Colon Cancer: Gene >> FGF23

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000237837
Start	4370365:4370365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200445443
CDS Mutation	c.734G>A
AA Mutation	p.Arg245His(p.R245H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000237837
Start	4372695:4372695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214G>T
AA Mutation	p.Ala72Ser(p.A72S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000237837
Start	4370572:4370572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104894347
CDS Mutation	c.527G>A
AA Mutation	p.Arg176Gln(p.R176Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000237837
Start	4370743:4370743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356C>T
AA Mutation	p.Thr119Met(p.T119M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000237837
Start	4379464:4379464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.119T>C
AA Mutation	p.Ile40Thr(p.I40T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237837
Start	4379424:4379424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237837
Start	4370775:4370775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201114020
CDS Mutation	c.324C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000237837
Start	4370513:4370513(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.586delC
AA Mutation	p.Arg196GlyfsTer4(p.R196Gfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000237837
Start	4370412:4370413(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.686dupG
AA Mutation	p.Gly230ArgfsTer32(p.G230Rfs*32)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FGF23

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000237837
Start	4370558:4370558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541G>A
AA Mutation	p.Ala181Thr(p.A181T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000237837
Start	4370707:4370707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.392A>C
AA Mutation	p.Gln131Pro(p.Q131P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237837
Start	4370460:4370460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756683570
CDS Mutation	c.639C>T
Mutation Classification	Silent
Feature Type	Transcript