Colon Cancer: Gene >> FTHL17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359202
Start	31071910:31071910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44C>T
AA Mutation	p.Thr15Ile(p.T15I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359202
Start	31071440:31071440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514G>T
AA Mutation	p.Asp172Tyr(p.D172Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359202
Start	31071755:31071755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199G>A
AA Mutation	p.Ala67Thr(p.A67T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359202
Start	31071723:31071723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FTHL17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359202
Start	31071500:31071500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454T>C
AA Mutation	p.Tyr152His(p.Y152H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359202
Start	31071934:31071934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771095024
CDS Mutation	c.20C>T
AA Mutation	p.Ser7Leu(p.S7L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript