Colon Cancer: Gene >> ARSH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381130
Start	3015123:3015123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.494T>C
AA Mutation	p.Ile165Thr(p.I165T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381130
Start	3029291:3029291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760186999
CDS Mutation	c.1244C>T
AA Mutation	p.Ala415Val(p.A415V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381130
Start	3027453:3027453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145391454
CDS Mutation	c.1177G>A
AA Mutation	p.Gly393Arg(p.G393R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381130
Start	3010085:3010085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758874207
CDS Mutation	c.148G>A
AA Mutation	p.Ala50Thr(p.A50T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381130
Start	3018542:3018542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773G>A
AA Mutation	p.Arg258Lys(p.R258K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381130
Start	3018616:3018616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746052942
CDS Mutation	c.847C>T
AA Mutation	p.Arg283Cys(p.R283C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381130
Start	3013117:3013117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.285T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ARSH

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381130
Start	3024115:3024115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143689139
CDS Mutation	c.996C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381130
Start	3027374:3027374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373570475
CDS Mutation	c.1098G>A
Mutation Classification	Silent
Feature Type	Transcript