Colon Cancer: Gene >> HIC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322941
Start	2056832:2056832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>A
AA Mutation	p.Ala67Thr(p.A67T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322941
Start	2057945:2057945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1312G>A
AA Mutation	p.Val438Met(p.V438M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322941
Start	2058362:2058362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1729C>T
AA Mutation	p.Arg577Cys(p.R577C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322941
Start	2056946:2056946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759366814
CDS Mutation	c.313C>T
AA Mutation	p.Arg105Cys(p.R105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322941
Start	2058324:2058324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1691C>T
AA Mutation	p.Ala564Val(p.A564V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322941
Start	2056774:2056774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322941
Start	2058799:2058799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2166C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HIC1

No Mutation Annotation!