Incidental Mutation 'R8985:Ccdc162'
| ID |
683977 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ccdc162
|
| Ensembl Gene |
ENSMUSG00000075225 |
| Gene Name |
coiled-coil domain containing 162 |
| Synonyms |
Gm29096, Gm6976, 5033413D22Rik |
| MMRRC Submission |
068818-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.070)
|
| Stock # |
R8985 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
10 |
| Chromosomal Location |
41414838-41592586 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 41432102 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 1797
(I1797T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000140774
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000019955]
[ENSMUST00000099932]
[ENSMUST00000179614]
[ENSMUST00000189488]
[ENSMUST00000219054]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000019955
AA Change: I5T
PolyPhen 2
Score 0.924 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000019955
Gene: ENSMUSG00000075225
AA Change: I5T
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
1 |
37 |
N/A |
INTRINSIC |
|
low complexity region
|
116 |
138 |
N/A |
INTRINSIC |
|
coiled coil region
|
177 |
217 |
N/A |
INTRINSIC |
|
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000092852
Gene: ENSMUSG00000075225
AA Change: I147T
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
140 |
179 |
N/A |
INTRINSIC |
|
low complexity region
|
304 |
326 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000099932
AA Change: I334T
PolyPhen 2
Score 0.963 (Sensitivity: 0.78; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000097516
Gene: ENSMUSG00000075225
AA Change: I334T
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
327 |
366 |
N/A |
INTRINSIC |
|
low complexity region
|
490 |
512 |
N/A |
INTRINSIC |
|
coiled coil region
|
551 |
607 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000179614
AA Change: I524T
PolyPhen 2
Score 0.963 (Sensitivity: 0.78; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000135966
Gene: ENSMUSG00000075225
AA Change: I524T
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
517 |
556 |
N/A |
INTRINSIC |
|
low complexity region
|
680 |
702 |
N/A |
INTRINSIC |
|
coiled coil region
|
741 |
797 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000189488
AA Change: I1797T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000140774
Gene: ENSMUSG00000075225
AA Change: I1797T
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
328 |
347 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000219054
AA Change: I524T
PolyPhen 2
Score 0.963 (Sensitivity: 0.78; Specificity: 0.95)
|
| Meta Mutation Damage Score |
0.6329 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.4%
|
| Validation Efficiency |
100% (74/74) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 72 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acad9 |
T |
A |
3: 36,141,860 (GRCm39) |
|
probably benign |
Het |
| Agbl1 |
C |
A |
7: 75,969,904 (GRCm39) |
S53R |
|
Het |
| Ahr |
T |
C |
12: 35,576,736 (GRCm39) |
K65R |
possibly damaging |
Het |
| AI429214 |
A |
T |
8: 37,460,820 (GRCm39) |
|
probably benign |
Het |
| Ankrd52 |
T |
C |
10: 128,222,978 (GRCm39) |
S643P |
probably damaging |
Het |
| Asz1 |
T |
C |
6: 18,051,336 (GRCm39) |
T448A |
probably benign |
Het |
| Atp10a |
A |
G |
7: 58,438,092 (GRCm39) |
I425V |
probably benign |
Het |
| Casd1 |
T |
A |
6: 4,624,399 (GRCm39) |
Y397* |
probably null |
Het |
| Cdc20b |
A |
T |
13: 113,196,330 (GRCm39) |
R152* |
probably null |
Het |
| Cdc25b |
T |
C |
2: 131,035,180 (GRCm39) |
C313R |
probably damaging |
Het |
| Cfap73 |
T |
A |
5: 120,768,123 (GRCm39) |
T212S |
probably benign |
Het |
| Chd9 |
G |
T |
8: 91,721,101 (GRCm39) |
R963L |
unknown |
Het |
| Clip4 |
G |
T |
17: 72,113,527 (GRCm39) |
V226F |
probably damaging |
Het |
| Cmya5 |
A |
G |
13: 93,233,664 (GRCm39) |
S475P |
possibly damaging |
Het |
| Cntn5 |
A |
G |
9: 10,171,960 (GRCm39) |
Y75H |
possibly damaging |
Het |
| Crtc1 |
T |
G |
8: 70,855,092 (GRCm39) |
H176P |
probably damaging |
Het |
| Cspg5 |
T |
C |
9: 110,085,502 (GRCm39) |
W558R |
unknown |
Het |
| Cyp2c39 |
A |
G |
19: 39,552,419 (GRCm39) |
T371A |
probably benign |
Het |
| Dcaf8 |
G |
A |
1: 172,000,199 (GRCm39) |
R119H |
probably benign |
Het |
| Drosha |
G |
T |
15: 12,924,187 (GRCm39) |
A1190S |
possibly damaging |
Het |
| Dst |
T |
C |
1: 34,288,886 (GRCm39) |
V5655A |
probably benign |
Het |
| Etnk1 |
C |
G |
6: 143,140,953 (GRCm39) |
|
probably benign |
Het |
| Flnc |
T |
A |
6: 29,440,499 (GRCm39) |
V269D |
probably benign |
Het |
| Foxs1 |
T |
A |
2: 152,775,058 (GRCm39) |
|
probably benign |
Het |
| Ftsj3 |
T |
C |
11: 106,141,595 (GRCm39) |
Y551C |
possibly damaging |
Het |
| Fzd6 |
A |
T |
15: 38,895,019 (GRCm39) |
H395L |
probably damaging |
Het |
| Grm6 |
C |
T |
11: 50,746,537 (GRCm39) |
A289V |
possibly damaging |
Het |
| Hook1 |
A |
G |
4: 95,910,468 (GRCm39) |
D694G |
probably benign |
Het |
| Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
| Igha |
T |
C |
12: 113,222,611 (GRCm39) |
E270G |
|
Het |
| Itga2b |
C |
A |
11: 102,356,288 (GRCm39) |
|
probably benign |
Het |
| Jade1 |
A |
C |
3: 41,568,148 (GRCm39) |
S739R |
probably benign |
Het |
| Lpin3 |
T |
C |
2: 160,738,674 (GRCm39) |
S209P |
probably benign |
Het |
| Ly6i |
A |
C |
15: 74,851,806 (GRCm39) |
L121R |
probably damaging |
Het |
| Ms4a1 |
C |
T |
19: 11,232,055 (GRCm39) |
V107I |
probably benign |
Het |
| Mycbpap |
T |
A |
11: 94,404,722 (GRCm39) |
T74S |
probably benign |
Het |
| Nlrp14 |
A |
G |
7: 106,796,436 (GRCm39) |
N921D |
probably benign |
Het |
| Nmur1 |
C |
T |
1: 86,314,103 (GRCm39) |
E388K |
probably benign |
Het |
| Nol4 |
T |
C |
18: 23,085,294 (GRCm39) |
Y40C |
probably damaging |
Het |
| Or1e1c |
T |
C |
11: 73,266,252 (GRCm39) |
S229P |
possibly damaging |
Het |
| Or51k1 |
A |
T |
7: 103,661,367 (GRCm39) |
C181S |
probably damaging |
Het |
| Or8b51 |
A |
T |
9: 38,569,621 (GRCm39) |
Y22* |
probably null |
Het |
| Pawr |
G |
A |
10: 108,247,861 (GRCm39) |
V283M |
possibly damaging |
Het |
| Pde6b |
T |
C |
5: 108,578,503 (GRCm39) |
Y814H |
probably benign |
Het |
| Pds5b |
T |
A |
5: 150,724,239 (GRCm39) |
L1272H |
probably benign |
Het |
| Pkd1l2 |
T |
C |
8: 117,764,849 (GRCm39) |
T1350A |
probably benign |
Het |
| Plcz1 |
T |
A |
6: 139,961,903 (GRCm39) |
Q216L |
possibly damaging |
Het |
| Prodh |
A |
T |
16: 17,890,362 (GRCm39) |
C522S |
probably null |
Het |
| Rasef |
G |
T |
4: 73,708,960 (GRCm39) |
P91Q |
possibly damaging |
Het |
| Rgs14 |
G |
A |
13: 55,531,234 (GRCm39) |
|
probably benign |
Het |
| Rnase6 |
A |
T |
14: 51,367,632 (GRCm39) |
Y8F |
unknown |
Het |
| Rnf216 |
T |
A |
5: 143,076,180 (GRCm39) |
T235S |
probably benign |
Het |
| Slco2a1 |
G |
A |
9: 102,949,834 (GRCm39) |
|
probably null |
Het |
| Smoc1 |
A |
G |
12: 81,226,261 (GRCm39) |
E362G |
probably damaging |
Het |
| Sncaip |
T |
C |
18: 53,002,169 (GRCm39) |
L230P |
probably benign |
Het |
| Tdrd3 |
A |
G |
14: 87,743,597 (GRCm39) |
E515G |
possibly damaging |
Het |
| Tipin |
T |
A |
9: 64,195,385 (GRCm39) |
|
probably null |
Het |
| Tmem9 |
T |
A |
1: 135,955,145 (GRCm39) |
V93D |
possibly damaging |
Het |
| Tpm3-rs7 |
A |
C |
14: 113,552,756 (GRCm39) |
I217L |
probably benign |
Het |
| Ttc41 |
A |
T |
10: 86,566,956 (GRCm39) |
I541F |
possibly damaging |
Het |
| Uck2 |
T |
C |
1: 167,070,681 (GRCm39) |
D16G |
probably benign |
Het |
| Vmn1r50 |
A |
G |
6: 90,085,017 (GRCm39) |
D254G |
probably benign |
Het |
| Vmn2r50 |
A |
C |
7: 9,779,974 (GRCm39) |
F469C |
probably damaging |
Het |
| Vmn2r57 |
A |
G |
7: 41,049,259 (GRCm39) |
V830A |
probably benign |
Het |
| Wwc2 |
T |
A |
8: 48,331,919 (GRCm39) |
R299S |
probably benign |
Het |
| Xdh |
C |
T |
17: 74,228,346 (GRCm39) |
G352R |
probably damaging |
Het |
| Xkr9 |
A |
T |
1: 13,770,990 (GRCm39) |
M169L |
probably benign |
Het |
| Zbtb10 |
A |
G |
3: 9,345,807 (GRCm39) |
D767G |
probably damaging |
Het |
| Zfp106 |
T |
C |
2: 120,366,077 (GRCm39) |
Y65C |
|
Het |
| Zfp536 |
A |
G |
7: 37,268,228 (GRCm39) |
L396P |
probably damaging |
Het |
| Znhit1 |
C |
A |
5: 137,011,408 (GRCm39) |
C135F |
probably damaging |
Het |
| Zscan5b |
A |
G |
7: 6,241,834 (GRCm39) |
E351G |
probably damaging |
Het |
|
| Other mutations in Ccdc162 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01013:Ccdc162
|
APN |
10 |
41,457,335 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01366:Ccdc162
|
APN |
10 |
41,456,302 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
IGL01924:Ccdc162
|
APN |
10 |
41,445,883 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02504:Ccdc162
|
APN |
10 |
41,428,384 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02678:Ccdc162
|
APN |
10 |
41,437,151 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02955:Ccdc162
|
APN |
10 |
41,437,123 (GRCm39) |
missense |
probably damaging |
1.00 |
|
beeswax
|
UTSW |
10 |
41,437,222 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
honeycomb
|
UTSW |
10 |
41,520,637 (GRCm39) |
missense |
probably benign |
0.35 |
|
FR4304:Ccdc162
|
UTSW |
10 |
41,432,117 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R0432:Ccdc162
|
UTSW |
10 |
41,417,856 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0585:Ccdc162
|
UTSW |
10 |
41,462,375 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0645:Ccdc162
|
UTSW |
10 |
41,462,407 (GRCm39) |
splice site |
probably benign |
|
|
R0731:Ccdc162
|
UTSW |
10 |
41,455,139 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1426:Ccdc162
|
UTSW |
10 |
41,429,178 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R1447:Ccdc162
|
UTSW |
10 |
41,456,243 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1712:Ccdc162
|
UTSW |
10 |
41,415,427 (GRCm39) |
missense |
probably benign |
0.35 |
|
R2138:Ccdc162
|
UTSW |
10 |
41,457,293 (GRCm39) |
missense |
probably benign |
0.15 |
|
R2351:Ccdc162
|
UTSW |
10 |
41,431,968 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2394:Ccdc162
|
UTSW |
10 |
41,445,894 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2431:Ccdc162
|
UTSW |
10 |
41,445,841 (GRCm39) |
missense |
probably benign |
|
|
R2571:Ccdc162
|
UTSW |
10 |
41,428,393 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2873:Ccdc162
|
UTSW |
10 |
41,531,095 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R2926:Ccdc162
|
UTSW |
10 |
41,437,203 (GRCm39) |
start gained |
probably benign |
|
|
R2999:Ccdc162
|
UTSW |
10 |
41,456,286 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3412:Ccdc162
|
UTSW |
10 |
41,415,545 (GRCm39) |
splice site |
probably benign |
|
|
R3712:Ccdc162
|
UTSW |
10 |
41,463,375 (GRCm39) |
missense |
probably benign |
|
|
R3736:Ccdc162
|
UTSW |
10 |
41,465,564 (GRCm39) |
splice site |
probably null |
|
|
R4112:Ccdc162
|
UTSW |
10 |
41,532,324 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R4557:Ccdc162
|
UTSW |
10 |
41,463,384 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4580:Ccdc162
|
UTSW |
10 |
41,437,136 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4685:Ccdc162
|
UTSW |
10 |
41,557,682 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R4837:Ccdc162
|
UTSW |
10 |
41,549,863 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5155:Ccdc162
|
UTSW |
10 |
41,455,147 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5155:Ccdc162
|
UTSW |
10 |
41,429,576 (GRCm39) |
splice site |
probably null |
|
|
R5645:Ccdc162
|
UTSW |
10 |
41,428,352 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5656:Ccdc162
|
UTSW |
10 |
41,445,930 (GRCm39) |
missense |
probably benign |
0.26 |
|
R5682:Ccdc162
|
UTSW |
10 |
41,432,799 (GRCm39) |
nonsense |
probably null |
|
|
R5808:Ccdc162
|
UTSW |
10 |
41,531,500 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R5909:Ccdc162
|
UTSW |
10 |
41,437,111 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6000:Ccdc162
|
UTSW |
10 |
41,437,159 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R6057:Ccdc162
|
UTSW |
10 |
41,510,037 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R6211:Ccdc162
|
UTSW |
10 |
41,506,141 (GRCm39) |
nonsense |
probably null |
|
|
R6264:Ccdc162
|
UTSW |
10 |
41,570,464 (GRCm39) |
missense |
probably benign |
0.31 |
|
R6329:Ccdc162
|
UTSW |
10 |
41,539,147 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R6349:Ccdc162
|
UTSW |
10 |
41,570,396 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6398:Ccdc162
|
UTSW |
10 |
41,503,145 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6453:Ccdc162
|
UTSW |
10 |
41,426,821 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6602:Ccdc162
|
UTSW |
10 |
41,491,976 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6627:Ccdc162
|
UTSW |
10 |
41,539,181 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6722:Ccdc162
|
UTSW |
10 |
41,520,637 (GRCm39) |
missense |
probably benign |
0.35 |
|
R6750:Ccdc162
|
UTSW |
10 |
41,437,222 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R6968:Ccdc162
|
UTSW |
10 |
41,549,840 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R6970:Ccdc162
|
UTSW |
10 |
41,491,954 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6989:Ccdc162
|
UTSW |
10 |
41,457,349 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7008:Ccdc162
|
UTSW |
10 |
41,428,411 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7135:Ccdc162
|
UTSW |
10 |
41,549,855 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7139:Ccdc162
|
UTSW |
10 |
41,542,717 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R7224:Ccdc162
|
UTSW |
10 |
41,437,187 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7230:Ccdc162
|
UTSW |
10 |
41,554,809 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7256:Ccdc162
|
UTSW |
10 |
41,431,997 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7261:Ccdc162
|
UTSW |
10 |
41,437,136 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7390:Ccdc162
|
UTSW |
10 |
41,510,044 (GRCm39) |
missense |
probably benign |
|
|
R7712:Ccdc162
|
UTSW |
10 |
41,503,223 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R7726:Ccdc162
|
UTSW |
10 |
41,429,071 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7754:Ccdc162
|
UTSW |
10 |
41,463,371 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7764:Ccdc162
|
UTSW |
10 |
41,566,109 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8053:Ccdc162
|
UTSW |
10 |
41,520,577 (GRCm39) |
missense |
probably benign |
|
|
R8088:Ccdc162
|
UTSW |
10 |
41,499,410 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R8094:Ccdc162
|
UTSW |
10 |
41,488,864 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8097:Ccdc162
|
UTSW |
10 |
41,510,115 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8321:Ccdc162
|
UTSW |
10 |
41,510,029 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8377:Ccdc162
|
UTSW |
10 |
41,457,306 (GRCm39) |
missense |
probably benign |
0.08 |
|
R8399:Ccdc162
|
UTSW |
10 |
41,415,517 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8669:Ccdc162
|
UTSW |
10 |
41,428,352 (GRCm39) |
missense |
probably benign |
0.06 |
|
R8772:Ccdc162
|
UTSW |
10 |
41,506,033 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8810:Ccdc162
|
UTSW |
10 |
41,542,737 (GRCm39) |
missense |
probably benign |
0.41 |
|
R8903:Ccdc162
|
UTSW |
10 |
41,531,440 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8928:Ccdc162
|
UTSW |
10 |
41,462,245 (GRCm39) |
splice site |
probably benign |
|
|
R8950:Ccdc162
|
UTSW |
10 |
41,474,507 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8960:Ccdc162
|
UTSW |
10 |
41,429,178 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9071:Ccdc162
|
UTSW |
10 |
41,457,174 (GRCm39) |
nonsense |
probably null |
|
|
R9254:Ccdc162
|
UTSW |
10 |
41,488,944 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R9297:Ccdc162
|
UTSW |
10 |
41,506,110 (GRCm39) |
missense |
probably benign |
|
|
R9318:Ccdc162
|
UTSW |
10 |
41,506,110 (GRCm39) |
missense |
probably benign |
|
|
R9518:Ccdc162
|
UTSW |
10 |
41,465,572 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9525:Ccdc162
|
UTSW |
10 |
41,559,222 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9539:Ccdc162
|
UTSW |
10 |
41,463,407 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R9638:Ccdc162
|
UTSW |
10 |
41,437,159 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1176:Ccdc162
|
UTSW |
10 |
41,530,993 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
Z1176:Ccdc162
|
UTSW |
10 |
41,481,104 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
Z1176:Ccdc162
|
UTSW |
10 |
41,429,127 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1176:Ccdc162
|
UTSW |
10 |
41,566,088 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1177:Ccdc162
|
UTSW |
10 |
41,559,191 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CAAAGTCCATTCTGCCATGGG -3'
(R):5'- GGACTGTTGAAAGGTCCTGAGC -3'
Sequencing Primer
(F):5'- CCTCGGTATGTAGCCATGGTC -3'
(R):5'- GAGCTTCTACCCAGTAGGCAATTTG -3'
|
| Posted On |
2021-10-11 |
Incidental Mutation