Incidental Mutation 'R9393:Ncapd3'
| ID |
710679 |
| 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 |
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.962)
|
| Stock # |
R9393 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
26941471-27006611 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 26962682 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 373
(T373A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000083374
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000073127]
[ENSMUST00000086198]
[ENSMUST00000216677]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000073127
AA Change: T373A
PolyPhen 2
Score 0.143 (Sensitivity: 0.92; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000072871
Gene: ENSMUSG00000035024
AA Change: T373A
| 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 |
possibly damaging
Transcript: ENSMUST00000086198
AA Change: T373A
PolyPhen 2
Score 0.538 (Sensitivity: 0.88; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000083374
Gene: ENSMUSG00000035024
AA Change: T373A
| 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 |
probably benign
Transcript: ENSMUST00000216677
AA Change: T373A
PolyPhen 2
Score 0.143 (Sensitivity: 0.92; Specificity: 0.86)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.7%
|
| Validation Efficiency |
|
| 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: 74 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A2m |
A |
G |
6: 121,616,270 (GRCm39) |
S133G |
possibly damaging |
Het |
| Agps |
A |
G |
2: 75,735,256 (GRCm39) |
E567G |
possibly damaging |
Het |
| Ak9 |
T |
C |
10: 41,285,068 (GRCm39) |
I1381T |
unknown |
Het |
| Apcdd1 |
C |
T |
18: 63,055,731 (GRCm39) |
|
probably benign |
Het |
| Arrb1 |
T |
A |
7: 99,238,891 (GRCm39) |
C150S |
probably damaging |
Het |
| Asz1 |
T |
C |
6: 18,051,330 (GRCm39) |
I450V |
probably benign |
Het |
| Atp10b |
A |
G |
11: 43,063,608 (GRCm39) |
N181S |
probably damaging |
Het |
| Bptf |
A |
C |
11: 106,965,134 (GRCm39) |
D1353E |
probably benign |
Het |
| Cacna2d1 |
T |
C |
5: 16,140,013 (GRCm39) |
M1T |
probably null |
Het |
| Ccdc106 |
T |
A |
7: 5,059,200 (GRCm39) |
I6N |
possibly damaging |
Het |
| Celf6 |
A |
T |
9: 59,510,525 (GRCm39) |
Q252L |
probably benign |
Het |
| Colgalt2 |
A |
T |
1: 152,360,598 (GRCm39) |
K212* |
probably null |
Het |
| Cryba4 |
T |
C |
5: 112,394,632 (GRCm39) |
S166G |
probably benign |
Het |
| Cyp2w1 |
A |
G |
5: 139,342,035 (GRCm39) |
E123G |
probably benign |
Het |
| Cyp4a10 |
G |
C |
4: 115,382,566 (GRCm39) |
K285N |
probably damaging |
Het |
| Cyth1 |
G |
T |
11: 118,074,710 (GRCm39) |
T197K |
probably benign |
Het |
| Ddhd1 |
A |
G |
14: 45,894,685 (GRCm39) |
W262R |
probably damaging |
Het |
| Dnah8 |
T |
A |
17: 30,872,361 (GRCm39) |
V450D |
possibly damaging |
Het |
| Eml5 |
C |
T |
12: 98,842,433 (GRCm39) |
V222I |
probably benign |
Het |
| Fbxw19 |
A |
G |
9: 109,324,873 (GRCm39) |
S15P |
probably damaging |
Het |
| Fhip2b |
G |
A |
14: 70,831,463 (GRCm39) |
Q24* |
probably null |
Het |
| Fignl2 |
C |
A |
15: 100,951,466 (GRCm39) |
R272L |
unknown |
Het |
| Gm10842 |
A |
T |
11: 105,037,885 (GRCm39) |
D56V |
unknown |
Het |
| Gmps |
T |
A |
3: 63,900,640 (GRCm39) |
N305K |
probably benign |
Het |
| Gnai1 |
A |
T |
5: 18,565,055 (GRCm39) |
L38Q |
|
Het |
| Golim4 |
A |
T |
3: 75,785,464 (GRCm39) |
D642E |
probably benign |
Het |
| Gp1ba |
A |
T |
11: 70,531,293 (GRCm39) |
Q353L |
unknown |
Het |
| Gpnmb |
T |
C |
6: 49,024,996 (GRCm39) |
S343P |
possibly damaging |
Het |
| Hexb |
G |
A |
13: 97,313,336 (GRCm39) |
R507* |
probably null |
Het |
| Ifitm10 |
A |
T |
7: 141,924,704 (GRCm39) |
V45D |
probably damaging |
Het |
| Khsrp |
T |
C |
17: 57,330,350 (GRCm39) |
Y585C |
probably damaging |
Het |
| Kif21a |
A |
T |
15: 90,853,981 (GRCm39) |
D795E |
probably benign |
Het |
| Klkb1 |
A |
T |
8: 45,729,392 (GRCm39) |
V309E |
probably benign |
Het |
| Krtap9-1 |
C |
A |
11: 99,764,664 (GRCm39) |
C133* |
probably null |
Het |
| Krtcap2 |
T |
C |
3: 89,153,578 (GRCm39) |
|
probably benign |
Het |
| Lilra5 |
T |
C |
7: 4,240,758 (GRCm39) |
M1T |
probably null |
Het |
| Magi1 |
G |
A |
6: 93,659,890 (GRCm39) |
T1019I |
probably benign |
Het |
| Mdn1 |
T |
A |
4: 32,713,825 (GRCm39) |
H1967Q |
|
Het |
| Mgat4f |
A |
G |
1: 134,318,596 (GRCm39) |
D456G |
probably benign |
Het |
| Mroh2b |
A |
T |
15: 4,980,666 (GRCm39) |
T1412S |
probably benign |
Het |
| Myh13 |
A |
T |
11: 67,242,894 (GRCm39) |
M936L |
probably benign |
Het |
| Nalf2 |
C |
T |
X: 98,889,097 (GRCm39) |
R321W |
probably damaging |
Het |
| Noc2l |
T |
C |
4: 156,320,784 (GRCm39) |
|
probably null |
Het |
| Nrg4 |
C |
T |
9: 55,149,420 (GRCm39) |
S59N |
probably benign |
Het |
| Nrip1 |
A |
G |
16: 76,091,353 (GRCm39) |
V68A |
probably benign |
Het |
| Or11g24 |
T |
C |
14: 50,662,255 (GRCm39) |
V93A |
probably benign |
Het |
| Or9k2 |
T |
C |
10: 129,999,016 (GRCm39) |
T60A |
probably benign |
Het |
| Pcdhga6 |
G |
T |
18: 37,840,212 (GRCm39) |
|
probably benign |
Het |
| Phf20l1 |
A |
G |
15: 66,475,955 (GRCm39) |
N196S |
probably damaging |
Het |
| Ppp4r4 |
T |
A |
12: 103,571,296 (GRCm39) |
Y787* |
probably null |
Het |
| Psma8 |
G |
A |
18: 14,839,298 (GRCm39) |
R4Q |
probably null |
Het |
| Reg4 |
A |
G |
3: 98,137,168 (GRCm39) |
K46E |
probably benign |
Het |
| Rnf14 |
T |
A |
18: 38,442,680 (GRCm39) |
M327K |
possibly damaging |
Het |
| Rtn1 |
A |
T |
12: 72,263,586 (GRCm39) |
Y753* |
probably null |
Het |
| Slc26a11 |
A |
G |
11: 119,259,627 (GRCm39) |
R275G |
probably benign |
Het |
| Stard9 |
A |
G |
2: 120,518,656 (GRCm39) |
T527A |
possibly damaging |
Het |
| Stk26 |
C |
T |
X: 49,930,618 (GRCm39) |
|
probably benign |
Het |
| Tas1r1 |
C |
T |
4: 152,116,413 (GRCm39) |
C407Y |
probably damaging |
Het |
| Tcstv1b |
A |
T |
13: 120,634,958 (GRCm39) |
Y80F |
probably benign |
Het |
| Tenm3 |
A |
G |
8: 49,127,559 (GRCm39) |
S40P |
probably damaging |
Het |
| Tespa1 |
T |
A |
10: 130,183,066 (GRCm39) |
S4T |
probably damaging |
Het |
| Tlr11 |
A |
G |
14: 50,599,547 (GRCm39) |
N511S |
probably benign |
Het |
| Tmprss15 |
A |
G |
16: 78,754,211 (GRCm39) |
I1014T |
probably benign |
Het |
| Tpte |
T |
A |
8: 22,774,990 (GRCm39) |
M20K |
probably benign |
Het |
| Ttn |
A |
G |
2: 76,612,390 (GRCm39) |
V17199A |
possibly damaging |
Het |
| Tubgcp3 |
A |
G |
8: 12,703,411 (GRCm39) |
Y305H |
probably damaging |
Het |
| Ubr4 |
T |
A |
4: 139,212,613 (GRCm39) |
V5081E |
unknown |
Het |
| Unkl |
T |
C |
17: 25,448,392 (GRCm39) |
S322P |
probably damaging |
Het |
| Uqcc6 |
A |
G |
10: 82,458,475 (GRCm39) |
S59P |
unknown |
Het |
| Vav3 |
T |
A |
3: 109,485,682 (GRCm39) |
|
probably null |
Het |
| Vmn1r76 |
A |
G |
7: 11,664,765 (GRCm39) |
S150P |
probably benign |
Het |
| Xpot |
A |
G |
10: 121,445,600 (GRCm39) |
|
probably null |
Het |
| Xylt1 |
A |
G |
7: 117,242,906 (GRCm39) |
I650V |
probably benign |
Het |
| Zan |
C |
A |
5: 137,403,682 (GRCm39) |
A3955S |
unknown |
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 |
|
R4675:Ncapd3
|
UTSW |
9 |
27,006,038 (GRCm39) |
unclassified |
probably benign |
|
|
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 |
|
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'- TCTGCATAGAGGCTTATAGTTTAGGC -3'
(R):5'- TGAAGACCCGGTGTGGAATC -3'
Sequencing Primer
(F):5'- ATAGTTTAGGCCTCAGTGGGATAAG -3'
(R):5'- CCGGTGTGGAATCTGGCAAG -3'
|
| Posted On |
2022-04-18 |
Incidental Mutation