Colon Cancer: Gene >> GART

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381815
Start	33528898:33528898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763C>A
AA Mutation	p.Leu255Ile(p.L255I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381815
Start	33511357:33511357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372288271
CDS Mutation	c.2209G>A
AA Mutation	p.Ala737Thr(p.A737T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381815
Start	33524976:33524976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767062634
CDS Mutation	c.1091G>A
AA Mutation	p.Gly364Glu(p.G364E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381815
Start	33504187:33504187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2970G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381815
Start	33524930:33524930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1137A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381815
Start	33504214:33504214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2943T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381815
Start	33517421:33517421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375498243
CDS Mutation	c.1890C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381815
Start	33522249:33522249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777303334
CDS Mutation	c.1332C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381815
Start	33509815:33509816(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2419_2420delAA
AA Mutation	p.Lys807GlyfsTer26(p.K807Gfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GART

No Mutation Annotation!