Incidental Mutation 'R9569:Yeats2'
| ID |
721874 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Yeats2
|
| Ensembl Gene |
ENSMUSG00000041215 |
| Gene Name |
YEATS domain containing 2 |
| Synonyms |
|
| MMRRC Submission |
068966-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.960)
|
| Stock # |
R9569 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
16 |
| Chromosomal Location |
19959813-20051323 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 19972902 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Tryptophan
at position 19
(R19W)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000087506
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000090052]
[ENSMUST00000115560]
[ENSMUST00000231705]
[ENSMUST00000232019]
[ENSMUST00000232338]
|
| AlphaFold |
Q3TUF7 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000090052
AA Change: R19W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000087506
Gene: ENSMUSG00000041215
AA Change: R19W
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:YEATS
|
179 |
262 |
2.6e-27 |
PFAM |
|
low complexity region
|
299 |
309 |
N/A |
INTRINSIC |
|
low complexity region
|
312 |
333 |
N/A |
INTRINSIC |
|
low complexity region
|
409 |
429 |
N/A |
INTRINSIC |
|
low complexity region
|
458 |
467 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
471 |
675 |
3.72e-6 |
PROSPERO |
|
low complexity region
|
683 |
702 |
N/A |
INTRINSIC |
|
low complexity region
|
738 |
775 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
785 |
978 |
3.72e-6 |
PROSPERO |
|
low complexity region
|
1240 |
1249 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000115560
AA Change: R72W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000111222
Gene: ENSMUSG00000041215
AA Change: R72W
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:YEATS
|
232 |
314 |
2.1e-28 |
PFAM |
|
low complexity region
|
352 |
362 |
N/A |
INTRINSIC |
|
low complexity region
|
365 |
386 |
N/A |
INTRINSIC |
|
low complexity region
|
462 |
482 |
N/A |
INTRINSIC |
|
low complexity region
|
511 |
520 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
524 |
728 |
4.68e-6 |
PROSPERO |
|
low complexity region
|
736 |
755 |
N/A |
INTRINSIC |
|
low complexity region
|
791 |
828 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
838 |
1031 |
4.68e-6 |
PROSPERO |
|
low complexity region
|
1293 |
1302 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000231705
AA Change: R72W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000232019
AA Change: R38W
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000232338
AA Change: R19W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] YEATS2 is a scaffolding subunit of the ADA2A (TADA2A; MIM 602276)-containing (ATAC) histone acetyltransferase complex (Wang et al., 2008 [PubMed 18838386]).[supplied by OMIM, Apr 2010]
|
| Allele List at MGI |
All alleles(34) : Targeted(1) Gene trapped(33)
|
| Other mutations in this stock |
Total: 76 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abi2 |
T |
A |
1: 60,503,763 (GRCm39) |
V356D |
probably damaging |
Het |
| Adgrd1 |
T |
C |
5: 129,256,701 (GRCm39) |
V690A |
possibly damaging |
Het |
| Apba2 |
T |
C |
7: 64,393,138 (GRCm39) |
M553T |
possibly damaging |
Het |
| Apeh |
C |
T |
9: 107,971,609 (GRCm39) |
V13M |
unknown |
Het |
| Apol11b |
C |
T |
15: 77,524,771 (GRCm39) |
E5K |
possibly damaging |
Het |
| Apol7e |
C |
T |
15: 77,601,933 (GRCm39) |
T177I |
probably damaging |
Het |
| Bltp1 |
T |
C |
3: 37,066,770 (GRCm39) |
M211T |
|
Het |
| Bub1b |
T |
C |
2: 118,468,884 (GRCm39) |
I883T |
probably damaging |
Het |
| C9 |
T |
C |
15: 6,489,062 (GRCm39) |
S140P |
probably damaging |
Het |
| Cbfa2t2 |
T |
A |
2: 154,346,485 (GRCm39) |
I64N |
probably benign |
Het |
| Cd180 |
A |
T |
13: 102,842,486 (GRCm39) |
I511F |
possibly damaging |
Het |
| Cic |
T |
C |
7: 24,972,120 (GRCm39) |
V617A |
possibly damaging |
Het |
| Clca3a2 |
A |
C |
3: 144,513,075 (GRCm39) |
|
probably null |
Het |
| D5Ertd579e |
T |
C |
5: 36,759,979 (GRCm39) |
T1394A |
probably damaging |
Het |
| Dclk1 |
A |
T |
3: 55,387,852 (GRCm39) |
E422D |
probably benign |
Het |
| Depdc5 |
A |
T |
5: 33,025,321 (GRCm39) |
D21V |
probably damaging |
Het |
| Dis3l |
A |
G |
9: 64,236,829 (GRCm39) |
F40S |
unknown |
Het |
| Duox1 |
T |
C |
2: 122,148,971 (GRCm39) |
V82A |
probably benign |
Het |
| Dus2 |
T |
C |
8: 106,771,507 (GRCm39) |
V211A |
probably damaging |
Het |
| Eif2ak4 |
G |
A |
2: 118,251,316 (GRCm39) |
S326N |
probably benign |
Het |
| Fat3 |
A |
C |
9: 15,830,495 (GRCm39) |
L153R |
|
Het |
| Gpx8 |
C |
T |
13: 113,182,125 (GRCm39) |
V103I |
probably damaging |
Het |
| Gtf2a1l |
A |
G |
17: 89,001,948 (GRCm39) |
D268G |
probably benign |
Het |
| Hc |
T |
C |
2: 34,926,359 (GRCm39) |
I342V |
probably benign |
Het |
| Hsp90ab1 |
T |
A |
17: 45,879,878 (GRCm39) |
D546V |
possibly damaging |
Het |
| Ifi206 |
T |
G |
1: 173,314,209 (GRCm39) |
D77A |
|
Het |
| Igfbp1 |
A |
G |
11: 7,147,881 (GRCm39) |
|
probably benign |
Het |
| Kdm3a |
T |
C |
6: 71,584,434 (GRCm39) |
D559G |
probably benign |
Het |
| Kif2a |
A |
G |
13: 107,105,246 (GRCm39) |
I565T |
probably benign |
Het |
| Krt1c |
T |
C |
15: 101,724,924 (GRCm39) |
T229A |
probably damaging |
Het |
| Lcmt2 |
G |
A |
2: 120,970,522 (GRCm39) |
A187V |
probably damaging |
Het |
| Mapk8ip1 |
A |
G |
2: 92,217,599 (GRCm39) |
M241T |
probably benign |
Het |
| Mup15 |
T |
C |
4: 61,357,875 (GRCm39) |
|
probably benign |
Het |
| Myo9b |
T |
C |
8: 71,811,629 (GRCm39) |
V1912A |
probably benign |
Het |
| Naip5 |
T |
A |
13: 100,356,338 (GRCm39) |
E1092D |
probably benign |
Het |
| Naip5 |
T |
C |
13: 100,359,821 (GRCm39) |
T472A |
probably benign |
Het |
| Net1 |
A |
G |
13: 3,938,518 (GRCm39) |
F123S |
probably benign |
Het |
| Or1j8 |
T |
C |
2: 36,191,946 (GRCm39) |
Y132H |
probably damaging |
Het |
| Or52n2 |
C |
T |
7: 104,542,525 (GRCm39) |
M103I |
possibly damaging |
Het |
| Or5h17 |
A |
G |
16: 58,820,228 (GRCm39) |
Y60C |
probably damaging |
Het |
| Pcdhb13 |
T |
C |
18: 37,576,153 (GRCm39) |
F177S |
probably damaging |
Het |
| Pclo |
T |
C |
5: 14,907,065 (GRCm39) |
|
probably null |
Het |
| Perm1 |
A |
G |
4: 156,303,039 (GRCm39) |
T528A |
probably benign |
Het |
| Pik3c2a |
C |
T |
7: 115,957,939 (GRCm39) |
A1116T |
possibly damaging |
Het |
| Prox2 |
G |
A |
12: 85,141,766 (GRCm39) |
Q146* |
probably null |
Het |
| Psd |
A |
T |
19: 46,308,717 (GRCm39) |
C639S |
possibly damaging |
Het |
| Rffl |
T |
A |
11: 82,703,264 (GRCm39) |
T220S |
probably benign |
Het |
| Scn2a |
A |
G |
2: 65,560,622 (GRCm39) |
D1284G |
probably damaging |
Het |
| Scube1 |
T |
C |
15: 83,513,605 (GRCm39) |
Y385C |
probably damaging |
Het |
| Sec14l3 |
A |
T |
11: 4,026,324 (GRCm39) |
D388V |
probably damaging |
Het |
| Slc26a1 |
G |
T |
5: 108,819,460 (GRCm39) |
Q596K |
probably benign |
Het |
| Slc6a19 |
T |
C |
13: 73,834,030 (GRCm39) |
T343A |
probably benign |
Het |
| Slc7a4 |
A |
G |
16: 17,393,262 (GRCm39) |
V179A |
|
Het |
| Sox14 |
T |
G |
9: 99,757,562 (GRCm39) |
D49A |
|
Het |
| Spata31g1 |
G |
C |
4: 42,971,740 (GRCm39) |
V358L |
probably benign |
Het |
| Timm22 |
A |
G |
11: 76,298,196 (GRCm39) |
S56G |
probably benign |
Het |
| Tmub2 |
G |
A |
11: 102,179,153 (GRCm39) |
W322* |
probably null |
Het |
| Tsc22d4 |
A |
G |
5: 137,756,428 (GRCm39) |
T8A |
probably benign |
Het |
| Ttn |
T |
C |
2: 76,539,652 (GRCm39) |
I34445V |
probably benign |
Het |
| Tyms |
A |
T |
5: 30,268,360 (GRCm39) |
Y196* |
probably null |
Het |
| Ube2o |
G |
A |
11: 116,434,823 (GRCm39) |
T546M |
probably damaging |
Het |
| Umodl1 |
A |
G |
17: 31,217,143 (GRCm39) |
Y1125C |
probably damaging |
Het |
| Unc13b |
CGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGC |
CGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGC |
4: 43,177,312 (GRCm39) |
|
probably benign |
Het |
| Unk |
A |
T |
11: 115,950,035 (GRCm39) |
Q747L |
probably damaging |
Het |
| Vmn1r170 |
A |
G |
7: 23,306,294 (GRCm39) |
E232G |
probably benign |
Het |
| Vps41 |
A |
G |
13: 19,013,396 (GRCm39) |
Y338C |
possibly damaging |
Het |
| Washc5 |
T |
C |
15: 59,215,980 (GRCm39) |
M800V |
probably benign |
Het |
| Wt1 |
T |
A |
2: 104,993,711 (GRCm39) |
I348N |
possibly damaging |
Het |
| Xirp2 |
A |
G |
2: 67,341,242 (GRCm39) |
Y1161C |
probably damaging |
Het |
| Xpo7 |
A |
G |
14: 70,906,140 (GRCm39) |
M1001T |
possibly damaging |
Het |
| Zfp142 |
T |
C |
1: 74,615,386 (GRCm39) |
T476A |
probably damaging |
Het |
| Zfp229 |
T |
C |
17: 21,964,573 (GRCm39) |
W268R |
possibly damaging |
Het |
| Zfp473 |
A |
G |
7: 44,388,971 (GRCm39) |
F50S |
probably damaging |
Het |
| Zfp975 |
A |
T |
7: 42,311,413 (GRCm39) |
M400K |
probably benign |
Het |
| Zkscan5 |
A |
G |
5: 145,144,419 (GRCm39) |
M150V |
probably benign |
Het |
| Znfx1 |
T |
A |
2: 166,897,875 (GRCm39) |
I350F |
|
Het |
|
| Other mutations in Yeats2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01118:Yeats2
|
APN |
16 |
20,005,054 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01128:Yeats2
|
APN |
16 |
19,980,718 (GRCm39) |
splice site |
probably benign |
|
|
IGL01139:Yeats2
|
APN |
16 |
20,033,143 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01394:Yeats2
|
APN |
16 |
19,980,782 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01482:Yeats2
|
APN |
16 |
20,041,671 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01924:Yeats2
|
APN |
16 |
20,024,917 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01925:Yeats2
|
APN |
16 |
19,998,430 (GRCm39) |
splice site |
probably benign |
|
|
IGL02106:Yeats2
|
APN |
16 |
20,011,970 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
IGL02370:Yeats2
|
APN |
16 |
19,969,221 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02447:Yeats2
|
APN |
16 |
20,012,429 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02669:Yeats2
|
APN |
16 |
20,005,033 (GRCm39) |
missense |
probably benign |
0.13 |
|
IGL03155:Yeats2
|
APN |
16 |
20,048,323 (GRCm39) |
critical splice donor site |
probably null |
|
|
tyrion
|
UTSW |
16 |
20,032,151 (GRCm39) |
splice site |
probably benign |
|
|
P0045:Yeats2
|
UTSW |
16 |
19,975,695 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R0051:Yeats2
|
UTSW |
16 |
20,012,474 (GRCm39) |
nonsense |
probably null |
|
|
R0051:Yeats2
|
UTSW |
16 |
20,012,474 (GRCm39) |
nonsense |
probably null |
|
|
R0118:Yeats2
|
UTSW |
16 |
19,975,692 (GRCm39) |
nonsense |
probably null |
|
|
R0157:Yeats2
|
UTSW |
16 |
20,040,427 (GRCm39) |
makesense |
probably null |
|
|
R0184:Yeats2
|
UTSW |
16 |
20,022,435 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R0194:Yeats2
|
UTSW |
16 |
19,971,719 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R0612:Yeats2
|
UTSW |
16 |
20,005,175 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0655:Yeats2
|
UTSW |
16 |
20,012,574 (GRCm39) |
nonsense |
probably null |
|
|
R0826:Yeats2
|
UTSW |
16 |
20,011,966 (GRCm39) |
nonsense |
probably null |
|
|
R1526:Yeats2
|
UTSW |
16 |
20,024,836 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1535:Yeats2
|
UTSW |
16 |
20,008,115 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1749:Yeats2
|
UTSW |
16 |
20,005,018 (GRCm39) |
nonsense |
probably null |
|
|
R1842:Yeats2
|
UTSW |
16 |
19,989,988 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1843:Yeats2
|
UTSW |
16 |
20,048,314 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1926:Yeats2
|
UTSW |
16 |
20,033,176 (GRCm39) |
missense |
probably benign |
|
|
R2000:Yeats2
|
UTSW |
16 |
20,005,141 (GRCm39) |
missense |
probably benign |
0.20 |
|
R2017:Yeats2
|
UTSW |
16 |
19,977,931 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2076:Yeats2
|
UTSW |
16 |
20,005,032 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R2153:Yeats2
|
UTSW |
16 |
19,972,916 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2167:Yeats2
|
UTSW |
16 |
20,032,151 (GRCm39) |
splice site |
probably benign |
|
|
R2981:Yeats2
|
UTSW |
16 |
20,005,051 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3160:Yeats2
|
UTSW |
16 |
20,012,395 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3161:Yeats2
|
UTSW |
16 |
20,012,395 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3162:Yeats2
|
UTSW |
16 |
20,012,395 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3774:Yeats2
|
UTSW |
16 |
19,969,245 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4250:Yeats2
|
UTSW |
16 |
19,975,685 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R4305:Yeats2
|
UTSW |
16 |
20,027,172 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4455:Yeats2
|
UTSW |
16 |
19,980,743 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R4458:Yeats2
|
UTSW |
16 |
20,032,071 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4811:Yeats2
|
UTSW |
16 |
19,971,645 (GRCm39) |
splice site |
probably null |
|
|
R4902:Yeats2
|
UTSW |
16 |
20,026,418 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5043:Yeats2
|
UTSW |
16 |
20,027,215 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5047:Yeats2
|
UTSW |
16 |
20,027,215 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5319:Yeats2
|
UTSW |
16 |
20,005,175 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5328:Yeats2
|
UTSW |
16 |
19,989,955 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5360:Yeats2
|
UTSW |
16 |
19,972,912 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5416:Yeats2
|
UTSW |
16 |
20,030,319 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5672:Yeats2
|
UTSW |
16 |
19,980,779 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5684:Yeats2
|
UTSW |
16 |
20,012,553 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5932:Yeats2
|
UTSW |
16 |
20,011,913 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5946:Yeats2
|
UTSW |
16 |
20,026,513 (GRCm39) |
nonsense |
probably null |
|
|
R6168:Yeats2
|
UTSW |
16 |
19,998,308 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6169:Yeats2
|
UTSW |
16 |
20,038,417 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6179:Yeats2
|
UTSW |
16 |
20,033,225 (GRCm39) |
missense |
probably benign |
0.16 |
|
R6371:Yeats2
|
UTSW |
16 |
20,040,460 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R6877:Yeats2
|
UTSW |
16 |
19,998,344 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7149:Yeats2
|
UTSW |
16 |
19,972,939 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7405:Yeats2
|
UTSW |
16 |
20,041,663 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8353:Yeats2
|
UTSW |
16 |
20,041,637 (GRCm39) |
nonsense |
probably null |
|
|
R8367:Yeats2
|
UTSW |
16 |
20,041,575 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8453:Yeats2
|
UTSW |
16 |
20,041,637 (GRCm39) |
nonsense |
probably null |
|
|
R8506:Yeats2
|
UTSW |
16 |
19,971,684 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8535:Yeats2
|
UTSW |
16 |
19,977,926 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8828:Yeats2
|
UTSW |
16 |
19,969,260 (GRCm39) |
missense |
probably benign |
0.45 |
|
R8905:Yeats2
|
UTSW |
16 |
20,009,144 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8924:Yeats2
|
UTSW |
16 |
19,969,312 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9087:Yeats2
|
UTSW |
16 |
20,030,500 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9276:Yeats2
|
UTSW |
16 |
19,975,786 (GRCm39) |
missense |
probably benign |
0.34 |
|
R9338:Yeats2
|
UTSW |
16 |
20,041,533 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9338:Yeats2
|
UTSW |
16 |
20,032,078 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R9378:Yeats2
|
UTSW |
16 |
20,033,228 (GRCm39) |
missense |
probably benign |
|
|
R9664:Yeats2
|
UTSW |
16 |
20,047,491 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- AAAAGCGTAGACTCCAGGGC -3'
(R):5'- GCCAGGCTTATCAAATGCTAAAG -3'
Sequencing Primer
(F):5'- AGACTCCAGGGCTTTGTTTATACAC -3'
(R):5'- GGCAATATAAGAAATGTCTGAATGGC -3'
|
| Posted On |
2022-08-09 |
Incidental Mutation