Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> INMT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000013222
Start	30753808:30753808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232T>C
AA Mutation	p.Phe78Leu(p.F78L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000013222
Start	30755507:30755507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.448G>C
AA Mutation	p.Ala150Pro(p.A150P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000013222
Start	30753868:30753868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292C>A
AA Mutation	p.Leu98Met(p.L98M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000013222
Start	30755540:30755540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481C>T
AA Mutation	p.Leu161Phe(p.L161F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000013222
Start	30753750:30753750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199553396
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> INMT

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000013222
Start	30753807:30753807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000013222
Start	30753753:30753753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.177G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000013222
Start	30753882:30753882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147050778
CDS Mutation	c.306G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000013222
Start	30753865:30753865(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.289delT
AA Mutation	p.Trp97GlyfsTer2(p.W97Gfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript