Incidental Mutation 'R5004:Myh15'
ID |
390113 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myh15
|
Ensembl Gene |
ENSMUSG00000092009 |
Gene Name |
myosin, heavy chain 15 |
Synonyms |
EG667772 |
MMRRC Submission |
042597-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.149)
|
Stock # |
R5004 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
16 |
Chromosomal Location |
48877849-49019467 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 48952411 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Asparagine
at position 827
(I827N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000127539
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000168680]
|
AlphaFold |
E9Q264 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000168680
AA Change: I827N
PolyPhen 2
Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000127539 Gene: ENSMUSG00000092009 AA Change: I827N
Domain | Start | End | E-Value | Type |
Pfam:Myosin_N
|
30 |
70 |
5.2e-12 |
PFAM |
MYSc
|
76 |
770 |
N/A |
SMART |
Pfam:Myosin_tail_1
|
836 |
1915 |
9.5e-118 |
PFAM |
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.8%
- 20x: 94.0%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029H14Rik |
A |
C |
8: 13,605,927 (GRCm39) |
D189E |
possibly damaging |
Het |
Abca5 |
C |
T |
11: 110,170,202 (GRCm39) |
E1298K |
probably damaging |
Het |
Actg1 |
C |
A |
11: 120,238,986 (GRCm39) |
|
probably benign |
Het |
Add2 |
A |
G |
6: 86,073,728 (GRCm39) |
T206A |
probably benign |
Het |
Alox12e |
A |
G |
11: 70,212,330 (GRCm39) |
V116A |
probably benign |
Het |
Ankrd27 |
T |
A |
7: 35,307,800 (GRCm39) |
D346E |
probably damaging |
Het |
Arfgap3 |
T |
A |
15: 83,194,497 (GRCm39) |
S391C |
possibly damaging |
Het |
Bcor |
C |
T |
X: 11,906,725 (GRCm39) |
R1551Q |
probably damaging |
Het |
Cars2 |
C |
T |
8: 11,568,956 (GRCm39) |
|
probably null |
Het |
Cav3 |
A |
G |
6: 112,436,885 (GRCm39) |
K38R |
probably damaging |
Het |
Ccdc159 |
G |
A |
9: 21,844,241 (GRCm39) |
R101H |
probably damaging |
Het |
Cops7b |
A |
G |
1: 86,515,132 (GRCm39) |
|
probably benign |
Het |
Cyp4a12b |
C |
T |
4: 115,295,310 (GRCm39) |
T472I |
probably benign |
Het |
Cyp4a32 |
T |
C |
4: 115,458,238 (GRCm39) |
S23P |
probably damaging |
Het |
Cyp4f13 |
T |
G |
17: 33,144,760 (GRCm39) |
I275L |
probably benign |
Het |
Dlgap1 |
T |
A |
17: 71,025,222 (GRCm39) |
|
probably null |
Het |
Dnajc12 |
A |
T |
10: 63,222,486 (GRCm39) |
I4L |
probably benign |
Het |
Ephb2 |
T |
A |
4: 136,387,010 (GRCm39) |
D739V |
possibly damaging |
Het |
Fam169a |
A |
G |
13: 97,234,100 (GRCm39) |
Y124C |
probably damaging |
Het |
Fbln5 |
T |
A |
12: 101,727,080 (GRCm39) |
N303I |
probably damaging |
Het |
Fdxr |
T |
C |
11: 115,160,399 (GRCm39) |
E352G |
probably benign |
Het |
Fhad1 |
T |
G |
4: 141,729,910 (GRCm39) |
|
probably null |
Het |
Fhod1 |
C |
T |
8: 106,063,577 (GRCm39) |
|
probably benign |
Het |
Fndc7 |
G |
A |
3: 108,790,789 (GRCm39) |
T79M |
probably damaging |
Het |
Fry |
A |
G |
5: 150,357,069 (GRCm39) |
Q1872R |
probably benign |
Het |
Gbx1 |
T |
C |
5: 24,709,837 (GRCm39) |
H336R |
probably damaging |
Het |
Gkn3 |
C |
T |
6: 87,360,507 (GRCm39) |
A163T |
probably damaging |
Het |
Gpr15lg |
A |
T |
14: 36,824,622 (GRCm39) |
C60S |
probably damaging |
Het |
Hacl1 |
C |
A |
14: 31,340,996 (GRCm39) |
C346F |
probably benign |
Het |
Hectd4 |
C |
A |
5: 121,466,262 (GRCm39) |
|
probably null |
Het |
Hectd4 |
C |
T |
5: 121,467,628 (GRCm39) |
P2526S |
possibly damaging |
Het |
Il3ra |
A |
T |
14: 14,355,381 (GRCm38) |
E289D |
probably benign |
Het |
Itih4 |
T |
G |
14: 30,614,629 (GRCm39) |
L497R |
probably damaging |
Het |
Kcnh3 |
A |
T |
15: 99,124,383 (GRCm39) |
K91* |
probably null |
Het |
Kiz |
C |
G |
2: 146,811,899 (GRCm39) |
D669E |
possibly damaging |
Het |
Klhl30 |
T |
A |
1: 91,287,046 (GRCm39) |
|
probably null |
Het |
Kndc1 |
C |
A |
7: 139,512,792 (GRCm39) |
C1514* |
probably null |
Het |
Lipo2 |
A |
G |
19: 33,699,076 (GRCm39) |
|
probably null |
Het |
Macf1 |
T |
C |
4: 123,279,268 (GRCm39) |
D5921G |
probably damaging |
Het |
Mau2 |
A |
G |
8: 70,478,537 (GRCm39) |
Y394H |
probably damaging |
Het |
Mctp1 |
T |
A |
13: 76,789,923 (GRCm39) |
S50R |
possibly damaging |
Het |
Mllt10 |
T |
C |
2: 18,175,079 (GRCm39) |
Y3H |
probably damaging |
Het |
Mon1b |
T |
C |
8: 114,365,859 (GRCm39) |
S396P |
probably damaging |
Het |
Mrgpra4 |
A |
C |
7: 47,631,535 (GRCm39) |
L22R |
probably benign |
Het |
Msln |
T |
G |
17: 25,973,193 (GRCm39) |
M1L |
possibly damaging |
Het |
Myh7 |
T |
C |
14: 55,209,140 (GRCm39) |
D1866G |
probably damaging |
Het |
Myo5b |
T |
G |
18: 74,877,844 (GRCm39) |
|
probably null |
Het |
Nlrc5 |
T |
G |
8: 95,247,844 (GRCm39) |
|
probably benign |
Het |
Nup210l |
A |
T |
3: 90,087,472 (GRCm39) |
R1082* |
probably null |
Het |
Or12k7 |
A |
G |
2: 36,958,422 (GRCm39) |
Y35C |
probably damaging |
Het |
Or4f4b |
G |
A |
2: 111,314,005 (GRCm39) |
V105I |
possibly damaging |
Het |
Or5p63 |
T |
A |
7: 107,811,323 (GRCm39) |
K138* |
probably null |
Het |
Or7e169 |
T |
C |
9: 19,757,398 (GRCm39) |
I172M |
probably benign |
Het |
Pi4ka |
A |
T |
16: 17,195,033 (GRCm39) |
C122S |
probably damaging |
Het |
Pkd2l1 |
G |
T |
19: 44,138,016 (GRCm39) |
A690E |
probably benign |
Het |
Pramel22 |
T |
C |
4: 143,380,706 (GRCm39) |
Q439R |
probably benign |
Het |
Prickle2 |
A |
T |
6: 92,393,736 (GRCm39) |
D312E |
probably benign |
Het |
Prrc2a |
T |
A |
17: 35,368,974 (GRCm39) |
N2021Y |
probably benign |
Het |
Prss3 |
T |
C |
6: 41,350,836 (GRCm39) |
Y218C |
probably damaging |
Het |
Psg20 |
T |
C |
7: 18,414,837 (GRCm39) |
T350A |
probably damaging |
Het |
Ptprg |
A |
T |
14: 12,220,667 (GRCm38) |
I1235F |
probably damaging |
Het |
Ptprk |
T |
A |
10: 28,462,059 (GRCm39) |
D1181E |
possibly damaging |
Het |
Rcc2 |
T |
A |
4: 140,444,977 (GRCm39) |
S415T |
possibly damaging |
Het |
Ripor1 |
CAA |
CA |
8: 106,345,452 (GRCm39) |
|
probably null |
Het |
Rnf31 |
T |
C |
14: 55,829,639 (GRCm39) |
L68P |
probably damaging |
Het |
Rsph6a |
A |
T |
7: 18,791,665 (GRCm39) |
E278V |
possibly damaging |
Het |
Rubcnl |
C |
T |
14: 75,269,617 (GRCm39) |
Q92* |
probably null |
Het |
Scfd1 |
A |
G |
12: 51,491,777 (GRCm39) |
R580G |
probably benign |
Het |
Sec31a |
A |
T |
5: 100,516,192 (GRCm39) |
N967K |
probably damaging |
Het |
Sema4b |
C |
A |
7: 79,866,093 (GRCm39) |
T154N |
probably benign |
Het |
Septin14 |
T |
A |
5: 129,770,040 (GRCm39) |
I219F |
possibly damaging |
Het |
Serpinb9c |
A |
T |
13: 33,334,338 (GRCm39) |
S235T |
probably benign |
Het |
Setd4 |
G |
T |
16: 93,388,133 (GRCm39) |
H118N |
probably benign |
Het |
Siglec1 |
C |
T |
2: 130,911,789 (GRCm39) |
V1697M |
probably benign |
Het |
Siglec1 |
A |
T |
2: 130,915,331 (GRCm39) |
L1420Q |
possibly damaging |
Het |
Soat2 |
T |
A |
15: 102,069,546 (GRCm39) |
H402Q |
probably damaging |
Het |
Sp3 |
A |
T |
2: 72,768,633 (GRCm39) |
V666D |
probably benign |
Het |
Spef2 |
T |
G |
15: 9,578,413 (GRCm39) |
S1704R |
probably benign |
Het |
Spidr |
A |
T |
16: 15,936,806 (GRCm39) |
W100R |
possibly damaging |
Het |
Steap1 |
G |
T |
5: 5,792,829 (GRCm39) |
Y27* |
probably null |
Het |
Svep1 |
G |
T |
4: 58,087,751 (GRCm39) |
T1776K |
probably benign |
Het |
Tdpoz1 |
T |
A |
3: 93,578,440 (GRCm39) |
T115S |
probably benign |
Het |
Tet2 |
A |
T |
3: 133,193,140 (GRCm39) |
H431Q |
possibly damaging |
Het |
Tnrc6c |
T |
G |
11: 117,611,872 (GRCm39) |
V170G |
probably benign |
Het |
Tom1 |
T |
C |
8: 75,778,630 (GRCm39) |
L99P |
probably damaging |
Het |
Trim11 |
C |
A |
11: 58,872,164 (GRCm39) |
|
probably benign |
Het |
Trio |
T |
C |
15: 27,755,264 (GRCm39) |
K955R |
probably damaging |
Het |
Tubd1 |
C |
T |
11: 86,452,146 (GRCm39) |
T371I |
probably damaging |
Het |
Usp17lb |
C |
T |
7: 104,490,884 (GRCm39) |
M13I |
probably benign |
Het |
Usp29 |
A |
G |
7: 6,965,158 (GRCm39) |
M334V |
probably benign |
Het |
Usp34 |
A |
G |
11: 23,414,586 (GRCm39) |
Y2843C |
probably damaging |
Het |
Utp20 |
A |
T |
10: 88,584,135 (GRCm39) |
I2674N |
probably damaging |
Het |
Vmn2r14 |
T |
G |
5: 109,368,246 (GRCm39) |
T249P |
probably benign |
Het |
Vmn2r43 |
A |
T |
7: 8,247,848 (GRCm39) |
F772I |
probably damaging |
Het |
Vmn2r51 |
T |
A |
7: 9,821,932 (GRCm39) |
E584D |
probably benign |
Het |
Zbtb22 |
G |
T |
17: 34,136,217 (GRCm39) |
A121S |
probably benign |
Het |
Zfp273 |
A |
T |
13: 67,973,673 (GRCm39) |
H267L |
probably damaging |
Het |
Zkscan2 |
C |
T |
7: 123,089,267 (GRCm39) |
V335M |
probably damaging |
Het |
|
Other mutations in Myh15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00943:Myh15
|
APN |
16 |
48,986,176 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01095:Myh15
|
APN |
16 |
48,952,378 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01343:Myh15
|
APN |
16 |
48,976,040 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01474:Myh15
|
APN |
16 |
48,952,461 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01572:Myh15
|
APN |
16 |
48,920,585 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01595:Myh15
|
APN |
16 |
48,993,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01632:Myh15
|
APN |
16 |
48,881,874 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01638:Myh15
|
APN |
16 |
48,889,843 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01667:Myh15
|
APN |
16 |
49,015,942 (GRCm39) |
missense |
probably benign |
0.20 |
IGL01715:Myh15
|
APN |
16 |
48,877,847 (GRCm39) |
unclassified |
probably benign |
|
IGL01833:Myh15
|
APN |
16 |
48,934,421 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02004:Myh15
|
APN |
16 |
48,930,892 (GRCm39) |
splice site |
probably benign |
|
IGL02033:Myh15
|
APN |
16 |
48,965,707 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02148:Myh15
|
APN |
16 |
48,936,678 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02225:Myh15
|
APN |
16 |
48,911,526 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02249:Myh15
|
APN |
16 |
48,930,847 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02505:Myh15
|
APN |
16 |
48,937,626 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02622:Myh15
|
APN |
16 |
48,997,317 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02814:Myh15
|
APN |
16 |
48,965,801 (GRCm39) |
splice site |
probably benign |
|
IGL02869:Myh15
|
APN |
16 |
48,965,767 (GRCm39) |
missense |
probably benign |
|
IGL02879:Myh15
|
APN |
16 |
48,993,422 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02881:Myh15
|
APN |
16 |
48,937,628 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03077:Myh15
|
APN |
16 |
48,916,901 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03354:Myh15
|
APN |
16 |
48,992,373 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03411:Myh15
|
APN |
16 |
48,980,330 (GRCm39) |
missense |
possibly damaging |
0.58 |
ANU74:Myh15
|
UTSW |
16 |
48,993,295 (GRCm39) |
missense |
possibly damaging |
0.58 |
P0027:Myh15
|
UTSW |
16 |
48,901,571 (GRCm39) |
missense |
possibly damaging |
0.77 |
PIT1430001:Myh15
|
UTSW |
16 |
49,017,254 (GRCm39) |
critical splice donor site |
probably null |
|
R0017:Myh15
|
UTSW |
16 |
48,983,423 (GRCm39) |
missense |
probably damaging |
0.97 |
R0038:Myh15
|
UTSW |
16 |
48,891,504 (GRCm39) |
splice site |
probably benign |
|
R0149:Myh15
|
UTSW |
16 |
48,934,368 (GRCm39) |
missense |
probably benign |
0.01 |
R0361:Myh15
|
UTSW |
16 |
48,934,368 (GRCm39) |
missense |
probably benign |
0.01 |
R0373:Myh15
|
UTSW |
16 |
49,003,322 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0433:Myh15
|
UTSW |
16 |
48,965,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R0525:Myh15
|
UTSW |
16 |
48,952,414 (GRCm39) |
missense |
probably benign |
0.03 |
R0586:Myh15
|
UTSW |
16 |
48,992,250 (GRCm39) |
splice site |
probably benign |
|
R0601:Myh15
|
UTSW |
16 |
48,881,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R0717:Myh15
|
UTSW |
16 |
48,963,356 (GRCm39) |
missense |
probably benign |
0.03 |
R0963:Myh15
|
UTSW |
16 |
48,952,512 (GRCm39) |
missense |
probably damaging |
0.97 |
R1075:Myh15
|
UTSW |
16 |
48,940,417 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1143:Myh15
|
UTSW |
16 |
48,885,449 (GRCm39) |
missense |
probably benign |
0.02 |
R1200:Myh15
|
UTSW |
16 |
48,916,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R1644:Myh15
|
UTSW |
16 |
48,952,566 (GRCm39) |
missense |
probably benign |
0.12 |
R1646:Myh15
|
UTSW |
16 |
49,015,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R1720:Myh15
|
UTSW |
16 |
48,913,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Myh15
|
UTSW |
16 |
48,983,498 (GRCm39) |
missense |
probably benign |
0.27 |
R1881:Myh15
|
UTSW |
16 |
48,891,446 (GRCm39) |
missense |
probably damaging |
0.98 |
R2048:Myh15
|
UTSW |
16 |
48,975,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R2064:Myh15
|
UTSW |
16 |
48,975,984 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2184:Myh15
|
UTSW |
16 |
48,957,874 (GRCm39) |
missense |
probably damaging |
0.99 |
R2212:Myh15
|
UTSW |
16 |
48,959,095 (GRCm39) |
missense |
probably benign |
0.02 |
R2216:Myh15
|
UTSW |
16 |
48,986,201 (GRCm39) |
nonsense |
probably null |
|
R2321:Myh15
|
UTSW |
16 |
48,933,436 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2327:Myh15
|
UTSW |
16 |
48,963,313 (GRCm39) |
missense |
probably benign |
0.01 |
R2395:Myh15
|
UTSW |
16 |
48,889,877 (GRCm39) |
missense |
probably benign |
0.04 |
R2399:Myh15
|
UTSW |
16 |
48,957,952 (GRCm39) |
missense |
probably damaging |
0.97 |
R3413:Myh15
|
UTSW |
16 |
48,959,095 (GRCm39) |
missense |
probably benign |
0.02 |
R4234:Myh15
|
UTSW |
16 |
48,983,405 (GRCm39) |
missense |
probably benign |
0.04 |
R4382:Myh15
|
UTSW |
16 |
48,963,306 (GRCm39) |
missense |
probably benign |
0.03 |
R4421:Myh15
|
UTSW |
16 |
48,929,707 (GRCm39) |
missense |
probably damaging |
0.99 |
R4580:Myh15
|
UTSW |
16 |
48,885,388 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4657:Myh15
|
UTSW |
16 |
48,992,421 (GRCm39) |
nonsense |
probably null |
|
R4780:Myh15
|
UTSW |
16 |
48,940,420 (GRCm39) |
missense |
probably benign |
0.13 |
R5175:Myh15
|
UTSW |
16 |
48,889,789 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5189:Myh15
|
UTSW |
16 |
48,921,870 (GRCm39) |
missense |
probably benign |
0.20 |
R5311:Myh15
|
UTSW |
16 |
48,986,204 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5318:Myh15
|
UTSW |
16 |
48,930,834 (GRCm39) |
missense |
probably damaging |
0.99 |
R5404:Myh15
|
UTSW |
16 |
48,980,341 (GRCm39) |
missense |
probably benign |
0.15 |
R5415:Myh15
|
UTSW |
16 |
48,937,658 (GRCm39) |
missense |
probably null |
1.00 |
R5558:Myh15
|
UTSW |
16 |
48,889,900 (GRCm39) |
missense |
probably benign |
0.32 |
R5977:Myh15
|
UTSW |
16 |
48,973,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R6004:Myh15
|
UTSW |
16 |
48,980,062 (GRCm39) |
missense |
probably benign |
0.00 |
R6275:Myh15
|
UTSW |
16 |
48,965,610 (GRCm39) |
missense |
probably benign |
0.00 |
R6381:Myh15
|
UTSW |
16 |
48,921,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R6448:Myh15
|
UTSW |
16 |
48,992,295 (GRCm39) |
missense |
probably damaging |
0.99 |
R6516:Myh15
|
UTSW |
16 |
48,957,996 (GRCm39) |
missense |
probably benign |
0.19 |
R6752:Myh15
|
UTSW |
16 |
49,003,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R6847:Myh15
|
UTSW |
16 |
48,965,451 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6868:Myh15
|
UTSW |
16 |
48,889,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R6889:Myh15
|
UTSW |
16 |
48,973,474 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6896:Myh15
|
UTSW |
16 |
48,933,434 (GRCm39) |
missense |
probably benign |
0.44 |
R6955:Myh15
|
UTSW |
16 |
48,901,598 (GRCm39) |
critical splice donor site |
probably null |
|
R6984:Myh15
|
UTSW |
16 |
48,930,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R7046:Myh15
|
UTSW |
16 |
48,929,662 (GRCm39) |
nonsense |
probably null |
|
R7095:Myh15
|
UTSW |
16 |
48,992,272 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7098:Myh15
|
UTSW |
16 |
48,997,420 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7134:Myh15
|
UTSW |
16 |
48,901,705 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7159:Myh15
|
UTSW |
16 |
48,881,937 (GRCm39) |
missense |
probably damaging |
0.97 |
R7244:Myh15
|
UTSW |
16 |
49,017,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Myh15
|
UTSW |
16 |
48,911,468 (GRCm39) |
missense |
probably damaging |
0.98 |
R7309:Myh15
|
UTSW |
16 |
48,916,828 (GRCm39) |
missense |
probably benign |
0.34 |
R7327:Myh15
|
UTSW |
16 |
48,993,369 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7418:Myh15
|
UTSW |
16 |
48,975,900 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7937:Myh15
|
UTSW |
16 |
48,976,009 (GRCm39) |
missense |
probably benign |
0.00 |
R8053:Myh15
|
UTSW |
16 |
48,963,302 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8313:Myh15
|
UTSW |
16 |
48,940,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R8315:Myh15
|
UTSW |
16 |
48,940,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R8316:Myh15
|
UTSW |
16 |
48,940,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R8317:Myh15
|
UTSW |
16 |
48,940,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R8342:Myh15
|
UTSW |
16 |
48,913,120 (GRCm39) |
missense |
probably benign |
|
R8379:Myh15
|
UTSW |
16 |
48,901,551 (GRCm39) |
missense |
probably benign |
|
R8445:Myh15
|
UTSW |
16 |
48,940,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R8707:Myh15
|
UTSW |
16 |
48,973,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R8729:Myh15
|
UTSW |
16 |
48,881,851 (GRCm39) |
missense |
probably damaging |
0.97 |
R8773:Myh15
|
UTSW |
16 |
49,015,900 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8869:Myh15
|
UTSW |
16 |
48,997,366 (GRCm39) |
missense |
probably benign |
|
R8890:Myh15
|
UTSW |
16 |
48,959,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R9026:Myh15
|
UTSW |
16 |
49,007,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R9063:Myh15
|
UTSW |
16 |
48,913,118 (GRCm39) |
missense |
probably benign |
0.00 |
R9290:Myh15
|
UTSW |
16 |
48,997,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R9630:Myh15
|
UTSW |
16 |
48,980,341 (GRCm39) |
missense |
probably benign |
0.15 |
R9710:Myh15
|
UTSW |
16 |
48,959,044 (GRCm39) |
missense |
probably damaging |
1.00 |
X0012:Myh15
|
UTSW |
16 |
48,963,341 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Myh15
|
UTSW |
16 |
48,986,237 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Myh15
|
UTSW |
16 |
48,916,894 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Myh15
|
UTSW |
16 |
48,980,189 (GRCm39) |
missense |
probably benign |
0.09 |
Z1177:Myh15
|
UTSW |
16 |
48,975,981 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Myh15
|
UTSW |
16 |
48,901,591 (GRCm39) |
missense |
probably benign |
0.02 |
|
Predicted Primers |
PCR Primer
(F):5'- CACAACCTGACTTTGTTGACTC -3'
(R):5'- GCCTGCAACTGAAGACGTAGATC -3'
Sequencing Primer
(F):5'- AACCTGACTTTGTTGACTCTGTGTC -3'
(R):5'- CATTCTTTTCTTGGACAAGGGAGAC -3'
|
Posted On |
2016-06-06 |