Incidental Mutation 'R7422:Cntnap5c'
| ID |
575787 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cntnap5c
|
| Ensembl Gene |
ENSMUSG00000038048 |
| Gene Name |
contactin associated protein-like 5C |
| Synonyms |
|
| MMRRC Submission |
045500-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.060)
|
| Stock # |
R7422 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
17 |
| Chromosomal Location |
58076565-58717350 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
T to A
at 58717226 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Stop codon
at position 1269
(Y1269*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000075416
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000076038]
|
| AlphaFold |
Q0V8T7 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000076038
AA Change: Y1269*
|
| SMART Domains |
Protein: ENSMUSP00000075416
Gene: ENSMUSG00000038048
AA Change: Y1269*
| 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: 100.0%
- 3x: 99.9%
- 10x: 99.1%
- 20x: 96.9%
|
| Validation Efficiency |
97% (98/101) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 99 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2810021J22Rik |
T |
A |
11: 58,771,885 (GRCm39) |
C456S |
probably damaging |
Het |
| 4930524J08Rik |
T |
C |
5: 100,127,068 (GRCm39) |
|
probably benign |
Het |
| Adam28 |
T |
G |
14: 68,864,326 (GRCm39) |
R492S |
probably damaging |
Het |
| Adarb2 |
G |
A |
13: 8,807,313 (GRCm39) |
A705T |
possibly damaging |
Het |
| Adprhl1 |
T |
C |
8: 13,272,873 (GRCm39) |
D1295G |
probably benign |
Het |
| Aldh3b3 |
A |
G |
19: 4,016,476 (GRCm39) |
I365V |
probably benign |
Het |
| Aldh8a1 |
T |
C |
10: 21,264,996 (GRCm39) |
F208L |
possibly damaging |
Het |
| Ap3b1 |
G |
A |
13: 94,664,673 (GRCm39) |
V871I |
unknown |
Het |
| Apol7e |
A |
T |
15: 77,598,552 (GRCm39) |
R6* |
probably null |
Het |
| Arfgap3 |
T |
C |
15: 83,191,150 (GRCm39) |
E456G |
probably damaging |
Het |
| Arhgef1 |
T |
C |
7: 24,615,461 (GRCm39) |
L285P |
probably benign |
Het |
| Arhgef7 |
T |
A |
8: 11,850,861 (GRCm39) |
C315S |
probably benign |
Het |
| Atp9a |
A |
T |
2: 168,490,513 (GRCm39) |
L829Q |
probably damaging |
Het |
| Babam2 |
T |
A |
5: 31,888,393 (GRCm39) |
|
probably null |
Het |
| Bptf |
C |
T |
11: 106,951,384 (GRCm39) |
R2185H |
probably damaging |
Het |
| Brd9 |
A |
C |
13: 74,102,697 (GRCm39) |
M473L |
probably benign |
Het |
| C7 |
T |
C |
15: 5,041,538 (GRCm39) |
H456R |
probably benign |
Het |
| Cabp7 |
C |
A |
11: 4,688,856 (GRCm39) |
A205S |
probably damaging |
Het |
| Catsperb |
A |
G |
12: 101,554,293 (GRCm39) |
I662M |
probably damaging |
Het |
| Ccl21a |
T |
C |
4: 42,773,906 (GRCm39) |
M5V |
probably benign |
Het |
| Cdyl |
G |
T |
13: 36,042,177 (GRCm39) |
R405L |
possibly damaging |
Het |
| Cep89 |
T |
C |
7: 35,127,672 (GRCm39) |
L538P |
probably damaging |
Het |
| Cercam |
A |
G |
2: 29,762,892 (GRCm39) |
M209V |
possibly damaging |
Het |
| Chfr |
T |
A |
5: 110,310,571 (GRCm39) |
|
probably null |
Het |
| Col6a2 |
G |
T |
10: 76,439,170 (GRCm39) |
C833* |
probably null |
Het |
| Cpeb3 |
T |
A |
19: 37,151,900 (GRCm39) |
I159F |
probably benign |
Het |
| Cplx2 |
G |
A |
13: 54,526,663 (GRCm39) |
E24K |
possibly damaging |
Het |
| Ctsb |
A |
G |
14: 63,379,752 (GRCm39) |
T332A |
probably benign |
Het |
| Cyp2j12 |
T |
A |
4: 96,029,222 (GRCm39) |
T20S |
probably benign |
Het |
| Dcst2 |
T |
A |
3: 89,273,993 (GRCm39) |
H181Q |
probably damaging |
Het |
| Dnm1l |
T |
C |
16: 16,136,338 (GRCm39) |
I411V |
probably benign |
Het |
| Dock5 |
T |
A |
14: 68,046,479 (GRCm39) |
I768F |
probably benign |
Het |
| Ecel1 |
A |
G |
1: 87,077,334 (GRCm39) |
Y625H |
probably damaging |
Het |
| Efl1 |
T |
G |
7: 82,330,587 (GRCm39) |
S253R |
probably damaging |
Het |
| Elmod1 |
T |
A |
9: 53,820,127 (GRCm39) |
D287V |
probably damaging |
Het |
| Fam171a2 |
T |
C |
11: 102,329,491 (GRCm39) |
S423G |
probably benign |
Het |
| Fbxo8 |
A |
T |
8: 57,022,317 (GRCm39) |
|
probably null |
Het |
| Flnc |
G |
T |
6: 29,455,470 (GRCm39) |
G2040W |
probably damaging |
Het |
| Fras1 |
C |
T |
5: 96,821,458 (GRCm39) |
A1405V |
probably benign |
Het |
| Frem3 |
A |
C |
8: 81,342,392 (GRCm39) |
I1562L |
probably benign |
Het |
| Fxr1 |
C |
T |
3: 34,103,369 (GRCm39) |
A233V |
probably damaging |
Het |
| H1f9 |
A |
G |
11: 94,859,184 (GRCm39) |
R160G |
possibly damaging |
Het |
| Helb |
A |
G |
10: 119,944,799 (GRCm39) |
F246L |
probably damaging |
Het |
| Hoxb6 |
G |
T |
11: 96,183,510 (GRCm39) |
|
probably benign |
Het |
| Hspa2 |
A |
G |
12: 76,452,884 (GRCm39) |
E526G |
probably damaging |
Het |
| Hyal5 |
A |
T |
6: 24,875,983 (GRCm39) |
|
probably benign |
Het |
| Ints6 |
A |
T |
14: 62,942,224 (GRCm39) |
V503E |
probably benign |
Het |
| Ints9 |
C |
T |
14: 65,269,747 (GRCm39) |
T479I |
possibly damaging |
Het |
| Jag1 |
C |
T |
2: 136,926,975 (GRCm39) |
R928H |
probably benign |
Het |
| Lman2 |
A |
T |
13: 55,499,338 (GRCm39) |
I179N |
probably damaging |
Het |
| Lta |
T |
C |
17: 35,422,805 (GRCm39) |
S173G |
probably benign |
Het |
| Mki67 |
G |
A |
7: 135,300,099 (GRCm39) |
P1645L |
probably damaging |
Het |
| Mrc2 |
A |
T |
11: 105,183,609 (GRCm39) |
|
probably benign |
Het |
| Muc4 |
T |
A |
16: 32,754,689 (GRCm38) |
M1521K |
probably benign |
Het |
| Mucl3 |
T |
A |
17: 35,949,312 (GRCm39) |
T96S |
probably benign |
Het |
| Mylk3 |
T |
G |
8: 86,081,873 (GRCm39) |
D438A |
probably benign |
Het |
| Myo7a |
T |
A |
7: 97,700,833 (GRCm39) |
|
probably null |
Het |
| Nsmce4a |
G |
T |
7: 130,135,547 (GRCm39) |
Q342K |
probably benign |
Het |
| Or10ac1 |
A |
G |
6: 42,515,053 (GRCm39) |
I301T |
possibly damaging |
Het |
| Or4c124 |
T |
A |
2: 89,156,423 (GRCm39) |
I34F |
probably benign |
Het |
| Or5p60 |
A |
G |
7: 107,724,068 (GRCm39) |
L134P |
probably damaging |
Het |
| Or6c65 |
A |
T |
10: 129,604,136 (GRCm39) |
Y257F |
possibly damaging |
Het |
| Osbpl6 |
T |
A |
2: 76,423,730 (GRCm39) |
F864L |
probably damaging |
Het |
| Pla2g4a |
A |
G |
1: 149,808,438 (GRCm39) |
S2P |
probably benign |
Het |
| Plce1 |
T |
C |
19: 38,640,329 (GRCm39) |
L525P |
probably damaging |
Het |
| Por |
A |
T |
5: 135,763,773 (GRCm39) |
M667L |
probably benign |
Het |
| Psma4 |
T |
C |
9: 54,862,166 (GRCm39) |
Y97H |
probably benign |
Het |
| Qtrt1 |
A |
T |
9: 21,323,753 (GRCm39) |
H126L |
probably benign |
Het |
| Rab3a |
A |
T |
8: 71,209,170 (GRCm39) |
Y102F |
possibly damaging |
Het |
| Rnf212 |
T |
A |
5: 108,879,555 (GRCm39) |
H87L |
probably benign |
Het |
| Rnf216 |
A |
G |
5: 143,076,591 (GRCm39) |
S98P |
probably benign |
Het |
| Ryr1 |
G |
T |
7: 28,785,295 (GRCm39) |
R1806S |
probably benign |
Het |
| Scgb1b3 |
A |
T |
7: 31,075,262 (GRCm39) |
L37F |
probably benign |
Het |
| Sds |
T |
C |
5: 120,617,254 (GRCm39) |
S37P |
probably damaging |
Het |
| Senp6 |
A |
G |
9: 80,021,159 (GRCm39) |
R280G |
probably damaging |
Het |
| She |
T |
A |
3: 89,761,864 (GRCm39) |
I441K |
possibly damaging |
Het |
| Slc6a20b |
A |
G |
9: 123,436,682 (GRCm39) |
S244P |
possibly damaging |
Het |
| Slc9a3 |
A |
T |
13: 74,299,004 (GRCm39) |
Y141F |
probably damaging |
Het |
| Slco6c1 |
A |
T |
1: 97,009,207 (GRCm39) |
H426Q |
probably benign |
Het |
| Smc2 |
C |
A |
4: 52,440,301 (GRCm39) |
Q16K |
probably benign |
Het |
| Sphkap |
A |
C |
1: 83,241,547 (GRCm39) |
V1535G |
probably benign |
Het |
| Stard9 |
C |
A |
2: 120,532,633 (GRCm39) |
N2963K |
probably benign |
Het |
| Sycp2 |
C |
T |
2: 178,035,944 (GRCm39) |
A248T |
probably damaging |
Het |
| Taar8a |
T |
C |
10: 23,952,762 (GRCm39) |
L122P |
probably damaging |
Het |
| Tab1 |
T |
A |
15: 80,044,445 (GRCm39) |
V491E |
probably benign |
Het |
| Tanc1 |
T |
C |
2: 59,636,688 (GRCm39) |
M857T |
probably benign |
Het |
| Tcirg1 |
C |
A |
19: 3,949,008 (GRCm39) |
R427L |
possibly damaging |
Het |
| Tmem109 |
A |
C |
19: 10,849,124 (GRCm39) |
*244G |
probably null |
Het |
| Tox2 |
A |
G |
2: 163,163,435 (GRCm39) |
Y136C |
|
Het |
| Tubb1 |
T |
C |
2: 174,298,825 (GRCm39) |
V169A |
possibly damaging |
Het |
| Ubr3 |
T |
C |
2: 69,783,886 (GRCm39) |
|
probably null |
Het |
| Vmn1r225 |
T |
A |
17: 20,723,059 (GRCm39) |
F167I |
probably benign |
Het |
| Vmn2r65 |
A |
C |
7: 84,595,569 (GRCm39) |
W372G |
probably damaging |
Het |
| Vps13a |
A |
T |
19: 16,727,537 (GRCm39) |
D188E |
probably damaging |
Het |
| Vsnl1 |
G |
T |
12: 11,376,439 (GRCm39) |
Q149K |
probably benign |
Het |
| Wdr35 |
A |
G |
12: 9,054,105 (GRCm39) |
N466S |
probably benign |
Het |
| Ywhae |
T |
A |
11: 75,650,169 (GRCm39) |
S210R |
probably damaging |
Het |
| Zfp28 |
T |
A |
7: 6,397,748 (GRCm39) |
S728T |
probably damaging |
Het |
| Zfpm1 |
A |
G |
8: 123,063,698 (GRCm39) |
D919G |
unknown |
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 |
|
|
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 |
|
|
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'- TGAAGTCAAGGAGTTCTGAGC -3'
(R):5'- TGTGTTCCAGAAAATGAATGGC -3'
Sequencing Primer
(F):5'- TCTGGATAGAGAGTAGAATTGTGC -3'
(R):5'- AAGTCTTCCTGCTTGCAC -3'
|
| Posted On |
2019-10-07 |
Incidental Mutation