Incidental Mutation 'R0133:Arap1'
ID |
21749 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Arap1
|
Ensembl Gene |
ENSMUSG00000032812 |
Gene Name |
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 |
Synonyms |
Centd2, 2410002L19Rik |
MMRRC Submission |
038418-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0133 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
7 |
Chromosomal Location |
100997296-101061793 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 101035436 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 30
(D30E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000121257
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000084895]
[ENSMUST00000084896]
[ENSMUST00000107010]
[ENSMUST00000127873]
[ENSMUST00000130016]
[ENSMUST00000134143]
[ENSMUST00000141083]
[ENSMUST00000148902]
|
AlphaFold |
Q4LDD4 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000084895
AA Change: D30E
PolyPhen 2
Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
|
SMART Domains |
Protein: ENSMUSP00000081957 Gene: ENSMUSG00000032812 AA Change: D30E
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
37 |
N/A |
INTRINSIC |
PH
|
82 |
175 |
2.62e-17 |
SMART |
PH
|
195 |
285 |
3.6e-6 |
SMART |
ArfGap
|
289 |
415 |
2.4e-22 |
SMART |
PH
|
498 |
606 |
1.23e-13 |
SMART |
PH
|
616 |
710 |
1.08e0 |
SMART |
RhoGAP
|
722 |
904 |
1.35e-63 |
SMART |
Pfam:RA
|
926 |
1015 |
1.5e-10 |
PFAM |
PH
|
1029 |
1141 |
8.58e-13 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000084896
AA Change: D278E
PolyPhen 2
Score 0.705 (Sensitivity: 0.86; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000081958 Gene: ENSMUSG00000032812 AA Change: D278E
Domain | Start | End | E-Value | Type |
SAM
|
3 |
70 |
1.72e-7 |
SMART |
low complexity region
|
92 |
104 |
N/A |
INTRINSIC |
low complexity region
|
115 |
126 |
N/A |
INTRINSIC |
low complexity region
|
135 |
146 |
N/A |
INTRINSIC |
low complexity region
|
151 |
167 |
N/A |
INTRINSIC |
low complexity region
|
197 |
227 |
N/A |
INTRINSIC |
low complexity region
|
267 |
285 |
N/A |
INTRINSIC |
PH
|
330 |
423 |
2.62e-17 |
SMART |
PH
|
443 |
533 |
3.6e-6 |
SMART |
ArfGap
|
537 |
663 |
2.4e-22 |
SMART |
PH
|
746 |
854 |
1.23e-13 |
SMART |
PH
|
864 |
958 |
1.08e0 |
SMART |
RhoGAP
|
970 |
1152 |
1.35e-63 |
SMART |
Pfam:RA
|
1174 |
1263 |
6.6e-13 |
PFAM |
PH
|
1277 |
1400 |
8e-13 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000107010
AA Change: D278E
PolyPhen 2
Score 0.705 (Sensitivity: 0.86; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000102624 Gene: ENSMUSG00000032812 AA Change: D278E
Domain | Start | End | E-Value | Type |
SAM
|
3 |
70 |
1.72e-7 |
SMART |
low complexity region
|
92 |
104 |
N/A |
INTRINSIC |
low complexity region
|
115 |
126 |
N/A |
INTRINSIC |
low complexity region
|
135 |
146 |
N/A |
INTRINSIC |
low complexity region
|
151 |
167 |
N/A |
INTRINSIC |
low complexity region
|
197 |
227 |
N/A |
INTRINSIC |
low complexity region
|
267 |
285 |
N/A |
INTRINSIC |
PH
|
330 |
423 |
2.62e-17 |
SMART |
PH
|
443 |
533 |
3.6e-6 |
SMART |
ArfGap
|
537 |
663 |
2.4e-22 |
SMART |
PH
|
746 |
854 |
1.23e-13 |
SMART |
PH
|
864 |
958 |
1.08e0 |
SMART |
RhoGAP
|
970 |
1152 |
1.35e-63 |
SMART |
Pfam:RA
|
1174 |
1263 |
1.9e-10 |
PFAM |
PH
|
1277 |
1389 |
8.58e-13 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000127873
AA Change: D30E
PolyPhen 2
Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000121257 Gene: ENSMUSG00000032812 AA Change: D30E
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
37 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000130016
AA Change: D30E
PolyPhen 2
Score 0.805 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000115850 Gene: ENSMUSG00000032812 AA Change: D30E
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
37 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000134143
AA Change: D30E
PolyPhen 2
Score 0.705 (Sensitivity: 0.86; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000115107 Gene: ENSMUSG00000032812 AA Change: D30E
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
37 |
N/A |
INTRINSIC |
SCOP:d1ki1b2
|
68 |
111 |
4e-4 |
SMART |
Blast:PH
|
82 |
111 |
6e-15 |
BLAST |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152082
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000141083
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000213314
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000148902
|
Meta Mutation Damage Score |
0.6467 |
Coding Region Coverage |
- 1x: 98.8%
- 3x: 97.9%
- 10x: 95.2%
- 20x: 89.4%
|
Validation Efficiency |
99% (83/84) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains SAM, ARF-GAP, RHO-GAP, ankyrin repeat, RAS-associating, and pleckstrin homology (PH) domains. In vitro, this protein displays RHO-GAP and phosphatidylinositol (3,4,5) trisphosphate (PIP3)-dependent ARF-GAP activity. The encoded protein associates with the Golgi, and the ARF-GAP activity mediates changes in the Golgi and the formation of filopodia. It is thought to regulate the cell-specific trafficking of a receptor protein involved in apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acbd4 |
T |
C |
11: 102,996,214 (GRCm39) |
S172P |
probably damaging |
Het |
Akap6 |
A |
T |
12: 53,186,254 (GRCm39) |
K1223* |
probably null |
Het |
Akna |
G |
A |
4: 63,297,598 (GRCm39) |
Q819* |
probably null |
Het |
Ankrd2 |
T |
C |
19: 42,032,510 (GRCm39) |
V257A |
probably benign |
Het |
Atp6v0d2 |
T |
C |
4: 19,910,578 (GRCm39) |
|
probably benign |
Het |
Blm |
T |
A |
7: 80,152,115 (GRCm39) |
I611F |
possibly damaging |
Het |
Ccng2 |
A |
G |
5: 93,421,240 (GRCm39) |
K250R |
probably benign |
Het |
Cdhr3 |
A |
G |
12: 33,142,751 (GRCm39) |
L8P |
possibly damaging |
Het |
Csf2rb |
T |
G |
15: 78,223,204 (GRCm39) |
|
probably benign |
Het |
Ctbs |
A |
G |
3: 146,163,223 (GRCm39) |
I204V |
probably benign |
Het |
Cxcl16 |
T |
A |
11: 70,349,596 (GRCm39) |
E76D |
possibly damaging |
Het |
Dhx15 |
T |
C |
5: 52,311,414 (GRCm39) |
I689V |
possibly damaging |
Het |
Dlk2 |
T |
C |
17: 46,609,868 (GRCm39) |
|
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,311,835 (GRCm39) |
M4452K |
probably damaging |
Het |
Dok4 |
T |
A |
8: 95,591,991 (GRCm39) |
I280F |
probably benign |
Het |
Dsc3 |
T |
C |
18: 20,104,639 (GRCm39) |
T563A |
probably damaging |
Het |
Dsg1b |
C |
T |
18: 20,537,935 (GRCm39) |
A617V |
probably damaging |
Het |
Eps8l2 |
C |
T |
7: 140,942,120 (GRCm39) |
P721S |
unknown |
Het |
Evx2 |
T |
C |
2: 74,489,426 (GRCm39) |
D112G |
possibly damaging |
Het |
Fam124a |
C |
A |
14: 62,843,782 (GRCm39) |
T430K |
possibly damaging |
Het |
Fbrs |
C |
T |
7: 127,088,782 (GRCm39) |
|
probably benign |
Het |
Fbxw14 |
T |
C |
9: 109,103,647 (GRCm39) |
T22A |
probably benign |
Het |
Fmo5 |
T |
G |
3: 97,552,952 (GRCm39) |
V300G |
probably damaging |
Het |
Gadl1 |
T |
C |
9: 115,770,411 (GRCm39) |
S75P |
probably benign |
Het |
Galnt2 |
T |
G |
8: 125,065,277 (GRCm39) |
I469S |
probably benign |
Het |
Gga3 |
T |
A |
11: 115,479,805 (GRCm39) |
|
probably benign |
Het |
Gm10647 |
T |
C |
9: 66,705,771 (GRCm39) |
|
probably benign |
Het |
Gm14180 |
C |
A |
11: 99,625,043 (GRCm39) |
C25F |
unknown |
Het |
Grid2 |
A |
T |
6: 64,297,116 (GRCm39) |
D493V |
probably damaging |
Het |
Gzmc |
T |
A |
14: 56,469,754 (GRCm39) |
Y182F |
possibly damaging |
Het |
Hecw2 |
A |
C |
1: 53,869,899 (GRCm39) |
L1443R |
probably damaging |
Het |
Igkv4-62 |
A |
G |
6: 69,377,053 (GRCm39) |
I32T |
probably benign |
Het |
Ikzf1 |
T |
A |
11: 11,691,015 (GRCm39) |
|
probably null |
Het |
Il27ra |
G |
A |
8: 84,760,571 (GRCm39) |
|
probably benign |
Het |
Jmjd1c |
C |
A |
10: 67,076,587 (GRCm39) |
A2137D |
probably benign |
Het |
Kcnc2 |
T |
C |
10: 112,294,502 (GRCm39) |
C579R |
probably damaging |
Het |
Kdr |
T |
C |
5: 76,112,498 (GRCm39) |
T862A |
probably damaging |
Het |
Kif17 |
T |
C |
4: 138,005,556 (GRCm39) |
S182P |
possibly damaging |
Het |
Klf5 |
A |
T |
14: 99,539,318 (GRCm39) |
T164S |
probably benign |
Het |
Ksr2 |
T |
G |
5: 117,693,359 (GRCm39) |
V269G |
possibly damaging |
Het |
Mcm5 |
T |
A |
8: 75,847,539 (GRCm39) |
D445E |
probably damaging |
Het |
Mlkl |
T |
C |
8: 112,054,580 (GRCm39) |
I186V |
probably damaging |
Het |
Muc4 |
A |
T |
16: 32,591,978 (GRCm39) |
S3017C |
possibly damaging |
Het |
Myo15a |
T |
C |
11: 60,368,676 (GRCm39) |
F479L |
possibly damaging |
Het |
Myo6 |
A |
G |
9: 80,181,257 (GRCm39) |
|
probably benign |
Het |
Myom1 |
T |
A |
17: 71,354,782 (GRCm39) |
V393E |
probably damaging |
Het |
Nup98 |
T |
A |
7: 101,788,859 (GRCm39) |
|
probably null |
Het |
Odf2l |
A |
G |
3: 144,854,302 (GRCm39) |
N383S |
probably damaging |
Het |
Olfml3 |
A |
C |
3: 103,644,342 (GRCm39) |
|
probably null |
Het |
Or10q1 |
T |
A |
19: 13,727,352 (GRCm39) |
I294N |
probably damaging |
Het |
Or7g17 |
G |
A |
9: 18,767,925 (GRCm39) |
M1I |
probably null |
Het |
Or8g18 |
A |
G |
9: 39,149,307 (GRCm39) |
Y141H |
probably benign |
Het |
Or8j3b |
A |
T |
2: 86,205,159 (GRCm39) |
V199E |
possibly damaging |
Het |
Plxna4 |
A |
T |
6: 32,174,009 (GRCm39) |
D1195E |
probably benign |
Het |
Ppp1r1a |
T |
A |
15: 103,446,247 (GRCm39) |
H20L |
probably damaging |
Het |
Prdm4 |
A |
G |
10: 85,746,085 (GRCm39) |
|
probably null |
Het |
Prom2 |
A |
G |
2: 127,380,258 (GRCm39) |
|
probably benign |
Het |
Rasal3 |
T |
C |
17: 32,622,357 (GRCm39) |
M1V |
probably null |
Het |
Rhoj |
A |
G |
12: 75,441,194 (GRCm39) |
|
probably null |
Het |
Rnf40 |
C |
T |
7: 127,196,032 (GRCm39) |
|
probably null |
Het |
Slc15a3 |
T |
C |
19: 10,820,614 (GRCm39) |
L77P |
probably damaging |
Het |
Slc26a6 |
T |
C |
9: 108,738,522 (GRCm39) |
V586A |
possibly damaging |
Het |
Slc30a10 |
T |
A |
1: 185,187,370 (GRCm39) |
L37Q |
probably damaging |
Het |
Slc43a2 |
T |
A |
11: 75,454,403 (GRCm39) |
M316K |
probably benign |
Het |
Smarcal1 |
T |
C |
1: 72,672,010 (GRCm39) |
F844L |
probably benign |
Het |
Snx19 |
A |
G |
9: 30,339,912 (GRCm39) |
E350G |
possibly damaging |
Het |
Tecta |
T |
A |
9: 42,278,524 (GRCm39) |
T995S |
probably benign |
Het |
Tmc3 |
T |
G |
7: 83,261,681 (GRCm39) |
N586K |
probably damaging |
Het |
Tmem107 |
T |
A |
11: 68,963,239 (GRCm39) |
|
probably benign |
Het |
Tmem247 |
A |
G |
17: 87,225,989 (GRCm39) |
Q51R |
probably benign |
Het |
Tmpo |
G |
T |
10: 90,999,900 (GRCm39) |
|
probably benign |
Het |
Ubr5 |
T |
A |
15: 37,996,815 (GRCm39) |
T1894S |
probably damaging |
Het |
Vmn2r92 |
C |
T |
17: 18,388,219 (GRCm39) |
A408V |
probably damaging |
Het |
Xirp2 |
T |
A |
2: 67,347,468 (GRCm39) |
H3236Q |
probably benign |
Het |
Zfand4 |
G |
A |
6: 116,291,700 (GRCm39) |
D545N |
probably benign |
Het |
Zkscan3 |
G |
T |
13: 21,578,944 (GRCm39) |
P155T |
possibly damaging |
Het |
|
Other mutations in Arap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00517:Arap1
|
APN |
7 |
101,037,256 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01311:Arap1
|
APN |
7 |
101,037,343 (GRCm39) |
nonsense |
probably null |
|
IGL01349:Arap1
|
APN |
7 |
101,036,359 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01521:Arap1
|
APN |
7 |
101,049,812 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01869:Arap1
|
APN |
7 |
101,049,490 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02156:Arap1
|
APN |
7 |
101,037,937 (GRCm39) |
unclassified |
probably benign |
|
IGL02320:Arap1
|
APN |
7 |
101,034,236 (GRCm39) |
missense |
probably benign |
|
IGL02478:Arap1
|
APN |
7 |
101,049,332 (GRCm39) |
splice site |
probably null |
|
R0233:Arap1
|
UTSW |
7 |
101,049,448 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0233:Arap1
|
UTSW |
7 |
101,049,448 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0412:Arap1
|
UTSW |
7 |
101,039,429 (GRCm39) |
missense |
probably damaging |
0.98 |
R0616:Arap1
|
UTSW |
7 |
101,050,857 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0838:Arap1
|
UTSW |
7 |
101,049,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R0962:Arap1
|
UTSW |
7 |
101,034,121 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1186:Arap1
|
UTSW |
7 |
101,053,476 (GRCm39) |
splice site |
probably benign |
|
R1405:Arap1
|
UTSW |
7 |
101,047,643 (GRCm39) |
splice site |
probably null |
|
R1405:Arap1
|
UTSW |
7 |
101,047,643 (GRCm39) |
splice site |
probably null |
|
R1724:Arap1
|
UTSW |
7 |
101,049,733 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1793:Arap1
|
UTSW |
7 |
101,037,829 (GRCm39) |
missense |
probably benign |
|
R1959:Arap1
|
UTSW |
7 |
101,022,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R1960:Arap1
|
UTSW |
7 |
101,022,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Arap1
|
UTSW |
7 |
101,050,725 (GRCm39) |
missense |
probably benign |
0.00 |
R2128:Arap1
|
UTSW |
7 |
101,058,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R3737:Arap1
|
UTSW |
7 |
101,049,484 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3851:Arap1
|
UTSW |
7 |
101,039,372 (GRCm39) |
nonsense |
probably null |
|
R4034:Arap1
|
UTSW |
7 |
101,049,484 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4386:Arap1
|
UTSW |
7 |
101,034,778 (GRCm39) |
missense |
probably benign |
|
R4435:Arap1
|
UTSW |
7 |
101,039,461 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4779:Arap1
|
UTSW |
7 |
101,053,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R4786:Arap1
|
UTSW |
7 |
101,034,212 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4850:Arap1
|
UTSW |
7 |
101,047,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R4942:Arap1
|
UTSW |
7 |
101,051,009 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5253:Arap1
|
UTSW |
7 |
101,037,851 (GRCm39) |
missense |
probably benign |
0.00 |
R5342:Arap1
|
UTSW |
7 |
101,054,167 (GRCm39) |
missense |
probably benign |
0.00 |
R5367:Arap1
|
UTSW |
7 |
101,058,337 (GRCm39) |
missense |
probably damaging |
0.99 |
R5397:Arap1
|
UTSW |
7 |
101,034,119 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5968:Arap1
|
UTSW |
7 |
101,043,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R6052:Arap1
|
UTSW |
7 |
101,053,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R6574:Arap1
|
UTSW |
7 |
101,053,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R6645:Arap1
|
UTSW |
7 |
101,057,318 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7060:Arap1
|
UTSW |
7 |
101,058,564 (GRCm39) |
splice site |
probably null |
|
R7191:Arap1
|
UTSW |
7 |
101,034,199 (GRCm39) |
missense |
probably benign |
0.31 |
R7323:Arap1
|
UTSW |
7 |
101,049,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R7349:Arap1
|
UTSW |
7 |
101,039,435 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7516:Arap1
|
UTSW |
7 |
101,058,538 (GRCm39) |
missense |
probably benign |
0.00 |
R7922:Arap1
|
UTSW |
7 |
101,053,621 (GRCm39) |
nonsense |
probably null |
|
R8034:Arap1
|
UTSW |
7 |
101,043,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R8293:Arap1
|
UTSW |
7 |
101,050,141 (GRCm39) |
missense |
probably benign |
|
R8493:Arap1
|
UTSW |
7 |
101,035,725 (GRCm39) |
nonsense |
probably null |
|
R8810:Arap1
|
UTSW |
7 |
101,053,585 (GRCm39) |
missense |
probably damaging |
0.99 |
R8811:Arap1
|
UTSW |
7 |
101,036,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Arap1
|
UTSW |
7 |
101,057,324 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8930:Arap1
|
UTSW |
7 |
101,057,324 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8931:Arap1
|
UTSW |
7 |
101,057,324 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8941:Arap1
|
UTSW |
7 |
101,057,324 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9014:Arap1
|
UTSW |
7 |
101,053,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R9144:Arap1
|
UTSW |
7 |
101,047,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R9164:Arap1
|
UTSW |
7 |
101,041,090 (GRCm39) |
nonsense |
probably null |
|
R9215:Arap1
|
UTSW |
7 |
101,049,214 (GRCm39) |
missense |
probably benign |
0.23 |
R9340:Arap1
|
UTSW |
7 |
101,037,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R9519:Arap1
|
UTSW |
7 |
101,043,946 (GRCm39) |
start gained |
probably benign |
|
R9790:Arap1
|
UTSW |
7 |
101,037,376 (GRCm39) |
missense |
probably benign |
0.00 |
R9791:Arap1
|
UTSW |
7 |
101,037,376 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GCCCTAGATCCATGTTTGCCAACAG -3'
(R):5'- CCAGCCTTGATGACAGGTGTGATG -3'
Sequencing Primer
(F):5'- GATCCATGTTTGCCAACAGTTCTC -3'
(R):5'- ATTCAGGCCACTCGTTGG -3'
|
Posted On |
2013-04-12 |