Colon Cancer: Gene >> RAP2B

Mutation ID	1
Mutation Consequence	coding_sequence_variant;3_prime_UTR_variant
Transcription ID	ENST00000323534
Start	153163244:153163266(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.552_*22delAGGCGGCCACCGCGCGCCGGCCG
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323534
Start	153162893:153162893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.200T>C
AA Mutation	p.Met67Thr(p.M67T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323534
Start	153163219:153163219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.526T>C
AA Mutation	p.Cys176Arg(p.C176R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323534
Start	153162912:153162912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323534
Start	153162808:153162809(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.117_118delTT
AA Mutation	p.Phe39LeufsTer6(p.F39Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RAP2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323534
Start	153162783:153162783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90G>T
AA Mutation	p.Glu30Asp(p.E30D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript