207A |
unknown |
Het |
Cfap57 |
C |
A |
4: 118,411,952 (GRCm39) |
G1231* |
probably null |
Het |
Chd7 |
A |
T |
4: 8,854,115 (GRCm39) |
T1896S |
probably benign |
Het |
Clk4 |
A |
T |
11: 51,171,956 (GRCm39) |
H412L |
probably benign |
Het |
Creld1 |
T |
C |
6: 113,465,100 (GRCm39) |
L109P |
probably damaging |
Het |
Cxxc4 |
A |
T |
3: 133,946,093 (GRCm39) |
I225L |
possibly damaging |
Het |
Cyp4f39 |
A |
T |
17: 32,702,291 (GRCm39) |
R263W |
probably benign |
Het |
Dennd10 |
G |
A |
19: 60,819,317 (GRCm39) |
A263T |
not run |
Het |
Dip2c |
T |
C |
13: 9,656,569 (GRCm39) |
|
probably null |
Het |
Dnah14 |
A |
G |
1: 181,455,463 (GRCm39) |
T863A |
probably damaging |
Het |
Dnah17 |
C |
A |
11: 117,970,508 (GRCm39) |
|
probably null |
Het |
Dnajc10 |
A |
G |
2: 80,175,409 (GRCm39) |
K599E |
probably benign |
Het |
Dnajc7 |
C |
A |
11: 100,489,544 (GRCm39) |
R101L |
probably benign |
Het |
Dnttip2 |
G |
A |
3: 122,069,990 (GRCm39) |
E402K |
probably benign |
Het |
Dusp22 |
T |
A |
13: 30,852,774 (GRCm39) |
|
probably null |
Het |
Egflam |
C |
A |
15: 7,280,675 (GRCm39) |
R450M |
probably null |
Het |
Eml5 |
C |
T |
12: 98,760,394 (GRCm39) |
R1785Q |
probably damaging |
Het |
Fam78b |
G |
T |
1: 166,829,178 (GRCm39) |
R15L |
probably damaging |
Het |
Fbxl5 |
A |
T |
5: 43,915,945 (GRCm39) |
I489N |
probably damaging |
Het |
Flt3 |
G |
A |
5: 147,271,263 (GRCm39) |
P893S |
probably damaging |
Het |
Gm17019 |
T |
C |
5: 15,081,049 (GRCm39) |
M131V |
possibly damaging |
Het |
Gm21560 |
T |
A |
14: 6,216,262 (GRCm38) |
I194F |
probably benign |
Het |
Gm28729 |
T |
C |
9: 96,399,705 (GRCm39) |
D158G |
probably damaging |
Het |
Gucy2c |
C |
T |
6: 136,746,814 (GRCm39) |
|
probably null |
Het |
Hectd1 |
C |
T |
12: 51,819,343 (GRCm39) |
G1247S |
probably damaging |
Het |
Ireb2 |
T |
A |
9: 54,816,970 (GRCm39) |
I946K |
probably benign |
Het |
Itgb4 |
A |
T |
11: 115,873,531 (GRCm39) |
D249V |
probably benign |
Het |
Klhdc7a |
A |
G |
4: 139,694,549 (GRCm39) |
S133P |
probably damaging |
Het |
Lsr |
A |
T |
7: 30,665,437 (GRCm39) |
D172E |
possibly damaging |
Het |
Macf1 |
T |
C |
4: 123,420,702 (GRCm39) |
E184G |
probably benign |
Het |
Map3k4 |
A |
T |
17: 12,490,030 (GRCm39) |
L467H |
possibly damaging |
Het |
Mogat1 |
T |
C |
1: 78,499,502 (GRCm39) |
|
probably null |
Het |
Mxra8 |
A |
G |
4: 155,927,367 (GRCm39) |
D384G |
probably damaging |
Het |
Myo15b |
A |
G |
11: 115,762,321 (GRCm39) |
T1214A |
|
Het |
Naip1 |
T |
C |
13: 100,563,506 (GRCm39) |
Y553C |
probably damaging |
Het |
Nln |
A |
T |
13: 104,189,137 (GRCm39) |
I278K |
probably benign |
Het |
Nsmaf |
T |
A |
4: 6,435,109 (GRCm39) |
|
probably null |
Het |
Nynrin |
A |
G |
14: 56,102,553 (GRCm39) |
R741G |
probably damaging |
Het |
Or4p8 |
A |
G |
2: 88,727,305 (GRCm39) |
V212A |
possibly damaging |
Het |
Or52e19b |
A |
G |
7: 103,032,783 (GRCm39) |
V142A |
probably benign |
Het |
Or5d38 |
C |
T |
2: 87,955,330 (GRCm39) |
|
probably benign |
Het |
Or8j3 |
G |
T |
2: 86,028,516 (GRCm39) |
Y193* |
probably null |
Het |
Orc1 |
A |
G |
4: 108,462,744 (GRCm39) |
H607R |
probably benign |
Het |
Pate2 |
A |
T |
9: 35,581,829 (GRCm39) |
Y41F |
probably damaging |
Het |
Pcdhb20 |
A |
T |
18: 37,638,112 (GRCm39) |
T213S |
possibly damaging |
Het |
Pcm1 |
G |
A |
8: 41,780,621 (GRCm39) |
E1858K |
possibly damaging |
Het |
Pla2g2d |
A |
G |
4: 138,506,089 (GRCm39) |
T59A |
probably damaging |
Het |
Ppl |
C |
T |
16: 4,906,725 (GRCm39) |
R1190H |
probably damaging |
Het |
Prl2c2 |
A |
G |
13: 13,179,907 (GRCm39) |
L2P |
probably benign |
Het |
Proz |
G |
A |
8: 13,113,406 (GRCm39) |
V76I |
probably benign |
Het |
Prr36 |
A |
G |
8: 4,260,953 (GRCm39) |
S955P |
probably benign |
Het |
Pter |
T |
C |
2: 12,983,352 (GRCm39) |
V119A |
probably damaging |
Het |
Qrich1 |
T |
A |
9: 108,433,567 (GRCm39) |
|
probably null |
Het |
Rbm15b |
T |
C |
9: 106,763,088 (GRCm39) |
E360G |
probably damaging |
Het |
Skint11 |
G |
A |
4: 114,101,968 (GRCm39) |
C327Y |
possibly damaging |
Het |
Spag17 |
T |
A |
3: 99,961,174 (GRCm39) |
S987T |
probably benign |
Het |
Spata31f3 |
TCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGTCATTCAACACTTTGG |
TCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGTCATTCAACACTTTGG |
4: 42,871,823 (GRCm39) |
|
probably benign |
Het |
Tbx1 |
T |
C |
16: 18,405,365 (GRCm39) |
S100G |
unknown |
Het |
Tiam2 |
C |
T |
17: 3,568,399 (GRCm39) |
S1515L |
possibly damaging |
Het |
Togaram1 |
C |
A |
12: 65,013,233 (GRCm39) |
D161E |
probably damaging |
Het |
Trhde |
A |
T |
10: 114,532,003 (GRCm39) |
S366T |
possibly damaging |
Het |
Ttc12 |
A |
G |
9: 49,349,724 (GRCm39) |
I691T |
possibly damaging |
Het |
Ube4a |
A |
G |
9: 44,861,025 (GRCm39) |
|
probably null |
Het |
Uggt2 |
A |
T |
14: 119,235,516 (GRCm39) |
I1453N |
probably damaging |
Het |
Unc79 |
T |
C |
12: 103,058,313 (GRCm39) |
S972P |
probably damaging |
Het |
Wdr20 |
G |
A |
12: 110,704,649 (GRCm39) |
D63N |
probably benign |
Het |
Wls |
T |
A |
3: 159,578,816 (GRCm39) |
I126N |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,355,289 (GRCm39) |
D3350G |
probably benign |
Het |
|
Other mutations in Map2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01518:Map2
|
APN |
1 |
66,464,490 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02135:Map2
|
APN |
1 |
66,419,920 (GRCm39) |
nonsense |
probably null |
|
IGL02526:Map2
|
APN |
1 |
66,419,876 (GRCm39) |
missense |
possibly damaging |
0.94 |
Annas
|
UTSW |
1 |
66,472,756 (GRCm39) |
critical splice donor site |
probably null |
|
calliope
|
UTSW |
1 |
66,464,457 (GRCm39) |
missense |
probably damaging |
1.00 |
carthage
|
UTSW |
1 |
66,453,807 (GRCm39) |
missense |
probably damaging |
1.00 |
costas
|
UTSW |
1 |
66,451,812 (GRCm39) |
missense |
possibly damaging |
0.94 |
Jacobin
|
UTSW |
1 |
66,438,578 (GRCm39) |
missense |
probably damaging |
1.00 |
Nectar
|
UTSW |
1 |
66,454,522 (GRCm39) |
nonsense |
probably null |
|
ruby_throat
|
UTSW |
1 |
66,454,043 (GRCm39) |
missense |
possibly damaging |
0.67 |
Rufous
|
UTSW |
1 |
66,419,927 (GRCm39) |
missense |
probably damaging |
1.00 |
Speckled
|
UTSW |
1 |
66,451,886 (GRCm39) |
nonsense |
probably null |
|
Sunbird
|
UTSW |
1 |
66,454,646 (GRCm39) |
missense |
probably benign |
0.01 |
swift
|
UTSW |
1 |
66,455,523 (GRCm39) |
missense |
probably damaging |
1.00 |
E0370:Map2
|
UTSW |
1 |
66,455,883 (GRCm39) |
unclassified |
probably benign |
|
PIT4362001:Map2
|
UTSW |
1 |
66,451,677 (GRCm39) |
missense |
probably benign |
0.05 |
R0067:Map2
|
UTSW |
1 |
66,452,322 (GRCm39) |
missense |
probably benign |
0.04 |
R0238:Map2
|
UTSW |
1 |
66,455,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0238:Map2
|
UTSW |
1 |
66,455,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Map2
|
UTSW |
1 |
66,455,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Map2
|
UTSW |
1 |
66,455,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:Map2
|
UTSW |
1 |
66,419,881 (GRCm39) |
nonsense |
probably null |
|
R0302:Map2
|
UTSW |
1 |
66,453,987 (GRCm39) |
missense |
probably benign |
0.15 |
R0305:Map2
|
UTSW |
1 |
66,452,253 (GRCm39) |
missense |
probably benign |
0.00 |
R0409:Map2
|
UTSW |
1 |
66,472,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0561:Map2
|
UTSW |
1 |
66,464,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R0674:Map2
|
UTSW |
1 |
66,452,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R0738:Map2
|
UTSW |
1 |
66,464,348 (GRCm39) |
splice site |
probably benign |
|
R0893:Map2
|
UTSW |
1 |
66,419,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R1305:Map2
|
UTSW |
1 |
66,464,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R1534:Map2
|
UTSW |
1 |
66,452,339 (GRCm39) |
missense |
probably benign |
0.33 |
R1632:Map2
|
UTSW |
1 |
66,454,245 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1682:Map2
|
UTSW |
1 |
66,454,781 (GRCm39) |
splice site |
probably null |
|
R1774:Map2
|
UTSW |
1 |
66,453,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Map2
|
UTSW |
1 |
66,455,295 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2017:Map2
|
UTSW |
1 |
66,451,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Map2
|
UTSW |
1 |
66,453,473 (GRCm39) |
missense |
probably damaging |
0.98 |
R2093:Map2
|
UTSW |
1 |
66,438,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R2214:Map2
|
UTSW |
1 |
66,459,345 (GRCm39) |
missense |
probably damaging |
0.99 |
R2284:Map2
|
UTSW |
1 |
66,453,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R3011:Map2
|
UTSW |
1 |
66,453,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R3105:Map2
|
UTSW |
1 |
66,472,756 (GRCm39) |
critical splice donor site |
probably null |
|
R3708:Map2
|
UTSW |
1 |
66,455,714 (GRCm39) |
unclassified |
probably benign |
|
R3709:Map2
|
UTSW |
1 |
66,455,015 (GRCm39) |
nonsense |
probably null |
|
R3729:Map2
|
UTSW |
1 |
66,451,605 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3760:Map2
|
UTSW |
1 |
66,478,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R3788:Map2
|
UTSW |
1 |
66,456,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R3789:Map2
|
UTSW |
1 |
66,456,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R4003:Map2
|
UTSW |
1 |
66,454,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Map2
|
UTSW |
1 |
66,455,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R4172:Map2
|
UTSW |
1 |
66,452,759 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4198:Map2
|
UTSW |
1 |
66,464,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R4200:Map2
|
UTSW |
1 |
66,464,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R4205:Map2
|
UTSW |
1 |
66,464,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Map2
|
UTSW |
1 |
66,464,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R4700:Map2
|
UTSW |
1 |
66,449,796 (GRCm39) |
missense |
probably damaging |
0.96 |
R4974:Map2
|
UTSW |
1 |
66,452,664 (GRCm39) |
missense |
probably benign |
0.15 |
R5007:Map2
|
UTSW |
1 |
66,452,448 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5039:Map2
|
UTSW |
1 |
66,477,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R5237:Map2
|
UTSW |
1 |
66,478,169 (GRCm39) |
unclassified |
probably benign |
|
R5313:Map2
|
UTSW |
1 |
66,464,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R5455:Map2
|
UTSW |
1 |
66,438,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R5490:Map2
|
UTSW |
1 |
66,452,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R5517:Map2
|
UTSW |
1 |
66,454,415 (GRCm39) |
missense |
probably benign |
0.00 |
R5532:Map2
|
UTSW |
1 |
66,453,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R5583:Map2
|
UTSW |
1 |
66,455,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R5764:Map2
|
UTSW |
1 |
66,454,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R5996:Map2
|
UTSW |
1 |
66,454,043 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6058:Map2
|
UTSW |
1 |
66,454,573 (GRCm39) |
missense |
probably benign |
0.05 |
R6199:Map2
|
UTSW |
1 |
66,464,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R6208:Map2
|
UTSW |
1 |
66,470,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R6276:Map2
|
UTSW |
1 |
66,438,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R6378:Map2
|
UTSW |
1 |
66,454,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R6424:Map2
|
UTSW |
1 |
66,453,946 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6743:Map2
|
UTSW |
1 |
66,454,766 (GRCm39) |
missense |
probably benign |
0.04 |
R6837:Map2
|
UTSW |
1 |
66,453,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R6901:Map2
|
UTSW |
1 |
66,460,932 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6984:Map2
|
UTSW |
1 |
66,454,395 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6989:Map2
|
UTSW |
1 |
66,454,065 (GRCm39) |
missense |
probably benign |
0.00 |
R7001:Map2
|
UTSW |
1 |
66,454,646 (GRCm39) |
missense |
probably benign |
0.01 |
R7055:Map2
|
UTSW |
1 |
66,455,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7094:Map2
|
UTSW |
1 |
66,451,886 (GRCm39) |
nonsense |
probably null |
|
R7106:Map2
|
UTSW |
1 |
66,449,903 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7182:Map2
|
UTSW |
1 |
66,451,812 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7235:Map2
|
UTSW |
1 |
66,453,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R7424:Map2
|
UTSW |
1 |
66,453,983 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7473:Map2
|
UTSW |
1 |
66,454,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R7642:Map2
|
UTSW |
1 |
66,452,466 (GRCm39) |
missense |
probably benign |
0.01 |
R7660:Map2
|
UTSW |
1 |
66,453,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R7673:Map2
|
UTSW |
1 |
66,452,933 (GRCm39) |
missense |
probably benign |
0.03 |
R7768:Map2
|
UTSW |
1 |
66,453,642 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7796:Map2
|
UTSW |
1 |
66,455,654 (GRCm39) |
splice site |
probably null |
|
R7834:Map2
|
UTSW |
1 |
66,455,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7955:Map2
|
UTSW |
1 |
66,452,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R8056:Map2
|
UTSW |
1 |
66,454,779 (GRCm39) |
missense |
probably damaging |
0.99 |
R8118:Map2
|
UTSW |
1 |
66,464,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R8135:Map2
|
UTSW |
1 |
66,452,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R8152:Map2
|
UTSW |
1 |
66,453,902 (GRCm39) |
missense |
probably benign |
0.00 |
R8223:Map2
|
UTSW |
1 |
66,464,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R8329:Map2
|
UTSW |
1 |
66,454,272 (GRCm39) |
missense |
probably benign |
0.01 |
R8344:Map2
|
UTSW |
1 |
66,460,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R8475:Map2
|
UTSW |
1 |
66,453,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R8548:Map2
|
UTSW |
1 |
66,452,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Map2
|
UTSW |
1 |
66,460,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R8713:Map2
|
UTSW |
1 |
66,453,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R8745:Map2
|
UTSW |
1 |
66,452,556 (GRCm39) |
missense |
probably benign |
0.00 |
R8786:Map2
|
UTSW |
1 |
66,472,755 (GRCm39) |
critical splice donor site |
probably benign |
|
R8790:Map2
|
UTSW |
1 |
66,477,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R8874:Map2
|
UTSW |
1 |
66,455,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R8887:Map2
|
UTSW |
1 |
66,454,758 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8948:Map2
|
UTSW |
1 |
66,419,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R8950:Map2
|
UTSW |
1 |
66,419,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R8998:Map2
|
UTSW |
1 |
66,452,473 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8999:Map2
|
UTSW |
1 |
66,452,473 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9072:Map2
|
UTSW |
1 |
66,453,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R9088:Map2
|
UTSW |
1 |
66,453,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R9089:Map2
|
UTSW |
1 |
66,452,098 (GRCm39) |
missense |
probably benign |
0.09 |
R9106:Map2
|
UTSW |
1 |
66,454,522 (GRCm39) |
nonsense |
probably null |
|
R9112:Map2
|
UTSW |
1 |
66,472,723 (GRCm39) |
nonsense |
probably null |
|
R9120:Map2
|
UTSW |
1 |
66,453,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R9161:Map2
|
UTSW |
1 |
66,477,503 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9464:Map2
|
UTSW |
1 |
66,454,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R9589:Map2
|
UTSW |
1 |
66,449,753 (GRCm39) |
missense |
probably benign |
|
V8831:Map2
|
UTSW |
1 |
66,455,004 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Map2
|
UTSW |
1 |
66,477,520 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Map2
|
UTSW |
1 |
66,419,839 (GRCm39) |
missense |
probably benign |
0.01 |
|