Colon Cancer: Gene >> DMP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87662874:87662874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096G>T
AA Mutation	p.Asp366Tyr(p.D366Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87662593:87662593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145237146
CDS Mutation	c.815G>A
AA Mutation	p.Arg272His(p.R272H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87662833:87662833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1055G>T
AA Mutation	p.Ser352Ile(p.S352I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87662481:87662481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703G>A
AA Mutation	p.Ala235Thr(p.A235T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87662085:87662085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307G>T
AA Mutation	p.Asp103Tyr(p.D103Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87662403:87662403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777148348
CDS Mutation	c.625G>A
AA Mutation	p.Glu209Lys(p.E209K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87662523:87662523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745G>A
AA Mutation	p.Ala249Thr(p.A249T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87663008:87663008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1230G>T
AA Mutation	p.Glu410Asp(p.E410D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87663047:87663047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1269G>T
AA Mutation	p.Glu423Asp(p.E423D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87662931:87662931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781781034
CDS Mutation	c.1153G>A
AA Mutation	p.Glu385Lys(p.E385K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339673
Start	87659469:87659469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000339673
Start	87662070:87662070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292G>T
AA Mutation	p.Gly98Ter(p.G98*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000339673
Start	87662818:87662818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040C>A
AA Mutation	p.Ser347Ter(p.S347*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DMP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87662883:87662883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540873212
CDS Mutation	c.1105G>A
AA Mutation	p.Asp369Asn(p.D369N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87663135:87663135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1357G>A
AA Mutation	p.Asp453Asn(p.D453N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339673
Start	87662202:87662202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201761802
CDS Mutation	c.424G>T
AA Mutation	p.Asp142Tyr(p.D142Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339673
Start	87663311:87663311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534492304
CDS Mutation	c.1533C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339673
Start	87662759:87662759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.981G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339673
Start	87662523:87662524(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.745_746insAACAACAT
AA Mutation	p.Ala249GlufsTer88(p.A249Efs*88)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript