Colon Cancer: Gene >> AGPAT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371696
Start	136677113:136677113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142145391
CDS Mutation	c.340C>T
AA Mutation	p.Arg114Cys(p.R114C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371696
Start	136677112:136677112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746314526
CDS Mutation	c.341G>A
AA Mutation	p.Arg114His(p.R114H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371696
Start	136677440:136677440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764260414
CDS Mutation	c.299G>A
AA Mutation	p.Ser100Asn(p.S100N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371696
Start	136676645:136676645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576185386
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371696
Start	136676612:136676612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756686507
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AGPAT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371696
Start	136677070:136677070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.383C>A
AA Mutation	p.Pro128His(p.P128H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript