Incidental Mutation 'R9629:Arhgap45'
ID |
725366 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Arhgap45
|
Ensembl Gene |
ENSMUSG00000035697 |
Gene Name |
Rho GTPase activating protein 45 |
Synonyms |
6330406L22Rik, Hmha1 |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R9629 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
10 |
Chromosomal Location |
79852505-79867305 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 79863694 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Glutamic Acid
at position 815
(K815E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000101012
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043311]
[ENSMUST00000099501]
[ENSMUST00000105373]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000043311
AA Change: K688E
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000041019 Gene: ENSMUSG00000035697 AA Change: K688E
Domain | Start | End | E-Value | Type |
low complexity region
|
142 |
153 |
N/A |
INTRINSIC |
FCH
|
157 |
244 |
4.14e-17 |
SMART |
low complexity region
|
255 |
269 |
N/A |
INTRINSIC |
low complexity region
|
309 |
324 |
N/A |
INTRINSIC |
low complexity region
|
330 |
345 |
N/A |
INTRINSIC |
low complexity region
|
527 |
536 |
N/A |
INTRINSIC |
C1
|
582 |
628 |
3.15e-8 |
SMART |
RhoGAP
|
653 |
852 |
2.73e-73 |
SMART |
low complexity region
|
856 |
869 |
N/A |
INTRINSIC |
Blast:RhoGAP
|
876 |
999 |
1e-21 |
BLAST |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000099501
AA Change: K804E
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000097100 Gene: ENSMUSG00000035697 AA Change: K804E
Domain | Start | End | E-Value | Type |
low complexity region
|
258 |
269 |
N/A |
INTRINSIC |
FCH
|
273 |
360 |
4.14e-17 |
SMART |
low complexity region
|
371 |
385 |
N/A |
INTRINSIC |
low complexity region
|
425 |
440 |
N/A |
INTRINSIC |
low complexity region
|
446 |
461 |
N/A |
INTRINSIC |
low complexity region
|
643 |
652 |
N/A |
INTRINSIC |
C1
|
698 |
744 |
3.15e-8 |
SMART |
RhoGAP
|
769 |
968 |
2.73e-73 |
SMART |
low complexity region
|
972 |
985 |
N/A |
INTRINSIC |
Blast:RhoGAP
|
992 |
1115 |
1e-21 |
BLAST |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000105373
AA Change: K815E
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000101012 Gene: ENSMUSG00000035697 AA Change: K815E
Domain | Start | End | E-Value | Type |
low complexity region
|
269 |
280 |
N/A |
INTRINSIC |
FCH
|
284 |
371 |
4.14e-17 |
SMART |
low complexity region
|
382 |
396 |
N/A |
INTRINSIC |
low complexity region
|
436 |
451 |
N/A |
INTRINSIC |
low complexity region
|
457 |
472 |
N/A |
INTRINSIC |
low complexity region
|
654 |
663 |
N/A |
INTRINSIC |
C1
|
709 |
755 |
3.15e-8 |
SMART |
RhoGAP
|
780 |
979 |
2.73e-73 |
SMART |
low complexity region
|
983 |
996 |
N/A |
INTRINSIC |
Blast:RhoGAP
|
1003 |
1126 |
1e-21 |
BLAST |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930596D02Rik |
T |
C |
14: 35,532,134 (GRCm39) |
E147G |
probably damaging |
Het |
Agrn |
G |
A |
4: 156,257,094 (GRCm39) |
Q1217* |
probably null |
Het |
Ankrd13c |
G |
C |
3: 157,653,313 (GRCm39) |
K50N |
probably benign |
Het |
Anks3 |
C |
T |
16: 4,775,565 (GRCm39) |
S144N |
probably damaging |
Het |
Apob |
A |
T |
12: 8,059,054 (GRCm39) |
D2512V |
probably damaging |
Het |
Atr |
T |
A |
9: 95,747,098 (GRCm39) |
C127S |
probably benign |
Het |
B4galnt4 |
A |
G |
7: 140,648,575 (GRCm39) |
D697G |
probably damaging |
Het |
C2cd3 |
C |
T |
7: 100,029,249 (GRCm39) |
L134F |
probably damaging |
Het |
Celsr2 |
C |
T |
3: 108,308,915 (GRCm39) |
G1697D |
probably damaging |
Het |
Cep170 |
A |
G |
1: 176,583,821 (GRCm39) |
S88P |
possibly damaging |
Het |
Cnot1 |
A |
G |
8: 96,455,874 (GRCm39) |
V1961A |
probably damaging |
Het |
Cntnap4 |
A |
G |
8: 113,568,349 (GRCm39) |
N795S |
probably damaging |
Het |
Cog2 |
T |
A |
8: 125,260,125 (GRCm39) |
V256D |
possibly damaging |
Het |
Col14a1 |
A |
G |
15: 55,382,545 (GRCm39) |
Y515C |
|
Het |
Cox7a1 |
A |
G |
7: 29,884,583 (GRCm39) |
Q30R |
probably damaging |
Het |
Cs |
T |
C |
10: 128,196,885 (GRCm39) |
S427P |
probably damaging |
Het |
Dbr1 |
T |
A |
9: 99,464,523 (GRCm39) |
C101S |
|
Het |
Dhcr7 |
C |
A |
7: 143,401,212 (GRCm39) |
Y461* |
probably null |
Het |
Dis3l2 |
T |
A |
1: 86,974,784 (GRCm39) |
M691K |
probably benign |
Het |
Dnah17 |
T |
C |
11: 117,979,804 (GRCm39) |
D1751G |
probably damaging |
Het |
Dock10 |
A |
T |
1: 80,481,389 (GRCm39) |
I536K |
|
Het |
Dok6 |
G |
T |
18: 89,491,988 (GRCm39) |
F196L |
possibly damaging |
Het |
Epx |
C |
T |
11: 87,755,651 (GRCm39) |
D678N |
probably damaging |
Het |
Fcrlb |
G |
C |
1: 170,739,735 (GRCm39) |
P56A |
probably benign |
Het |
Flrt3 |
T |
C |
2: 140,502,816 (GRCm39) |
R271G |
possibly damaging |
Het |
Galnt15 |
T |
A |
14: 31,774,301 (GRCm39) |
L479Q |
probably damaging |
Het |
Gfy |
G |
A |
7: 44,827,785 (GRCm39) |
L104F |
probably benign |
Het |
Gltp |
C |
T |
5: 114,814,382 (GRCm39) |
M80I |
probably benign |
Het |
Gm21560 |
G |
A |
14: 6,218,250 (GRCm38) |
T76I |
probably benign |
Het |
Gm5150 |
A |
G |
3: 16,044,829 (GRCm39) |
I132T |
probably benign |
Het |
Hdac9 |
T |
C |
12: 34,439,389 (GRCm39) |
H437R |
probably damaging |
Het |
Hpgd |
C |
A |
8: 56,751,419 (GRCm39) |
F82L |
|
Het |
Ifi207 |
GAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATGAAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATGAAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGACTATTGGATGGTGTTGATAGAGTTGCTTGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATGAAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATACAGTTGCTTGTGGAGCCAGGAGGTTGCTAGATGCTGTTGAT |
GAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATGAAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGACTATTGGATGGTGTTGATAGAGTTGCTTGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATGAAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATACAGTTGCTTGTGGAGCCAGGAGGTTGCTAGATGCTGTTGAT |
1: 173,556,561 (GRCm39) |
|
probably benign |
Het |
Ilrun |
A |
T |
17: 28,012,913 (GRCm39) |
F95I |
probably damaging |
Het |
Itgb5 |
C |
T |
16: 33,696,295 (GRCm39) |
T162I |
probably damaging |
Het |
Jakmip3 |
G |
A |
7: 138,625,118 (GRCm39) |
|
probably null |
Het |
Kctd1 |
A |
T |
18: 15,196,611 (GRCm39) |
M4K |
unknown |
Het |
Kirrel1 |
C |
A |
3: 87,003,025 (GRCm39) |
E123* |
probably null |
Het |
Krt87 |
G |
C |
15: 101,389,048 (GRCm39) |
P95A |
probably benign |
Het |
Man1a |
A |
T |
10: 53,796,158 (GRCm39) |
H511Q |
probably damaging |
Het |
Megf8 |
A |
G |
7: 25,043,194 (GRCm39) |
D1372G |
possibly damaging |
Het |
Mrgprd |
A |
G |
7: 144,875,189 (GRCm39) |
D20G |
probably benign |
Het |
Mrpl54 |
C |
T |
10: 81,101,528 (GRCm39) |
G78S |
probably damaging |
Het |
Myl1 |
T |
A |
1: 66,969,448 (GRCm39) |
E61D |
probably benign |
Het |
Myo7a |
G |
T |
7: 97,712,937 (GRCm39) |
H1679Q |
probably benign |
Het |
Naca |
A |
G |
10: 127,878,226 (GRCm39) |
E1086G |
unknown |
Het |
Nagpa |
C |
G |
16: 5,017,829 (GRCm39) |
D258H |
probably damaging |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nr2f6 |
G |
A |
8: 71,827,171 (GRCm39) |
L377F |
probably damaging |
Het |
Ntsr1 |
G |
A |
2: 180,183,274 (GRCm39) |
R328H |
probably damaging |
Het |
Nup93 |
G |
A |
8: 95,033,267 (GRCm39) |
S592N |
probably damaging |
Het |
Or10a2 |
A |
T |
7: 106,673,164 (GRCm39) |
N43I |
probably damaging |
Het |
Or4k40 |
T |
A |
2: 111,251,137 (GRCm39) |
H53L |
probably benign |
Het |
Or8g36 |
T |
C |
9: 39,422,497 (GRCm39) |
D173G |
probably benign |
Het |
Pard3 |
T |
C |
8: 128,136,153 (GRCm39) |
V842A |
possibly damaging |
Het |
Phospho2 |
T |
A |
2: 69,626,295 (GRCm39) |
N150K |
probably damaging |
Het |
Piwil1 |
T |
C |
5: 128,831,051 (GRCm39) |
S791P |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,462,437 (GRCm39) |
V2039A |
possibly damaging |
Het |
Ppp1r3c |
A |
G |
19: 36,711,404 (GRCm39) |
I122T |
probably benign |
Het |
Prrc2c |
A |
G |
1: 162,519,959 (GRCm39) |
Y2131H |
possibly damaging |
Het |
Qtrt2 |
T |
C |
16: 43,683,540 (GRCm39) |
M311V |
possibly damaging |
Het |
Rbbp4 |
T |
C |
4: 129,212,243 (GRCm39) |
D346G |
probably damaging |
Het |
Slc13a5 |
A |
G |
11: 72,138,578 (GRCm39) |
I455T |
probably damaging |
Het |
Slc28a3 |
A |
T |
13: 58,717,187 (GRCm39) |
Y366* |
probably null |
Het |
Srgap1 |
T |
A |
10: 121,705,746 (GRCm39) |
Q226L |
probably benign |
Het |
Syt17 |
A |
G |
7: 118,007,379 (GRCm39) |
V362A |
probably damaging |
Het |
Tas2r117 |
T |
C |
6: 132,780,374 (GRCm39) |
S171P |
probably benign |
Het |
Tfap2b |
A |
T |
1: 19,289,468 (GRCm39) |
I198F |
probably damaging |
Het |
Tg |
A |
T |
15: 66,555,587 (GRCm39) |
I760F |
possibly damaging |
Het |
Tmem123 |
T |
C |
9: 7,790,984 (GRCm39) |
V95A |
possibly damaging |
Het |
Tmem198b |
C |
A |
10: 128,638,386 (GRCm39) |
G59V |
probably damaging |
Het |
Tmem30c |
T |
G |
16: 57,096,585 (GRCm39) |
I179L |
probably benign |
Het |
Tmprss2 |
A |
T |
16: 97,369,702 (GRCm39) |
D357E |
probably benign |
Het |
Tns3 |
G |
A |
11: 8,401,142 (GRCm39) |
T1052M |
possibly damaging |
Het |
Trex1 |
A |
T |
9: 108,887,632 (GRCm39) |
C120S |
probably damaging |
Het |
Ttc8 |
A |
G |
12: 98,886,965 (GRCm39) |
S13G |
possibly damaging |
Het |
Ttll7 |
T |
C |
3: 146,621,487 (GRCm39) |
I362T |
probably damaging |
Het |
Usp34 |
A |
T |
11: 23,314,364 (GRCm39) |
T769S |
|
Het |
Vmn1r185 |
G |
T |
7: 26,311,439 (GRCm39) |
T22K |
probably damaging |
Het |
Vmn1r39 |
T |
G |
6: 66,781,578 (GRCm39) |
M247L |
probably benign |
Het |
Vmn2r96 |
A |
G |
17: 18,803,257 (GRCm39) |
D389G |
probably benign |
Het |
Xirp1 |
C |
T |
9: 119,846,379 (GRCm39) |
V835I |
probably benign |
Het |
Ylpm1 |
T |
G |
12: 85,044,036 (GRCm39) |
I258S |
unknown |
Het |
Zfp971 |
A |
T |
2: 177,675,417 (GRCm39) |
S339C |
probably damaging |
Het |
|
Other mutations in Arhgap45 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01360:Arhgap45
|
APN |
10 |
79,864,482 (GRCm39) |
splice site |
probably benign |
|
IGL01414:Arhgap45
|
APN |
10 |
79,862,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01505:Arhgap45
|
APN |
10 |
79,862,376 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02203:Arhgap45
|
APN |
10 |
79,863,387 (GRCm39) |
nonsense |
probably null |
|
IGL02557:Arhgap45
|
APN |
10 |
79,857,472 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02858:Arhgap45
|
APN |
10 |
79,853,768 (GRCm39) |
missense |
probably benign |
0.20 |
IGL03292:Arhgap45
|
APN |
10 |
79,856,803 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03352:Arhgap45
|
APN |
10 |
79,866,585 (GRCm39) |
missense |
probably damaging |
0.96 |
Celt
|
UTSW |
10 |
79,856,652 (GRCm39) |
missense |
probably damaging |
1.00 |
celtic
|
UTSW |
10 |
79,863,423 (GRCm39) |
nonsense |
probably null |
|
druid
|
UTSW |
10 |
79,862,181 (GRCm39) |
critical splice donor site |
probably null |
|
Mistletoe
|
UTSW |
10 |
79,862,936 (GRCm39) |
nonsense |
probably null |
|
Roman
|
UTSW |
10 |
79,863,431 (GRCm39) |
missense |
probably damaging |
1.00 |
stonehenge
|
UTSW |
10 |
79,861,316 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03048:Arhgap45
|
UTSW |
10 |
79,852,851 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4677001:Arhgap45
|
UTSW |
10 |
79,856,583 (GRCm39) |
missense |
probably benign |
|
R0532:Arhgap45
|
UTSW |
10 |
79,857,917 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1233:Arhgap45
|
UTSW |
10 |
79,863,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R1579:Arhgap45
|
UTSW |
10 |
79,864,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R1666:Arhgap45
|
UTSW |
10 |
79,864,584 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1668:Arhgap45
|
UTSW |
10 |
79,864,584 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1688:Arhgap45
|
UTSW |
10 |
79,864,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R1710:Arhgap45
|
UTSW |
10 |
79,853,932 (GRCm39) |
nonsense |
probably null |
|
R1902:Arhgap45
|
UTSW |
10 |
79,861,300 (GRCm39) |
missense |
probably damaging |
0.99 |
R1912:Arhgap45
|
UTSW |
10 |
79,856,524 (GRCm39) |
missense |
probably benign |
0.08 |
R1935:Arhgap45
|
UTSW |
10 |
79,866,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R1936:Arhgap45
|
UTSW |
10 |
79,866,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R1955:Arhgap45
|
UTSW |
10 |
79,862,326 (GRCm39) |
missense |
probably benign |
0.15 |
R1968:Arhgap45
|
UTSW |
10 |
79,863,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R1977:Arhgap45
|
UTSW |
10 |
79,856,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R1986:Arhgap45
|
UTSW |
10 |
79,856,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R2074:Arhgap45
|
UTSW |
10 |
79,863,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R2081:Arhgap45
|
UTSW |
10 |
79,863,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R2162:Arhgap45
|
UTSW |
10 |
79,852,813 (GRCm39) |
start codon destroyed |
probably null |
0.02 |
R2937:Arhgap45
|
UTSW |
10 |
79,864,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R2938:Arhgap45
|
UTSW |
10 |
79,864,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R3081:Arhgap45
|
UTSW |
10 |
79,862,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4695:Arhgap45
|
UTSW |
10 |
79,861,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R4736:Arhgap45
|
UTSW |
10 |
79,862,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4758:Arhgap45
|
UTSW |
10 |
79,866,127 (GRCm39) |
missense |
probably benign |
0.00 |
R4860:Arhgap45
|
UTSW |
10 |
79,862,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R4860:Arhgap45
|
UTSW |
10 |
79,862,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R4934:Arhgap45
|
UTSW |
10 |
79,856,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R4943:Arhgap45
|
UTSW |
10 |
79,862,337 (GRCm39) |
missense |
probably benign |
0.00 |
R5102:Arhgap45
|
UTSW |
10 |
79,857,262 (GRCm39) |
missense |
probably benign |
0.01 |
R5128:Arhgap45
|
UTSW |
10 |
79,866,793 (GRCm39) |
missense |
probably benign |
0.16 |
R5667:Arhgap45
|
UTSW |
10 |
79,861,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Arhgap45
|
UTSW |
10 |
79,861,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R5920:Arhgap45
|
UTSW |
10 |
79,864,965 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5998:Arhgap45
|
UTSW |
10 |
79,866,784 (GRCm39) |
missense |
probably damaging |
0.99 |
R6276:Arhgap45
|
UTSW |
10 |
79,862,068 (GRCm39) |
missense |
probably benign |
0.25 |
R6675:Arhgap45
|
UTSW |
10 |
79,853,938 (GRCm39) |
missense |
probably null |
0.98 |
R6738:Arhgap45
|
UTSW |
10 |
79,863,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R6783:Arhgap45
|
UTSW |
10 |
79,853,698 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6863:Arhgap45
|
UTSW |
10 |
79,853,616 (GRCm39) |
missense |
probably benign |
0.03 |
R6978:Arhgap45
|
UTSW |
10 |
79,857,682 (GRCm39) |
missense |
probably benign |
0.00 |
R7089:Arhgap45
|
UTSW |
10 |
79,862,181 (GRCm39) |
critical splice donor site |
probably null |
|
R7215:Arhgap45
|
UTSW |
10 |
79,861,316 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7307:Arhgap45
|
UTSW |
10 |
79,865,016 (GRCm39) |
missense |
probably benign |
0.14 |
R7308:Arhgap45
|
UTSW |
10 |
79,862,392 (GRCm39) |
critical splice donor site |
probably null |
|
R7480:Arhgap45
|
UTSW |
10 |
79,862,936 (GRCm39) |
nonsense |
probably null |
|
R7481:Arhgap45
|
UTSW |
10 |
79,858,134 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7649:Arhgap45
|
UTSW |
10 |
79,866,835 (GRCm39) |
missense |
probably benign |
0.00 |
R7652:Arhgap45
|
UTSW |
10 |
79,864,672 (GRCm39) |
missense |
probably benign |
0.01 |
R7748:Arhgap45
|
UTSW |
10 |
79,852,766 (GRCm39) |
unclassified |
probably benign |
|
R7883:Arhgap45
|
UTSW |
10 |
79,863,423 (GRCm39) |
nonsense |
probably null |
|
R8121:Arhgap45
|
UTSW |
10 |
79,853,909 (GRCm39) |
missense |
probably damaging |
0.99 |
R8169:Arhgap45
|
UTSW |
10 |
79,863,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R8170:Arhgap45
|
UTSW |
10 |
79,863,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R8175:Arhgap45
|
UTSW |
10 |
79,863,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R8178:Arhgap45
|
UTSW |
10 |
79,863,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R8186:Arhgap45
|
UTSW |
10 |
79,863,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R8187:Arhgap45
|
UTSW |
10 |
79,863,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R8687:Arhgap45
|
UTSW |
10 |
79,852,621 (GRCm39) |
unclassified |
probably benign |
|
R8866:Arhgap45
|
UTSW |
10 |
79,853,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:Arhgap45
|
UTSW |
10 |
79,855,570 (GRCm39) |
missense |
probably benign |
0.00 |
R9299:Arhgap45
|
UTSW |
10 |
79,862,565 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9412:Arhgap45
|
UTSW |
10 |
79,855,564 (GRCm39) |
start codon destroyed |
probably null |
0.66 |
R9579:Arhgap45
|
UTSW |
10 |
79,853,843 (GRCm39) |
missense |
probably benign |
|
R9710:Arhgap45
|
UTSW |
10 |
79,857,635 (GRCm39) |
missense |
probably damaging |
0.99 |
X0023:Arhgap45
|
UTSW |
10 |
79,866,634 (GRCm39) |
missense |
probably damaging |
0.98 |
X0063:Arhgap45
|
UTSW |
10 |
79,866,190 (GRCm39) |
missense |
possibly damaging |
0.51 |
Z1176:Arhgap45
|
UTSW |
10 |
79,864,886 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Arhgap45
|
UTSW |
10 |
79,861,370 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TTGGACAAGACTTCAGCCAGG -3'
(R):5'- GTCCCCTACCATGCTAATGC -3'
Sequencing Primer
(F):5'- AGACTTCAGCCAGGCAGCC -3'
(R):5'- TACCATGCTAATGCCCCGC -3'
|
Posted On |
2022-09-12 |