Colon Cancer: Gene >> FGFR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292408
Start	177096075:177096075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1840G>T
AA Mutation	p.Ala614Ser(p.A614S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292408
Start	177097320:177097320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777207919
CDS Mutation	c.2182G>A
AA Mutation	p.Ala728Thr(p.A728T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292408
Start	177097305:177097305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201490532
CDS Mutation	c.2167C>T
AA Mutation	p.Arg723Cys(p.R723C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292408
Start	177093661:177093661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1405C>T
AA Mutation	p.Leu469Phe(p.L469F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292408
Start	177092377:177092377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148292303
CDS Mutation	c.784G>A
AA Mutation	p.Val262Met(p.V262M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292408
Start	177093758:177093758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1502C>T
AA Mutation	p.Ala501Val(p.A501V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292408
Start	177093735:177093735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1479G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292408
Start	177092418:177092418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11954456
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292408
Start	177091720:177091720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292408
Start	177090622:177090622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781632034
CDS Mutation	c.324C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292408
Start	177089659:177089659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.57C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292408
Start	177096644:177096644(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2060delG
AA Mutation	p.Gly687AlafsTer35(p.G687Afs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292408
Start	177096729:177096730(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2147dupC
AA Mutation	p.Glu717ArgfsTer8(p.E717Rfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FGFR4

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000292408
Start	177091103:177091103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147846257
CDS Mutation	c.602G>A
AA Mutation	p.Arg201Gln(p.R201Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript