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PIONEERING CANCER RESEARCH
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Pancreas
BCM-PDAC-13
Model Details
Patient
PDX Model
Histology
Metastasis
Patient Treatment
Patient Information for Model: BCM-PDAC-13
Contact Model Developer
Model Contact
Model: BCM-PDAC-13
Model Contact: Qizhi Cathy Yao
Institution: BCM Pancreas PDX Program
Email:
qizhiyao@bcm.edu
Patient Information
Clinical Timeline
Clinical Information at Collection
Clinical Biomarkers/Mutations at Collection
Pathology Information at Collection
Model Information for Model: BCM-PDAC-13
Model Details - Initial Implantation of Patient Tissue
Mutations (Cancer Gene Census List)
Show/Hide Columns
The number of models in this collection with mutations in the listed gene;
may include models that are not publicly available for distribution.
The number of models in this collection with mutations at the listed site;
may include models that are not publicly available for distribution.
Total mutations showing: 435
F
P
1
2
3
4
5
6
7
8
9
10
N
E
Rows Per Page
10
15
25
50
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Gene
Filter by Gene
Chr
Filter by Chr
Start
End
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Alt
cDNA Change
Codon Change
Protein Change
TVAF
Gene Mutation Freq.
Site Mutation Freq.
Most Severe Effect
All Effects
Mutation Impact
Transcript ID
ClinVar Clinical Significance
COSMIC ID
gnomAD Non-Cancer AF
dbSNP ID
Gene Mutation Freq.
Site Mutation Freq.
Transcript ID
ClinVar Clinical Significance
COSMIC ID
dbSNP ID
A1CF
chr10
50809906
50809909
TAGC
T
c.1594_1596del
GCT/-
p.A532del
0.024
5
4
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000373997.8
COSV50964203
rs747104061
5
4
ENST00000373997.8
COSV50964203
rs747104061
ABL1
chr9
130884102
130884105
CAAG
C
c.1826_1828del
AAG/-
p.K609del
0.047
5
4
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000318560.6
COSV59324524
rs201725154
5
4
ENST00000318560.6
COSV59324524
rs201725154
AFDN
chr6
167966011
167966014
TGAG
T
c.5091_5093del
GAG/-
p.E1697del
0.029
5
4
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000366806.6
COSV60040388
.
5
4
ENST00000366806.6
COSV60040388
.
AFF3
chr2
99593618
99593620
CAG
C
c.2116_2117del
CTg/g
p.L706Gfs*24
0.011
5
1
Frameshift Mutation
Frameshift Mutation
HIGH
ENST00000409579.5
.
5
1
ENST00000409579.5
.
AFF3
chr2
99601548
99601551
CGCT
C
c.1330_1332del
AGC/-
p.S444del
0.049
5
5
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000409579.5
COSV57843239
.
5
5
ENST00000409579.5
COSV57843239
.
AFF3
chr2
99593652
99593652
G
C
c.2084C>G
tCg/tGg
p.S695W
0.581
5
1
Missense Variant
Missense Variant
MODERATE
ENST00000409579.5
rs1436457705
5
1
ENST00000409579.5
rs1436457705
AFF3
chr2
99593623
99593623
C
CCT
c.2112_2113insAG
-/AG
p.D705Rfs*30
0.011
5
1
Frameshift Mutation
Frameshift Mutation
HIGH
ENST00000409579.5
.
5
1
ENST00000409579.5
.
AFF3
chr2
99593622
99593622
T
A
c.2114A>T
gAc/gTc
p.D705V
0.01
5
1
Missense Variant
Missense Variant
MODERATE
ENST00000409579.5
.
5
1
ENST00000409579.5
.
AKAP9
chr7
92042077
92042079
CAG
C
c.4960_4961del
tcAGag/tcag
p.R1654Gfs*23
0.027
8
2
Frameshift Mutation
Frameshift Mutation
HIGH
ENST00000356239.8
COSV62338254
rs779447911
8
2
ENST00000356239.8
COSV62338254
rs779447911
AKAP9
chr7
92085597
92085597
C
T
c.8935C>T
Cct/Tct
p.P2979S
0.998
8
8
Missense Variant
Missense Variant
MODERATE
ENST00000356239.8
Benign/Likely_benign
COSV104663065
0.996325000000
rs1063242
8
8
ENST00000356239.8
Benign/Likely_benign
COSV104663065
rs1063242
AKAP9
chr7
92042077
92042077
C
CAG
c.4960_4961dup
tca/tcAGa
p.V1655Gfs*4
0.017
8
1
Frameshift Mutation
Frameshift Mutation
HIGH
ENST00000356239.8
COSV62350299
.
8
1
ENST00000356239.8
COSV62350299
.
ALK
chr2
29193500
29193500
G
C
c.4587C>G
gaC/gaG
p.D1529E
0.249
8
7
Missense Variant
Missense Variant
MODERATE
ENST00000389048.8
Benign
COSV66569695
0.472160000000
rs1881421
8
7
ENST00000389048.8
Benign
COSV66569695
rs1881421
ALK
chr2
29193706
29193706
T
C
c.4381A>G
Atc/Gtc
p.I1461V
0.999
8
8
Missense Variant
Missense Variant
MODERATE
ENST00000389048.8
Benign
COSV101201052
0.997594000000
rs1670283
8
8
ENST00000389048.8
Benign
COSV101201052
rs1670283
ALK
chr2
29193615
29193615
T
C
c.4472A>G
aAg/aGg
p.K1491R
0.24
8
7
Missense Variant
Missense Variant
MODERATE
ENST00000389048.8
Benign
COSV66555753
0.349007000000
rs1881420
8
7
ENST00000389048.8
Benign
COSV66555753
rs1881420
ANK1
chr8
41708920
41708920
C
T
c.1856G>A
cGt/cAt
p.R619H
0.266
5
3
Missense Variant
Missense Variant
MODERATE
ENST00000289734.13
Benign/Likely_benign
COSV55882618
0.044445800000
rs2304877
5
3
ENST00000289734.13
Benign/Likely_benign
COSV55882618
rs2304877
Total mutations showing: 435
F
P
1
2
3
4
5
6
7
8
9
10
N
E
Rows Per Page
10
15
25
50
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CNV
Histology Information for Model: BCM-PDAC-13
There are no histology images for this model.
Metastasis Information for Model: BCM-PDAC-13
Patient
PDX
Liver
Local
Local recurrence
Lung
Rectum
lymph node
Patient Treatment Information for Model: BCM-PDAC-13
Event Id
Treatment
Treatment Setting
Age at Start
Age at End
Duration
Clinical Response
Pathologic Response
Reason Stopped
5
Gemcitabine/Abraxane
Neoadjuvant
64.9
65.09
69 days
Stable Disease (SD); CA 19-9 dropped from 504-184
No Response (NR)
Treatment Completed
15
Gemcitabine/Abraxane
Adjuvant
65.46
65.48
7 days
Poor performance status
Please wait...