Incidental Mutation 'R7365:Clca4b'
| ID |
571689 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Clca4b
|
| Ensembl Gene |
ENSMUSG00000074195 |
| Gene Name |
chloride channel accessory 4B |
| Synonyms |
AI747448 |
| MMRRC Submission |
045449-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.060)
|
| Stock # |
R7365 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
3 |
| Chromosomal Location |
144616682-144638290 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 144628529 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 393
(T393A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000096149
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000098549]
|
| AlphaFold |
Q3UW98 |
| Predicted Effect |
not run
Transcript: ENSMUST00000098549
AA Change: T393A
|
| SMART Domains |
Protein: ENSMUSP00000096149
Gene: ENSMUSG00000074195
AA Change: T393A
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
|
VWA
|
306 |
480 |
1.03e-15 |
SMART |
|
Blast:VWA
|
513 |
552 |
6e-16 |
BLAST |
|
Blast:FN3
|
757 |
838 |
5e-35 |
BLAST |
|
low complexity region
|
882 |
906 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.3%
|
| Validation Efficiency |
100% (96/96) |
| MGI Phenotype |
PHENOTYPE: No notable phenotype was detected in a high throughput screen of homozyogus mutant null mice. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 96 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700123K08Rik |
T |
C |
5: 138,561,198 (GRCm39) |
S155G |
probably benign |
Het |
| Abcc4 |
T |
C |
14: 118,865,066 (GRCm39) |
N320S |
probably damaging |
Het |
| Akr1c19 |
G |
A |
13: 4,287,069 (GRCm39) |
R96H |
probably benign |
Het |
| Ankrd17 |
T |
C |
5: 90,439,010 (GRCm39) |
D451G |
possibly damaging |
Het |
| Ano8 |
T |
A |
8: 71,937,754 (GRCm39) |
D36V |
probably damaging |
Het |
| Aqp3 |
A |
G |
4: 41,098,003 (GRCm39) |
V36A |
probably benign |
Het |
| Atf7ip |
A |
G |
6: 136,537,708 (GRCm39) |
T314A |
probably benign |
Het |
| Atp2c1 |
A |
T |
9: 105,300,198 (GRCm39) |
D700E |
probably damaging |
Het |
| Axin2 |
G |
A |
11: 108,830,202 (GRCm39) |
V341M |
possibly damaging |
Het |
| Bin3 |
A |
G |
14: 70,371,976 (GRCm39) |
Q139R |
probably damaging |
Het |
| Brca2 |
A |
G |
5: 150,455,802 (GRCm39) |
D181G |
probably damaging |
Het |
| Capn3 |
A |
G |
2: 120,325,295 (GRCm39) |
E466G |
probably damaging |
Het |
| Ccdc14 |
T |
A |
16: 34,543,989 (GRCm39) |
Y830* |
probably null |
Het |
| Cdk12 |
T |
C |
11: 98,111,910 (GRCm39) |
F723L |
unknown |
Het |
| Cep89 |
G |
A |
7: 35,129,353 (GRCm39) |
R630H |
probably damaging |
Het |
| Cip2a |
T |
A |
16: 48,822,016 (GRCm39) |
S215T |
probably benign |
Het |
| Clca3a2 |
T |
A |
3: 144,804,545 (GRCm39) |
I61F |
probably damaging |
Het |
| Cldn5 |
G |
A |
16: 18,595,845 (GRCm39) |
A34T |
probably damaging |
Het |
| Cobll1 |
A |
T |
2: 64,928,717 (GRCm39) |
S870T |
probably damaging |
Het |
| Col12a1 |
T |
C |
9: 79,613,642 (GRCm39) |
K68E |
probably damaging |
Het |
| Crnn |
A |
T |
3: 93,055,841 (GRCm39) |
Q209L |
probably damaging |
Het |
| Cwf19l1 |
A |
T |
19: 44,120,579 (GRCm39) |
F45I |
probably damaging |
Het |
| Cyfip2 |
T |
A |
11: 46,098,267 (GRCm39) |
K1052* |
probably null |
Het |
| D930020B18Rik |
G |
A |
10: 121,503,716 (GRCm39) |
|
probably null |
Het |
| Dcc |
G |
A |
18: 71,959,194 (GRCm39) |
P193S |
probably damaging |
Het |
| Dda1 |
T |
A |
8: 71,927,137 (GRCm39) |
C48S |
probably benign |
Het |
| Disc1 |
A |
G |
8: 125,881,780 (GRCm39) |
R572G |
probably damaging |
Het |
| Dnah7a |
A |
T |
1: 53,536,297 (GRCm39) |
M2582K |
probably benign |
Het |
| Dsel |
C |
T |
1: 111,789,303 (GRCm39) |
G411S |
probably damaging |
Het |
| Dynlrb2 |
T |
C |
8: 117,241,696 (GRCm39) |
V80A |
probably benign |
Het |
| Eif3a |
A |
T |
19: 60,755,082 (GRCm39) |
D1033E |
unknown |
Het |
| Enam |
C |
A |
5: 88,649,347 (GRCm39) |
H285Q |
possibly damaging |
Het |
| Ep400 |
T |
C |
5: 110,867,480 (GRCm39) |
D980G |
unknown |
Het |
| Epha7 |
C |
T |
4: 28,871,937 (GRCm39) |
S422L |
probably benign |
Het |
| Erc2 |
A |
C |
14: 27,762,346 (GRCm39) |
D703A |
probably damaging |
Het |
| Ezh2 |
G |
T |
6: 47,510,692 (GRCm39) |
S639* |
probably null |
Het |
| Fbn1 |
G |
A |
2: 125,193,969 (GRCm39) |
H1333Y |
probably damaging |
Het |
| Flad1 |
A |
G |
3: 89,315,972 (GRCm39) |
S197P |
possibly damaging |
Het |
| Foxl3 |
A |
G |
5: 138,806,736 (GRCm39) |
H82R |
probably damaging |
Het |
| Gfm2 |
G |
T |
13: 97,279,529 (GRCm39) |
C26F |
probably benign |
Het |
| Golga2 |
C |
T |
2: 32,193,013 (GRCm39) |
Q444* |
probably null |
Het |
| Gp5 |
A |
T |
16: 30,127,426 (GRCm39) |
V416D |
probably damaging |
Het |
| Gpat2 |
A |
G |
2: 127,268,901 (GRCm39) |
|
probably null |
Het |
| Gpr137c |
A |
G |
14: 45,516,471 (GRCm39) |
D353G |
probably damaging |
Het |
| Hoxa13 |
A |
C |
6: 52,236,862 (GRCm39) |
W133G |
probably damaging |
Het |
| Hydin |
A |
T |
8: 111,284,294 (GRCm39) |
I3189F |
probably damaging |
Het |
| Hydin |
A |
T |
8: 111,327,905 (GRCm39) |
K4804M |
probably damaging |
Het |
| Ice2 |
T |
C |
9: 69,307,794 (GRCm39) |
F26S |
probably damaging |
Het |
| Ints11 |
T |
C |
4: 155,956,687 (GRCm39) |
|
probably null |
Het |
| Ipo5 |
A |
G |
14: 121,157,497 (GRCm39) |
I112V |
probably benign |
Het |
| Itgax |
T |
A |
7: 127,734,481 (GRCm39) |
S346R |
probably damaging |
Het |
| Kcnj13 |
T |
A |
1: 87,316,739 (GRCm39) |
M125L |
probably damaging |
Het |
| Lmbrd1 |
T |
A |
1: 24,783,948 (GRCm39) |
V359E |
possibly damaging |
Het |
| Lrrc7 |
T |
G |
3: 157,903,798 (GRCm39) |
K287N |
probably damaging |
Het |
| Mau2 |
C |
T |
8: 70,481,884 (GRCm39) |
A191T |
possibly damaging |
Het |
| Mkx |
C |
A |
18: 7,000,747 (GRCm39) |
R65L |
possibly damaging |
Het |
| Mroh4 |
T |
A |
15: 74,482,220 (GRCm39) |
K746* |
probably null |
Het |
| Myh4 |
A |
G |
11: 67,133,674 (GRCm39) |
T238A |
probably damaging |
Het |
| Nlrp9c |
T |
A |
7: 26,070,822 (GRCm39) |
N920Y |
possibly damaging |
Het |
| Nr4a3 |
T |
G |
4: 48,051,290 (GRCm39) |
S15A |
possibly damaging |
Het |
| Ntn4 |
T |
C |
10: 93,480,666 (GRCm39) |
L130P |
probably damaging |
Het |
| Or2ag13 |
A |
G |
7: 106,313,171 (GRCm39) |
V239A |
probably benign |
Het |
| Or4a68 |
A |
G |
2: 89,270,542 (GRCm39) |
V27A |
probably benign |
Het |
| Or4f59 |
A |
T |
2: 111,873,359 (GRCm39) |
V6E |
possibly damaging |
Het |
| Or56a42-ps1 |
T |
A |
7: 104,777,552 (GRCm39) |
I21F |
probably benign |
Het |
| Or8d23 |
A |
T |
9: 38,842,072 (GRCm39) |
I202F |
probably damaging |
Het |
| Otog |
T |
C |
7: 45,947,732 (GRCm39) |
L110P |
probably damaging |
Het |
| Platr25 |
G |
A |
13: 62,848,719 (GRCm39) |
H48Y |
probably benign |
Het |
| Plcxd2 |
T |
C |
16: 45,800,789 (GRCm39) |
E145G |
probably damaging |
Het |
| Pltp |
A |
T |
2: 164,696,242 (GRCm39) |
N143K |
probably damaging |
Het |
| Pnpt1 |
T |
C |
11: 29,111,334 (GRCm39) |
Y735H |
probably damaging |
Het |
| Prom1 |
A |
G |
5: 44,178,173 (GRCm39) |
Y520H |
probably damaging |
Het |
| Rag2 |
A |
G |
2: 101,461,118 (GRCm39) |
Y476C |
probably damaging |
Het |
| Rdh16f2 |
A |
G |
10: 127,712,893 (GRCm39) |
Y297C |
probably damaging |
Het |
| Ryr1 |
T |
C |
7: 28,785,180 (GRCm39) |
E1844G |
probably benign |
Het |
| Ryr2 |
A |
G |
13: 11,655,161 (GRCm39) |
C3679R |
probably damaging |
Het |
| Sirt1 |
A |
G |
10: 63,157,782 (GRCm39) |
I544T |
probably benign |
Het |
| Slc26a10 |
A |
T |
10: 127,012,716 (GRCm39) |
I382N |
possibly damaging |
Het |
| Sox2 |
C |
A |
3: 34,705,121 (GRCm39) |
P186Q |
possibly damaging |
Het |
| Spata31e5 |
A |
T |
1: 28,819,233 (GRCm39) |
M16K |
probably benign |
Het |
| Tnpo3 |
A |
G |
6: 29,556,995 (GRCm39) |
L752P |
probably damaging |
Het |
| Top2b |
T |
A |
14: 16,416,649 (GRCm38) |
N1136K |
probably benign |
Het |
| Tpsg1 |
G |
T |
17: 25,592,184 (GRCm39) |
G86V |
probably damaging |
Het |
| Ttf2 |
C |
A |
3: 100,870,618 (GRCm39) |
D152Y |
possibly damaging |
Het |
| Txndc15 |
T |
C |
13: 55,862,601 (GRCm39) |
L4P |
unknown |
Het |
| Unc5a |
T |
C |
13: 55,144,386 (GRCm39) |
V237A |
possibly damaging |
Het |
| Urb1 |
CACTTAC |
CAC |
16: 90,569,461 (GRCm39) |
|
probably benign |
Het |
| Vav3 |
C |
A |
3: 109,535,415 (GRCm39) |
P616T |
possibly damaging |
Het |
| Vmn2r15 |
T |
A |
5: 109,441,105 (GRCm39) |
D251V |
probably benign |
Het |
| Vmn2r15 |
A |
G |
5: 109,445,388 (GRCm39) |
L12S |
probably benign |
Het |
| Wfs1 |
A |
C |
5: 37,125,076 (GRCm39) |
I605S |
probably benign |
Het |
| Wif1 |
G |
A |
10: 120,919,814 (GRCm39) |
R187Q |
possibly damaging |
Het |
| Yipf1 |
A |
G |
4: 107,207,738 (GRCm39) |
|
probably null |
Het |
| Zdhhc20 |
G |
T |
14: 58,111,377 (GRCm39) |
F74L |
possibly damaging |
Het |
| Zfp507 |
T |
C |
7: 35,475,843 (GRCm39) |
T303A |
unknown |
Het |
| Zfp763 |
A |
T |
17: 33,252,352 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Clca4b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00228:Clca4b
|
APN |
3 |
144,638,152 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL00391:Clca4b
|
APN |
3 |
144,621,322 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
IGL00576:Clca4b
|
APN |
3 |
144,631,108 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01484:Clca4b
|
APN |
3 |
144,633,996 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01539:Clca4b
|
APN |
3 |
144,631,918 (GRCm39) |
missense |
probably benign |
|
|
IGL01726:Clca4b
|
APN |
3 |
144,634,103 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01903:Clca4b
|
APN |
3 |
144,634,020 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01967:Clca4b
|
APN |
3 |
144,633,951 (GRCm39) |
splice site |
probably benign |
|
|
IGL02002:Clca4b
|
APN |
3 |
144,638,194 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02323:Clca4b
|
APN |
3 |
144,619,082 (GRCm39) |
missense |
probably benign |
|
|
IGL02379:Clca4b
|
APN |
3 |
144,627,619 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02638:Clca4b
|
APN |
3 |
144,631,939 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02859:Clca4b
|
APN |
3 |
144,617,800 (GRCm39) |
missense |
probably benign |
|
|
R0110:Clca4b
|
UTSW |
3 |
144,619,112 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0266:Clca4b
|
UTSW |
3 |
144,628,547 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0311:Clca4b
|
UTSW |
3 |
144,638,257 (GRCm39) |
missense |
probably benign |
0.04 |
|
R0348:Clca4b
|
UTSW |
3 |
144,627,741 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0450:Clca4b
|
UTSW |
3 |
144,619,112 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0510:Clca4b
|
UTSW |
3 |
144,619,112 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0538:Clca4b
|
UTSW |
3 |
144,627,717 (GRCm39) |
missense |
probably benign |
0.15 |
|
R0551:Clca4b
|
UTSW |
3 |
144,634,387 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0552:Clca4b
|
UTSW |
3 |
144,622,536 (GRCm39) |
missense |
probably benign |
|
|
R0570:Clca4b
|
UTSW |
3 |
144,631,110 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0591:Clca4b
|
UTSW |
3 |
144,621,353 (GRCm39) |
nonsense |
probably null |
|
|
R0627:Clca4b
|
UTSW |
3 |
144,634,020 (GRCm39) |
missense |
probably benign |
0.20 |
|
R0729:Clca4b
|
UTSW |
3 |
144,634,111 (GRCm39) |
splice site |
probably benign |
|
|
R0844:Clca4b
|
UTSW |
3 |
144,622,532 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0964:Clca4b
|
UTSW |
3 |
144,621,337 (GRCm39) |
missense |
probably benign |
|
|
R1388:Clca4b
|
UTSW |
3 |
144,622,415 (GRCm39) |
missense |
probably benign |
|
|
R1479:Clca4b
|
UTSW |
3 |
144,621,229 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1603:Clca4b
|
UTSW |
3 |
144,627,780 (GRCm39) |
missense |
probably benign |
0.20 |
|
R2045:Clca4b
|
UTSW |
3 |
144,630,924 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2162:Clca4b
|
UTSW |
3 |
144,634,348 (GRCm39) |
missense |
probably benign |
0.19 |
|
R2185:Clca4b
|
UTSW |
3 |
144,634,317 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2241:Clca4b
|
UTSW |
3 |
144,616,987 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2300:Clca4b
|
UTSW |
3 |
144,622,432 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2321:Clca4b
|
UTSW |
3 |
144,638,134 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2359:Clca4b
|
UTSW |
3 |
144,631,003 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R3105:Clca4b
|
UTSW |
3 |
144,622,432 (GRCm39) |
missense |
probably benign |
0.02 |
|
R3151:Clca4b
|
UTSW |
3 |
144,621,272 (GRCm39) |
missense |
probably benign |
0.05 |
|
R3158:Clca4b
|
UTSW |
3 |
144,617,878 (GRCm39) |
missense |
probably benign |
0.04 |
|
R3177:Clca4b
|
UTSW |
3 |
144,617,120 (GRCm39) |
missense |
probably benign |
0.15 |
|
R3277:Clca4b
|
UTSW |
3 |
144,617,120 (GRCm39) |
missense |
probably benign |
0.15 |
|
R3981:Clca4b
|
UTSW |
3 |
144,631,797 (GRCm39) |
missense |
probably benign |
0.27 |
|
R4601:Clca4b
|
UTSW |
3 |
144,632,945 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R4646:Clca4b
|
UTSW |
3 |
144,634,286 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4647:Clca4b
|
UTSW |
3 |
144,634,286 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4696:Clca4b
|
UTSW |
3 |
144,617,146 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4893:Clca4b
|
UTSW |
3 |
144,630,934 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R4998:Clca4b
|
UTSW |
3 |
144,621,269 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5053:Clca4b
|
UTSW |
3 |
144,616,882 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5060:Clca4b
|
UTSW |
3 |
144,617,267 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5319:Clca4b
|
UTSW |
3 |
144,630,940 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R5409:Clca4b
|
UTSW |
3 |
144,622,452 (GRCm39) |
nonsense |
probably null |
|
|
R5534:Clca4b
|
UTSW |
3 |
144,621,227 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5578:Clca4b
|
UTSW |
3 |
144,638,196 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5667:Clca4b
|
UTSW |
3 |
144,627,624 (GRCm39) |
missense |
probably benign |
|
|
R5671:Clca4b
|
UTSW |
3 |
144,627,624 (GRCm39) |
missense |
probably benign |
|
|
R5715:Clca4b
|
UTSW |
3 |
144,619,018 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5875:Clca4b
|
UTSW |
3 |
144,628,650 (GRCm39) |
missense |
probably benign |
0.38 |
|
R5876:Clca4b
|
UTSW |
3 |
144,617,821 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6122:Clca4b
|
UTSW |
3 |
144,631,927 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R6294:Clca4b
|
UTSW |
3 |
144,630,946 (GRCm39) |
missense |
probably null |
|
|
R6408:Clca4b
|
UTSW |
3 |
144,625,036 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6418:Clca4b
|
UTSW |
3 |
144,633,996 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6458:Clca4b
|
UTSW |
3 |
144,617,088 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R6536:Clca4b
|
UTSW |
3 |
144,622,490 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R6567:Clca4b
|
UTSW |
3 |
144,638,100 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R6781:Clca4b
|
UTSW |
3 |
144,628,562 (GRCm39) |
missense |
probably benign |
|
|
R6799:Clca4b
|
UTSW |
3 |
144,621,388 (GRCm39) |
splice site |
probably null |
|
|
R7046:Clca4b
|
UTSW |
3 |
144,621,367 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7431:Clca4b
|
UTSW |
3 |
144,616,894 (GRCm39) |
missense |
probably benign |
0.28 |
|
R7462:Clca4b
|
UTSW |
3 |
144,628,621 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7611:Clca4b
|
UTSW |
3 |
144,627,757 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7806:Clca4b
|
UTSW |
3 |
144,638,157 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7918:Clca4b
|
UTSW |
3 |
144,619,033 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7962:Clca4b
|
UTSW |
3 |
144,622,421 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R7990:Clca4b
|
UTSW |
3 |
144,634,103 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8198:Clca4b
|
UTSW |
3 |
144,638,167 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8327:Clca4b
|
UTSW |
3 |
144,627,762 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R8370:Clca4b
|
UTSW |
3 |
144,631,824 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8434:Clca4b
|
UTSW |
3 |
144,631,917 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8493:Clca4b
|
UTSW |
3 |
144,617,911 (GRCm39) |
missense |
probably benign |
|
|
R9027:Clca4b
|
UTSW |
3 |
144,617,827 (GRCm39) |
nonsense |
probably null |
|
|
R9211:Clca4b
|
UTSW |
3 |
144,638,214 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9371:Clca4b
|
UTSW |
3 |
144,631,845 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R9400:Clca4b
|
UTSW |
3 |
144,616,953 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9446:Clca4b
|
UTSW |
3 |
144,638,134 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9474:Clca4b
|
UTSW |
3 |
144,616,927 (GRCm39) |
missense |
probably benign |
0.04 |
|
R9479:Clca4b
|
UTSW |
3 |
144,617,100 (GRCm39) |
missense |
probably benign |
0.44 |
|
R9493:Clca4b
|
UTSW |
3 |
144,632,964 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9730:Clca4b
|
UTSW |
3 |
144,632,979 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9733:Clca4b
|
UTSW |
3 |
144,621,272 (GRCm39) |
missense |
probably benign |
0.05 |
|
| Predicted Primers |
|
| Posted On |
2019-09-13 |
Incidental Mutation