Incidental Mutation 'R1789:Cntnap5c'
ID |
201679 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cntnap5c
|
Ensembl Gene |
ENSMUSG00000038048 |
Gene Name |
contactin associated protein-like 5C |
Synonyms |
|
MMRRC Submission |
039820-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.060)
|
Stock # |
R1789 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
17 |
Chromosomal Location |
58076565-58717350 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 58320916 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glycine to Arginine
at position 163
(G163R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000075416
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000076038]
|
AlphaFold |
Q0V8T7 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000076038
AA Change: G163R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000075416 Gene: ENSMUSG00000038048 AA Change: G163R
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: 97.4%
- 3x: 96.8%
- 10x: 95.2%
- 20x: 92.1%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
G |
A |
16: 20,184,701 (GRCm39) |
P986L |
probably damaging |
Het |
Acad10 |
A |
T |
5: 121,769,456 (GRCm39) |
Y667N |
possibly damaging |
Het |
Ahi1 |
G |
A |
10: 20,839,014 (GRCm39) |
G121D |
probably benign |
Het |
Ampd1 |
T |
A |
3: 103,006,442 (GRCm39) |
I690N |
possibly damaging |
Het |
Amy1 |
C |
A |
3: 113,351,814 (GRCm39) |
W425L |
possibly damaging |
Het |
Arhgap27 |
A |
T |
11: 103,223,831 (GRCm39) |
V823E |
probably damaging |
Het |
Arhgef17 |
A |
G |
7: 100,579,077 (GRCm39) |
S624P |
probably damaging |
Het |
Arid5b |
T |
C |
10: 68,021,897 (GRCm39) |
H231R |
probably damaging |
Het |
Aspscr1 |
C |
A |
11: 120,579,386 (GRCm39) |
T78N |
probably damaging |
Het |
Auts2 |
T |
A |
5: 131,501,288 (GRCm39) |
T42S |
probably damaging |
Het |
Ccdc171 |
A |
G |
4: 83,473,045 (GRCm39) |
D158G |
probably damaging |
Het |
Ces4a |
G |
A |
8: 105,864,729 (GRCm39) |
G69S |
probably damaging |
Het |
Cfap61 |
T |
C |
2: 145,781,913 (GRCm39) |
|
probably null |
Het |
Chrna5 |
T |
C |
9: 54,911,935 (GRCm39) |
V245A |
possibly damaging |
Het |
Col5a2 |
A |
G |
1: 45,417,465 (GRCm39) |
|
probably null |
Het |
Col5a2 |
T |
C |
1: 45,433,936 (GRCm39) |
Q759R |
probably damaging |
Het |
Comp |
A |
G |
8: 70,829,796 (GRCm39) |
D340G |
probably benign |
Het |
Cyfip1 |
T |
A |
7: 55,576,143 (GRCm39) |
D1104E |
probably damaging |
Het |
Dnah11 |
A |
T |
12: 118,002,515 (GRCm39) |
S308T |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,270,572 (GRCm39) |
H958R |
probably benign |
Het |
Elp3 |
A |
G |
14: 65,785,368 (GRCm39) |
Y478H |
probably damaging |
Het |
Fam237b |
A |
T |
5: 5,625,652 (GRCm39) |
Q116L |
possibly damaging |
Het |
Fat3 |
T |
C |
9: 16,288,281 (GRCm39) |
Y414C |
probably benign |
Het |
Fbxo10 |
C |
A |
4: 45,046,389 (GRCm39) |
A574S |
probably damaging |
Het |
Fsip2 |
G |
T |
2: 82,807,906 (GRCm39) |
L1408F |
probably benign |
Het |
Fubp3 |
T |
C |
2: 31,501,747 (GRCm39) |
V425A |
possibly damaging |
Het |
Gm7168 |
A |
T |
17: 14,169,846 (GRCm39) |
R404S |
probably benign |
Het |
Gpd1 |
T |
G |
15: 99,621,083 (GRCm39) |
F299C |
probably damaging |
Het |
Gpr137 |
C |
T |
19: 6,919,425 (GRCm39) |
|
probably benign |
Het |
Grin3b |
T |
C |
10: 79,809,242 (GRCm39) |
S331P |
probably benign |
Het |
Grk3 |
T |
A |
5: 113,089,584 (GRCm39) |
I281F |
probably damaging |
Het |
Hoxb7 |
T |
A |
11: 96,177,607 (GRCm39) |
S18R |
probably damaging |
Het |
Igf1r |
C |
T |
7: 67,864,681 (GRCm39) |
R1160* |
probably null |
Het |
Itfg1 |
A |
G |
8: 86,452,141 (GRCm39) |
|
probably null |
Het |
Itgb8 |
T |
C |
12: 119,166,190 (GRCm39) |
I114V |
probably benign |
Het |
Kcnk1 |
A |
G |
8: 126,752,123 (GRCm39) |
E243G |
possibly damaging |
Het |
Kif27 |
A |
G |
13: 58,491,822 (GRCm39) |
L439P |
probably damaging |
Het |
Kif2c |
T |
A |
4: 117,024,558 (GRCm39) |
Q279L |
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,749,955 (GRCm39) |
|
probably benign |
Het |
L3mbtl1 |
A |
G |
2: 162,816,422 (GRCm39) |
T821A |
probably benign |
Het |
Lrrc24 |
A |
T |
15: 76,606,778 (GRCm39) |
M206K |
probably benign |
Het |
Mamdc4 |
T |
G |
2: 25,457,634 (GRCm39) |
K460Q |
possibly damaging |
Het |
Maml2 |
C |
G |
9: 13,608,641 (GRCm39) |
L30V |
probably damaging |
Het |
Mc5r |
C |
G |
18: 68,471,741 (GRCm39) |
|
probably null |
Het |
Myo10 |
T |
G |
15: 25,726,611 (GRCm39) |
|
probably null |
Het |
Myo1e |
T |
A |
9: 70,246,066 (GRCm39) |
L419Q |
probably damaging |
Het |
Myo6 |
C |
A |
9: 80,207,854 (GRCm39) |
H1115Q |
probably damaging |
Het |
Myo7a |
A |
G |
7: 97,756,302 (GRCm39) |
V10A |
probably damaging |
Het |
Myoz2 |
C |
T |
3: 122,819,776 (GRCm39) |
R61H |
probably damaging |
Het |
Ncdn |
G |
A |
4: 126,645,796 (GRCm39) |
R38C |
probably damaging |
Het |
Nckap1 |
T |
A |
2: 80,350,900 (GRCm39) |
T736S |
probably benign |
Het |
Ncor2 |
G |
A |
5: 125,096,954 (GRCm39) |
A2325V |
probably damaging |
Het |
Nid2 |
T |
A |
14: 19,802,499 (GRCm39) |
V140E |
possibly damaging |
Het |
Nlrp9c |
C |
A |
7: 26,079,915 (GRCm39) |
D704Y |
probably benign |
Het |
Notch3 |
T |
A |
17: 32,377,699 (GRCm39) |
S126C |
probably damaging |
Het |
Or2g7 |
T |
C |
17: 38,378,839 (GRCm39) |
I259T |
probably damaging |
Het |
Or5p60 |
A |
G |
7: 107,724,122 (GRCm39) |
F116S |
probably benign |
Het |
Or5w10 |
A |
T |
2: 87,375,327 (GRCm39) |
L187H |
probably damaging |
Het |
Or6c219 |
A |
T |
10: 129,781,451 (GRCm39) |
L160* |
probably null |
Het |
Or6c6c |
T |
C |
10: 129,541,476 (GRCm39) |
M243T |
possibly damaging |
Het |
Or6d15 |
A |
C |
6: 116,559,658 (GRCm39) |
F83C |
probably damaging |
Het |
Pdzd7 |
A |
G |
19: 45,027,667 (GRCm39) |
I269T |
probably damaging |
Het |
Phf3 |
A |
T |
1: 30,845,287 (GRCm39) |
D1299E |
probably damaging |
Het |
Pitx2 |
T |
A |
3: 129,012,403 (GRCm39) |
Y271N |
probably damaging |
Het |
Polk |
T |
C |
13: 96,633,140 (GRCm39) |
E301G |
probably damaging |
Het |
Prkdc |
C |
A |
16: 15,557,388 (GRCm39) |
N2230K |
probably damaging |
Het |
Prlr |
A |
G |
15: 10,322,622 (GRCm39) |
E170G |
probably benign |
Het |
Prss55 |
A |
G |
14: 64,313,179 (GRCm39) |
I235T |
probably damaging |
Het |
Psd3 |
T |
C |
8: 68,413,217 (GRCm39) |
I724V |
probably benign |
Het |
Rabep2 |
A |
G |
7: 126,037,971 (GRCm39) |
T248A |
possibly damaging |
Het |
Rbm26 |
T |
A |
14: 105,354,509 (GRCm39) |
K949N |
probably benign |
Het |
Rnf213 |
T |
A |
11: 119,331,047 (GRCm39) |
D2085E |
probably damaging |
Het |
Serpinb7 |
A |
T |
1: 107,378,003 (GRCm39) |
H232L |
possibly damaging |
Het |
Slu7 |
A |
G |
11: 43,336,069 (GRCm39) |
Q484R |
probably benign |
Het |
Smg1 |
A |
G |
7: 117,745,021 (GRCm39) |
S3044P |
possibly damaging |
Het |
Snrnp48 |
A |
G |
13: 38,405,336 (GRCm39) |
D248G |
possibly damaging |
Het |
Snrpc |
C |
A |
17: 28,064,193 (GRCm39) |
P66Q |
unknown |
Het |
Snrpn |
T |
A |
7: 59,633,207 (GRCm39) |
|
probably benign |
Het |
Spag17 |
T |
A |
3: 99,846,672 (GRCm39) |
S65R |
possibly damaging |
Het |
Srsf6 |
C |
A |
2: 162,776,408 (GRCm39) |
|
probably benign |
Het |
Stil |
T |
A |
4: 114,898,979 (GRCm39) |
M1203K |
probably benign |
Het |
Syt17 |
T |
C |
7: 118,036,061 (GRCm39) |
T106A |
probably benign |
Het |
Tbx15 |
C |
T |
3: 99,259,562 (GRCm39) |
Q478* |
probably null |
Het |
Tg |
A |
T |
15: 66,609,397 (GRCm39) |
Q319L |
probably benign |
Het |
Thada |
A |
G |
17: 84,755,461 (GRCm39) |
L243P |
probably damaging |
Het |
Thada |
G |
T |
17: 84,755,462 (GRCm39) |
L243I |
probably damaging |
Het |
Tnnt3 |
A |
G |
7: 142,066,101 (GRCm39) |
R211G |
probably damaging |
Het |
Togaram1 |
A |
T |
12: 65,049,409 (GRCm39) |
Q1282L |
possibly damaging |
Het |
Tpm3-rs7 |
T |
G |
14: 113,552,379 (GRCm39) |
M91R |
probably damaging |
Het |
Trappc9 |
G |
A |
15: 72,897,816 (GRCm39) |
R377W |
probably damaging |
Het |
Ttll7 |
T |
G |
3: 146,621,535 (GRCm39) |
L378R |
probably damaging |
Het |
Tyw1 |
T |
G |
5: 130,287,834 (GRCm39) |
I22R |
probably damaging |
Het |
Ubr3 |
T |
C |
2: 69,846,711 (GRCm39) |
S1645P |
possibly damaging |
Het |
Ubr4 |
T |
C |
4: 139,120,364 (GRCm39) |
L263P |
probably damaging |
Het |
Unc13c |
T |
C |
9: 73,663,621 (GRCm39) |
E1071G |
possibly damaging |
Het |
Vmn2r44 |
G |
T |
7: 8,383,122 (GRCm39) |
D157E |
possibly damaging |
Het |
Vps16 |
C |
T |
2: 130,285,520 (GRCm39) |
T821I |
probably benign |
Het |
Washc4 |
T |
C |
10: 83,415,389 (GRCm39) |
V793A |
possibly damaging |
Het |
Wdr35 |
G |
T |
12: 9,027,435 (GRCm39) |
|
probably null |
Het |
Zfp277 |
A |
G |
12: 40,414,084 (GRCm39) |
F254L |
probably benign |
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 |
R1758:Cntnap5c
|
UTSW |
17 |
58,349,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Cntnap5c
|
UTSW |
17 |
58,469,286 (GRCm39) |
missense |
probably benign |
0.00 |
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'- GTGGATAAGCATGCATACTTGTGA -3'
(R):5'- TTCTCAGCTGAGGTACACATTTTC -3'
Sequencing Primer
(F):5'- GCATGCATACTTGTGATTATATGGC -3'
(R):5'- ATGACCAGACCTTTGTGGATCACTG -3'
|
Posted On |
2014-06-23 |