Colon Cancer: Gene >> HFE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357618
Start	26091359:26091359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.386A>G
AA Mutation	p.Asp129Gly(p.D129G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357618
Start	26091081:26091081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317T>G
AA Mutation	p.Met106Arg(p.M106R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357618
Start	26090921:26090921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28934889
CDS Mutation	c.157G>A
AA Mutation	p.Val53Met(p.V53M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357618
Start	26092752:26092752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684G>T
AA Mutation	p.Leu228Phe(p.L228F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357618
Start	26092767:26092767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699G>T
AA Mutation	p.Gln233His(p.Q233H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HFE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357618
Start	26090976:26090976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776741897
CDS Mutation	c.212G>A
AA Mutation	p.Arg71Gln(p.R71Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357618
Start	26090855:26090855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.91C>G
AA Mutation	p.His31Asp(p.H31D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript