Colon Cancer: Gene >> CD177

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618265
Start	43361466:43361466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757644378
CDS Mutation	c.968G>A
AA Mutation	p.Arg323Gln(p.R323Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618265
Start	43361155:43361155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773C>A
AA Mutation	p.Thr258Asn(p.T258N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000618265
Start	43354387:43354387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771651317
CDS Mutation	c.374C>T
AA Mutation	p.Pro125Leu(p.P125L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618265
Start	43354280:43354280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000618265
Start	43361514:43361514(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1021delC
AA Mutation	p.Arg341GlufsTer2(p.R341Efs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CD177

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618265
Start	43362181:43362181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541810499
CDS Mutation	c.1175C>T
AA Mutation	p.Ala392Val(p.A392V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618265
Start	43353940:43353940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140C>T
AA Mutation	p.Thr47Ile(p.T47I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript