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PIONEERING CANCER RESEARCH
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Pancreas
BCM-PDAC-11
Model Details
Patient
PDX Model
Histology
Metastasis
Patient Treatment
Patient Information for Model: BCM-PDAC-11
Contact Model Developer
Model Contact
Model: BCM-PDAC-11
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-11
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: 561
F
P
1
2
3
4
5
6
7
8
9
10
N
E
Rows Per Page
10
15
25
50
Download
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
0.016
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
0.037
5
4
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000318560.6
COSV59324524
rs201725154
5
4
ENST00000318560.6
COSV59324524
rs201725154
ACVR1
chr2
157780555
157780555
T
TCA
c.111_112dup
gaa/gTGaa
p.E38Vfs*21
0.008778
2
1
Frameshift Mutation
Frameshift Mutation
HIGH
ENST00000434821.7
COSV55118029
.
2
1
ENST00000434821.7
COSV55118029
.
ACVR1
chr2
157780555
157780557
TCA
T
c.111_112del
tgTGaa/tgaa
p.C37*
0.01
2
1
Frameshift Mutation
Frameshift Mutation; Nonsense Mutation
HIGH
ENST00000434821.7
COSV55117690
rs141073095
2
1
ENST00000434821.7
COSV55117690
rs141073095
AFDN
chr6
167966011
167966014
TGAG
T
c.5091_5093del
GAG/-
p.E1697del
0.031
5
4
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000366806.6
COSV60040388
.
5
4
ENST00000366806.6
COSV60040388
.
AFF3
chr2
99601548
99601551
CGCT
C
c.1330_1332del
AGC/-
p.S444del
0.041
5
5
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000409579.5
COSV57843239
.
5
5
ENST00000409579.5
COSV57843239
.
AKAP9
chr7
92001306
92001306
G
T
c.1389G>T
atG/atT
p.M463I
0.993
8
4
Missense Variant
Missense Variant
MODERATE
ENST00000356239.8
Benign
COSV62345589
0.376835000000
rs6964587
8
4
ENST00000356239.8
Benign
COSV62345589
rs6964587
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
92083384
92083384
A
G
c.8375A>G
aAt/aGt
p.N2792S
0.999
8
4
Missense Variant
Missense Variant
MODERATE
ENST00000356239.8
Benign/Likely_benign
COSV62339152
0.357813000000
rs6960867
8
4
ENST00000356239.8
Benign/Likely_benign
COSV62339152
rs6960867
AKAP9
chr7
92042077
92042079
CAG
C
c.4960_4961del
tcAGag/tcag
p.R1654Gfs*23
0.015
8
2
Frameshift Mutation
Frameshift Mutation
HIGH
ENST00000356239.8
COSV62338254
rs779447911
8
2
ENST00000356239.8
COSV62338254
rs779447911
AKAP9
chr7
92022864
92022864
A
AAAC
c.4004_4006dup
aaa/aAACaa
p.K1335_L1336insQ
0.991
8
4
In-frame Insertion
In-frame Insertion
MODERATE
ENST00000356239.8
COSV62337888
rs10644111
8
4
ENST00000356239.8
COSV62337888
rs10644111
AKT1
chr14
104775735
104775738
TCTC
T
c.349_351del
GAG/-
p.E117del
0.007498
3
2
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000554581.5
COSV62573212
rs768025881
3
2
ENST00000554581.5
COSV62573212
rs768025881
ALK
chr2
29193500
29193500
G
C
c.4587C>G
gaC/gaG
p.D1529E
0.489
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
0.496
8
7
Missense Variant
Missense Variant
MODERATE
ENST00000389048.8
Benign
COSV66555753
0.349007000000
rs1881420
8
7
ENST00000389048.8
Benign
COSV66555753
rs1881420
Total mutations showing: 561
F
P
1
2
3
4
5
6
7
8
9
10
N
E
Rows Per Page
10
15
25
50
Download
CNV
Histology Information for Model: BCM-PDAC-11
There are no histology images for this model.
Metastasis Information for Model: BCM-PDAC-11
Patient
PDX
Liver
Local
Local recurrence
Lung
Rectum
lymph node
Patient Treatment Information for Model: BCM-PDAC-11
Event Id
Treatment
Treatment Setting
Age at Start
Age at End
Duration
Clinical Response
Reason Stopped
25
Gemcitabine
Adjuvant
60.17
60.6
157 days
No evidence of disease
Treatment completed
30
Folfirinox
Adjuvant
60.99
61.07
29 days
Side Effects
35
Folfox
Adjuvant
61.13
61.23
36 days
Stable Disease (SD)
Treatment completed
40
Capecitabine/radiation
Adjuvant
61.3
61.4
37 days
Stable Disease (SD)
Treatment completed
45
Capecitabine
Adjuvant
61.51
61.73
80 days
Progressive Disease (PD)
Stopped due to disease progression
50
Gemcitabine/Abraxane
Adjuvant
61.8
61.85
18 days
Progressive Disease (PD)
Disease progression and clinical decompensation
Please wait...