Incidental Mutation 'R9294:Virma'
| ID |
704439 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Virma
|
| Ensembl Gene |
ENSMUSG00000040720 |
| Gene Name |
vir like m6A methyltransferase associated |
| Synonyms |
1110037F02Rik |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R9294 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
4 |
| Chromosomal Location |
11485958-11550684 bp(+) (GRCm38) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to T
at 11513507 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Stop codon
at position 454
(R454*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000063188
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055372]
[ENSMUST00000059914]
[ENSMUST00000108307]
|
| AlphaFold |
A2AIV2 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000055372
AA Change: R454*
|
| SMART Domains |
Protein: ENSMUSP00000063188
Gene: ENSMUSG00000040720
AA Change: R454*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
139 |
153 |
N/A |
INTRINSIC |
|
low complexity region
|
172 |
198 |
N/A |
INTRINSIC |
|
low complexity region
|
236 |
267 |
N/A |
INTRINSIC |
|
low complexity region
|
276 |
297 |
N/A |
INTRINSIC |
|
low complexity region
|
615 |
625 |
N/A |
INTRINSIC |
|
low complexity region
|
1008 |
1020 |
N/A |
INTRINSIC |
|
low complexity region
|
1112 |
1124 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000059914
AA Change: R454*
|
| SMART Domains |
Protein: ENSMUSP00000058078
Gene: ENSMUSG00000040720
AA Change: R454*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
139 |
153 |
N/A |
INTRINSIC |
|
low complexity region
|
172 |
198 |
N/A |
INTRINSIC |
|
low complexity region
|
236 |
267 |
N/A |
INTRINSIC |
|
low complexity region
|
276 |
297 |
N/A |
INTRINSIC |
|
low complexity region
|
615 |
625 |
N/A |
INTRINSIC |
|
low complexity region
|
1008 |
1020 |
N/A |
INTRINSIC |
|
low complexity region
|
1112 |
1124 |
N/A |
INTRINSIC |
|
low complexity region
|
1224 |
1232 |
N/A |
INTRINSIC |
|
low complexity region
|
1443 |
1458 |
N/A |
INTRINSIC |
|
low complexity region
|
1460 |
1474 |
N/A |
INTRINSIC |
|
low complexity region
|
1618 |
1634 |
N/A |
INTRINSIC |
|
low complexity region
|
1684 |
1697 |
N/A |
INTRINSIC |
|
low complexity region
|
1750 |
1757 |
N/A |
INTRINSIC |
|
low complexity region
|
1796 |
1808 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000108307
AA Change: R454*
|
| SMART Domains |
Protein: ENSMUSP00000103943
Gene: ENSMUSG00000040720
AA Change: R454*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:VIR_N
|
5 |
266 |
2e-110 |
PFAM |
|
low complexity region
|
276 |
297 |
N/A |
INTRINSIC |
|
low complexity region
|
615 |
625 |
N/A |
INTRINSIC |
|
low complexity region
|
1058 |
1070 |
N/A |
INTRINSIC |
|
low complexity region
|
1162 |
1174 |
N/A |
INTRINSIC |
|
low complexity region
|
1274 |
1282 |
N/A |
INTRINSIC |
|
low complexity region
|
1493 |
1508 |
N/A |
INTRINSIC |
|
low complexity region
|
1510 |
1524 |
N/A |
INTRINSIC |
|
low complexity region
|
1668 |
1684 |
N/A |
INTRINSIC |
|
low complexity region
|
1734 |
1747 |
N/A |
INTRINSIC |
|
low complexity region
|
1800 |
1807 |
N/A |
INTRINSIC |
|
low complexity region
|
1846 |
1858 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.8%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 87 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 0610009O20Rik |
T |
G |
18: 38,261,076 (GRCm38) |
L442R |
probably damaging |
Het |
| 1700067K01Rik |
A |
G |
8: 84,003,379 (GRCm38) |
Y165C |
probably damaging |
Het |
| 2410089E03Rik |
T |
C |
15: 8,203,327 (GRCm38) |
V1110A |
probably benign |
Het |
| 2810474O19Rik |
T |
A |
6: 149,326,432 (GRCm38) |
N325K |
probably benign |
Het |
| 4930452B06Rik |
A |
G |
14: 8,578,361 (GRCm38) |
I127T |
possibly damaging |
Het |
| Abcb11 |
T |
A |
2: 69,265,496 (GRCm38) |
K833N |
possibly damaging |
Het |
| Abcb1a |
T |
A |
5: 8,686,171 (GRCm38) |
M188K |
probably benign |
Het |
| Akap1 |
A |
T |
11: 88,837,140 (GRCm38) |
V672D |
probably damaging |
Het |
| Anapc4 |
A |
G |
5: 52,864,525 (GRCm38) |
T650A |
possibly damaging |
Het |
| Ash1l |
C |
A |
3: 88,982,990 (GRCm38) |
S725R |
possibly damaging |
Het |
| Axdnd1 |
T |
A |
1: 156,420,347 (GRCm38) |
K28* |
probably null |
Het |
| C8b |
C |
A |
4: 104,786,995 (GRCm38) |
H286Q |
probably benign |
Het |
| Cacna2d1 |
A |
G |
5: 16,012,398 (GRCm38) |
K34E |
probably damaging |
Het |
| Ccdc14 |
T |
A |
16: 34,697,358 (GRCm38) |
H154Q |
probably damaging |
Het |
| Ccdc184 |
A |
G |
15: 98,168,512 (GRCm38) |
D66G |
probably damaging |
Het |
| Ccdc62 |
A |
G |
5: 123,954,709 (GRCm38) |
I586V |
possibly damaging |
Het |
| Chadl |
A |
T |
15: 81,694,490 (GRCm38) |
C313S |
probably damaging |
Het |
| Clec14a |
C |
A |
12: 58,268,750 (GRCm38) |
A29S |
probably damaging |
Het |
| Col26a1 |
C |
T |
5: 136,757,754 (GRCm38) |
G161D |
probably benign |
Het |
| Ctbp2 |
A |
G |
7: 133,014,232 (GRCm38) |
S325P |
probably damaging |
Het |
| Dcaf13 |
A |
G |
15: 39,130,292 (GRCm38) |
D260G |
possibly damaging |
Het |
| Dhx37 |
G |
A |
5: 125,422,672 (GRCm38) |
P575L |
probably benign |
Het |
| Dnajc6 |
T |
C |
4: 101,550,857 (GRCm38) |
|
probably null |
Het |
| Eapp |
T |
C |
12: 54,690,276 (GRCm38) |
T145A |
unknown |
Het |
| Efcab5 |
A |
G |
11: 77,121,238 (GRCm38) |
M730T |
probably benign |
Het |
| Eif4g3 |
T |
A |
4: 138,190,657 (GRCm38) |
D1305E |
probably damaging |
Het |
| Endou |
A |
T |
15: 97,712,065 (GRCm38) |
V450E |
probably benign |
Het |
| F10 |
A |
T |
8: 13,048,177 (GRCm38) |
K127* |
probably null |
Het |
| Fbxw21 |
A |
G |
9: 109,143,762 (GRCm38) |
F368S |
probably damaging |
Het |
| Fezf1 |
A |
T |
6: 23,245,798 (GRCm38) |
L456Q |
possibly damaging |
Het |
| Foxo3 |
C |
T |
10: 42,197,025 (GRCm38) |
V499M |
probably damaging |
Het |
| Fyco1 |
A |
C |
9: 123,794,813 (GRCm38) |
C1384G |
probably damaging |
Het |
| Galnt6 |
G |
T |
15: 100,704,151 (GRCm38) |
S258R |
possibly damaging |
Het |
| Gemin5 |
A |
G |
11: 58,137,748 (GRCm38) |
V882A |
probably benign |
Het |
| Gm10750 |
A |
G |
2: 149,016,187 (GRCm38) |
L48P |
unknown |
Het |
| Gm11639 |
A |
G |
11: 104,831,300 (GRCm38) |
I1913V |
probably benign |
Het |
| Gm16503 |
T |
A |
4: 147,541,114 (GRCm38) |
F22I |
unknown |
Het |
| Hdac10 |
A |
G |
15: 89,126,277 (GRCm38) |
C281R |
probably damaging |
Het |
| Hikeshi |
T |
C |
7: 89,935,760 (GRCm38) |
S79G |
probably damaging |
Het |
| Ifitm2 |
AG |
A |
7: 140,955,901 (GRCm38) |
|
probably null |
Het |
| Itpr3 |
A |
G |
17: 27,111,217 (GRCm38) |
E1603G |
probably damaging |
Het |
| Lrrc37a |
A |
T |
11: 103,504,533 (GRCm38) |
V22E |
probably benign |
Het |
| Man1a |
C |
T |
10: 53,933,491 (GRCm38) |
|
probably null |
Het |
| Mdga1 |
A |
G |
17: 29,839,897 (GRCm38) |
L5P |
probably damaging |
Het |
| Mettl7a1 |
A |
G |
15: 100,313,133 (GRCm38) |
E213G |
probably damaging |
Het |
| Mup6 |
A |
G |
4: 60,004,838 (GRCm38) |
I76M |
probably benign |
Het |
| Nbea |
A |
T |
3: 56,091,092 (GRCm38) |
M98K |
probably benign |
Het |
| Nckap1l |
A |
G |
15: 103,473,539 (GRCm38) |
E454G |
probably damaging |
Het |
| Notch3 |
A |
T |
17: 32,143,691 (GRCm38) |
L1320Q |
probably benign |
Het |
| Nrn1 |
A |
T |
13: 36,726,674 (GRCm38) |
L128H |
probably damaging |
Het |
| Numa1 |
A |
G |
7: 102,012,796 (GRCm38) |
D1898G |
probably damaging |
Het |
| Numa1 |
T |
C |
7: 101,995,416 (GRCm38) |
S200P |
possibly damaging |
Het |
| Olfr1124 |
G |
A |
2: 87,434,666 (GRCm38) |
A60T |
probably benign |
Het |
| Olfr152 |
A |
C |
2: 87,782,523 (GRCm38) |
|
probably null |
Het |
| Olfr366 |
T |
C |
2: 37,220,110 (GRCm38) |
I207T |
possibly damaging |
Het |
| Olfr700 |
A |
T |
7: 106,806,398 (GRCm38) |
S21R |
possibly damaging |
Het |
| P2ry6 |
A |
T |
7: 100,938,926 (GRCm38) |
Y75* |
probably null |
Het |
| Pbrm1 |
T |
A |
14: 31,084,803 (GRCm38) |
C1062* |
probably null |
Het |
| Pcdh15 |
A |
G |
10: 74,643,728 (GRCm38) |
E557G |
unknown |
Het |
| Pcdh7 |
T |
C |
5: 57,721,335 (GRCm38) |
L744P |
probably benign |
Het |
| Plekhg3 |
A |
T |
12: 76,562,278 (GRCm38) |
I142L |
possibly damaging |
Het |
| Plk4 |
C |
T |
3: 40,811,891 (GRCm38) |
H695Y |
probably damaging |
Het |
| Pms1 |
T |
C |
1: 53,208,057 (GRCm38) |
H243R |
probably benign |
Het |
| Prdm14 |
T |
C |
1: 13,122,483 (GRCm38) |
D344G |
possibly damaging |
Het |
| R3hdml |
A |
G |
2: 163,502,332 (GRCm38) |
I214V |
probably benign |
Het |
| Rab11fip5 |
T |
C |
6: 85,348,710 (GRCm38) |
N238S |
probably benign |
Het |
| Sacs |
T |
A |
14: 61,240,319 (GRCm38) |
Y732N |
possibly damaging |
Het |
| Scfd1 |
T |
A |
12: 51,393,866 (GRCm38) |
M187K |
possibly damaging |
Het |
| Serpina1d |
A |
G |
12: 103,767,998 (GRCm38) |
C16R |
probably damaging |
Het |
| Slc2a12 |
T |
C |
10: 22,665,095 (GRCm38) |
I283T |
possibly damaging |
Het |
| Smarca5 |
A |
G |
8: 80,719,803 (GRCm38) |
Y423H |
probably damaging |
Het |
| Srrm3 |
C |
A |
5: 135,868,261 (GRCm38) |
A366E |
unknown |
Het |
| St7 |
A |
T |
6: 17,844,914 (GRCm38) |
K134* |
probably null |
Het |
| St8sia5 |
T |
G |
18: 77,254,829 (GRCm38) |
C412G |
probably damaging |
Het |
| Tanc2 |
A |
T |
11: 105,886,458 (GRCm38) |
I821F |
probably damaging |
Het |
| Tbrg4 |
A |
G |
11: 6,624,204 (GRCm38) |
M6T |
probably benign |
Het |
| Tcf20 |
A |
T |
15: 82,852,696 (GRCm38) |
I1518N |
probably benign |
Het |
| Tctn3 |
A |
G |
19: 40,607,276 (GRCm38) |
V355A |
probably benign |
Het |
| Tenm2 |
A |
T |
11: 36,024,500 (GRCm38) |
F2070Y |
probably damaging |
Het |
| Tex2 |
A |
G |
11: 106,568,535 (GRCm38) |
V23A |
probably damaging |
Het |
| Thrsp |
C |
G |
7: 97,417,074 (GRCm38) |
E144Q |
probably damaging |
Het |
| Top2a |
A |
C |
11: 99,001,078 (GRCm38) |
S1114A |
probably benign |
Het |
| Tpm1 |
A |
G |
9: 67,029,716 (GRCm38) |
Y267H |
probably benign |
Het |
| Txndc2 |
G |
T |
17: 65,639,024 (GRCm38) |
P53T |
unknown |
Het |
| Ugt2b36 |
A |
T |
5: 87,081,017 (GRCm38) |
I389N |
probably damaging |
Het |
| Vwa3b |
T |
A |
1: 37,035,801 (GRCm38) |
H16Q |
probably damaging |
Het |
| Zbp1 |
A |
G |
2: 173,210,643 (GRCm38) |
M240T |
possibly damaging |
Het |
|
| Other mutations in Virma |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00428:Virma
|
APN |
4 |
11,519,424 (GRCm38) |
splice site |
probably benign |
|
|
IGL00477:Virma
|
APN |
4 |
11,519,006 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL01293:Virma
|
APN |
4 |
11,521,114 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01410:Virma
|
APN |
4 |
11,518,929 (GRCm38) |
nonsense |
probably null |
|
|
IGL01531:Virma
|
APN |
4 |
11,528,753 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01672:Virma
|
APN |
4 |
11,527,792 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01724:Virma
|
APN |
4 |
11,528,672 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01747:Virma
|
APN |
4 |
11,526,877 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01776:Virma
|
APN |
4 |
11,527,792 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02064:Virma
|
APN |
4 |
11,513,163 (GRCm38) |
missense |
possibly damaging |
0.87 |
|
IGL02243:Virma
|
APN |
4 |
11,546,031 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02244:Virma
|
APN |
4 |
11,546,031 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02445:Virma
|
APN |
4 |
11,527,029 (GRCm38) |
missense |
probably damaging |
0.97 |
|
IGL02546:Virma
|
APN |
4 |
11,494,804 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL02807:Virma
|
APN |
4 |
11,507,079 (GRCm38) |
splice site |
probably benign |
|
|
IGL02967:Virma
|
APN |
4 |
11,514,096 (GRCm38) |
missense |
probably benign |
0.01 |
|
IGL03211:Virma
|
APN |
4 |
11,548,770 (GRCm38) |
nonsense |
probably null |
|
|
IGL03242:Virma
|
APN |
4 |
11,527,669 (GRCm38) |
missense |
possibly damaging |
0.70 |
|
IGL03256:Virma
|
APN |
4 |
11,542,207 (GRCm38) |
splice site |
probably benign |
|
|
IGL03327:Virma
|
APN |
4 |
11,518,984 (GRCm38) |
missense |
probably benign |
0.00 |
|
IGL03346:Virma
|
APN |
4 |
11,518,984 (GRCm38) |
missense |
probably benign |
0.00 |
|
PIT4802001:Virma
|
UTSW |
4 |
11,546,008 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R0142:Virma
|
UTSW |
4 |
11,548,783 (GRCm38) |
missense |
probably benign |
0.04 |
|
R0355:Virma
|
UTSW |
4 |
11,528,626 (GRCm38) |
nonsense |
probably null |
|
|
R0522:Virma
|
UTSW |
4 |
11,519,416 (GRCm38) |
critical splice donor site |
probably null |
|
|
R0600:Virma
|
UTSW |
4 |
11,498,769 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R1435:Virma
|
UTSW |
4 |
11,528,621 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1489:Virma
|
UTSW |
4 |
11,521,164 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1568:Virma
|
UTSW |
4 |
11,528,776 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R1616:Virma
|
UTSW |
4 |
11,544,954 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1655:Virma
|
UTSW |
4 |
11,494,786 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1695:Virma
|
UTSW |
4 |
11,494,814 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R1835:Virma
|
UTSW |
4 |
11,540,511 (GRCm38) |
missense |
probably benign |
0.02 |
|
R1951:Virma
|
UTSW |
4 |
11,513,907 (GRCm38) |
missense |
probably benign |
0.00 |
|
R1991:Virma
|
UTSW |
4 |
11,519,242 (GRCm38) |
missense |
probably benign |
0.06 |
|
R2145:Virma
|
UTSW |
4 |
11,548,726 (GRCm38) |
splice site |
probably benign |
|
|
R2172:Virma
|
UTSW |
4 |
11,527,843 (GRCm38) |
missense |
possibly damaging |
0.82 |
|
R2217:Virma
|
UTSW |
4 |
11,544,924 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2218:Virma
|
UTSW |
4 |
11,544,924 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2248:Virma
|
UTSW |
4 |
11,518,927 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2342:Virma
|
UTSW |
4 |
11,501,316 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R3424:Virma
|
UTSW |
4 |
11,513,177 (GRCm38) |
nonsense |
probably null |
|
|
R4397:Virma
|
UTSW |
4 |
11,513,901 (GRCm38) |
missense |
possibly damaging |
0.81 |
|
R4449:Virma
|
UTSW |
4 |
11,498,828 (GRCm38) |
critical splice donor site |
probably null |
|
|
R4660:Virma
|
UTSW |
4 |
11,513,505 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4698:Virma
|
UTSW |
4 |
11,528,636 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4878:Virma
|
UTSW |
4 |
11,544,971 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4937:Virma
|
UTSW |
4 |
11,521,147 (GRCm38) |
nonsense |
probably null |
|
|
R5031:Virma
|
UTSW |
4 |
11,542,116 (GRCm38) |
nonsense |
probably null |
|
|
R5040:Virma
|
UTSW |
4 |
11,528,746 (GRCm38) |
missense |
probably benign |
0.01 |
|
R5061:Virma
|
UTSW |
4 |
11,494,840 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R5091:Virma
|
UTSW |
4 |
11,519,392 (GRCm38) |
missense |
probably benign |
0.00 |
|
R5137:Virma
|
UTSW |
4 |
11,546,297 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5262:Virma
|
UTSW |
4 |
11,539,926 (GRCm38) |
missense |
probably benign |
0.01 |
|
R5297:Virma
|
UTSW |
4 |
11,494,819 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5730:Virma
|
UTSW |
4 |
11,542,154 (GRCm38) |
missense |
probably benign |
0.44 |
|
R5818:Virma
|
UTSW |
4 |
11,513,319 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
R5835:Virma
|
UTSW |
4 |
11,514,036 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6125:Virma
|
UTSW |
4 |
11,521,172 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R6197:Virma
|
UTSW |
4 |
11,505,498 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R6222:Virma
|
UTSW |
4 |
11,527,820 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6793:Virma
|
UTSW |
4 |
11,539,968 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7028:Virma
|
UTSW |
4 |
11,519,249 (GRCm38) |
missense |
possibly damaging |
0.50 |
|
R7356:Virma
|
UTSW |
4 |
11,513,595 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7383:Virma
|
UTSW |
4 |
11,514,026 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R7391:Virma
|
UTSW |
4 |
11,508,099 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7425:Virma
|
UTSW |
4 |
11,546,211 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R7556:Virma
|
UTSW |
4 |
11,518,927 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7715:Virma
|
UTSW |
4 |
11,513,016 (GRCm38) |
splice site |
probably null |
|
|
R7715:Virma
|
UTSW |
4 |
11,549,682 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7986:Virma
|
UTSW |
4 |
11,540,023 (GRCm38) |
missense |
probably benign |
0.01 |
|
R7990:Virma
|
UTSW |
4 |
11,513,983 (GRCm38) |
missense |
probably benign |
0.00 |
|
R8048:Virma
|
UTSW |
4 |
11,539,918 (GRCm38) |
nonsense |
probably null |
|
|
R8050:Virma
|
UTSW |
4 |
11,528,643 (GRCm38) |
missense |
probably benign |
0.22 |
|
R8165:Virma
|
UTSW |
4 |
11,542,128 (GRCm38) |
missense |
probably benign |
0.00 |
|
R8412:Virma
|
UTSW |
4 |
11,521,261 (GRCm38) |
critical splice donor site |
probably null |
|
|
R8544:Virma
|
UTSW |
4 |
11,516,949 (GRCm38) |
missense |
probably benign |
|
|
R8551:Virma
|
UTSW |
4 |
11,513,397 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8699:Virma
|
UTSW |
4 |
11,528,678 (GRCm38) |
missense |
probably benign |
0.04 |
|
R8739:Virma
|
UTSW |
4 |
11,540,643 (GRCm38) |
critical splice donor site |
probably null |
|
|
R8950:Virma
|
UTSW |
4 |
11,519,047 (GRCm38) |
nonsense |
probably null |
|
|
R9015:Virma
|
UTSW |
4 |
11,540,494 (GRCm38) |
missense |
probably benign |
0.27 |
|
R9038:Virma
|
UTSW |
4 |
11,526,922 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R9115:Virma
|
UTSW |
4 |
11,498,744 (GRCm38) |
missense |
probably benign |
0.15 |
|
R9404:Virma
|
UTSW |
4 |
11,513,626 (GRCm38) |
missense |
probably benign |
0.17 |
|
R9477:Virma
|
UTSW |
4 |
11,528,753 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9532:Virma
|
UTSW |
4 |
11,507,078 (GRCm38) |
critical splice donor site |
probably null |
|
|
R9649:Virma
|
UTSW |
4 |
11,486,045 (GRCm38) |
start codon destroyed |
probably null |
0.08 |
|
R9657:Virma
|
UTSW |
4 |
11,544,898 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R9780:Virma
|
UTSW |
4 |
11,513,442 (GRCm38) |
missense |
possibly damaging |
0.75 |
|
R9800:Virma
|
UTSW |
4 |
11,546,007 (GRCm38) |
missense |
probably damaging |
0.99 |
|
X0020:Virma
|
UTSW |
4 |
11,486,055 (GRCm38) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GAAGCCTCGGTGAAGTTAACTG -3'
(R):5'- ATGCTAATGACACTGTCCAAAGC -3'
Sequencing Primer
(F):5'- CTGAACTGCTAGACCTGTATCAG -3'
(R):5'- TGACACTGTCCAAAGCTTTAAAAG -3'
|
| Posted On |
2022-03-25 |
Incidental Mutation