Incidental Mutation 'R9433:Magi3'
| ID |
713085 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Magi3
|
| Ensembl Gene |
ENSMUSG00000052539 |
| Gene Name |
membrane associated guanylate kinase, WW and PDZ domain containing 3 |
| Synonyms |
4732496O19Rik, 6530407C02Rik |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.435)
|
| Stock # |
R9433 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
3 |
| Chromosomal Location |
103920575-104127690 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 103922473 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Threonine
at position 1415
(A1415T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000112934
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000064371]
[ENSMUST00000121198]
[ENSMUST00000122303]
[ENSMUST00000145727]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000064371
|
| SMART Domains |
Protein: ENSMUSP00000067932
Gene: ENSMUSG00000052539
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
14 |
N/A |
INTRINSIC |
|
PDZ
|
27 |
108 |
1.94e-1 |
SMART |
|
GuKc
|
114 |
281 |
8.56e-10 |
SMART |
|
WW
|
297 |
329 |
9.14e-12 |
SMART |
|
WW
|
343 |
375 |
2.47e-8 |
SMART |
|
PDZ
|
421 |
497 |
1.48e-17 |
SMART |
|
PDZ
|
589 |
659 |
3.07e-10 |
SMART |
|
low complexity region
|
664 |
674 |
N/A |
INTRINSIC |
|
low complexity region
|
683 |
698 |
N/A |
INTRINSIC |
|
PDZ
|
737 |
813 |
1.34e-15 |
SMART |
|
PDZ
|
861 |
939 |
7.65e-20 |
SMART |
|
PDZ
|
1030 |
1104 |
1.55e-20 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000121198
AA Change: A1415T
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
| SMART Domains |
Protein: ENSMUSP00000112934
Gene: ENSMUSG00000052539
AA Change: A1415T
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
14 |
N/A |
INTRINSIC |
|
PDZ
|
27 |
108 |
1.94e-1 |
SMART |
|
GuKc
|
114 |
281 |
8.56e-10 |
SMART |
|
WW
|
297 |
329 |
9.14e-12 |
SMART |
|
WW
|
343 |
375 |
2.47e-8 |
SMART |
|
PDZ
|
421 |
497 |
1.48e-17 |
SMART |
|
PDZ
|
589 |
659 |
3.07e-10 |
SMART |
|
low complexity region
|
664 |
674 |
N/A |
INTRINSIC |
|
low complexity region
|
683 |
698 |
N/A |
INTRINSIC |
|
PDZ
|
737 |
813 |
1.34e-15 |
SMART |
|
PDZ
|
861 |
939 |
7.65e-20 |
SMART |
|
PDZ
|
1030 |
1104 |
1.55e-20 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000122303
|
| SMART Domains |
Protein: ENSMUSP00000113713
Gene: ENSMUSG00000052539
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
14 |
N/A |
INTRINSIC |
|
PDZ
|
27 |
108 |
1.94e-1 |
SMART |
|
GuKc
|
114 |
281 |
8.56e-10 |
SMART |
|
WW
|
297 |
329 |
9.14e-12 |
SMART |
|
WW
|
343 |
375 |
2.47e-8 |
SMART |
|
PDZ
|
421 |
497 |
1.48e-17 |
SMART |
|
PDZ
|
589 |
659 |
3.07e-10 |
SMART |
|
low complexity region
|
664 |
674 |
N/A |
INTRINSIC |
|
low complexity region
|
683 |
698 |
N/A |
INTRINSIC |
|
PDZ
|
737 |
813 |
1.34e-15 |
SMART |
|
PDZ
|
861 |
939 |
7.65e-20 |
SMART |
|
PDZ
|
1030 |
1104 |
1.55e-20 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000145727
|
| SMART Domains |
Protein: ENSMUSP00000114722
Gene: ENSMUSG00000058388
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Phtf-FEM1B_bdg
|
3 |
158 |
1.6e-88 |
PFAM |
|
low complexity region
|
170 |
181 |
N/A |
INTRINSIC |
|
low complexity region
|
347 |
370 |
N/A |
INTRINSIC |
|
transmembrane domain
|
473 |
492 |
N/A |
INTRINSIC |
|
transmembrane domain
|
512 |
534 |
N/A |
INTRINSIC |
|
transmembrane domain
|
610 |
632 |
N/A |
INTRINSIC |
|
transmembrane domain
|
647 |
664 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.2%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 79 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam4 |
T |
C |
12: 81,466,723 (GRCm39) |
T633A |
possibly damaging |
Het |
| Adgrv1 |
A |
T |
13: 81,714,471 (GRCm39) |
F937L |
probably benign |
Het |
| Adipor2 |
A |
T |
6: 119,336,486 (GRCm39) |
F159Y |
probably damaging |
Het |
| Ahcyl1 |
A |
G |
3: 107,575,645 (GRCm39) |
V380A |
probably damaging |
Het |
| Akp3 |
A |
G |
1: 87,053,517 (GRCm39) |
K157E |
probably benign |
Het |
| Arpc1a |
T |
A |
5: 145,045,203 (GRCm39) |
I364N |
possibly damaging |
Het |
| Bach1 |
C |
G |
16: 87,516,603 (GRCm39) |
S381R |
probably benign |
Het |
| Brms1l |
G |
A |
12: 55,912,863 (GRCm39) |
|
probably null |
Het |
| Camk1d |
A |
G |
2: 5,680,777 (GRCm39) |
S6P |
unknown |
Het |
| Ccdc112 |
C |
A |
18: 46,424,040 (GRCm39) |
V233L |
probably benign |
Het |
| Ccdc113 |
A |
T |
8: 96,272,613 (GRCm39) |
N240I |
possibly damaging |
Het |
| Ccdc168 |
A |
T |
1: 44,095,668 (GRCm39) |
V1810E |
possibly damaging |
Het |
| Ccdc6 |
T |
C |
10: 70,004,951 (GRCm39) |
V232A |
possibly damaging |
Het |
| Cct5 |
A |
G |
15: 31,592,883 (GRCm39) |
I409T |
possibly damaging |
Het |
| Cd96 |
A |
G |
16: 45,856,298 (GRCm39) |
Y583H |
probably damaging |
Het |
| Cdh22 |
C |
T |
2: 164,954,329 (GRCm39) |
V731M |
probably benign |
Het |
| Clcn1 |
C |
T |
6: 42,282,494 (GRCm39) |
P521S |
probably damaging |
Het |
| Clec18a |
C |
T |
8: 111,808,322 (GRCm39) |
A27T |
probably benign |
Het |
| Cnnm2 |
C |
T |
19: 46,750,807 (GRCm39) |
A199V |
probably benign |
Het |
| Copg1 |
G |
A |
6: 87,880,478 (GRCm39) |
A494T |
possibly damaging |
Het |
| Cpsf2 |
A |
G |
12: 101,948,252 (GRCm39) |
E16G |
probably damaging |
Het |
| Cyp2j5 |
T |
A |
4: 96,552,244 (GRCm39) |
I2F |
probably benign |
Het |
| Dgkg |
T |
A |
16: 22,384,065 (GRCm39) |
N463Y |
probably damaging |
Het |
| Dnah11 |
T |
C |
12: 117,976,007 (GRCm39) |
D2804G |
probably damaging |
Het |
| Efcab12 |
T |
C |
6: 115,792,995 (GRCm39) |
N488D |
probably benign |
Het |
| Etv5 |
G |
A |
16: 22,254,668 (GRCm39) |
P64L |
probably damaging |
Het |
| Fbrs |
A |
G |
7: 127,084,272 (GRCm39) |
E468G |
probably benign |
Het |
| Fcho1 |
A |
T |
8: 72,169,468 (GRCm39) |
M146K |
probably benign |
Het |
| Gad1 |
A |
T |
2: 70,423,807 (GRCm39) |
M405L |
|
Het |
| Gcc2 |
T |
A |
10: 58,106,592 (GRCm39) |
H609Q |
probably benign |
Het |
| Gm11983 |
A |
T |
11: 6,786,902 (GRCm39) |
M75K |
unknown |
Het |
| Gm4353 |
T |
A |
7: 115,682,871 (GRCm39) |
I237F |
probably damaging |
Het |
| H1f0 |
C |
T |
15: 78,912,947 (GRCm39) |
P9L |
probably damaging |
Het |
| Hcn4 |
A |
G |
9: 58,731,222 (GRCm39) |
D143G |
unknown |
Het |
| Id1 |
T |
A |
2: 152,578,430 (GRCm39) |
V57D |
probably damaging |
Het |
| Ifna13 |
T |
C |
4: 88,562,540 (GRCm39) |
Q28R |
probably benign |
Het |
| Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
| Lonrf2 |
G |
A |
1: 38,875,538 (GRCm39) |
|
probably benign |
Het |
| Mia2 |
A |
G |
12: 59,148,371 (GRCm39) |
E77G |
probably damaging |
Het |
| Muc16 |
T |
A |
9: 18,483,937 (GRCm39) |
Q6945L |
probably benign |
Het |
| Nos2 |
G |
A |
11: 78,850,490 (GRCm39) |
R1116H |
probably damaging |
Het |
| Or2w4 |
C |
T |
13: 21,795,224 (GRCm39) |
C305Y |
probably benign |
Het |
| Parpbp |
A |
C |
10: 87,975,858 (GRCm39) |
V85G |
probably benign |
Het |
| Pcmtd2 |
C |
T |
2: 181,496,837 (GRCm39) |
H273Y |
possibly damaging |
Het |
| Pcp4l1 |
C |
T |
1: 171,001,998 (GRCm39) |
G54D |
probably damaging |
Het |
| Pkdrej |
T |
C |
15: 85,704,070 (GRCm39) |
H622R |
probably benign |
Het |
| Plxnd1 |
G |
T |
6: 115,945,754 (GRCm39) |
D906E |
probably benign |
Het |
| Pnpla8 |
T |
C |
12: 44,330,305 (GRCm39) |
S286P |
probably damaging |
Het |
| Prss36 |
C |
T |
7: 127,533,339 (GRCm39) |
V631I |
probably benign |
Het |
| Ptpn9 |
A |
T |
9: 56,964,010 (GRCm39) |
N381I |
possibly damaging |
Het |
| Ranbp9 |
A |
T |
13: 43,576,041 (GRCm39) |
I222N |
probably damaging |
Het |
| Rev1 |
T |
C |
1: 38,092,173 (GRCm39) |
T1249A |
probably damaging |
Het |
| Ripply2 |
G |
T |
9: 86,901,715 (GRCm39) |
W80C |
probably damaging |
Het |
| Rnaseh2b |
C |
A |
14: 62,602,722 (GRCm39) |
P235Q |
probably benign |
Het |
| Sacs |
T |
A |
14: 61,443,997 (GRCm39) |
F2014L |
probably damaging |
Het |
| Serpinb9f |
A |
G |
13: 33,518,238 (GRCm39) |
N246S |
probably benign |
Het |
| Sh3pxd2a |
A |
T |
19: 47,255,539 (GRCm39) |
S1088T |
probably damaging |
Het |
| Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
| Skint3 |
A |
G |
4: 112,137,432 (GRCm39) |
I367V |
probably benign |
Het |
| Slc20a2 |
G |
T |
8: 23,051,211 (GRCm39) |
E415* |
probably null |
Het |
| Slc5a1 |
T |
A |
5: 33,310,025 (GRCm39) |
S418T |
probably benign |
Het |
| Spats2 |
G |
T |
15: 99,076,446 (GRCm39) |
G175* |
probably null |
Het |
| Srebf1 |
A |
T |
11: 60,095,015 (GRCm39) |
F485L |
possibly damaging |
Het |
| St8sia4 |
A |
G |
1: 95,555,364 (GRCm39) |
V222A |
|
Het |
| Stab1 |
C |
T |
14: 30,865,531 (GRCm39) |
E1786K |
probably benign |
Het |
| Stat2 |
A |
G |
10: 128,112,657 (GRCm39) |
M58V |
probably benign |
Het |
| Stat5a |
A |
G |
11: 100,765,870 (GRCm39) |
T319A |
probably benign |
Het |
| Sufu |
A |
G |
19: 46,385,532 (GRCm39) |
|
probably benign |
Het |
| Tle6 |
T |
A |
10: 81,426,880 (GRCm39) |
I579F |
probably damaging |
Het |
| Tmem131l |
A |
T |
3: 83,845,459 (GRCm39) |
D390E |
probably benign |
Het |
| Trim33 |
T |
A |
3: 103,228,979 (GRCm39) |
|
probably null |
Het |
| Usp54 |
A |
G |
14: 20,611,678 (GRCm39) |
V1046A |
probably benign |
Het |
| Vit |
G |
A |
17: 78,932,413 (GRCm39) |
G507R |
probably damaging |
Het |
| Vmn2r59 |
A |
G |
7: 41,695,590 (GRCm39) |
I274T |
probably damaging |
Het |
| Vmn2r67 |
T |
A |
7: 84,804,917 (GRCm39) |
K65M |
possibly damaging |
Het |
| Vmn2r86 |
C |
T |
10: 130,282,567 (GRCm39) |
G683E |
possibly damaging |
Het |
| Vwa8 |
T |
C |
14: 79,335,871 (GRCm39) |
|
probably null |
Het |
| Zdhhc14 |
A |
G |
17: 5,781,779 (GRCm39) |
D333G |
probably benign |
Het |
| Zup1 |
G |
A |
10: 33,795,355 (GRCm39) |
S568L |
probably damaging |
Het |
|
| Other mutations in Magi3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00429:Magi3
|
APN |
3 |
103,922,294 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00933:Magi3
|
APN |
3 |
103,923,163 (GRCm39) |
missense |
probably benign |
|
|
IGL01151:Magi3
|
APN |
3 |
103,958,690 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01674:Magi3
|
APN |
3 |
104,013,037 (GRCm39) |
splice site |
probably benign |
|
|
IGL01790:Magi3
|
APN |
3 |
103,992,560 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01903:Magi3
|
APN |
3 |
103,958,526 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
IGL01939:Magi3
|
APN |
3 |
103,961,778 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02142:Magi3
|
APN |
3 |
103,923,219 (GRCm39) |
missense |
probably benign |
0.32 |
|
IGL02183:Magi3
|
APN |
3 |
103,992,663 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02887:Magi3
|
APN |
3 |
104,002,473 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03071:Magi3
|
APN |
3 |
103,923,202 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
IGL03085:Magi3
|
APN |
3 |
103,922,655 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
IGL03192:Magi3
|
APN |
3 |
103,950,562 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03204:Magi3
|
APN |
3 |
104,013,151 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03227:Magi3
|
APN |
3 |
103,958,435 (GRCm39) |
missense |
probably benign |
|
|
IGL03388:Magi3
|
APN |
3 |
103,923,157 (GRCm39) |
missense |
probably benign |
0.30 |
|
PIT4280001:Magi3
|
UTSW |
3 |
103,961,668 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4504001:Magi3
|
UTSW |
3 |
103,922,842 (GRCm39) |
missense |
probably benign |
0.05 |
|
R0092:Magi3
|
UTSW |
3 |
103,958,280 (GRCm39) |
nonsense |
probably null |
|
|
R0514:Magi3
|
UTSW |
3 |
103,922,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0569:Magi3
|
UTSW |
3 |
103,923,358 (GRCm39) |
missense |
probably benign |
0.43 |
|
R0608:Magi3
|
UTSW |
3 |
103,924,873 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0920:Magi3
|
UTSW |
3 |
103,941,507 (GRCm39) |
splice site |
probably null |
|
|
R1173:Magi3
|
UTSW |
3 |
103,968,946 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1256:Magi3
|
UTSW |
3 |
103,935,126 (GRCm39) |
missense |
probably benign |
0.08 |
|
R1391:Magi3
|
UTSW |
3 |
103,922,374 (GRCm39) |
nonsense |
probably null |
|
|
R1559:Magi3
|
UTSW |
3 |
103,954,169 (GRCm39) |
splice site |
probably benign |
|
|
R1568:Magi3
|
UTSW |
3 |
103,996,843 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1631:Magi3
|
UTSW |
3 |
103,958,493 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1747:Magi3
|
UTSW |
3 |
103,941,489 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R1930:Magi3
|
UTSW |
3 |
103,996,920 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1964:Magi3
|
UTSW |
3 |
103,927,718 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2151:Magi3
|
UTSW |
3 |
103,992,554 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2151:Magi3
|
UTSW |
3 |
103,954,198 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2266:Magi3
|
UTSW |
3 |
103,928,382 (GRCm39) |
intron |
probably benign |
|
|
R2267:Magi3
|
UTSW |
3 |
103,928,382 (GRCm39) |
intron |
probably benign |
|
|
R2268:Magi3
|
UTSW |
3 |
103,928,382 (GRCm39) |
intron |
probably benign |
|
|
R2519:Magi3
|
UTSW |
3 |
103,923,081 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3104:Magi3
|
UTSW |
3 |
103,958,636 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3105:Magi3
|
UTSW |
3 |
103,958,636 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3619:Magi3
|
UTSW |
3 |
103,961,721 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4158:Magi3
|
UTSW |
3 |
103,958,277 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4160:Magi3
|
UTSW |
3 |
103,958,277 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4284:Magi3
|
UTSW |
3 |
103,923,184 (GRCm39) |
nonsense |
probably null |
|
|
R4285:Magi3
|
UTSW |
3 |
103,923,184 (GRCm39) |
nonsense |
probably null |
|
|
R4397:Magi3
|
UTSW |
3 |
104,127,030 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4512:Magi3
|
UTSW |
3 |
103,996,871 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4676:Magi3
|
UTSW |
3 |
103,923,141 (GRCm39) |
missense |
probably benign |
|
|
R4758:Magi3
|
UTSW |
3 |
103,922,637 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4940:Magi3
|
UTSW |
3 |
103,958,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5039:Magi3
|
UTSW |
3 |
104,013,107 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5160:Magi3
|
UTSW |
3 |
103,935,224 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R5422:Magi3
|
UTSW |
3 |
103,958,684 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5509:Magi3
|
UTSW |
3 |
103,922,818 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5839:Magi3
|
UTSW |
3 |
104,127,047 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5924:Magi3
|
UTSW |
3 |
103,961,854 (GRCm39) |
splice site |
probably null |
|
|
R6018:Magi3
|
UTSW |
3 |
104,013,128 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6189:Magi3
|
UTSW |
3 |
103,958,181 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6235:Magi3
|
UTSW |
3 |
103,923,384 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6244:Magi3
|
UTSW |
3 |
103,923,013 (GRCm39) |
missense |
probably benign |
0.16 |
|
R6258:Magi3
|
UTSW |
3 |
103,996,912 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6358:Magi3
|
UTSW |
3 |
103,958,268 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6534:Magi3
|
UTSW |
3 |
103,992,536 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R6806:Magi3
|
UTSW |
3 |
103,954,285 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6816:Magi3
|
UTSW |
3 |
103,997,227 (GRCm39) |
splice site |
probably null |
|
|
R6897:Magi3
|
UTSW |
3 |
103,996,873 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7011:Magi3
|
UTSW |
3 |
104,013,070 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7039:Magi3
|
UTSW |
3 |
103,958,699 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7196:Magi3
|
UTSW |
3 |
103,956,484 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7237:Magi3
|
UTSW |
3 |
103,935,227 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7285:Magi3
|
UTSW |
3 |
103,941,430 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7709:Magi3
|
UTSW |
3 |
103,941,354 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7724:Magi3
|
UTSW |
3 |
103,923,243 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7797:Magi3
|
UTSW |
3 |
103,958,618 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7950:Magi3
|
UTSW |
3 |
103,924,005 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8140:Magi3
|
UTSW |
3 |
103,941,402 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8204:Magi3
|
UTSW |
3 |
103,958,502 (GRCm39) |
missense |
probably benign |
|
|
R8229:Magi3
|
UTSW |
3 |
103,923,018 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8229:Magi3
|
UTSW |
3 |
103,923,017 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R8260:Magi3
|
UTSW |
3 |
103,922,625 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8348:Magi3
|
UTSW |
3 |
103,958,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8368:Magi3
|
UTSW |
3 |
104,002,379 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8543:Magi3
|
UTSW |
3 |
104,126,984 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8762:Magi3
|
UTSW |
3 |
103,958,169 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8826:Magi3
|
UTSW |
3 |
103,992,662 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8847:Magi3
|
UTSW |
3 |
103,922,334 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8892:Magi3
|
UTSW |
3 |
103,958,141 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8939:Magi3
|
UTSW |
3 |
103,996,748 (GRCm39) |
intron |
probably benign |
|
|
R9090:Magi3
|
UTSW |
3 |
103,923,264 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R9187:Magi3
|
UTSW |
3 |
103,923,073 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R9271:Magi3
|
UTSW |
3 |
103,923,264 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R9439:Magi3
|
UTSW |
3 |
103,922,473 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9557:Magi3
|
UTSW |
3 |
103,924,933 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9557:Magi3
|
UTSW |
3 |
103,922,473 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9697:Magi3
|
UTSW |
3 |
103,956,458 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9796:Magi3
|
UTSW |
3 |
103,928,291 (GRCm39) |
missense |
probably benign |
|
|
X0026:Magi3
|
UTSW |
3 |
103,927,736 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTTGTCAGCCATGCCAGTAG -3'
(R):5'- TCTGAAGCAGAGTCAGCCAG -3'
Sequencing Primer
(F):5'- ATGCCAGTAGTGCCTGTGAC -3'
(R):5'- CCAAGTCTCCAGAGAAAAAGAGCAG -3'
|
| Posted On |
2022-05-16 |
Incidental Mutation