Incidental Mutation 'R4675:Stag1'
| ID |
349507 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Stag1
|
| Ensembl Gene |
ENSMUSG00000037286 |
| Gene Name |
STAG1 cohesin complex component |
| Synonyms |
SA-1, Scc3 |
| MMRRC Submission |
041930-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R4675 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
9 |
| Chromosomal Location |
100479762-100840597 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 100730758 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 391
(V391A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000116205
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000041418]
[ENSMUST00000123302]
[ENSMUST00000129269]
[ENSMUST00000138405]
[ENSMUST00000155108]
|
| AlphaFold |
Q9D3E6 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000041418
AA Change: V391A
PolyPhen 2
Score 0.946 (Sensitivity: 0.80; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000040724
Gene: ENSMUSG00000037286
AA Change: V391A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
32 |
44 |
N/A |
INTRINSIC |
|
low complexity region
|
59 |
72 |
N/A |
INTRINSIC |
|
Pfam:STAG
|
157 |
276 |
1.5e-50 |
PFAM |
|
SCOP:d1qbkb_
|
279 |
850 |
4e-5 |
SMART |
|
low complexity region
|
1062 |
1081 |
N/A |
INTRINSIC |
|
low complexity region
|
1107 |
1120 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000122824
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000123302
AA Change: V391A
PolyPhen 2
Score 0.946 (Sensitivity: 0.80; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000117879
Gene: ENSMUSG00000037286
AA Change: V391A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
32 |
44 |
N/A |
INTRINSIC |
|
low complexity region
|
59 |
72 |
N/A |
INTRINSIC |
|
Pfam:STAG
|
157 |
276 |
2.9e-51 |
PFAM |
|
low complexity region
|
303 |
315 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000129269
AA Change: V391A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000116205
Gene: ENSMUSG00000037286
AA Change: V391A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
32 |
44 |
N/A |
INTRINSIC |
|
low complexity region
|
59 |
72 |
N/A |
INTRINSIC |
|
Pfam:STAG
|
160 |
274 |
3.8e-41 |
PFAM |
|
SCOP:d1qbkb_
|
279 |
850 |
3e-5 |
SMART |
|
low complexity region
|
1062 |
1081 |
N/A |
INTRINSIC |
|
low complexity region
|
1107 |
1120 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000138405
|
| SMART Domains |
Protein: ENSMUSP00000116322
Gene: ENSMUSG00000037286
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
32 |
44 |
N/A |
INTRINSIC |
|
low complexity region
|
59 |
72 |
N/A |
INTRINSIC |
|
Pfam:STAG
|
157 |
276 |
1.5e-51 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000143150
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000146934
AA Change: V37A
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000120974
Gene: ENSMUSG00000037286
AA Change: V37A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
673 |
692 |
N/A |
INTRINSIC |
|
low complexity region
|
718 |
731 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000149771
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000155108
|
| SMART Domains |
Protein: ENSMUSP00000118952
Gene: ENSMUSG00000037286
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
32 |
44 |
N/A |
INTRINSIC |
|
low complexity region
|
59 |
72 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.3125 |
| 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.] This gene is a member of the SCC3 family and is expressed in the nucleus. It encodes a component of cohesin, a multisubunit protein complex that provides sister chromatid cohesion along the length of a chromosome from DNA replication through prophase and prometaphase, after which it is dissociated in preparation for segregation during anaphase. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mouse embryos homozygous for a null mutation show developmental delay and die before birth. Heterozygous animals have shorter lifespan and earlier onset of tumourigenesis. [provided by MGI curators]
|
| 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 |
| Ncapd3 |
T |
C |
9: 27,006,038 (GRCm39) |
|
probably benign |
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 |
A |
AGGGCGACGG |
7: 97,229,111 (GRCm39) |
|
probably null |
Het |
| Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
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 |
| 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 Stag1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00649:Stag1
|
APN |
9 |
100,658,861 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01010:Stag1
|
APN |
9 |
100,827,986 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL01012:Stag1
|
APN |
9 |
100,737,912 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
IGL01025:Stag1
|
APN |
9 |
100,833,710 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL01307:Stag1
|
APN |
9 |
100,833,841 (GRCm39) |
intron |
probably benign |
|
|
IGL02149:Stag1
|
APN |
9 |
100,769,442 (GRCm39) |
missense |
probably benign |
0.09 |
|
IGL02608:Stag1
|
APN |
9 |
100,639,822 (GRCm39) |
missense |
probably null |
0.99 |
|
IGL03008:Stag1
|
APN |
9 |
100,658,844 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03210:Stag1
|
APN |
9 |
100,727,129 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
eto_o
|
UTSW |
9 |
100,678,769 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4280001:Stag1
|
UTSW |
9 |
100,824,769 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0070:Stag1
|
UTSW |
9 |
100,838,461 (GRCm39) |
missense |
probably null |
1.00 |
|
R0070:Stag1
|
UTSW |
9 |
100,838,461 (GRCm39) |
missense |
probably null |
1.00 |
|
R0349:Stag1
|
UTSW |
9 |
100,658,837 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0479:Stag1
|
UTSW |
9 |
100,810,144 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0531:Stag1
|
UTSW |
9 |
100,836,300 (GRCm39) |
makesense |
probably null |
|
|
R0962:Stag1
|
UTSW |
9 |
100,678,880 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0976:Stag1
|
UTSW |
9 |
100,812,069 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0976:Stag1
|
UTSW |
9 |
100,658,877 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1170:Stag1
|
UTSW |
9 |
100,770,506 (GRCm39) |
intron |
probably benign |
|
|
R1499:Stag1
|
UTSW |
9 |
100,769,426 (GRCm39) |
intron |
probably benign |
|
|
R1499:Stag1
|
UTSW |
9 |
100,737,885 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R1644:Stag1
|
UTSW |
9 |
100,762,953 (GRCm39) |
intron |
probably benign |
|
|
R1747:Stag1
|
UTSW |
9 |
100,770,353 (GRCm39) |
missense |
probably benign |
|
|
R1799:Stag1
|
UTSW |
9 |
100,835,515 (GRCm39) |
splice site |
probably null |
|
|
R1807:Stag1
|
UTSW |
9 |
100,790,719 (GRCm39) |
missense |
probably benign |
0.34 |
|
R1978:Stag1
|
UTSW |
9 |
100,770,139 (GRCm39) |
missense |
probably benign |
0.03 |
|
R2029:Stag1
|
UTSW |
9 |
100,668,740 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2161:Stag1
|
UTSW |
9 |
100,771,648 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2300:Stag1
|
UTSW |
9 |
100,594,553 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R2327:Stag1
|
UTSW |
9 |
100,668,666 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R2426:Stag1
|
UTSW |
9 |
100,727,169 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2448:Stag1
|
UTSW |
9 |
100,770,462 (GRCm39) |
missense |
probably benign |
0.42 |
|
R2504:Stag1
|
UTSW |
9 |
100,748,263 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3713:Stag1
|
UTSW |
9 |
100,771,671 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3835:Stag1
|
UTSW |
9 |
100,620,035 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R3862:Stag1
|
UTSW |
9 |
100,826,838 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4398:Stag1
|
UTSW |
9 |
100,838,659 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R4568:Stag1
|
UTSW |
9 |
100,730,722 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4651:Stag1
|
UTSW |
9 |
100,678,769 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4652:Stag1
|
UTSW |
9 |
100,678,769 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4653:Stag1
|
UTSW |
9 |
100,678,769 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4709:Stag1
|
UTSW |
9 |
100,620,092 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4924:Stag1
|
UTSW |
9 |
100,678,808 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R5018:Stag1
|
UTSW |
9 |
100,833,672 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5435:Stag1
|
UTSW |
9 |
100,835,603 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5460:Stag1
|
UTSW |
9 |
100,838,506 (GRCm39) |
splice site |
probably null |
|
|
R5805:Stag1
|
UTSW |
9 |
100,678,831 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6127:Stag1
|
UTSW |
9 |
100,833,750 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6313:Stag1
|
UTSW |
9 |
100,639,786 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6597:Stag1
|
UTSW |
9 |
100,769,473 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6807:Stag1
|
UTSW |
9 |
100,826,903 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7099:Stag1
|
UTSW |
9 |
100,826,879 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7167:Stag1
|
UTSW |
9 |
100,827,942 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7395:Stag1
|
UTSW |
9 |
100,678,781 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7504:Stag1
|
UTSW |
9 |
100,770,381 (GRCm39) |
missense |
probably benign |
0.09 |
|
R7663:Stag1
|
UTSW |
9 |
100,620,191 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7769:Stag1
|
UTSW |
9 |
100,826,880 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R8245:Stag1
|
UTSW |
9 |
100,811,946 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8343:Stag1
|
UTSW |
9 |
100,639,819 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8473:Stag1
|
UTSW |
9 |
100,762,840 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8709:Stag1
|
UTSW |
9 |
100,772,975 (GRCm39) |
intron |
probably benign |
|
|
R8925:Stag1
|
UTSW |
9 |
100,587,298 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R8927:Stag1
|
UTSW |
9 |
100,587,298 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R8951:Stag1
|
UTSW |
9 |
100,762,854 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9138:Stag1
|
UTSW |
9 |
100,829,335 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9233:Stag1
|
UTSW |
9 |
100,812,024 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9246:Stag1
|
UTSW |
9 |
100,770,329 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9419:Stag1
|
UTSW |
9 |
100,811,967 (GRCm39) |
missense |
probably benign |
|
|
R9442:Stag1
|
UTSW |
9 |
100,836,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9694:Stag1
|
UTSW |
9 |
100,810,151 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9740:Stag1
|
UTSW |
9 |
100,587,288 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- CCCCACTTAAATAAGATGGTTTCAAG -3'
(R):5'- GACTGCACAAACAAACTTTTATACG -3'
Sequencing Primer
(F):5'- GCTTTAATCCTGGCACTAGGGAAC -3'
(R):5'- CCGAACCTGGGCTTCATTATAAG -3'
|
| Posted On |
2015-10-08 |
Incidental Mutation