Incidental Mutation 'RF020:Abca16'
| ID |
603812 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Abca16
|
| Ensembl Gene |
ENSMUSG00000051900 |
| Gene Name |
ATP-binding cassette, sub-family A member 16 |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
RF020 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
120008870-120144036 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 120132880 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Lysine to Glutamic Acid
at position 1270
(K1270E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000112736
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000056042]
[ENSMUST00000120490]
|
| AlphaFold |
E9PWJ7 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000056042
AA Change: K1269E
PolyPhen 2
Score 0.715 (Sensitivity: 0.86; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000061094
Gene: ENSMUSG00000051900
AA Change: K1269E
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ABC2_membrane_3
|
26 |
455 |
2.7e-23 |
PFAM |
|
AAA
|
537 |
720 |
2.01e-7 |
SMART |
|
Pfam:ABC2_membrane_3
|
898 |
1287 |
4.6e-25 |
PFAM |
|
low complexity region
|
1325 |
1336 |
N/A |
INTRINSIC |
|
low complexity region
|
1342 |
1353 |
N/A |
INTRINSIC |
|
AAA
|
1378 |
1563 |
4.23e-6 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000120490
AA Change: K1270E
PolyPhen 2
Score 0.902 (Sensitivity: 0.82; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000112736
Gene: ENSMUSG00000051900
AA Change: K1270E
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ABC2_membrane_3
|
25 |
456 |
2.4e-22 |
PFAM |
|
AAA
|
538 |
721 |
2.01e-7 |
SMART |
|
Pfam:ABC2_membrane_3
|
899 |
1288 |
1.1e-27 |
PFAM |
|
low complexity region
|
1326 |
1337 |
N/A |
INTRINSIC |
|
low complexity region
|
1343 |
1354 |
N/A |
INTRINSIC |
|
AAA
|
1379 |
1564 |
4.23e-6 |
SMART |
|
| Coding Region Coverage |
- 1x: 99.8%
- 3x: 99.7%
- 10x: 99.3%
- 20x: 98.5%
|
| Validation Efficiency |
|
| Allele List at MGI |
All alleles(4) : Targeted(3) Gene trapped(1)
|
| Other mutations in this stock |
Total: 90 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrb2 |
T |
C |
4: 129,903,877 (GRCm39) |
S668P |
probably damaging |
Het |
| Ahdc1 |
T |
G |
4: 132,791,588 (GRCm39) |
L943R |
possibly damaging |
Het |
| Ank2 |
T |
C |
3: 126,739,125 (GRCm39) |
K2253R |
unknown |
Het |
| Arhgap23 |
T |
C |
11: 97,354,387 (GRCm39) |
S767P |
probably damaging |
Het |
| Arhgef12 |
A |
G |
9: 42,901,285 (GRCm39) |
I839T |
possibly damaging |
Het |
| Begain |
CGCCGC |
CGCCGCGGCCGC |
12: 108,999,350 (GRCm39) |
|
probably benign |
Het |
| Btbd19 |
A |
T |
4: 116,979,472 (GRCm39) |
C116S |
probably damaging |
Het |
| Cbr1 |
C |
T |
16: 93,407,067 (GRCm39) |
A261V |
probably benign |
Het |
| Ccdc137 |
A |
G |
11: 120,349,022 (GRCm39) |
R18G |
probably benign |
Het |
| Cdsn |
AG |
AGACAGGAAGTAGTAGCTCTCAG |
17: 35,865,876 (GRCm39) |
|
probably benign |
Het |
| Celsr3 |
C |
T |
9: 108,726,256 (GRCm39) |
R3162C |
probably benign |
Het |
| Cep350 |
A |
T |
1: 155,791,224 (GRCm39) |
V1300E |
probably benign |
Het |
| Cluh |
G |
GCCAGAT |
11: 74,560,364 (GRCm39) |
|
probably benign |
Het |
| Cmya5 |
G |
T |
13: 93,205,799 (GRCm39) |
Q3357K |
possibly damaging |
Het |
| Col6a2 |
T |
G |
10: 76,442,043 (GRCm39) |
|
probably null |
Het |
| Cyp2j9 |
T |
A |
4: 96,465,889 (GRCm39) |
T315S |
probably damaging |
Het |
| Cyp3a13 |
CATTATT |
CATT |
5: 137,892,525 (GRCm39) |
|
probably null |
Het |
| Dnah6 |
T |
A |
6: 73,095,040 (GRCm39) |
Y2181F |
probably benign |
Het |
| Dnah7b |
A |
G |
1: 46,412,421 (GRCm39) |
D4010G |
possibly damaging |
Het |
| E4f1 |
CCG |
CCGACG |
17: 24,674,169 (GRCm39) |
|
probably benign |
Het |
| Ep300 |
A |
T |
15: 81,470,772 (GRCm39) |
|
probably benign |
Het |
| Fam234a |
A |
G |
17: 26,437,725 (GRCm39) |
V90A |
probably benign |
Het |
| Gab3 |
TCT |
TCTGCT |
X: 74,043,623 (GRCm39) |
|
probably benign |
Het |
| Gal3st1 |
A |
G |
11: 3,948,153 (GRCm39) |
Y120C |
possibly damaging |
Het |
| Garin5a |
GGA |
GGAAGGGTGGATCCTGGATACCTGGGTCTGAGGGAAGA |
7: 44,149,959 (GRCm39) |
|
probably null |
Het |
| Gm5475 |
GTGGAAGGAAAGGT |
G |
15: 100,325,030 (GRCm39) |
|
probably null |
Het |
| Gm6665 |
T |
TC |
18: 31,953,430 (GRCm39) |
|
probably null |
Het |
| Hdlbp |
T |
C |
1: 93,368,456 (GRCm39) |
T8A |
probably benign |
Het |
| Hnrnpa2b1 |
T |
A |
6: 51,443,674 (GRCm39) |
K92N |
probably damaging |
Het |
| Hsdl2 |
GGAGCAGCCACAGCTGCAGGAGAAGCCACAGCTGCAGGAGCAGCCACAGC |
GGAGCAGCCACAGCTGCAGGAGCAGCCACAGCTGCAGGAGAAGCCACAGCTGCAGGAGCAGCCACAGC |
4: 59,610,640 (GRCm39) |
|
probably benign |
Het |
| Klhl10 |
C |
G |
11: 100,332,896 (GRCm39) |
Q14E |
probably benign |
Het |
| Klra2 |
GAAAGAAATCCA |
GAAAGAAATCCAAAGAAATCCA |
6: 131,198,801 (GRCm39) |
|
probably null |
Het |
| Kmt2b |
CC |
CCTCCTGC |
7: 30,285,807 (GRCm39) |
|
probably benign |
Het |
| Krt1c |
A |
G |
15: 101,726,403 (GRCm39) |
I45T |
unknown |
Het |
| Ksr2 |
T |
C |
5: 117,693,283 (GRCm39) |
S244P |
probably benign |
Het |
| Lama5 |
A |
T |
2: 179,837,971 (GRCm39) |
M915K |
probably benign |
Het |
| Lrp1b |
A |
C |
2: 41,660,858 (GRCm39) |
H197Q |
|
Het |
| Lrrc1 |
T |
C |
9: 77,359,913 (GRCm39) |
E293G |
probably damaging |
Het |
| Med12l |
AACA |
AACAACA |
3: 59,183,379 (GRCm39) |
|
probably benign |
Het |
| Mgam |
T |
A |
6: 40,662,243 (GRCm39) |
Y1179N |
probably damaging |
Het |
| Mgat4c |
A |
G |
10: 102,224,928 (GRCm39) |
I381V |
probably benign |
Het |
| Mrgprx1 |
A |
AGAC |
7: 47,671,259 (GRCm39) |
|
probably benign |
Het |
| Myc |
A |
T |
15: 61,857,672 (GRCm39) |
|
probably benign |
Het |
| Nipbl |
A |
G |
15: 8,388,418 (GRCm39) |
S401P |
probably damaging |
Het |
| Nlrp9c |
A |
T |
7: 26,084,649 (GRCm39) |
I310N |
probably benign |
Het |
| Nwd2 |
C |
A |
5: 63,963,066 (GRCm39) |
Y883* |
probably null |
Het |
| Oas1e |
T |
A |
5: 120,932,383 (GRCm39) |
T87S |
possibly damaging |
Het |
| Or10n7-ps1 |
GA |
GATACA |
9: 39,598,049 (GRCm39) |
|
probably null |
Het |
| Or51a5 |
A |
T |
7: 102,771,098 (GRCm39) |
C294S |
probably benign |
Het |
| Or52d3 |
A |
G |
7: 104,229,497 (GRCm39) |
M215V |
probably benign |
Het |
| Or8b38 |
G |
A |
9: 37,972,620 (GRCm39) |
M1I |
probably null |
Het |
| Pappa |
T |
G |
4: 65,123,282 (GRCm39) |
S872R |
possibly damaging |
Het |
| Parp4 |
T |
C |
14: 56,884,806 (GRCm39) |
L1295P |
unknown |
Het |
| Pcdh15 |
A |
T |
10: 74,021,242 (GRCm39) |
Y152F |
probably damaging |
Het |
| Pdk1 |
A |
T |
2: 71,714,240 (GRCm39) |
I217L |
possibly damaging |
Het |
| Phldb1 |
A |
C |
9: 44,609,243 (GRCm39) |
C450W |
probably damaging |
Het |
| Pnma8a |
C |
CCATGATGCACCTGCTTCAACATCA |
7: 16,695,376 (GRCm39) |
|
probably benign |
Het |
| Prl2c5 |
G |
A |
13: 13,360,497 (GRCm39) |
G55S |
probably benign |
Het |
| Psme2b |
A |
T |
11: 48,836,397 (GRCm39) |
H183Q |
probably damaging |
Het |
| Ptms |
CCTCCTC |
CCTCCTCCTC |
6: 124,891,412 (GRCm39) |
|
probably benign |
Het |
| Rln3 |
T |
C |
8: 84,769,931 (GRCm39) |
T73A |
probably benign |
Het |
| Rprd1a |
T |
A |
18: 24,663,062 (GRCm39) |
Q21L |
probably damaging |
Het |
| Septin3 |
A |
T |
15: 82,168,662 (GRCm39) |
D155V |
probably damaging |
Het |
| Sh3rf3 |
T |
A |
10: 58,649,590 (GRCm39) |
V65E |
probably damaging |
Het |
| Shank3 |
A |
G |
15: 89,384,593 (GRCm39) |
N155S |
probably benign |
Het |
| Shox2 |
G |
T |
3: 66,881,146 (GRCm39) |
P278Q |
probably damaging |
Het |
| Slc1a1 |
T |
C |
19: 28,856,555 (GRCm39) |
|
probably null |
Het |
| Slc39a10 |
A |
T |
1: 46,849,175 (GRCm39) |
F814I |
probably damaging |
Het |
| Slc5a1 |
T |
C |
5: 33,290,773 (GRCm39) |
I119T |
probably damaging |
Het |
| Slc6a13 |
T |
C |
6: 121,301,310 (GRCm39) |
|
probably null |
Het |
| Spmap2l |
CAGCGATCCTCCCCAGTCCCGCAAGGC |
CAGCGATCCTCCCCAGTCCCGCAAGGCGAGCGATCCTCCCCAGTCCCGCAAGGC |
5: 77,164,247 (GRCm39) |
|
probably benign |
Het |
| Spta1 |
A |
G |
1: 174,041,010 (GRCm39) |
D1270G |
probably benign |
Het |
| Spta1 |
T |
A |
1: 174,045,469 (GRCm39) |
F1542L |
probably damaging |
Het |
| Tacc3 |
T |
A |
5: 33,818,568 (GRCm39) |
M1K |
probably null |
Het |
| Tax1bp1 |
T |
C |
6: 52,698,339 (GRCm39) |
V17A |
probably damaging |
Het |
| Tmem156 |
T |
A |
5: 65,248,890 (GRCm39) |
E3D |
probably benign |
Het |
| Tmem209 |
T |
A |
6: 30,487,417 (GRCm39) |
M530L |
probably benign |
Het |
| Trpc2 |
A |
G |
7: 101,745,433 (GRCm39) |
D883G |
unknown |
Het |
| Tsen34 |
GGAGCCAAAAT |
G |
7: 3,698,795 (GRCm39) |
|
probably null |
Het |
| Uhrf2 |
T |
C |
19: 30,063,791 (GRCm39) |
Y585H |
probably damaging |
Het |
| Vmn1r26 |
T |
A |
6: 57,985,705 (GRCm39) |
K161N |
probably benign |
Het |
| Vmn1r29 |
A |
G |
6: 58,284,528 (GRCm39) |
S83G |
probably benign |
Het |
| Vps13b |
G |
T |
15: 35,925,552 (GRCm39) |
W3829L |
probably null |
Het |
| Vwce |
G |
A |
19: 10,630,449 (GRCm39) |
G503R |
probably damaging |
Het |
| Zc3h11a |
T |
C |
1: 133,554,735 (GRCm39) |
E415G |
possibly damaging |
Het |
| Zc3h14 |
T |
A |
12: 98,746,541 (GRCm39) |
|
probably null |
Het |
| Zfp119b |
A |
T |
17: 56,246,499 (GRCm39) |
M229K |
probably benign |
Het |
| Zfp384 |
CCAAGCTCAAGC |
CCAAGC |
6: 125,013,418 (GRCm39) |
|
probably benign |
Het |
| Zfp384 |
GGCCCAGGC |
GGCCCAGGCCCACGCCCAGGC |
6: 125,013,451 (GRCm39) |
|
probably benign |
Het |
| Zyx |
T |
A |
6: 42,334,330 (GRCm39) |
L518Q |
probably damaging |
Het |
|
| Other mutations in Abca16 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00417:Abca16
|
APN |
7 |
120,022,982 (GRCm39) |
missense |
probably benign |
0.08 |
|
IGL00590:Abca16
|
APN |
7 |
120,023,038 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01320:Abca16
|
APN |
7 |
120,038,422 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01322:Abca16
|
APN |
7 |
120,038,422 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01613:Abca16
|
APN |
7 |
120,140,500 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL01774:Abca16
|
APN |
7 |
120,021,024 (GRCm39) |
splice site |
probably benign |
|
|
IGL01774:Abca16
|
APN |
7 |
120,077,058 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01797:Abca16
|
APN |
7 |
120,113,760 (GRCm39) |
missense |
probably benign |
0.15 |
|
IGL02406:Abca16
|
APN |
7 |
120,139,825 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02437:Abca16
|
APN |
7 |
120,132,952 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02541:Abca16
|
APN |
7 |
120,113,881 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL02576:Abca16
|
APN |
7 |
120,032,678 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL02578:Abca16
|
APN |
7 |
120,023,179 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL03156:Abca16
|
APN |
7 |
120,023,074 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
IGL03381:Abca16
|
APN |
7 |
120,127,041 (GRCm39) |
missense |
probably benign |
0.12 |
|
PIT4802001:Abca16
|
UTSW |
7 |
120,139,351 (GRCm39) |
missense |
probably benign |
0.31 |
|
R0024:Abca16
|
UTSW |
7 |
120,032,608 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0026:Abca16
|
UTSW |
7 |
120,077,146 (GRCm39) |
splice site |
probably benign |
|
|
R0026:Abca16
|
UTSW |
7 |
120,077,146 (GRCm39) |
splice site |
probably benign |
|
|
R0123:Abca16
|
UTSW |
7 |
120,139,378 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0134:Abca16
|
UTSW |
7 |
120,139,378 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0225:Abca16
|
UTSW |
7 |
120,139,378 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0346:Abca16
|
UTSW |
7 |
120,035,155 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0355:Abca16
|
UTSW |
7 |
120,023,021 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R0358:Abca16
|
UTSW |
7 |
120,143,939 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0525:Abca16
|
UTSW |
7 |
120,065,033 (GRCm39) |
nonsense |
probably null |
|
|
R0617:Abca16
|
UTSW |
7 |
120,032,834 (GRCm39) |
splice site |
probably benign |
|
|
R0625:Abca16
|
UTSW |
7 |
120,035,116 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0835:Abca16
|
UTSW |
7 |
120,065,007 (GRCm39) |
missense |
probably benign |
0.42 |
|
R1445:Abca16
|
UTSW |
7 |
120,119,256 (GRCm39) |
missense |
probably benign |
0.41 |
|
R1535:Abca16
|
UTSW |
7 |
120,139,928 (GRCm39) |
missense |
probably benign |
0.30 |
|
R1567:Abca16
|
UTSW |
7 |
120,030,352 (GRCm39) |
missense |
probably benign |
0.08 |
|
R1694:Abca16
|
UTSW |
7 |
120,119,307 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1860:Abca16
|
UTSW |
7 |
120,133,986 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1876:Abca16
|
UTSW |
7 |
120,032,608 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1913:Abca16
|
UTSW |
7 |
120,140,463 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1940:Abca16
|
UTSW |
7 |
120,032,832 (GRCm39) |
splice site |
probably benign |
|
|
R2042:Abca16
|
UTSW |
7 |
120,143,941 (GRCm39) |
missense |
probably benign |
|
|
R2115:Abca16
|
UTSW |
7 |
120,139,868 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2122:Abca16
|
UTSW |
7 |
120,119,184 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2265:Abca16
|
UTSW |
7 |
120,030,383 (GRCm39) |
missense |
probably benign |
0.03 |
|
R2267:Abca16
|
UTSW |
7 |
120,030,383 (GRCm39) |
missense |
probably benign |
0.03 |
|
R2269:Abca16
|
UTSW |
7 |
120,030,383 (GRCm39) |
missense |
probably benign |
0.03 |
|
R2993:Abca16
|
UTSW |
7 |
120,134,384 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3055:Abca16
|
UTSW |
7 |
120,035,074 (GRCm39) |
missense |
probably benign |
0.05 |
|
R3956:Abca16
|
UTSW |
7 |
120,126,975 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4114:Abca16
|
UTSW |
7 |
120,126,290 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4441:Abca16
|
UTSW |
7 |
120,127,024 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4601:Abca16
|
UTSW |
7 |
120,035,920 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4706:Abca16
|
UTSW |
7 |
120,064,988 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4807:Abca16
|
UTSW |
7 |
120,139,832 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4824:Abca16
|
UTSW |
7 |
120,074,702 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R4937:Abca16
|
UTSW |
7 |
120,126,309 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5152:Abca16
|
UTSW |
7 |
120,139,846 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5257:Abca16
|
UTSW |
7 |
120,035,992 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5258:Abca16
|
UTSW |
7 |
120,035,992 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5330:Abca16
|
UTSW |
7 |
120,102,600 (GRCm39) |
missense |
probably benign |
0.15 |
|
R5388:Abca16
|
UTSW |
7 |
120,139,969 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5590:Abca16
|
UTSW |
7 |
120,143,995 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5810:Abca16
|
UTSW |
7 |
120,035,155 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6030:Abca16
|
UTSW |
7 |
120,133,021 (GRCm39) |
missense |
probably benign |
|
|
R6030:Abca16
|
UTSW |
7 |
120,133,021 (GRCm39) |
missense |
probably benign |
|
|
R6161:Abca16
|
UTSW |
7 |
120,139,934 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6313:Abca16
|
UTSW |
7 |
120,126,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6485:Abca16
|
UTSW |
7 |
120,026,390 (GRCm39) |
nonsense |
probably null |
|
|
R6527:Abca16
|
UTSW |
7 |
120,076,995 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6772:Abca16
|
UTSW |
7 |
120,126,276 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6885:Abca16
|
UTSW |
7 |
120,119,332 (GRCm39) |
missense |
probably benign |
0.07 |
|
R6899:Abca16
|
UTSW |
7 |
120,126,264 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6941:Abca16
|
UTSW |
7 |
120,140,370 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6990:Abca16
|
UTSW |
7 |
120,126,950 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7059:Abca16
|
UTSW |
7 |
120,020,971 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7144:Abca16
|
UTSW |
7 |
120,032,796 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7146:Abca16
|
UTSW |
7 |
120,126,974 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R7193:Abca16
|
UTSW |
7 |
120,026,409 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7308:Abca16
|
UTSW |
7 |
120,022,993 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7449:Abca16
|
UTSW |
7 |
120,035,131 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7571:Abca16
|
UTSW |
7 |
120,119,211 (GRCm39) |
missense |
probably benign |
0.11 |
|
R7617:Abca16
|
UTSW |
7 |
120,102,694 (GRCm39) |
nonsense |
probably null |
|
|
R7646:Abca16
|
UTSW |
7 |
120,113,937 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7750:Abca16
|
UTSW |
7 |
120,113,928 (GRCm39) |
missense |
probably benign |
0.09 |
|
R7763:Abca16
|
UTSW |
7 |
120,113,825 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7840:Abca16
|
UTSW |
7 |
120,074,689 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7946:Abca16
|
UTSW |
7 |
120,126,398 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8018:Abca16
|
UTSW |
7 |
120,132,866 (GRCm39) |
missense |
probably benign |
0.04 |
|
R8170:Abca16
|
UTSW |
7 |
120,065,005 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8413:Abca16
|
UTSW |
7 |
120,023,123 (GRCm39) |
missense |
probably benign |
0.06 |
|
R8461:Abca16
|
UTSW |
7 |
120,035,918 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8858:Abca16
|
UTSW |
7 |
120,052,327 (GRCm39) |
missense |
probably benign |
|
|
R8881:Abca16
|
UTSW |
7 |
120,074,794 (GRCm39) |
missense |
probably benign |
0.18 |
|
R9272:Abca16
|
UTSW |
7 |
120,076,993 (GRCm39) |
missense |
probably benign |
0.13 |
|
R9303:Abca16
|
UTSW |
7 |
120,126,989 (GRCm39) |
missense |
probably benign |
0.25 |
|
R9305:Abca16
|
UTSW |
7 |
120,126,989 (GRCm39) |
missense |
probably benign |
0.25 |
|
R9320:Abca16
|
UTSW |
7 |
120,139,320 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9413:Abca16
|
UTSW |
7 |
120,126,422 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9512:Abca16
|
UTSW |
7 |
120,022,963 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9559:Abca16
|
UTSW |
7 |
120,021,019 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9615:Abca16
|
UTSW |
7 |
120,126,404 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9641:Abca16
|
UTSW |
7 |
120,126,308 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R9643:Abca16
|
UTSW |
7 |
120,065,023 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R9674:Abca16
|
UTSW |
7 |
120,074,668 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R9714:Abca16
|
UTSW |
7 |
120,030,383 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9799:Abca16
|
UTSW |
7 |
120,132,998 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9800:Abca16
|
UTSW |
7 |
120,119,283 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
X0066:Abca16
|
UTSW |
7 |
120,102,609 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CAGCCTCAACTGAGATGTCTC -3'
(R):5'- TGACCAAACGGTTTGCTTTC -3'
Sequencing Primer
(F):5'- ATTCATTTTACATCCCATTCCCAATC -3'
(R):5'- TCGAAAGACAAAGCTCTTC -3'
|
| Posted On |
2019-12-04 |
Incidental Mutation