Incidental Mutation 'R8094:Ccdc162'
| ID |
630091 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ccdc162
|
| Ensembl Gene |
ENSMUSG00000075225 |
| Gene Name |
coiled-coil domain containing 162 |
| Synonyms |
Gm29096, Gm6976, 5033413D22Rik |
| MMRRC Submission |
067526-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.070)
|
| Stock # |
R8094 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
10 |
| Chromosomal Location |
41414838-41592586 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 41488864 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 1208
(D1208E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000140774
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000019955]
[ENSMUST00000099932]
[ENSMUST00000189488]
[ENSMUST00000219054]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000019955
|
| SMART Domains |
Protein: ENSMUSP00000019955
Gene: ENSMUSG00000075225
| 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 |
probably benign
Transcript: ENSMUST00000099932
|
| SMART Domains |
Protein: ENSMUSP00000097516
Gene: ENSMUSG00000075225
| 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 benign
Transcript: ENSMUST00000189488
AA Change: D1208E
PolyPhen 2
Score 0.023 (Sensitivity: 0.95; Specificity: 0.81)
|
| SMART Domains |
Protein: ENSMUSP00000140774
Gene: ENSMUSG00000075225
AA Change: D1208E
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
328 |
347 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000219054
|
| Coding Region Coverage |
- 1x: 99.8%
- 3x: 99.7%
- 10x: 99.2%
- 20x: 98.0%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 94 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A230072I06Rik |
T |
A |
8: 12,329,824 (GRCm39) |
L93H |
unknown |
Het |
| A2ml1 |
A |
G |
6: 128,549,045 (GRCm39) |
Y246H |
probably damaging |
Het |
| Akap11 |
C |
A |
14: 78,750,413 (GRCm39) |
C658F |
|
Het |
| Arid2 |
T |
G |
15: 96,266,592 (GRCm39) |
S547A |
possibly damaging |
Het |
| Atf1 |
C |
A |
15: 100,143,170 (GRCm39) |
D46E |
probably damaging |
Het |
| Brca2 |
T |
A |
5: 150,459,634 (GRCm39) |
F303Y |
possibly damaging |
Het |
| Btbd18 |
T |
A |
2: 84,498,260 (GRCm39) |
S633T |
possibly damaging |
Het |
| Btg4 |
T |
G |
9: 51,030,445 (GRCm39) |
F182V |
probably benign |
Het |
| Cacna1e |
G |
A |
1: 154,437,516 (GRCm39) |
S340F |
probably damaging |
Het |
| Camta2 |
A |
G |
11: 70,576,903 (GRCm39) |
W41R |
probably damaging |
Het |
| Cbl |
A |
T |
9: 44,074,696 (GRCm39) |
D455E |
probably benign |
Het |
| Cd177 |
A |
T |
7: 24,443,842 (GRCm39) |
M752K |
probably damaging |
Het |
| Cep290 |
A |
T |
10: 100,380,793 (GRCm39) |
H100L |
possibly damaging |
Het |
| Chrnb2 |
T |
A |
3: 89,668,698 (GRCm39) |
I206F |
probably damaging |
Het |
| Cyp2c40 |
A |
G |
19: 39,791,009 (GRCm39) |
L274S |
probably benign |
Het |
| Cyp2c40 |
T |
A |
19: 39,791,015 (GRCm39) |
Y272F |
probably benign |
Het |
| Cyp2d22 |
C |
A |
15: 82,258,556 (GRCm39) |
A102S |
probably benign |
Het |
| Cyp51 |
C |
T |
5: 4,136,490 (GRCm39) |
E435K |
probably benign |
Het |
| Dchs2 |
T |
C |
3: 83,262,929 (GRCm39) |
F3066L |
probably benign |
Het |
| Disp1 |
C |
A |
1: 182,869,192 (GRCm39) |
R1076L |
probably damaging |
Het |
| Dkk2 |
C |
T |
3: 131,791,801 (GRCm39) |
A3V |
probably benign |
Het |
| Dnah7b |
T |
C |
1: 46,165,964 (GRCm39) |
F543S |
probably benign |
Het |
| Dpt |
A |
T |
1: 164,624,481 (GRCm39) |
S61C |
probably damaging |
Het |
| Drg2 |
A |
T |
11: 60,353,096 (GRCm39) |
Y243F |
probably damaging |
Het |
| Dsg2 |
A |
G |
18: 20,716,061 (GRCm39) |
|
probably benign |
Het |
| Dst |
T |
G |
1: 34,228,040 (GRCm39) |
L1878V |
possibly damaging |
Het |
| F5 |
A |
G |
1: 164,036,509 (GRCm39) |
Y1890C |
probably benign |
Het |
| Fat1 |
T |
C |
8: 45,405,739 (GRCm39) |
V830A |
probably damaging |
Het |
| Fat2 |
C |
T |
11: 55,186,965 (GRCm39) |
D1294N |
probably benign |
Het |
| Fbxo15 |
A |
G |
18: 84,983,618 (GRCm39) |
Y322C |
probably benign |
Het |
| Fcsk |
A |
G |
8: 111,622,604 (GRCm39) |
F108S |
probably damaging |
Het |
| Fhit |
A |
T |
14: 10,751,666 (GRCm38) |
N7K |
unknown |
Het |
| Gabrb2 |
A |
G |
11: 42,488,370 (GRCm39) |
I279V |
probably damaging |
Het |
| Galk2 |
T |
C |
2: 125,773,189 (GRCm39) |
F207S |
probably damaging |
Het |
| Gtpbp3 |
C |
T |
8: 71,941,480 (GRCm39) |
L17F |
possibly damaging |
Het |
| Gucy2c |
T |
A |
6: 136,714,446 (GRCm39) |
D460V |
probably benign |
Het |
| Herc1 |
G |
A |
9: 66,400,462 (GRCm39) |
V4329I |
probably damaging |
Het |
| Iqcn |
T |
C |
8: 71,162,067 (GRCm39) |
V420A |
probably benign |
Het |
| Kirrel3 |
G |
A |
9: 34,946,460 (GRCm39) |
V740M |
probably damaging |
Het |
| Macf1 |
C |
A |
4: 123,263,660 (GRCm39) |
V6956L |
probably damaging |
Het |
| Mill1 |
C |
T |
7: 17,989,835 (GRCm39) |
A39V |
probably benign |
Het |
| Mkln1 |
T |
A |
6: 31,469,588 (GRCm39) |
Y599* |
probably null |
Het |
| Mrpl14 |
T |
A |
17: 46,009,039 (GRCm39) |
L46Q |
possibly damaging |
Het |
| Myom2 |
G |
T |
8: 15,119,418 (GRCm39) |
R103L |
possibly damaging |
Het |
| Naip2 |
A |
C |
13: 100,298,290 (GRCm39) |
I582S |
probably benign |
Het |
| Ndst2 |
A |
T |
14: 20,778,232 (GRCm39) |
V449D |
probably damaging |
Het |
| Nell1 |
T |
A |
7: 49,770,335 (GRCm39) |
H131Q |
probably benign |
Het |
| Nos3 |
G |
C |
5: 24,572,218 (GRCm39) |
R97P |
probably benign |
Het |
| Npc1 |
A |
T |
18: 12,327,297 (GRCm39) |
F1099L |
probably benign |
Het |
| Nxpe5 |
T |
A |
5: 138,249,802 (GRCm39) |
W531R |
probably damaging |
Het |
| Ogfr |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
2: 180,237,059 (GRCm39) |
|
probably benign |
Het |
| Or1j1 |
A |
T |
2: 36,702,330 (GRCm39) |
L258H |
probably damaging |
Het |
| Or4c110 |
T |
C |
2: 88,832,712 (GRCm39) |
|
probably benign |
Het |
| Or5b98 |
A |
T |
19: 12,931,366 (GRCm39) |
T138S |
probably benign |
Het |
| Or6c210 |
A |
G |
10: 129,495,933 (GRCm39) |
D86G |
probably damaging |
Het |
| Osmr |
T |
C |
15: 6,845,102 (GRCm39) |
N889S |
possibly damaging |
Het |
| Oxct2b |
A |
G |
4: 123,010,301 (GRCm39) |
I74V |
possibly damaging |
Het |
| Pakap |
A |
G |
4: 57,886,319 (GRCm39) |
T859A |
possibly damaging |
Het |
| Phldb3 |
C |
A |
7: 24,326,134 (GRCm39) |
A572D |
probably damaging |
Het |
| Pigr |
A |
G |
1: 130,774,247 (GRCm39) |
E409G |
probably damaging |
Het |
| Ptprs |
T |
C |
17: 56,735,947 (GRCm39) |
E674G |
probably benign |
Het |
| Ptpru |
G |
A |
4: 131,520,903 (GRCm39) |
T801I |
possibly damaging |
Het |
| Ralgapa1 |
T |
A |
12: 55,829,631 (GRCm39) |
D200V |
probably damaging |
Het |
| Rb1cc1 |
A |
T |
1: 6,333,448 (GRCm39) |
R1429* |
probably null |
Het |
| Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
| Rnpep |
A |
T |
1: 135,211,514 (GRCm39) |
L78Q |
probably damaging |
Het |
| Rtn2 |
A |
T |
7: 19,027,791 (GRCm39) |
I394F |
probably damaging |
Het |
| Satb2 |
A |
T |
1: 56,870,623 (GRCm39) |
V572D |
possibly damaging |
Het |
| Sds |
T |
C |
5: 120,617,001 (GRCm39) |
|
probably benign |
Het |
| Serpina10 |
TTCCTCCTCCTCCTCCTCCTCCTCC |
TTCCTCCTCCTCCTCCTCCTCC |
12: 103,595,032 (GRCm39) |
|
probably benign |
Het |
| Sgo2a |
T |
C |
1: 58,056,300 (GRCm39) |
I828T |
possibly damaging |
Het |
| Slc25a33 |
T |
A |
4: 149,840,609 (GRCm39) |
K79N |
probably benign |
Het |
| Slc25a51 |
A |
C |
4: 45,399,783 (GRCm39) |
F136V |
probably benign |
Het |
| Slfn14 |
T |
A |
11: 83,174,119 (GRCm39) |
K291* |
probably null |
Het |
| Sp100 |
A |
G |
1: 85,624,819 (GRCm39) |
K403E |
possibly damaging |
Het |
| Spaca1 |
C |
T |
4: 34,049,837 (GRCm39) |
E54K |
possibly damaging |
Het |
| Sympk |
T |
G |
7: 18,787,373 (GRCm39) |
|
probably null |
Het |
| Syne1 |
A |
T |
10: 5,067,031 (GRCm39) |
V7078D |
probably damaging |
Het |
| Tas2r121 |
T |
A |
6: 132,677,772 (GRCm39) |
I67L |
probably benign |
Het |
| Tha1 |
T |
C |
11: 117,759,323 (GRCm39) |
K389E |
probably benign |
Het |
| Thbs2 |
T |
A |
17: 14,900,584 (GRCm39) |
Q541L |
probably benign |
Het |
| Tmem161b |
C |
A |
13: 84,370,537 (GRCm39) |
|
probably benign |
Het |
| Tmem94 |
T |
C |
11: 115,679,218 (GRCm39) |
|
probably null |
Het |
| Tnfsf13 |
A |
G |
11: 69,575,983 (GRCm39) |
C35R |
probably damaging |
Het |
| Trcg1 |
C |
A |
9: 57,149,564 (GRCm39) |
Q379K |
probably benign |
Het |
| Ubr4 |
T |
C |
4: 139,168,007 (GRCm39) |
S1507P |
probably damaging |
Het |
| Uckl1 |
A |
G |
2: 181,215,049 (GRCm39) |
I268T |
probably damaging |
Het |
| Uvrag |
T |
C |
7: 98,641,174 (GRCm39) |
K289E |
possibly damaging |
Het |
| Vmn2r104 |
C |
A |
17: 20,250,483 (GRCm39) |
C596F |
possibly damaging |
Het |
| Vmn2r11 |
A |
T |
5: 109,201,626 (GRCm39) |
F293I |
probably damaging |
Het |
| Vps13b |
T |
A |
15: 35,669,052 (GRCm39) |
|
probably null |
Het |
| Wipf1 |
G |
A |
2: 73,267,879 (GRCm39) |
P173L |
possibly damaging |
Het |
| Zfp217 |
G |
A |
2: 169,961,571 (GRCm39) |
S252F |
possibly damaging |
Het |
| Zscan4f |
T |
A |
7: 11,135,154 (GRCm39) |
C187S |
possibly 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 |
|
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 |
|
R8985:Ccdc162
|
UTSW |
10 |
41,432,102 (GRCm39) |
missense |
probably damaging |
1.00 |
|
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'- TGTGTGCTGTACTTAACGCTCC -3'
(R):5'- GCAATGCCAGCCTTACCAAG -3'
Sequencing Primer
(F):5'- GTACTTAACGCTCCTCTCTGGG -3'
(R):5'- CAAGGTGGCCATGCTTTCTCAG -3'
|
| Posted On |
2020-06-30 |
Incidental Mutation