Incidental Mutation 'R7289:Bahcc1'
| ID |
566262 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Bahcc1
|
| Ensembl Gene |
ENSMUSG00000039741 |
| Gene Name |
BAH domain and coiled-coil containing 1 |
| Synonyms |
|
| MMRRC Submission |
045396-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.838)
|
| Stock # |
R7289 (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 120171000 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Valine
at position 1514
(A1514V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000112827
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044985]
[ENSMUST00000118987]
[ENSMUST00000122148]
|
| AlphaFold |
Q3UHR0 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000044985
AA Change: A1514V
PolyPhen 2
Score 0.128 (Sensitivity: 0.93; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000043643
Gene: ENSMUSG00000039741
AA Change: A1514V
| 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 |
probably benign
Transcript: ENSMUST00000118987
AA Change: A1514V
PolyPhen 2
Score 0.077 (Sensitivity: 0.93; Specificity: 0.85)
|
| SMART Domains |
Protein: ENSMUSP00000112784
Gene: ENSMUSG00000039741
AA Change: A1514V
| 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 |
probably benign
Transcript: ENSMUST00000122148
AA Change: A1514V
PolyPhen 2
Score 0.077 (Sensitivity: 0.93; Specificity: 0.85)
|
| SMART Domains |
Protein: ENSMUSP00000112827
Gene: ENSMUSG00000039741
AA Change: A1514V
| 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: 100.0%
- 10x: 99.7%
- 20x: 99.0%
|
| 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: 93 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aars2 |
G |
A |
17: 45,818,550 (GRCm39) |
D112N |
probably damaging |
Het |
| Abca7 |
T |
A |
10: 79,845,778 (GRCm39) |
I1580K |
probably damaging |
Het |
| Aebp1 |
A |
G |
11: 5,815,059 (GRCm39) |
D234G |
probably damaging |
Het |
| Agap1 |
T |
A |
1: 89,383,153 (GRCm39) |
M1K |
probably null |
Het |
| Agrn |
A |
T |
4: 156,263,389 (GRCm39) |
L345H |
probably damaging |
Het |
| Amfr |
A |
G |
8: 94,725,754 (GRCm39) |
M209T |
possibly damaging |
Het |
| Angel2 |
G |
A |
1: 190,673,371 (GRCm39) |
R338H |
possibly damaging |
Het |
| Ankrd27 |
C |
T |
7: 35,330,674 (GRCm39) |
A866V |
probably damaging |
Het |
| Apc |
G |
A |
18: 34,448,324 (GRCm39) |
R1740Q |
probably damaging |
Het |
| Arhgap32 |
A |
T |
9: 32,168,233 (GRCm39) |
S739C |
possibly damaging |
Het |
| Arhgap32 |
G |
C |
9: 32,168,234 (GRCm39) |
S739T |
probably benign |
Het |
| Arhgef2 |
C |
T |
3: 88,543,192 (GRCm39) |
S418L |
probably benign |
Het |
| Arhgef25 |
T |
C |
10: 127,019,641 (GRCm39) |
T472A |
possibly damaging |
Het |
| Atrnl1 |
C |
T |
19: 57,638,846 (GRCm39) |
S328F |
probably benign |
Het |
| Calcoco2 |
C |
T |
11: 95,990,823 (GRCm39) |
E305K |
unknown |
Het |
| Ccn1 |
C |
T |
3: 145,354,428 (GRCm39) |
W161* |
probably null |
Het |
| Cdc42bpa |
A |
T |
1: 179,889,362 (GRCm39) |
K203* |
probably null |
Het |
| Cmc1 |
A |
T |
9: 117,904,250 (GRCm39) |
I47N |
possibly damaging |
Het |
| Cntln |
A |
G |
4: 84,964,540 (GRCm39) |
E656G |
possibly damaging |
Het |
| Dcun1d3 |
T |
C |
7: 119,458,864 (GRCm39) |
K57R |
possibly damaging |
Het |
| Ddx23 |
T |
C |
15: 98,546,492 (GRCm39) |
E559G |
probably damaging |
Het |
| Dennd6a |
G |
A |
14: 26,333,193 (GRCm39) |
R367Q |
probably damaging |
Het |
| Desi2 |
A |
T |
1: 178,083,702 (GRCm39) |
|
probably benign |
Het |
| Dido1 |
T |
C |
2: 180,301,424 (GRCm39) |
D2160G |
unknown |
Het |
| Efcab3 |
T |
C |
11: 104,929,184 (GRCm39) |
M4838T |
probably benign |
Het |
| Epb41 |
A |
G |
4: 131,718,520 (GRCm39) |
|
probably null |
Het |
| Esrrb |
T |
A |
12: 86,517,331 (GRCm39) |
|
probably null |
Het |
| Fabp1 |
C |
A |
6: 71,180,111 (GRCm39) |
T94N |
probably benign |
Het |
| Fam120a |
A |
T |
13: 49,045,482 (GRCm39) |
C785S |
probably damaging |
Het |
| Fam243 |
T |
C |
16: 92,117,710 (GRCm39) |
I193V |
probably damaging |
Het |
| Foxc1 |
A |
G |
13: 31,991,243 (GRCm39) |
Y18C |
probably damaging |
Het |
| Fshr |
T |
C |
17: 89,293,272 (GRCm39) |
T469A |
probably benign |
Het |
| Gm14399 |
T |
A |
2: 174,972,204 (GRCm39) |
H517L |
unknown |
Het |
| Gm39115 |
G |
T |
7: 141,689,297 (GRCm39) |
Q159K |
unknown |
Het |
| Gm7347 |
T |
A |
5: 26,262,306 (GRCm39) |
I72F |
possibly damaging |
Het |
| Hmcn1 |
A |
G |
1: 150,559,466 (GRCm39) |
V2395A |
possibly damaging |
Het |
| Ighv5-17 |
T |
G |
12: 113,822,858 (GRCm39) |
T88P |
probably damaging |
Het |
| Insm2 |
T |
A |
12: 55,647,329 (GRCm39) |
Y358N |
probably damaging |
Het |
| Kazn |
A |
T |
4: 141,844,486 (GRCm39) |
L409Q |
|
Het |
| Kcnj5 |
A |
C |
9: 32,234,045 (GRCm39) |
L90R |
probably damaging |
Het |
| Kcnv2 |
A |
T |
19: 27,311,084 (GRCm39) |
T484S |
probably damaging |
Het |
| Kdm3b |
T |
C |
18: 34,927,557 (GRCm39) |
Y140H |
probably benign |
Het |
| Kifbp |
A |
C |
10: 62,401,895 (GRCm39) |
C261W |
probably damaging |
Het |
| Krt25 |
C |
T |
11: 99,212,098 (GRCm39) |
A180T |
probably benign |
Het |
| Mmp1a |
A |
G |
9: 7,467,294 (GRCm39) |
E290G |
probably damaging |
Het |
| Muc21 |
G |
A |
17: 35,929,761 (GRCm39) |
A1475V |
unknown |
Het |
| Nr3c1 |
T |
C |
18: 39,547,654 (GRCm39) |
T755A |
probably benign |
Het |
| Nr3c1 |
A |
T |
18: 39,555,786 (GRCm39) |
I517N |
probably benign |
Het |
| Nxpe2 |
A |
G |
9: 48,234,339 (GRCm39) |
|
probably null |
Het |
| Oaz1 |
C |
A |
10: 80,662,673 (GRCm39) |
T27K |
possibly damaging |
Het |
| Or4p7 |
A |
T |
2: 88,222,050 (GRCm39) |
H153L |
probably damaging |
Het |
| Or51f5 |
T |
C |
7: 102,424,634 (GRCm39) |
I301T |
probably damaging |
Het |
| Or5t5 |
G |
T |
2: 86,617,034 (GRCm39) |
C320F |
probably benign |
Het |
| Or6z3 |
T |
A |
7: 6,463,777 (GRCm39) |
W90R |
probably benign |
Het |
| Or8k21 |
A |
G |
2: 86,145,369 (GRCm39) |
M87T |
probably benign |
Het |
| Or8s5 |
A |
G |
15: 98,237,943 (GRCm39) |
V309A |
probably damaging |
Het |
| Pafah2 |
A |
T |
4: 134,147,308 (GRCm39) |
K319M |
probably damaging |
Het |
| Pask |
A |
T |
1: 93,259,309 (GRCm39) |
V236E |
probably damaging |
Het |
| Pcdh1 |
T |
C |
18: 38,322,966 (GRCm39) |
T956A |
probably damaging |
Het |
| Pcdhb18 |
C |
A |
18: 37,623,700 (GRCm39) |
N343K |
probably damaging |
Het |
| Pcsk2 |
A |
T |
2: 143,532,343 (GRCm39) |
I164F |
probably damaging |
Het |
| Phf1 |
T |
C |
17: 27,154,289 (GRCm39) |
Y169H |
probably damaging |
Het |
| Pkdrej |
T |
A |
15: 85,705,301 (GRCm39) |
I212F |
probably benign |
Het |
| Pnkp |
T |
A |
7: 44,508,114 (GRCm39) |
W146R |
probably damaging |
Het |
| Prkcb |
A |
T |
7: 122,143,910 (GRCm39) |
I325F |
probably benign |
Het |
| Ptpn21 |
C |
T |
12: 98,670,450 (GRCm39) |
D239N |
probably benign |
Het |
| Ptprb |
A |
G |
10: 116,164,070 (GRCm39) |
T626A |
probably damaging |
Het |
| Pttg1 |
T |
C |
11: 43,311,916 (GRCm39) |
N180D |
probably benign |
Het |
| Raly |
G |
A |
2: 154,703,774 (GRCm39) |
R115Q |
probably damaging |
Het |
| Rims2 |
A |
T |
15: 39,301,114 (GRCm39) |
M474L |
probably benign |
Het |
| Sash1 |
A |
T |
10: 8,605,960 (GRCm39) |
I810N |
probably damaging |
Het |
| Scnn1g |
T |
A |
7: 121,337,304 (GRCm39) |
L55* |
probably null |
Het |
| Sema6b |
A |
T |
17: 56,432,573 (GRCm39) |
D543E |
possibly damaging |
Het |
| Serpina11 |
C |
T |
12: 103,952,761 (GRCm39) |
G5E |
unknown |
Het |
| Sesn3 |
A |
T |
9: 14,187,848 (GRCm39) |
M1L |
probably benign |
Het |
| Sez6 |
T |
A |
11: 77,865,149 (GRCm39) |
I632N |
possibly damaging |
Het |
| Sgo2b |
A |
T |
8: 64,394,192 (GRCm39) |
I49N |
probably damaging |
Het |
| Slc30a2 |
A |
T |
4: 134,071,524 (GRCm39) |
I86F |
possibly damaging |
Het |
| Slc38a6 |
T |
A |
12: 73,333,786 (GRCm39) |
W30R |
probably benign |
Het |
| Spata31g1 |
A |
T |
4: 42,972,379 (GRCm39) |
T571S |
probably benign |
Het |
| Spata31g1 |
A |
T |
4: 42,973,252 (GRCm39) |
I862F |
possibly damaging |
Het |
| Stk31 |
T |
G |
6: 49,415,393 (GRCm39) |
V576G |
probably benign |
Het |
| Szt2 |
G |
A |
4: 118,233,075 (GRCm39) |
T2297I |
unknown |
Het |
| Tmem208 |
T |
C |
8: 106,061,418 (GRCm39) |
F148S |
possibly damaging |
Het |
| Tprg1l |
A |
G |
4: 154,245,031 (GRCm39) |
L19P |
possibly damaging |
Het |
| Tubg2 |
C |
A |
11: 101,050,897 (GRCm39) |
N207K |
probably damaging |
Het |
| Ube2n |
G |
T |
10: 95,377,612 (GRCm39) |
K130N |
probably benign |
Het |
| Usp36 |
T |
C |
11: 118,164,355 (GRCm39) |
Y384C |
probably damaging |
Het |
| Vcan |
A |
T |
13: 89,840,852 (GRCm39) |
L1564* |
probably null |
Het |
| Xkr6 |
A |
T |
14: 64,035,748 (GRCm39) |
D283V |
unknown |
Het |
| Zfp654 |
T |
C |
16: 64,605,523 (GRCm39) |
H352R |
probably benign |
Het |
| Zfp819 |
T |
A |
7: 43,266,506 (GRCm39) |
C330S |
probably damaging |
Het |
| Zfp970 |
G |
T |
2: 177,167,086 (GRCm39) |
C220F |
probably 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 |
|
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 |
|
R9328:Bahcc1
|
UTSW |
11 |
120,165,885 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
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'- TCTGAGAGCACTACTGACCG -3'
(R):5'- CTCTATCTGCAGGACATGTGTC -3'
Sequencing Primer
(F):5'- ACATTCCTCTGCAGGGCAATG -3'
(R):5'- ACATGTGTCATGGCCTCAG -3'
|
| Posted On |
2019-06-26 |
Incidental Mutation