Colon Cancer: Gene >> CHGA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216492
Start	92931336:92931336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150244309
CDS Mutation	c.442G>A
AA Mutation	p.Gly148Arg(p.G148R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216492
Start	92932553:92932553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552215557
CDS Mutation	c.992G>A
AA Mutation	p.Arg331Gln(p.R331Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216492
Start	92926635:92926635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147517274
CDS Mutation	c.124G>A
AA Mutation	p.Asp42Asn(p.D42N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000216492
Start	92929719:92929719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200937569
CDS Mutation	c.259G>A
AA Mutation	p.Ala87Thr(p.A87T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216492
Start	92931581:92931581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.687G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216492
Start	92932377:92932377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772213323
CDS Mutation	c.816G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000216492
Start	92931684:92931684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790G>T
AA Mutation	p.Glu264Ter(p.E264*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000216492
Start	92931578:92931579(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs371452136
CDS Mutation	c.707_709dupAGG
AA Mutation	p.Glu236dup(p.E236dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CHGA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216492
Start	92931699:92931699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780810744
CDS Mutation	c.805G>A
AA Mutation	p.Glu269Lys(p.E269K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216492
Start	92927574:92927574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212G>T
AA Mutation	p.Arg71Ile(p.R71I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216492
Start	92931292:92931292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398G>T
AA Mutation	p.Arg133Ile(p.R133I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript