Colon Cancer: Gene >> RHPN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254260
Start	33002953:33002953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749216712
CDS Mutation	c.808G>A
AA Mutation	p.Asp270Asn(p.D270N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254260
Start	32980181:32980181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753102976
CDS Mutation	c.1876G>A
AA Mutation	p.Asp626Asn(p.D626N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254260
Start	32991867:32991867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753950362
CDS Mutation	c.1600G>A
AA Mutation	p.Ala534Thr(p.A534T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254260
Start	32990605:32990605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752356242
CDS Mutation	c.1709C>T
AA Mutation	p.Thr570Met(p.T570M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254260
Start	32990638:32990638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1676T>C
AA Mutation	p.Val559Ala(p.V559A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254260
Start	32996173:32996173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761330344
CDS Mutation	c.1273C>T
AA Mutation	p.Arg425Trp(p.R425W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254260
Start	32999595:32999595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1216C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254260
Start	33011691:33011691(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.581delT
AA Mutation	p.Leu194ProfsTer53(p.L194Pfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RHPN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254260
Start	32996044:32996044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148084786
CDS Mutation	c.1402G>A
AA Mutation	p.Asp468Asn(p.D468N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254260
Start	32996042:32996042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766920434
CDS Mutation	c.1404C>T
Mutation Classification	Silent
Feature Type	Transcript