Incidental Mutation 'R7422:Sphkap'
| ID |
575699 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Sphkap
|
| Ensembl Gene |
ENSMUSG00000026163 |
| Gene Name |
SPHK1 interactor, AKAP domain containing |
| Synonyms |
SKIP, A930009L15Rik, 4930544G21Rik |
| MMRRC Submission |
045500-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.074)
|
| Stock # |
R7422 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
83233163-83385853 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to C
at 83241547 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Glycine
at position 1535
(V1535G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000124872
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000159078]
[ENSMUST00000160953]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000159078
AA Change: V1277G
PolyPhen 2
Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000124384
Gene: ENSMUSG00000026163
AA Change: V1277G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
303 |
314 |
N/A |
INTRINSIC |
|
SCOP:d1ash__
|
382 |
462 |
5e-3 |
SMART |
|
low complexity region
|
809 |
819 |
N/A |
INTRINSIC |
|
low complexity region
|
854 |
865 |
N/A |
INTRINSIC |
|
low complexity region
|
1202 |
1221 |
N/A |
INTRINSIC |
|
low complexity region
|
1243 |
1254 |
N/A |
INTRINSIC |
|
Pfam:AKAP_110
|
1281 |
1398 |
7.5e-13 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000160953
AA Change: V1535G
PolyPhen 2
Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000124872
Gene: ENSMUSG00000026163
AA Change: V1535G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
590 |
601 |
N/A |
INTRINSIC |
|
SCOP:d1ash__
|
669 |
749 |
6e-3 |
SMART |
|
low complexity region
|
1096 |
1106 |
N/A |
INTRINSIC |
|
low complexity region
|
1141 |
1152 |
N/A |
INTRINSIC |
|
low complexity region
|
1489 |
1508 |
N/A |
INTRINSIC |
|
Pfam:AKAP_110
|
1540 |
1655 |
6.4e-12 |
PFAM |
|
| Meta Mutation Damage Score |
0.0638 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.1%
- 20x: 96.9%
|
| Validation Efficiency |
97% (98/101) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 99 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2810021J22Rik |
T |
A |
11: 58,771,885 (GRCm39) |
C456S |
probably damaging |
Het |
| 4930524J08Rik |
T |
C |
5: 100,127,068 (GRCm39) |
|
probably benign |
Het |
| Adam28 |
T |
G |
14: 68,864,326 (GRCm39) |
R492S |
probably damaging |
Het |
| Adarb2 |
G |
A |
13: 8,807,313 (GRCm39) |
A705T |
possibly damaging |
Het |
| Adprhl1 |
T |
C |
8: 13,272,873 (GRCm39) |
D1295G |
probably benign |
Het |
| Aldh3b3 |
A |
G |
19: 4,016,476 (GRCm39) |
I365V |
probably benign |
Het |
| Aldh8a1 |
T |
C |
10: 21,264,996 (GRCm39) |
F208L |
possibly damaging |
Het |
| Ap3b1 |
G |
A |
13: 94,664,673 (GRCm39) |
V871I |
unknown |
Het |
| Apol7e |
A |
T |
15: 77,598,552 (GRCm39) |
R6* |
probably null |
Het |
| Arfgap3 |
T |
C |
15: 83,191,150 (GRCm39) |
E456G |
probably damaging |
Het |
| Arhgef1 |
T |
C |
7: 24,615,461 (GRCm39) |
L285P |
probably benign |
Het |
| Arhgef7 |
T |
A |
8: 11,850,861 (GRCm39) |
C315S |
probably benign |
Het |
| Atp9a |
A |
T |
2: 168,490,513 (GRCm39) |
L829Q |
probably damaging |
Het |
| Babam2 |
T |
A |
5: 31,888,393 (GRCm39) |
|
probably null |
Het |
| Bptf |
C |
T |
11: 106,951,384 (GRCm39) |
R2185H |
probably damaging |
Het |
| Brd9 |
A |
C |
13: 74,102,697 (GRCm39) |
M473L |
probably benign |
Het |
| C7 |
T |
C |
15: 5,041,538 (GRCm39) |
H456R |
probably benign |
Het |
| Cabp7 |
C |
A |
11: 4,688,856 (GRCm39) |
A205S |
probably damaging |
Het |
| Catsperb |
A |
G |
12: 101,554,293 (GRCm39) |
I662M |
probably damaging |
Het |
| Ccl21a |
T |
C |
4: 42,773,906 (GRCm39) |
M5V |
probably benign |
Het |
| Cdyl |
G |
T |
13: 36,042,177 (GRCm39) |
R405L |
possibly damaging |
Het |
| Cep89 |
T |
C |
7: 35,127,672 (GRCm39) |
L538P |
probably damaging |
Het |
| Cercam |
A |
G |
2: 29,762,892 (GRCm39) |
M209V |
possibly damaging |
Het |
| Chfr |
T |
A |
5: 110,310,571 (GRCm39) |
|
probably null |
Het |
| Cntnap5c |
T |
A |
17: 58,717,226 (GRCm39) |
Y1269* |
probably null |
Het |
| Col6a2 |
G |
T |
10: 76,439,170 (GRCm39) |
C833* |
probably null |
Het |
| Cpeb3 |
T |
A |
19: 37,151,900 (GRCm39) |
I159F |
probably benign |
Het |
| Cplx2 |
G |
A |
13: 54,526,663 (GRCm39) |
E24K |
possibly damaging |
Het |
| Ctsb |
A |
G |
14: 63,379,752 (GRCm39) |
T332A |
probably benign |
Het |
| Cyp2j12 |
T |
A |
4: 96,029,222 (GRCm39) |
T20S |
probably benign |
Het |
| Dcst2 |
T |
A |
3: 89,273,993 (GRCm39) |
H181Q |
probably damaging |
Het |
| Dnm1l |
T |
C |
16: 16,136,338 (GRCm39) |
I411V |
probably benign |
Het |
| Dock5 |
T |
A |
14: 68,046,479 (GRCm39) |
I768F |
probably benign |
Het |
| Ecel1 |
A |
G |
1: 87,077,334 (GRCm39) |
Y625H |
probably damaging |
Het |
| Efl1 |
T |
G |
7: 82,330,587 (GRCm39) |
S253R |
probably damaging |
Het |
| Elmod1 |
T |
A |
9: 53,820,127 (GRCm39) |
D287V |
probably damaging |
Het |
| Fam171a2 |
T |
C |
11: 102,329,491 (GRCm39) |
S423G |
probably benign |
Het |
| Fbxo8 |
A |
T |
8: 57,022,317 (GRCm39) |
|
probably null |
Het |
| Flnc |
G |
T |
6: 29,455,470 (GRCm39) |
G2040W |
probably damaging |
Het |
| Fras1 |
C |
T |
5: 96,821,458 (GRCm39) |
A1405V |
probably benign |
Het |
| Frem3 |
A |
C |
8: 81,342,392 (GRCm39) |
I1562L |
probably benign |
Het |
| Fxr1 |
C |
T |
3: 34,103,369 (GRCm39) |
A233V |
probably damaging |
Het |
| H1f9 |
A |
G |
11: 94,859,184 (GRCm39) |
R160G |
possibly damaging |
Het |
| Helb |
A |
G |
10: 119,944,799 (GRCm39) |
F246L |
probably damaging |
Het |
| Hoxb6 |
G |
T |
11: 96,183,510 (GRCm39) |
|
probably benign |
Het |
| Hspa2 |
A |
G |
12: 76,452,884 (GRCm39) |
E526G |
probably damaging |
Het |
| Hyal5 |
A |
T |
6: 24,875,983 (GRCm39) |
|
probably benign |
Het |
| Ints6 |
A |
T |
14: 62,942,224 (GRCm39) |
V503E |
probably benign |
Het |
| Ints9 |
C |
T |
14: 65,269,747 (GRCm39) |
T479I |
possibly damaging |
Het |
| Jag1 |
C |
T |
2: 136,926,975 (GRCm39) |
R928H |
probably benign |
Het |
| Lman2 |
A |
T |
13: 55,499,338 (GRCm39) |
I179N |
probably damaging |
Het |
| Lta |
T |
C |
17: 35,422,805 (GRCm39) |
S173G |
probably benign |
Het |
| Mki67 |
G |
A |
7: 135,300,099 (GRCm39) |
P1645L |
probably damaging |
Het |
| Mrc2 |
A |
T |
11: 105,183,609 (GRCm39) |
|
probably benign |
Het |
| Muc4 |
T |
A |
16: 32,754,689 (GRCm38) |
M1521K |
probably benign |
Het |
| Mucl3 |
T |
A |
17: 35,949,312 (GRCm39) |
T96S |
probably benign |
Het |
| Mylk3 |
T |
G |
8: 86,081,873 (GRCm39) |
D438A |
probably benign |
Het |
| Myo7a |
T |
A |
7: 97,700,833 (GRCm39) |
|
probably null |
Het |
| Nsmce4a |
G |
T |
7: 130,135,547 (GRCm39) |
Q342K |
probably benign |
Het |
| Or10ac1 |
A |
G |
6: 42,515,053 (GRCm39) |
I301T |
possibly damaging |
Het |
| Or4c124 |
T |
A |
2: 89,156,423 (GRCm39) |
I34F |
probably benign |
Het |
| Or5p60 |
A |
G |
7: 107,724,068 (GRCm39) |
L134P |
probably damaging |
Het |
| Or6c65 |
A |
T |
10: 129,604,136 (GRCm39) |
Y257F |
possibly damaging |
Het |
| Osbpl6 |
T |
A |
2: 76,423,730 (GRCm39) |
F864L |
probably damaging |
Het |
| Pla2g4a |
A |
G |
1: 149,808,438 (GRCm39) |
S2P |
probably benign |
Het |
| Plce1 |
T |
C |
19: 38,640,329 (GRCm39) |
L525P |
probably damaging |
Het |
| Por |
A |
T |
5: 135,763,773 (GRCm39) |
M667L |
probably benign |
Het |
| Psma4 |
T |
C |
9: 54,862,166 (GRCm39) |
Y97H |
probably benign |
Het |
| Qtrt1 |
A |
T |
9: 21,323,753 (GRCm39) |
H126L |
probably benign |
Het |
| Rab3a |
A |
T |
8: 71,209,170 (GRCm39) |
Y102F |
possibly damaging |
Het |
| Rnf212 |
T |
A |
5: 108,879,555 (GRCm39) |
H87L |
probably benign |
Het |
| Rnf216 |
A |
G |
5: 143,076,591 (GRCm39) |
S98P |
probably benign |
Het |
| Ryr1 |
G |
T |
7: 28,785,295 (GRCm39) |
R1806S |
probably benign |
Het |
| Scgb1b3 |
A |
T |
7: 31,075,262 (GRCm39) |
L37F |
probably benign |
Het |
| Sds |
T |
C |
5: 120,617,254 (GRCm39) |
S37P |
probably damaging |
Het |
| Senp6 |
A |
G |
9: 80,021,159 (GRCm39) |
R280G |
probably damaging |
Het |
| She |
T |
A |
3: 89,761,864 (GRCm39) |
I441K |
possibly damaging |
Het |
| Slc6a20b |
A |
G |
9: 123,436,682 (GRCm39) |
S244P |
possibly damaging |
Het |
| Slc9a3 |
A |
T |
13: 74,299,004 (GRCm39) |
Y141F |
probably damaging |
Het |
| Slco6c1 |
A |
T |
1: 97,009,207 (GRCm39) |
H426Q |
probably benign |
Het |
| Smc2 |
C |
A |
4: 52,440,301 (GRCm39) |
Q16K |
probably benign |
Het |
| Stard9 |
C |
A |
2: 120,532,633 (GRCm39) |
N2963K |
probably benign |
Het |
| Sycp2 |
C |
T |
2: 178,035,944 (GRCm39) |
A248T |
probably damaging |
Het |
| Taar8a |
T |
C |
10: 23,952,762 (GRCm39) |
L122P |
probably damaging |
Het |
| Tab1 |
T |
A |
15: 80,044,445 (GRCm39) |
V491E |
probably benign |
Het |
| Tanc1 |
T |
C |
2: 59,636,688 (GRCm39) |
M857T |
probably benign |
Het |
| Tcirg1 |
C |
A |
19: 3,949,008 (GRCm39) |
R427L |
possibly damaging |
Het |
| Tmem109 |
A |
C |
19: 10,849,124 (GRCm39) |
*244G |
probably null |
Het |
| Tox2 |
A |
G |
2: 163,163,435 (GRCm39) |
Y136C |
|
Het |
| Tubb1 |
T |
C |
2: 174,298,825 (GRCm39) |
V169A |
possibly damaging |
Het |
| Ubr3 |
T |
C |
2: 69,783,886 (GRCm39) |
|
probably null |
Het |
| Vmn1r225 |
T |
A |
17: 20,723,059 (GRCm39) |
F167I |
probably benign |
Het |
| Vmn2r65 |
A |
C |
7: 84,595,569 (GRCm39) |
W372G |
probably damaging |
Het |
| Vps13a |
A |
T |
19: 16,727,537 (GRCm39) |
D188E |
probably damaging |
Het |
| Vsnl1 |
G |
T |
12: 11,376,439 (GRCm39) |
Q149K |
probably benign |
Het |
| Wdr35 |
A |
G |
12: 9,054,105 (GRCm39) |
N466S |
probably benign |
Het |
| Ywhae |
T |
A |
11: 75,650,169 (GRCm39) |
S210R |
probably damaging |
Het |
| Zfp28 |
T |
A |
7: 6,397,748 (GRCm39) |
S728T |
probably damaging |
Het |
| Zfpm1 |
A |
G |
8: 123,063,698 (GRCm39) |
D919G |
unknown |
Het |
|
| Other mutations in Sphkap |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00332:Sphkap
|
APN |
1 |
83,258,237 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00337:Sphkap
|
APN |
1 |
83,317,329 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00470:Sphkap
|
APN |
1 |
83,255,631 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
IGL00577:Sphkap
|
APN |
1 |
83,256,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00657:Sphkap
|
APN |
1 |
83,254,096 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01868:Sphkap
|
APN |
1 |
83,258,120 (GRCm39) |
splice site |
probably null |
|
|
IGL02101:Sphkap
|
APN |
1 |
83,268,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02471:Sphkap
|
APN |
1 |
83,253,897 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02943:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02945:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03008:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03031:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03059:Sphkap
|
APN |
1 |
83,234,963 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL03085:Sphkap
|
APN |
1 |
83,258,075 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL03355:Sphkap
|
APN |
1 |
83,258,224 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03356:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03368:Sphkap
|
APN |
1 |
83,253,397 (GRCm39) |
missense |
probably benign |
0.14 |
|
R0294:Sphkap
|
UTSW |
1 |
83,255,966 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R0308:Sphkap
|
UTSW |
1 |
83,254,690 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0478:Sphkap
|
UTSW |
1 |
83,256,432 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0606:Sphkap
|
UTSW |
1 |
83,258,145 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0678:Sphkap
|
UTSW |
1 |
83,256,349 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1216:Sphkap
|
UTSW |
1 |
83,268,698 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1253:Sphkap
|
UTSW |
1 |
83,256,619 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R1532:Sphkap
|
UTSW |
1 |
83,234,924 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1635:Sphkap
|
UTSW |
1 |
83,256,121 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1655:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
|
R1657:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
|
R1700:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
|
R1701:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
|
R1734:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
|
R1736:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
|
R1743:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
|
R1744:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
|
R1760:Sphkap
|
UTSW |
1 |
83,255,265 (GRCm39) |
missense |
probably benign |
0.29 |
|
R1893:Sphkap
|
UTSW |
1 |
83,256,687 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1937:Sphkap
|
UTSW |
1 |
83,245,162 (GRCm39) |
nonsense |
probably null |
|
|
R1986:Sphkap
|
UTSW |
1 |
83,255,643 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1993:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
|
R1995:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
|
R2001:Sphkap
|
UTSW |
1 |
83,254,383 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2004:Sphkap
|
UTSW |
1 |
83,255,632 (GRCm39) |
missense |
probably benign |
0.04 |
|
R2111:Sphkap
|
UTSW |
1 |
83,253,602 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2112:Sphkap
|
UTSW |
1 |
83,253,602 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2156:Sphkap
|
UTSW |
1 |
83,255,710 (GRCm39) |
missense |
probably benign |
0.03 |
|
R2182:Sphkap
|
UTSW |
1 |
83,254,405 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2271:Sphkap
|
UTSW |
1 |
83,234,942 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3712:Sphkap
|
UTSW |
1 |
83,254,833 (GRCm39) |
missense |
probably benign |
0.27 |
|
R3919:Sphkap
|
UTSW |
1 |
83,254,179 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3980:Sphkap
|
UTSW |
1 |
83,245,215 (GRCm39) |
splice site |
probably null |
|
|
R4130:Sphkap
|
UTSW |
1 |
83,255,619 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4539:Sphkap
|
UTSW |
1 |
83,255,514 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4602:Sphkap
|
UTSW |
1 |
83,256,782 (GRCm39) |
nonsense |
probably null |
|
|
R4735:Sphkap
|
UTSW |
1 |
83,256,838 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4793:Sphkap
|
UTSW |
1 |
83,255,805 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R4849:Sphkap
|
UTSW |
1 |
83,255,105 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4880:Sphkap
|
UTSW |
1 |
83,266,538 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5213:Sphkap
|
UTSW |
1 |
83,258,224 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5277:Sphkap
|
UTSW |
1 |
83,253,885 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5331:Sphkap
|
UTSW |
1 |
83,254,503 (GRCm39) |
missense |
probably benign |
0.08 |
|
R5632:Sphkap
|
UTSW |
1 |
83,256,006 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5647:Sphkap
|
UTSW |
1 |
83,385,720 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5751:Sphkap
|
UTSW |
1 |
83,253,618 (GRCm39) |
missense |
probably benign |
0.27 |
|
R5935:Sphkap
|
UTSW |
1 |
83,317,320 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5999:Sphkap
|
UTSW |
1 |
83,245,126 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6232:Sphkap
|
UTSW |
1 |
83,258,200 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6318:Sphkap
|
UTSW |
1 |
83,256,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6474:Sphkap
|
UTSW |
1 |
83,256,544 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6602:Sphkap
|
UTSW |
1 |
83,253,479 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R6674:Sphkap
|
UTSW |
1 |
83,255,555 (GRCm39) |
missense |
probably benign |
0.37 |
|
R6716:Sphkap
|
UTSW |
1 |
83,339,949 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6803:Sphkap
|
UTSW |
1 |
83,258,231 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6880:Sphkap
|
UTSW |
1 |
83,234,978 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6941:Sphkap
|
UTSW |
1 |
83,385,811 (GRCm39) |
start gained |
probably benign |
|
|
R7170:Sphkap
|
UTSW |
1 |
83,243,706 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7263:Sphkap
|
UTSW |
1 |
83,254,399 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7640:Sphkap
|
UTSW |
1 |
83,256,649 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7722:Sphkap
|
UTSW |
1 |
83,256,642 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7810:Sphkap
|
UTSW |
1 |
83,254,021 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7887:Sphkap
|
UTSW |
1 |
83,255,133 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7974:Sphkap
|
UTSW |
1 |
83,256,683 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7990:Sphkap
|
UTSW |
1 |
83,245,066 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8096:Sphkap
|
UTSW |
1 |
83,255,279 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8110:Sphkap
|
UTSW |
1 |
83,256,492 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R8125:Sphkap
|
UTSW |
1 |
83,241,303 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8153:Sphkap
|
UTSW |
1 |
83,255,730 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8245:Sphkap
|
UTSW |
1 |
83,256,492 (GRCm39) |
missense |
probably benign |
0.14 |
|
R8394:Sphkap
|
UTSW |
1 |
83,253,797 (GRCm39) |
missense |
probably benign |
0.08 |
|
R8443:Sphkap
|
UTSW |
1 |
83,255,953 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8508:Sphkap
|
UTSW |
1 |
83,254,221 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8531:Sphkap
|
UTSW |
1 |
83,254,909 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8673:Sphkap
|
UTSW |
1 |
83,253,561 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8674:Sphkap
|
UTSW |
1 |
83,255,565 (GRCm39) |
missense |
probably benign |
0.04 |
|
R8682:Sphkap
|
UTSW |
1 |
83,256,997 (GRCm39) |
missense |
probably benign |
0.21 |
|
R8837:Sphkap
|
UTSW |
1 |
83,253,384 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R8857:Sphkap
|
UTSW |
1 |
83,258,288 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8902:Sphkap
|
UTSW |
1 |
83,256,685 (GRCm39) |
missense |
probably benign |
0.21 |
|
R8916:Sphkap
|
UTSW |
1 |
83,255,108 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R8944:Sphkap
|
UTSW |
1 |
83,256,927 (GRCm39) |
missense |
probably benign |
0.39 |
|
R9154:Sphkap
|
UTSW |
1 |
83,234,982 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9579:Sphkap
|
UTSW |
1 |
83,255,295 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9616:Sphkap
|
UTSW |
1 |
83,254,989 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9781:Sphkap
|
UTSW |
1 |
83,255,772 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
Z1088:Sphkap
|
UTSW |
1 |
83,256,325 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1088:Sphkap
|
UTSW |
1 |
83,254,329 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Sphkap
|
UTSW |
1 |
83,258,163 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
Z1176:Sphkap
|
UTSW |
1 |
83,253,754 (GRCm39) |
nonsense |
probably null |
|
|
Z1177:Sphkap
|
UTSW |
1 |
83,254,152 (GRCm39) |
missense |
probably damaging |
0.96 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTCTGGCTCCAGGTCAAAGTTG -3'
(R):5'- GGAGAACACTAATGGCAGACCC -3'
Sequencing Primer
(F):5'- GTCAAAGTTGATCACCAGTAGGCTC -3'
(R):5'- GCAGACCCAAATGCCCTGTG -3'
|
| Posted On |
2019-10-07 |
Incidental Mutation