Incidental Mutation 'R4675:Ncapd3'
| ID |
349503 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ncapd3
|
| Ensembl Gene |
ENSMUSG00000035024 |
| Gene Name |
non-SMC condensin II complex, subunit D3 |
| Synonyms |
4632407J06Rik, 2810487N22Rik, B130055D15Rik |
| MMRRC Submission |
041930-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.962)
|
| Stock # |
R4675 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
9 |
| Chromosomal Location |
26941471-27006611 bp(+) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
T to C
at 27006038 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000034472
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034472]
[ENSMUST00000073127]
[ENSMUST00000086198]
[ENSMUST00000216677]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000034472
|
| SMART Domains |
Protein: ENSMUSP00000034472
Gene: ENSMUSG00000031990
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
31 |
N/A |
INTRINSIC |
|
IG
|
38 |
136 |
2.7e-9 |
SMART |
|
IGc2
|
151 |
226 |
8.12e-13 |
SMART |
|
transmembrane domain
|
245 |
267 |
N/A |
INTRINSIC |
|
| Predicted Effect |
silent
Transcript: ENSMUST00000073127
|
| SMART Domains |
Protein: ENSMUSP00000072871
Gene: ENSMUSG00000035024
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
159 |
170 |
N/A |
INTRINSIC |
|
low complexity region
|
173 |
184 |
N/A |
INTRINSIC |
|
Pfam:Cnd1
|
949 |
1148 |
1.7e-46 |
PFAM |
|
low complexity region
|
1192 |
1200 |
N/A |
INTRINSIC |
|
coiled coil region
|
1213 |
1270 |
N/A |
INTRINSIC |
|
low complexity region
|
1290 |
1315 |
N/A |
INTRINSIC |
|
low complexity region
|
1393 |
1410 |
N/A |
INTRINSIC |
|
low complexity region
|
1485 |
1498 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000086198
AA Change: S1212P
|
| SMART Domains |
Protein: ENSMUSP00000083374
Gene: ENSMUSG00000035024
AA Change: S1212P
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
159 |
170 |
N/A |
INTRINSIC |
|
low complexity region
|
173 |
184 |
N/A |
INTRINSIC |
|
Pfam:Cohesin_HEAT
|
536 |
560 |
4.6e-5 |
PFAM |
|
Pfam:Cnd1
|
949 |
1148 |
6.6e-59 |
PFAM |
|
low complexity region
|
1192 |
1200 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000214432
|
| Predicted Effect |
silent
Transcript: ENSMUST00000216677
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000217654
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.9%
|
| Validation Efficiency |
95% (89/94) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Condensin complexes I and II play essential roles in mitotic chromosome assembly and segregation. Both condensins contain 2 invariant structural maintenance of chromosome (SMC) subunits, SMC2 (MIM 605576) and SMC4 (MIM 605575), but they contain different sets of non-SMC subunits. NCAPD3 is 1 of 3 non-SMC subunits that define condensin II (Ono et al., 2003 [PubMed 14532007]).[supplied by OMIM, Mar 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 88 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310061I04Rik |
C |
A |
17: 36,203,820 (GRCm39) |
K291N |
probably damaging |
Het |
| Adgra1 |
A |
G |
7: 139,456,102 (GRCm39) |
T577A |
probably damaging |
Het |
| Akip1 |
T |
A |
7: 109,308,188 (GRCm39) |
I152N |
possibly damaging |
Het |
| Armc9 |
A |
G |
1: 86,130,240 (GRCm39) |
Y8C |
probably damaging |
Het |
| Atp1a4 |
A |
T |
1: 172,085,223 (GRCm39) |
V66E |
possibly damaging |
Het |
| Atp2a3 |
A |
T |
11: 72,872,623 (GRCm39) |
T724S |
probably damaging |
Het |
| Bmp1 |
C |
A |
14: 70,730,284 (GRCm39) |
R416L |
probably damaging |
Het |
| Bmt2 |
G |
T |
6: 13,663,300 (GRCm39) |
A66E |
probably benign |
Het |
| Bscl2 |
A |
T |
19: 8,825,523 (GRCm39) |
D403V |
possibly damaging |
Het |
| Cbx2 |
T |
A |
11: 118,919,935 (GRCm39) |
I500N |
probably damaging |
Het |
| Cd84 |
A |
T |
1: 171,700,887 (GRCm39) |
H216L |
possibly damaging |
Het |
| Cdhr18 |
A |
T |
14: 13,856,724 (GRCm38) |
D462E |
probably benign |
Het |
| Ceacam15 |
T |
C |
7: 16,407,410 (GRCm39) |
T36A |
probably benign |
Het |
| Cebpd |
A |
G |
16: 15,705,385 (GRCm39) |
D66G |
probably damaging |
Het |
| Cntnap4 |
A |
G |
8: 113,512,468 (GRCm39) |
Y610C |
probably damaging |
Het |
| Col11a2 |
T |
C |
17: 34,283,267 (GRCm39) |
|
probably null |
Het |
| Col17a1 |
T |
C |
19: 47,651,497 (GRCm39) |
|
probably null |
Het |
| Cracr2b |
A |
G |
7: 141,043,451 (GRCm39) |
D43G |
probably damaging |
Het |
| Dgkz |
T |
A |
2: 91,768,691 (GRCm39) |
K697* |
probably null |
Het |
| Dnah7b |
T |
A |
1: 46,256,317 (GRCm39) |
D1873E |
possibly damaging |
Het |
| Dst |
G |
A |
1: 34,314,784 (GRCm39) |
E6472K |
possibly damaging |
Het |
| Duox2 |
T |
C |
2: 122,111,414 (GRCm39) |
D1428G |
probably damaging |
Het |
| Elmod2 |
T |
C |
8: 84,043,537 (GRCm39) |
N210S |
probably damaging |
Het |
| Ephx1 |
A |
G |
1: 180,822,256 (GRCm39) |
F220S |
probably damaging |
Het |
| F13b |
A |
G |
1: 139,429,542 (GRCm39) |
Y20C |
unknown |
Het |
| Fbn2 |
T |
A |
18: 58,173,265 (GRCm39) |
N2051I |
possibly damaging |
Het |
| Gabrg2 |
G |
A |
11: 41,859,650 (GRCm39) |
H201Y |
probably damaging |
Het |
| Gbgt1 |
T |
C |
2: 28,388,453 (GRCm39) |
F46S |
possibly damaging |
Het |
| Gjd4 |
A |
G |
18: 9,280,578 (GRCm39) |
S167P |
probably damaging |
Het |
| Heatr5a |
T |
C |
12: 51,924,130 (GRCm39) |
N2028D |
probably benign |
Het |
| Heca |
T |
C |
10: 17,791,057 (GRCm39) |
H333R |
probably benign |
Het |
| Herc1 |
T |
C |
9: 66,298,740 (GRCm39) |
S625P |
probably damaging |
Het |
| Ighv1-55 |
T |
C |
12: 115,172,175 (GRCm39) |
|
probably benign |
Het |
| Ighv5-8 |
G |
A |
12: 113,618,777 (GRCm39) |
S64N |
probably benign |
Het |
| Itga1 |
G |
T |
13: 115,138,227 (GRCm39) |
|
probably null |
Het |
| Kif21a |
C |
A |
15: 90,824,748 (GRCm39) |
R1342L |
possibly damaging |
Het |
| Ksr1 |
G |
A |
11: 78,965,186 (GRCm39) |
P118S |
possibly damaging |
Het |
| Lat2 |
T |
C |
5: 134,634,911 (GRCm39) |
N100S |
probably damaging |
Het |
| Lrit3 |
T |
A |
3: 129,582,121 (GRCm39) |
D501V |
probably damaging |
Het |
| Lrrfip1 |
T |
A |
1: 91,031,042 (GRCm39) |
|
probably null |
Het |
| Lyst |
G |
A |
13: 13,809,968 (GRCm39) |
R546H |
probably damaging |
Het |
| Med21 |
T |
A |
6: 146,551,691 (GRCm39) |
L114H |
probably damaging |
Het |
| Mfap4 |
A |
T |
11: 61,376,336 (GRCm39) |
|
probably benign |
Het |
| Mpdz |
G |
A |
4: 81,302,049 (GRCm39) |
R233W |
probably damaging |
Het |
| Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
| Neto2 |
T |
G |
8: 86,396,333 (GRCm39) |
H104P |
probably damaging |
Het |
| Nr1h2 |
T |
C |
7: 44,201,979 (GRCm39) |
T36A |
possibly damaging |
Het |
| Nudt16l2 |
T |
C |
9: 105,021,647 (GRCm39) |
D133G |
probably benign |
Het |
| Or13a20 |
A |
T |
7: 140,232,074 (GRCm39) |
M61L |
probably damaging |
Het |
| Or4a79 |
T |
C |
2: 89,551,838 (GRCm39) |
I206V |
probably benign |
Het |
| Or51ab3 |
T |
G |
7: 103,201,183 (GRCm39) |
L64V |
probably damaging |
Het |
| Or51g2 |
A |
G |
7: 102,623,013 (GRCm39) |
M62T |
probably damaging |
Het |
| Or52p1 |
T |
A |
7: 104,267,631 (GRCm39) |
C248* |
probably null |
Het |
| Or5p52 |
A |
G |
7: 107,502,567 (GRCm39) |
I214M |
probably damaging |
Het |
| Or5p72 |
T |
C |
7: 108,022,309 (GRCm39) |
V177A |
possibly damaging |
Het |
| Or8b4 |
T |
C |
9: 37,830,882 (GRCm39) |
*310R |
probably null |
Het |
| Pcbp3 |
A |
G |
10: 76,606,869 (GRCm39) |
L241S |
possibly damaging |
Het |
| Pcf11 |
G |
A |
7: 92,308,985 (GRCm39) |
|
probably benign |
Het |
| Podxl |
G |
A |
6: 31,503,579 (GRCm39) |
T254M |
possibly damaging |
Het |
| Prr27 |
A |
C |
5: 87,991,100 (GRCm39) |
E237D |
possibly damaging |
Het |
| Rdh16 |
G |
T |
10: 127,637,316 (GRCm39) |
V84F |
probably damaging |
Het |
| Rnf26 |
A |
T |
9: 44,023,428 (GRCm39) |
D273E |
probably benign |
Het |
| Rpl13a |
A |
T |
7: 44,776,242 (GRCm39) |
|
probably benign |
Het |
| Rpl3l |
A |
G |
17: 24,952,584 (GRCm39) |
K239E |
probably benign |
Het |
| Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
| Rsf1 |
A |
AGGGCGACGG |
7: 97,229,111 (GRCm39) |
|
probably null |
Het |
| Ryk |
A |
G |
9: 102,768,415 (GRCm39) |
D352G |
possibly damaging |
Het |
| Setd1b |
T |
A |
5: 123,299,061 (GRCm39) |
|
probably benign |
Het |
| Sh2b1 |
G |
A |
7: 126,070,618 (GRCm39) |
A361V |
possibly damaging |
Het |
| Slc35f3 |
A |
T |
8: 127,047,935 (GRCm39) |
K92* |
probably null |
Het |
| Slc39a10 |
A |
G |
1: 46,857,144 (GRCm39) |
|
probably benign |
Het |
| Slc47a1 |
G |
A |
11: 61,253,857 (GRCm39) |
T194I |
probably benign |
Het |
| Slc6a3 |
C |
A |
13: 73,692,936 (GRCm39) |
N185K |
probably damaging |
Het |
| Stag1 |
T |
C |
9: 100,730,758 (GRCm39) |
V391A |
probably damaging |
Het |
| Syne2 |
A |
C |
12: 75,996,075 (GRCm39) |
N2206T |
probably damaging |
Het |
| Tbc1d23 |
C |
A |
16: 57,003,325 (GRCm39) |
R481I |
possibly damaging |
Het |
| Tcstv7b |
T |
C |
13: 120,702,362 (GRCm39) |
W53R |
probably damaging |
Het |
| Tfam |
A |
G |
10: 71,069,225 (GRCm39) |
S166P |
probably benign |
Het |
| Tmem63a |
A |
G |
1: 180,784,056 (GRCm39) |
H212R |
probably benign |
Het |
| Txndc11 |
T |
A |
16: 10,902,745 (GRCm39) |
Q634L |
possibly damaging |
Het |
| Usp31 |
T |
C |
7: 121,306,548 (GRCm39) |
|
probably benign |
Het |
| Vmn1r204 |
A |
T |
13: 22,740,962 (GRCm39) |
M198L |
probably damaging |
Het |
| Vmn2r17 |
A |
T |
5: 109,575,049 (GRCm39) |
T119S |
probably benign |
Het |
| Vsig1 |
A |
G |
X: 139,833,861 (GRCm39) |
D227G |
probably damaging |
Het |
| Zfhx2 |
G |
A |
14: 55,304,678 (GRCm39) |
P1102L |
probably benign |
Het |
| Zfp715 |
T |
C |
7: 42,949,444 (GRCm39) |
Q172R |
probably benign |
Het |
| Zfp872 |
A |
G |
9: 22,108,701 (GRCm39) |
D53G |
probably damaging |
Het |
| Zswim8 |
G |
A |
14: 20,764,681 (GRCm39) |
D684N |
probably benign |
Het |
|
| Other mutations in Ncapd3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00339:Ncapd3
|
APN |
9 |
26,963,649 (GRCm39) |
missense |
probably benign |
|
|
IGL00544:Ncapd3
|
APN |
9 |
26,974,634 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL01657:Ncapd3
|
APN |
9 |
26,983,120 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
IGL01979:Ncapd3
|
APN |
9 |
26,983,261 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02073:Ncapd3
|
APN |
9 |
26,974,612 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02083:Ncapd3
|
APN |
9 |
26,963,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02383:Ncapd3
|
APN |
9 |
26,961,624 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02429:Ncapd3
|
APN |
9 |
27,000,598 (GRCm39) |
missense |
probably benign |
0.08 |
|
IGL02437:Ncapd3
|
APN |
9 |
26,975,264 (GRCm39) |
splice site |
probably benign |
|
|
IGL02861:Ncapd3
|
APN |
9 |
26,981,195 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03202:Ncapd3
|
APN |
9 |
26,983,011 (GRCm39) |
splice site |
probably benign |
|
|
IGL03219:Ncapd3
|
APN |
9 |
26,975,169 (GRCm39) |
splice site |
probably benign |
|
|
IGL03252:Ncapd3
|
APN |
9 |
26,962,745 (GRCm39) |
missense |
probably damaging |
1.00 |
|
pevensie
|
UTSW |
9 |
26,997,342 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0015:Ncapd3
|
UTSW |
9 |
26,963,105 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0015:Ncapd3
|
UTSW |
9 |
26,963,105 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0084:Ncapd3
|
UTSW |
9 |
26,967,407 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0491:Ncapd3
|
UTSW |
9 |
26,969,179 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0513:Ncapd3
|
UTSW |
9 |
26,975,401 (GRCm39) |
splice site |
probably benign |
|
|
R0565:Ncapd3
|
UTSW |
9 |
26,999,294 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0601:Ncapd3
|
UTSW |
9 |
26,952,803 (GRCm39) |
missense |
probably benign |
0.05 |
|
R0671:Ncapd3
|
UTSW |
9 |
26,998,773 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0673:Ncapd3
|
UTSW |
9 |
26,998,773 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0842:Ncapd3
|
UTSW |
9 |
26,948,380 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1178:Ncapd3
|
UTSW |
9 |
26,952,717 (GRCm39) |
missense |
probably benign |
|
|
R1366:Ncapd3
|
UTSW |
9 |
26,969,236 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1432:Ncapd3
|
UTSW |
9 |
26,981,168 (GRCm39) |
splice site |
probably benign |
|
|
R1439:Ncapd3
|
UTSW |
9 |
26,998,862 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1532:Ncapd3
|
UTSW |
9 |
26,994,656 (GRCm39) |
nonsense |
probably null |
|
|
R2131:Ncapd3
|
UTSW |
9 |
26,994,642 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2178:Ncapd3
|
UTSW |
9 |
26,999,845 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2238:Ncapd3
|
UTSW |
9 |
26,978,320 (GRCm39) |
missense |
probably benign |
|
|
R2258:Ncapd3
|
UTSW |
9 |
26,967,368 (GRCm39) |
missense |
probably benign |
0.16 |
|
R2259:Ncapd3
|
UTSW |
9 |
26,967,368 (GRCm39) |
missense |
probably benign |
0.16 |
|
R2260:Ncapd3
|
UTSW |
9 |
26,967,368 (GRCm39) |
missense |
probably benign |
0.16 |
|
R2297:Ncapd3
|
UTSW |
9 |
26,952,797 (GRCm39) |
nonsense |
probably null |
|
|
R2877:Ncapd3
|
UTSW |
9 |
26,955,783 (GRCm39) |
splice site |
probably null |
|
|
R3612:Ncapd3
|
UTSW |
9 |
26,961,653 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3709:Ncapd3
|
UTSW |
9 |
26,963,645 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3791:Ncapd3
|
UTSW |
9 |
26,963,931 (GRCm39) |
missense |
probably benign |
0.27 |
|
R4052:Ncapd3
|
UTSW |
9 |
27,000,679 (GRCm39) |
splice site |
probably null |
|
|
R4297:Ncapd3
|
UTSW |
9 |
26,963,623 (GRCm39) |
missense |
probably benign |
|
|
R4299:Ncapd3
|
UTSW |
9 |
26,963,623 (GRCm39) |
missense |
probably benign |
|
|
R4441:Ncapd3
|
UTSW |
9 |
26,962,941 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R4572:Ncapd3
|
UTSW |
9 |
27,005,911 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4790:Ncapd3
|
UTSW |
9 |
26,963,146 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4835:Ncapd3
|
UTSW |
9 |
26,997,342 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4919:Ncapd3
|
UTSW |
9 |
26,963,071 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4928:Ncapd3
|
UTSW |
9 |
26,983,031 (GRCm39) |
nonsense |
probably null |
|
|
R4939:Ncapd3
|
UTSW |
9 |
26,975,165 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4980:Ncapd3
|
UTSW |
9 |
26,974,591 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5030:Ncapd3
|
UTSW |
9 |
26,983,062 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5052:Ncapd3
|
UTSW |
9 |
26,963,015 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5180:Ncapd3
|
UTSW |
9 |
26,962,941 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R5343:Ncapd3
|
UTSW |
9 |
26,999,349 (GRCm39) |
small deletion |
probably benign |
|
|
R5656:Ncapd3
|
UTSW |
9 |
26,962,941 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R5840:Ncapd3
|
UTSW |
9 |
27,006,054 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5900:Ncapd3
|
UTSW |
9 |
26,978,265 (GRCm39) |
missense |
probably benign |
0.26 |
|
R6093:Ncapd3
|
UTSW |
9 |
26,967,454 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6122:Ncapd3
|
UTSW |
9 |
26,975,278 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6249:Ncapd3
|
UTSW |
9 |
26,999,349 (GRCm39) |
small deletion |
probably benign |
|
|
R6428:Ncapd3
|
UTSW |
9 |
26,963,960 (GRCm39) |
splice site |
probably null |
|
|
R6432:Ncapd3
|
UTSW |
9 |
26,955,805 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6441:Ncapd3
|
UTSW |
9 |
26,974,712 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6459:Ncapd3
|
UTSW |
9 |
26,963,051 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6567:Ncapd3
|
UTSW |
9 |
26,978,300 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R6722:Ncapd3
|
UTSW |
9 |
26,998,852 (GRCm39) |
missense |
probably benign |
|
|
R6862:Ncapd3
|
UTSW |
9 |
26,942,105 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7234:Ncapd3
|
UTSW |
9 |
26,961,655 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7286:Ncapd3
|
UTSW |
9 |
26,981,254 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7404:Ncapd3
|
UTSW |
9 |
26,978,315 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7541:Ncapd3
|
UTSW |
9 |
26,978,336 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7583:Ncapd3
|
UTSW |
9 |
26,983,144 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7655:Ncapd3
|
UTSW |
9 |
26,966,801 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R7656:Ncapd3
|
UTSW |
9 |
26,966,801 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R7815:Ncapd3
|
UTSW |
9 |
26,974,736 (GRCm39) |
nonsense |
probably null |
|
|
R7876:Ncapd3
|
UTSW |
9 |
26,956,519 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7913:Ncapd3
|
UTSW |
9 |
26,959,522 (GRCm39) |
nonsense |
probably null |
|
|
R8068:Ncapd3
|
UTSW |
9 |
26,974,657 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R8147:Ncapd3
|
UTSW |
9 |
26,942,014 (GRCm39) |
start gained |
probably benign |
|
|
R8197:Ncapd3
|
UTSW |
9 |
26,997,329 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8264:Ncapd3
|
UTSW |
9 |
27,006,038 (GRCm39) |
unclassified |
probably benign |
|
|
R8353:Ncapd3
|
UTSW |
9 |
26,983,100 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8539:Ncapd3
|
UTSW |
9 |
26,959,520 (GRCm39) |
missense |
probably benign |
|
|
R8839:Ncapd3
|
UTSW |
9 |
27,005,730 (GRCm39) |
missense |
|
|
|
R8917:Ncapd3
|
UTSW |
9 |
26,999,297 (GRCm39) |
missense |
probably benign |
|
|
R8997:Ncapd3
|
UTSW |
9 |
26,959,577 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9215:Ncapd3
|
UTSW |
9 |
26,975,386 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R9393:Ncapd3
|
UTSW |
9 |
26,962,682 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R9412:Ncapd3
|
UTSW |
9 |
26,967,451 (GRCm39) |
nonsense |
probably null |
|
|
R9688:Ncapd3
|
UTSW |
9 |
26,967,349 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9746:Ncapd3
|
UTSW |
9 |
26,974,655 (GRCm39) |
missense |
probably benign |
|
|
R9749:Ncapd3
|
UTSW |
9 |
26,956,873 (GRCm39) |
missense |
probably benign |
0.14 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTGTCAGAGAAACACGAAGCC -3'
(R):5'- GTTGGTTAGACAAACACAAGCTG -3'
Sequencing Primer
(F):5'- GCCCAAGAACAAGGAAGTGAC -3'
(R):5'- GACACACTGATGTCCTAGGCAG -3'
|
| Posted On |
2015-10-08 |
Incidental Mutation