Incidental Mutation 'R1655:Virma'
| ID |
189008 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Virma
|
| Ensembl Gene |
ENSMUSG00000040720 |
| Gene Name |
vir like m6A methyltransferase associated |
| Synonyms |
1110037F02Rik |
| MMRRC Submission |
039691-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R1655 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
4 |
| Chromosomal Location |
11485958-11550684 bp(+) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 11494786 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 29
(V29A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000103943
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055372]
[ENSMUST00000059914]
[ENSMUST00000108307]
|
| AlphaFold |
A2AIV2 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000055372
AA Change: V29A
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000063188
Gene: ENSMUSG00000040720
AA Change: V29A
| 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 damaging
Transcript: ENSMUST00000059914
AA Change: V29A
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000058078
Gene: ENSMUSG00000040720
AA Change: V29A
| 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 damaging
Transcript: ENSMUST00000108307
AA Change: V29A
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000103943
Gene: ENSMUSG00000040720
AA Change: V29A
| 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: 99.1%
- 3x: 98.3%
- 10x: 96.0%
- 20x: 91.3%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 73 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4833427G06Rik |
A |
T |
9: 51,083,621 (GRCm38) |
I136N |
probably damaging |
Het |
| 9530053A07Rik |
A |
T |
7: 28,147,110 (GRCm38) |
N1076Y |
probably damaging |
Het |
| A730061H03Rik |
A |
T |
14: 55,560,333 (GRCm38) |
|
probably benign |
Het |
| Abca1 |
C |
T |
4: 53,050,964 (GRCm38) |
A1582T |
probably benign |
Het |
| Acot8 |
A |
T |
2: 164,803,108 (GRCm38) |
S52T |
probably benign |
Het |
| Atcay |
C |
T |
10: 81,213,397 (GRCm38) |
V124M |
probably damaging |
Het |
| Cep295 |
C |
T |
9: 15,340,883 (GRCm38) |
E397K |
probably damaging |
Het |
| Cfap46 |
A |
T |
7: 139,642,520 (GRCm38) |
Y1180* |
probably null |
Het |
| Clptm1 |
T |
A |
7: 19,645,867 (GRCm38) |
H148L |
probably benign |
Het |
| Clstn3 |
A |
G |
6: 124,437,427 (GRCm38) |
L743P |
probably damaging |
Het |
| Crtc3 |
A |
T |
7: 80,598,776 (GRCm38) |
M313K |
possibly damaging |
Het |
| Csgalnact1 |
T |
A |
8: 68,373,689 (GRCm38) |
I326F |
possibly damaging |
Het |
| Dennd6b |
G |
T |
15: 89,196,340 (GRCm38) |
T19K |
unknown |
Het |
| Disp1 |
A |
T |
1: 183,087,004 (GRCm38) |
I1284N |
probably benign |
Het |
| Dnah2 |
A |
G |
11: 69,473,854 (GRCm38) |
Y1992H |
probably damaging |
Het |
| Dnah6 |
C |
T |
6: 73,205,732 (GRCm38) |
V205I |
possibly damaging |
Het |
| Dst |
G |
T |
1: 34,282,576 (GRCm38) |
G4391* |
probably null |
Het |
| Dytn |
A |
G |
1: 63,661,198 (GRCm38) |
S258P |
probably damaging |
Het |
| Emilin3 |
T |
A |
2: 160,910,866 (GRCm38) |
|
probably null |
Het |
| Ermn |
C |
T |
2: 58,052,584 (GRCm38) |
V45I |
probably benign |
Het |
| Fat4 |
T |
C |
3: 38,957,318 (GRCm38) |
V2189A |
probably damaging |
Het |
| Filip1l |
T |
C |
16: 57,571,851 (GRCm38) |
I934T |
probably damaging |
Het |
| Gbp9 |
T |
A |
5: 105,081,692 (GRCm38) |
Q472L |
possibly damaging |
Het |
| Gimap5 |
G |
T |
6: 48,753,176 (GRCm38) |
E227* |
probably null |
Het |
| Gsdmc |
C |
T |
15: 63,780,043 (GRCm38) |
V240M |
probably benign |
Het |
| H2-Q4 |
G |
T |
17: 35,382,905 (GRCm38) |
V248F |
probably damaging |
Het |
| Helz2 |
T |
C |
2: 181,234,147 (GRCm38) |
E1518G |
probably damaging |
Het |
| Hmcn1 |
A |
G |
1: 150,630,333 (GRCm38) |
V3814A |
probably benign |
Het |
| Ifna7 |
A |
G |
4: 88,816,660 (GRCm38) |
T145A |
probably benign |
Het |
| Itgam |
T |
A |
7: 128,115,163 (GRCm38) |
M947K |
probably benign |
Het |
| Itpr2 |
T |
G |
6: 146,376,148 (GRCm38) |
N608H |
probably damaging |
Het |
| Klra2 |
T |
A |
6: 131,220,211 (GRCm38) |
N242I |
probably damaging |
Het |
| Lonrf2 |
A |
T |
1: 38,811,824 (GRCm38) |
L219Q |
probably damaging |
Het |
| Ly6c2 |
T |
C |
15: 75,108,563 (GRCm38) |
I126V |
probably benign |
Het |
| Mr1 |
G |
A |
1: 155,132,455 (GRCm38) |
T258M |
probably benign |
Het |
| Mrps35 |
T |
G |
6: 147,060,228 (GRCm38) |
D200E |
possibly damaging |
Het |
| Nbeal2 |
A |
C |
9: 110,632,872 (GRCm38) |
S1506A |
probably damaging |
Het |
| Ncoa7 |
T |
C |
10: 30,698,245 (GRCm38) |
|
probably null |
Het |
| Nlrp4a |
A |
T |
7: 26,449,651 (GRCm38) |
I228F |
possibly damaging |
Het |
| Olfr1047 |
A |
G |
2: 86,228,080 (GRCm38) |
V297A |
possibly damaging |
Het |
| Olfr1339 |
A |
G |
4: 118,734,999 (GRCm38) |
S157G |
probably benign |
Het |
| Olfr368 |
A |
G |
2: 37,331,939 (GRCm38) |
Y64C |
probably damaging |
Het |
| Olfr483 |
A |
T |
7: 108,103,464 (GRCm38) |
I52F |
probably damaging |
Het |
| Paxx |
T |
C |
2: 25,460,316 (GRCm38) |
E93G |
probably damaging |
Het |
| Per2 |
C |
A |
1: 91,448,768 (GRCm38) |
G128W |
probably damaging |
Het |
| Piezo1 |
A |
G |
8: 122,496,822 (GRCm38) |
I796T |
probably benign |
Het |
| Pkhd1 |
A |
G |
1: 20,584,129 (GRCm38) |
S235P |
probably damaging |
Het |
| Pole |
T |
A |
5: 110,335,922 (GRCm38) |
F259Y |
probably damaging |
Het |
| Pus7 |
T |
A |
5: 23,747,800 (GRCm38) |
K512* |
probably null |
Het |
| Ralyl |
A |
T |
3: 14,107,236 (GRCm38) |
Y55F |
probably damaging |
Het |
| Rgs14 |
T |
A |
13: 55,383,534 (GRCm38) |
M451K |
probably benign |
Het |
| Rhag |
T |
C |
17: 40,831,596 (GRCm38) |
F231L |
probably damaging |
Het |
| Ric8a |
T |
C |
7: 140,860,895 (GRCm38) |
C94R |
probably benign |
Het |
| Rictor |
T |
A |
15: 6,772,212 (GRCm38) |
D460E |
probably benign |
Het |
| Rpn1 |
T |
C |
6: 88,100,944 (GRCm38) |
V454A |
possibly damaging |
Het |
| Sacs |
A |
G |
14: 61,191,782 (GRCm38) |
D427G |
probably benign |
Het |
| Scai |
A |
T |
2: 39,080,117 (GRCm38) |
V545D |
possibly damaging |
Het |
| Serpinb3a |
A |
G |
1: 107,046,212 (GRCm38) |
V323A |
probably damaging |
Het |
| Slc13a5 |
C |
A |
11: 72,257,378 (GRCm38) |
C277F |
probably benign |
Het |
| Slc15a1 |
A |
T |
14: 121,465,899 (GRCm38) |
Y557N |
probably benign |
Het |
| Slc34a2 |
T |
C |
5: 53,069,419 (GRCm38) |
V628A |
probably benign |
Het |
| Slc8a2 |
G |
T |
7: 16,141,135 (GRCm38) |
G436V |
probably damaging |
Het |
| Sphkap |
G |
A |
1: 83,277,515 (GRCm38) |
R838* |
probably null |
Het |
| Supt5 |
T |
C |
7: 28,330,024 (GRCm38) |
I103V |
probably benign |
Het |
| Tdrd1 |
T |
A |
19: 56,843,216 (GRCm38) |
Y346* |
probably null |
Het |
| Tg |
T |
G |
15: 66,828,568 (GRCm38) |
|
probably null |
Het |
| Top1 |
T |
A |
2: 160,703,696 (GRCm38) |
|
probably null |
Het |
| Trmt12 |
T |
C |
15: 58,873,227 (GRCm38) |
L158P |
probably damaging |
Het |
| Tssk4 |
A |
G |
14: 55,651,695 (GRCm38) |
N226S |
probably damaging |
Het |
| Unc80 |
G |
T |
1: 66,672,756 (GRCm38) |
V2746F |
possibly damaging |
Het |
| Usp34 |
T |
A |
11: 23,375,051 (GRCm38) |
V999E |
probably benign |
Het |
| Zfp40 |
A |
T |
17: 23,177,266 (GRCm38) |
Y48N |
probably benign |
Het |
| Zfp609 |
A |
G |
9: 65,703,554 (GRCm38) |
V709A |
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 |
|
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 |
|
R9294:Virma
|
UTSW |
4 |
11,513,507 (GRCm38) |
nonsense |
probably null |
|
|
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'- GGTTTTAGTGATGAGGGTTCAACCCAG -3'
(R):5'- TCTATCTCCAACACATAGGGGCTGC -3'
Sequencing Primer
(F):5'- cccaagtgccaggattagag -3'
(R):5'- CTCTGTTGTCAGGTAAGCCA -3'
|
| Posted On |
2014-05-09 |
Incidental Mutation