Colon Cancer: Gene >> DPPA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000478945
Start	109309277:109309277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.235A>G
AA Mutation	p.Lys79Glu(p.K79E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000478945
Start	109312596:109312596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757394035
CDS Mutation	c.130G>A
AA Mutation	p.Val44Ile(p.V44I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000478945
Start	109308280:109308280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.410T>C
AA Mutation	p.Met137Thr(p.M137T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000478945
Start	109304668:109304668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199811743
CDS Mutation	c.661G>A
AA Mutation	p.Val221Ile(p.V221I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000478945
Start	109312545:109312545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181G>T
AA Mutation	p.Gly61Cys(p.G61C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000478945
Start	109312687:109312687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39C>A
AA Mutation	p.Phe13Leu(p.F13L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000478945
Start	109314557:109314557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.-13-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000478945
Start	109314557:109314557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.-13-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DPPA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000478945
Start	109304520:109304520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809C>T
AA Mutation	p.Ser270Phe(p.S270F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000478945
Start	109312687:109312687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39C>A
AA Mutation	p.Phe13Leu(p.F13L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript