Colon Cancer: Gene >> FGF16

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000439435
Start	77456279:77456279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.381G>T
AA Mutation	p.Lys127Asn(p.K127N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000439435
Start	77456325:77456325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.427T>G
AA Mutation	p.Trp143Gly(p.W143G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439435
Start	77454182:77454182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439435
Start	77456409:77456409(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.514delC
AA Mutation	p.Arg172GlyfsTer20(p.R172Gfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439435
Start	77456453:77456454(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.560dupT
AA Mutation	p.Leu187PhefsTer9(p.L187Ffs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FGF16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439435
Start	77456476:77456476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578C>T
AA Mutation	p.Pro193Leu(p.P193L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript