Incidental Mutation 'R9090:Ifi207'
| ID |
690865 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ifi207
|
| Ensembl Gene |
ENSMUSG00000073490 |
| Gene Name |
interferon activated gene 207 |
| Synonyms |
AI607873, Pyhin-A |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.086)
|
| Stock # |
R9090 (G1)
|
| Quality Score |
136.467 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
173550993-173569313 bp(-) (GRCm39) |
| Type of Mutation |
small deletion (14 aa in frame mutation) |
| DNA Base Change (assembly) |
CTGTTGATGAAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATACAGTTGCTTGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATAGAGTTGCATATGGAGCCAGGAGGATGCTATATGTTGTTGATGAAGTTGCATGTGGAGCCAGGAG to CTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATACAGTTGCTTGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATAGAGTTGCATATGGAGCCAGGAGGATGCTATATGTTGTTGATGAAGTTGCATGTGGAGCCAGGAG
at 173556762 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000119350
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042610]
[ENSMUST00000127730]
|
| AlphaFold |
E9Q3L4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000042610
|
| SMART Domains |
Protein: ENSMUSP00000048129
Gene: ENSMUSG00000073490
| Domain | Start | End | E-Value | Type |
|---|
|
PYRIN
|
6 |
84 |
3.2e-15 |
SMART |
|
low complexity region
|
121 |
133 |
N/A |
INTRINSIC |
|
low complexity region
|
136 |
162 |
N/A |
INTRINSIC |
|
low complexity region
|
207 |
215 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
286 |
472 |
4.17e-7 |
PROSPERO |
|
low complexity region
|
476 |
496 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
565 |
782 |
4.17e-7 |
PROSPERO |
|
Pfam:HIN
|
788 |
954 |
4.9e-76 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000127730
|
| SMART Domains |
Protein: ENSMUSP00000119350
Gene: ENSMUSG00000073490
| Domain | Start | End | E-Value | Type |
|---|
|
PYRIN
|
6 |
84 |
3.2e-15 |
SMART |
|
low complexity region
|
121 |
133 |
N/A |
INTRINSIC |
|
low complexity region
|
136 |
155 |
N/A |
INTRINSIC |
|
low complexity region
|
200 |
208 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
279 |
465 |
6.41e-7 |
PROSPERO |
|
low complexity region
|
469 |
489 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
558 |
775 |
6.41e-7 |
PROSPERO |
|
Pfam:HIN
|
781 |
948 |
1.8e-78 |
PFAM |
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.2%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 106 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aatk |
A |
T |
11: 119,901,940 (GRCm39) |
S819T |
probably damaging |
Het |
| Abca13 |
A |
T |
11: 9,241,698 (GRCm39) |
D1187V |
probably damaging |
Het |
| Ak9 |
C |
A |
10: 41,300,623 (GRCm39) |
T1611K |
unknown |
Het |
| Als2 |
G |
T |
1: 59,242,189 (GRCm39) |
T622K |
probably benign |
Het |
| Ankrd40 |
G |
A |
11: 94,225,262 (GRCm39) |
A98T |
probably benign |
Het |
| Ap1b1 |
T |
C |
11: 4,973,174 (GRCm39) |
L339P |
probably damaging |
Het |
| Appl1 |
A |
C |
14: 26,669,084 (GRCm39) |
H363Q |
probably benign |
Het |
| Atf6 |
T |
C |
1: 170,622,245 (GRCm39) |
N459D |
probably damaging |
Het |
| Ccdc6 |
A |
T |
10: 70,024,993 (GRCm39) |
Q432L |
unknown |
Het |
| Ccl21a |
T |
A |
4: 42,773,486 (GRCm39) |
Q84L |
probably damaging |
Het |
| Cct4 |
A |
G |
11: 22,951,389 (GRCm39) |
I348V |
probably benign |
Het |
| Cd300ld2 |
A |
G |
11: 114,904,550 (GRCm39) |
Y106H |
probably damaging |
Het |
| Cdh19 |
C |
T |
1: 110,876,947 (GRCm39) |
E131K |
probably damaging |
Het |
| Cdon |
A |
G |
9: 35,403,175 (GRCm39) |
D1095G |
probably damaging |
Het |
| Cep85l |
T |
A |
10: 53,157,670 (GRCm39) |
R678* |
probably null |
Het |
| Chst3 |
T |
A |
10: 60,021,465 (GRCm39) |
S461C |
probably damaging |
Het |
| Clk1 |
A |
G |
1: 58,459,312 (GRCm39) |
I149T |
possibly damaging |
Het |
| Clvs2 |
T |
A |
10: 33,389,301 (GRCm39) |
D313V |
possibly damaging |
Het |
| Dap3 |
T |
C |
3: 88,840,913 (GRCm39) |
T75A |
probably benign |
Het |
| Dnaaf1 |
T |
A |
8: 120,324,392 (GRCm39) |
F631L |
probably benign |
Het |
| Dnah14 |
A |
T |
1: 181,597,325 (GRCm39) |
N3549I |
probably benign |
Het |
| Dnah17 |
A |
T |
11: 117,931,870 (GRCm39) |
Y3701N |
probably damaging |
Het |
| Dock6 |
A |
G |
9: 21,752,796 (GRCm39) |
V339A |
possibly damaging |
Het |
| Dpp6 |
T |
A |
5: 27,803,832 (GRCm39) |
C259* |
probably null |
Het |
| Dqx1 |
A |
G |
6: 83,036,024 (GRCm39) |
T119A |
probably benign |
Het |
| Dync1h1 |
G |
T |
12: 110,583,310 (GRCm39) |
R469L |
probably benign |
Het |
| Eno4 |
C |
T |
19: 58,951,260 (GRCm39) |
A424V |
probably benign |
Het |
| Entrep1 |
A |
T |
19: 23,972,221 (GRCm39) |
I161N |
possibly damaging |
Het |
| Fads1 |
T |
A |
19: 10,163,162 (GRCm39) |
D146E |
probably damaging |
Het |
| Fam171a1 |
C |
T |
2: 3,224,543 (GRCm39) |
T303M |
probably damaging |
Het |
| Fbxw20 |
C |
T |
9: 109,050,423 (GRCm39) |
D401N |
probably benign |
Het |
| Fcho1 |
T |
A |
8: 72,163,068 (GRCm39) |
T654S |
possibly damaging |
Het |
| Flad1 |
C |
A |
3: 89,315,858 (GRCm39) |
E235* |
probably null |
Het |
| Flrt2 |
G |
T |
12: 95,745,907 (GRCm39) |
A82S |
probably benign |
Het |
| Gabrg3 |
A |
T |
7: 56,829,386 (GRCm39) |
S124T |
probably benign |
Het |
| Galt |
C |
T |
4: 41,756,777 (GRCm39) |
T139I |
probably benign |
Het |
| Garin4 |
A |
G |
1: 190,895,153 (GRCm39) |
S497P |
probably damaging |
Het |
| Gfod1 |
T |
C |
13: 43,456,861 (GRCm39) |
E38G |
possibly damaging |
Het |
| Gm10330 |
A |
G |
12: 23,829,992 (GRCm39) |
I63T |
possibly damaging |
Het |
| Gm49359 |
A |
G |
13: 62,602,867 (GRCm39) |
V111A |
probably benign |
Het |
| Gpank1 |
C |
T |
17: 35,340,734 (GRCm39) |
|
probably benign |
Het |
| Hck |
T |
C |
2: 152,973,185 (GRCm39) |
L156P |
probably damaging |
Het |
| Hcn3 |
G |
T |
3: 89,057,267 (GRCm39) |
R444S |
probably damaging |
Het |
| Hephl1 |
T |
C |
9: 14,988,236 (GRCm39) |
N624S |
probably damaging |
Het |
| Hmcn1 |
A |
G |
1: 150,632,309 (GRCm39) |
I876T |
probably damaging |
Het |
| Itga9 |
T |
A |
9: 118,500,859 (GRCm39) |
D377E |
possibly damaging |
Het |
| Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
| Itprid1 |
G |
T |
6: 55,944,051 (GRCm39) |
R417L |
probably benign |
Het |
| Klk1b11 |
C |
T |
7: 43,425,954 (GRCm39) |
L32F |
probably benign |
Het |
| Lta4h |
A |
G |
10: 93,310,412 (GRCm39) |
S427G |
probably benign |
Het |
| Lxn |
T |
A |
3: 67,368,651 (GRCm39) |
I122F |
probably damaging |
Het |
| Lyz1 |
A |
G |
10: 117,124,492 (GRCm39) |
V148A |
possibly damaging |
Het |
| Mael |
G |
T |
1: 166,032,424 (GRCm39) |
Q326K |
probably benign |
Het |
| Magi3 |
T |
C |
3: 103,923,264 (GRCm39) |
D1151G |
possibly damaging |
Het |
| Map3k9 |
C |
A |
12: 81,769,261 (GRCm39) |
G929V |
probably benign |
Het |
| Mcoln1 |
A |
G |
8: 3,555,771 (GRCm39) |
Y22C |
probably damaging |
Het |
| Mier3 |
G |
T |
13: 111,827,870 (GRCm39) |
M45I |
probably benign |
Het |
| Mrpl1 |
T |
C |
5: 96,371,746 (GRCm39) |
V91A |
probably damaging |
Het |
| Myo7a |
T |
C |
7: 97,740,281 (GRCm39) |
H571R |
probably benign |
Het |
| Myom1 |
T |
A |
17: 71,374,325 (GRCm39) |
W601R |
probably damaging |
Het |
| Myom3 |
C |
T |
4: 135,505,479 (GRCm39) |
T456I |
probably benign |
Het |
| Nags |
A |
T |
11: 102,037,584 (GRCm39) |
H225L |
probably benign |
Het |
| Ncaph |
C |
A |
2: 126,958,554 (GRCm39) |
K488N |
probably damaging |
Het |
| Nkain3 |
C |
T |
4: 20,484,897 (GRCm39) |
R60H |
probably damaging |
Het |
| Nlrp9a |
A |
T |
7: 26,261,944 (GRCm39) |
M698L |
probably benign |
Het |
| Nmur2 |
A |
C |
11: 55,931,308 (GRCm39) |
I134M |
probably benign |
Het |
| Nrp2 |
A |
C |
1: 62,784,670 (GRCm39) |
E273A |
probably benign |
Het |
| Nup85 |
A |
G |
11: 115,468,787 (GRCm39) |
D210G |
possibly damaging |
Het |
| Obscn |
A |
G |
11: 59,006,643 (GRCm39) |
F1173S |
probably damaging |
Het |
| Or5ac24 |
A |
T |
16: 59,165,145 (GRCm39) |
C306* |
probably null |
Het |
| Otogl |
T |
A |
10: 107,652,974 (GRCm39) |
E1126V |
probably null |
Het |
| Pfkl |
T |
C |
10: 77,833,426 (GRCm39) |
I259V |
probably benign |
Het |
| Phkg1 |
A |
T |
5: 129,893,863 (GRCm39) |
Y291N |
probably benign |
Het |
| Piezo2 |
T |
G |
18: 63,163,450 (GRCm39) |
H2156P |
probably damaging |
Het |
| Piezo2 |
C |
A |
18: 63,208,790 (GRCm39) |
V1408L |
probably damaging |
Het |
| Pira13 |
T |
A |
7: 3,819,997 (GRCm39) |
E640V |
unknown |
Het |
| Plekhg3 |
A |
G |
12: 76,622,694 (GRCm39) |
T646A |
probably benign |
Het |
| Plk5 |
C |
G |
10: 80,193,830 (GRCm39) |
R40G |
probably damaging |
Het |
| Ppp1r12a |
T |
C |
10: 108,098,224 (GRCm39) |
S838P |
probably damaging |
Het |
| Rarb |
A |
T |
14: 16,435,235 (GRCm38) |
Y270* |
probably null |
Het |
| Rbm15 |
T |
C |
3: 107,239,312 (GRCm39) |
E362G |
possibly damaging |
Het |
| Rcan1 |
A |
G |
16: 92,262,741 (GRCm39) |
F76L |
|
Het |
| Rdh19 |
T |
C |
10: 127,696,142 (GRCm39) |
L298P |
probably damaging |
Het |
| Rims1 |
T |
A |
1: 22,498,773 (GRCm39) |
H57L |
|
Het |
| Rlf |
T |
C |
4: 121,004,751 (GRCm39) |
T1520A |
probably benign |
Het |
| Rnase1 |
T |
A |
14: 51,382,964 (GRCm39) |
H130L |
possibly damaging |
Het |
| Samd8 |
T |
A |
14: 21,842,569 (GRCm39) |
M360K |
probably damaging |
Het |
| Samhd1 |
A |
G |
2: 156,956,205 (GRCm39) |
L329P |
probably damaging |
Het |
| Scube1 |
C |
T |
15: 83,494,394 (GRCm39) |
E878K |
probably damaging |
Het |
| Sema3b |
T |
C |
9: 107,476,154 (GRCm39) |
Y689C |
probably damaging |
Het |
| Semp2l2a |
T |
C |
8: 13,886,697 (GRCm39) |
T465A |
possibly damaging |
Het |
| Sh3pxd2b |
A |
T |
11: 32,373,361 (GRCm39) |
N843Y |
possibly damaging |
Het |
| Slco1a6 |
C |
T |
6: 142,035,575 (GRCm39) |
C583Y |
probably damaging |
Het |
| Smg1 |
A |
C |
7: 117,811,786 (GRCm39) |
V88G |
unknown |
Het |
| Spata24 |
T |
A |
18: 35,790,054 (GRCm39) |
N146Y |
probably damaging |
Het |
| Tcf3 |
C |
A |
10: 80,253,191 (GRCm39) |
V258L |
probably benign |
Het |
| Tiam2 |
T |
C |
17: 3,465,011 (GRCm39) |
Y247H |
probably damaging |
Het |
| Ticrr |
T |
C |
7: 79,310,604 (GRCm39) |
F173L |
possibly damaging |
Het |
| Tpp2 |
A |
G |
1: 43,993,811 (GRCm39) |
E232G |
probably damaging |
Het |
| Trank1 |
T |
A |
9: 111,174,547 (GRCm39) |
V138E |
probably damaging |
Het |
| Ttll3 |
T |
C |
6: 113,369,596 (GRCm39) |
S47P |
probably benign |
Het |
| Utp4 |
C |
T |
8: 107,632,857 (GRCm39) |
T280M |
probably damaging |
Het |
| Vmn1r123 |
A |
T |
7: 20,896,794 (GRCm39) |
N229Y |
probably benign |
Het |
| Vmn1r85 |
A |
T |
7: 12,818,942 (GRCm39) |
Y67* |
probably null |
Het |
| Zbtb12 |
T |
A |
17: 35,114,320 (GRCm39) |
V35E |
possibly damaging |
Het |
| Zmym6 |
T |
A |
4: 127,017,854 (GRCm39) |
F1212I |
probably damaging |
Het |
|
| Other mutations in Ifi207 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01776:Ifi207
|
APN |
1 |
173,552,610 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01864:Ifi207
|
APN |
1 |
173,564,007 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
IGL02293:Ifi207
|
APN |
1 |
173,551,314 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02402:Ifi207
|
APN |
1 |
173,555,159 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03160:Ifi207
|
APN |
1 |
173,562,670 (GRCm39) |
splice site |
probably benign |
|
|
PIT4458001:Ifi207
|
UTSW |
1 |
173,562,738 (GRCm39) |
missense |
unknown |
|
|
R0043:Ifi207
|
UTSW |
1 |
173,556,678 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R0212:Ifi207
|
UTSW |
1 |
173,563,964 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R0395:Ifi207
|
UTSW |
1 |
173,557,431 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R0506:Ifi207
|
UTSW |
1 |
173,563,878 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R0843:Ifi207
|
UTSW |
1 |
173,555,143 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1302:Ifi207
|
UTSW |
1 |
173,562,861 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R1373:Ifi207
|
UTSW |
1 |
173,557,913 (GRCm39) |
missense |
unknown |
|
|
R1462:Ifi207
|
UTSW |
1 |
173,552,513 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1462:Ifi207
|
UTSW |
1 |
173,552,513 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1471:Ifi207
|
UTSW |
1 |
173,557,629 (GRCm39) |
missense |
unknown |
|
|
R1502:Ifi207
|
UTSW |
1 |
173,556,872 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R1533:Ifi207
|
UTSW |
1 |
173,555,306 (GRCm39) |
missense |
probably benign |
0.30 |
|
R1831:Ifi207
|
UTSW |
1 |
173,559,992 (GRCm39) |
missense |
unknown |
|
|
R1928:Ifi207
|
UTSW |
1 |
173,557,211 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R1982:Ifi207
|
UTSW |
1 |
173,562,805 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2132:Ifi207
|
UTSW |
1 |
173,557,337 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R2248:Ifi207
|
UTSW |
1 |
173,564,036 (GRCm39) |
splice site |
probably benign |
|
|
R3703:Ifi207
|
UTSW |
1 |
173,555,029 (GRCm39) |
nonsense |
probably null |
|
|
R3741:Ifi207
|
UTSW |
1 |
173,555,128 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3846:Ifi207
|
UTSW |
1 |
173,562,869 (GRCm39) |
missense |
probably benign |
0.33 |
|
R4747:Ifi207
|
UTSW |
1 |
173,556,633 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4772:Ifi207
|
UTSW |
1 |
173,555,253 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4776:Ifi207
|
UTSW |
1 |
173,557,622 (GRCm39) |
missense |
unknown |
|
|
R4855:Ifi207
|
UTSW |
1 |
173,557,381 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5170:Ifi207
|
UTSW |
1 |
173,558,064 (GRCm39) |
missense |
unknown |
|
|
R5244:Ifi207
|
UTSW |
1 |
173,557,503 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5280:Ifi207
|
UTSW |
1 |
173,557,870 (GRCm39) |
missense |
unknown |
|
|
R5301:Ifi207
|
UTSW |
1 |
173,556,977 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R5334:Ifi207
|
UTSW |
1 |
173,555,097 (GRCm39) |
missense |
probably benign |
0.21 |
|
R5445:Ifi207
|
UTSW |
1 |
173,555,363 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5691:Ifi207
|
UTSW |
1 |
173,559,992 (GRCm39) |
missense |
unknown |
|
|
R5838:Ifi207
|
UTSW |
1 |
173,559,953 (GRCm39) |
missense |
unknown |
|
|
R6060:Ifi207
|
UTSW |
1 |
173,558,093 (GRCm39) |
missense |
unknown |
|
|
R6220:Ifi207
|
UTSW |
1 |
173,557,112 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6264:Ifi207
|
UTSW |
1 |
173,555,111 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6307:Ifi207
|
UTSW |
1 |
173,552,619 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6326:Ifi207
|
UTSW |
1 |
173,557,532 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6394:Ifi207
|
UTSW |
1 |
173,556,581 (GRCm39) |
missense |
probably benign |
0.43 |
|
R6532:Ifi207
|
UTSW |
1 |
173,557,211 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R6660:Ifi207
|
UTSW |
1 |
173,556,972 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6893:Ifi207
|
UTSW |
1 |
173,555,208 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7190:Ifi207
|
UTSW |
1 |
173,557,818 (GRCm39) |
missense |
unknown |
|
|
R7192:Ifi207
|
UTSW |
1 |
173,556,584 (GRCm39) |
missense |
not run |
|
|
R7194:Ifi207
|
UTSW |
1 |
173,557,490 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R7327:Ifi207
|
UTSW |
1 |
173,556,581 (GRCm39) |
missense |
probably benign |
0.43 |
|
R7348:Ifi207
|
UTSW |
1 |
173,556,762 (GRCm39) |
small deletion |
probably benign |
|
|
R7404:Ifi207
|
UTSW |
1 |
173,556,494 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R7442:Ifi207
|
UTSW |
1 |
173,554,997 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7784:Ifi207
|
UTSW |
1 |
173,557,698 (GRCm39) |
missense |
unknown |
|
|
R8041:Ifi207
|
UTSW |
1 |
173,555,268 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R8116:Ifi207
|
UTSW |
1 |
173,557,746 (GRCm39) |
missense |
unknown |
|
|
R8166:Ifi207
|
UTSW |
1 |
173,557,504 (GRCm39) |
missense |
probably benign |
0.10 |
|
R8166:Ifi207
|
UTSW |
1 |
173,557,166 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8168:Ifi207
|
UTSW |
1 |
173,557,504 (GRCm39) |
missense |
probably benign |
0.10 |
|
R8383:Ifi207
|
UTSW |
1 |
173,556,770 (GRCm39) |
small deletion |
probably benign |
|
|
R8388:Ifi207
|
UTSW |
1 |
173,557,016 (GRCm39) |
frame shift |
probably null |
|
|
R8389:Ifi207
|
UTSW |
1 |
173,557,016 (GRCm39) |
frame shift |
probably null |
|
|
R8390:Ifi207
|
UTSW |
1 |
173,557,016 (GRCm39) |
frame shift |
probably null |
|
|
R8399:Ifi207
|
UTSW |
1 |
173,557,844 (GRCm39) |
missense |
unknown |
|
|
R8431:Ifi207
|
UTSW |
1 |
173,558,070 (GRCm39) |
missense |
unknown |
|
|
R8474:Ifi207
|
UTSW |
1 |
173,556,605 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R8505:Ifi207
|
UTSW |
1 |
173,557,016 (GRCm39) |
frame shift |
probably null |
|
|
R9009:Ifi207
|
UTSW |
1 |
173,555,382 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9061:Ifi207
|
UTSW |
1 |
173,564,153 (GRCm39) |
intron |
probably benign |
|
|
R9071:Ifi207
|
UTSW |
1 |
173,557,764 (GRCm39) |
missense |
unknown |
|
|
R9323:Ifi207
|
UTSW |
1 |
173,555,143 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9407:Ifi207
|
UTSW |
1 |
173,555,234 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9493:Ifi207
|
UTSW |
1 |
173,556,522 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9629:Ifi207
|
UTSW |
1 |
173,556,561 (GRCm39) |
small deletion |
probably benign |
|
|
RF009:Ifi207
|
UTSW |
1 |
173,556,558 (GRCm39) |
missense |
probably benign |
0.00 |
|
RF011:Ifi207
|
UTSW |
1 |
173,556,687 (GRCm39) |
missense |
not run |
|
|
RF032:Ifi207
|
UTSW |
1 |
173,562,723 (GRCm39) |
small deletion |
probably benign |
|
|
X0003:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0004:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0005:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0009:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0010:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0011:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0012:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0013:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0014:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0017:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0018:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0019:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0020:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0021:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0022:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0023:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0024:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0025:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0026:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0027:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0028:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0033:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0034:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0035:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0036:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0037:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0038:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0039:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0040:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0050:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0052:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0053:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0054:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0057:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0058:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0060:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0061:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0062:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0063:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0064:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0065:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0066:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0067:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1177:Ifi207
|
UTSW |
1 |
173,557,145 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1187:Ifi207
|
UTSW |
1 |
173,558,093 (GRCm39) |
missense |
unknown |
|
|
Z1192:Ifi207
|
UTSW |
1 |
173,558,093 (GRCm39) |
missense |
unknown |
|
|
| Predicted Primers |
PCR Primer
(F):5'- ACTGTGGAGCCAGAAGATTGC -3'
(R):5'- ATCTAGCAACCTCCTGGCTC -3'
Sequencing Primer
(F):5'- CCAGAAGATTGCTGGATGCTG -3'
(R):5'- ACCTCCTGGCTCCACAAG -3'
|
| Posted On |
2021-12-30 |
Incidental Mutation