Colon Cancer: Gene >> GH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323322
Start	63917422:63917422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371051668
CDS Mutation	c.541G>A
AA Mutation	p.Ala181Thr(p.A181T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323322
Start	63917884:63917884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781692092
CDS Mutation	c.332C>T
AA Mutation	p.Ser111Leu(p.S111L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323322
Start	63917347:63917347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616G>A
AA Mutation	p.Val206Met(p.V206M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323322
Start	63917448:63917448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515T>G
AA Mutation	p.Phe172Cys(p.F172C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323322
Start	63917376:63917376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587T>C
AA Mutation	p.Met196Thr(p.M196T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000323322
Start	63917467:63917467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496A>G
AA Mutation	p.Lys166Glu(p.K166E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323322
Start	63918110:63918110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.198G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323322
Start	63917820:63917820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763501141
CDS Mutation	c.396T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323322
Start	63917829:63917829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370785603
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323322
Start	63917803:63917803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413A>C
AA Mutation	p.Asp138Ala(p.D138A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript