Colon Cancer: Gene >> FKBP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357266
Start	35620179:35620179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346G>A
AA Mutation	p.Ala116Thr(p.A116T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357266
Start	35637126:35637126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138645077
CDS Mutation	c.138G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357266
Start	35580135:35580135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764691592
CDS Mutation	c.927G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357266
Start	35591136:35591136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148575731
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357266
Start	35642733:35642734(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781180464
CDS Mutation	c.91_92delAG
AA Mutation	p.Arg31GlyfsTer13(p.R31Gfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000357266
Start	35587111:35587111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763G>T
AA Mutation	p.Glu255Ter(p.E255*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FKBP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357266
Start	35620159:35620159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366T>G
AA Mutation	p.Ile122Met(p.I122M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357266
Start	35591191:35591191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.695A>C
AA Mutation	p.Lys232Thr(p.K232T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript