Colon Cancer: Gene >> EXOC7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335146
Start	76089251:76089251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1124C>T
AA Mutation	p.Ala375Val(p.A375V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335146
Start	76091166:76091166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878G>A
AA Mutation	p.Gly293Asp(p.G293D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335146
Start	76089227:76089227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1148C>T
AA Mutation	p.Ala383Val(p.A383V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335146
Start	76088556:76088556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1360G>A
AA Mutation	p.Ala454Thr(p.A454T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335146
Start	76091204:76091204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.840A>C
AA Mutation	p.Lys280Asn(p.K280N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335146
Start	76101749:76101749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.241C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335146
Start	76087673:76087673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530110887
CDS Mutation	c.1563C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335146
Start	76088108:76088108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1467G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335146
Start	76103394:76103394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.93C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EXOC7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335146
Start	76089189:76089189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372862629
CDS Mutation	c.1186G>A
AA Mutation	p.Asp396Asn(p.D396N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript