Colon Cancer: Gene >> HAS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306560
Start	69114593:69114593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773346129
CDS Mutation	c.989G>A
AA Mutation	p.Arg330Gln(p.R330Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306560
Start	69109543:69109543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148G>A
AA Mutation	p.Ala50Thr(p.A50T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306560
Start	69114685:69114685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1081T>C
AA Mutation	p.Tyr361His(p.Y361H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306560
Start	69114819:69114819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1215C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306560
Start	69113446:69113446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306560
Start	69115098:69115098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1494A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HAS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306560
Start	69110026:69110026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631A>G
AA Mutation	p.Ile211Val(p.I211V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript