Colon Cancer: Gene >> REG1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233735
Start	79121628:79121628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777579151
CDS Mutation	c.131G>A
AA Mutation	p.Arg44His(p.R44H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233735
Start	79122916:79122916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397A>G
AA Mutation	p.Asn133Asp(p.N133D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233735
Start	79122931:79122931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412G>A
AA Mutation	p.Val138Met(p.V138M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233735
Start	79122848:79122848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200685695
CDS Mutation	c.329G>A
AA Mutation	p.Arg110His(p.R110H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233735
Start	79122878:79122878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359C>T
AA Mutation	p.Ser120Phe(p.S120F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000233735
Start	79123166:79123166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452A>G
AA Mutation	p.Asp151Gly(p.D151G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> REG1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233735
Start	79122010:79122010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200969301
CDS Mutation	c.206C>T
AA Mutation	p.Ser69Leu(p.S69L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233735
Start	79122106:79122106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302G>A
AA Mutation	p.Gly101Asp(p.G101D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript