Colon Cancer: Gene >> DPH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263083
Start	2036922:2036922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769281060
CDS Mutation	c.661T>C
AA Mutation	p.Ser221Pro(p.S221P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263083
Start	2033507:2033507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753008362
CDS Mutation	c.79C>T
AA Mutation	p.Arg27Trp(p.R27W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263083
Start	2039816:2039816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371816907
CDS Mutation	c.757G>A
AA Mutation	p.Ala253Thr(p.A253T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263083
Start	2039771:2039771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712C>A
AA Mutation	p.Arg238Ser(p.R238S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263083
Start	2036569:2036569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263083
Start	2035976:2035976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573260759
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DPH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263083
Start	2040518:2040518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764906514
CDS Mutation	c.935G>A
AA Mutation	p.Arg312Gln(p.R312Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263083
Start	2039816:2039816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371816907
CDS Mutation	c.757G>A
AA Mutation	p.Ala253Thr(p.A253T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript