Colon Cancer: Gene >> GHDC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301671
Start	42193569:42193569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13C>T
AA Mutation	p.Pro5Ser(p.P5S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000301671
Start	42192907:42192907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200346068
CDS Mutation	c.386A>G
AA Mutation	p.Gln129Arg(p.Q129R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301671
Start	42192408:42192408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149036800
CDS Mutation	c.722G>A
AA Mutation	p.Arg241Gln(p.R241Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301671
Start	42192963:42192963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301671
Start	42192909:42192909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301671
Start	42193497:42193497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000301671
Start	42190881:42190881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105C>T
AA Mutation	p.Arg369Ter(p.R369*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301671
Start	42193019:42193020(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.273_274insCTAGATT
AA Mutation	p.Thr92LeufsTer94(p.T92Lfs*94)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GHDC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301671
Start	42192625:42192625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505A>G
AA Mutation	p.Asn169Asp(p.N169D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301671
Start	42192517:42192517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148046976
CDS Mutation	c.613G>A
AA Mutation	p.Glu205Lys(p.E205K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript