Colon Cancer: Gene >> VSX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261980
Start	74239640:74239640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79G>A
AA Mutation	p.Ala27Thr(p.A27T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261980
Start	74260670:74260670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837G>T
AA Mutation	p.Lys279Asn(p.K279N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261980
Start	74259683:74259683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.661C>T
AA Mutation	p.Leu221Phe(p.L221F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261980
Start	74239649:74239649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88A>G
AA Mutation	p.Thr30Ala(p.T30A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261980
Start	74259683:74259683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.661C>A
AA Mutation	p.Leu221Ile(p.L221I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261980
Start	74260609:74260609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751455710
CDS Mutation	c.776C>T
AA Mutation	p.Ser259Leu(p.S259L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261980
Start	74245232:74245232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777493485
CDS Mutation	c.523G>A
AA Mutation	p.Val175Ile(p.V175I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261980
Start	74259682:74259682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.660G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261980
Start	74239639:74239639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261980
Start	74260754:74260754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768286032
CDS Mutation	c.921G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261980
Start	74260610:74260610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371707151
CDS Mutation	c.777G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261980
Start	74239627:74239627(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.71delG
AA Mutation	p.Gly24AlafsTer17(p.G24Afs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> VSX2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261980
Start	74260838:74260838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1005G>A
Mutation Classification	Silent
Feature Type	Transcript