Colon Cancer: Gene >> HEY2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368364
Start	125759206:125759206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs3734638
CDS Mutation	c.418G>A
AA Mutation	p.Val140Met(p.V140M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368364
Start	125759242:125759242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Trp(p.R152W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368364
Start	125759278:125759278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Trp(p.R164W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368364
Start	125759128:125759128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340G>A
AA Mutation	p.Ala114Thr(p.A114T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368364
Start	125759583:125759583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368364
Start	125759664:125759664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146693390
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368364
Start	125759346:125759346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.558C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000368364
Start	125751835:125751836(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.127_129dupACA
AA Mutation	p.Thr43dup(p.T43dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HEY2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368364
Start	125759257:125759257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.469C>A
AA Mutation	p.Leu157Ile(p.L157I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368364
Start	125759664:125759664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146693390
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript