Incidental Mutation 'R1542:Ccdc18'
| ID |
171805 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ccdc18
|
| Ensembl Gene |
ENSMUSG00000056531 |
| Gene Name |
coiled-coil domain containing 18 |
| Synonyms |
1700021E15Rik, 4932411G06Rik |
| MMRRC Submission |
039581-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R1542 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
5 |
| Chromosomal Location |
108280741-108381494 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 108360054 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Serine
at position 1146
(N1146S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000036507
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047677]
|
| AlphaFold |
Q640L5 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000047677
AA Change: N1146S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000036507
Gene: ENSMUSG00000056531
AA Change: N1146S
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
109 |
140 |
N/A |
INTRINSIC |
|
coiled coil region
|
168 |
320 |
N/A |
INTRINSIC |
|
coiled coil region
|
344 |
405 |
N/A |
INTRINSIC |
|
coiled coil region
|
507 |
1307 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000199594
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.3%
- 20x: 92.5%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 92 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700006A11Rik |
A |
G |
3: 124,208,055 (GRCm39) |
M208T |
possibly damaging |
Het |
| Acsbg2 |
T |
A |
17: 57,156,791 (GRCm39) |
I416F |
probably damaging |
Het |
| Adam6b |
G |
A |
12: 113,454,559 (GRCm39) |
D459N |
possibly damaging |
Het |
| Adprh |
A |
T |
16: 38,266,286 (GRCm39) |
D285E |
probably damaging |
Het |
| Aggf1 |
A |
T |
13: 95,507,450 (GRCm39) |
C112S |
probably benign |
Het |
| Als2cl |
T |
C |
9: 110,723,102 (GRCm39) |
V602A |
probably benign |
Het |
| Angptl2 |
G |
T |
2: 33,118,897 (GRCm39) |
V224F |
probably benign |
Het |
| Ap3b2 |
A |
T |
7: 81,127,825 (GRCm39) |
|
probably null |
Het |
| Aqp2 |
A |
C |
15: 99,481,723 (GRCm39) |
I206L |
probably benign |
Het |
| Asap2 |
A |
G |
12: 21,315,998 (GRCm39) |
D930G |
probably damaging |
Het |
| Cacna1e |
T |
A |
1: 154,353,525 (GRCm39) |
M682L |
probably benign |
Het |
| Ccr4 |
G |
A |
9: 114,321,073 (GRCm39) |
H331Y |
probably benign |
Het |
| Cd33 |
A |
G |
7: 43,181,530 (GRCm39) |
L210P |
probably damaging |
Het |
| Cep85l |
T |
C |
10: 53,177,680 (GRCm39) |
E351G |
probably damaging |
Het |
| Cntn6 |
C |
A |
6: 104,825,061 (GRCm39) |
T867K |
probably damaging |
Het |
| Cpeb2 |
C |
T |
5: 43,443,218 (GRCm39) |
R970C |
probably damaging |
Het |
| Cul7 |
T |
A |
17: 46,974,116 (GRCm39) |
L1467H |
probably damaging |
Het |
| Dscaml1 |
T |
A |
9: 45,660,738 (GRCm39) |
I1693K |
possibly damaging |
Het |
| Ebf4 |
A |
T |
2: 130,207,418 (GRCm39) |
M621L |
probably benign |
Het |
| Elp4 |
G |
T |
2: 105,624,954 (GRCm39) |
T313N |
probably benign |
Het |
| Epas1 |
T |
A |
17: 87,131,918 (GRCm39) |
I373N |
possibly damaging |
Het |
| Etnk1 |
A |
T |
6: 143,126,367 (GRCm39) |
M71L |
probably benign |
Het |
| Fry |
C |
T |
5: 150,328,431 (GRCm39) |
T1257I |
probably benign |
Het |
| Gm21834 |
A |
G |
17: 58,048,946 (GRCm39) |
F90S |
possibly damaging |
Het |
| Gm8674 |
T |
A |
13: 50,054,039 (GRCm39) |
|
noncoding transcript |
Het |
| Gna11 |
T |
C |
10: 81,369,162 (GRCm39) |
T134A |
probably benign |
Het |
| Golga5 |
C |
T |
12: 102,440,979 (GRCm39) |
S238F |
probably damaging |
Het |
| Grin2a |
T |
A |
16: 9,397,067 (GRCm39) |
N1007Y |
probably damaging |
Het |
| H3c6 |
A |
G |
13: 23,746,338 (GRCm39) |
F68L |
probably damaging |
Het |
| Ifnar2 |
G |
A |
16: 91,196,153 (GRCm39) |
V253M |
possibly damaging |
Het |
| Insl5 |
A |
T |
4: 102,875,382 (GRCm39) |
S123T |
probably damaging |
Het |
| Itgb2 |
T |
C |
10: 77,395,320 (GRCm39) |
S474P |
probably benign |
Het |
| Kcnb2 |
A |
G |
1: 15,781,012 (GRCm39) |
H628R |
probably benign |
Het |
| L3mbtl2 |
G |
A |
15: 81,566,352 (GRCm39) |
D392N |
probably null |
Het |
| Lrp1b |
G |
T |
2: 41,013,724 (GRCm39) |
T1813K |
probably damaging |
Het |
| Map3k4 |
A |
G |
17: 12,454,793 (GRCm39) |
L1399P |
probably damaging |
Het |
| Mbtps1 |
A |
C |
8: 120,272,986 (GRCm39) |
|
probably null |
Het |
| Mettl25 |
A |
T |
10: 105,661,981 (GRCm39) |
S330T |
probably benign |
Het |
| Mical2 |
T |
C |
7: 111,908,675 (GRCm39) |
L211P |
probably damaging |
Het |
| Mmrn1 |
T |
A |
6: 60,922,102 (GRCm39) |
S186R |
probably damaging |
Het |
| Mob3b |
C |
A |
4: 35,084,046 (GRCm39) |
V48L |
possibly damaging |
Het |
| Napsa |
A |
T |
7: 44,231,113 (GRCm39) |
H114L |
probably damaging |
Het |
| Nsmce4a |
A |
T |
7: 130,147,623 (GRCm39) |
|
probably null |
Het |
| Nup62 |
A |
G |
7: 44,479,353 (GRCm39) |
K456R |
possibly damaging |
Het |
| Nwd2 |
T |
A |
5: 63,964,318 (GRCm39) |
W1301R |
probably damaging |
Het |
| Oprm1 |
G |
T |
10: 6,738,960 (GRCm39) |
W29L |
probably damaging |
Het |
| Or10al2 |
A |
T |
17: 37,983,142 (GRCm39) |
E76V |
probably damaging |
Het |
| Or1l4b |
T |
A |
2: 37,036,978 (GRCm39) |
S251R |
probably damaging |
Het |
| Or2c1 |
T |
A |
16: 3,657,696 (GRCm39) |
N286K |
probably damaging |
Het |
| Or5w17 |
A |
G |
2: 87,583,662 (GRCm39) |
V225A |
probably damaging |
Het |
| Pals2 |
A |
G |
6: 50,175,306 (GRCm39) |
Y539C |
probably damaging |
Het |
| Pcnt |
T |
G |
10: 76,225,221 (GRCm39) |
N1761T |
probably benign |
Het |
| Pcnt |
C |
T |
10: 76,237,220 (GRCm39) |
M1355I |
probably benign |
Het |
| Pde11a |
A |
T |
2: 75,877,199 (GRCm39) |
S757T |
probably benign |
Het |
| Pde6a |
T |
A |
18: 61,390,116 (GRCm39) |
I490N |
possibly damaging |
Het |
| Pgap1 |
A |
G |
1: 54,531,249 (GRCm39) |
V742A |
probably benign |
Het |
| Pik3c2b |
T |
C |
1: 133,017,772 (GRCm39) |
L915P |
probably damaging |
Het |
| Pkd1l1 |
A |
G |
11: 8,824,179 (GRCm39) |
C1129R |
possibly damaging |
Het |
| Pkhd1l1 |
A |
T |
15: 44,391,587 (GRCm39) |
H1551L |
probably benign |
Het |
| Plxnb2 |
C |
T |
15: 89,050,124 (GRCm39) |
C491Y |
probably damaging |
Het |
| Ppt1 |
C |
A |
4: 122,751,402 (GRCm39) |
H300N |
probably benign |
Het |
| Prpf3 |
T |
A |
3: 95,743,782 (GRCm39) |
Q457L |
probably benign |
Het |
| Ranbp17 |
C |
T |
11: 33,214,672 (GRCm39) |
V914I |
probably benign |
Het |
| Rasal2 |
T |
C |
1: 157,003,421 (GRCm39) |
I413V |
possibly damaging |
Het |
| Rb1cc1 |
G |
A |
1: 6,314,473 (GRCm39) |
V382I |
possibly damaging |
Het |
| Rere |
T |
A |
4: 150,700,399 (GRCm39) |
F1125I |
probably damaging |
Het |
| Rprd2 |
A |
T |
3: 95,672,988 (GRCm39) |
V805E |
possibly damaging |
Het |
| Septin10 |
T |
G |
10: 59,002,428 (GRCm39) |
E162A |
probably damaging |
Het |
| Septin12 |
G |
T |
16: 4,810,159 (GRCm39) |
D125E |
probably benign |
Het |
| Serpina6 |
A |
G |
12: 103,620,732 (GRCm39) |
Y6H |
probably benign |
Het |
| Serpinb3c |
T |
C |
1: 107,200,517 (GRCm39) |
M209V |
probably damaging |
Het |
| Slc2a7 |
A |
T |
4: 150,252,928 (GRCm39) |
T523S |
probably damaging |
Het |
| Smdt1 |
T |
C |
15: 82,230,376 (GRCm39) |
V31A |
possibly damaging |
Het |
| Snrnp48 |
T |
C |
13: 38,404,680 (GRCm39) |
I245T |
probably damaging |
Het |
| Spink2 |
G |
A |
5: 77,354,812 (GRCm39) |
T33I |
probably damaging |
Het |
| Sptan1 |
A |
G |
2: 29,917,139 (GRCm39) |
T2204A |
probably damaging |
Het |
| Synj2 |
A |
G |
17: 6,075,292 (GRCm39) |
D306G |
probably benign |
Het |
| Tas2r109 |
A |
G |
6: 132,957,873 (GRCm39) |
I19T |
possibly damaging |
Het |
| Tbk1 |
C |
T |
10: 121,395,840 (GRCm39) |
V418M |
probably benign |
Het |
| Tcerg1 |
A |
G |
18: 42,686,495 (GRCm39) |
E684G |
probably damaging |
Het |
| Tenm2 |
T |
C |
11: 36,191,047 (GRCm39) |
N308S |
probably damaging |
Het |
| Tfb2m |
A |
T |
1: 179,365,426 (GRCm39) |
|
probably null |
Het |
| Tmc1 |
T |
A |
19: 20,793,486 (GRCm39) |
L558F |
probably damaging |
Het |
| Tmprss5 |
T |
A |
9: 49,020,434 (GRCm39) |
I80N |
possibly damaging |
Het |
| Trappc2l |
G |
A |
8: 123,342,146 (GRCm39) |
V131M |
probably damaging |
Het |
| Trpm7 |
A |
C |
2: 126,664,519 (GRCm39) |
Y953* |
probably null |
Het |
| Ttn |
T |
C |
2: 76,583,859 (GRCm39) |
R22383G |
probably damaging |
Het |
| Ugt1a6b |
G |
A |
1: 88,034,983 (GRCm39) |
G107D |
probably benign |
Het |
| Vmn1r197 |
A |
T |
13: 22,512,520 (GRCm39) |
Y147F |
probably benign |
Het |
| Zfp507 |
A |
T |
7: 35,494,226 (GRCm39) |
N272K |
possibly damaging |
Het |
| Zfp526 |
G |
A |
7: 24,925,687 (GRCm39) |
E649K |
probably benign |
Het |
| Zswim6 |
G |
A |
13: 107,863,769 (GRCm39) |
|
noncoding transcript |
Het |
|
| Other mutations in Ccdc18 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00836:Ccdc18
|
APN |
5 |
108,328,391 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01380:Ccdc18
|
APN |
5 |
108,328,753 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL01405:Ccdc18
|
APN |
5 |
108,350,052 (GRCm39) |
splice site |
probably benign |
|
|
IGL01718:Ccdc18
|
APN |
5 |
108,349,214 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
IGL02098:Ccdc18
|
APN |
5 |
108,349,977 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02227:Ccdc18
|
APN |
5 |
108,296,788 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL02391:Ccdc18
|
APN |
5 |
108,283,918 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02794:Ccdc18
|
APN |
5 |
108,319,614 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02808:Ccdc18
|
APN |
5 |
108,283,835 (GRCm39) |
splice site |
probably benign |
|
|
IGL02880:Ccdc18
|
APN |
5 |
108,283,310 (GRCm39) |
missense |
probably benign |
0.31 |
|
IGL03069:Ccdc18
|
APN |
5 |
108,376,767 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03390:Ccdc18
|
APN |
5 |
108,359,997 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4402001:Ccdc18
|
UTSW |
5 |
108,306,485 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0004:Ccdc18
|
UTSW |
5 |
108,309,566 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R0112:Ccdc18
|
UTSW |
5 |
108,321,627 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0295:Ccdc18
|
UTSW |
5 |
108,321,655 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0546:Ccdc18
|
UTSW |
5 |
108,322,830 (GRCm39) |
missense |
probably benign |
0.06 |
|
R0619:Ccdc18
|
UTSW |
5 |
108,328,282 (GRCm39) |
missense |
probably benign |
0.04 |
|
R0648:Ccdc18
|
UTSW |
5 |
108,322,853 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0648:Ccdc18
|
UTSW |
5 |
108,283,426 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0666:Ccdc18
|
UTSW |
5 |
108,311,530 (GRCm39) |
missense |
probably benign |
0.19 |
|
R1271:Ccdc18
|
UTSW |
5 |
108,349,982 (GRCm39) |
nonsense |
probably null |
|
|
R1509:Ccdc18
|
UTSW |
5 |
108,336,844 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R1539:Ccdc18
|
UTSW |
5 |
108,339,843 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1663:Ccdc18
|
UTSW |
5 |
108,363,956 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1865:Ccdc18
|
UTSW |
5 |
108,341,668 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1870:Ccdc18
|
UTSW |
5 |
108,368,703 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R1897:Ccdc18
|
UTSW |
5 |
108,343,908 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1946:Ccdc18
|
UTSW |
5 |
108,376,861 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2420:Ccdc18
|
UTSW |
5 |
108,376,454 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2421:Ccdc18
|
UTSW |
5 |
108,376,454 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2422:Ccdc18
|
UTSW |
5 |
108,376,454 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4078:Ccdc18
|
UTSW |
5 |
108,306,394 (GRCm39) |
nonsense |
probably null |
|
|
R4079:Ccdc18
|
UTSW |
5 |
108,306,394 (GRCm39) |
nonsense |
probably null |
|
|
R4244:Ccdc18
|
UTSW |
5 |
108,296,838 (GRCm39) |
nonsense |
probably null |
|
|
R4409:Ccdc18
|
UTSW |
5 |
108,368,708 (GRCm39) |
nonsense |
probably null |
|
|
R4428:Ccdc18
|
UTSW |
5 |
108,283,943 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4455:Ccdc18
|
UTSW |
5 |
108,309,395 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R4499:Ccdc18
|
UTSW |
5 |
108,376,826 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R4612:Ccdc18
|
UTSW |
5 |
108,283,307 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4907:Ccdc18
|
UTSW |
5 |
108,284,007 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4972:Ccdc18
|
UTSW |
5 |
108,339,869 (GRCm39) |
missense |
probably benign |
|
|
R5039:Ccdc18
|
UTSW |
5 |
108,306,514 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5835:Ccdc18
|
UTSW |
5 |
108,288,740 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5854:Ccdc18
|
UTSW |
5 |
108,354,594 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6128:Ccdc18
|
UTSW |
5 |
108,311,625 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R6229:Ccdc18
|
UTSW |
5 |
108,319,484 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6271:Ccdc18
|
UTSW |
5 |
108,322,753 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R6315:Ccdc18
|
UTSW |
5 |
108,309,448 (GRCm39) |
missense |
probably benign |
|
|
R6359:Ccdc18
|
UTSW |
5 |
108,283,391 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6375:Ccdc18
|
UTSW |
5 |
108,322,820 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6388:Ccdc18
|
UTSW |
5 |
108,349,214 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R6415:Ccdc18
|
UTSW |
5 |
108,309,612 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6560:Ccdc18
|
UTSW |
5 |
108,339,790 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6645:Ccdc18
|
UTSW |
5 |
108,286,796 (GRCm39) |
missense |
probably benign |
|
|
R6664:Ccdc18
|
UTSW |
5 |
108,315,966 (GRCm39) |
nonsense |
probably null |
|
|
R6836:Ccdc18
|
UTSW |
5 |
108,345,833 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6947:Ccdc18
|
UTSW |
5 |
108,309,401 (GRCm39) |
missense |
probably benign |
0.26 |
|
R7009:Ccdc18
|
UTSW |
5 |
108,321,728 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7052:Ccdc18
|
UTSW |
5 |
108,309,554 (GRCm39) |
missense |
probably benign |
0.15 |
|
R7058:Ccdc18
|
UTSW |
5 |
108,341,664 (GRCm39) |
missense |
probably benign |
|
|
R7087:Ccdc18
|
UTSW |
5 |
108,343,988 (GRCm39) |
missense |
probably benign |
|
|
R7117:Ccdc18
|
UTSW |
5 |
108,296,835 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7176:Ccdc18
|
UTSW |
5 |
108,315,972 (GRCm39) |
missense |
probably benign |
|
|
R7382:Ccdc18
|
UTSW |
5 |
108,286,873 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7477:Ccdc18
|
UTSW |
5 |
108,368,716 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7493:Ccdc18
|
UTSW |
5 |
108,354,483 (GRCm39) |
nonsense |
probably null |
|
|
R7506:Ccdc18
|
UTSW |
5 |
108,311,605 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R7635:Ccdc18
|
UTSW |
5 |
108,376,915 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7690:Ccdc18
|
UTSW |
5 |
108,376,528 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7748:Ccdc18
|
UTSW |
5 |
108,296,907 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7812:Ccdc18
|
UTSW |
5 |
108,328,699 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8017:Ccdc18
|
UTSW |
5 |
108,376,511 (GRCm39) |
nonsense |
probably null |
|
|
R8019:Ccdc18
|
UTSW |
5 |
108,376,511 (GRCm39) |
nonsense |
probably null |
|
|
R8172:Ccdc18
|
UTSW |
5 |
108,311,640 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8177:Ccdc18
|
UTSW |
5 |
108,345,661 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R8344:Ccdc18
|
UTSW |
5 |
108,309,369 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R8351:Ccdc18
|
UTSW |
5 |
108,303,663 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8415:Ccdc18
|
UTSW |
5 |
108,363,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8451:Ccdc18
|
UTSW |
5 |
108,303,663 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8547:Ccdc18
|
UTSW |
5 |
108,345,725 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8725:Ccdc18
|
UTSW |
5 |
108,328,283 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R9137:Ccdc18
|
UTSW |
5 |
108,296,856 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9391:Ccdc18
|
UTSW |
5 |
108,376,770 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9418:Ccdc18
|
UTSW |
5 |
108,303,669 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9536:Ccdc18
|
UTSW |
5 |
108,286,792 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9565:Ccdc18
|
UTSW |
5 |
108,339,800 (GRCm39) |
missense |
probably damaging |
0.99 |
|
RF013:Ccdc18
|
UTSW |
5 |
108,368,582 (GRCm39) |
missense |
probably benign |
0.05 |
|
X0024:Ccdc18
|
UTSW |
5 |
108,339,788 (GRCm39) |
missense |
probably benign |
0.01 |
|
X0063:Ccdc18
|
UTSW |
5 |
108,360,063 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TGAACTTCTctctttctctgcccact -3'
(R):5'- GTCAAACCCACCCAACACCAATCAC -3'
Sequencing Primer
(F):5'- tcccacctgtttcttctgtc -3'
(R):5'- GTGACAAGCATTATTATCTGCCTTC -3'
|
| Posted On |
2014-04-13 |
Incidental Mutation