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PIONEERING CANCER RESEARCH
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Pancreas
BCM-PDAC-19
Model Details
Patient
PDX Model
Histology
Metastasis
Patient Treatment
Patient Information for Model: BCM-PDAC-19
Contact Model Developer
Model Contact
Model: BCM-PDAC-19
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-19
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: 59
F
P
1
2
3
4
N
E
Rows Per Page
10
15
25
50
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Gene
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Chr
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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
AR
chrX
67546752
67546752
G
A
c.1606G>A
Ggg/Agg
p.G536R
0.083
17
2
Missense Variant
Missense Variant
MODERATE
ENST00000374690.9
17
2
ENST00000374690.9
AR
chrX
67546514
67546523
TGGCGGCGGC
T
c.1412_1420del
GGCGGCGGC/-
p.G471_G473del
0.898
17
3
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000374690.9
COSV65963320
17
3
ENST00000374690.9
COSV65963320
ARHGAP26
chr5
143222445
143222445
A
C
c.2279A>C
tAa/tCa
p.*760Sext*15
0.062
1
1
Loss of Stop Codon
Loss of Stop Codon
HIGH
ENST00000645722.2
rs1811331649
1
1
ENST00000645722.2
rs1811331649
ARID1A
chr1
26697364
26697364
C
T
c.961C>T
Cag/Tag
p.Q321*
0.981
12
2
Nonsense Mutation
Nonsense Mutation
HIGH
ENST00000324856.13
12
2
ENST00000324856.13
ARID1A
chr1
26779717
26779717
C
T
c.5819C>T
cCa/cTa
p.P1940L
0.475
12
2
Missense Variant
Missense Variant
MODERATE
ENST00000324856.13
COSV61376744
0.000004220440
rs773088565
12
2
ENST00000324856.13
COSV61376744
rs773088565
ATRX
chrX
77682471
77682471
C
G
c.2785G>C
Gag/Cag
p.E929Q
0.949
20
20
Missense Variant
Missense Variant
MODERATE
ENST00000373344.10
Benign
rs3088074
20
20
ENST00000373344.10
Benign
rs3088074
AXIN2
chr17
65536947
65536947
C
T
c.1829G>A
cGg/cAg
p.R610Q
0.306
8
2
Missense Variant
Missense Variant
MODERATE
ENST00000307078.10
Uncertain_significance
COSV61058100
0.000050762700
rs376248072
8
2
ENST00000307078.10
Uncertain_significance
COSV61058100
rs376248072
BAZ1A
chr14
34773613
34773613
C
G
c.3111G>C
gaG/gaC
p.E1037D
0.798
1
1
Missense Variant
Missense Variant
MODERATE
ENST00000360310.6
1
1
ENST00000360310.6
BCR
chr22
23181025
23181025
G
T
c.65G>T
cGc/cTc
p.R22L
0.657
7
2
Missense Variant
Missense Variant
MODERATE
ENST00000305877.13
COSV99045372
0.000041740700
rs376532812
7
2
ENST00000305877.13
COSV99045372
rs376532812
BIRC3
chr11
102331127
102331127
C
G
c.1210C>G
Cta/Gta
p.L404V
0.45
2
2
Missense Variant
Missense Variant
MODERATE
ENST00000263464.9
2
2
ENST00000263464.9
CBLC
chr19
44793589
44793589
A
AC
c.1255dup
gac/gaCc
p.Q419Pfs*81
0.326
3
3
Frameshift Mutation
Frameshift Mutation
HIGH
ENST00000647358.2
COSV54322503
3
3
ENST00000647358.2
COSV54322503
CDH11
chr16
64988331
64988331
C
T
c.825G>A
atG/atA
p.M275I
0.687
2
1
Missense Variant
Missense Variant
MODERATE
ENST00000268603.9
Benign
COSV51754932
0.196252000000
rs1130821
2
1
ENST00000268603.9
Benign
COSV51754932
rs1130821
CIITA
chr16
10909070
10909070
A
G
c.2702A>G
cAg/cGg
p.Q901R
0.982
24
24
Missense Variant
Missense Variant
MODERATE
ENST00000618327.4
Benign
0.983235000000
rs7197779
24
24
ENST00000618327.4
Benign
rs7197779
CLTCL1
chr22
19253972
19253972
C
T
c.506G>A
gGc/gAc
p.G169D
0.326
2
2
Missense Variant
Missense Variant
MODERATE
ENST00000427926.6
COSV54241275
0.000146219000
rs564477345
2
2
ENST00000427926.6
COSV54241275
rs564477345
CREB3L2
chr7
137928167
137928170
CTGG
C
c.299_301del
aCCAgt/agt
p.T100del
0.258
10
10
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000330387.11
COSV57791862
rs3217268
10
10
ENST00000330387.11
COSV57791862
rs3217268
Total mutations showing: 59
F
P
1
2
3
4
N
E
Rows Per Page
10
15
25
50
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CNV
Histology Information for Model: BCM-PDAC-19
There are no histology images for this model.
Metastasis Information for Model: BCM-PDAC-19
Patient
PDX
Liver
Local recurrence
Lung
Rectum
lymph node
Patient Treatment Information for Model: BCM-PDAC-19
Event Id
Treatment
Treatment Setting
Age at Start
Age at End
Duration
Clinical Response
Pathologic Response
Reason Stopped
10
Gemcitabine
Adjuvant
72.2
1Unknown
Not Reported
Not Reported
Not Reported
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