Incidental Mutation 'R9328:Bahcc1'
| ID |
706670 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Bahcc1
|
| Ensembl Gene |
ENSMUSG00000039741 |
| Gene Name |
BAH domain and coiled-coil containing 1 |
| Synonyms |
|
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.871)
|
| Stock # |
R9328 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
120123773-120183108 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 120165885 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 1047
(T1047I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000112827
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044985]
[ENSMUST00000118987]
[ENSMUST00000122148]
|
| AlphaFold |
Q3UHR0 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000044985
AA Change: T1047I
PolyPhen 2
Score 0.612 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000043643
Gene: ENSMUSG00000039741
AA Change: T1047I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
46 |
N/A |
INTRINSIC |
|
low complexity region
|
219 |
233 |
N/A |
INTRINSIC |
|
low complexity region
|
351 |
366 |
N/A |
INTRINSIC |
|
low complexity region
|
756 |
778 |
N/A |
INTRINSIC |
|
low complexity region
|
811 |
821 |
N/A |
INTRINSIC |
|
low complexity region
|
882 |
890 |
N/A |
INTRINSIC |
|
coiled coil region
|
931 |
976 |
N/A |
INTRINSIC |
|
low complexity region
|
1042 |
1059 |
N/A |
INTRINSIC |
|
low complexity region
|
1127 |
1139 |
N/A |
INTRINSIC |
|
low complexity region
|
1172 |
1183 |
N/A |
INTRINSIC |
|
low complexity region
|
1267 |
1277 |
N/A |
INTRINSIC |
|
coiled coil region
|
1346 |
1373 |
N/A |
INTRINSIC |
|
coiled coil region
|
1437 |
1486 |
N/A |
INTRINSIC |
|
low complexity region
|
1706 |
1711 |
N/A |
INTRINSIC |
|
low complexity region
|
1729 |
1740 |
N/A |
INTRINSIC |
|
low complexity region
|
1746 |
1764 |
N/A |
INTRINSIC |
|
low complexity region
|
1865 |
1891 |
N/A |
INTRINSIC |
|
low complexity region
|
2088 |
2104 |
N/A |
INTRINSIC |
|
low complexity region
|
2135 |
2158 |
N/A |
INTRINSIC |
|
low complexity region
|
2209 |
2224 |
N/A |
INTRINSIC |
|
low complexity region
|
2225 |
2245 |
N/A |
INTRINSIC |
|
low complexity region
|
2317 |
2332 |
N/A |
INTRINSIC |
|
low complexity region
|
2348 |
2387 |
N/A |
INTRINSIC |
|
low complexity region
|
2401 |
2410 |
N/A |
INTRINSIC |
|
low complexity region
|
2429 |
2447 |
N/A |
INTRINSIC |
|
BAH
|
2517 |
2637 |
4.19e-20 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000118987
AA Change: T1047I
PolyPhen 2
Score 0.612 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000112784
Gene: ENSMUSG00000039741
AA Change: T1047I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
46 |
N/A |
INTRINSIC |
|
low complexity region
|
219 |
233 |
N/A |
INTRINSIC |
|
low complexity region
|
351 |
366 |
N/A |
INTRINSIC |
|
low complexity region
|
756 |
778 |
N/A |
INTRINSIC |
|
low complexity region
|
811 |
821 |
N/A |
INTRINSIC |
|
low complexity region
|
882 |
890 |
N/A |
INTRINSIC |
|
coiled coil region
|
931 |
976 |
N/A |
INTRINSIC |
|
low complexity region
|
1042 |
1059 |
N/A |
INTRINSIC |
|
low complexity region
|
1127 |
1139 |
N/A |
INTRINSIC |
|
low complexity region
|
1172 |
1183 |
N/A |
INTRINSIC |
|
low complexity region
|
1267 |
1277 |
N/A |
INTRINSIC |
|
coiled coil region
|
1346 |
1373 |
N/A |
INTRINSIC |
|
coiled coil region
|
1437 |
1486 |
N/A |
INTRINSIC |
|
low complexity region
|
1706 |
1711 |
N/A |
INTRINSIC |
|
low complexity region
|
1729 |
1740 |
N/A |
INTRINSIC |
|
low complexity region
|
1746 |
1764 |
N/A |
INTRINSIC |
|
low complexity region
|
1865 |
1891 |
N/A |
INTRINSIC |
|
low complexity region
|
2088 |
2104 |
N/A |
INTRINSIC |
|
low complexity region
|
2135 |
2158 |
N/A |
INTRINSIC |
|
low complexity region
|
2209 |
2224 |
N/A |
INTRINSIC |
|
low complexity region
|
2225 |
2245 |
N/A |
INTRINSIC |
|
low complexity region
|
2317 |
2332 |
N/A |
INTRINSIC |
|
low complexity region
|
2348 |
2387 |
N/A |
INTRINSIC |
|
low complexity region
|
2401 |
2410 |
N/A |
INTRINSIC |
|
low complexity region
|
2429 |
2447 |
N/A |
INTRINSIC |
|
BAH
|
2517 |
2637 |
4.19e-20 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000122148
AA Change: T1047I
PolyPhen 2
Score 0.612 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000112827
Gene: ENSMUSG00000039741
AA Change: T1047I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
46 |
N/A |
INTRINSIC |
|
low complexity region
|
219 |
233 |
N/A |
INTRINSIC |
|
low complexity region
|
351 |
366 |
N/A |
INTRINSIC |
|
low complexity region
|
756 |
778 |
N/A |
INTRINSIC |
|
low complexity region
|
811 |
821 |
N/A |
INTRINSIC |
|
low complexity region
|
882 |
890 |
N/A |
INTRINSIC |
|
coiled coil region
|
931 |
976 |
N/A |
INTRINSIC |
|
low complexity region
|
1042 |
1059 |
N/A |
INTRINSIC |
|
low complexity region
|
1127 |
1139 |
N/A |
INTRINSIC |
|
low complexity region
|
1172 |
1183 |
N/A |
INTRINSIC |
|
low complexity region
|
1267 |
1277 |
N/A |
INTRINSIC |
|
coiled coil region
|
1346 |
1373 |
N/A |
INTRINSIC |
|
coiled coil region
|
1437 |
1486 |
N/A |
INTRINSIC |
|
low complexity region
|
1706 |
1711 |
N/A |
INTRINSIC |
|
low complexity region
|
1729 |
1740 |
N/A |
INTRINSIC |
|
low complexity region
|
1746 |
1764 |
N/A |
INTRINSIC |
|
low complexity region
|
1865 |
1891 |
N/A |
INTRINSIC |
|
low complexity region
|
2088 |
2104 |
N/A |
INTRINSIC |
|
low complexity region
|
2135 |
2158 |
N/A |
INTRINSIC |
|
low complexity region
|
2209 |
2224 |
N/A |
INTRINSIC |
|
low complexity region
|
2225 |
2245 |
N/A |
INTRINSIC |
|
low complexity region
|
2317 |
2332 |
N/A |
INTRINSIC |
|
low complexity region
|
2348 |
2387 |
N/A |
INTRINSIC |
|
low complexity region
|
2401 |
2410 |
N/A |
INTRINSIC |
|
low complexity region
|
2429 |
2447 |
N/A |
INTRINSIC |
|
BAH
|
2517 |
2637 |
4.19e-20 |
SMART |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Homozygous mutation of this gene results in perinatal lethality for the majority of mutants. Those that survive exhibit hind leg motor dysfunction. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(26) : Targeted, knock-out(2) Gene trapped(24) |
| Other mutations in this stock |
Total: 80 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1600014C10Rik |
A |
G |
7: 37,894,272 (GRCm39) |
T102A |
probably benign |
Het |
| 1700109H08Rik |
A |
G |
5: 3,632,161 (GRCm39) |
K164E |
possibly damaging |
Het |
| 2610042L04Rik |
C |
T |
14: 4,350,013 (GRCm38) |
Q74* |
probably null |
Het |
| Aadacl4fm4 |
T |
A |
4: 144,401,256 (GRCm39) |
H76L |
probably benign |
Het |
| Adgrb2 |
T |
A |
4: 129,915,363 (GRCm39) |
M1381K |
probably damaging |
Het |
| Adgrv1 |
C |
A |
13: 81,620,523 (GRCm39) |
D3975Y |
probably damaging |
Het |
| Ano10 |
C |
T |
9: 122,090,168 (GRCm39) |
E382K |
possibly damaging |
Het |
| Ascc3 |
T |
C |
10: 50,535,015 (GRCm39) |
V636A |
probably damaging |
Het |
| AU040320 |
T |
C |
4: 126,729,332 (GRCm39) |
V498A |
possibly damaging |
Het |
| BC004004 |
A |
T |
17: 29,501,682 (GRCm39) |
T74S |
possibly damaging |
Het |
| Bend3 |
A |
G |
10: 43,387,419 (GRCm39) |
D604G |
possibly damaging |
Het |
| Brinp3 |
T |
A |
1: 146,707,455 (GRCm39) |
V373E |
probably damaging |
Het |
| Bsph2 |
A |
T |
7: 13,290,764 (GRCm39) |
D38E |
probably benign |
Het |
| Castor1 |
T |
C |
11: 4,170,423 (GRCm39) |
F140L |
probably benign |
Het |
| Catsperd |
A |
G |
17: 56,965,074 (GRCm39) |
I474V |
possibly damaging |
Het |
| Ccdc180 |
A |
G |
4: 45,902,447 (GRCm39) |
N292S |
possibly damaging |
Het |
| Cd1d1 |
A |
T |
3: 86,905,459 (GRCm39) |
V178E |
possibly damaging |
Het |
| Cdca2 |
T |
A |
14: 67,931,131 (GRCm39) |
R521W |
probably damaging |
Het |
| Champ1 |
A |
G |
8: 13,929,392 (GRCm39) |
K517E |
probably damaging |
Het |
| Chrna9 |
T |
C |
5: 66,128,569 (GRCm39) |
F259S |
probably damaging |
Het |
| Chuk |
A |
T |
19: 44,085,422 (GRCm39) |
C241* |
probably null |
Het |
| Clns1a |
A |
G |
7: 97,363,240 (GRCm39) |
Y204C |
probably benign |
Het |
| Cplane1 |
A |
G |
15: 8,215,692 (GRCm39) |
D416G |
probably damaging |
Het |
| Cyp2j7 |
A |
T |
4: 96,115,869 (GRCm39) |
N192K |
probably damaging |
Het |
| Ddr2 |
A |
G |
1: 169,829,504 (GRCm39) |
V250A |
probably benign |
Het |
| Dlgap2 |
A |
G |
8: 14,777,441 (GRCm39) |
S229G |
probably damaging |
Het |
| Dmrt1 |
A |
T |
19: 25,523,231 (GRCm39) |
H194L |
probably damaging |
Het |
| Dock7 |
A |
T |
4: 98,968,064 (GRCm39) |
F138I |
|
Het |
| Dsg2 |
T |
C |
18: 20,715,847 (GRCm39) |
V263A |
possibly damaging |
Het |
| Dusp16 |
A |
G |
6: 134,716,902 (GRCm39) |
L135P |
probably damaging |
Het |
| Dysf |
A |
G |
6: 84,050,895 (GRCm39) |
N414S |
probably damaging |
Het |
| Efhc1 |
A |
G |
1: 21,030,598 (GRCm39) |
Y177C |
probably damaging |
Het |
| Fam83e |
A |
T |
7: 45,372,912 (GRCm39) |
R174S |
probably benign |
Het |
| Fgf4 |
C |
T |
7: 144,416,664 (GRCm39) |
L199F |
probably damaging |
Het |
| Fignl2 |
A |
G |
15: 100,951,271 (GRCm39) |
L337P |
unknown |
Het |
| Gm4353 |
T |
C |
7: 115,682,724 (GRCm39) |
R286G |
probably damaging |
Het |
| Gm5142 |
T |
C |
14: 59,416,126 (GRCm39) |
S11G |
probably benign |
Het |
| Gpr151 |
A |
G |
18: 42,712,270 (GRCm39) |
V136A |
probably damaging |
Het |
| Ift80 |
T |
A |
3: 68,847,483 (GRCm39) |
I338F |
probably damaging |
Het |
| Itgb4 |
A |
G |
11: 115,880,625 (GRCm39) |
S693G |
probably benign |
Het |
| Kif13a |
T |
A |
13: 46,951,838 (GRCm39) |
I812F |
probably damaging |
Het |
| Krit1 |
T |
C |
5: 3,862,577 (GRCm39) |
|
probably null |
Het |
| Mapk6 |
T |
C |
9: 75,305,252 (GRCm39) |
D55G |
possibly damaging |
Het |
| Matn3 |
A |
G |
12: 9,002,033 (GRCm39) |
I82V |
possibly damaging |
Het |
| Mecom |
T |
A |
3: 30,063,994 (GRCm39) |
D32V |
unknown |
Het |
| Nacad |
T |
C |
11: 6,552,417 (GRCm39) |
H258R |
possibly damaging |
Het |
| Ndufaf5 |
T |
A |
2: 140,030,752 (GRCm39) |
S213T |
possibly damaging |
Het |
| Nphp1 |
C |
T |
2: 127,582,892 (GRCm39) |
D674N |
possibly damaging |
Het |
| Nsmaf |
A |
G |
4: 6,426,412 (GRCm39) |
L250P |
probably damaging |
Het |
| Ogdh |
T |
C |
11: 6,297,838 (GRCm39) |
S571P |
probably benign |
Het |
| Or1e31 |
T |
C |
11: 73,690,478 (GRCm39) |
Y35C |
probably damaging |
Het |
| Or51i2 |
T |
A |
7: 103,689,268 (GRCm39) |
D88E |
|
Het |
| Or8g27 |
T |
C |
9: 39,129,175 (GRCm39) |
I174T |
probably damaging |
Het |
| Osbpl11 |
A |
G |
16: 33,047,245 (GRCm39) |
I403V |
probably damaging |
Het |
| Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
| Pira13 |
T |
A |
7: 3,827,580 (GRCm39) |
R192S |
unknown |
Het |
| Plat |
A |
G |
8: 23,268,133 (GRCm39) |
R300G |
probably damaging |
Het |
| Ppid |
T |
C |
3: 79,505,059 (GRCm39) |
I134T |
probably damaging |
Het |
| Rad51ap2 |
A |
G |
12: 11,507,772 (GRCm39) |
I565V |
probably benign |
Het |
| Rasa1 |
T |
C |
13: 85,403,575 (GRCm39) |
|
probably null |
Het |
| Sema4a |
C |
T |
3: 88,345,613 (GRCm39) |
W490* |
probably null |
Het |
| Septin3 |
A |
G |
15: 82,173,439 (GRCm39) |
Y257C |
probably damaging |
Het |
| Sh3rf2 |
C |
A |
18: 42,274,161 (GRCm39) |
F442L |
probably benign |
Het |
| Sipa1l1 |
A |
G |
12: 82,388,792 (GRCm39) |
I339M |
possibly damaging |
Het |
| Six2 |
T |
C |
17: 85,995,196 (GRCm39) |
N62S |
possibly damaging |
Het |
| Slc44a5 |
T |
C |
3: 153,964,678 (GRCm39) |
I526T |
probably benign |
Het |
| Smarca5 |
T |
C |
8: 81,447,378 (GRCm39) |
S402G |
probably benign |
Het |
| Son |
T |
A |
16: 91,452,645 (GRCm39) |
V464E |
possibly damaging |
Het |
| Sorcs3 |
A |
G |
19: 48,785,950 (GRCm39) |
K1144E |
probably damaging |
Het |
| Stxbp6 |
A |
G |
12: 44,902,659 (GRCm39) |
L204P |
probably damaging |
Het |
| Tchh |
A |
G |
3: 93,351,570 (GRCm39) |
R337G |
unknown |
Het |
| Tgm4 |
T |
C |
9: 122,885,697 (GRCm39) |
V413A |
possibly damaging |
Het |
| Tmem131 |
G |
A |
1: 36,858,236 (GRCm39) |
Q704* |
probably null |
Het |
| Tmpo |
T |
C |
10: 90,998,825 (GRCm39) |
K321E |
probably damaging |
Het |
| Trim75 |
G |
T |
8: 65,435,315 (GRCm39) |
N378K |
probably benign |
Het |
| Tspan18 |
T |
A |
2: 93,036,065 (GRCm39) |
I227F |
probably benign |
Het |
| Ttn |
C |
T |
2: 76,541,526 (GRCm39) |
W33820* |
probably null |
Het |
| Urb2 |
T |
A |
8: 124,774,034 (GRCm39) |
Y1522N |
probably damaging |
Het |
| Zbtb40 |
T |
C |
4: 136,745,620 (GRCm39) |
N138D |
probably benign |
Het |
| Zfp715 |
A |
T |
7: 42,947,328 (GRCm39) |
H877Q |
possibly damaging |
Het |
|
| Other mutations in Bahcc1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00341:Bahcc1
|
APN |
11 |
120,163,130 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00536:Bahcc1
|
APN |
11 |
120,175,871 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL01339:Bahcc1
|
APN |
11 |
120,180,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01695:Bahcc1
|
APN |
11 |
120,167,435 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01744:Bahcc1
|
APN |
11 |
120,162,563 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01769:Bahcc1
|
APN |
11 |
120,171,030 (GRCm39) |
splice site |
probably benign |
|
|
IGL01982:Bahcc1
|
APN |
11 |
120,178,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02341:Bahcc1
|
APN |
11 |
120,163,346 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02535:Bahcc1
|
APN |
11 |
120,178,362 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
IGL02559:Bahcc1
|
APN |
11 |
120,175,998 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL02579:Bahcc1
|
APN |
11 |
120,176,175 (GRCm39) |
splice site |
probably benign |
|
|
IGL02609:Bahcc1
|
APN |
11 |
120,180,224 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL02678:Bahcc1
|
APN |
11 |
120,163,697 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02800:Bahcc1
|
APN |
11 |
120,163,760 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02963:Bahcc1
|
APN |
11 |
120,165,758 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL03128:Bahcc1
|
APN |
11 |
120,159,260 (GRCm39) |
splice site |
probably benign |
|
|
IGL03242:Bahcc1
|
APN |
11 |
120,159,126 (GRCm39) |
splice site |
probably benign |
|
|
IGL03248:Bahcc1
|
APN |
11 |
120,159,235 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Dimensionality
|
UTSW |
11 |
120,163,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
G1citation:Bahcc1
|
UTSW |
11 |
120,178,547 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0019:Bahcc1
|
UTSW |
11 |
120,180,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0040:Bahcc1
|
UTSW |
11 |
120,159,196 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0040:Bahcc1
|
UTSW |
11 |
120,159,196 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0148:Bahcc1
|
UTSW |
11 |
120,159,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0164:Bahcc1
|
UTSW |
11 |
120,175,900 (GRCm39) |
splice site |
probably benign |
|
|
R0321:Bahcc1
|
UTSW |
11 |
120,164,251 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0671:Bahcc1
|
UTSW |
11 |
120,178,146 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0737:Bahcc1
|
UTSW |
11 |
120,163,667 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1452:Bahcc1
|
UTSW |
11 |
120,173,065 (GRCm39) |
splice site |
probably benign |
|
|
R1570:Bahcc1
|
UTSW |
11 |
120,163,009 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R1914:Bahcc1
|
UTSW |
11 |
120,176,225 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2010:Bahcc1
|
UTSW |
11 |
120,163,604 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2075:Bahcc1
|
UTSW |
11 |
120,162,515 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2085:Bahcc1
|
UTSW |
11 |
120,178,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3552:Bahcc1
|
UTSW |
11 |
120,167,598 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R3711:Bahcc1
|
UTSW |
11 |
120,165,923 (GRCm39) |
missense |
probably benign |
0.27 |
|
R3804:Bahcc1
|
UTSW |
11 |
120,174,184 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4349:Bahcc1
|
UTSW |
11 |
120,150,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4557:Bahcc1
|
UTSW |
11 |
120,165,914 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4801:Bahcc1
|
UTSW |
11 |
120,173,051 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4802:Bahcc1
|
UTSW |
11 |
120,173,051 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4908:Bahcc1
|
UTSW |
11 |
120,178,580 (GRCm39) |
missense |
probably benign |
0.36 |
|
R4941:Bahcc1
|
UTSW |
11 |
120,177,491 (GRCm39) |
missense |
probably benign |
|
|
R5217:Bahcc1
|
UTSW |
11 |
120,165,285 (GRCm39) |
nonsense |
probably null |
|
|
R5241:Bahcc1
|
UTSW |
11 |
120,162,229 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5432:Bahcc1
|
UTSW |
11 |
120,178,814 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5696:Bahcc1
|
UTSW |
11 |
120,164,813 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5724:Bahcc1
|
UTSW |
11 |
120,176,192 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R5725:Bahcc1
|
UTSW |
11 |
120,165,714 (GRCm39) |
missense |
probably benign |
|
|
R5788:Bahcc1
|
UTSW |
11 |
120,177,178 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5893:Bahcc1
|
UTSW |
11 |
120,176,256 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5900:Bahcc1
|
UTSW |
11 |
120,175,319 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6014:Bahcc1
|
UTSW |
11 |
120,180,615 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6058:Bahcc1
|
UTSW |
11 |
120,178,211 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6107:Bahcc1
|
UTSW |
11 |
120,163,714 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6302:Bahcc1
|
UTSW |
11 |
120,167,634 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6525:Bahcc1
|
UTSW |
11 |
120,176,048 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6550:Bahcc1
|
UTSW |
11 |
120,167,477 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6822:Bahcc1
|
UTSW |
11 |
120,178,547 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6836:Bahcc1
|
UTSW |
11 |
120,162,583 (GRCm39) |
nonsense |
probably null |
|
|
R6846:Bahcc1
|
UTSW |
11 |
120,162,422 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R6916:Bahcc1
|
UTSW |
11 |
120,163,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6966:Bahcc1
|
UTSW |
11 |
120,173,985 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7097:Bahcc1
|
UTSW |
11 |
120,163,472 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7289:Bahcc1
|
UTSW |
11 |
120,171,000 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7441:Bahcc1
|
UTSW |
11 |
120,177,132 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7520:Bahcc1
|
UTSW |
11 |
120,167,031 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R7556:Bahcc1
|
UTSW |
11 |
120,178,589 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7672:Bahcc1
|
UTSW |
11 |
120,174,172 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R7791:Bahcc1
|
UTSW |
11 |
120,159,203 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7794:Bahcc1
|
UTSW |
11 |
120,163,507 (GRCm39) |
nonsense |
probably null |
|
|
R7802:Bahcc1
|
UTSW |
11 |
120,165,518 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7946:Bahcc1
|
UTSW |
11 |
120,163,325 (GRCm39) |
missense |
probably benign |
|
|
R7985:Bahcc1
|
UTSW |
11 |
120,163,717 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8128:Bahcc1
|
UTSW |
11 |
120,163,216 (GRCm39) |
nonsense |
probably null |
|
|
R8131:Bahcc1
|
UTSW |
11 |
120,163,664 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8353:Bahcc1
|
UTSW |
11 |
120,165,251 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8439:Bahcc1
|
UTSW |
11 |
120,165,415 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8710:Bahcc1
|
UTSW |
11 |
120,174,953 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8799:Bahcc1
|
UTSW |
11 |
120,177,173 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8810:Bahcc1
|
UTSW |
11 |
120,164,587 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R8920:Bahcc1
|
UTSW |
11 |
120,175,331 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8924:Bahcc1
|
UTSW |
11 |
120,167,591 (GRCm39) |
missense |
probably benign |
0.09 |
|
R9014:Bahcc1
|
UTSW |
11 |
120,173,048 (GRCm39) |
missense |
probably benign |
|
|
R9014:Bahcc1
|
UTSW |
11 |
120,163,715 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9195:Bahcc1
|
UTSW |
11 |
120,167,337 (GRCm39) |
missense |
probably benign |
|
|
R9216:Bahcc1
|
UTSW |
11 |
120,177,514 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9392:Bahcc1
|
UTSW |
11 |
120,163,513 (GRCm39) |
nonsense |
probably null |
|
|
R9562:Bahcc1
|
UTSW |
11 |
120,150,035 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R9680:Bahcc1
|
UTSW |
11 |
120,163,286 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R9797:Bahcc1
|
UTSW |
11 |
120,159,147 (GRCm39) |
nonsense |
probably null |
|
|
X0026:Bahcc1
|
UTSW |
11 |
120,162,578 (GRCm39) |
missense |
probably benign |
0.20 |
|
Z1176:Bahcc1
|
UTSW |
11 |
120,175,220 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1176:Bahcc1
|
UTSW |
11 |
120,167,435 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
Z1177:Bahcc1
|
UTSW |
11 |
120,163,747 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGTCTCTCACCAAGCAGTG -3'
(R):5'- TTGCCAGGCCAAAGAGACTC -3'
Sequencing Primer
(F):5'- AAGCCTGAGGATCGCCACATG -3'
(R):5'- AGAGACTCCCTCCCTCACCTG -3'
|
| Posted On |
2022-04-18 |
Incidental Mutation