Colon Cancer: Gene >> FKBP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000001008
Start	2800044:2800044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768G>T
AA Mutation	p.Lys256Asn(p.K256N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000001008
Start	2803221:2803221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766636474
CDS Mutation	c.1343C>T
AA Mutation	p.Thr448Met(p.T448M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000001008
Start	2800102:2800102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372836178
CDS Mutation	c.826C>T
AA Mutation	p.Arg276Trp(p.R276W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000001008
Start	2799202:2799202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766142249
CDS Mutation	c.629G>A
AA Mutation	p.Arg210His(p.R210H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000001008
Start	2798756:2798756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000001008
Start	2797859:2797859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370885732
CDS Mutation	c.381G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000001008
Start	2801213:2801213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1129C>T
AA Mutation	p.Gln377Ter(p.Q377*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FKBP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000001008
Start	2801286:2801286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199923813
CDS Mutation	c.1202G>A
AA Mutation	p.Arg401Gln(p.R401Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000001008
Start	2799090:2799090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517G>A
AA Mutation	p.Ala173Thr(p.A173T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript