Incidental Mutation 'R1920:Arhgef10'
ID |
212949 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Arhgef10
|
Ensembl Gene |
ENSMUSG00000071176 |
Gene Name |
Rho guanine nucleotide exchange factor 10 |
Synonyms |
6430549H08Rik |
MMRRC Submission |
039938-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1920 (G1)
|
Quality Score |
141 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
14961663-15051085 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
C to T
at 15006987 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000125526
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000084207]
[ENSMUST00000110800]
[ENSMUST00000161162]
[ENSMUST00000163062]
|
AlphaFold |
Q8C033 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000084207
|
SMART Domains |
Protein: ENSMUSP00000081225 Gene: ENSMUSG00000071176
Domain | Start | End | E-Value | Type |
low complexity region
|
73 |
82 |
N/A |
INTRINSIC |
low complexity region
|
155 |
165 |
N/A |
INTRINSIC |
low complexity region
|
236 |
245 |
N/A |
INTRINSIC |
low complexity region
|
247 |
265 |
N/A |
INTRINSIC |
coiled coil region
|
308 |
335 |
N/A |
INTRINSIC |
RhoGEF
|
401 |
583 |
9.79e-58 |
SMART |
Blast:PH
|
617 |
829 |
6e-47 |
BLAST |
low complexity region
|
1256 |
1272 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000110800
|
SMART Domains |
Protein: ENSMUSP00000106424 Gene: ENSMUSG00000071176
Domain | Start | End | E-Value | Type |
low complexity region
|
73 |
82 |
N/A |
INTRINSIC |
low complexity region
|
155 |
165 |
N/A |
INTRINSIC |
low complexity region
|
236 |
245 |
N/A |
INTRINSIC |
low complexity region
|
247 |
265 |
N/A |
INTRINSIC |
low complexity region
|
280 |
291 |
N/A |
INTRINSIC |
RhoGEF
|
362 |
544 |
9.79e-58 |
SMART |
Blast:PH
|
578 |
790 |
8e-47 |
BLAST |
low complexity region
|
1217 |
1233 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000161162
|
SMART Domains |
Protein: ENSMUSP00000125606 Gene: ENSMUSG00000071176
Domain | Start | End | E-Value | Type |
low complexity region
|
73 |
82 |
N/A |
INTRINSIC |
low complexity region
|
155 |
165 |
N/A |
INTRINSIC |
low complexity region
|
235 |
244 |
N/A |
INTRINSIC |
low complexity region
|
246 |
264 |
N/A |
INTRINSIC |
coiled coil region
|
307 |
334 |
N/A |
INTRINSIC |
RhoGEF
|
400 |
579 |
2.2e-51 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162958
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000163062
|
SMART Domains |
Protein: ENSMUSP00000125526 Gene: ENSMUSG00000071176
Domain | Start | End | E-Value | Type |
RhoGEF
|
73 |
255 |
9.79e-58 |
SMART |
Blast:PH
|
289 |
501 |
2e-47 |
BLAST |
low complexity region
|
899 |
915 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.7%
- 20x: 93.4%
|
Validation Efficiency |
98% (101/103) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a Rho guanine nucleotide exchange factor (GEF). Rho GEFs regulate the activity of small Rho GTPases by stimulating the exchange of guanine diphosphate (GDP) for guanine triphosphate (GTP) and may play a role in neural morphogenesis. Mutations in this gene are associated with slowed nerve conduction velocity (SNCV). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700056E22Rik |
A |
G |
1: 183,765,828 (GRCm39) |
V77A |
probably benign |
Het |
Actl7a |
G |
A |
4: 56,744,135 (GRCm39) |
V221M |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Asgr2 |
T |
C |
11: 69,989,123 (GRCm39) |
L86P |
possibly damaging |
Het |
Atp12a |
A |
G |
14: 56,624,308 (GRCm39) |
R919G |
probably benign |
Het |
Atrn |
A |
G |
2: 130,836,971 (GRCm39) |
Y1145C |
probably damaging |
Het |
B3gnt5 |
T |
G |
16: 19,588,294 (GRCm39) |
L171R |
probably benign |
Het |
Bbof1 |
T |
A |
12: 84,457,859 (GRCm39) |
N41K |
possibly damaging |
Het |
Bdp1 |
A |
T |
13: 100,235,097 (GRCm39) |
W166R |
probably benign |
Het |
Bean1 |
A |
T |
8: 104,937,742 (GRCm39) |
H107L |
possibly damaging |
Het |
Brd4 |
T |
C |
17: 32,417,060 (GRCm39) |
|
probably benign |
Het |
Cadps |
T |
C |
14: 12,465,859 (GRCm38) |
K1017R |
possibly damaging |
Het |
Cep78 |
G |
A |
19: 15,951,715 (GRCm39) |
|
probably benign |
Het |
Cfap70 |
C |
T |
14: 20,445,020 (GRCm39) |
A1087T |
probably damaging |
Het |
Cideb |
A |
G |
14: 55,992,700 (GRCm39) |
V72A |
probably benign |
Het |
Cpz |
T |
C |
5: 35,675,012 (GRCm39) |
E79G |
probably damaging |
Het |
Crybg1 |
A |
G |
10: 43,873,544 (GRCm39) |
L1188P |
probably damaging |
Het |
Cuzd1 |
G |
A |
7: 130,911,425 (GRCm39) |
P518L |
probably benign |
Het |
Cyp2j5 |
A |
T |
4: 96,551,491 (GRCm39) |
N77K |
probably damaging |
Het |
Cyp4f39 |
T |
G |
17: 32,702,265 (GRCm39) |
F254C |
probably benign |
Het |
Dkk1 |
C |
A |
19: 30,524,731 (GRCm39) |
V225L |
probably damaging |
Het |
Dlg5 |
T |
C |
14: 24,226,639 (GRCm39) |
Y421C |
probably damaging |
Het |
Dll3 |
T |
C |
7: 27,998,348 (GRCm39) |
T206A |
probably benign |
Het |
Dnhd1 |
T |
C |
7: 105,362,614 (GRCm39) |
C3766R |
probably benign |
Het |
Dock9 |
G |
T |
14: 121,820,792 (GRCm39) |
S1534Y |
probably damaging |
Het |
Dst |
T |
C |
1: 34,200,110 (GRCm39) |
V96A |
probably damaging |
Het |
F2r |
A |
G |
13: 95,740,698 (GRCm39) |
F279S |
probably damaging |
Het |
Farp1 |
C |
A |
14: 121,492,908 (GRCm39) |
N503K |
probably benign |
Het |
Fbxw2 |
G |
A |
2: 34,712,776 (GRCm39) |
T95I |
probably damaging |
Het |
Fis1 |
A |
G |
5: 136,994,461 (GRCm39) |
T50A |
probably benign |
Het |
Frzb |
T |
G |
2: 80,276,772 (GRCm39) |
E138A |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,817,164 (GRCm39) |
D4299V |
probably benign |
Het |
Fyco1 |
C |
T |
9: 123,659,478 (GRCm39) |
D233N |
probably damaging |
Het |
Gmpr |
A |
G |
13: 45,667,997 (GRCm39) |
|
probably benign |
Het |
Hc |
C |
T |
2: 34,919,407 (GRCm39) |
|
probably benign |
Het |
Hnrnpa1 |
T |
C |
15: 103,150,699 (GRCm39) |
M186T |
possibly damaging |
Het |
Kl |
A |
G |
5: 150,906,132 (GRCm39) |
K501E |
probably benign |
Het |
Klhl42 |
A |
G |
6: 147,009,427 (GRCm39) |
N422S |
probably damaging |
Het |
Kmt2d |
C |
G |
15: 98,753,471 (GRCm39) |
K127N |
probably damaging |
Het |
Kmt2d |
T |
A |
15: 98,753,472 (GRCm39) |
K127M |
probably damaging |
Het |
Krt39 |
T |
A |
11: 99,405,461 (GRCm39) |
T480S |
probably benign |
Het |
Lims2 |
T |
A |
18: 32,088,395 (GRCm39) |
C198* |
probably null |
Het |
Mctp1 |
A |
G |
13: 76,532,729 (GRCm39) |
N26D |
possibly damaging |
Het |
Mdm4 |
A |
G |
1: 132,931,538 (GRCm39) |
S168P |
probably benign |
Het |
Myo3a |
A |
G |
2: 22,455,008 (GRCm39) |
Y71C |
probably benign |
Het |
Nlrp9c |
T |
A |
7: 26,084,319 (GRCm39) |
D420V |
probably damaging |
Het |
Ntf3 |
A |
T |
6: 126,079,485 (GRCm39) |
I7N |
possibly damaging |
Het |
Or10ag52 |
G |
A |
2: 87,043,721 (GRCm39) |
G162S |
probably benign |
Het |
Or13c25 |
G |
T |
4: 52,910,849 (GRCm39) |
T315K |
probably benign |
Het |
Or4c119 |
A |
G |
2: 88,986,925 (GRCm39) |
V198A |
probably benign |
Het |
Or8b38 |
T |
C |
9: 37,972,981 (GRCm39) |
Y122H |
probably damaging |
Het |
Papln |
C |
A |
12: 83,836,028 (GRCm39) |
Y1222* |
probably null |
Het |
Pgm3 |
T |
G |
9: 86,440,531 (GRCm39) |
I387L |
possibly damaging |
Het |
Pira12 |
G |
C |
7: 3,900,871 (GRCm39) |
P20R |
probably damaging |
Het |
Pkd1 |
C |
A |
17: 24,814,131 (GRCm39) |
P4167Q |
probably damaging |
Het |
Plcb4 |
T |
A |
2: 135,854,947 (GRCm39) |
V1174E |
probably damaging |
Het |
Polr1b |
A |
G |
2: 128,943,031 (GRCm39) |
N9D |
probably benign |
Het |
Prkaa2 |
G |
A |
4: 104,893,950 (GRCm39) |
Q456* |
probably null |
Het |
Ptch2 |
G |
T |
4: 116,965,858 (GRCm39) |
V425L |
probably benign |
Het |
Ptprh |
A |
T |
7: 4,552,394 (GRCm39) |
S957T |
probably benign |
Het |
Riok1 |
A |
G |
13: 38,241,177 (GRCm39) |
D444G |
probably benign |
Het |
Rrbp1 |
A |
T |
2: 143,830,211 (GRCm39) |
V652E |
probably benign |
Het |
Rrp36 |
C |
T |
17: 46,983,671 (GRCm39) |
R47Q |
possibly damaging |
Het |
Sec24c |
T |
C |
14: 20,736,955 (GRCm39) |
S304P |
probably damaging |
Het |
Serpinb6b |
A |
T |
13: 33,158,991 (GRCm39) |
D64V |
possibly damaging |
Het |
Serpinb9b |
A |
T |
13: 33,223,531 (GRCm39) |
|
probably null |
Het |
Six6 |
T |
A |
12: 72,988,538 (GRCm39) |
I237N |
probably damaging |
Het |
Slc25a36 |
A |
T |
9: 96,975,135 (GRCm39) |
M127K |
probably benign |
Het |
Slc2a10 |
A |
G |
2: 165,356,550 (GRCm39) |
D70G |
probably damaging |
Het |
Slc2a3 |
T |
A |
6: 122,713,700 (GRCm39) |
I171F |
probably damaging |
Het |
Smc4 |
A |
G |
3: 68,940,401 (GRCm39) |
T1087A |
probably damaging |
Het |
Spg21 |
A |
G |
9: 65,391,779 (GRCm39) |
Y242C |
probably damaging |
Het |
St14 |
A |
G |
9: 31,001,166 (GRCm39) |
V855A |
possibly damaging |
Het |
Stx2 |
G |
A |
5: 129,065,903 (GRCm39) |
T251M |
probably damaging |
Het |
Svs3b |
A |
T |
2: 164,097,848 (GRCm39) |
S158T |
probably benign |
Het |
Synpo |
C |
T |
18: 60,736,661 (GRCm39) |
M428I |
probably benign |
Het |
Tasor2 |
A |
T |
13: 3,626,612 (GRCm39) |
Y1113N |
possibly damaging |
Het |
Tbc1d31 |
G |
A |
15: 57,775,760 (GRCm39) |
R17H |
probably damaging |
Het |
Tbl3 |
G |
A |
17: 24,923,477 (GRCm39) |
T284I |
probably benign |
Het |
Tcof1 |
T |
C |
18: 60,971,927 (GRCm39) |
T127A |
possibly damaging |
Het |
Tgoln1 |
T |
C |
6: 72,593,084 (GRCm39) |
E132G |
probably benign |
Het |
Timeless |
T |
C |
10: 128,077,583 (GRCm39) |
I221T |
probably damaging |
Het |
Tmem176b |
C |
T |
6: 48,815,138 (GRCm39) |
A52T |
possibly damaging |
Het |
Tmem192 |
C |
T |
8: 65,418,235 (GRCm39) |
L207F |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,176,996 (GRCm39) |
|
probably null |
Het |
Ttc7b |
C |
T |
12: 100,381,389 (GRCm39) |
|
probably null |
Het |
Tubb5 |
T |
C |
17: 36,146,190 (GRCm39) |
Y340C |
probably benign |
Het |
Ubr1 |
G |
A |
2: 120,761,449 (GRCm39) |
T576I |
probably benign |
Het |
Vcan |
T |
C |
13: 89,841,134 (GRCm39) |
E1470G |
probably damaging |
Het |
Vmn1r200 |
T |
A |
13: 22,579,663 (GRCm39) |
N146K |
probably damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,831,839 (GRCm39) |
I317F |
probably benign |
Het |
Vmn2r61 |
T |
C |
7: 41,949,710 (GRCm39) |
I710T |
possibly damaging |
Het |
Wipf1 |
T |
A |
2: 73,270,499 (GRCm39) |
K61N |
probably benign |
Het |
Zfp112 |
T |
C |
7: 23,824,662 (GRCm39) |
V210A |
probably benign |
Het |
Zfp612 |
G |
A |
8: 110,815,095 (GRCm39) |
V101M |
probably benign |
Het |
Zfp637 |
A |
G |
6: 117,822,681 (GRCm39) |
R270G |
probably damaging |
Het |
Zfp652 |
A |
G |
11: 95,654,851 (GRCm39) |
E418G |
possibly damaging |
Het |
Zfp97 |
A |
G |
17: 17,365,265 (GRCm39) |
I255V |
probably benign |
Het |
|
Other mutations in Arhgef10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00766:Arhgef10
|
APN |
8 |
15,025,006 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00823:Arhgef10
|
APN |
8 |
14,990,378 (GRCm39) |
unclassified |
probably benign |
|
IGL01012:Arhgef10
|
APN |
8 |
15,029,977 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01311:Arhgef10
|
APN |
8 |
15,041,054 (GRCm39) |
splice site |
probably null |
|
IGL01596:Arhgef10
|
APN |
8 |
15,049,468 (GRCm39) |
nonsense |
probably null |
|
IGL01888:Arhgef10
|
APN |
8 |
15,012,577 (GRCm39) |
nonsense |
probably null |
|
IGL01938:Arhgef10
|
APN |
8 |
15,041,062 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02151:Arhgef10
|
APN |
8 |
14,978,889 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02274:Arhgef10
|
APN |
8 |
14,997,205 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02369:Arhgef10
|
APN |
8 |
15,047,551 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02411:Arhgef10
|
APN |
8 |
15,004,819 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02500:Arhgef10
|
APN |
8 |
15,011,238 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02597:Arhgef10
|
APN |
8 |
14,980,198 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02602:Arhgef10
|
APN |
8 |
14,980,198 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02743:Arhgef10
|
APN |
8 |
14,980,198 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02744:Arhgef10
|
APN |
8 |
14,980,198 (GRCm39) |
missense |
probably benign |
0.27 |
IGL03113:Arhgef10
|
APN |
8 |
15,004,505 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03248:Arhgef10
|
APN |
8 |
14,978,847 (GRCm39) |
missense |
probably benign |
0.00 |
P0028:Arhgef10
|
UTSW |
8 |
14,978,925 (GRCm39) |
missense |
possibly damaging |
0.79 |
P4748:Arhgef10
|
UTSW |
8 |
14,978,925 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0049:Arhgef10
|
UTSW |
8 |
15,004,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R0197:Arhgef10
|
UTSW |
8 |
15,012,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R0479:Arhgef10
|
UTSW |
8 |
15,041,070 (GRCm39) |
missense |
probably damaging |
0.98 |
R0701:Arhgef10
|
UTSW |
8 |
15,012,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R0966:Arhgef10
|
UTSW |
8 |
14,990,343 (GRCm39) |
missense |
probably benign |
0.01 |
R1367:Arhgef10
|
UTSW |
8 |
14,990,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Arhgef10
|
UTSW |
8 |
15,041,211 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1631:Arhgef10
|
UTSW |
8 |
14,997,157 (GRCm39) |
missense |
probably damaging |
0.98 |
R1766:Arhgef10
|
UTSW |
8 |
15,029,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R2051:Arhgef10
|
UTSW |
8 |
14,995,320 (GRCm39) |
missense |
probably null |
1.00 |
R2088:Arhgef10
|
UTSW |
8 |
15,033,898 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2118:Arhgef10
|
UTSW |
8 |
14,984,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R2120:Arhgef10
|
UTSW |
8 |
14,984,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R2121:Arhgef10
|
UTSW |
8 |
14,984,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R2122:Arhgef10
|
UTSW |
8 |
14,984,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R2124:Arhgef10
|
UTSW |
8 |
14,984,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R2318:Arhgef10
|
UTSW |
8 |
14,978,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Arhgef10
|
UTSW |
8 |
15,025,666 (GRCm39) |
missense |
probably benign |
0.01 |
R2870:Arhgef10
|
UTSW |
8 |
15,025,666 (GRCm39) |
missense |
probably benign |
0.01 |
R2870:Arhgef10
|
UTSW |
8 |
15,025,093 (GRCm39) |
critical splice donor site |
probably null |
|
R2870:Arhgef10
|
UTSW |
8 |
15,025,093 (GRCm39) |
critical splice donor site |
probably null |
|
R2872:Arhgef10
|
UTSW |
8 |
15,025,666 (GRCm39) |
missense |
probably benign |
0.01 |
R2872:Arhgef10
|
UTSW |
8 |
15,025,666 (GRCm39) |
missense |
probably benign |
0.01 |
R2872:Arhgef10
|
UTSW |
8 |
15,025,093 (GRCm39) |
critical splice donor site |
probably null |
|
R2872:Arhgef10
|
UTSW |
8 |
15,025,093 (GRCm39) |
critical splice donor site |
probably null |
|
R2874:Arhgef10
|
UTSW |
8 |
15,025,666 (GRCm39) |
missense |
probably benign |
0.01 |
R2874:Arhgef10
|
UTSW |
8 |
15,025,093 (GRCm39) |
critical splice donor site |
probably null |
|
R3522:Arhgef10
|
UTSW |
8 |
15,004,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R4049:Arhgef10
|
UTSW |
8 |
15,029,998 (GRCm39) |
missense |
probably benign |
0.05 |
R4324:Arhgef10
|
UTSW |
8 |
14,990,335 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4351:Arhgef10
|
UTSW |
8 |
15,041,145 (GRCm39) |
nonsense |
probably null |
|
R4384:Arhgef10
|
UTSW |
8 |
14,980,157 (GRCm39) |
nonsense |
probably null |
|
R4385:Arhgef10
|
UTSW |
8 |
14,980,157 (GRCm39) |
nonsense |
probably null |
|
R4685:Arhgef10
|
UTSW |
8 |
15,006,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R5111:Arhgef10
|
UTSW |
8 |
14,982,408 (GRCm39) |
missense |
probably benign |
0.00 |
R5169:Arhgef10
|
UTSW |
8 |
14,980,051 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5670:Arhgef10
|
UTSW |
8 |
15,004,774 (GRCm39) |
missense |
probably benign |
0.01 |
R5945:Arhgef10
|
UTSW |
8 |
15,030,028 (GRCm39) |
critical splice donor site |
probably null |
|
R6593:Arhgef10
|
UTSW |
8 |
15,012,564 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6593:Arhgef10
|
UTSW |
8 |
15,012,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R6734:Arhgef10
|
UTSW |
8 |
15,025,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R6859:Arhgef10
|
UTSW |
8 |
15,025,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R6890:Arhgef10
|
UTSW |
8 |
14,978,786 (GRCm39) |
missense |
probably benign |
0.27 |
R7068:Arhgef10
|
UTSW |
8 |
15,008,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R7081:Arhgef10
|
UTSW |
8 |
15,047,547 (GRCm39) |
nonsense |
probably null |
|
R7157:Arhgef10
|
UTSW |
8 |
14,980,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R7232:Arhgef10
|
UTSW |
8 |
14,990,323 (GRCm39) |
missense |
probably benign |
0.10 |
R7514:Arhgef10
|
UTSW |
8 |
15,025,956 (GRCm39) |
missense |
probably benign |
0.16 |
R7544:Arhgef10
|
UTSW |
8 |
15,029,854 (GRCm39) |
missense |
probably benign |
0.34 |
R7657:Arhgef10
|
UTSW |
8 |
15,029,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R7736:Arhgef10
|
UTSW |
8 |
15,030,583 (GRCm39) |
nonsense |
probably null |
|
R7777:Arhgef10
|
UTSW |
8 |
14,995,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R8000:Arhgef10
|
UTSW |
8 |
14,980,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R8060:Arhgef10
|
UTSW |
8 |
15,004,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R8441:Arhgef10
|
UTSW |
8 |
15,041,237 (GRCm39) |
splice site |
probably benign |
|
R8545:Arhgef10
|
UTSW |
8 |
15,025,931 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8545:Arhgef10
|
UTSW |
8 |
14,978,868 (GRCm39) |
missense |
probably benign |
0.00 |
R8702:Arhgef10
|
UTSW |
8 |
14,992,638 (GRCm39) |
missense |
probably benign |
|
R8846:Arhgef10
|
UTSW |
8 |
15,025,956 (GRCm39) |
missense |
probably benign |
0.16 |
R8854:Arhgef10
|
UTSW |
8 |
15,029,798 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9076:Arhgef10
|
UTSW |
8 |
15,024,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R9384:Arhgef10
|
UTSW |
8 |
15,041,067 (GRCm39) |
missense |
probably damaging |
0.99 |
R9479:Arhgef10
|
UTSW |
8 |
15,047,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R9799:Arhgef10
|
UTSW |
8 |
14,990,268 (GRCm39) |
missense |
probably damaging |
0.99 |
X0024:Arhgef10
|
UTSW |
8 |
15,028,486 (GRCm39) |
missense |
probably benign |
0.01 |
X0027:Arhgef10
|
UTSW |
8 |
15,047,631 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1088:Arhgef10
|
UTSW |
8 |
15,014,191 (GRCm39) |
missense |
probably benign |
0.01 |
|
Predicted Primers |
PCR Primer
(F):5'- AAGAGCTCCTGCAGTCATAGC -3'
(R):5'- ATCTATGATCCAGCCTAGAGCC -3'
Sequencing Primer
(F):5'- TCCTGCAGTCATAGCCGTCG -3'
(R):5'- GCCTAGAGCCCCTGAACCTC -3'
|
Posted On |
2014-07-14 |