Incidental Mutation 'R1758:Cntnap5c'
ID |
195133 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cntnap5c
|
Ensembl Gene |
ENSMUSG00000038048 |
Gene Name |
contactin associated protein-like 5C |
Synonyms |
|
MMRRC Submission |
039790-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.060)
|
Stock # |
R1758 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
17 |
Chromosomal Location |
58076565-58717350 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 58349545 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glycine
at position 286
(D286G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000075416
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000076038]
|
AlphaFold |
Q0V8T7 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000076038
AA Change: D286G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000075416 Gene: ENSMUSG00000038048 AA Change: D286G
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
FA58C
|
29 |
174 |
1.26e-10 |
SMART |
LamG
|
201 |
338 |
1.57e-29 |
SMART |
LamG
|
387 |
521 |
3e-26 |
SMART |
EGF
|
549 |
583 |
1.88e-1 |
SMART |
Blast:FBG
|
586 |
769 |
8e-83 |
BLAST |
LamG
|
811 |
938 |
4.37e-28 |
SMART |
EGF
|
959 |
995 |
6.55e-1 |
SMART |
LamG
|
1036 |
1172 |
2.08e-11 |
SMART |
transmembrane domain
|
1240 |
1262 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.6%
- 20x: 93.2%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029H14Rik |
T |
C |
8: 13,612,237 (GRCm39) |
R38G |
possibly damaging |
Het |
4930590J08Rik |
T |
C |
6: 91,892,203 (GRCm39) |
V155A |
possibly damaging |
Het |
Adgb |
A |
G |
10: 10,302,349 (GRCm39) |
S406P |
probably damaging |
Het |
Adgrb2 |
C |
A |
4: 129,905,668 (GRCm39) |
T893N |
probably damaging |
Het |
Adgrf5 |
T |
C |
17: 43,735,484 (GRCm39) |
|
probably null |
Het |
Alms1 |
T |
A |
6: 85,605,487 (GRCm39) |
I2379N |
probably damaging |
Het |
Arap3 |
C |
T |
18: 38,122,965 (GRCm39) |
V512I |
probably benign |
Het |
Atf4 |
C |
T |
15: 80,141,414 (GRCm39) |
T268I |
probably benign |
Het |
Cblif |
G |
A |
19: 11,735,179 (GRCm39) |
M266I |
probably damaging |
Het |
Ccdc154 |
T |
C |
17: 25,382,156 (GRCm39) |
L25P |
probably damaging |
Het |
Ccdc9 |
G |
A |
7: 16,010,161 (GRCm39) |
S381F |
probably damaging |
Het |
Cdk17 |
C |
T |
10: 93,044,112 (GRCm39) |
T17M |
probably damaging |
Het |
Cep128 |
T |
C |
12: 91,314,352 (GRCm39) |
N142S |
probably benign |
Het |
Cep78 |
A |
G |
19: 15,936,900 (GRCm39) |
I602T |
probably damaging |
Het |
Clasp1 |
C |
T |
1: 118,475,755 (GRCm39) |
T935I |
probably damaging |
Het |
Cnr1 |
T |
C |
4: 33,945,000 (GRCm39) |
S463P |
probably damaging |
Het |
Cntnap1 |
T |
A |
11: 101,075,449 (GRCm39) |
W876R |
probably damaging |
Het |
Copa |
C |
T |
1: 171,931,711 (GRCm39) |
R321C |
probably damaging |
Het |
Cspg4b |
A |
G |
13: 113,505,266 (GRCm39) |
T2132A |
possibly damaging |
Het |
Ctla2a |
T |
G |
13: 61,083,256 (GRCm39) |
E98A |
probably damaging |
Het |
Cux1 |
A |
T |
5: 136,421,176 (GRCm39) |
D183E |
probably damaging |
Het |
Cxcl15 |
A |
C |
5: 90,949,323 (GRCm39) |
T163P |
unknown |
Het |
Ddias |
T |
C |
7: 92,508,571 (GRCm39) |
N448S |
probably benign |
Het |
Dhx8 |
T |
C |
11: 101,657,564 (GRCm39) |
F1152S |
probably damaging |
Het |
Dnah12 |
C |
A |
14: 26,488,071 (GRCm39) |
Q992K |
probably benign |
Het |
Eno3 |
G |
T |
11: 70,552,251 (GRCm39) |
W301L |
possibly damaging |
Het |
Faap100 |
A |
T |
11: 120,268,059 (GRCm39) |
V238E |
probably damaging |
Het |
Fgf4 |
A |
G |
7: 144,416,049 (GRCm39) |
S137G |
probably benign |
Het |
Fhod3 |
A |
C |
18: 25,253,367 (GRCm39) |
D1439A |
possibly damaging |
Het |
Frem2 |
A |
G |
3: 53,560,778 (GRCm39) |
L1243P |
probably damaging |
Het |
Gkn3 |
T |
G |
6: 87,365,817 (GRCm39) |
M1L |
probably benign |
Het |
Gm10250 |
T |
C |
15: 5,150,509 (GRCm39) |
|
probably benign |
Het |
Gm12185 |
T |
C |
11: 48,798,859 (GRCm39) |
T545A |
possibly damaging |
Het |
Gm14226 |
T |
A |
2: 154,867,378 (GRCm39) |
L445H |
probably damaging |
Het |
Gm3404 |
A |
T |
5: 146,463,036 (GRCm39) |
M73L |
probably benign |
Het |
Gm973 |
G |
T |
1: 59,673,169 (GRCm39) |
R976S |
unknown |
Het |
Gpr146 |
A |
T |
5: 139,379,137 (GRCm39) |
H313L |
probably benign |
Het |
Gys2 |
T |
A |
6: 142,418,432 (GRCm39) |
E32D |
probably damaging |
Het |
Igsf10 |
G |
A |
3: 59,236,617 (GRCm39) |
T1188I |
probably benign |
Het |
Igsf9b |
A |
T |
9: 27,245,548 (GRCm39) |
T1172S |
possibly damaging |
Het |
Itga8 |
T |
A |
2: 12,270,144 (GRCm39) |
N114I |
possibly damaging |
Het |
Itsn2 |
T |
A |
12: 4,708,160 (GRCm39) |
V795E |
possibly damaging |
Het |
Kdm1b |
T |
A |
13: 47,214,244 (GRCm39) |
S197T |
probably benign |
Het |
Kif5c |
G |
A |
2: 49,613,145 (GRCm39) |
R161Q |
probably benign |
Het |
Krt33b |
T |
C |
11: 99,916,361 (GRCm39) |
Y232C |
probably damaging |
Het |
Lonrf2 |
G |
A |
1: 38,852,357 (GRCm39) |
P165S |
probably benign |
Het |
Lrp1 |
A |
T |
10: 127,424,453 (GRCm39) |
N744K |
possibly damaging |
Het |
Mcm10 |
C |
A |
2: 5,008,861 (GRCm39) |
L369F |
probably damaging |
Het |
Muc5ac |
T |
A |
7: 141,355,268 (GRCm39) |
I1018N |
possibly damaging |
Het |
Myom2 |
T |
C |
8: 15,115,795 (GRCm39) |
L70P |
probably benign |
Het |
Myt1l |
T |
A |
12: 29,877,241 (GRCm39) |
N297K |
unknown |
Het |
Ncr1 |
C |
T |
7: 4,343,807 (GRCm39) |
T98I |
probably benign |
Het |
Nek3 |
T |
C |
8: 22,650,278 (GRCm39) |
E78G |
probably damaging |
Het |
Nfatc3 |
T |
A |
8: 106,825,768 (GRCm39) |
N606K |
probably damaging |
Het |
Nup107 |
T |
G |
10: 117,597,248 (GRCm39) |
D669A |
probably damaging |
Het |
Or10ag52 |
A |
T |
2: 87,043,758 (GRCm39) |
Q174L |
probably benign |
Het |
Or10c1 |
A |
T |
17: 37,522,204 (GRCm39) |
I180N |
possibly damaging |
Het |
Or4c3 |
T |
C |
2: 89,851,673 (GRCm39) |
T246A |
probably benign |
Het |
Or8b55 |
A |
T |
9: 38,726,871 (GRCm39) |
H24L |
probably benign |
Het |
Pcnx1 |
T |
C |
12: 82,030,258 (GRCm39) |
V1711A |
probably benign |
Het |
Pik3c3 |
A |
G |
18: 30,410,063 (GRCm39) |
D99G |
probably damaging |
Het |
Pinx1 |
C |
A |
14: 64,157,024 (GRCm39) |
T317K |
probably benign |
Het |
Ppargc1b |
G |
T |
18: 61,431,857 (GRCm39) |
|
probably null |
Het |
Pradc1 |
T |
A |
6: 85,424,203 (GRCm39) |
I119F |
possibly damaging |
Het |
Psat1 |
G |
T |
19: 15,892,243 (GRCm39) |
T242K |
probably damaging |
Het |
Psma6 |
G |
A |
12: 55,454,317 (GRCm39) |
C28Y |
probably damaging |
Het |
Pyurf |
A |
T |
6: 57,668,817 (GRCm39) |
C58* |
probably null |
Het |
Rab3gap2 |
C |
A |
1: 185,016,081 (GRCm39) |
A1331E |
probably benign |
Het |
Rnase4 |
T |
C |
14: 51,342,722 (GRCm39) |
*149Q |
probably null |
Het |
Ruvbl2 |
T |
C |
7: 45,074,586 (GRCm39) |
K184R |
probably benign |
Het |
Scn7a |
T |
G |
2: 66,510,527 (GRCm39) |
M1292L |
probably benign |
Het |
Scn7a |
A |
T |
2: 66,531,231 (GRCm39) |
Y549N |
probably damaging |
Het |
Selp |
A |
G |
1: 163,959,854 (GRCm39) |
D370G |
possibly damaging |
Het |
Slc22a15 |
G |
A |
3: 101,767,769 (GRCm39) |
Q386* |
probably null |
Het |
Slc22a29 |
A |
G |
19: 8,195,126 (GRCm39) |
|
probably null |
Het |
Slc26a7 |
A |
C |
4: 14,548,491 (GRCm39) |
I266S |
possibly damaging |
Het |
Smpd4 |
T |
C |
16: 17,443,872 (GRCm39) |
S112P |
probably damaging |
Het |
Smpd4 |
T |
A |
16: 17,458,744 (GRCm39) |
L165Q |
probably damaging |
Het |
Snx33 |
A |
G |
9: 56,833,982 (GRCm39) |
I29T |
probably benign |
Het |
Spen |
G |
A |
4: 141,203,686 (GRCm39) |
P1647L |
unknown |
Het |
Strip2 |
T |
C |
6: 29,941,940 (GRCm39) |
|
probably null |
Het |
Swsap1 |
C |
T |
9: 21,867,280 (GRCm39) |
R75* |
probably null |
Het |
Tesl1 |
A |
G |
X: 23,772,990 (GRCm39) |
I164V |
probably benign |
Het |
Tmem210 |
C |
T |
2: 25,178,435 (GRCm39) |
T32I |
probably damaging |
Het |
Tnn |
C |
T |
1: 159,975,154 (GRCm39) |
R91H |
possibly damaging |
Het |
Tnni1 |
G |
A |
1: 135,736,420 (GRCm39) |
R94H |
probably damaging |
Het |
Tnrc6c |
T |
A |
11: 117,651,556 (GRCm39) |
V1693D |
probably benign |
Het |
Trip4 |
G |
A |
9: 65,782,259 (GRCm39) |
Q158* |
probably null |
Het |
Ttc39b |
T |
C |
4: 83,155,586 (GRCm39) |
E474G |
probably damaging |
Het |
Usp50 |
C |
A |
2: 126,617,782 (GRCm39) |
C221F |
probably damaging |
Het |
Vmn1r171 |
T |
C |
7: 23,331,781 (GRCm39) |
I2T |
probably benign |
Het |
Wdr62 |
T |
A |
7: 29,967,328 (GRCm39) |
I309F |
probably damaging |
Het |
Xdh |
A |
T |
17: 74,217,204 (GRCm39) |
V688E |
probably damaging |
Het |
Zfyve26 |
A |
G |
12: 79,285,718 (GRCm39) |
L2353P |
probably damaging |
Het |
Zgpat |
C |
A |
2: 181,020,633 (GRCm39) |
R269S |
probably damaging |
Het |
|
Other mutations in Cntnap5c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00495:Cntnap5c
|
APN |
17 |
58,469,272 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00543:Cntnap5c
|
APN |
17 |
58,601,345 (GRCm39) |
missense |
probably benign |
|
IGL00679:Cntnap5c
|
APN |
17 |
58,362,673 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00942:Cntnap5c
|
APN |
17 |
58,076,593 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01352:Cntnap5c
|
APN |
17 |
58,600,896 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01822:Cntnap5c
|
APN |
17 |
58,362,700 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01864:Cntnap5c
|
APN |
17 |
58,717,237 (GRCm39) |
missense |
probably benign |
|
IGL01922:Cntnap5c
|
APN |
17 |
58,637,114 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02111:Cntnap5c
|
APN |
17 |
58,409,103 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02112:Cntnap5c
|
APN |
17 |
58,620,853 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02259:Cntnap5c
|
APN |
17 |
58,341,857 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02270:Cntnap5c
|
APN |
17 |
58,341,848 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02312:Cntnap5c
|
APN |
17 |
58,445,694 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02456:Cntnap5c
|
APN |
17 |
58,714,739 (GRCm39) |
splice site |
probably benign |
|
IGL02755:Cntnap5c
|
APN |
17 |
58,671,189 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02955:Cntnap5c
|
APN |
17 |
58,199,097 (GRCm39) |
splice site |
probably benign |
|
IGL03001:Cntnap5c
|
APN |
17 |
58,362,634 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03012:Cntnap5c
|
APN |
17 |
58,666,229 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03243:Cntnap5c
|
APN |
17 |
58,409,171 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03375:Cntnap5c
|
APN |
17 |
58,469,200 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02802:Cntnap5c
|
UTSW |
17 |
58,612,679 (GRCm39) |
missense |
probably benign |
0.04 |
LCD18:Cntnap5c
|
UTSW |
17 |
58,469,155 (GRCm39) |
intron |
probably benign |
|
R0003:Cntnap5c
|
UTSW |
17 |
58,506,012 (GRCm39) |
missense |
probably benign |
|
R0041:Cntnap5c
|
UTSW |
17 |
58,183,464 (GRCm39) |
missense |
probably benign |
0.00 |
R0041:Cntnap5c
|
UTSW |
17 |
58,183,464 (GRCm39) |
missense |
probably benign |
0.00 |
R0046:Cntnap5c
|
UTSW |
17 |
58,666,295 (GRCm39) |
missense |
probably benign |
|
R0046:Cntnap5c
|
UTSW |
17 |
58,666,295 (GRCm39) |
missense |
probably benign |
|
R0179:Cntnap5c
|
UTSW |
17 |
58,076,620 (GRCm39) |
missense |
probably benign |
0.19 |
R0244:Cntnap5c
|
UTSW |
17 |
58,409,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R0445:Cntnap5c
|
UTSW |
17 |
58,411,738 (GRCm39) |
missense |
probably benign |
0.01 |
R0626:Cntnap5c
|
UTSW |
17 |
58,349,422 (GRCm39) |
missense |
probably benign |
0.29 |
R0675:Cntnap5c
|
UTSW |
17 |
58,341,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R0681:Cntnap5c
|
UTSW |
17 |
58,612,550 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0699:Cntnap5c
|
UTSW |
17 |
58,349,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R0927:Cntnap5c
|
UTSW |
17 |
58,349,553 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1081:Cntnap5c
|
UTSW |
17 |
58,612,520 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1132:Cntnap5c
|
UTSW |
17 |
58,601,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R1175:Cntnap5c
|
UTSW |
17 |
58,671,241 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1640:Cntnap5c
|
UTSW |
17 |
58,702,289 (GRCm39) |
missense |
probably benign |
0.01 |
R1664:Cntnap5c
|
UTSW |
17 |
58,600,985 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Cntnap5c
|
UTSW |
17 |
58,469,286 (GRCm39) |
missense |
probably benign |
0.00 |
R1789:Cntnap5c
|
UTSW |
17 |
58,320,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Cntnap5c
|
UTSW |
17 |
58,666,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R2041:Cntnap5c
|
UTSW |
17 |
58,505,984 (GRCm39) |
missense |
probably benign |
0.02 |
R2041:Cntnap5c
|
UTSW |
17 |
58,411,765 (GRCm39) |
critical splice donor site |
probably null |
|
R2073:Cntnap5c
|
UTSW |
17 |
58,612,547 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2093:Cntnap5c
|
UTSW |
17 |
58,505,995 (GRCm39) |
missense |
probably benign |
0.00 |
R2134:Cntnap5c
|
UTSW |
17 |
58,714,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Cntnap5c
|
UTSW |
17 |
58,362,666 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2176:Cntnap5c
|
UTSW |
17 |
58,320,941 (GRCm39) |
missense |
probably benign |
0.04 |
R2256:Cntnap5c
|
UTSW |
17 |
58,637,310 (GRCm39) |
missense |
probably benign |
0.00 |
R2847:Cntnap5c
|
UTSW |
17 |
58,183,387 (GRCm39) |
missense |
probably damaging |
0.99 |
R2848:Cntnap5c
|
UTSW |
17 |
58,183,387 (GRCm39) |
missense |
probably damaging |
0.99 |
R2850:Cntnap5c
|
UTSW |
17 |
58,717,343 (GRCm39) |
utr 3 prime |
probably benign |
|
R3008:Cntnap5c
|
UTSW |
17 |
58,666,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R3714:Cntnap5c
|
UTSW |
17 |
58,199,062 (GRCm39) |
nonsense |
probably null |
|
R3720:Cntnap5c
|
UTSW |
17 |
58,637,197 (GRCm39) |
missense |
probably benign |
|
R3755:Cntnap5c
|
UTSW |
17 |
58,411,594 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4001:Cntnap5c
|
UTSW |
17 |
58,714,735 (GRCm39) |
critical splice donor site |
probably null |
|
R4619:Cntnap5c
|
UTSW |
17 |
58,717,263 (GRCm39) |
missense |
probably benign |
|
R5146:Cntnap5c
|
UTSW |
17 |
58,320,842 (GRCm39) |
missense |
probably damaging |
0.96 |
R5309:Cntnap5c
|
UTSW |
17 |
58,666,249 (GRCm39) |
missense |
probably benign |
0.05 |
R5312:Cntnap5c
|
UTSW |
17 |
58,666,249 (GRCm39) |
missense |
probably benign |
0.05 |
R5722:Cntnap5c
|
UTSW |
17 |
58,620,852 (GRCm39) |
missense |
probably benign |
0.01 |
R5974:Cntnap5c
|
UTSW |
17 |
58,183,480 (GRCm39) |
missense |
probably benign |
0.00 |
R6017:Cntnap5c
|
UTSW |
17 |
58,411,693 (GRCm39) |
missense |
probably benign |
0.41 |
R6059:Cntnap5c
|
UTSW |
17 |
58,620,707 (GRCm39) |
missense |
probably damaging |
0.99 |
R6152:Cntnap5c
|
UTSW |
17 |
58,593,881 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6182:Cntnap5c
|
UTSW |
17 |
58,183,390 (GRCm39) |
missense |
probably benign |
0.00 |
R6298:Cntnap5c
|
UTSW |
17 |
58,411,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R6301:Cntnap5c
|
UTSW |
17 |
58,199,032 (GRCm39) |
missense |
probably benign |
0.01 |
R6514:Cntnap5c
|
UTSW |
17 |
58,637,165 (GRCm39) |
missense |
probably damaging |
0.96 |
R6583:Cntnap5c
|
UTSW |
17 |
58,637,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R6688:Cntnap5c
|
UTSW |
17 |
58,600,899 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6781:Cntnap5c
|
UTSW |
17 |
58,445,648 (GRCm39) |
nonsense |
probably null |
|
R6866:Cntnap5c
|
UTSW |
17 |
58,399,289 (GRCm39) |
missense |
probably benign |
|
R6906:Cntnap5c
|
UTSW |
17 |
58,702,302 (GRCm39) |
missense |
probably benign |
0.18 |
R6911:Cntnap5c
|
UTSW |
17 |
58,199,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R6919:Cntnap5c
|
UTSW |
17 |
58,600,948 (GRCm39) |
missense |
probably benign |
0.02 |
R6923:Cntnap5c
|
UTSW |
17 |
58,399,345 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6925:Cntnap5c
|
UTSW |
17 |
58,702,261 (GRCm39) |
missense |
probably benign |
0.39 |
R6982:Cntnap5c
|
UTSW |
17 |
58,399,247 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7144:Cntnap5c
|
UTSW |
17 |
58,593,883 (GRCm39) |
missense |
probably benign |
|
R7422:Cntnap5c
|
UTSW |
17 |
58,717,226 (GRCm39) |
nonsense |
probably null |
|
R7797:Cntnap5c
|
UTSW |
17 |
58,666,270 (GRCm39) |
missense |
probably benign |
0.11 |
R7830:Cntnap5c
|
UTSW |
17 |
58,469,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R8169:Cntnap5c
|
UTSW |
17 |
58,411,765 (GRCm39) |
critical splice donor site |
probably null |
|
R8351:Cntnap5c
|
UTSW |
17 |
58,362,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R8352:Cntnap5c
|
UTSW |
17 |
58,362,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R8451:Cntnap5c
|
UTSW |
17 |
58,362,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R8452:Cntnap5c
|
UTSW |
17 |
58,362,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R8696:Cntnap5c
|
UTSW |
17 |
58,601,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Cntnap5c
|
UTSW |
17 |
58,362,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R8838:Cntnap5c
|
UTSW |
17 |
58,198,964 (GRCm39) |
missense |
|
|
R8901:Cntnap5c
|
UTSW |
17 |
58,637,156 (GRCm39) |
missense |
probably benign |
0.03 |
R8911:Cntnap5c
|
UTSW |
17 |
58,506,043 (GRCm39) |
missense |
probably damaging |
0.98 |
R9010:Cntnap5c
|
UTSW |
17 |
58,671,159 (GRCm39) |
missense |
probably benign |
0.00 |
R9065:Cntnap5c
|
UTSW |
17 |
58,445,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R9082:Cntnap5c
|
UTSW |
17 |
58,637,335 (GRCm39) |
missense |
probably damaging |
0.98 |
R9122:Cntnap5c
|
UTSW |
17 |
58,411,601 (GRCm39) |
missense |
probably benign |
0.01 |
R9137:Cntnap5c
|
UTSW |
17 |
58,601,203 (GRCm39) |
splice site |
probably benign |
|
R9176:Cntnap5c
|
UTSW |
17 |
58,620,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R9179:Cntnap5c
|
UTSW |
17 |
58,600,912 (GRCm39) |
missense |
probably benign |
0.14 |
R9352:Cntnap5c
|
UTSW |
17 |
58,399,463 (GRCm39) |
missense |
probably benign |
0.01 |
R9485:Cntnap5c
|
UTSW |
17 |
58,409,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R9558:Cntnap5c
|
UTSW |
17 |
58,671,157 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9792:Cntnap5c
|
UTSW |
17 |
58,409,192 (GRCm39) |
missense |
probably benign |
0.03 |
R9793:Cntnap5c
|
UTSW |
17 |
58,409,192 (GRCm39) |
missense |
probably benign |
0.03 |
R9795:Cntnap5c
|
UTSW |
17 |
58,409,192 (GRCm39) |
missense |
probably benign |
0.03 |
RF010:Cntnap5c
|
UTSW |
17 |
58,593,790 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TTCCAAGCTGCTCAAGCTAAGACTC -3'
(R):5'- AGTTGATACCTCATCAGGGACCCAG -3'
Sequencing Primer
(F):5'- TGCTCAAGCTAAGACTCCATTC -3'
(R):5'- CAATTCCAGACCTTAGAGCGGG -3'
|
Posted On |
2014-05-23 |