Incidental Mutation 'R2073:Cntnap5c'
| ID |
227377 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cntnap5c
|
| Ensembl Gene |
ENSMUSG00000038048 |
| Gene Name |
contactin associated protein-like 5C |
| Synonyms |
|
| MMRRC Submission |
040078-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.060)
|
| Stock # |
R2073 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
17 |
| Chromosomal Location |
58076565-58717350 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 58612547 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Proline
at position 862
(L862P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000075416
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000076038]
|
| AlphaFold |
Q0V8T7 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000076038
AA Change: L862P
PolyPhen 2
Score 0.577 (Sensitivity: 0.88; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000075416
Gene: ENSMUSG00000038048
AA Change: L862P
| 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: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.2%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 86 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310057M21Rik |
T |
C |
7: 130,959,242 (GRCm39) |
R153G |
probably benign |
Het |
| 5730596B20Rik |
C |
A |
6: 52,155,962 (GRCm39) |
Y9* |
probably null |
Het |
| Aco1 |
G |
A |
4: 40,183,605 (GRCm39) |
G508S |
probably damaging |
Het |
| Acot3 |
A |
G |
12: 84,100,230 (GRCm39) |
H2R |
possibly damaging |
Het |
| Adamts13 |
T |
A |
2: 26,896,326 (GRCm39) |
C1240S |
probably damaging |
Het |
| Adra1b |
T |
C |
11: 43,726,698 (GRCm39) |
N73S |
probably damaging |
Het |
| Aebp2 |
G |
A |
6: 140,579,420 (GRCm39) |
S219N |
probably benign |
Het |
| Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
| Ank |
T |
C |
15: 27,565,108 (GRCm39) |
S270P |
probably benign |
Het |
| Ankle1 |
G |
A |
8: 71,861,973 (GRCm39) |
R492H |
possibly damaging |
Het |
| Ankub1 |
G |
A |
3: 57,599,713 (GRCm39) |
H19Y |
possibly damaging |
Het |
| Anln |
C |
A |
9: 22,244,464 (GRCm39) |
W1083L |
probably benign |
Het |
| Apaf1 |
G |
T |
10: 90,867,556 (GRCm39) |
S763* |
probably null |
Het |
| Apba3 |
A |
G |
10: 81,105,128 (GRCm39) |
T134A |
probably benign |
Het |
| Armh3 |
A |
T |
19: 45,953,820 (GRCm39) |
I188K |
probably damaging |
Het |
| Bod1l |
C |
T |
5: 41,976,532 (GRCm39) |
S1594N |
probably benign |
Het |
| C7 |
T |
C |
15: 5,019,910 (GRCm39) |
M746V |
probably benign |
Het |
| Cdkn2a |
T |
A |
4: 89,212,730 (GRCm39) |
I11F |
possibly damaging |
Het |
| Cideb |
T |
C |
14: 55,992,617 (GRCm39) |
M100V |
possibly damaging |
Het |
| Coch |
A |
T |
12: 51,649,472 (GRCm39) |
D261V |
probably benign |
Het |
| Cyp2ab1 |
A |
G |
16: 20,132,639 (GRCm39) |
F220L |
possibly damaging |
Het |
| Ddx10 |
A |
T |
9: 53,151,805 (GRCm39) |
D73E |
probably benign |
Het |
| Dgkg |
A |
G |
16: 22,384,067 (GRCm39) |
F462S |
probably damaging |
Het |
| Dlgap3 |
C |
T |
4: 127,089,159 (GRCm39) |
H252Y |
probably damaging |
Het |
| Dmd |
G |
C |
X: 83,356,089 (GRCm39) |
A2257P |
probably benign |
Het |
| Dnaaf6rt |
A |
G |
1: 31,262,077 (GRCm39) |
S20G |
probably benign |
Het |
| Dnai4 |
G |
A |
4: 102,907,390 (GRCm39) |
T632M |
probably damaging |
Het |
| Dtnb |
A |
G |
12: 3,831,273 (GRCm39) |
T658A |
probably benign |
Het |
| Duox2 |
T |
A |
2: 122,125,639 (GRCm39) |
S323C |
probably damaging |
Het |
| Dync1h1 |
T |
A |
12: 110,581,026 (GRCm39) |
I251N |
probably damaging |
Het |
| Eml5 |
A |
G |
12: 98,768,705 (GRCm39) |
S1457P |
probably damaging |
Het |
| Fam114a1 |
T |
A |
5: 65,153,247 (GRCm39) |
|
probably null |
Het |
| Fcho1 |
A |
T |
8: 72,163,133 (GRCm39) |
L632Q |
probably damaging |
Het |
| Gm12695 |
T |
C |
4: 96,612,182 (GRCm39) |
Y527C |
possibly damaging |
Het |
| Gm16223 |
T |
C |
5: 42,371,942 (GRCm39) |
C111R |
unknown |
Het |
| H2-Q4 |
T |
A |
17: 35,599,378 (GRCm39) |
S154T |
possibly damaging |
Het |
| Hhat |
A |
G |
1: 192,409,687 (GRCm39) |
F125L |
possibly damaging |
Het |
| Ier5l |
T |
A |
2: 30,363,068 (GRCm39) |
D319V |
probably damaging |
Het |
| Kif5a |
T |
C |
10: 127,081,238 (GRCm39) |
D232G |
probably damaging |
Het |
| M1ap |
A |
G |
6: 82,958,863 (GRCm39) |
I165V |
probably benign |
Het |
| Map2k4 |
A |
C |
11: 65,584,282 (GRCm39) |
F334V |
probably damaging |
Het |
| Mmp19 |
G |
A |
10: 128,630,848 (GRCm39) |
R156H |
probably damaging |
Het |
| Mpped2 |
T |
A |
2: 106,575,147 (GRCm39) |
Y77* |
probably null |
Het |
| Nhs |
T |
A |
X: 160,625,717 (GRCm39) |
H544L |
probably damaging |
Het |
| Nr4a1 |
C |
A |
15: 101,171,948 (GRCm39) |
H541N |
probably damaging |
Het |
| Or4a74 |
A |
G |
2: 89,439,822 (GRCm39) |
V208A |
probably benign |
Het |
| Or5b122 |
A |
T |
19: 13,562,965 (GRCm39) |
Q99L |
probably damaging |
Het |
| Pak6 |
A |
C |
2: 118,519,332 (GRCm39) |
N17T |
probably damaging |
Het |
| Pcnt |
T |
A |
10: 76,216,214 (GRCm39) |
T2225S |
possibly damaging |
Het |
| Pdzd2 |
A |
G |
15: 12,385,905 (GRCm39) |
L955P |
probably damaging |
Het |
| Phf21a |
A |
G |
2: 92,178,381 (GRCm39) |
D357G |
probably damaging |
Het |
| Pkhd1l1 |
G |
T |
15: 44,422,035 (GRCm39) |
A3102S |
probably damaging |
Het |
| Plch2 |
A |
T |
4: 155,074,366 (GRCm39) |
L754Q |
probably damaging |
Het |
| Plekhd1 |
A |
G |
12: 80,768,066 (GRCm39) |
N335D |
probably benign |
Het |
| Pole |
C |
A |
5: 110,473,417 (GRCm39) |
T1737N |
probably damaging |
Het |
| Potefam1 |
T |
C |
2: 111,030,763 (GRCm39) |
E382G |
probably damaging |
Het |
| Pramel6 |
G |
A |
2: 87,339,088 (GRCm39) |
S96N |
probably damaging |
Het |
| Prdm14 |
A |
C |
1: 13,195,954 (GRCm39) |
Y36D |
possibly damaging |
Het |
| Psg27 |
T |
C |
7: 18,294,342 (GRCm39) |
D355G |
probably damaging |
Het |
| Rfc1 |
A |
T |
5: 65,459,282 (GRCm39) |
D225E |
probably damaging |
Het |
| Sec16a |
A |
G |
2: 26,330,251 (GRCm39) |
I588T |
probably damaging |
Het |
| Setd6 |
G |
A |
8: 96,443,416 (GRCm39) |
V60M |
probably damaging |
Het |
| Sgk3 |
A |
G |
1: 9,961,649 (GRCm39) |
I432V |
probably benign |
Het |
| Six2 |
A |
G |
17: 85,994,933 (GRCm39) |
S150P |
probably damaging |
Het |
| Slc1a6 |
T |
C |
10: 78,635,964 (GRCm39) |
V343A |
possibly damaging |
Het |
| Slc43a3 |
T |
C |
2: 84,774,956 (GRCm39) |
|
probably null |
Het |
| Smc3 |
A |
G |
19: 53,619,964 (GRCm39) |
D620G |
probably benign |
Het |
| Smg6 |
C |
G |
11: 74,821,120 (GRCm39) |
P464A |
probably damaging |
Het |
| Sox11 |
T |
C |
12: 27,392,278 (GRCm39) |
T44A |
possibly damaging |
Het |
| Spata22 |
A |
G |
11: 73,227,052 (GRCm39) |
R89G |
possibly damaging |
Het |
| Spmip6 |
A |
G |
4: 41,507,519 (GRCm39) |
|
probably null |
Het |
| Stk3 |
T |
C |
15: 34,959,195 (GRCm39) |
M256V |
possibly damaging |
Het |
| Syne2 |
A |
G |
12: 76,062,353 (GRCm39) |
D4226G |
possibly damaging |
Het |
| Tecpr2 |
T |
C |
12: 110,934,863 (GRCm39) |
S1370P |
possibly damaging |
Het |
| Tek |
A |
G |
4: 94,715,966 (GRCm39) |
I463V |
probably benign |
Het |
| Trib1 |
T |
A |
15: 59,526,189 (GRCm39) |
I253N |
probably damaging |
Het |
| Triobp |
G |
T |
15: 78,858,095 (GRCm39) |
G1232V |
probably damaging |
Het |
| Trpm6 |
G |
A |
19: 18,853,406 (GRCm39) |
V1809M |
probably damaging |
Het |
| Tsc22d4 |
A |
G |
5: 137,760,749 (GRCm39) |
K57E |
possibly damaging |
Het |
| Vmn2r109 |
T |
A |
17: 20,784,974 (GRCm39) |
K15N |
probably benign |
Het |
| Wnt9a |
A |
G |
11: 59,222,055 (GRCm39) |
N318D |
probably damaging |
Het |
| Wwp1 |
A |
G |
4: 19,662,181 (GRCm39) |
V138A |
possibly damaging |
Het |
| Zfp37 |
A |
T |
4: 62,109,945 (GRCm39) |
M411K |
probably damaging |
Het |
| Zfp715 |
T |
A |
7: 42,960,544 (GRCm39) |
T16S |
probably benign |
Het |
| Zfp932 |
A |
G |
5: 110,157,684 (GRCm39) |
T461A |
possibly damaging |
Het |
| Zscan29 |
A |
T |
2: 120,991,336 (GRCm39) |
C817* |
probably null |
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 |
|
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 |
|
|
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'- GTTCAGAAATGTCCTCTCCACATTG -3'
(R):5'- TGAGCTAGAGCACTCTTGTAGG -3'
Sequencing Primer
(F):5'- GAAATGTCCTCTCCACATTGATGGAG -3'
(R):5'- GCTAGAGCACTCTTGTAGGTATTTAG -3'
|
| Posted On |
2014-09-17 |
Incidental Mutation