Incidental Mutation 'IGL01920:Vcan'
ID |
180070 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vcan
|
Ensembl Gene |
ENSMUSG00000021614 |
Gene Name |
versican |
Synonyms |
PG-M, hdf, DPEAAE, heart defect, Cspg2, 5430420N07Rik |
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
IGL01920
|
Quality Score |
|
Status
|
|
Chromosome |
13 |
Chromosomal Location |
89655312-89742509 bp(-) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 89689205 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glycine to Glutamic Acid
at position 2740
(G2740E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000105173
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000109543]
[ENSMUST00000109544]
[ENSMUST00000109546]
[ENSMUST00000159910]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000109543
|
SMART Domains |
Protein: ENSMUSP00000105170 Gene: ENSMUSG00000021614
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
IG
|
29 |
148 |
1.4e-7 |
SMART |
LINK
|
148 |
245 |
1.4e-53 |
SMART |
LINK
|
249 |
347 |
8.8e-60 |
SMART |
EGF
|
351 |
384 |
2.72e-7 |
SMART |
EGF_CA
|
386 |
422 |
1.16e-10 |
SMART |
CLECT
|
428 |
549 |
3.08e-34 |
SMART |
CCP
|
555 |
611 |
1.04e-8 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000109544
|
SMART Domains |
Protein: ENSMUSP00000105171 Gene: ENSMUSG00000021614
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
IG
|
29 |
148 |
1.4e-7 |
SMART |
LINK
|
148 |
245 |
1.4e-53 |
SMART |
LINK
|
249 |
347 |
8.8e-60 |
SMART |
low complexity region
|
728 |
743 |
N/A |
INTRINSIC |
low complexity region
|
1205 |
1219 |
N/A |
INTRINSIC |
EGF
|
1311 |
1344 |
2.72e-7 |
SMART |
EGF_CA
|
1346 |
1382 |
1.16e-10 |
SMART |
CLECT
|
1388 |
1509 |
3.08e-34 |
SMART |
CCP
|
1515 |
1571 |
1.04e-8 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000109546
AA Change: G2740E
PolyPhen 2
Score 0.036 (Sensitivity: 0.94; Specificity: 0.82)
|
SMART Domains |
Protein: ENSMUSP00000105173 Gene: ENSMUSG00000021614 AA Change: G2740E
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
IG
|
29 |
148 |
1.4e-7 |
SMART |
LINK
|
148 |
245 |
1.4e-53 |
SMART |
LINK
|
249 |
347 |
8.8e-60 |
SMART |
low complexity region
|
728 |
743 |
N/A |
INTRINSIC |
low complexity region
|
1205 |
1219 |
N/A |
INTRINSIC |
low complexity region
|
1322 |
1333 |
N/A |
INTRINSIC |
low complexity region
|
1546 |
1569 |
N/A |
INTRINSIC |
low complexity region
|
1837 |
1852 |
N/A |
INTRINSIC |
low complexity region
|
2013 |
2026 |
N/A |
INTRINSIC |
low complexity region
|
2354 |
2367 |
N/A |
INTRINSIC |
low complexity region
|
2468 |
2482 |
N/A |
INTRINSIC |
low complexity region
|
2719 |
2728 |
N/A |
INTRINSIC |
EGF
|
3050 |
3083 |
2.72e-7 |
SMART |
EGF_CA
|
3085 |
3121 |
1.16e-10 |
SMART |
CLECT
|
3127 |
3248 |
3.08e-34 |
SMART |
CCP
|
3254 |
3310 |
1.04e-8 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000159910
AA Change: G1780E
PolyPhen 2
Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
|
SMART Domains |
Protein: ENSMUSP00000125446 Gene: ENSMUSG00000021614 AA Change: G1780E
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
IG
|
29 |
148 |
1.4e-7 |
SMART |
LINK
|
148 |
245 |
1.4e-53 |
SMART |
LINK
|
249 |
347 |
8.8e-60 |
SMART |
low complexity region
|
362 |
373 |
N/A |
INTRINSIC |
low complexity region
|
586 |
609 |
N/A |
INTRINSIC |
low complexity region
|
877 |
892 |
N/A |
INTRINSIC |
low complexity region
|
1053 |
1066 |
N/A |
INTRINSIC |
low complexity region
|
1394 |
1407 |
N/A |
INTRINSIC |
low complexity region
|
1508 |
1522 |
N/A |
INTRINSIC |
low complexity region
|
1759 |
1768 |
N/A |
INTRINSIC |
EGF
|
2090 |
2123 |
2.72e-7 |
SMART |
EGF_CA
|
2125 |
2161 |
1.16e-10 |
SMART |
CLECT
|
2167 |
2288 |
3.08e-34 |
SMART |
CCP
|
2294 |
2350 |
1.04e-8 |
SMART |
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the aggrecan/versican proteoglycan family. The protein encoded is a large chondroitin sulfate proteoglycan and is a major component of the extracellular matrix. This protein is involved in cell adhesion, proliferation, proliferation, migration and angiogenesis and plays a central role in tissue morphogenesis and maintenance. Mutations in this gene are the cause of Wagner syndrome type 1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009] PHENOTYPE: Homozygotes for an insertional mutation exhibit anterior-posterior segmental defects of the heart, lack endocardial cushions of the conus and atrioventricular region, and die and around embryonic day 10.5. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 24 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars |
C |
T |
8: 111,043,246 |
R326W |
probably damaging |
Het |
Acad11 |
T |
C |
9: 104,063,905 |
|
probably null |
Het |
Acat2 |
A |
G |
17: 12,944,025 |
I312T |
probably benign |
Het |
Adgrl3 |
T |
C |
5: 81,465,296 |
V192A |
probably damaging |
Het |
Akap1 |
T |
C |
11: 88,839,633 |
H643R |
probably damaging |
Het |
Akap7 |
A |
T |
10: 25,289,603 |
C85* |
probably null |
Het |
Ankrd11 |
T |
C |
8: 122,915,897 |
|
probably benign |
Het |
Ano1 |
G |
A |
7: 144,611,454 |
|
probably benign |
Het |
C130026I21Rik |
A |
G |
1: 85,254,186 |
|
probably benign |
Het |
Csnk1g2 |
T |
C |
10: 80,638,428 |
L161P |
probably damaging |
Het |
Dvl2 |
A |
G |
11: 70,008,047 |
H420R |
probably benign |
Het |
Fam135b |
G |
T |
15: 71,622,036 |
H15N |
possibly damaging |
Het |
Foxj1 |
G |
T |
11: 116,331,920 |
H352Q |
possibly damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 |
S67L |
probably benign |
Het |
Gm10718 |
A |
T |
9: 3,025,118 |
Y194F |
probably benign |
Het |
Hectd1 |
T |
C |
12: 51,782,554 |
I969M |
probably damaging |
Het |
Kcnh3 |
C |
A |
15: 99,233,377 |
P544T |
probably benign |
Het |
Olfr855 |
A |
C |
9: 19,585,022 |
M162L |
probably benign |
Het |
Pcnt |
A |
G |
10: 76,404,528 |
L1224P |
probably damaging |
Het |
Prss2 |
A |
G |
6: 41,524,543 |
N182S |
possibly damaging |
Het |
Sgsm1 |
A |
T |
5: 113,273,605 |
W594R |
probably damaging |
Het |
Slc38a1 |
C |
T |
15: 96,586,897 |
A261T |
probably benign |
Het |
Vmn2r-ps159 |
C |
T |
4: 156,338,254 |
|
noncoding transcript |
Het |
Vwa7 |
G |
A |
17: 35,024,603 |
V729I |
probably benign |
Het |
|
Other mutations in Vcan |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00434:Vcan
|
APN |
13 |
89704702 |
missense |
probably damaging |
1.00 |
IGL00502:Vcan
|
APN |
13 |
89692319 |
missense |
probably benign |
|
IGL00504:Vcan
|
APN |
13 |
89691275 |
missense |
possibly damaging |
0.70 |
IGL00566:Vcan
|
APN |
13 |
89688979 |
missense |
probably benign |
0.01 |
IGL00701:Vcan
|
APN |
13 |
89703726 |
missense |
probably benign |
|
IGL00743:Vcan
|
APN |
13 |
89725306 |
missense |
probably damaging |
0.98 |
IGL00962:Vcan
|
APN |
13 |
89662052 |
missense |
probably damaging |
1.00 |
IGL01085:Vcan
|
APN |
13 |
89679958 |
missense |
probably damaging |
1.00 |
IGL01317:Vcan
|
APN |
13 |
89691668 |
missense |
probably benign |
0.00 |
IGL01349:Vcan
|
APN |
13 |
89703943 |
missense |
probably damaging |
0.98 |
IGL01391:Vcan
|
APN |
13 |
89704169 |
missense |
probably benign |
0.19 |
IGL01644:Vcan
|
APN |
13 |
89688675 |
missense |
probably benign |
0.13 |
IGL01657:Vcan
|
APN |
13 |
89690586 |
missense |
probably damaging |
1.00 |
IGL01707:Vcan
|
APN |
13 |
89689745 |
missense |
probably damaging |
1.00 |
IGL01764:Vcan
|
APN |
13 |
89725388 |
missense |
probably damaging |
1.00 |
IGL01989:Vcan
|
APN |
13 |
89689359 |
missense |
possibly damaging |
0.86 |
IGL01999:Vcan
|
APN |
13 |
89684438 |
missense |
probably damaging |
1.00 |
IGL02083:Vcan
|
APN |
13 |
89725565 |
missense |
probably damaging |
1.00 |
IGL02160:Vcan
|
APN |
13 |
89684493 |
missense |
probably damaging |
1.00 |
IGL02217:Vcan
|
APN |
13 |
89703077 |
missense |
probably damaging |
1.00 |
IGL02522:Vcan
|
APN |
13 |
89704849 |
missense |
probably benign |
0.00 |
IGL02527:Vcan
|
APN |
13 |
89690657 |
missense |
possibly damaging |
0.95 |
IGL02926:Vcan
|
APN |
13 |
89688623 |
missense |
probably damaging |
0.98 |
IGL03061:Vcan
|
APN |
13 |
89703275 |
missense |
probably benign |
0.25 |
IGL03331:Vcan
|
APN |
13 |
89661932 |
missense |
probably damaging |
1.00 |
IGL03352:Vcan
|
APN |
13 |
89705006 |
missense |
probably benign |
0.00 |
R0041:Vcan
|
UTSW |
13 |
89661985 |
missense |
probably damaging |
1.00 |
R0102:Vcan
|
UTSW |
13 |
89703668 |
missense |
probably benign |
0.01 |
R0102:Vcan
|
UTSW |
13 |
89703668 |
missense |
probably benign |
0.01 |
R0109:Vcan
|
UTSW |
13 |
89678073 |
critical splice donor site |
probably null |
|
R0139:Vcan
|
UTSW |
13 |
89691261 |
missense |
probably damaging |
1.00 |
R0295:Vcan
|
UTSW |
13 |
89712191 |
missense |
probably benign |
0.06 |
R0375:Vcan
|
UTSW |
13 |
89691275 |
missense |
probably damaging |
0.99 |
R0379:Vcan
|
UTSW |
13 |
89703546 |
missense |
probably damaging |
0.99 |
R0457:Vcan
|
UTSW |
13 |
89703199 |
missense |
possibly damaging |
0.78 |
R0482:Vcan
|
UTSW |
13 |
89678145 |
missense |
probably damaging |
1.00 |
R0485:Vcan
|
UTSW |
13 |
89704660 |
missense |
possibly damaging |
0.92 |
R0532:Vcan
|
UTSW |
13 |
89703772 |
missense |
probably damaging |
0.99 |
R0561:Vcan
|
UTSW |
13 |
89712253 |
missense |
probably damaging |
1.00 |
R0561:Vcan
|
UTSW |
13 |
89731464 |
missense |
possibly damaging |
0.86 |
R0636:Vcan
|
UTSW |
13 |
89704706 |
missense |
probably damaging |
0.99 |
R0636:Vcan
|
UTSW |
13 |
89712267 |
missense |
probably damaging |
1.00 |
R0680:Vcan
|
UTSW |
13 |
89679822 |
missense |
probably damaging |
1.00 |
R0849:Vcan
|
UTSW |
13 |
89704953 |
missense |
possibly damaging |
0.75 |
R1006:Vcan
|
UTSW |
13 |
89685077 |
critical splice donor site |
probably null |
|
R1104:Vcan
|
UTSW |
13 |
89692410 |
missense |
probably damaging |
1.00 |
R1118:Vcan
|
UTSW |
13 |
89705663 |
missense |
probably damaging |
1.00 |
R1137:Vcan
|
UTSW |
13 |
89704303 |
missense |
probably damaging |
1.00 |
R1199:Vcan
|
UTSW |
13 |
89679794 |
splice site |
probably null |
|
R1219:Vcan
|
UTSW |
13 |
89679904 |
missense |
probably damaging |
1.00 |
R1296:Vcan
|
UTSW |
13 |
89657556 |
missense |
probably damaging |
1.00 |
R1332:Vcan
|
UTSW |
13 |
89693055 |
missense |
probably damaging |
1.00 |
R1336:Vcan
|
UTSW |
13 |
89693055 |
missense |
probably damaging |
1.00 |
R1403:Vcan
|
UTSW |
13 |
89688484 |
missense |
probably benign |
0.00 |
R1403:Vcan
|
UTSW |
13 |
89688484 |
missense |
probably benign |
0.00 |
R1546:Vcan
|
UTSW |
13 |
89692956 |
missense |
probably damaging |
0.99 |
R1604:Vcan
|
UTSW |
13 |
89689661 |
missense |
probably benign |
0.42 |
R1616:Vcan
|
UTSW |
13 |
89705663 |
missense |
probably damaging |
1.00 |
R1636:Vcan
|
UTSW |
13 |
89703667 |
missense |
possibly damaging |
0.90 |
R1654:Vcan
|
UTSW |
13 |
89661946 |
missense |
probably damaging |
1.00 |
R1680:Vcan
|
UTSW |
13 |
89703547 |
missense |
probably benign |
0.19 |
R1694:Vcan
|
UTSW |
13 |
89688483 |
missense |
probably damaging |
0.98 |
R1712:Vcan
|
UTSW |
13 |
89721775 |
missense |
probably damaging |
1.00 |
R1754:Vcan
|
UTSW |
13 |
89704735 |
missense |
probably benign |
0.01 |
R1756:Vcan
|
UTSW |
13 |
89691681 |
missense |
probably benign |
0.05 |
R1824:Vcan
|
UTSW |
13 |
89705212 |
missense |
possibly damaging |
0.75 |
R1852:Vcan
|
UTSW |
13 |
89705392 |
missense |
probably damaging |
0.99 |
R1868:Vcan
|
UTSW |
13 |
89690871 |
missense |
probably benign |
0.12 |
R1920:Vcan
|
UTSW |
13 |
89693015 |
missense |
probably damaging |
1.00 |
R1932:Vcan
|
UTSW |
13 |
89705534 |
missense |
possibly damaging |
0.78 |
R1934:Vcan
|
UTSW |
13 |
89702926 |
missense |
probably damaging |
1.00 |
R1942:Vcan
|
UTSW |
13 |
89703424 |
missense |
probably benign |
0.01 |
R1964:Vcan
|
UTSW |
13 |
89692742 |
missense |
probably benign |
0.02 |
R1970:Vcan
|
UTSW |
13 |
89689038 |
missense |
probably damaging |
1.00 |
R2045:Vcan
|
UTSW |
13 |
89690985 |
missense |
probably benign |
0.00 |
R2110:Vcan
|
UTSW |
13 |
89693303 |
missense |
probably damaging |
1.00 |
R2111:Vcan
|
UTSW |
13 |
89693303 |
missense |
probably damaging |
1.00 |
R2112:Vcan
|
UTSW |
13 |
89693303 |
missense |
probably damaging |
1.00 |
R2136:Vcan
|
UTSW |
13 |
89689737 |
missense |
probably damaging |
1.00 |
R2158:Vcan
|
UTSW |
13 |
89703529 |
missense |
possibly damaging |
0.68 |
R2376:Vcan
|
UTSW |
13 |
89703410 |
missense |
possibly damaging |
0.80 |
R2385:Vcan
|
UTSW |
13 |
89689449 |
missense |
probably damaging |
1.00 |
R2443:Vcan
|
UTSW |
13 |
89704675 |
missense |
probably damaging |
1.00 |
R2876:Vcan
|
UTSW |
13 |
89704237 |
missense |
probably damaging |
1.00 |
R3607:Vcan
|
UTSW |
13 |
89703301 |
missense |
probably damaging |
0.98 |
R4042:Vcan
|
UTSW |
13 |
89692543 |
missense |
probably benign |
0.35 |
R4043:Vcan
|
UTSW |
13 |
89692543 |
missense |
probably benign |
0.35 |
R4044:Vcan
|
UTSW |
13 |
89692543 |
missense |
probably benign |
0.35 |
R4065:Vcan
|
UTSW |
13 |
89679887 |
missense |
probably damaging |
1.00 |
R4161:Vcan
|
UTSW |
13 |
89685158 |
missense |
probably damaging |
1.00 |
R4178:Vcan
|
UTSW |
13 |
89725547 |
missense |
probably damaging |
1.00 |
R4290:Vcan
|
UTSW |
13 |
89725486 |
missense |
probably damaging |
1.00 |
R4530:Vcan
|
UTSW |
13 |
89704028 |
missense |
probably damaging |
0.97 |
R4666:Vcan
|
UTSW |
13 |
89679934 |
missense |
probably damaging |
1.00 |
R4785:Vcan
|
UTSW |
13 |
89705789 |
missense |
probably damaging |
1.00 |
R4870:Vcan
|
UTSW |
13 |
89704739 |
missense |
probably benign |
0.01 |
R4973:Vcan
|
UTSW |
13 |
89688842 |
missense |
probably benign |
0.30 |
R5037:Vcan
|
UTSW |
13 |
89703977 |
missense |
probably damaging |
1.00 |
R5104:Vcan
|
UTSW |
13 |
89657472 |
intron |
probably benign |
|
R5124:Vcan
|
UTSW |
13 |
89725517 |
missense |
probably damaging |
1.00 |
R5129:Vcan
|
UTSW |
13 |
89690240 |
missense |
probably damaging |
1.00 |
R5198:Vcan
|
UTSW |
13 |
89690872 |
missense |
probably damaging |
1.00 |
R5240:Vcan
|
UTSW |
13 |
89692532 |
missense |
probably benign |
0.08 |
R5254:Vcan
|
UTSW |
13 |
89691600 |
missense |
probably damaging |
0.99 |
R5280:Vcan
|
UTSW |
13 |
89690286 |
missense |
probably benign |
0.00 |
R5522:Vcan
|
UTSW |
13 |
89691810 |
missense |
possibly damaging |
0.62 |
R5557:Vcan
|
UTSW |
13 |
89703112 |
missense |
possibly damaging |
0.77 |
R5568:Vcan
|
UTSW |
13 |
89688671 |
missense |
probably damaging |
1.00 |
R5578:Vcan
|
UTSW |
13 |
89691503 |
missense |
probably benign |
0.01 |
R5627:Vcan
|
UTSW |
13 |
89691135 |
frame shift |
probably null |
|
R5687:Vcan
|
UTSW |
13 |
89678134 |
missense |
probably damaging |
1.00 |
R5752:Vcan
|
UTSW |
13 |
89679950 |
missense |
probably damaging |
1.00 |
R5879:Vcan
|
UTSW |
13 |
89703952 |
missense |
probably damaging |
0.99 |
R5941:Vcan
|
UTSW |
13 |
89692691 |
missense |
probably damaging |
0.98 |
R6113:Vcan
|
UTSW |
13 |
89657536 |
nonsense |
probably null |
|
R6135:Vcan
|
UTSW |
13 |
89689926 |
missense |
probably benign |
0.36 |
R6252:Vcan
|
UTSW |
13 |
89691220 |
nonsense |
probably null |
|
R6280:Vcan
|
UTSW |
13 |
89725373 |
missense |
probably damaging |
1.00 |
R6317:Vcan
|
UTSW |
13 |
89691597 |
missense |
probably benign |
0.22 |
R6327:Vcan
|
UTSW |
13 |
89704832 |
missense |
probably damaging |
0.99 |
R6460:Vcan
|
UTSW |
13 |
89690687 |
missense |
possibly damaging |
0.61 |
R6669:Vcan
|
UTSW |
13 |
89704731 |
missense |
probably benign |
0.21 |
R6744:Vcan
|
UTSW |
13 |
89705182 |
missense |
probably damaging |
1.00 |
R6819:Vcan
|
UTSW |
13 |
89705125 |
missense |
probably benign |
0.00 |
R6880:Vcan
|
UTSW |
13 |
89712381 |
missense |
probably damaging |
1.00 |
R6956:Vcan
|
UTSW |
13 |
89689431 |
missense |
probably damaging |
0.99 |
R6971:Vcan
|
UTSW |
13 |
89678133 |
missense |
probably damaging |
1.00 |
R6985:Vcan
|
UTSW |
13 |
89679956 |
missense |
probably damaging |
1.00 |
R6994:Vcan
|
UTSW |
13 |
89693407 |
missense |
possibly damaging |
0.94 |
R6997:Vcan
|
UTSW |
13 |
89690618 |
missense |
probably damaging |
0.98 |
R7029:Vcan
|
UTSW |
13 |
89690241 |
missense |
probably damaging |
1.00 |
R7066:Vcan
|
UTSW |
13 |
89705686 |
missense |
probably damaging |
1.00 |
R7156:Vcan
|
UTSW |
13 |
89689110 |
missense |
possibly damaging |
0.95 |
R7171:Vcan
|
UTSW |
13 |
89725591 |
missense |
probably damaging |
1.00 |
R7176:Vcan
|
UTSW |
13 |
89688936 |
missense |
probably benign |
0.01 |
R7229:Vcan
|
UTSW |
13 |
89705270 |
missense |
possibly damaging |
0.87 |
R7250:Vcan
|
UTSW |
13 |
89721686 |
missense |
probably damaging |
1.00 |
R7250:Vcan
|
UTSW |
13 |
89731457 |
critical splice donor site |
probably null |
|
R7262:Vcan
|
UTSW |
13 |
89705161 |
missense |
possibly damaging |
0.62 |
R7289:Vcan
|
UTSW |
13 |
89692733 |
nonsense |
probably null |
|
R7299:Vcan
|
UTSW |
13 |
89705266 |
missense |
probably benign |
|
R7301:Vcan
|
UTSW |
13 |
89705266 |
missense |
probably benign |
|
R7425:Vcan
|
UTSW |
13 |
89689832 |
missense |
probably damaging |
0.99 |
R7514:Vcan
|
UTSW |
13 |
89704118 |
missense |
probably damaging |
0.97 |
R7579:Vcan
|
UTSW |
13 |
89692458 |
missense |
probably damaging |
1.00 |
R7618:Vcan
|
UTSW |
13 |
89692223 |
missense |
probably damaging |
0.99 |
R7655:Vcan
|
UTSW |
13 |
89685114 |
missense |
probably damaging |
1.00 |
R7656:Vcan
|
UTSW |
13 |
89685114 |
missense |
probably damaging |
1.00 |
R7676:Vcan
|
UTSW |
13 |
89691789 |
missense |
probably damaging |
1.00 |
R7719:Vcan
|
UTSW |
13 |
89704619 |
missense |
probably damaging |
0.98 |
R7753:Vcan
|
UTSW |
13 |
89689323 |
missense |
probably damaging |
1.00 |
R7762:Vcan
|
UTSW |
13 |
89692937 |
missense |
probably damaging |
1.00 |
R7778:Vcan
|
UTSW |
13 |
89688654 |
missense |
probably damaging |
1.00 |
R7824:Vcan
|
UTSW |
13 |
89688654 |
missense |
probably damaging |
1.00 |
R7995:Vcan
|
UTSW |
13 |
89691858 |
missense |
probably benign |
|
R7998:Vcan
|
UTSW |
13 |
89704327 |
missense |
probably damaging |
1.00 |
R8033:Vcan
|
UTSW |
13 |
89704360 |
missense |
probably benign |
0.04 |
R8061:Vcan
|
UTSW |
13 |
89657290 |
missense |
probably benign |
0.45 |
R8103:Vcan
|
UTSW |
13 |
89657658 |
missense |
probably damaging |
1.00 |
R8103:Vcan
|
UTSW |
13 |
89703320 |
nonsense |
probably null |
|
R8124:Vcan
|
UTSW |
13 |
89704254 |
missense |
possibly damaging |
0.93 |
R8162:Vcan
|
UTSW |
13 |
89704987 |
nonsense |
probably null |
|
R8166:Vcan
|
UTSW |
13 |
89692736 |
missense |
probably benign |
0.02 |
R8274:Vcan
|
UTSW |
13 |
89704970 |
missense |
probably benign |
0.02 |
R8284:Vcan
|
UTSW |
13 |
89704335 |
missense |
possibly damaging |
0.68 |
R8417:Vcan
|
UTSW |
13 |
89688743 |
missense |
probably benign |
0.19 |
R8696:Vcan
|
UTSW |
13 |
89691098 |
missense |
probably benign |
0.00 |
R8738:Vcan
|
UTSW |
13 |
89692320 |
missense |
probably benign |
0.17 |
R8792:Vcan
|
UTSW |
13 |
89692111 |
missense |
possibly damaging |
0.91 |
R8887:Vcan
|
UTSW |
13 |
89704907 |
missense |
probably benign |
|
R9049:Vcan
|
UTSW |
13 |
89678105 |
missense |
probably damaging |
1.00 |
R9074:Vcan
|
UTSW |
13 |
89691027 |
missense |
possibly damaging |
0.95 |
R9095:Vcan
|
UTSW |
13 |
89704525 |
missense |
probably benign |
0.32 |
R9172:Vcan
|
UTSW |
13 |
89679931 |
missense |
probably damaging |
1.00 |
R9199:Vcan
|
UTSW |
13 |
89690496 |
nonsense |
probably null |
|
R9259:Vcan
|
UTSW |
13 |
89690870 |
missense |
probably damaging |
0.99 |
R9455:Vcan
|
UTSW |
13 |
89689333 |
missense |
probably damaging |
1.00 |
R9476:Vcan
|
UTSW |
13 |
89703412 |
missense |
possibly damaging |
0.95 |
R9477:Vcan
|
UTSW |
13 |
89693009 |
missense |
probably damaging |
1.00 |
R9555:Vcan
|
UTSW |
13 |
89691540 |
missense |
|
|
R9579:Vcan
|
UTSW |
13 |
89689594 |
missense |
possibly damaging |
0.67 |
R9606:Vcan
|
UTSW |
13 |
89705372 |
missense |
probably damaging |
1.00 |
R9645:Vcan
|
UTSW |
13 |
89692962 |
missense |
probably benign |
0.00 |
R9659:Vcan
|
UTSW |
13 |
89691741 |
missense |
probably damaging |
0.99 |
R9766:Vcan
|
UTSW |
13 |
89691128 |
missense |
probably benign |
0.00 |
R9778:Vcan
|
UTSW |
13 |
89689811 |
missense |
probably damaging |
1.00 |
X0058:Vcan
|
UTSW |
13 |
89692493 |
missense |
probably benign |
0.21 |
X0065:Vcan
|
UTSW |
13 |
89705749 |
missense |
probably damaging |
0.96 |
Z1176:Vcan
|
UTSW |
13 |
89692571 |
missense |
probably benign |
0.10 |
Z1177:Vcan
|
UTSW |
13 |
89703524 |
missense |
probably benign |
0.00 |
Z1177:Vcan
|
UTSW |
13 |
89703788 |
nonsense |
probably null |
|
Z1177:Vcan
|
UTSW |
13 |
89704073 |
missense |
probably damaging |
1.00 |
|
Posted On |
2014-05-07 |